Improving the TiO2 electron transport layer in perovskite solar cells using acetylacetonate-based additives

被引:105
作者
Wang, Hsin-Hua [1 ,2 ]
Chen, Qi [1 ,2 ]
Zhou, Huanping [1 ,2 ]
Song, Luo [1 ,2 ]
St Louis, Zac [1 ,2 ]
De Marco, Nicholas [1 ,2 ]
Fang, Yihao [1 ,2 ]
Sun, Pengyu [1 ]
Song, Tze-Bin [1 ,2 ]
Chen, Huajun [1 ]
Yang, Yang [1 ,2 ]
机构
[1] Univ Calif Los Angeles, Dept Mat Sci & Engn, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Calif NanoSyst Inst, Los Angeles, CA 90095 USA
基金
美国国家科学基金会;
关键词
HIGH-PERFORMANCE; EFFICIENCY; INTERFACE; DYNAMICS; ORIGINS; LENGTHS;
D O I
10.1039/c4ta06394e
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 developed a facile and quantitative method to improve the electron transport properties and resulting device performances of perovskite solar cells based on post-incorporation of various acetylacetonate additives. Previous studies rely on synthesis or soaking processes with limited additive control. Here, our acetylacetonated-based additives are used as effective intermediate gels to interact with TiO2 nanocrystals using a simple approach. The incorporation process can be controlled effectively and quantitatively using a range of additives from divalent (II), trivalent (III), and tetravalent (IV) to hexavalent (VI) acetylacetonate. Electronic parameters of solar cell devices, such as short circuit current (J(sc)) and fill factor (FF), are enhanced, regardless of the different valencies of the additives. Zirconium( IV) acetylacetonate was found to be the most effective additive, with average PCE improved from 15.0% to 15.8%. Detailed characterization experiments including transient photoluminescence spectra, ultra-violet photoelectron spectroscopy, photovoltage decay, and photocurrent decay indicate an improved interface with improved carrier extraction originating from the TiO2 modification.
引用
收藏
页码:9108 / 9115
页数:8
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