新型高效双供体型有机染料的设计及理论研究
[1] Grtzel M. Recent Advances in Sensitized Mesoscopic Solar Cells[J]. Accounts of Chemical Research, 2009, 42(11): 1788-1798.
[2] O'regan B, Grtzel M. A Low-cost,High-efficiency Solar Cell Based on Dye-sensitized Colloidal TiO2 Films[J]. Nature, 1991, 353(6346): 737-740.
[3] 于利成, 李洪飞. 染料敏化太阳能电池研究进展[J]. 材料导报, 2011, 11(2): 7-18.
[4] Yu Q, Wang Y, Yi Z, et al. High-efficiency Dye-sensitized Solar Cells: the Influence of Lithium Ions on Exciton Dissociation, Charge Recombination, and Surface States[J]. ACS Nano, 2010, 4(10): 6032-6038.
[5] Wen Y, Wu W, Li Y, et al. First Principles Study of Thieno[2,3-b] Indole-based Organic Dyes for Dye-sensitized Solar Cells: Screen Novel π-linkers and Explore the Interface Between Photosensitizers and TiO2[J]. Journal of Power Sources, 2016, 326(15): 193-202.
[6] Chaurasia S, Lin J T. Metal-free Sensitizers for Dye-sensitized Solar Cells[J]. Chemical Record, 2016, 16(3): 1311-1336.
[7] Wang P, Yao Z, Wu H, et al. Dithienopicenocarbazole as the Kernel Module of Low-energy-gap Organic Dyes for Efficient Conversion of Sunlight to Electricit[J]. Energy & Environmental Science, 2015, 8 (11): 3192-3197.
[8] Kakiage K, Aoyama Y, Yano T, et al. Highly-efficient Dye-sensitized Solar Cells with Collaborative Sensitization by Silyl-anchor and Carboxy-anchor Dyes[J]. Chemical Communications, 2015, 51(88): 15894.
[9] Zhong C, Gao J, Cui Y, et al. Coumarin-bearing Triarylamine Sensitizers with High Molar Extinction Coefficient for Dye-sensitized Solar Cells[J]. Journal of Power Sources, 2015, 273(6): 831-838.
[10] Tian H, Yang X, Chen R, et al. Phenothiazine Derivatives for Efficient Organic Dye-sensitized Solar Cells[J]. Chemical Communications, 2007, 36(36): 3741.
[11] Zeng W, Cao Y, Bai Y, et al. Efficient Dye-sensitized Solar Cells with an Organic Photosensitizer Featuring Orderly Conjugated Ethylenedioxythiophene and dithienosilole blocks[J]. Chemistry of Materials, 2010, 22 (5): 1915-1925.
[12] Feng H, Li R, Song Y, et al. Novel D-π-A-π-A Coumarin Dyes for Highly Efficient Dye-sensitized Solar Cells: Effect of π-bridge on Optical, Electrochemical, and Photovoltaic performance[J]. Journal of Power Sources, 2017, 345: 59-66.
[13] Iqbal Z, Wu W Q. Trilateral π-conjugation Extensions of Phenothiazine-based Dyes Enhance the Photovoltaic Performance of the Dye-sensitized Solar Cells[J]. Dyes & Pigments, 2016, 124(124): 63-71.
[14] Cai N, Moon S J, Cevey-Ha L, et al. An Organic D-π-A Dye for Record Efficiency Solid-state Sensitized Heterojunction Solar Cells[J]. Nano Letters, 2011, 11(4): 1452.
[15] Yang J B, Ganesan P, Teuscher J, et al. Influence of the Donor Size in D-pi-A Organic Dyes for Dye-sensitized Solar Cells[J]. Journal of the American Chemical Society, 2014, 136(15): 5722-5730.
[16] Wang S, Wang H R, Guo J C, et al. Influence of the Terminal Electron Donor in D-D-π-A Phenothiazine Dyes for Dye-sensitized Solar Cells[J]. Dyes & Pigments, 2014, 109: 96-104.
