To provide orthogonal solvent processable surface modification and improve the device stability of bulk-heterojunction polymer solar cells (PSCs), n-type semiconducting material naphthalene diimide (NDI) was chemically introduced onto the ITO surface as a cathode interlayer (CIL) using 3-bromopropyltrimethoxysilane (BrTMS) as a coupling agent. After modification, the work function of ITO can be decreased from 4.70 to 4.23 eV. The modified ITO cathode was applied in inverted PSCs based on PTB7-Th:PC71BM. With the CIL modification, a champion power conversion efficiency (PCE) of 5.87% was achieved, showing a dramatic improvement compared to that of devices (PCE = 3.58%) without CIL. More importantly, with these chemical bonded interlayers, the stability of inverted PSCs was greatly enhanced. The improved PCE and stability can be attributed to the increased open-circuit voltage and the formation of robust chemical bonds in NDI-TMS films, respectively. This study demonstrated that chemical modification of ITO with n-type semiconducting materials provides an avenue for not only solving the solvent orthogonal problem but also improving the device performance in terms of the PCE and the stability.

Different contents of fluorine in side alkyl chains were incorporated into three conjugated polymers (namely, PBDTTT-f13, PBDTTT-f9, and PBDTTT-f5) whose backbones consist of benzodithiophene donors and thienothiophene acceptors. These three fluorinated polymers, in comparison with the well-known analogue PTB7-Th, show comparable energy levels and optical band gaps. However, the fluorination of side alkyl chains significantly changed the surface energy of bulk materials, which leads to distinctly different self-assembly behaviors and phase separations as being mixed with PC71BM. The increased mismatch in surface energies between the polymer and PC71BM causes larger scale phase domains, which makes a sound explanation for the difference in their photovoltaic properties.Topics: Contact angle; Electric properties; Electric transport processes and properties; Electronic structure; Energy level; Heterojunction solar cells; Molecular structure-property relationship; Organic solar cells; Physical and chemical processes; Polymer morphology; Polymers; Quantum mechanics; Quantum mechanics; Self-assembly; Separation science; Spectra; Surface energy; Thin films; Thin films;

•A new 2D-conjugated molecule DR3TBDTTVT was synthesized, and OSCs based on DR3TBDTTVT:PC71BM achieved a best PCE of 5.71%.•DR3TBDTTVT shows complementary absorption to PTB7-Th & PC71BM, and was introduced as third component to ternary OSCs.•The ternary OSCs displayed improved device performance compared with the binary OSCs based on PTB7-Th:PC71BM.Ternary organic solar cells (OSCs) are burgeoning as one of the effective strategies to achieve high power conversion efficiencies (PCEs) by incorporating a third component with a complementary absorption into the binary blends. In this study, we presented a new two-dimension-conjugated small molecule denoted by DR3TBDTTVT, which alone gave rise to a best PCE of 5.71% with acceptor PC71BM as active layer. Given the complementary absorption with PTB7-Th, DR3TBDTTVT was doped into (PTB7-Th:PC71BM)-based binary blends, and ternary OSCs were developed. The ternary OSCs with 10 wt% of DR3TBDTTVT displayed improved hole-mobility, reduced device resistance and better phase separation of active layer, thus leading to an impressive PCE of 7.77% with open-circuit voltage of 0.77 V, short-circuit density of 14.52 mA cm−2 and fill factor of 70.3%. Ternary OSCs well make up for the light-harvesting insufficiency of binary OSCs, and this research provides a new material for the improvement of PCEs for single-junction OSCs.Download high-res image (328KB)Download full-size image

The self-assembly behavior of a molecule composed of an azobenzene segment, carboxylic-acid group and flexible alkyl chains (denoted by ABA11) was studied as an extension of our proceeding work. We have previously reported that in DMSO solution ABA11 self-assembled into nanotubes starting from nanosheets and experiencing a meta-state of helical ribbons. Herein, we found that changing the solvent can also affect the self-assembly pathway of ABA11 to nanotubes. When DMSO was replaced by ethanol, the nanosheets formed by ABA11 bilayers either directly scrolled up to form nanotubes without a meta-state of helical ribbons at low concentrations, or stacked up to form nanobricks at higher concentrations. In addition, increasing the water content in ethanol can significantly facilitate the formation of the assembled nanostructures.

