Co-reporter:Yanhui Wei;Xianqing Lin;Cong Wei;Wei Zhang;Yongli Yan;Yong Sheng Zhao
ACS Nano January 24, 2017 Volume 11(Issue 1) pp:597-602
Publication Date(Web):December 13, 2016
DOI:10.1021/acsnano.6b06772
Microlasers with good biocompatibility are of great significance to the detection of tiny changes in biological systems. Most current biolasers were realized through the introduction of biomaterials into various external resonators, resulting in an increase of difficulties in application. Here, we used starch as the host to build dye@starch microlasers by encapsulating guest organic laser dye into the interhelical structure of starch granules. The as-prepared dye@starch system with high transparency and ultrasmooth spherical surface functions as an efficient whispering gallery mode resonator for low threshold lasing. The obtained laser signal is closely related to the structural transformation of the starch matrix. Our results would provide a deep insight into the relationship between biostructure and lasing properties, facilitating the monitoring of the structural variances in biological processes through lasing signals.Keywords: bio-nanophotonics; biological composite material; organic laser; organic nanophotonic material; starch laser;
Co-reporter:Haiyun Dong;Chunhuan Zhang;Zhonghao Zhou;Xianqing Lin;Jiannian Yao;Yong Sheng Zhao
Nano Letters January 11, 2017 Volume 17(Issue 1) pp:91-96
Publication Date(Web):December 5, 2016
DOI:10.1021/acs.nanolett.6b03499
Wavelength switchable micro/nanoscale laser is essential to construct various ultracompact photonic devices. However, traditional semiconductors as the gain media generally provide only monochromatic laser output due to their continuous energy band structures. For luminescent conjugated molecules, the broad emission band usually contains a series of vibronic peaks, which is very helpful for extending the lasing spectrum to several different wavelengths. Here we propose a novel strategy to realize wavelength switchable lasers based on the controlled competition of dual-wavelength vibronic lasing in single-component organic microcrystals. The vibrationally structured fluorescence property of the single-crystal organic microdisks brings dual-wavelength lasing at different vibronic bands. Their relative optical gain intensity was modulated by controlling the population on the certain vibronic level of the ground state with varied temperature, which consequently enabled the reversible switching of the dual-wavelength vibronic lasing. The results point out a promising route to the rational design of miniaturized lasers and other photonic elements with desired performances.Keywords: laser switch; nanophotonic material; organic microlaser; Organic nanomaterial; WGM laser;
Co-reporter:Yuanchao Lv, Yong Jun Li, Jing Li, Yongli Yan, Jiannian Yao, and Yong Sheng Zhao
Journal of the American Chemical Society August 23, 2017 Volume 139(Issue 33) pp:11329-11329
Publication Date(Web):August 10, 2017
DOI:10.1021/jacs.7b06174
All-color subwavelength output of lasers was demonstrated in a rationally designed organic microdisk/silver nanowire heterostructures. The dye-doped flexible microdisks served as the wavelength tunable whispering-gallery-mode lasers with low lasing thresholds, whereas the silver nanowires supported the output of the lasing mode as subwavelength coherent light sources. The wavelength of the outcoupled laser was tuned over the full visible spectrum scope owing to the flexibility of the microdisks and their compatibility with various organic laser dyes. Furthermore, a multicolor subwavelength laser was achieved in a single heterostructure and the laser output was successfully modulated by varying the surface plasmon polariton propagation length.
Co-reporter:Xiaogang Yang;Xianqing Lin;Yibing Zhao; Yong Sheng Zhao; Dongpeng Yan
Angewandte Chemie 2017 Volume 129(Issue 27) pp:7961-7965
Publication Date(Web):2017/06/26
DOI:10.1002/ange.201703917
AbstractLanthanide metal–organic frameworks (Ln-MOFs) have received much attention owing to their structural tunability and widely photofunctional applications. However, successful examples of Ln-MOFs with well-defined photonic performances at micro-/nanometer size are still quite limited. Herein, self-assemblies of 1,3,5-benzenetricarboxylic acid (BTC) and lanthanide ions afford isostructural crystalline Ln-MOFs. Tb-BTC, Eu@Tb-BTC, and Eu-BTC have 1D microrod morphologies, high photoluminescence (PL) quantum yields, and different emission colors (green, orange, and red). Spatially PL resolved spectra confirm that Ln-MOF microrods exhibit an optical waveguide effect with low waveguide loss coefficient (0.012≈0.033 dB μm−1) during propagation. Furthermore, these microrods feature both linear and chiral polarized photoemission with high anisotropy.
Co-reporter:Xiaogang Yang;Xianqing Lin;Yibing Zhao; Yong Sheng Zhao; Dongpeng Yan
Angewandte Chemie International Edition 2017 Volume 56(Issue 27) pp:7853-7857
Publication Date(Web):2017/06/26
DOI:10.1002/anie.201703917
AbstractLanthanide metal–organic frameworks (Ln-MOFs) have received much attention owing to their structural tunability and widely photofunctional applications. However, successful examples of Ln-MOFs with well-defined photonic performances at micro-/nanometer size are still quite limited. Herein, self-assemblies of 1,3,5-benzenetricarboxylic acid (BTC) and lanthanide ions afford isostructural crystalline Ln-MOFs. Tb-BTC, Eu@Tb-BTC, and Eu-BTC have 1D microrod morphologies, high photoluminescence (PL) quantum yields, and different emission colors (green, orange, and red). Spatially PL resolved spectra confirm that Ln-MOF microrods exhibit an optical waveguide effect with low waveguide loss coefficient (0.012≈0.033 dB μm−1) during propagation. Furthermore, these microrods feature both linear and chiral polarized photoemission with high anisotropy.
Co-reporter:Miaomiao Gao;Cong Wei;Xianqing Lin;Yuan Liu;Fengqin Hu;Yong Sheng Zhao
Chemical Communications 2017 vol. 53(Issue 21) pp:3102-3105
Publication Date(Web):2017/03/09
DOI:10.1039/C6CC08094D
We demonstrate the fabrication of organic high Q active whispering-gallery-mode (WGM) resonators from π-conjugated polymer by a controlled emulsion-solvent-evaporation method, which can simultaneously provide optical gain and act as an effective resonant cavity. By measuring the shift of their lasing modes on exposure to organic vapor, we successfully monitored the slight concentration variation in the chemical gas. These microlaser sensors demonstrated high detection sensitivity and good signal repeatability under continuous chemical gas treatments. The results offer an effective strategy to design miniaturized optical sensors.
Co-reporter:Haiyun Dong;Chunhuan Zhang;Yong Sheng Zhao
Journal of Materials Chemistry C 2017 vol. 5(Issue 23) pp:5600-5609
Publication Date(Web):2017/06/15
DOI:10.1039/C6TC05474A
Organic microlasers are miniaturized coherent light sources with great promise for advancing the field of optoelectronics. Recently, host–guest composite organic microlasers, where the host materials provide spatial confinement for the organic gain materials, have captured much research interest because the host–guest composite material systems endow the organic microlasers with improved lasing performances, such as low threshold, high stability, and excellent tunability. In this Review, we explore the latest advancements in the development of host–guest composite organic microlasers, and offer our perspective on future improvements and trends. Special emphasis is put on the construction strategies and the unique laser properties of the organic microlasers based on host–guest confinement systems. The comprehensive understanding of the relationship between laser performances and the synergistic interactions of the host and guest materials would provide a useful guidance for the design and fabrication of novel organic microlasers.
Co-reporter:Jianmin Gu, Zhenpan Bian, Baipeng Yin, Cuihong Jin, ... Yong Sheng Zhao
Science Bulletin 2017 Volume 62, Issue 18(Volume 62, Issue 18) pp:
Publication Date(Web):30 September 2017
DOI:10.1016/j.scib.2017.09.002
Rare earth doping has been widely applied in many functional nanomaterials with desirable properties and functions, which would have a significant effect on the growth process of the materials. However, the controlling strategy is limited into high concentration of lanthanide doping, which produces concentration quenching of the lanthanide ion luminescence with an increase in the Ln3+ concentration, resulting in lowering the fluorescence quantum yield of lanthanide ion. Herein, for the first time, we demonstrate simultaneous control of the structures and luminescence properties of BaCO3 nanocrystals via a small amount of Tb3+ doping strategy. In fact, Tb3+ would partially occupy Ba2+ sites, resulting in the changes to the structures of the BaCO3 nanocrystals, which is primarily determined by charge modulation, including the contributions from the surfaces of crystal nuclei and building blocks. These structurally modified nanocrystals exhibit tunable luminescence properties, thus emerging as potential candidates for photonic devices such as light-emitting diodes and color displays.We demonstrate that small amount of Tb3+ doping, mainly occupied Ba2+ sites in BaCO3 lattice, can give simultaneous control over the structures and luminescence properties of the nanocrystals, which could primarily arise from the charge modulation on the surfaces of crystal nuclei and self-assembly building blocks.Download high-res image (90KB)Download full-size image
Co-reporter:Qing Li;Caihong Kang;Kunjie Li;Aibing Chen;Wei Zhang
Science China Chemistry 2017 Volume 60( Issue 5) pp:642-648
Publication Date(Web):07 March 2017
DOI:10.1007/s11426-016-0457-9
In this work, we chose tris(2,2′-bipyridyl)ruthenium(II)hexafluorophosphate (Ru(bpy)3(PF6)2), a metal-organic complex material, to prepare nanowires, which were subsequently applied for the construction of electrochemiluminescence (ECL) biosensor by immobilizing them onto a glassy carbon electrode (GCE) with graphene-Nafion composite films. The graphene therein, being a two-dimensional carbon nanomaterial with outstanding electronic properties, can obviously improve the conductivity of the Nafion film, as well as enhance the electrochemical signal and ECL intensity of the Ru(bpy)3(PF6)2 nanowires (RuNWs) at low graphene concentration. The developed biosensor exhibited excellent ECL stability with tripropylamine (TPrA) as co-reactant. The ECL biosensor exhibited high sensitive ECL response in a wide linear range and low detection limit for the detection of proline. It is considered that the oxidation products of proline would be responsible for the ECL enhancement. The large electro-active area of the nanowires and the enhancement effect of the graphene played critical roles in the high detection performance of the ECL biosensor. The results demonstrated herein may provide a useful enlightenment for the design of more sensitive ECL biosensors.
