Electron Diffusion and Back Reaction in Dye-Sensitized Solar Cells: The Effect of Nonlinear Recombination Kinetics

被引:110
作者
Villanueva-Cab, Julio [2 ]
Wang, Hongxia [1 ]
Oskam, Gerko [2 ]
Peter, Laurence M. [1 ]
机构
[1] Univ Bath, Dept Chem, Bath BA2 7AY, Avon, England
[2] IPN, CINVESTAV, Dept Fis Aplicada, Merida 97310, Yuc, Mexico
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2010年 / 1卷 / 04期
基金
英国工程与自然科学研究理事会;
关键词
PHOTOVOLTAGE; INJECTION; LENGTH;
D O I
10.1021/jz1000243
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The electron collection efficiency in dye-sensitized solar cells (DSCs) is usually related, to the electron diffusion length, L = (D tau)(1/2), where D is the diffusion coefficient of mobile electrons and r is their lifetime, which is determined by electron transfer to the redox electrolyte. Analysis of incident photon-to-current efficiency (IPCE) spectra for front and rear illumination consistently gives smaller values of L than those derived from small amplitude methods. We show that the IPCE analysis is incorrect if recombination is not first-order in free electron concentration, and we demonstrate that the intensity dependence of the apparent L derived by first-order analysis of IPCE measurements and the voltage dependence of L derived from perturbation experiments can be fitted using the same reaction order, gamma approximate to 0.8. The new analysis presented in this letter resolves the controversy over why L values derived from small amplitude methods are larger than those obtained from IPCE data.
引用
收藏
页码:748 / 751
页数:4
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