For planar p–i–n perovskite solar cells (Pero-SCs), the bottom hole transporting layer (HTL) material is crucially important, since it can greatly affect the device performance in two aspects: (1) hole collection and transportation and (2) the crystallinity of the perovskite layer formed on it. Herein, a series of catechol derivatives, L-3,4-dihydroxyphenylalanine (DOPA), norepinephrine (NE) and 3,4-dihydroxybenzhydrazide (DOBD), were employed as dopants in PEDOT:PSS and applied as HTLs, and the influence on performance of p–i–n Pero-SCs was systematically studied. It is found that all these three catechols can improve the power conversion efficiency (PCE) of the Pero-SCs, among which DOBD shows far better performance than the other two. Under optimized conditions, a PCE of 17.46% was achieved for the p–i–n Pero-SCs using DOBD-doped PEDOT:PSS as the HTL. The investigations on morphology, fluorescence and electrochemical impedance spectra indicate that the PCE improvement should be mainly attributed to the facilitated charge collection and transportation due to the doped HTL and the enhanced crystallinity of the perovskite films. This line of research demonstrates that the easily accessible catechols can be employed as an excellent dopant in PEDOT:PSS for application as HTLs in Pero-SCs and opens a novel avenue for further improving the performance of the devices.

A methanol-soluble diamine-modified fullerene derivative (denoted as PCBDANI) was applied as an efficient cathode buffer layer (CBL) in planar p-i-n perovskite solar cells (pero-SCs) based on the CH3NH3PbI3–xClx absorber. The device with PCBDANI single CBL exhibited significantly improved performance with a power conversion efficiency (PCE) of 15.45%, which is approximately 17% higher than that of the control device without the CBL. The dramatic improvement in PCE can be attributed to the formation of an interfacial dipole at the PCBM/Al interface originating from the amine functional group and the suppression of interfacial recombination by the PCBDANI interlayer. To further improve the PCE of pero-SCs, PCBDANI/LiF double CBLs were introduced between PCBM and the top Al electrode. An impressive PCE of 15.71% was achieved, which is somewhat higher than that of the devices with LiF or PCBDANI single CBL. Besides the PCE, the long-term stability of the device with PCBDANI/LiF double CBLs is also superior to that of the device with LiF single CBL.

In this study, two fullerenes (C60, C70) and their methano-substitutions (PC61BM, PC71BM), as electron transport materials (ETMs) in perovskite solar cells (Pero-SCs), were systematically studied. As being used as ETMs, methanofullerenes, though with lower electron mobility compared to the counterpart pristine fullerenes, lead to higher power conversion efficiencies (PCEs) of Pero-SCs. The difference is likely caused by the fill-out vacancies and smoother morphology of the interfaces between ETM and perovskite layers, as they were prepared by different methods. In addition, compared to C60 and PC61BM, C70 and PC71BM showed priority in terms of short-circuit current density, which should be attributed to fast free charge extraction abilities.

In this paper, we introduce a room-temperature mixed-solvent-vapor annealing (rtMSVA) method to fabricate high performance perovskite solar cells (pero-SCs) based on MAPbI3−xClx without the need for thermal annealing (TA). An ultra-smooth perovskite thin-film with high crystallinity was obtained by the DMF/CB mixed-solvent (1:20, v/v) vapor annealing at room-temperature without TA and the power conversion efficiency (PCE) of the pero-SCs reached 16.4%. More importantly, the reproducibility of the PCEs is quite good among 40 different devices. Furthermore, large active area pero-SCs were fabricated with the rtMSVA method. The PCEs of the pero-SCs based on ITO and flexible PET/Ag mesh electrodes with an active area of 1.21 cm2 reached 11.01% and 7.5%, respectively. We anticipate that rtMSVA would very possibly become a promising crystallization method for the fabrication of large area pero-SCs in the near future.

For perovskite solar cells (Pero-SCs), one of the key issues with respect to the power conversion efficiency (PCE) is the morphology control of the perovskite thin-films. In this study, an easily-accessible additive polyethylenimine (PEI) is utilized to tune the morphology of CH3NH3PbI3−xClx. With addition of 1.00 wt% of PEI, the smoothness and crystallinity of the perovskite were greatly improved, which were characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD). A summit PCE of 14.07% was achieved for the p-i-n type Pero-SC, indicating a 26% increase compared to those of the devices without the additive. Both photoluminescence (PL) and alternating current impedance spectroscopy (ACIS) analyses confirm the efficiency results after the addition of PEI. This study provides a low-cost polymer additive candidate for tuning the morphology of perovskite thin-films, and might be a new clue for the mass production of Pero-SCs.

