Dye-Sensitized Solar Cells: Progress on Robust Anchor Groups in Dyes

doi:10.6023/cjoc201709014

Chin. J. Org. Chem. ›› 2018, Vol. 38 ›› Issue (5): 1085-1106.DOI: 10.6023/cjoc201709014 Previous Articles Next Articles

Reviews

染料敏化太阳电池:染料中稳定锚基团的研究进展

田亚娟^a, 蔡宁^a, 陈亚通^a, 钱赛男^a, 霍延平^a,b

a 广东工业大学轻工化工学院广州 510006;
b 中国科学院上海有机化学研究所有机氟化学中国科学院重点实验室上海 200032

收稿日期:2017-09-08 修回日期:2017-11-16 发布日期:2017-12-08
通讯作者: 蔡宁,E-mail:ning.cai@gdut.edu.cn;霍延平,E-mail:organicteacherhuo@126.com E-mail:ning.cai@gdut.edu.cn;organicteacherhuo@126.com
基金资助:
广东省自然科学基金（No.2017A030310039）、国家自然科学基金（Nos.61671162，21372051）、广东省科技计划（No.2016A010103031）资助项目.

Dye-Sensitized Solar Cells: Progress on Robust Anchor Groups in Dyes

Tian Yajuan^a, Cai Ning^a, Chen Yatong^a, Qian Sainan^a, Huo Yanping^a,b

a School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006;
b Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Cheimstry, Chinese Academy of Sciences, Shanghai 200032

Received:2017-09-08 Revised:2017-11-16 Published:2017-12-08
Contact: 10.6023/cjoc201709014 E-mail:ning.cai@gdut.edu.cn;organicteacherhuo@126.com
Supported by:
Project supported by the Natural Science Foundation of Guangdong Province (No. 2017A030310039), the National Natural Science Foundation of China (Nos. 61671162, 21372051) and the Science and Technology Planning Project of Guangdong Province (No. 2016A010103031).

As a type of potential photovoltaic device, dye-sensitized solar cells (DSSCs) have attracted tremendous attention due to its high cost-effective and simple manufacturing process. In the device, dye molecules attach on the metal oxide surface via chemical bonds between anchor substituents and metal oxide substrate, realizing the light harvesting and photoelectron injection. Traditionally, carboxylic acids, such as benzoic acid and cyanoacrylic acid groups, have been widely utilized as the anchor groups in DSSCs. However, the detachment of dye molecules from metal oxide surface during device operation and consequent long-term stability issues cannot be ignored. Therefore, in view of durability of DSSCs in practical application, various anchor groups with a better ability to graft on the metal oxide have been explored. Several robust anchor groups in recent years and corresponding photovoltaic parameters are reviewed and the relationship between molecular structures and device performance is also discussed. The research progress of anchoring groups in photocatalytic hydrogen and quantum dot sensitized solar cells (QDSSCs) is also examined.

Key words: dye-sensitized solar cell, dye sensitizer, anchor group, stability

Cite this article

Tian Yajuan, Cai Ning, Chen Yatong, Qian Sainan, Huo Yanping. Dye-Sensitized Solar Cells: Progress on Robust Anchor Groups in Dyes[J]. Chin. J. Org. Chem., 2018, 38(5): 1085-1106.