Co-reporter:Wei Zhang, Jiannian Yao, and Yong Sheng Zhao
Accounts of Chemical Research 2016 Volume 49(Issue 9) pp:1691
Publication Date(Web):August 25, 2016
DOI:10.1021/acs.accounts.6b00209
Micro/nanoscale lasers that can deliver intense coherent light signals at (sub)wavelength scale have recently captured broad research interest because of their potential applications ranging from on-chip information processing to high-throughput sensing. Organic molecular materials are a promising kind of ideal platform to construct high-performance microlasers, mainly because of their superiority in abundant excited-state processes with large active cross sections for high gain emissions and flexibly assembled structures for high-quality microcavities. In recent years, ever-increasing efforts have been dedicated to developing such organic microlasers toward low threshold, multicolor output, broadband tunability, and easy integration. Therefore, it is increasingly important to summarize this research field and give deep insight into the structure–property relationships of organic microlasers to accelerate the future development.In this Account, we will review the recent advances in organic miniaturized lasers, with an emphasis on tunable laser performances based on the tailorable microcavity structures and controlled excited-state gain processes of organic materials toward integrated photonic applications. Organic π-conjugated molecules with weak intermolecular interactions readily assemble into regular nanostructures that can serve as high-quality optical microcavities for the strong confinement of photons. On the basis of rational material design, a series of optical microcavities with different structures have been controllably synthesized. These microcavity nanostructures can be endowed with effective four-level dynamic gain processes, such as excited-state intramolecular charge transfer, excited-state intramolecular proton transfer, and excimer processes, that exhibit large dipole optical transitions for strongly active gain behaviors. By tailoring these excited-state processes with molecular/crystal engineering and external stimuli, people have effectively modulated the performances of organic micro/nanolasers. Furthermore, by means of controlled assembly and tunable laser performances, efficient outcoupling of microlasers has been successfully achieved in various organic hybrid microstructures, showing considerable potential for the integrated photonic applications.This Account starts by presenting an overview of the research evolution of organic microlasers in terms of microcavity resonators and energy-level gain. Then a series of strategies to tailor the microcavity structures and excited-state dynamics of organic nanomaterials for the modulation of lasing performances are highlighted. In the following part, we introduce the construction and advanced photonic functionalities of organic-microlaser-based hybrid structures and their applications in integrated nanophotonics. Finally, we provide our outlook on the current challenges as well as the future development of organic microlasers. It is anticipated that this Account will provide inspiration for the development of miniaturized lasers with desired performances by tailoring of excited-state processes and microcavity structures toward integrated photonic applications.
Co-reporter:Wei Zhang;Lan Peng;Jie Liu;Aiwei Tang;Jin-Song Hu;Jiannian Yao;Yong Sheng Zhao
Advanced Materials 2016 Volume 28( Issue 21) pp:4040-4046
Publication Date(Web):
DOI:10.1002/adma.201505927
Co-reporter:Yong Jun Li;Yongli Yan;Yong Sheng Zhao;Jiannian Yao
Advanced Materials 2016 Volume 28( Issue 6) pp:1319-1326
Publication Date(Web):
DOI:10.1002/adma.201502577
Nanophotonics has received broad research interest because it may provide an alternative opportunity to overcome the fundamental limitations of electronic circuits. So far, diverse photonic functions, such as light generation, modulation, and detection, have been realized based on various nanomaterials. The exact structural features of these material systems, including geometric characteristics, surface morphology, and material composition, play a key role in determining the photonic functions. Therefore, rational designs and constructions of materials on both morphological and componential levels, namely nanoarchitectonics, are indispensable for any photonic device with specific functionalities. Recently, a series of nanowire heterojunctions (NWHJs), which are usually made from two or more kinds of material compositions, were constructed for novel photonic applications based on various interactions between different materials at the junctions, for instance, energy transfer, exciton–plasmon coupling, or photon–plasmon coupling. A summary of these works is necessary to get a more comprehensive understanding of the relationship between photonic functions and architectonics of NWHJs, which will be instructive for designing novel photonic devices towards integrated circuits. Here, photonic function oriented nanoarchitectonics based on recent breakthroughs in nanophotonic devices are discussed, with emphasis on the design mechanisms, fabrication strategies, and excellent performances.
Co-reporter:Yong Jun Li; Yuanchao Lv; Chang-Ling Zou; Wei Zhang; Jiannian Yao;Yong Sheng Zhao
Journal of the American Chemical Society 2016 Volume 138(Issue 7) pp:2122-2125
Publication Date(Web):February 5, 2016
DOI:10.1021/jacs.5b12755
Nanoscale lasers are ideal light-signal sources for integrated photonic devices. Most of the present lasers made of dielectric materials are restricted to being larger than half the wavelength of the optical field. Plasmon lasers made from metallic nanostructures can help to break the diffraction limit, yet they suffer from low optical pump efficiencies and low quality factors. Integrating dielectric lasers with plasmonic waveguides to construct hybrid material systems may circumvent these problems and combine the advantages of the two components. Here we demonstrate the nanoscale output of dielectric lasers via photon–plasmon coupling in rationally designed perovskite/silver heterostructures. The perovskite crystals offer the gain and high-Q cavity for low-threshold laser generation, while the embedded silver nanowires (AgNWs) help to output the lasing modes efficiently in the form of surface plasmons. The output coupling can be modulated by controlling the resonant modes of the two-dimensional perovskite microcavities. The results would pave an alternative avenue to ultrasmall light sources as well as fundamental studies of light–matter interactions.
Co-reporter:Haiyun Dong; Yanhui Wei; Wei Zhang; Cong Wei; Chunhuan Zhang; Jiannian Yao;Yong Sheng Zhao
Journal of the American Chemical Society 2016 Volume 138(Issue 4) pp:1118-1121
Publication Date(Web):January 12, 2016
DOI:10.1021/jacs.5b11525
Wavelength tunable micro/nanolasers are indispensable components for various photonic devices. Here, we report broadband tunable microlasers built by incorporating a highly polarized organic intramolecular charge-transfer (ICT) compound with a supramolecular host. The spatial confinement of the ICT dye generates an optimized energy level system that favors controlled population distribution between the locally excited (LE) state and the twisted intramolecular charge-transfer (TICT) state, which is beneficial for significantly broadening the tailorable gain region. As a result, we realized a wide tuning of lasing wavelength in the organic supramolecular microcrystals based on temperature-controlled population transfer from the LE to TICT state. The results will provide a useful enlightenment for the rational design of miniaturized lasers with desired performances.
Co-reporter:Cong Wei and Yong Sheng Zhao
ACS Applied Materials & Interfaces 2016 Volume 8(Issue 6) pp:3703
Publication Date(Web):November 4, 2015
DOI:10.1021/acsami.5b08086
Metal materials, supporting plasmon modes on their surface, can confine the optical field at deep subwavelength scale, which is desired for photonic integration. However, their intrinsic high Ohmic losses make it impossible to construct the whole circuit solely with the metal materials. Integrating the plasmonic components with dielectric materials may offer a solution to this dilemma. With outstanding active optical performance, these dielectric components not only can greatly reduce the optical losses of the entire circuits but also offer an efficient way to launch the surface plasmon polaritons through the evanescent field coupling or the direct exciton–plasmon conversion. Furthermore, the cooperative interaction between metal and dielectric materials would bring vast novel optical phenomena and functional photonic devices. In this review, the synergistic effects among metal and dielectric materials in various heterostructures as well as their related applications are highlighted. Comprehensive understanding on their synergistic interactions would offer useful guidance for the design and fabrication of the ultracompact novel optical devices.Keywords: diffraction limit; metal-dielectric structures; photon-plasmon coupling; subwavelength photonic devices; surface plasmon polaritons
Co-reporter:Wei Zhang and Yong Sheng Zhao
Chemical Communications 2016 vol. 52(Issue 58) pp:8906-8917
Publication Date(Web):03 Feb 2016
DOI:10.1039/C6CC00018E
Nanophotonics have recently captured broad attention because of their great potential in information processing and communication, which may allow rates and bandwidth beyond what is feasible in the realm of electronics. Organic materials could be well suitable for such applications due to their ability to generate, transmit, modulate and detect light in their lightweight and flexible nanoarchitectures. Their distinct nanophotonic properties strongly depend on their extrinsic morphologies and intrinsic molecular excited-state processes. In this feature article, we mainly focus on a comprehensive understanding of the relationship between molecular excited-state processes and the advanced photonic functionalities of organic micro/nano-crystals in recent organic nanophotonic research, and then expect to provide enlightenment for the design and development of tiny photonic devices with broadband tunable properties by tailoring the excited-state processes of organic microcrystals.