[17] Liu X, Cao Z, Huang H, et al. Novel D-D-π-A Organic Dyes Based on Triphenylamine and Indole-derivatives for High Performance Dye-sensitized Solar Cells[J]. Journal of Power Sources, 2014, 248(15): 400-406.
[18] Ning Z, Zhang Q, Wu W, et al. Starburst Triarylamine Based Dyes for Efficient Dye-sensitized Solar Cells[J]. Journal of Organic Chemistry, 2008, 73(10): 3791.
[19] Chai Q, Li W, Zhu S, et al. Influence of Donor Configurations on Photophysical, Electrochemical, and Photovoltaic Performances in D-π-A Organic Sensitizers[J]. Acs Sustainable Chemistry & Engineering, 2014, 2(2): 239-247.
[20] Yuan R, Liu Z, Wan Y, et al. New D-D-p-A-type Indol-triarylamine Sensitizers for Ef cient Dye-sensitized Solar Cells[J]. Synthetic Metals, 2016, 215(215): 21-27.
[21] He J, Liu Y, Gao J, et al. New D-D-π-A Triphenylamine-coumarin Sensitizers for Dye-sensitized Solar Cells[J]. Photochemical & Photobiological Sciences Official Journal of the European Photochemistry Association & the European Society for Photobiology, 2017, 16(7): 1049-1056.
[22] Dai P, Yang L, Liang M, et al. Influence of the Terminal Electron Donor in D-D-π-A Organic Dye-sensitized Solar Cells: Dithieno[3,2-b:2,3-d]pyrrole Versus Bis(amine)[J]. Acs Applied Materials & Interfaces, 2015, 7(40): 22436-22447.
[23] Frisch M. et al. DJ Fox. Gaussian 09[CP]. Revision C. 01. Gaussian, Inc.: Wallingford, CT, 2009.
[24] Becke A D. Density‐functional thermochemistry. III. The role of exact exchange[J]. The Journal of Chemical Physics, 98(1993): 5648-5652.
[25] Zhang M, Wang Y, Xu M, et al. Design of High-efficiency Organic Dyes for Titania Solar Cells Based on the Chromophoric Core of Cyclopentadithiophene-benzothiadiazole[J]. Energy & Environmental Science, 2013, 6(10): 2944-2949.
[26] Chattopadhyay D, Lastella S, Kim S, et al. Length Separation of Zwitterion-functionalized Single Wall Carbon Nanotubes by GPC[J]. Journal of the American Chemical Society, 2002, 124(5): 728-729.
[27] Yanai T, Tew D P, Handy N C. A New Hybrid Exchange-correlation Functional Using the Coulomb-attenuating Method (CAM-B3LYP)[J]. Chemical Physics Letters, 2004, 393(1-3): 51-57.
[28] Chaitanya K, Ju X -H, Heron B M. Can Elongation of the p-system in Triarylamine Derived Sensitizers with Either Benzothiadiazole and/or Ortho-fluorophenyl Moieties Enrich Their Light Harvesting Efficiency -a theoretical Study[J]. Rsc Advances, 2014, 5(6): 3978-3998.
[29] Delley B. An All Electron Numerical Method for Solving the Local Density Functional for Polyatomic Molecules[J]. Journal of Chemical Physics, 1990, 92(1): 508-517.
[30] Perdew J, Burke K, Ernzerh M. Generalized Gradient Approximation Made Simple[J]. Physical Review Letters, 1997, 78(18).
邵迪, 唐炼, 邵长金. 新型高效双供体型有机染料的设计及理论研究[J]. 红外, 2018, 39(3): 36. SHAO Di, TANG Lian, SHAO Chang-Jin. Design and Theoretical Study of New Type of High Efficiency Dual Donors Type Organic Dyes[J]. INFRARED, 2018, 39(3): 36.