Hongxiang Li

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Organization: Institute of Chemistry
Department: Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids
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Co-reporter:Qing Meng, Jianhua Gao, Rongjin Li, Lang Jiang, Chengliang Wang, Huaping Zhao, Caiming Liu, Hongxiang Li and Wenping Hu  
Journal of Materials Chemistry A 2009 vol. 19(Issue 10) pp:1477-1482
Publication Date(Web):28 Jan 2009
DOI:10.1039/B816590D
A series of thiophene-phenylene semiconductors containing –CC– bonds were designed and synthesized. Their thermal, optical, electrochemical and FET properties were fully characterized. The crystal structure of 5,5′-bis(phenylethynyl)-2,2′-bithiophene (1c) revealed that the introduction of carbon-carbon triple bonds efficiently eliminated the steric repulsions between adjacent aromatic rings. TGA, UV-vis spectra and electrochemical measurements showed that all compounds had good thermal and environmental stability. FET devices based on these materials exhibited high performance and stability. All the results suggested the introduction of carbon-carbon triple bonds provided an efficient route to high performance organic semiconductors.
Co-reporter:Erjing Wang, Qing Meng, Chengliang Wang, Liqiang Li, Hongxiang Li, Wenping Hu
Synthetic Metals 2009 Volume 159(Issue 13) pp:1298-1301
Publication Date(Web):July 2009
DOI:10.1016/j.synthmet.2009.02.032
Thiophene-phenylene co-oligomers with cyano and dicyanovinyl substituents at different positions were synthesized. Their stability and energy levels were estimated through thermal gravimetric analysis, UV–vis absorption spectra and electrochemistry. Interestingly, the absorption of BTCV covered the range of 430–610 nm, and thin film transistors of BTCV exhibited p-type behavior with high stability, suggesting BTCV a good candidate for solar cell.
Co-reporter:Qingxin Tang;Yanhong Tong;Zhuoyu Ji;Liqiang Li;Wenping Hu;Yunqi Liu;Daoben Zhu
Advanced Materials 2008 Volume 20( Issue 8) pp:1511-1515
Publication Date(Web):
DOI:10.1002/adma.200702145
Co-reporter:Qingxin Tang;Lang Jiang;Yanhong Tong;Yaling Liu;Zhaohui Wang;Wenping Hu;Yunqi Liu;Daoben Zhu
Advanced Materials 2008 Volume 20( Issue 15) pp:2947-2951
Publication Date(Web):
DOI:10.1002/adma.200800669

Abstract

The use of micrometer and nanometer-sized organic single crystals to fabricate devices can retain all the advantages of single crystals, avoid the difficulties of growing large crystals, and provide a way to characterize organic semiconductors more efficiently. Moreover, the effective use of such “small” crystals will be beneficial to nanoelectronics. Here we review the recent progress of organic single-crystalline transistors based on micro-/nanometer-sized structures, namely fabrication methods and related technical issues, device properties, and current challenges.

Co-reporter:Lang Jiang;Jianhua Gao;Erjing Wang;Zhaohui Wang;Wenping Hu;Lei Jiang
Advanced Materials 2008 Volume 20( Issue 14) pp:2735-2740
Publication Date(Web):
DOI:10.1002/adma.200800341
Co-reporter:Er Jing Wang, Cheng Liang Wang, Qing Meng, Hong Xiang Li, Wen Ping Hu, Dao Ben Zhu
Chinese Chemical Letters 2008 Volume 19(Issue 11) pp:1285-1289
Publication Date(Web):November 2008
DOI:10.1016/j.cclet.2008.06.056
Molecular wires with tetrathiafulvalene (TTF) as redox center were synthesized and characterized. UV–vis spectra and cyclic voltammetry showed these wires had good reversible redox behavior under ambient conditions and their HOMO energy levels (∼−5.0 eV) matched well with the Fermi level of Au (∼−5.1 eV).
Co-reporter:Yanyan Fu, Hongxiang Li, Wenping Hu
Sensors and Actuators B: Chemical 2008 Volume 131(Issue 1) pp:167-173
Publication Date(Web):14 April 2008
DOI:10.1016/j.snb.2007.11.010
In this paper, two chemosensing ensemble probes – 2*Cu for histidine and 1*Fe for fluoride ion – obtained by simple modification of a known fluorescent probe 1*Cu were reported. Both probes showed high selectivity, sensitivity and real-time detection to the target analyte. Their working mechanism was studied by UV–vis spectra, fluorescent spectra and/or mass spectra. The potential application of these probes was also investigated. The successful performance of these probes suggested chemosensing ensemble method had great advantage and should play more roles in sensor design.
Co-reporter:Liqiang Li, Qingxin Tang, Hongxiang Li and Wenping Hu
The Journal of Physical Chemistry B 2008 Volume 112(Issue 34) pp:10405-10410
Publication Date(Web):August 1, 2008
DOI:10.1021/jp800879g
Organic thin film field-effect transistors (OTFTs) with mobility up to 1.0 cm2 V−1 s−1 and on/off ratio of 106−108 as well as good environmental stability were demonstrated by using vanadyl phthalocyanine (VOPc), a pyramid-like compound with an ultra closely π-stacked structure. The high performance, remarkable stability, low price, easy availability and nontoxicity of VOPc enabled it to be a promising candidate for OTFTs. Furthermore, we found that the mobility of the devices on OTS-modified Si/SiO2 substrates was 2 orders of magnitude higher than that of devices on Si/SiO2 substrates. Significantly, the relationship between field effect property and insulator surface property was explained from two new aspects of distribution of molecular orientation and interface compatibility, which might provide not only a useful model to explain why the surface modification with OTS could largely improve the field-effect performance but also a guide for rational optimization of device structure for higher performance. In addition, the field effect property of VOPc devices under vacuum, i.e., the oxygen doping effect on the VOPc devices, was measured. We found that the hole mobility decreased by several orders of magnitude with decreasing pressure. At a pressure below 10−2 Pa, the device on OTS-modified substrates exhibited ambipolar conduction. These results indicated that the oxygen doping exerted essential effect on the field-effect property of VOPc, which was clearly distinct from that observed for pentacene-based OFETs.
Co-reporter:J. H. Gao;R. J. Li;L. Q. Li;Q. Meng;H. Jiang;H. X. Li;W. P. Hu
Advanced Materials 2007 Volume 19(Issue 19) pp:3008-3011
Publication Date(Web):6 SEP 2007
DOI:10.1002/adma.200701167