Co-reporter:Cong Wei;Miaomiao Gao;Fengqin Hu;Jiannian Yao;Yong Sheng Zhao
Advanced Optical Materials 2016 Volume 4( Issue 7) pp:1009-1014
Publication Date(Web):
DOI:10.1002/adom.201600048
Co-reporter:Jian Zhang, Yanlin Lv, Wei Zhang, Hui Ding, Rongji Liu, Yongsheng Zhao, Guangjin Zhang, Zhiyuan Tian
Talanta 2016 Volume 146() pp:41-48
Publication Date(Web):1 January 2016
DOI:10.1016/j.talanta.2015.08.025
•Flavone-based highly selective fluorescent probe for Cys/Hcy sensing was developed.•The ability of the probe for micromolar level Cys/Hcy sensing was confirmed.•The practicability of the probe for intracellular Cys/Hcy sensing was validated.A new type of flavone-based fluorescent probe (DMAF) capable of cysteine (Cys)/homocysteine (Hcy) sensing with high selectivity over other amino acids was developed. Such type of probe undergoes Cys/Hcy-mediated cyclization reaction with the involvement of its aldehyde group, which suppresses of the photoinduced electron transfer (PET) process of the probe molecule and consequently leads to the enhancement of fluorescence emission upon excitation using visible light. The formation of product of the Cys/Hcy-mediated cyclization reaction was confirmed and the preliminary fluorescence imaging experiments revealed the biocompatibility of the as-prepared probe and validated its practicability for intracellular Cys/Hcy sensing.A new type of flavone-based fluorescent probe (DMAF) capable of cysteine (Cys)/homocysteine (Hcy) sensing with high selectivity over other amino acids was developed. Such type of probe undergoes Cys/Hcy-mediated cyclization reaction with the involvement of its aldehyde group, which suppresses of the photoinduced electron transfer (PET) process of the probe molecule and consequently leads to the enhancement of fluorescence emission upon excitation using visible light. The formation of product of the Cys/Hcy-mediated cyclization reaction was confirmed and the preliminary fluorescence imaging experiments revealed the biocompatibility of the as-prepared probe and validated its practicability for intracellular Cys/Hcy sensing.
Co-reporter:Yanlin Lv, Peng Liu, Hui Ding, Yishi Wu, Yongli Yan, Heng Liu, Xuefei Wang, Fei Huang, Yongsheng Zhao, and Zhiyuan Tian
ACS Applied Materials & Interfaces 2015 Volume 7(Issue 37) pp:20640
Publication Date(Web):September 4, 2015
DOI:10.1021/acsami.5b05150
Hybrid fluorescent nanoparticles (NPs) capable of fluorescing near-infrared (NIR) light (centered ∼730 nm) upon excitation of 800 nm laser light were constructed. A new type of conjugated polymer with two-photon excited fluorescence (TPEF) feature, P-F8-DPSB, was used as the NIR-light harvesting component and the energy donor while a NIR fluorescent dye, DPA-PR-PDI, was used as the energy acceptor and the NIR-light emitting component for the construction of the fluorescent NPs. The hybrid NPs possess δ value up to 2.3 × 106 GM per particle upon excitation of 800 nm pulse laser. The excellent two-photon absorption (TPA) property of the conjugated polymer component, together with its high fluorescence quantum yield (ϕ) up to 45% and the efficient energy transfer from the conjugated polymer to NIR-emitting fluorophore with efficiency up to 90%, imparted the hybrid NPs with TPEF-based NIR-input-NIR-output fluorescence imaging ability with penetration depth up to 1200 μm. The practicability of the hybrid NPs for fluorescence imaging in Hela cells was validated.Keywords: conjugated polymer; energy transfer; multiphoton fluorescence bioimaging; near-infrared (NIR) fluorescence; two-photon absorption
Co-reporter:Wei Yao;Guangchao Han;Fu Huang;Manman Chu;Qian Peng;Fengqin Hu;Yuanping Yi;Hua Jiang;Jiannian Yao;Yong Sheng Zhao
Advanced Science 2015 Volume 2( Issue 11) pp:
Publication Date(Web):
DOI:10.1002/advs.201500130
Co-reporter:Wei Zhang;Dr. Yongli Yan;Dr. Jianmin Gu; Jiannian Yao ; Yong Sheng Zhao
Angewandte Chemie 2015 Volume 127( Issue 24) pp:7231-7235
Publication Date(Web):
DOI:10.1002/ange.201502684
Abstract
Coherent light signals generated at the nanoscale are crucial to the realization of photonic integrated circuits. Self-assembled nanowires from organic dyes can provide both a gain medium and an effective resonant cavity, which have been utilized for fulfilling miniaturized lasers. Excited-state intramolecular proton transfer (ESIPT), a classical molecular photoisomerization process, can be used to build a typical four-level system, which is more favorable for population inversion. Low-power driven lasing in proton-transfer molecular nanowires with an optimized ESIPT energy-level process has been achieved. With high gain and low loss from the ESIPT, the wires can be applied as effective FP-type resonators, which generated single-mode lasing with a very low threshold. The lasing wavelength can be reversibly switched based on a conformation conversion of the excited keto form in the ESIPT process.
Co-reporter:Wei Zhang;Dr. Yongli Yan;Dr. Jianmin Gu; Jiannian Yao ; Yong Sheng Zhao
Angewandte Chemie International Edition 2015 Volume 54( Issue 24) pp:7125-7129
Publication Date(Web):
DOI:10.1002/anie.201502684
Abstract
Coherent light signals generated at the nanoscale are crucial to the realization of photonic integrated circuits. Self-assembled nanowires from organic dyes can provide both a gain medium and an effective resonant cavity, which have been utilized for fulfilling miniaturized lasers. Excited-state intramolecular proton transfer (ESIPT), a classical molecular photoisomerization process, can be used to build a typical four-level system, which is more favorable for population inversion. Low-power driven lasing in proton-transfer molecular nanowires with an optimized ESIPT energy-level process has been achieved. With high gain and low loss from the ESIPT, the wires can be applied as effective FP-type resonators, which generated single-mode lasing with a very low threshold. The lasing wavelength can be reversibly switched based on a conformation conversion of the excited keto form in the ESIPT process.
Co-reporter:Chuang Zhang;Chang-Ling Zou;Yan Zhao;Chun-Hua Dong;Cong Wei;Hanlin Wang;Yunqi Liu;Guang-Can Guo;Jiannian Yao;Yong Sheng Zhao
Science Advances 2015 Vol 1(8) pp:e1500257
Publication Date(Web):18 Sep 2015
DOI:10.1126/sciadv.1500257
Flexible organic photonic devices for high-performance optical information processing can be produced via ink-jet printing.
Co-reporter:Yongli Yan and Yong Sheng Zhao
Chemical Society Reviews 2014 vol. 43(Issue 13) pp:4325-4340
Publication Date(Web):03 Apr 2014
DOI:10.1039/C4CS00098F
Nanophotonics, which is mainly the study of the behavior of light–matter interaction at the wavelength scale, has developed into one of the most important branches in optics-related disciplines. Utilizing organic functional molecules as the building blocks of nanophotonic materials and devices has great potential due to the multiple advantages, including the molecular designability, good processability, tailorable properties, and so on. Small molecules exhibit a strong tendency to aggregate into low-dimensional structures through an assembly process. The morphologies of the formed products, which are tightly related to the stacking modes of the molecules, can be precisely controlled through the modulation of various intermolecular interactions. The optical properties of organic complex structures, assembled from one or more types of small molecules, show heavy dependence on the composition, distribution, as well as the topological structures, manifesting a strategy to acquire desired photonic properties via rational structural design and/or componential modulation. This tutorial review focuses on the relationship among various molecules, diverse structures and photonic properties, with emphasis on the controllable assembly processes to fabricate low-dimensional structures and assembly strategies to achieve requisite optofunctional properties.