TiO2 is widely used in perovskite solar cells (Pero-SCs), but its low electrical conductivity remains a drawback for application in electron transport layer (ETL). To overcome this problem, an easily accessible hydroxylated fullerene, fullerenol, was employed herein as ETL modified on ITO in n-i-p type (ITO as cathode) Pero-SCs for the first time. The results showed that the insertion of a single layer of fullerenol between perovskite and TiO2 dramatically facilitates the charge transportation and decreases the interfacial resistance. As a consequence, the device performance was greatly improved, and a higher power conversion efficiency of 14.69% was achieved, which is ∼17.5% enhancement compared with that (12.50%) of the control device without the fullerenol interlayer. This work provides a new candidate of interfacial engineering for facilitating the electron transportation in Pero-SCs.

•The effect of DIO on the photovoltaic performance of polymer/PC71BM blends is studied.•The addition of DIO can optimize the morphology of the active layer and enhance hole and electron mobilities.•The impact of chalcogen atom on the intrinsic properties of donor materials has been studied.Two donor-acceptor polymers P8 and P9 based on 5,6-difluoro-benzo[1,2,5]thiadiazole unit have been prepared and applied as the donor materials in polymer solar cells. Due to the slight difference between electronic structures of thiophene and selenophene, P8 and P9 show similar absorption spectra and similar frontier energy levels. However, the pristine P8:PC71BM and P9:PC71BM blend films display distinct morphologies as revealed by AFM measurement. After the addition of DIO, both blend films feature a nanoscale interconnected-network structure, which leads to the enhancement in solar cells performance with PCE up to 6.73% and 6.84% for P8 and P9, respectively. Alternating current impedance spectrometry measurements revealed that high surface roughness could improve the PCE of P8-based PSCs, while in P9-based PSCs DIO can enhance hole and electron mobilities of the active layer.Two donor-acceptor polymers based on 5,6-difluoro-benzo[1,2,5]thiadiazole have been prepared as donor materials for high efficiency polymer solar cells.

•Two novel copolymers, with priorities in light absorption and hole mobility, were applied as HTL materials in perovskite solar cells.•To balance the charge transportation, pristine C60 was employed as interlayer at the cathode side.•With the two above-mentioned interlayers, a PCE as high as 15.83% was achieved.The interlayers, including hole transporting layer (HTL) and electron transporting layer (ETL), segregating photoactive layer and the electrodes play an important role in charge extraction and transportation in perovskite solar cells (pero-SCs). Two novel copolymers, PDTSTTz and PDTSTTz-4, for the first time were applied as HTL in the n-i-p type pero-SCs, with the device structure of ITO/compact TiO2/CH3NH3PbI3-xClx/HTL/MoO3/Ag. The highest occupied molecular orbitals (HOMO) levels of PDTSTTz and PDTSTTz-4 exhibit a suitable band alignment with the valence band edge of the perovskite. Both of them lead to improved device performances compared with reference pero-SCs based on P3HT as HTL. To further balance the charge extraction and the diffusion length of charge carriers, pristine C60 was introduced at the cathode side of the pero-SCs, working together with TiO2 as ETL. With insertion of both the HTL and ETL, the performance of pero-SCs was greatly enhanced. The optimized devices exhibited impressive PCEs of 14.4% and 15.8% for devices based on PDTSTTz and PDTSTTz-4. The improved performance is attributed to better light harvest ability, decreased interface resistance and faster decay time due to the introduction of the interlayers.

•To solve the solvent orthogonal problem, buffer layers based on AOB were chemically modified on ITO through BrTMS.•This buffer layers can efficiently lower the work function of the ITO, and greatly improve the performance of PSCs.•After insertion of this interlayer, the PCE of PSCs based on PBDTTT-C-T:PCBM was enhanced from 4.10% to 7.56%.In order to avoid an interpenetration of the buffer and the photoactive layers during preparation of polymer solar cells (PSCs), solvent-resistant buffer films were chemically modified on indium tin oxide (ITO) surface. The conjugated aromatics acridine orange base (AOB) was introduced into the films using 3-bromopropyltrimethoxysilane (BrTMS) as coupling agent. Upon ITO surface modification, the respective work functions show a significant decrease. The modified ITO substrates were implemented in inverted PSCs based on PBDTTT-C-T:PC71BM. With the modification, the power conversion efficiency (PCE) was improved significantly from 4.10% (for the inverted PSC without this buffer layer) to 7.56%. The PCE enhancement is mainly caused by the increase of the open-circuit voltage (43%). These results indicate that the solvent-resistant film is able to facilitate electron collection and transportation, thus providing a novel route to high efficient PSCs by surface engineering.

