Sensitized solar cells with colloidal PbS-CdS core-shell quantum dots

被引:118
作者
Lai, Lai-Hung [1 ]
Protesescu, Loredana [2 ,3 ]
Kovalenko, Maksym V. [2 ,3 ]
Loi, Maria A. [1 ]
机构
[1] Univ Groningen, Zernike Inst Adv Mat, NL-9747 AG Groningen, Netherlands
[2] ETH, Dept Chem & Appl Biosci, CH-8093 Zurich, Switzerland
[3] EMPA Swiss Fed Labs Mat Sci & Technol, CH-8600 Dubendorf, Switzerland
关键词
MULTIPLE EXCITON GENERATION; INTERFACIAL CHARGE-TRANSFER; TIO2; IMPEDANCE; TRANSPORT; RECOMBINATION; ELECTROLYTE; COLLECTION; EFFICIENCY; DIFFUSION;
D O I
10.1039/c3cp54145b
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 report on the fabrication of PbS-CdS (core-shell) quantum dot (QD)-sensitized solar cells by direct adsorption of core-shell QDs on mesoporous TiO2 followed by 3-mercaptopropionic acid ligand exchange. PbS-CdS QD-sensitized solar cells show 4 times higher efficiency with respect to solar cells sensitized with PbS QDs. The significantly enhanced mean electron lifetime and electron diffusion length provide crucial evidence for the higher efficiency of the cell. The average electron lifetime increases with the thickness of the CdS shell, demonstrating that the CdS shell plays an important role in preventing carrier recombination. However, owing to the barrier provided by the offset between the conduction bands of CdS and the PbS core, the CdS shell also hinders carrier injection from PbS to TiO2. Herein, we studied the effect of the shell thickness on cell's performance, showing a power conversion efficiency of 1.28% for PbS QDs with a 0.5 nm CdS shell. In addition, we demonstrate that the CdS shell effectively prevents photo-corrosion of PbS, resulting in devices with highly stable photocurrent.
引用
收藏
页码:736 / 742
页数:7
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