Export EndNote|Reference Manager|ProCite|BibTeX|RefWorks

share this article

References

[1] Sorensen, B. Renewable Energy, 1st ed, Academic Press, London, 1979.
[2] O'Regan, B.; Grätzel, M. Nature 1991, 353, 737.
[3] Yella, A.; Lee, H. W.; Tsao, H. N.; Yi, C.; Chandiran, A. K.; Nazeeruddin, M. K.; Diau, E. W. G.; Yeh, C. Y.; Zakeeruddin, S. M.; Grätzel, M. Science 2011, 334, 629.
[4] (a) Wang, Y.; Chen, B.; Wu, W.; Li, X.; Zhu, W.; Tian, H.; Xie, Y. Angew. Chem., Int. Ed. 2014, 53, 10779.
(b) Wei, T.; Sun, X.; Li, X.; Ågren, H.; Xie, Y. ACS Appl. Mater. Interfaces 2015, 39, 21956.
(c) Xie, Y.; Tang, Y.; Wu, W.; Wang, Y.; Liu, J.; Liu, X.; Tian, H.; Zhu, W. J. Am. Chem. Soc. 2015, 44. 14055.
(d) Tang, Y.; Wang, Y.; Li, X.; Ågren, H.; Zhu, W.; Xie, Y. ACS Appl. Mater. Interfaces 2015, 50, 27976.
(e) Song, H.; Li, X.; Ågren, H.; Xie, Y. Dyes Pigm. 2017, 137, 421.
[5] (a) Yang, H. W.; Guan, J. J.; Gao, F. X.; He, X. P.; Wang, A.; Sun, B. D.; Zhang, X. Q.; Zhang, B.; Feng, Y. Q. Chin. J. Org. Chem. 2015, 35, 2237(in Chinese). (杨贺玮, 官俊杰, 高峰贤, 何欣平, 王安, 孙宝德, 张学强, 张宝, 冯亚青, 有机化学, 2015, 35, 2237.)
(b) Zhou, D.; Cai, N.; Long, H.; Zhang, M.; Wang, Y.; Wang, P. J. Phys. Chem. C 2011, 115, 3163.
(c) Xu, M.; Zhou, D.; Cai, N.; Liu, J.; Li, R.; Wang, P. Energy Environ. Sci. 2011, 4, 4735.
(d) Li, R.; Liu, J.; Cai, N.; Zhang, M.; Wang, P. J. Phys. Chem. B 2010, 114, 4461.
(e) Cai, N.; Moon, S. J.; Cevey-Ha, L.; Moehl, T.; Humphry-Baker, R.; Wang, P.; Zakeeruddin, S. M.; Grätzel, M. Nano Lett. 2011, 11, 1452.
[6] (a) Cao, Y.; Cai, N.; Wang, Y.; Li, R.; Yuan, Y.; Wang, P. Phys. Chem. Chem. Phys. 2012, 14, 8282.
(b) Cai, N.; Zhang, J.; Xu, M.; Zhang, M.; Wang, P. Adv. Funct. Mater. 2013, 23, 3539.
(c) Cai, N.; Wang, Y.; Xu, M.; Fan, Y.; Li, R.; Zhang, M.; Wang, P. Adv. Funct. Mater. 2013, 23, 1846.
(d) Cai, N.; Li, R.; Wang, Y.; Zhang, M.; Wang, P. Energy Environ. Sci. 2013, 6, 139.
[7] Kalyanasundaram, K.; Grätzel, M. Coord. Chem. Rev. 1998, 177, 347.
[8] Mathew, S.; Yella, A.; Gao, P.; Humphry-Baker, R.; Curchod, B. F. E.; Ashari-Astani, N.; Tavernelli, I.; Rothlisberger, U.; Nazeeruddin, M. K.; Grätzel, M. Nat. Chem. 2014, 6, 242.
[9] Hagfeldt, A.; Boschloo, G.; Sun, L.; Kloo, L.; Pettersson, H. Chem. Rev. 2010, 110, 6595.
[10] Galoppini, E. Coord. Chem. Rev. 2004, 248, 1283.