Co-reporter:Chuang Zhang, Yongli Yan, Yong Sheng Zhao, and Jiannian Yao
Accounts of Chemical Research 2014 Volume 47(Issue 12) pp:3448
Publication Date(Web):October 24, 2014
DOI:10.1021/ar500192v
Nanophotonics has recently received broad research interest, since it may provide an alternative opportunity to overcome the fundamental limitations in electronic circuits. Diverse optical materials down to the wavelength scale are required to develop nanophotonic devices, including functional components for light emission, transmission, and detection. During the past decade, the chemists have made their own contributions to this interdisciplinary field, especially from the controlled fabrication of nanophotonic molecules and materials. In this context, organic micro- or nanocrystals have been developed as a very promising kind of building block in the construction of novel units for integrated nanophotonics, mainly due to the great versatility in organic molecular structures and their flexibility for the subsequent processing. Following the pioneering works on organic nanolasers and optical waveguides, the organic nanophotonic materials and devices have attracted increasing interest and developed rapidly during the past few years.In this Account, we review our research on the photonic performance of molecular micro- or nanostructures and the latest breakthroughs toward organic nanophotonic devices. Overall, the versatile features of organic materials are highlighted, because they brings tunable optical properties based on molecular design, size-dependent light confinement in low-dimensional structures, and various device geometries for nanophotonic integration. The molecular diversity enables abundant optical transitions in conjugated π-electron systems, and thus brings specific photonic functions into molecular aggregates. The morphology of these micro- or nanostructures can be further controlled based on the weak intermolecular interactions during molecular assembly process, making the aggregates show photon confinement or light guiding properties as nanophotonic materials. By adoption of some active processes in the composite of two or more materials, such as energy transfer, charge separation, and exciton–plasmon coupling, a series of novel nanophotonic devices could be achieved for light signal manipulation.First, we provide an overview of the research evolution of organic nanophotonics, which arises from attempts to explore the photonic potentials of low-dimensional structures assembled from organic molecules. Then, recent advances in this field are described from the viewpoints of molecules, materials, and devices. Many kinds of optofunctional molecules are designed and synthesized according to the demands in high luminescence yield, nonlinear optical response, and other optical properties. Due to the weak interactions between these molecules, numerous micro- or nanostructures could be prepared via self-assembly or vapor-deposition, bringing the capabilities of light transport and confinement at the wavelength scale. The above advantages provide great possibilities in the fabrication of organic nanophotonic devices, by rationally combining these functional components to manipulate light signals. Finally, we present our views on the current challenges as well as the future development of organic nanophotonic materials and devices. This Account gives a comprehensive understanding of organic nanophotonics, including the design and fabrication of organic micro- or nanocrystals with specific photonic properties and their promising applications in functional nanophotonic components and integrated circuits.
Co-reporter:Qiu Hong Cui;Yong Sheng Zhao;Jiannian Yao
Advanced Materials 2014 Volume 26( Issue 40) pp:6852-6870
Publication Date(Web):
DOI:10.1002/adma.201305913
Organic nanomaterials have drawn great interest for their potential applications in high-speed miniaturized photonic integration due to their high photoluminescence quantum efficiency, structural processability, ultrafast photoresponse, and excellent property engineering. Based on the rational design on morphological and componential levels, a series of organic nanomaterials have been controllably synthesized in recent years, and their excitonic/photonic behaviors has been fine-tuned to steer the light flow for specific optical applications. This review presents a comprehensive summary of recent breakthroughs in the controlled synthesis of organic nanomaterials with specific structures and compositions, whose tunable photonic properties would provide a novel platform for multifunctional applications. First, we give a general overview of the tailored construction of novel nanostructures with various photonic properties. Then, we summarize the design and controllable synthesis of composite materials for the modulation of their functionalities. Subsequently, special emphasis is put on the fabrication of complex nanostructures towards wide applications in isolated photonic devices. We conclude with our personal viewpoints on the development directions in the novel design and controllable construction of organic nanomaterials for future applications in highly integrated photonic devices and chips.
Co-reporter:Jian Ye;Chuang Zhang;Chang-Ling Zou;Yongli Yan;Jianmin Gu;Yong Sheng Zhao;Jiannian Yao
Advanced Materials 2014 Volume 26( Issue 4) pp:620-624
Publication Date(Web):
DOI:10.1002/adma.201303482
Co-reporter:Cong Wei; Si-Yun Liu; Chang-Ling Zou; Yingying Liu; Jiannian Yao;Yong Sheng Zhao
Journal of the American Chemical Society 2014 Volume 137(Issue 1) pp:62-65
Publication Date(Web):December 24, 2014
DOI:10.1021/ja5112817
Flexible microdisk whispering-gallery-mode (WGM) resonators with high quality factors were achieved through the controlled assembly of organic materials with an emulsion-solvent-evaporation method. The high material compatibility of the assembled microdisks enabled us to realize low-threshold WGM lasers by doping with organic dyes as gain media. Furthermore, the emulsion-assisted self-assembly provided a strategy for the one-step fabrication of microwire-waveguide-connected microdisk heterostructures, which can be utilized for the efficient output of the isotropic WGM lasers from the coupled waveguides. We hope that these results will pave an avenue for the construction of new types of flexible WGM-based components for photonic integration.
Co-reporter:Qiu Hong Cui, Yong Sheng Zhao and Jiannian Yao
Chemical Science 2014 vol. 5(Issue 1) pp:52-57
Publication Date(Web):14 Aug 2013
DOI:10.1039/C3SC51798E
One-dimensional (1D) organic nanostructures and their hierarchical assemblies have sparked great interest in sensing applications recently owing to convenient detection, high sensitivity and selectivity, and real-time monitoring with fast response time afforded by systems that utilize them. In this mini-review, we focus on the construction and modulation of 1D nanostructures from single- or multicomponent organic compounds, and the relevant approaches that have employed them into sensing applications. Furthermore, major obstacles and future steps towards ultimate organic nanosensors based on 1D structures are discussed.
Co-reporter:Cong Wei and Yong Sheng Zhao
Journal of Materials Chemistry A 2014 vol. 2(Issue 13) pp:2295-2297
Publication Date(Web):07 Jan 2014
DOI:10.1039/C3TC32427C
Exciton–polaritons arising from strong coupling between excitons and photons are composite bosons which are half light and half matter. Due to their relatively light effective mass (seven orders of magnitude less than the mass of a hydrogen atom), they could potentially condense at temperatures much higher than those required for atom Bose–Einstein condensations (tens of nanokelvins). This makes them not only a perfect model for fundamental studies of dynamical Bose–Einstein condensates, but also a suitable system for the design of novel optical components. Various polaritonic devices such as polariton parametric amplifiers, optically pumped polariton lasers and polariton light-emitting diodes have been achieved. With the recently reported electrically pumped polariton lasers added to the list, the polaritons seem to have made their way out of the laboratory and have a bright, white future ahead.
Co-reporter:Wei Yao and Yong Sheng Zhao
Nanoscale 2014 vol. 6(Issue 7) pp:3467-3473
Publication Date(Web):28 Nov 2013
DOI:10.1039/C3NR04654K
Organic nanomaterials have attracted more and more attention for their applications in nano-photonics due to their high photoluminescence quantum efficiencies, color tunabilities, and size-dependent optical properties. With the distinctive features of photoluminescence, waveguiding and dimensional confinement, different organic nanostructures, such as 0D nanoparticles, 1D nanowires and 2D nanosheets, have a significant influence on their photonic properties. Therefore, it is of great importance and scientific interest to develop the strategy for tailoring the self-assembled structures with specific photonic behaviors in desired manners. In this mini review, we give a brief review of the recent work on the control of self-assembled organic nanostructures, and the tunable photonic properties of the predetermined structures.
Co-reporter:Meng Li, Wei Yao, Jun-Dao Chen, Hai-Yan Lu, YongSheng Zhao and Chuan-Feng Chen
Journal of Materials Chemistry A 2014 vol. 2(Issue 39) pp:8373-8380
Publication Date(Web):18 Aug 2014
DOI:10.1039/C4TC01562B
A series of tetrahydro[5]helicene-based dye molecules were efficiently synthesized and the helical structural features of their tetrahydro[5]helicene skeletons were confirmed by the crystal structures. The substituent effect of the dyes on their photophysical properties was then investigated. Consequently, it was found that compared with hydroxymethyl and ester groups, the introduction of imide to the tetrahydro[5]helicene skeleton could result in not only red shifts of their absorption and emission bands, but also higher quantum yields and larger Stokes shift. Especially, intense full-color fluorescence emissions in both solution and solid states could be achieved just by changing the substituents with different electron-donating abilities in the tetrahydro[5]helicene imide skeleton. Moreover, a significant solvent-effect on the emissions of the tetrahydro[5]helicene-based organic dyes was also found. The density functional theory calculations further demonstrated that with the increase of the electron-donating ability of the substituents, the energy gaps of the tetrahydro[5]helicene-based dyes gradually decreased, which theoretically elucidated the substituent effect of the dyes on their photophysical properties. Additionally, an optical waveguide application of the tetrahydro[5]helicene-based imide dye is shown as well.
