[1] Hagfeldt A, Gratzel M. Light-induced redox reactions in nanocrystalline systems[J]. Chemical Reviews, 1995, 95(1):49-68.
[2] Wang Z S,Cui Y,Danoh Y, Kasada C, Shinpo A A, Hara K. Thiophene-functionalized coumarin dye for efficient dye-sensitized solar cells:electron lifetime improved by coadsorption of deoxycholic acid[J]. The Journal of Physical Chemistry C, 2007, 111(19):7224-7230.
[3] Yang H Y, Yen Y S, Hsu Y C, Chou H H, Lin J T.Organic dyes incorporating the dithieno[3, 2-b:2', 3'-d] thiophene moiety for efficient dye-sensitized solar cells[J]. Organic Letters, 2009, 12(1):16-19.
[4] Im H B, Kim S K, Park C M, Jang S H, Kim C J, Kim K K, Park N G, Kim C H. High performance organic photosensitizers for dye-sensitized solar cells[J]. Chemical Communications, 2010, 46(8):1335-1337.
[5] Nazeeruddin M K, Péchy P, Renouard T, Zakeeruddin S M, Humphry-Baker R, Comte P, Liska P, Cevey L, Costa E, Shklover V, Spiccia L, Deacon G B,Bignozzi C A, Grätzel M. Engineering of efficient panchromatic sensitizers for nanocrystalline TiO2-based solar cells[J]. Journal of the American Chemical Society, 2001, 123(8):1613-1624.
[6] Mishra A, Fischer M K R, Bäuerle P. Metal-free organic dyes for dye-sensitized solar cells:from structure:property relationships to design rules[J]. Angewandte Chemie International Edition, 2009, 48(14):2474-2499.
[7] 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. D-A-π-A结构染料敏化剂研究进展[J]. 有机化学, 2015, 35(11):2237-2258. Yang H W,Guan J J, Gao F X, He X P, Wang A, Sun B D, Zhang X Q, Zhang B, Feng Y G. The research progress of dye sensitizer with D-A-π-A structure[J].Organic Chemi-stry, 2015, 35(11):2237-2258.
[8] 李晶,武文俊,贺锦香,花建丽. 基于苯并噻二唑的菁染料敏化剂的合成与光伏性能研究[J]. 化学学报,2010, 68(24):2551-2558. Li J, Wu W J, He J X, Hua J L. Synthesis and photovoltaic properties of benzothiadiazole based cyanine dyes for dye-sensitized solar cells[J]. Acta Chimica Sinica, 2010, 68(24):2551-2558.
[9] Chen B S, Chen D Y, Chen C L, Hsu C W, Hsu H C, Wu K L, Liu S H, Chou P T, Chi Y. Donor-acceptor dyes with fluorine substituted phenylene spacer for dye-sensitized solar cells[J]. Journal of Materials Chemistry, 2011, 21(6):1937-1945.
[10] Hua Y, Chang S, Huang D D, Zhou X, Zhu X J, Zhao J Z, Chen T, Wong W Y, Wong W K. Significant improvement of dye-sensitized solar cell performance using simple phenothiazine-based dyes[J]. Chemistry of Materials, 2013, 25(10):2146-2153.
[11] Cao D R, Peng J N, Hong Y P, Fang X M, Wang L Y, Herbert M. Enhanced performance of the dye-sensitized solar cells with phenothiazine-based dyes containing double D-A branches[J]. Organic Letters, 2011, 13(7):1610-1613.
[12] Zang X F, Xu Y F, Iqbal Z, Huang Z S, Kuang D B, Wang L Y, Herbert Meierc, Ying Lid, Cao D R. Synthesis and photovoltaic performance of dihydrodibenzoazepine-based sensitizers with additional lateral anchor[J]. Dyes and Pigments, 2013, 99(3):1072-1081.
[13] Hart A S, K C CB, Subbaiyan N K, Karr P A, D'Souza F. Phenothiazine-sensitized organic solar cells:effect of dye anchor group positioning on the cell performance[J]. ACS Applied Materials & Interfaces, 2012, 4(11):5813-5820.
[14] Li H Y, Hou Y Q, Yang Y Z, Tang R L, Chen J N, Wang H, Han H W, Peng T Y, Li Q Q, Li Z. Attempt to improve the performance of pyrrole-containing dyes in dye sensitized solar cells by adjusting isolation groups[J]. ACS Applied Materials & Interfaces, 2013, 5(23):12469-12477.