[11] Péchy, P.; Rotzinger, F. P.; Nazeeruddin, M. K.; Kohle, O.; Zakeeruddin, S. M.; Humphry-Baker, R.; Grätzel, M. J. Chem. Soc. Chem. Commun. 1995, 65.
[12] Park, H.; Bae, E.; Lee, J. J.; Park, J.; Choi, W. J. Phys. Chem. B 2006, 110, 8740.
[13] Odobel, F.; Blart, E.; Lagree, M.; Villieras, M.; Boujtita, H.; EIMurr, N.; Caramori, S.; Alberto Bignozzi, C. J. Mater. Chem. 2003, 13, 502.
[14] Lopez-Duarte, I.; Wang, M.; Humphry-Baker, R.; Ince, M.; Martínez-Díaz, M. V.; Nazeeruddin, M. K.; Torres, T.; Grätzel, M. Angew. Chem., Int. Ed. 2012, 51, 1895.
[15] Mulhern, K. R.; Orchard, A.; Watson, D. F.; Detty, M. R. Langmuir 2012, 28, 7071.
[16] Brown, D. G.; Schauer, P. A.; Borau-Garcia, J.; Fancy, B. R.; Berlinguette, C. P. J. Am. Chem. Soc. 2013, 135, 1692.
[17] He, H.; Gurunga, A.; Si, L. Chem. Commun. 2012, 48, 5910.
[18] Si, L.; He, H.; Zhu, K. New J. Chem. 2014, 38, 1565.
[19] Mao, J.; He, N.; Ning, Z.; Zhang, Q.; Guo, F.; Chen, L.; Wu, W.; Hua, J.; Tian, H. Angew. Chem., Int. Ed. 2012, 51, 9873.
[20] Zhang, J.; Li, H.-B.; Zhang, J.-Z.; Wu, Y.; Geng, Y.; Fu, Q.; Su, Z.-M. J. Mater. Chem. A 2013, 1, 14000.
[21] Mao, J.; Zhang, X.; Liu, S.-H.; Shen, Z.; Li, X.; Wu, W.; Chou, P.-T.; Hua, J. Electrochim. Acta 2015, 179, 179.
[22] Matsui, M.; Tanaka, N.; Kubota, Y.; Funabiki, K.; Jin, J.; Higashijima, S.; Miura, H.; Manseki, K. RSC Adv. 2016, 6, 33111.
[23] Qian, X.; Yan, R.; Hang, Y.; Lv, Y.; Zheng, L.; Xu, C.; Hou, L. Dyes Pigm. 2017, 139, 274.
[24] Qian, X.; Lan, X.; Yan, R.; He, Y.; Huang, J.; Hou, L. Electrochim. Acta 2017, 232, 377.
[25] Yu, F.; Cui, S.-C.; Li, X.; Peng, Y.; Yu, Y.; Kang, Y.; Zhang, S.-C.; Li, J.; Liu, J.-G.; Hua, J. Dyes Pigm. 2017, 139, 7.
[26] Horiuchi, T.; Miuraa, H.; Uchida, S. Chem. Commun. 2003, 3036.
[27] Horiuchi, T.; Miura, H.; Uchida, S. J. Photochem. Photobiol., A Chem. 2004, 164, 29.
[28] Horiuchi, T.; Miura, H.; Sumioka, K.; Uchida, S. J. Am. Chem. Soc. 2004, 126, 12218.
[29] Chen, Y.; Li, C.; Zeng, Z.; Wang, W.; Wang, X.; Zhang, B. Chem. Lett. 2005, 6, 762.
[30] Li, S.-L.; Jiang, K.-J.; Shao, K.-F.; Yang, L.-M. Chem. Commun. 2006, 2792.
[31] Tian, H.; Yang, X.; Chen, R.; Pan, Y.; Li, L.; Hagfeldt, A.; Sun, L. Chem. Commun. 2007, 3741.
[32] Liang, M.; Xu, W.; Cai, F.; Chen, P.; Peng, B.; Chen, J.; Li, Z. J. Phys. Chem. C 2007, 111, 4465.
[33] Tian, H.; Yang, X.; Pan, J.; Chen, R.; Liu, M.; Zhang, Q.; Hagfeldt, A.; Sun, L. Adv. Funct. Mater. 2008, 18, 3461.