•A benzothiazole dye bearing a long alkyl chain (BTA-12) was synthesized and used as chemosensor to detect Zn2+.•In presence of Zn2+, due to the formation of coordination complex and further aggregation, the fluorescence of BTA-12 was significantly enhanced.•This chemosensor shows a very good selectivity to Zn2+ and a detection limit as low as 7.5 × 10−7 mol L−1.Chemical detection of Zn2+ ion plays an important role in both environmental and biological systems. In this paper, a new chemosensor based on benzothiazole was designed and synthesized. The fluorescent intensity of the chemosensor enhanced significantly with existence of Zn2+ ion. The control experiments show that the analogous ions (Pb2+, Co2+, Ni2+, Mn2+, Cu2+, Mg2+, Cd2+, Na+ and K+) do not have fluorescence enhancement effect; and some of them even quench the fluorescence dramatically. The intensity increase upon addition of Zn2+ is due to the coordination between Zn2+ and benzothiazole. This chemosensor shows a high sensitivity for Zn2+ with a detection limit as low as 7.5 × 10−7 mol L−1 and high selectivity through a ‘turn-on’ fluorescence response over the other tested metal ions.

Doping of semiconductors by introducing foreign atoms enables their widespread applications in microelectronics and optoelectronics. We show that this strategy can be applied to direct bandgap lead-halide perovskites, leading to the realization of ultrawide photoluminescence (PL) at new wavelengths enabled by doping bismuth (Bi) into lead-halide perovskites. Structural and photophysical characterization reveals that the PL stems from one class of Bi doping-induced optically active center, which is attributed to distorted [PbI6] units coupled with spatially localized bipolarons. Additionally, we find that compositional engineering of these semiconductors can be employed as an additional way to rationally tune the PL properties of doped perovskites. Finally, we accomplished the electroluminescence at cryogenic temperatures by using this system as an emissive layer, marking the first electrically driven devices using Bi-doped photonic materials. Our results suggest that low-cost, earth-abundant, solution-processable Bi-doped perovskite semiconductors could be promising candidate materials for developing optical sources operating at new wavelengths.

An alcohol-soluble fullerene derivative functionalized with a crown-ether end group in its side chain (denoted as PCBC) was synthesized and applied as a cathode buffer layer in planar p–i–n perovskite solar cells and bulk-heterojunction polymer solar cells. It is found that the introduction of the PCBC cathode buffer layer can greatly improve the photovoltaic performance of the planar p–i–n perovskite solar cells based on CH3NH3PbI3−xClx with power conversion efficiency (PCE) reaching 15.08%. In addition, the bulk-heterojunction polymer solar cells based on PBDTTT-C-T:PC70BM with the PCBC cathode buffer layer also showed a higher PCE of 7.67%, which is improved in comparison with the traditional device with the Ca/Al cathode. This work indicates that PCBC is a promising solution-processable cathode buffer layer material for application in both planar p–i–n perovskite solar cells and bulk-heterojunction polymer solar cells.

Nano-fluorogens with a mono-molecule layered structure are fabricated by self-assembly of a new bolaamphiphile bearing a tetraphenylethene moiety. The nano-fluorogens show good water-solubility, biocompatibility, and strong emission with a quantum yield as high as 15%. The nano-fluorogens, as prepared, are successfully applied to label and map HeLa cells. The images obtained have high contrast and resolution, showing a promising potential for fluorescence detection in bio-related systems.

In this paper, nanotubes with a uniform diameter were prepared by self-assembly of an achiral azobenzene-containing fatty acid. The polymorphic transformation of the assemblies during the cooling process was systematically studied. By controlling the incubation temperature, different morphologies, such as membranes, stripes, helical ribbons and tubes, were all obtained in our experiment. These elements were all predicted by Selinger et al. in the theoretical model of the formation of nanotubes. To the best of our knowledge, this is the first experimental example to fully support their theory.