Co-reporter:Jianmin Gu, Yongli Yan, Chuang Zhang, Jiannian Yao and Yong Sheng Zhao
Journal of Materials Chemistry A 2014 vol. 2(Issue 17) pp:3199-3203
Publication Date(Web):17 Sep 2013
DOI:10.1039/C3TC31399A
A host–guest inclusion complexation self-assembly strategy was developed for the synthesis of SHG-active low dimensional supramolecular crystals (LDSCs). p-Nitroaniline guest molecules with high inherent second-order polarizability were introduced into the cavities of the β-cyclodextrin host to form supramolecular inclusion complexes, which were then assembled into microscale crystalline structures with an anti-solvent diffusion combined solvent-evaporation-induced self-assembly method. Two distinct types of LDSCs with controllable dimensions were obtained by altering the polarity of anti-solvents and the concentration of supramolecular monomers. Each type of LDSCs exhibited its characteristic SHG response to the polarized incident signals, which is attributed to the inherent crystal structures.
Co-reporter:Yong Jun Li;Yongli Yan;Chuang Zhang;Yong Sheng Zhao;Jiannian Yao
Advanced Materials 2013 Volume 25( Issue 20) pp:2784-2788
Publication Date(Web):
DOI:10.1002/adma.201203829
Co-reporter:Yongli Yan;Chuang Zhang;Jiannian Yao ;Yong Sheng Zhao
Advanced Materials 2013 Volume 25( Issue 27) pp:3627-3638
Publication Date(Web):
DOI:10.1002/adma.201300325
Abstract
Many recent activities in the use of one-dimensional nanostructures as photonic elements for optical information processing are explained by huge advantages that photonic circuits possess over traditional silicon-based electronic ones in bandwidth, heat dissipation, and resistance to electromagnetic wave interference. Organic materials are a promising candidate to support these optical-related applications, as they combine the properties of plastics with broad spectral tunability, high optical cross-section, easy fabrication, as well as low cost. Their outstanding compatibility allows organic composite structures which are made of two or more kinds of materials combined together, showing great superiority to single-component materials due to the introduced interactions among multiple constituents, such as energy transfer, electron transfer, exciton coupling, etc. The easy processability of organic 1D crystalline heterostructures enables a fine topological control of both composition and geometry, which offsets the intrinsic deficiencies of individual material. At the same time, the strong exciton-photon coupling and exciton-exciton interaction impart the excellent confinement of photons in organic microstructures, thus light can be manipulated according to our intention to realize specific functions. These collective properties indicate a potential utility of organic heterogeneous material for miniaturized photonic circuitry. Herein, focus is given on recent advances of 1D organic crystalline heterostructures, with special emphasis on the novel design, controllable construction, diverse performance, as well as wide applications in isolated photonic elements for integration. It is proposed that the highly coupled, hybrid optical networks would be an important material basis towards the creation of on-chip optical information processing.
Co-reporter:Yong Jun Li;Yongli Yan;Chuang Zhang;Yong Sheng Zhao;Jiannian Yao
Advanced Materials 2013 Volume 25( Issue 20) pp:
Publication Date(Web):
DOI:10.1002/adma.201370130
Co-reporter:Chuanxing Shi, Zhiqian Guo, Yongli Yan, Shiqin Zhu, Yongshu Xie, Yong Sheng Zhao, Weihong Zhu, and He Tian
ACS Applied Materials & Interfaces 2013 Volume 5(Issue 1) pp:192
Publication Date(Web):December 6, 2012
DOI:10.1021/am302466m
The fluorescence of luminescent emitters is often quenched in the solid state, because of the typical aggregation-caused quenching (ACQ) effect, which is a thorny obstacle to high-performance organic optoelectronic materials. The exploration of solid-state enhanced long wavelength, red-emitting chromophores, especially possessing one-dimensional (1D) assembly features, is of great importance. Interestingly, an excellent solid-state enhanced red emission system (denoted as ED) based on quinolinemalononitrile has been developed via the delicate modification of the conventional ACQ dicyanomethylene-4H-pyran (DCM) derivative (denoted as BD) through crystal engineering. ED exhibits extraordinary self-assembly property in a variety of solvents, even realizing the “waving ribbons” with a length of 6 mm and a diameter of 10 μm. Crystal analysis shows that the CH···π and CH···N supramolecular interactions of ED contribute to the twisted self-assembly solid-state enhanced emission phenomenon. However, for BD, strong face-to-face stacking leads to fluorescence quenching in the solid state. Because of such easy assembly and strong solid-state emission properties, application for optical waveguides of ED is realized with a low optical loss. Stimuli-responsive behavior is also elaborated with color change between orange and red by grinding/fuming or pressing/heating.Keywords: cell imaging; crystal structures; optical waveguides; self-assembly; solid-state fluorescence; stimuli-response;
Co-reporter:Chuang Zhang;Chang-Ling Zou;Yongli Yan;Cong Wei;Jin-Ming Cui;Fang-Wen Sun;Jiannian Yao;Yong Sheng Zhao
Advanced Optical Materials 2013 Volume 1( Issue 5) pp:357-361
Publication Date(Web):
DOI:10.1002/adom.201200065
Co-reporter:Wei Yao;Dr. Yongli Yan;Dr. Lin Xue;Chuang Zhang;Guoping Li; Qingdong Zheng; Yong Sheng Zhao; Hua Jiang; Jiannian Yao
Angewandte Chemie 2013 Volume 125( Issue 33) pp:8875-8879
Publication Date(Web):
DOI:10.1002/ange.201302894
Co-reporter:Wei Yao;Dr. Yongli Yan;Dr. Lin Xue;Chuang Zhang;Guoping Li; Qingdong Zheng; Yong Sheng Zhao; Hua Jiang; Jiannian Yao
Angewandte Chemie International Edition 2013 Volume 52( Issue 33) pp:8713-8717
Publication Date(Web):
DOI:10.1002/anie.201302894
Co-reporter:Yongli Yan;Chuang Zhang;Jian Yao Zheng;Jiannian Yao ;Yong Sheng Zhao
Advanced Materials 2012 Volume 24( Issue 42) pp:5681-5686
Publication Date(Web):
DOI:10.1002/adma.201202698
Co-reporter:Qing Li;Jian Yao Zheng;Yongli Yan;Yong Sheng Zhao;Jiannian Yao
Advanced Materials 2012 Volume 24( Issue 35) pp:4745-4749
Publication Date(Web):
DOI:10.1002/adma.201201931
Co-reporter:Jianmin Gu;Yongli Yan;Yong Sheng Zhao;Jiannian Yao
Advanced Materials 2012 Volume 24( Issue 17) pp:2249-2253
Publication Date(Web):
DOI:10.1002/adma.201104297
Co-reporter:Qiu Hong Cui;Lang Jiang;Chuang Zhang;Yong Sheng Zhao;Wenping Hu;Jiannian Yao
Advanced Materials 2012 Volume 24( Issue 17) pp:2332-2336
Publication Date(Web):
DOI:10.1002/adma.201104594
Co-reporter:Chuang Zhang;Yongli Yan;Yuan-Yuan Jing;Qiang Shi;Yong Sheng Zhao;Jiannian Yao
Advanced Materials 2012 Volume 24( Issue 13) pp:1703-1708
Publication Date(Web):
DOI:10.1002/adma.201104326
Co-reporter:Chuang Zhang;Yongli Yan;Yuan-Yuan Jing;Qiang Shi;Yong Sheng Zhao;Jiannian Yao
Advanced Materials 2012 Volume 24( Issue 13) pp:
Publication Date(Web):
DOI:10.1002/adma.201290073
Co-reporter:Jian Yao Zheng;Yongli Yan;Xiaopeng Wang;Wen Shi;Huimin Ma;Yong Sheng Zhao;Jiannian Yao
Advanced Materials 2012 Volume 24( Issue 35) pp:OP194-OP199
Publication Date(Web):
DOI:10.1002/adma.201200867
Co-reporter:Jian Yao Zheng;Yongli Yan;Xiaopeng Wang;Wen Shi;Huimin Ma;Yong Sheng Zhao;Jiannian Yao
Advanced Materials 2012 Volume 24( Issue 35) pp:
Publication Date(Web):
DOI:10.1002/adma.201290212
Co-reporter:Yongli Yan;Chuang Zhang;Jian Yao Zheng;Jiannian Yao ;Yong Sheng Zhao
Advanced Materials 2012 Volume 24( Issue 42) pp:
Publication Date(Web):
DOI:10.1002/adma.201290261
Co-reporter:Jian Yao Zheng ; Yongli Yan ; Xiaopeng Wang ; Yong Sheng Zhao ; Jiaxing Huang ;Jiannian Yao
Journal of the American Chemical Society 2012 Volume 134(Issue 6) pp:2880-2883
Publication Date(Web):January 30, 2012
DOI:10.1021/ja209815f
Dendritic organic heterojunctions with aluminum tris(8-hydroxyquinoline) (Alq3) microwire trunks and 1,5-diaminoanthraquinone (DAAQ) nanowire branches were prepared by a two-step growth process. The prefabricated Alq3 microwires act as nucleation centers for site-specific secondary vapor growth of DAAQ nanowires, resulting in the unique dendritic heterostructures. When the trunk was excited with a focused laser beam, emitted light of various colors was simultaneously channeled from the branched nanowires via both waveguiding and energy transfer. The intensity of the out-coupled emissions was modulated effectively by changing the polarization of the incident light.