[34] Ito, S.; Miura, H.; Uchida, S.; Takata, M.; Sumioka, K.; Liska, P.; Comte, P.; Péchy, P.; Grätzel, M. Chem. Commun. 2008, 5194.
[35] Zhang, X.-H.; Yao, Y.-S.; Li, C.; Wang, W.-B.; Cheng, X.-X.; Wang, X.-S.; Zhang, B.-W. Chin. J. Chem. 2008, 26, 929.
[36] Marinado, T.; Hagberg, D. P.; Hedlund, M.; Edvinsson, T.; Johansson, E. M. J.; Boschloo, G.; Rensmo, H.; Brinck, T.; Sun, L.; Hagfeldt, A. Phys. Chem. Chem. Phys. 2009, 11, 133.
[37] Pei, J.; Peng, S.; Shi, J.; Liang, Y.; Tao, Z.; Liang, J.; Chen, J. J. Power Sources 2009, 187, 620.
[38] Ahn, H. J.; Thogiti, S.; Cho, J. M.; Jang, B. Y.; Kim, J. H. Electron. Mater. Lett. 2015, 5, 882.
[39] Gupta, K. S. V.; Singh, S. P.; Islam, A.; Han, L.; Chandrasekharam, M. Electrochim. Acta 2015, 174, 581.
[40] Kathiravan, A.; Panneerselvam, M.; Sundaravel, K.; Pavithra, N.; Srinivasan, V.; Anandand, S.; Jaccob, M. Phys. Chem. Chem. Phys. 2016, 18, 13332.
[41] Kathiravan, A.; Srinivasan, V.; Khamrang, T.; Velusamy, M.; Jaccob, M.; Pavithra, N.; Anandane, S.; Velappan, K. Phys. Chem. Chem. Phys. 2017, 19, 3125.
[42] Hai, N. T.; Bao, L. Q.; Thogiti, S.; Cheruku, R.; Ahn, K.-S.; Kim, J. H. J. Nanosci. Nanotechnol. 2017, 5, 3181.
[43] Ooyama, Y.; Inoue, S.; Nagano, T.; Kushimoto, K.; Ohshita, J.; Imae, I.; Komaguchi, K.; Harima, Y. Angew. Chem., Int. Ed. 2011, 50, 7429.
[44] Ooyama, Y.; Nagano, T.; Inoue, S.; Imae, I.; Komaguchi, K.; Ohshita, J.; Harima, Y. Chem.-Eur. J. 2011, 17, 14837.
[45] Zhang, M.-D.; Xie, H.-X.; Ju, X.-H.; Qin, L.; Yang, Q.-X.; Zheng, H.-G.; Zhou, X.-F. Phys. Chem. Chem. Phys. 2013, 15, 634.
[46] Ooyama, Y.; Yamaguchi, N.; Imae, I.; Komaguchi, K.; Ohshita, J.; Harima, Y. Chem. Commun. 2013, 49, 2548.
[47] Wang, L.; Yang, X.; Li, S.; Cheng, M.; Sun, L. RSC Adv. 2013, 3, 13677.
[48] Wang, L.; Yang, X.; Zhao, J.; Zhang, F.; Wang, X.; Sun, L. ChemSusChem 2014, 7, 2640.
[49] Mao, J.; Wang, D.; Liu, S.-H.; Hang, Y.; Xu, Y.; Zhang, Q.; Wu, W.; Chou, P.-T.; Hua, J. Asian J. Org. Chem. 2014, 3, 153.
[50] (a) Cong, J.; Yang, X.; Liu, J.; Zhao, J.; Hao, Y.; Wang, Y.; Sun, L. Chem. Commun. 2012, 48, 6663.
(b) Ooyama, Y.; Hagiwara, Y.; Oda, Y.; Mizumo, T.; Harima, Y.; Ohshita, J. New J. Chem. 2013, 37, 2336.
[51] Massin, J.; Ducasse, L.; Toupance, T.; Olivier, C. J. Phys. Chem. C 2014, 118, 10677.
[52] Zhang, L.; Cole, J. M.; Dai, C. Appl. Mater. Interfaces 2014, 6, 7535.