In this paper, triple cathode buffer layers (CBLs) composed of phenyl-C61-butyric acid methyl ester (PCBM), C60, and LiF layers were introduced into the planar p–i–n perovskite solar cells (p–i–n PSCs) with a device structure of ITO/PEDOT:PSS/CH3NH3PbI3–xClx/CBLs/Al. For comparison, a single CBL of PCBM and a double CBL of PCBM/LiF were also investigated in the p–i–n PSCs. On the basis of the PCBM buffer layer, the addition of a thin LiF layer facilitated the charge collection process and led to the dramatic improvement of the power conversion efficiency (PCE) of the PSCs up to 14.69% under an illumination of AM 1.5G, 100 mW/cm2, which is to date one of the highest efficiencies of the p–i–n PSCs. By further insertion of a C60 layer between PCBM and LiF in the triple CBLs, a PCE of 14.24% was obtained, and more importantly, the PCBM/C60/LiF triple CBLs are very helpful for improving the stability of the devices and making the LiF layer less thickness-sensitive for achieving high performances of the p–i–n PSCs.Keywords: cathode buffer layers; CH3NH3PbI3−xClx; PCBM/C60/LiF triple CBLs; planar perovskite solar cells; stability

In this paper, a pyrene moiety is incorporated into a bolaamphiphile to form a novel molecule denoted PRB. Above the critical micelle concentration, PRB forms nanodisks in the aqueous solution. The addition of acetate ions induces a morphological change in self-assembled aggregates, which convert into nanofibers with a diameter of several nanometers. More interestingly, along with the morphological change, the fluorescence of the assemblies was enhanced concomitantly, which can be attributed to the binding effect of acetate ions on pyridinium head groups of PRB.

In this paper, a new bolaamphiphile bearing 1-cyano-1,2-bis(phenyl)ethene (CNBE) has been synthesized. The self-assembly of this molecule in aqueous solution is concentration-dependent. Two distinct morphologies, monomolecular layered lamellas and helical nanofibres have been obtained with the as-prepared molecular configuration. Note worthily, the helical nanofibres provide an experimental evidence for the pure twisted structure in the liquid crystals, which is theoretically proposed by De Gennes. Due to the photoisomerization of CNBE, the self-assembled nanostructures undergo morphological changes upon irradiation. Although various nanostructures were observed in the solution-state, only nanofibres were obtained after the solution was cast on a substrate, which was attributed to a strong dewetting effect. This work illustrates concentration-dependent and light-responsive self-assembly and provides a novel avenue for fabricating smart soft materials.

•In this manuscript, regarding to the effect of PEI as cathode interlayer, we have studied the work function and resistance of the ITO electrode correlating to the device performance of the inverted polymer solar cells (PSCs) based on PBDTTT-C-T:PC70BM.•It is found that a very thin layer of PEI (⩽5.5 nm), either linear PEI (l-PEI) or branched PEI (b-PEI) with different molecular weights, is enough to lower the work function of the ITO electrode and to enhance the photovoltaic performance of the devices.•However, a thicker PEI interlayer (⩾10 nm) results in abrupt decrease of the PCEs due to the increase of the interface resistance.•Interestingly, for the thicker interlayers, the l-PEI shows better photovoltaic performance than that of b-PEI, which can also be explained by their difference in the interface resistances.•This work from the experimental basis supplies an insight into the function of PEI cathode interlayer, and provides some instruction on the future design of interlayer materials in PSCs.In this paper, we investigated the effect of PEI cathode interlayer on the work function and the interface resistance of ITO electrode in the inverted polymer solar cells (PSCs) based on PBDTTT-C-T:PC70BM. It is found that a very thin layer of PEI (⩽5.5 nm), either linear PEI (l-PEI) or branched PEI (b-PEI) with different molecular weights, is enough to lower the work function of the ITO electrode and to enhance the photovoltaic performance of the devices. The champion power conversion efficiency (PCE) of the devices with the PEI cathode interlayer is 7.84%, more than doubled of that without the interlayer. However, a thicker PEI interlayer (⩾10 nm) results in abrupt decrease of the PCEs due to the increase of the resistance. Interestingly, for the thicker interlayers, the l-PEI shows high photovoltaic performance than that of b-PEI, which can also be explained by their difference in the resistances. This work supplies an insight into the function of PEI cathode interlayer on improving the work function and resistance of ITO electrode in the inverted PSCs, and provides some instructions on the future design of interlayer materials in PSCs.

Amphiphilic molecules generally tend to organize spontaneously into spherical or cylindrical micelles/vesicles in appropriate liquid media and conditions, and seldom form two dimensional (2D) planar structures with a regular shape, due to their energetically unfavorable state. Herein, the self-assembly of a new bolaamphiphile bearing a bistriazole-pyrene unit leads to the formation of mono-molecule-layer nano-ribbons. The π–π stacking interaction between the rigid bistriazole-pyrene units and electrostatic screening contributed by the aromatic counterion tosyl groups are responsible for the 2D alignment of the molecules in the aggregate. Partial replacement of the tosyl groups causes a reduction in the width of the nano-ribbons and the coordination of triazole with Pd2+ ions results in the collapse of the self-assembled structure. This study supplies new clues for fabricating molecular level 2D nanostructures by bottom-up supramolecular assembly.