Co-reporter:Yongli Yan ;Yong Sheng Zhao
Advanced Functional Materials 2012 Volume 22( Issue 7) pp:1330-1332
Publication Date(Web):
DOI:10.1002/adfm.201102173
Co-reporter:Qiu Hong Cui, Yong Sheng Zhao and Jiannian Yao
Journal of Materials Chemistry A 2012 vol. 22(Issue 10) pp:4136-4140
Publication Date(Web):07 Dec 2011
DOI:10.1039/C1JM14721H
Due to their potential performances in photonic integrations, one-dimensional single-crystalline nanostructures constructed from organic luminescent molecules have generated wide research interests during the past few years. Here, we highlight the two main kinds of applications in the future of miniaturized photonic circuits: optical waveguides and optically pumped lasers. This article concludes with a summary and our personal view about the direction of future development in organic opto-functional waveguides and lasers as photonic devices.
Co-reporter:Jian Ye, Jidong Jiang, Yong Sheng Zhao and Jiannian Yao
Journal of Materials Chemistry A 2012 vol. 22(Issue 36) pp:19202-19206
Publication Date(Web):30 Jul 2012
DOI:10.1039/C2JM33846G
We have demonstrated a new fabrication methodology for gold nano- and microtubes with regular cylinders by vapor-induced strain of porous thin films, which exhibit highly sensitive SERS signals for Rhodamine 6G detection. The strain originates from the temperature difference in the top and bottom of the gold film, which is brought about by the vapor of the Se powder, because Selenium has a low melting point. Around its melting point, Se appears in the vapor state, while the gold nanofilms remain in the solid phase. By exploiting such vapor-driven self-rolling of the gold film, shrinkage or collapse of the tube wall by capillary forces can be effectively avoided. Moreover, the diameter and the length of the obtained gold tubes can be well controlled by changing the Se powder evaporation temperature and the thickness of the gold film. The wall number of the tubes varied with the evaporation time and speed of the Se powder. Attributed to the larger surface area of the porous structures, the tubes exhibit SERS signals nearly 20 times larger than those of the gold film. This means that the detection limit of gold film is enhanced by over one order of magnitude.
Co-reporter:Fengqin Hu and Yong Sheng Zhao
Nanoscale 2012 vol. 4(Issue 20) pp:6235-6243
Publication Date(Web):24 Aug 2012
DOI:10.1039/C2NR31865B
Magnetic resonance imaging (MRI) yields high spatially resolved contrast with anatomical details for diagnosis, deeper penetration depth and rapid 3D scanning. To improve imaging sensitivity, adding contrast agents accelerates the relaxation rate of water molecules, thereby greatly increasing the contrast between specific issues or organs of interest. Currently, the majority of T1 contrast agents are paramagnetic molecular complexes, typically Gd(III) chelates. Various nanoparticulate T1 and T1/T2 contrast agents have recently been investigated as novel agents possessing the advantages of both the T1 contrast effect and nanostructural characteristics. In this minireview, we describe the recent progress of these inorganic nanoparticle-based MRI contrast agents. Specifically, we mainly report on Gd and Mn-based inorganic nanoparticles and ultrasmall iron oxide/ferrite nanoparticles.
Co-reporter:Qing Li, Chuang Zhang, Jian Yao Zheng, Yong Sheng Zhao and Jiannian Yao
Chemical Communications 2012 vol. 48(Issue 1) pp:85-87
Publication Date(Web):04 Nov 2011
DOI:10.1039/C1CC15632B
The electrogenerated upconversion was achieved in the uniformly doped organic nanowires based on triplet energy transfer from tris(2,2′-bipyridyl)ruthenium(II) to 9,10-diphenylanthracene.
Co-reporter:Taifeng Liu, Yongjun Li, Yongli Yan, Yuliang Li, Yanwen Yu, Nan Chen, Songhua Chen, Chao Liu, Yongsheng Zhao, and Huibiao Liu
The Journal of Physical Chemistry C 2012 Volume 116(Issue 26) pp:14134-14138
Publication Date(Web):June 11, 2012
DOI:10.1021/jp301998d
A novel amphiphilic porphyrin derivative DOCP-Zn has been synthesized and utilized to construct tunable nanostructures from 0D to 1D by controlling the axial coordination of zinc porphyrin with 4,4′-bipyridine. SEM images indicated that patterns between 0D nanospheres and 1D nanorods or nanoslices can be reversibly converted by the construction or destroy of the axial coordination interaction. This facile approach provided a new method for controlling the nanostructure morphologies and dimension by patterns conversion. The photoluminescence microscopy images indicated the 1D nanorods material has the potential application as nanoscale photonic elements.
Co-reporter:Chuang Zhang;Jian Yao Zheng;Yong Sheng Zhao;Jiannian Yao
Advanced Materials 2011 Volume 23( Issue 11) pp:1380-1384
Publication Date(Web):
DOI:10.1002/adma.201003829
Co-reporter:Chuang Zhang ; Chang-Ling Zou ; Yongli Yan ; Rui Hao ; Fang-Wen Sun ; Zheng-Fu Han ; Yong Sheng Zhao ;Jiannian Yao
Journal of the American Chemical Society 2011 Volume 133(Issue 19) pp:7276-7279
Publication Date(Web):April 25, 2011
DOI:10.1021/ja200549v
Single-crystal organic nanowires were fabricated with a soft-template-assisted self-assembly method in liquid phase. These nanowires with rectangular cross section can serve as resonators for exciton–photon coupling, leading to a microcavity effect and a relatively low threshold of laser actions. Two-photon-pumped blue lasing was observed in these organic waveguiding nanostructures above a threshold of 60 nJ, excited with a 750 nm near-infrared femtosecond pulse laser at 77 K.
Co-reporter:Jidong Jiang, Qing Liao, Yong Sheng Zhao and Jiannian Yao
Journal of Materials Chemistry A 2011 vol. 21(Issue 13) pp:4837-4842
Publication Date(Web):22 Feb 2011
DOI:10.1039/C0JM04437G
Single-crystal ZnS1−xSexnanoribbons with various compositions were synthesized through an Au-catalyzed vapor transport method. Under two-photon pumping with an 800 nm femtosecond pulsed laser, the spontaneous emission peak of the ternary nanoribbons undergoes a gradual red-shift from 422 to 464 nm with the increase of Se content. When the pump energy densities are increased above the thresholds, the nanoribbons exhibit a tunable upconverted laser emission accompanied by a dramatic decrease in spectral linewidth as a set of sharp peaks on the corresponding wavelengths of each sample, featuring the occurrence of stimulated emission. Two components appear in the fluorescence lifetimes, which indicate that the ZnS1−xSexnanoribbons have two different recombination centers. Both lifetime components decrease with the increase of pump energy, further confirming the occurrence of stimulated emission. The two-photon pumped lasing behavior was also observed from single nanoribbons, in which the photoluminescence (PL) spectra are composed of multimode of lasing. The distinct modes show gain competition and pronounced shifts as a function of excitation density.
Co-reporter:Chuang Zhang, Yong Sheng Zhao and Jiannian Yao
Physical Chemistry Chemical Physics 2011 vol. 13(Issue 20) pp:9060-9073
Publication Date(Web):31 Jan 2011
DOI:10.1039/C0CP02376K
Optical waveguides synthesized at the micro/nanoscale have drawn great interest for their potential applications in high speed miniaturized photonic integrations. In this Perspective article, we mainly focus on the related works on active optical waveguides based on functional small organic molecules in micro/nano regime. We begin with a general overview of recent progress in sub-wavelength optical waveguides, including the development of waveguide materials of inorganic semiconductors, polymers, and small organic molecules. Then brief highlights are put on the recently reported organic optical waveguides with various unique optical properties induced by the ordered molecular aggregations in the micro/nano-sized solid-state structures, such as polarized emission, lasing, aggregation-induced enhanced emission, etc. This article concludes with a summary and our personal view about the direction of future development in organic opto-functional waveguides as photonic devices.
Co-reporter:Chuang Zhang, Yong Sheng Zhao and Jiannian Yao
New Journal of Chemistry 2011 vol. 35(Issue 5) pp:973-978
Publication Date(Web):09 Mar 2011
DOI:10.1039/C1NJ20012G
Composite nanomaterials fabricated from organic luminescent molecules have generated wide research interests during the past few years. These optically active binary nanostructures are of great importance not only for fundamental investigations on energy transfers, but also for various practical applications in light emitting, optical waveguiding, fluorescence switching and chemical sensing. Therefore, many kinds of organic composite nanostructures have been synthesized by different techniques, including liquid-phase mixing, vapor-phase doping, chemical reaction and surface modification. In this Focus, we describe the recent progress in our group toward the construction of organic composite nanomaterials and studies on their tunable luminescent behaviors via energy transfers.
