钙钛矿(结构)
钝化
开路电压
晶界
光致发光
光电子学
载流子寿命
材料科学
载流子
能量转换效率
电压
带隙
化学物理
化学
纳米技术
硅
电气工程
结晶学
冶金
工程类
微观结构
图层(电子)
作者
Nicholas De Marco,Huanping Zhou,Qi Chen,Pengyu Sun,Zonghao Liu,Lei Meng,En‐Ping Yao,Yongsheng Liu,Andy Schiffer,Yang Yang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2016-01-20
卷期号:16 (2): 1009-1016
被引量:520
标识
DOI:10.1021/acs.nanolett.5b04060
摘要
Hybrid perovskites have shown astonishing power conversion efficiencies owed to their remarkable absorber characteristics including long carrier lifetimes, and a relatively substantial defect tolerance for solution-processed polycrystalline films. However, nonradiative charge carrier recombination at grain boundaries limits open circuit voltages and consequent performance improvements of perovskite solar cells. Here we address such recombination pathways and demonstrate a passivation effect through guanidinium-based additives to achieve extraordinarily enhanced carrier lifetimes and higher obtainable open circuit voltages. Time-resolved photoluminescence measurements yield carrier lifetimes in guanidinium-based films an order of magnitude greater than pure-methylammonium counterparts, giving rise to higher device open circuit voltages and power conversion efficiencies exceeding 17%. A reduction in defect activation energy of over 30% calculated via admittance spectroscopy and confocal fluorescence intensity mapping indicates successful passivation of recombination/trap centers at grain boundaries. We speculate that guanidinium ions serve to suppress formation of iodide vacancies and passivate under-coordinated iodine species at grain boundaries and within the bulk through their hydrogen bonding capability. These results present a simple method for suppressing nonradiative carrier loss in hybrid perovskites to further improve performances toward highly efficient solar cells.
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