Direct Spectroscopic Evidence of Ultrafast Electron Transfer from a Low Band Gap Polymer to CdSe Quantum Dots in Hybrid Photovoltaic Thin Films

被引:34
作者
Couderc, Elsa
Greaney, Matthew J.
Brutchey, Richard L. [1 ]
Bradforth, Stephen E.
机构
[1] Univ So Calif, Dept Chem, Los Angeles, CA 90089 USA
关键词
HETEROJUNCTION SOLAR-CELLS; CHARGE-TRANSFER STATE; TERT-BUTYLTHIOL; GENERATION; ENERGY; PHOTOCURRENT; EFFICIENCY; RELAXATION; DYNAMICS; PHOTOGENERATION;
D O I
10.1021/ja406884h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ultrafast transient absorption spectroscopy is used to study charge transfer dynamics in hybrid films composed of the low band gap polymer PCPDTBT and CdSe quantum dots capped with tert-butylthiol ligands. By selectively exciting the polymer, a spectral signature for electrons on the quantum dots appears on ultrafast time scales (less than or similar to 65 fs), which indicates ultrafast electron transfer. From this time scale, the coupling between the polymer chains and the quantum dots is estimated to be J greater than or similar to 17 meV. The reduced quantum dot acceptors exhibit an unambiguous spectral bleach signature, whose amplitude allows for the first direct calculation of the absolute electron transfer yield in a hybrid solar cell (82 +/- 5%). We also show that a limitation of the hybrid system is rapid and measurable geminate recombination due to the small separation of the initial charge pair. The fast recombination is consistent with the internal quantum efficiency corresponding solar cell. We therefore have identified and quantified a main loss mechanism in this type of third generation solar cell.
引用
收藏
页码:18418 / 18426
页数:9
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