[53] Daphnomili, D.; Landrou, G.; Prakash Singh, S.; Thomas, A.; Yesudas, K.; Bhanuprakash, K.; Sharma, G. D.; Coutsolelos, A. G. RSC Adv. 2012, 2, 12899.
[54] Daphnomili, D.; Sharma, G. D.; Biswas, S.; Justin Thomas, K. R.; Coutsolelos, A. G. J. Photochem. Photobiol., A:Chem. 2013, 253, 88.
[55] Mai, C.-L.; Moehl, T.; Hsieh, C.-H.; Decoppet, J. D.; Zakeeruddin, S. M.; Grätzel, M.; Yeh, C. Y. ACS Appl. Mater. Interfaces 2015, 7, 14975.
[56] Li, T.-Y.; Su, C.; Akula, S. B.; Sun, W.-G.; Chien, H.-M.; Li, W.-R. Org. Lett. 2016, 18, 3386.
[57] Asao, T.; Kikuchi, Y. Chem. Lett. 1972, 413.
[58] Barret, M. C.; Mahon, M. F.; Molloy, K. C.; Steed, J. W.; Wright, P. Inorg. Chem. 2001, 40, 4384.
[59] Nomiya, K.; Onodera, K.; Sukagoshi, K.; Shimada, K.; Yoshizawa, A.; Itoyanagi, T. A.; Sugie, A.; Tsuruta, S.; Sato, R.; Kasuga, N. C. Inorg. Chim. Acta 2009, 362, 43.
[60] Higashino, T.; Fujimori, Y.; Sugiura, K.; Tsuji, Y.;Ito, S.; Imahori, H. Angew. Chem., Int. Ed. 2015, 54, 9052.
[61] Cocozza, C.; Tsao, C. C. G.; Cheah, S. F.; Kraemer, S. M.; Raymond, K. N.; Miano, T. M.; Sposito, G. Geochim. Cosmochim. Acta 2002, 66, 431.
[62] Yang, J.; Bremer, P. J.; Lamont, I. L.; McQuillan, A. J. Langmuir 2006, 22, 10109.
[63] Upritchard, H. G.; Yang, J.; Bremer, P. J.; Lamont, I. L.; McQuillan, A. J. Langmuir 2007, 23, 7189.
[64] McNamara, W. R.; Snoeberger Ⅲ, R. C.; Li, G.; Richter, C.; Allen, L. J.; Milot, R. L.; Schmuttenmaer, C. A.; Crabtree, R. H.; Brudvig, G. W.; Batista, V. S. Energy Environ. Sci. 2009, 2, 1173.
[65] McNamara, W. R.; Milot, R. L.; Song, H.; Snoeberger, R. C.; Batista, V. S.; Schmuttenmaer, C. A.; Brudvig, G. W.; Crabtree, R. H. Energy Environ. Sci. 2010, 3, 917.
[66] Brewster, T. P.; Konezny, S. J.; Sheehan, S. W.; Martini, L. A.; Schmuttenmaer, C. A.; Batista, V. S.; Crabtree, R. H. Inorg. Chem. 2013, 52, 6752.
[67] Koenigsmann, C.; Ripolles, T. S.; Brennan, B. J.; Negre, C. F. A.; Koepf, M.; Durrell, A. C.; Milot, R. L.; Torre, J. A.; Crabtree, R. H.; Batista, V. S.; Brudvig, G.; Bisquert, J.; Schmuttenmaer, C. Phys. Chem. Chem. Phys. 2014, 16, 16629.
[68] Brennan, B. J.; Koenigsmann, C.; Materna, K. L.; Kim, P. M.; Koepf, M.; Crabtree, R. H.; Schmuttenmaer, C. A.; Brudvig, G. W. J. Phys. Chem. C 2016, 23, 12495.
[69] Bowman, D. N.; Mukherjee, S.; Barnes, L. J.; Jakubikova, E. J. Phys.:Condens. Matter. 2015, 27, 134205.