[15] Xu Y J, Liang M, Liu X J, Han H Y, Sun Z, Xue S. Synthesis of triarylamine dyes containing secondary electron-donating groups and application in the dye-sensitized solar cells[J]. Synthetic Metals, 2011, 161(5):496-503.
[16] Tan H J, Pan C Y, Wang G, Wu Y Y, Zhang Y P, Yu G P, Zhang M. A comparative study on properties of two phenoxazine-based dyes for dye-sensitized solar cells[J]. Dyes and Pigments, 2014, 101:67-73.
[17] Chang Y J, Chou P T, Lin Y Z, Watanabe M, Yang C J, Chin T M, Chow T J. Organic dyes containing oligo-phenothiazine for dye-sensitized solar cells[J]. Journal of Materials Chemistry, 2012, 22(40):21704-21712.
[18] Wu Y, Zhu W. Organic sensitizers from D-π-A to D-A-π-A:effect of the internal electron-withdrawing units on molecular absorption, energy levels and photovoltaic perfor-mances[J]. Chemical Society Reviews, 2013, 42(5):2039-2058.
[19] Li H Y, Yang L Y, Tang R L, Hou Y Q, Yang Y Z, Wang H, Han H W, Qin J G, Li Q Q, Li Z. Organic dyes incorporating N-functionalized pyrrole as conjugated bridge for dye-sensitized solar cells:convenient synthesis, additional withdrawing group on the π-bridge and the suppressed aggregation[J]. Dyes and Pigments, 2013, 99(3):863-870.
[20] Zafar I, Wu W Q, Zhang H, Han L J, Fang X M, Wang L Y, Kuang D B, Meier H, Cao D R. Influence of spatial arrangements of π-spacer and accepter of phenothiazine based dyes on the performance of dye-sensitized solar cells[J]. Organic Electronics, 2014, 14:2662-2672.
[21] Geng Y, Flavia P, Yi C Y, Avarvari N, Grätzel M, Decurtins S, Liu S X. Electronic tuning effects via π-linkers in tetrathiafulvalene-based dyes[J]. New Journal of Chemistry, 2014, 38(7):3269-3274.
[22] Hong Y P, Liao J Y, Cao D R, Zang X F, Kuang D B, Wang L Y, Meier H, Su C Y. Organic dye bearing asymmetric double donor-π-acceptor chains for dye-sensitized solar cells[J]. The Journal of Organic Chemistry, 2011, 76(19):8015-8021.
[23] Kumar C V, Raptis D, Koukaras E N, Sygellou L, Lianos P. Study of an indoline-phenothiazine based organic dye for dye-sensitized solar cells theoretical calculations and experimental data[J]. Organic Electronics, 2015, 25:66-73.
[24] Chen R K, Yang X C, Tian H N, Wang X N, Hagfeldt A, Sun L C. Effect of tetrahydroquinoline dyes structure on the performance of organic dye-sensitized solar cells[J]. Chemistry of Materials, 2007, 19(16):4007-4015.
[25] Pommerehne J, Vestweber H, Guss W, Mahrt R F, Bässler H, Porsch M, Daub J. Efficient two layer leds on a polymer blend basis[J]. Advanced Materials, 1995, 7:551-554.
[26] Wei L G, Yang Y L, Fan R Q, Wang P, Dong Y W, Zhou W, Luan T Z. Enhance the performance of co-sensitized solar cell by a series efficient pyridine-anchor co-adsorbents of N,N'-bis((pyridin-2-yl) methylene)-p-phenylenediimine and a ruthenium dye of N719[J]. Journal of Power Sources, 2015, 293:203-212.
[27] O 'Regan B C, López-Duarte I, Martínez-Díaz M V, Forneli A, Albero J, Morandeira A, Palomares E, Torres T, Durrant J R. Catalysis of recombination and its limitation on open circuit voltage for dye sensitized photovoltaic cells using phthalocyanine dyes[J]. Journal of the American Chemical Society, 2008, 130(10):2906-2907.
[28] O Regan B C, Walley K, Juozapavicius M, Anderson A, Matar F, Ghaddar T, Zakeeruddin S M, Klein C, Durrant J R. Structure/function relationships in dyes for solar energy conversion:a two-atom change in dye structure and the mechanism for its effect on cell voltage[J]. Journal of the American Chemical Society, 2009, 131(10):3541-3548.
[29] Kumar C V, Raptis D, Koukaras E N, Sygellou L, Lianos P. Study of an indoline-phenothiazine based organic dye for dye-sensitized solar cells. Theoretical calculations and experimental data[J]. Organic Electronics, 2015, 25:66-73. |