钙钛矿(结构)
材料科学
表面光电压
离子
带材弯曲
重组
再分配(选举)
光电子学
化学物理
可见光谱
化学
结晶学
光谱学
物理
生物化学
有机化学
量子力学
政治
政治学
法学
基因
作者
Jiangang Hu,Ronen Gottesman,Laxman Gouda,Adi Kama,Maayan Priel,Shay Tirosh,Juan Bisquert,Arie Zaban
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2017-04-07
卷期号:2 (5): 950-956
被引量:96
标识
DOI:10.1021/acsenergylett.7b00212
摘要
The photovoltage of perovskite solar cells (PSCs) was studied over a wide range of light intensities, showing changes from pristine to light-soaking (LS) conditions, explained using a specific model of spatial charge distribution. Migration of ions and vacancies under photovoltage conditions results in localized charge redistribution manifested as positive charge accumulation at the TiO2 or TiO2–MgO interlayer–perovskite interface, signifying photoinduced interfacial upward band bending. Consequentially, generation of an electrostatic potential (Velec) and an increase in interfacial recombination rate are confirmed. The magnitude and effect of Velec and interfacial recombination on the photovoltage depend on the illumination intensity and on the LS duration. PSCs with mesoporous Al2O3 showed similar changes, validating the role of the compact TiO2. Faster generation and a gradual increase of Velec are apparent under LS, which expresses the constant migration of ions and vacancies toward the interface. The nonrigid TiO2–perovskite interface calls for a vital perspective change of PSCs.
科研通智能强力驱动
Strongly Powered by AbleSci AI