Three simple, controlled steps are all it takes to synthesize the title pentacene analogue DBTDT (see figure). The material's high ionization potential, high thermal and photostability, high mobilities, and an on/off ratio larger than 106 at a substrate temperature of ca. 36 °C, as reported here, suggest that DBTDT will be extremely valuable for applications in plastic organic electronics.

Co-reporter:Y. Song;Q. Tang;L. Li;Y. Liu;W. Xu;Y. Liu;H. Li;W. Hu;D. Zhu
Advanced Materials 2007 Volume 19(Issue 18) pp:2624-2628
Publication Date(Web):15 AUG 2007
DOI:10.1002/adma.200700208

Ribbons of an air-stable, n-type organic single-crystal semiconductor, F16CuPc, are used to study photoswitches and phototransistors. High-quality, reversibly switching, fast photoswitches together with strongly photodependent field-effect phototransistors (see figure) of F16CuPc are made. The high light sensitivity and large on/off ratio of the phototransistors realize a new way to detect light and magnify signals in a single organic device, indicating a future in low-cost, ultrahigh density, organic photoelectric integration.

Co-reporter:Jianhua Gao, Liqiang Li, Qing Meng, Rongjin Li, Hui Jiang, Hongxiang Li and Wenping Hu  
Journal of Materials Chemistry A 2007 vol. 17(Issue 14) pp:1421-1426
Publication Date(Web):26 Jan 2007
DOI:10.1039/B616381E
New prototype semiconductor materials based on dibenzothiophene (DBT) derivatives were successfully synthesized by a convergent approach using palladium catalyzed Stille coupling reactions. Thermogravimetric analysis, UV-vis spectra and electrochemistry results indicated these materials had good thermal and photooxidation stability. X-Ray diffraction measurements of the vacuum-evaporated films showed enhanced crystalline order with increasing substrate deposition temperature. The ordered vacuum-evaporated films with charge carrier mobility as high as 7.7 × 10−2 cm2 V−1 s−1 and an on/off ratio of nearly 1 × 107 had been achieved with 3,7-bis(5′-hexyl-thiophen-2′-yl)-dibenzothiophene (3,7-DHTDBTT). These results suggest that the 3,7-substituted DBT system is a good prototype for new type organic semiconductors and will play a more important role in organic semiconductors.
Co-reporter:Yanyan Fu;Wenping Hu
European Journal of Organic Chemistry 2007 Volume 2007(Issue 15) pp:2459-2463
Publication Date(Web):30 MAR 2007
DOI:10.1002/ejoc.200601086

Two small molecular chromogenic sensors 1 and 2 for detection of Hg2+ are described. After coordination with Hg2+, a red shift of about 100 nm was observed in the UV/Vis spectra and the color of the solution changed from pale yellow to red which could easily be detected by the naked eye. The results indicate a strong push-pull system was formed after coordination of Hg2+. The 1H NMR spectra and control experiments showed the binding sites of 1 and 2 to be the aniline groups rather than the azine bridge. Moreover, mercury test papers were made by adsorbing 1 onto filter paper, allowing heterogeneous sensing of Hg2+ in aqueous solution.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)

Co-reporter:Erjing Wang;Wenping Hu;Daoben Zhu
Journal of Polymer Science Part A: Polymer Chemistry 2006 Volume 44(Issue 8) pp:2707-2713
Publication Date(Web):10 MAR 2006
DOI:10.1002/pola.21390