[70] Higashino, T.; Kurumisawa, Y.; Cai, N.; Fujimori, Y.; Tsuji, Y.; Nimura, S.; Packwood, D.; Jaehong Park, J.; Imahori, H. ChemSusChem 2017, 10, 3347.
[71] Politano, A.; Cattelan, M.; Boukhvalov, D. W.; Campi, D.; Cupolillo, A.; Agnoli, S.; Apostol, N. G.; Lacovig, P.; Lizzit, S.; Farías, D.; Chiarello, G.; Granozzi, G.; Larciprete, R. ACS Nano 2016, 10, 4543.
[72] Tsuji, K.; Tomita, O.; Higashi, M.; Abe, R. ChemSusChem 2016, 9, 2201.
[73] Zhang, Y.; Sun, Z.; Cheng, S.; Yan, F. ChemSusChem 2016, 9, 813.
[74] Kim, H. G.; Borse, P. H.; Choi, W.; Choi, W.; Lee, J. S. Angew. Chem., Int. Ed. 2005, 44, 4585.
[75] Zhang, X.; Peng, T.; Song, S. J. Mater. Chem. A 2016, 4, 2365.
[76] Fan, K.; Li, F. S.; Wang, L.; Daniel, Q.; Gabrielsson, E.; Sun, L. Phys. Chem. Chem. Phys. 2014, 16, 25234.
[77] Fan, K.; Li, F.; Wang, L.; Daniel, Q.; Gabrielsson, E.; Sun, L. J. Am. Chem. Soc. 2015, 137, 9153.
[78] Li, X.; Hu, Y.; Sanchez-Molina, I.; Zhou, Y.; Yu, F.; Haque, S. A.; Wu, W.; Hua, J.; Tian, H.; Robertson, N. J. Mater. Chem. A 2015, 3, 21733.
[79] Rao, C. N. R.; Lingampalli, S. R. Small 2016, 12, 16.
[80] Manfredi, N.; Cecconi, B.; Calabrese, V.; Minotti, A.; Peri, F.; Ruffo, R.; Monai, M.; Romero-Ocaña, I.; Montini, T.; Fornasiero, P.; Abbotto, A. Chem. Commun. 2016, 52, 6977.
[81] Maeda, K.; Eguchi, M.; Youngblood, W. J.; Mallouk, T. E. Chem Mater. 2008, 20, 6770.
[82] Bae, E. Y.; Choi, W.; Park, J.; Shin, H. S.; Kim, S. B.; Lee, J. S. J. Phys. Chem. B 2004, 108, 14093.
[83] Yu, F.; Cui, S.-C.; Li, X.; Peng, Y.; Yu, Y.; Yun, K.; Zhang, S.-C.; Li, J.; Liu, J.-G.; Hua, J. Dyes Pigm. 2017, 139, 7.
[84] Guerrero, G.; Alauzun, J. G.; Granier, M.; Laurencin, D.; Mutin, P. H. Dalton Trans. 2013, 42, 12569.
[85] Baker, D. R.; Kamat, P. V. Adv. Funct. Mater. 2009, 19, 805.
[86] Meng, Q. B. Acta Chim. Sinica 2015, 73, 161(in Chinese). (孟庆波, 化学学报, 2015, 73, 161.)
[87] Robel, I.; Subramanian, V.; Kuno, M.; Kamat, P. V. J. Am. Chem. Soc. 2006, 128, 2385.
[88] Ardalan, P.; Brennan, T. P.; Lee, H. B. R.; Bakke, J. R.; Ding, I. K.; McGehee, M. D.; Bent, S. F. ACS Nano 2011, 5, 1495.
[89] Yu, L.; Li, Z.; Song, H. J. Mater. Sci.:Mater. Electron. 2017, 28, 2867.
[90] Mora-Seró, I.; Giménez, S.; Moehl, T.; Fabregat-Santiago, F.; Lana-Villareal, T.; Gómez, R.; Bisquert, J. Nanotechnology 2008, 19, 424007.

