Quantifying Regeneration in Dye-Sensitized Solar Cells

被引:180
|
作者
Anderson, Assaf Y. [1 ]
Barnes, Piers R. F. [1 ]
Durrant, James R. [1 ]
O'Regan, Brian C. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Chem, London SW7 2AZ, England
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2011年 / 115卷 / 05期
基金
英国工程与自然科学研究理事会;
关键词
NANOCRYSTALLINE TITANIUM-DIOXIDE; ELECTRON-TRANSFER; TRANSIENT ABSORPTION; TIO2; FILMS; CHARGE RECOMBINATION; RUTHENIUM; EFFICIENCY; DYNAMICS; IODIDE; INJECTION;
D O I
10.1021/jp1101048
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
We propose and apply a new experimental protocol for determining the kinetics of the oxidation of iodide (aka dye regeneration) in dye sensitized solar cells (DSSCs) using measurements on full cells under operating conditions. Transient absorption (TA) decays of the oxidized dye after a laser pulse are correlated with the short circuit current (J(sc)) and electron concentration in the TiO2, measured during the TA experiment. Results for a series of cells with N719 [(Bu4N)(2)][Ru(dcbpyH)(2)-(NCS)(2)] (dcbpy = 4,4'-dicarboxy-2,2'-bipyridyl), a standard electrolyte, and varying iodide concentration allow us to fit for the fundamental regeneration rate constant (k(rg) = 7.8 x 10(5)M(-1) s(-1)) and to determine that the order in iodide, in these cells, is near 1 (0.98 +/- 0.16) and dearly not 2. The rate and order allow us to rank various reaction mechanisms and to discuss possible rate-limiting steps that could be catalyzed to improve regeneration. The method can also give estimates of the fundamental rate constant for electron dye recombination (EDR) and the apparent reaction order in total electron concentration.
引用
收藏
页码:2439 / 2447
页数:9
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