A new type of molecular wire 1ac with tetrathiafulvalene (TTF) units was synthesized and characterized. The UV–vis spectra and electrochemistry results showed that comparing with PPE, these polymers had smaller HOMO–LUMO band gap, and the HOMO level of polymer 1a (−5.05 eV) was closer to the work function energy of Au electrode. Thermal stability analyses indicated that these polymers had good thermal stability. All of the results showed that the introduction of TTF units made polymers 1ac better candidates for molecular wires than PPE. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 2707–2713, 2006

Co-reporter:Y. Liu;Z. Ji;Q. Tang;L. Jiang;H. Li;M. He;W. Hu;D. Zhang;L. Jiang;X. Wang;C. Wang;Y. Liu;D. Zhu
Advanced Materials 2005 Volume 17(Issue 24) pp:
Publication Date(Web):3 NOV 2005
DOI:10.1002/adma.200500809

Nanostructures with tunable size and shapes are produced using a charge-transfer complex, copper tetracyanoquinodimethane (CuTCNQ). Surfaces can be coated with the charge-transfer complex nanoparticles (see Figure). These superhydrophobic coatings may be useful for constructing water/moisture-resistant and contamination-free electronic devices.

Co-reporter:Yanyan Fu, Hongxiang Li, Wenping Hu and Daoben Zhu  
Chemical Communications 2005 (Issue 25) pp:3189-3191
Publication Date(Web):24 May 2005
DOI:10.1039/B503772G
A new fluorescence probe is described using the “chemosensing ensemble” method. The probe shows high selectivity and sensitivity for thiol-containing amino acids and peptides, and can detect cysteine and homocysteine from healthy to abnormal levels under physiologically-relevant conditions.
Co-reporter:Yanyan Fu, Hongxiang Li, Wenping Hu
Sensors and Actuators B: Chemical (14 April 2008) Volume 131(Issue 1) pp:167-173
Publication Date(Web):14 April 2008
DOI:10.1016/j.snb.2007.11.010
In this paper, two chemosensing ensemble probes – 2*Cu for histidine and 1*Fe for fluoride ion – obtained by simple modification of a known fluorescent probe 1*Cu were reported. Both probes showed high selectivity, sensitivity and real-time detection to the target analyte. Their working mechanism was studied by UV–vis spectra, fluorescent spectra and/or mass spectra. The potential application of these probes was also investigated. The successful performance of these probes suggested chemosensing ensemble method had great advantage and should play more roles in sensor design.
Co-reporter:Qing Meng, Jianhua Gao, Rongjin Li, Lang Jiang, Chengliang Wang, Huaping Zhao, Caiming Liu, Hongxiang Li and Wenping Hu
Journal of Materials Chemistry A 2009 - vol. 19(Issue 10) pp:NaN1482-1482
Publication Date(Web):2009/01/28
DOI:10.1039/B816590D
A series of thiophene-phenylene semiconductors containing –CC– bonds were designed and synthesized. Their thermal, optical, electrochemical and FET properties were fully characterized. The crystal structure of 5,5′-bis(phenylethynyl)-2,2′-bithiophene (1c) revealed that the introduction of carbon-carbon triple bonds efficiently eliminated the steric repulsions between adjacent aromatic rings. TGA, UV-vis spectra and electrochemical measurements showed that all compounds had good thermal and environmental stability. FET devices based on these materials exhibited high performance and stability. All the results suggested the introduction of carbon-carbon triple bonds provided an efficient route to high performance organic semiconductors.
Co-reporter:Jianhua Gao, Liqiang Li, Qing Meng, Rongjin Li, Hui Jiang, Hongxiang Li and Wenping Hu
Journal of Materials Chemistry A 2007 - vol. 17(Issue 14) pp:NaN1426-1426
Publication Date(Web):2007/01/26
DOI:10.1039/B616381E
New prototype semiconductor materials based on dibenzothiophene (DBT) derivatives were successfully synthesized by a convergent approach using palladium catalyzed Stille coupling reactions. Thermogravimetric analysis, UV-vis spectra and electrochemistry results indicated these materials had good thermal and photooxidation stability. X-Ray diffraction measurements of the vacuum-evaporated films showed enhanced crystalline order with increasing substrate deposition temperature. The ordered vacuum-evaporated films with charge carrier mobility as high as 7.7 × 10−2 cm2 V−1 s−1 and an on/off ratio of nearly 1 × 107 had been achieved with 3,7-bis(5′-hexyl-thiophen-2′-yl)-dibenzothiophene (3,7-DHTDBTT). These results suggest that the 3,7-substituted DBT system is a good prototype for new type organic semiconductors and will play a more important role in organic semiconductors.
3,6-Bis(5-bromothiophen-2-yl)-2,5-dihexylpyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione
(4,8-Bis(octyloxy)benzo[1,2-b:4,5-b']dithiophene-2,6-diyl)bis(trimethylstannane)
4,8-Bis(octyloxy)benzo[1,2-b:4,5-b']dithiophene
Thiazolo[5,4-d]thiazole, bis(5'-hexyl[2,2'-bithiophen]-5-yl)-
Di-tert-butyl(methyl)phosphonium tetrafluoroborate
furan-2,5-diylbis(tributylstannane)
2,2':5',2''-Terthiophene, 5,5''-dibromo-3,3''-dioctyl-