Co-reporter:Chuang Zhang, Jian Yao Zheng, Yong Sheng Zhao and Jiannian Yao
Chemical Communications 2010 vol. 46(Issue 27) pp:4959-4961
Publication Date(Web):28 May 2010
DOI:10.1039/C0CC00347F
Organic core–shell nanostructures with upconverted emission property were synthesized with a microemulsion–assisted chemical reaction method.
Co-reporter:Jian Yao Zheng, Chuang Zhang, Yong Sheng Zhao and Jiannian Yao
Physical Chemistry Chemical Physics 2010 vol. 12(Issue 40) pp:12935-12938
Publication Date(Web):31 Aug 2010
DOI:10.1039/C0CP00300J
Tunable emission of binary organic nanobelts was realized via the fluorescence resonance energy transfer (FRET) process, which can be exploited for the detection of acid and basic chemical vapors.
Co-reporter:Yong Sheng Zhao;Aidong Peng;Hongbing Fu;Ying Ma;Jiannian Yao
Advanced Materials 2008 Volume 20( Issue 9) pp:1661-1665
Publication Date(Web):
DOI:10.1002/adma.200800123
Co-reporter:Y. S. Zhao;H. B. Fu;F. Q. Hu;A. D. Peng;W. S. Yang;J. N. Yao
Advanced Materials 2008 Volume 20( Issue 1) pp:79-83
Publication Date(Web):
DOI:10.1002/adma.200700542
Co-reporter:Yong Sheng Zhao, Zhibin Yu, Ali Douraghy, Arion F. Chatziioannou, Yueqi Mo and Qibing Pei
Chemical Communications 2008 (Issue 45) pp:6008-6010
Publication Date(Web):14 Oct 2008
DOI:10.1039/B813571A
Two classes of bulk high-Zpolymer composites were prepared, which exhibit scintillation properties for γ-radiation detection.
Co-reporter:Yuan Liu, Haiyun Dong, Fengqin Hu, Yong Sheng Zhao
Science Bulletin (15 January 2017) Volume 62(Issue 1) pp:3-4
Publication Date(Web):15 January 2017
DOI:10.1016/j.scib.2016.12.002
Co-reporter:Zheng-Feng Chang, Ling-Min Jing, Ying-Ying Liu, Jun-Jie Liu, Yan-Chun Ye, Yong Sheng Zhao, Si-Chun Yuan and Jin-Liang Wang
Journal of Materials Chemistry A 2016 - vol. 4(Issue 36) pp:NaN8415-8415
Publication Date(Web):2016/07/27
DOI:10.1039/C6TC02395A
In this work, we employ the Corey–Fuchs reaction followed by coupling reactions to develop a series of π-conjugated aggregation-induced emission (AIE) small-molecule luminophores (DT2A, DT3A and DT4A) through a 2,2-(2,2-diphenylethene-1,1-diyl)dithiophene (DPDT) core with different amounts and different strengths of TPA peripheral moieties. Interestingly, these molecules give obviously higher solid fluorescent quantum efficiency and AIE phenomena. In particular, the thin film of DT3A exhibited the highest fluorescent quantum efficiency of ca. 25% and the DT2A showed the highest αAIE of 78. Moreover, the excellent optical waveguide applications of DT2A and DT4A were achieved because of their excellent self-assembly properties. Meanwhile, piezofluorochromic behavior with a large red shift of 35 nm only appeared when DT4A was ground using a pestle, because DT4A inserted more TPA and changed the twisting conformation. The piezofluorochromic behavior can be recovered to its original color by fuming with solvent. Finally, DT2A and DT4A were utilized as fluorescent probes to detect nitroaromatic/nitroaliphatic compounds and showed evident fluorescence quenching. These results indicate a huge potential to develop bright AIEgens based on DPDT core units and also provide insights into understanding how piezofluorochromism, optical waveguides and explosive detection properties are influenced by alternating the spatial symmetry of AIE materials with different numbers of TPA terminal groups.
Co-reporter:Haiyun Dong, Chunhuan Zhang and Yong Sheng Zhao
Journal of Materials Chemistry A 2017 - vol. 5(Issue 23) pp:NaN5609-5609
Publication Date(Web):2017/02/13
DOI:10.1039/C6TC05474A
Organic microlasers are miniaturized coherent light sources with great promise for advancing the field of optoelectronics. Recently, host–guest composite organic microlasers, where the host materials provide spatial confinement for the organic gain materials, have captured much research interest because the host–guest composite material systems endow the organic microlasers with improved lasing performances, such as low threshold, high stability, and excellent tunability. In this Review, we explore the latest advancements in the development of host–guest composite organic microlasers, and offer our perspective on future improvements and trends. Special emphasis is put on the construction strategies and the unique laser properties of the organic microlasers based on host–guest confinement systems. The comprehensive understanding of the relationship between laser performances and the synergistic interactions of the host and guest materials would provide a useful guidance for the design and fabrication of novel organic microlasers.
Co-reporter:Meng Li, Wei Yao, Jun-Dao Chen, Hai-Yan Lu, YongSheng Zhao and Chuan-Feng Chen
Journal of Materials Chemistry A 2014 - vol. 2(Issue 39) pp:NaN8380-8380
Publication Date(Web):2014/08/18
DOI:10.1039/C4TC01562B
A series of tetrahydro[5]helicene-based dye molecules were efficiently synthesized and the helical structural features of their tetrahydro[5]helicene skeletons were confirmed by the crystal structures. The substituent effect of the dyes on their photophysical properties was then investigated. Consequently, it was found that compared with hydroxymethyl and ester groups, the introduction of imide to the tetrahydro[5]helicene skeleton could result in not only red shifts of their absorption and emission bands, but also higher quantum yields and larger Stokes shift. Especially, intense full-color fluorescence emissions in both solution and solid states could be achieved just by changing the substituents with different electron-donating abilities in the tetrahydro[5]helicene imide skeleton. Moreover, a significant solvent-effect on the emissions of the tetrahydro[5]helicene-based organic dyes was also found. The density functional theory calculations further demonstrated that with the increase of the electron-donating ability of the substituents, the energy gaps of the tetrahydro[5]helicene-based dyes gradually decreased, which theoretically elucidated the substituent effect of the dyes on their photophysical properties. Additionally, an optical waveguide application of the tetrahydro[5]helicene-based imide dye is shown as well.
Co-reporter:Jianmin Gu, Yongli Yan, Chuang Zhang, Jiannian Yao and Yong Sheng Zhao
Journal of Materials Chemistry A 2014 - vol. 2(Issue 17) pp:NaN3203-3203
Publication Date(Web):2013/09/17
DOI:10.1039/C3TC31399A
A host–guest inclusion complexation self-assembly strategy was developed for the synthesis of SHG-active low dimensional supramolecular crystals (LDSCs). p-Nitroaniline guest molecules with high inherent second-order polarizability were introduced into the cavities of the β-cyclodextrin host to form supramolecular inclusion complexes, which were then assembled into microscale crystalline structures with an anti-solvent diffusion combined solvent-evaporation-induced self-assembly method. Two distinct types of LDSCs with controllable dimensions were obtained by altering the polarity of anti-solvents and the concentration of supramolecular monomers. Each type of LDSCs exhibited its characteristic SHG response to the polarized incident signals, which is attributed to the inherent crystal structures.
Co-reporter:Yongli Yan and Yong Sheng Zhao
Chemical Society Reviews 2014 - vol. 43(Issue 13) pp:NaN4340-4340
Publication Date(Web):2014/04/03
DOI:10.1039/C4CS00098F
Nanophotonics, which is mainly the study of the behavior of light–matter interaction at the wavelength scale, has developed into one of the most important branches in optics-related disciplines. Utilizing organic functional molecules as the building blocks of nanophotonic materials and devices has great potential due to the multiple advantages, including the molecular designability, good processability, tailorable properties, and so on. Small molecules exhibit a strong tendency to aggregate into low-dimensional structures through an assembly process. The morphologies of the formed products, which are tightly related to the stacking modes of the molecules, can be precisely controlled through the modulation of various intermolecular interactions. The optical properties of organic complex structures, assembled from one or more types of small molecules, show heavy dependence on the composition, distribution, as well as the topological structures, manifesting a strategy to acquire desired photonic properties via rational structural design and/or componential modulation. This tutorial review focuses on the relationship among various molecules, diverse structures and photonic properties, with emphasis on the controllable assembly processes to fabricate low-dimensional structures and assembly strategies to achieve requisite optofunctional properties.
Co-reporter:Yong Sheng Zhao, Zhibin Yu, Ali Douraghy, Arion F. Chatziioannou, Yueqi Mo and Qibing Pei
Chemical Communications 2008(Issue 45) pp:NaN6010-6010
Publication Date(Web):2008/10/14
DOI:10.1039/B813571A
Two classes of bulk high-Zpolymer composites were prepared, which exhibit scintillation properties for γ-radiation detection.