染料敏化太阳电池:染料中稳定锚基团的研究进展

Dye-Sensitized Solar Cells: Progress on Robust Anchor Groups in Dyes

PDF

Knowledge

Abstract

Cite this article

share this article

References

Related Articles 15

Recommended Articles

Metrics

Comments

[1]	Liping Pang, Changjie Yang, Hongmin Lin, Xinyu Li, Haitao Tang, Yingming Pan. Porous Organophosphine Ligand Polymers as Recyclable Ligands for the Synthesis of Isoindolinone Compounds [J]. Chinese Journal of Organic Chemistry, 2022, 42(7): 2117-2123.
[2]	Mouxin Huang, Zongbin Jia, Sanzhong Luo, Jin-Pei Cheng. Quantitative Thermodynamic and Kinetic Parameters of Radical [J]. Chinese Journal of Organic Chemistry, 2021, 41(10): 3892-3902.
[3]	Jiang Hongji, He Xu, Li Xiong. Synthesis and Characterization of Blue Light Emitting Polymer Based on 2,4,6-Triphenyl-1,3,5-triazine and 1-(4-Hexyloxy)-benzene Functionalized Fluorene Units [J]. Chinese Journal of Organic Chemistry, 2020, 40(3): 763-773.
[4]	Tang Yue, Wang Min, Ding Yong, Li Jine, Chen Yihua. Improvement of Paulomycin Stability by Addition of Paulic Acid [J]. Chin. J. Org. Chem., 2018, 38(9): 2420-2426.
[5]	Jiang Shaoliang, Liu Jie, Cui Yanhong, Wu Huabiao, Han Liang. Syntheses and Photovoltaic Performance of Nitrogen-Containing Rigid Heterocycle Substituted Coumarin Sensitizing Dyes [J]. Chin. J. Org. Chem., 2018, 38(12): 3219-3226.
[6]	Chen Lei, Tang Xiang, Jia Kun, Tang Xianzhong. Synthesis and Properties of Organic Nonlinear Optical Chromophores Containing Azo- and Furan-Based Conjugated Bridge [J]. Chin. J. Org. Chem., 2016, 36(9): 2197-2203.
[7]	Li Lei, Zhu Zhitian, Jin Kaikai, Wang Jiajia, Zheng Shijun, Fang Qiang. Synthesis, Thermostability and Mechanical Properties of the Ether- Based Benzoxazine Resin with Benzoyl Moiety in the Side Chain [J]. Chin. J. Org. Chem., 2016, 36(4): 844-849.
[8]	Chen Huajie. Recent Advances in High-Mobility Polymeric Semiconductor Materials [J]. Chin. J. Org. Chem., 2016, 36(3): 460-479.
[9]	Cao Jie, Liao Chaoqiang, Yang Ling, Zhang Xuejun. Synthesis and Characterization of the Coumarin-Binuclear Zinc Phthalocyanine Formed by Droxynaphthyl Bridge [J]. Chin. J. Org. Chem., 2016, 36(1): 213-217.
[10]	Sun Jian, Jin Zheming, Wang Chengyun, Shen Yongjia. Synthesis and Properties of Extended Bis-1,2-dithiolene Nickel Complexes Substituted with Unsaturated Group [J]. Chin. J. Org. Chem., 2015, 35(9): 1948-1954.
[11]	Gu Chengzhi, Meng Shuxian, Feng Yaqing. Progress of Porphyrin Sensitizers for Dye-Sensitized Solar Cells [J]. Chin. J. Org. Chem., 2015, 35(6): 1229-1237.
[12]	Li Baolin. Furan Derivatives: An Emerging Class of Organic Semiconductors [J]. Chin. J. Org. Chem., 2015, 35(12): 2487-2506.
[13]	Cao Zhencai, He Zhou, Deng Lijun, Tan Songting. Synthesis and Photovoltaic Properties of Two Dimensional Organic Dyes Containing Benzothiadiazole Unit [J]. Chin. J. Org. Chem., 2014, 34(2): 340-348.
[14]	Zhang Yiliang, Zhang Gang. Vibrational Frequencies and Determination of Stability of Aromatic Molecules [J]. Chin. J. Org. Chem., 2014, 34(1): 178-189.
[15]	Wu Jianping, Lai Hua, Diao Shen, Jin Kaikai, Yuan Chao, Fang Qiang. Synthesis and Properties of the Polymer Based on Benzoxazine with Two Perfluorohexyl Side Chains [J]. Chin. J. Org. Chem., 2013, 33(05): 1042-1046.