In this article, we have synthesized a polymer containing regulated azobenzene groups by one-pot multi-component polymerization (MCP) based on Passerini reaction, and investigated its self-assembly behavior and photo-induced deformation properties. We found that this molecule can form spherical structures with sizes ranging from hundreds of nanometers to several micrometers when dissolved in THF. NMR and FTIR studies indicate that there are associated hydrogen bonds among the molecules in the aggregates, which are responsible for the formation of the nanospheres. By controlling the stirring rate as the THF suspension is dropped into water, the nanospheres can be sorted according to their size. In this way, we have obtained nanospheres with relatively uniform diameter. When irradiated by UV light in the aqueous medium, the nanospheres tend to aggregate into large clusters, while in dry state they are ready to merge into island-like structures, showing a good photo-induced deformation property.

The adsorption of lysozyme is difficult to control by pH because of the relatively high isoelectric point of this protein (11.1). In this article, we demonstrate good control of lysozyme adsorption by pH in the range of 4–10 on silicon surfaces through modification with poly(2-(dimethylamino ethyl) methacrylate)-block-poly(methacrylic acid) (PDMAEMA-b-PMAA) diblock copolymer brushes. We show that the thickness of the outer PMAA block (lPMAA) is critical to the adsorption. When lPMAA was less than 10 nm, adsorption increased with increasing pH, and the difference in adsorption between high and low pH increased with lPMAA. The ratio of adsorption at pH 10 and pH 4 reached values as high as 16.4. When lPMAA was more than 10 nm, the adsorption tendency on the PDMAEMA-b-PMAA diblock copolymer brushes was similar to that on PMAA homopolymer brushes. These results indicate that the combination of PDMAEMA and PMAA gives adsorption behavior reflecting the properties of both polymers. However, if the outer PMAA block is thicker than a critical value, then the protein-resistant effect of the inner PDMAEMA block is screened.

An alcohol-soluble fullerene derivative functionalized with a crown-ether end group in its side chain (denoted as PCBC) was synthesized and applied as a cathode buffer layer in planar p–i–n perovskite solar cells and bulk-heterojunction polymer solar cells. It is found that the introduction of the PCBC cathode buffer layer can greatly improve the photovoltaic performance of the planar p–i–n perovskite solar cells based on CH3NH3PbI3−xClx with power conversion efficiency (PCE) reaching 15.08%. In addition, the bulk-heterojunction polymer solar cells based on PBDTTT-C-T:PC70BM with the PCBC cathode buffer layer also showed a higher PCE of 7.67%, which is improved in comparison with the traditional device with the Ca/Al cathode. This work indicates that PCBC is a promising solution-processable cathode buffer layer material for application in both planar p–i–n perovskite solar cells and bulk-heterojunction polymer solar cells.

Nano-fluorogens with a mono-molecule layered structure are fabricated by self-assembly of a new bolaamphiphile bearing a tetraphenylethene moiety. The nano-fluorogens show good water-solubility, biocompatibility, and strong emission with a quantum yield as high as 15%. The nano-fluorogens, as prepared, are successfully applied to label and map HeLa cells. The images obtained have high contrast and resolution, showing a promising potential for fluorescence detection in bio-related systems.

In this paper, we introduce a room-temperature mixed-solvent-vapor annealing (rtMSVA) method to fabricate high performance perovskite solar cells (pero-SCs) based on MAPbI3−xClx without the need for thermal annealing (TA). An ultra-smooth perovskite thin-film with high crystallinity was obtained by the DMF/CB mixed-solvent (1:20, v/v) vapor annealing at room-temperature without TA and the power conversion efficiency (PCE) of the pero-SCs reached 16.4%. More importantly, the reproducibility of the PCEs is quite good among 40 different devices. Furthermore, large active area pero-SCs were fabricated with the rtMSVA method. The PCEs of the pero-SCs based on ITO and flexible PET/Ag mesh electrodes with an active area of 1.21 cm2 reached 11.01% and 7.5%, respectively. We anticipate that rtMSVA would very possibly become a promising crystallization method for the fabrication of large area pero-SCs in the near future.