Co-reporter:Miaomiao Gao, Cong Wei, Xianqing Lin, Yuan Liu, Fengqin Hu and Yong Sheng Zhao
Chemical Communications 2017 - vol. 53(Issue 21) pp:NaN3105-3105
Publication Date(Web):2017/02/14
DOI:10.1039/C6CC08094D
We demonstrate the fabrication of organic high Q active whispering-gallery-mode (WGM) resonators from π-conjugated polymer by a controlled emulsion-solvent-evaporation method, which can simultaneously provide optical gain and act as an effective resonant cavity. By measuring the shift of their lasing modes on exposure to organic vapor, we successfully monitored the slight concentration variation in the chemical gas. These microlaser sensors demonstrated high detection sensitivity and good signal repeatability under continuous chemical gas treatments. The results offer an effective strategy to design miniaturized optical sensors.
Co-reporter:Wei Zhang and Yong Sheng Zhao
Chemical Communications 2016 - vol. 52(Issue 58) pp:NaN8917-8917
Publication Date(Web):2016/02/03
DOI:10.1039/C6CC00018E
Nanophotonics have recently captured broad attention because of their great potential in information processing and communication, which may allow rates and bandwidth beyond what is feasible in the realm of electronics. Organic materials could be well suitable for such applications due to their ability to generate, transmit, modulate and detect light in their lightweight and flexible nanoarchitectures. Their distinct nanophotonic properties strongly depend on their extrinsic morphologies and intrinsic molecular excited-state processes. In this feature article, we mainly focus on a comprehensive understanding of the relationship between molecular excited-state processes and the advanced photonic functionalities of organic micro/nano-crystals in recent organic nanophotonic research, and then expect to provide enlightenment for the design and development of tiny photonic devices with broadband tunable properties by tailoring the excited-state processes of organic microcrystals.
Co-reporter:Qing Li, Chuang Zhang, Jian Yao Zheng, Yong Sheng Zhao and Jiannian Yao
Chemical Communications 2012 - vol. 48(Issue 1) pp:NaN87-87
Publication Date(Web):2011/11/04
DOI:10.1039/C1CC15632B
The electrogenerated upconversion was achieved in the uniformly doped organic nanowires based on triplet energy transfer from tris(2,2′-bipyridyl)ruthenium(II) to 9,10-diphenylanthracene.
Co-reporter:Chuang Zhang, Jian Yao Zheng, Yong Sheng Zhao and Jiannian Yao
Chemical Communications 2010 - vol. 46(Issue 27) pp:NaN4961-4961
Publication Date(Web):2010/05/28
DOI:10.1039/C0CC00347F
Organic core–shell nanostructures with upconverted emission property were synthesized with a microemulsion–assisted chemical reaction method.
Co-reporter:Qiu Hong Cui, Yong Sheng Zhao and Jiannian Yao
Chemical Science (2010-Present) 2014 - vol. 5(Issue 1) pp:NaN57-57
Publication Date(Web):2013/08/14
DOI:10.1039/C3SC51798E
One-dimensional (1D) organic nanostructures and their hierarchical assemblies have sparked great interest in sensing applications recently owing to convenient detection, high sensitivity and selectivity, and real-time monitoring with fast response time afforded by systems that utilize them. In this mini-review, we focus on the construction and modulation of 1D nanostructures from single- or multicomponent organic compounds, and the relevant approaches that have employed them into sensing applications. Furthermore, major obstacles and future steps towards ultimate organic nanosensors based on 1D structures are discussed.
Co-reporter:Cong Wei and Yong Sheng Zhao
Journal of Materials Chemistry A 2014 - vol. 2(Issue 13) pp:NaN2297-2297
Publication Date(Web):2014/01/07
DOI:10.1039/C3TC32427C
Exciton–polaritons arising from strong coupling between excitons and photons are composite bosons which are half light and half matter. Due to their relatively light effective mass (seven orders of magnitude less than the mass of a hydrogen atom), they could potentially condense at temperatures much higher than those required for atom Bose–Einstein condensations (tens of nanokelvins). This makes them not only a perfect model for fundamental studies of dynamical Bose–Einstein condensates, but also a suitable system for the design of novel optical components. Various polaritonic devices such as polariton parametric amplifiers, optically pumped polariton lasers and polariton light-emitting diodes have been achieved. With the recently reported electrically pumped polariton lasers added to the list, the polaritons seem to have made their way out of the laboratory and have a bright, white future ahead.
Co-reporter:Qiu Hong Cui, Yong Sheng Zhao and Jiannian Yao
Journal of Materials Chemistry A 2012 - vol. 22(Issue 10) pp:NaN4140-4140
Publication Date(Web):2011/12/07
DOI:10.1039/C1JM14721H
Due to their potential performances in photonic integrations, one-dimensional single-crystalline nanostructures constructed from organic luminescent molecules have generated wide research interests during the past few years. Here, we highlight the two main kinds of applications in the future of miniaturized photonic circuits: optical waveguides and optically pumped lasers. This article concludes with a summary and our personal view about the direction of future development in organic opto-functional waveguides and lasers as photonic devices.
Co-reporter:Jian Ye, Jidong Jiang, Yong Sheng Zhao and Jiannian Yao
Journal of Materials Chemistry A 2012 - vol. 22(Issue 36) pp:NaN19206-19206
Publication Date(Web):2012/07/30
DOI:10.1039/C2JM33846G
We have demonstrated a new fabrication methodology for gold nano- and microtubes with regular cylinders by vapor-induced strain of porous thin films, which exhibit highly sensitive SERS signals for Rhodamine 6G detection. The strain originates from the temperature difference in the top and bottom of the gold film, which is brought about by the vapor of the Se powder, because Selenium has a low melting point. Around its melting point, Se appears in the vapor state, while the gold nanofilms remain in the solid phase. By exploiting such vapor-driven self-rolling of the gold film, shrinkage or collapse of the tube wall by capillary forces can be effectively avoided. Moreover, the diameter and the length of the obtained gold tubes can be well controlled by changing the Se powder evaporation temperature and the thickness of the gold film. The wall number of the tubes varied with the evaporation time and speed of the Se powder. Attributed to the larger surface area of the porous structures, the tubes exhibit SERS signals nearly 20 times larger than those of the gold film. This means that the detection limit of gold film is enhanced by over one order of magnitude.
Co-reporter:Jidong Jiang, Qing Liao, Yong Sheng Zhao and Jiannian Yao
Journal of Materials Chemistry A 2011 - vol. 21(Issue 13) pp:NaN4842-4842
Publication Date(Web):2011/02/22
DOI:10.1039/C0JM04437G
Single-crystal ZnS1−xSexnanoribbons with various compositions were synthesized through an Au-catalyzed vapor transport method. Under two-photon pumping with an 800 nm femtosecond pulsed laser, the spontaneous emission peak of the ternary nanoribbons undergoes a gradual red-shift from 422 to 464 nm with the increase of Se content. When the pump energy densities are increased above the thresholds, the nanoribbons exhibit a tunable upconverted laser emission accompanied by a dramatic decrease in spectral linewidth as a set of sharp peaks on the corresponding wavelengths of each sample, featuring the occurrence of stimulated emission. Two components appear in the fluorescence lifetimes, which indicate that the ZnS1−xSexnanoribbons have two different recombination centers. Both lifetime components decrease with the increase of pump energy, further confirming the occurrence of stimulated emission. The two-photon pumped lasing behavior was also observed from single nanoribbons, in which the photoluminescence (PL) spectra are composed of multimode of lasing. The distinct modes show gain competition and pronounced shifts as a function of excitation density.
Co-reporter:Chuang Zhang, Yong Sheng Zhao and Jiannian Yao
Physical Chemistry Chemical Physics 2011 - vol. 13(Issue 20) pp:NaN9073-9073
Publication Date(Web):2011/01/31
DOI:10.1039/C0CP02376K
Optical waveguides synthesized at the micro/nanoscale have drawn great interest for their potential applications in high speed miniaturized photonic integrations. In this Perspective article, we mainly focus on the related works on active optical waveguides based on functional small organic molecules in micro/nano regime. We begin with a general overview of recent progress in sub-wavelength optical waveguides, including the development of waveguide materials of inorganic semiconductors, polymers, and small organic molecules. Then brief highlights are put on the recently reported organic optical waveguides with various unique optical properties induced by the ordered molecular aggregations in the micro/nano-sized solid-state structures, such as polarized emission, lasing, aggregation-induced enhanced emission, etc. This article concludes with a summary and our personal view about the direction of future development in organic opto-functional waveguides as photonic devices.
Co-reporter:Jian Yao Zheng, Chuang Zhang, Yong Sheng Zhao and Jiannian Yao
Physical Chemistry Chemical Physics 2010 - vol. 12(Issue 40) pp:NaN12938-12938
Publication Date(Web):2010/08/31
DOI:10.1039/C0CP00300J
Tunable emission of binary organic nanobelts was realized via the fluorescence resonance energy transfer (FRET) process, which can be exploited for the detection of acid and basic chemical vapors.