Novel D-π-A structured porphyrin dyes containing various diarylamino moieties for dye-sensitized solar cells

被引:24
作者
Liang, Yuxia [1 ,2 ]
Xue, Xiaodong [1 ]
Zhang, Weihong [1 ]
Fan, Chencheng [1 ]
Li, Yuanchao [1 ]
Zhang, Bao [1 ]
Feng, Yaqing [1 ,2 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Tianjin 300072, Peoples R China
[2] Tianjin Univ, Tianjin Coinnovat Ctr Chem Sci & Engn, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
Dye-sensitized solar cells; Porphyrin; Photovoltaic; Meso position; Fukui function; Charge transfer; MOLECULAR DESIGN; HIGHLY-EFFICIENT; ORGANIC-DYES; DENSITY; PERFORMANCE; DERIVATIVES; OXIDE; ZN; MG;
D O I
10.1016/j.dyepig.2014.12.006
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A series of novel zinc porphyrins which are featured with a donor-pi-acceptor structure have been synthesized for use in the dye-sensitized solar cells. Various diarylamine moiety, such as diphenylamine, iminodibenzyl or iminostilbene, is introduced at porphyrin mesa position as an electron donating group. The cell fabricated with the iminodibenzyl-substituted porphyrin sensitizer yields a short circuit photocurrent density of 9.68 mA/cm(2), an open-circuit voltage of 740 mV, and a fill factor of 73.48%, corresponding to an overall conversion efficiency (eta) up to 5.26%, which is greater than those obtained by diphenylamine- and iminostilbene-substituted porphyrin-sensitized solar cells (eta = 4.05% and 2.62%, respectively). The theoretical studies reveal that the iminodibenzyl donor has the strongest electron donating ability among all three diarylamine substituents employed, which is believed to play a significant role in influencing the photovoltaic properties of these sensitizer-based solar cells. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7 / 16
页数:10
相关论文
共 49 条
[1]   DFT/TD-DFT molecular design of porphyrin analogues for use in dye-sensitized solar cells [J].
Balanay, Mannix P. ;
Kim, Dong Hee .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2008, 10 (33) :5121-5127
[2]   Electron Lifetime in Dye-Sensitized Solar Cells: Theory and Interpretation of Measurements [J].
Bisquert, Juan ;
Fabregat-Santiago, Francisco ;
Mora-Sero, Ivan ;
Garcia-Belmonte, Germa ;
Gimenez, Sixto .
JOURNAL OF PHYSICAL CHEMISTRY C, 2009, 113 (40) :17278-17290
[3]   A strategy to design highly efficient porphyrin sensitizers for dye-sensitized solar cells [J].
Chang, Yu-Cheng ;
Wang, Chin-Li ;
Pan, Tsung-Yu ;
Hong, Shang-Hao ;
Lan, Chi-Ming ;
Kuo, Hshin-Hui ;
Lo, Chen-Fu ;
Hsu, Hung-Yu ;
Lin, Ching-Yao ;
Diau, Eric Wei-Guang .
CHEMICAL COMMUNICATIONS, 2011, 47 (31) :8910-8912
[4]   Opp-Dibenzoporphyrins as a Light-Harvester for Dye-Sensitized Solar Cells [J].
Deshpande, Rohit ;
Wang, Bo ;
Dai, Lin ;
Jiang, Lin ;
Hartley, C. Scott ;
Zou, Shouzhong ;
Wang, Hong ;
Kerr, Lei .
CHEMISTRY-AN ASIAN JOURNAL, 2012, 7 (11) :2662-2669
[5]   Tetrakis(thiadiazole)porphyrazines.: 5.: Electrochemical and DFT/TDDFT studies of the free-base macrocycle and its MgII, ZnII, and CuII complexes [J].
Donzello, Maria Pia ;
Ercolani, Claudio ;
Kadish, Karl M. ;
Ricciardi, Giampaolo ;
Rosa, Angela ;
Stuzhin, Pavel A. .
INORGANIC CHEMISTRY, 2007, 46 (10) :4145-4157
[6]   Electron Transport and Recombination in Solid-State Dye Solar Cell with Spiro-OMeTAD as Hole Conductor [J].
Fabregat-Santiago, Francisco ;
Bisquert, Juan ;
Cevey, Le ;
Chen, Peter ;
Wang, Mingkui ;
Zakeeruddin, Shaik M. ;
Graetzel, Michael .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (02) :558-562
[7]  
Frisch M. J., 2004, GAUSSIAN 03 REVISION
[8]   Molecular design of coumarin dyes for efficient dye-sensitized solar cells [J].
Hara, K ;
Sato, T ;
Katoh, R ;
Furube, A ;
Ohga, Y ;
Shinpo, A ;
Suga, S ;
Sayama, K ;
Sugihara, H ;
Arakawa, H .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (02) :597-606
[9]   High efficiency of dye-sensitized solar cells based on metal-free indoline dyes [J].
Horiuchi, T ;
Miura, H ;
Sumioka, K ;
Uchida, S .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (39) :12218-12219
[10]   Highly-efficient metal-free organic dyes for dye-sensitized solar cells [J].
Horiuchi, T ;
Miura, H ;
Uchida, S .
CHEMICAL COMMUNICATIONS, 2003, (24) :3036-3037