钝化
钙钛矿(结构)
光电流
材料科学
纳秒
光谱学
化学物理
载流子寿命
扩散
光电子学
超快激光光谱学
化学
纳米技术
光学
物理
硅
结晶学
热力学
量子力学
激光器
图层(电子)
作者
Jiaxin Pan,Ziming Chen,Tiankai Zhang,Beier Hu,Haoqing Ning,Z. Meng,Zhicheng Su,Davide Nodari,Weidong Xu,Ganghong Min,Mengyun Chen,Xianjie Liu,Nicola Gasparini,Saif A. Haque,Piers R. F. Barnes,Feng Gao,Artem A. Bakulin
标识
DOI:10.1038/s41467-023-43852-5
摘要
Conventional spectroscopies are not sufficiently selective to comprehensively understand the behaviour of trapped carriers in perovskite solar cells, particularly under their working conditions. Here we use infrared optical activation spectroscopy (i.e., pump-push-photocurrent), to observe the properties and real-time dynamics of trapped carriers within operando perovskite solar cells. We compare behaviour differences of trapped holes in pristine and surface-passivated FA0.99Cs0.01PbI3 devices using a combination of quasi-steady-state and nanosecond time-resolved pump-push-photocurrent, as well as kinetic and drift-diffusion models. We find a two-step trap-filling process: the rapid filling (~10 ns) of low-density traps in the bulk of perovskite, followed by the slower filling (~100 ns) of high-density traps at the perovskite/hole transport material interface. Surface passivation by n-octylammonium iodide dramatically reduces the number of trap states (~50 times), improving the device performance substantially. Moreover, the activation energy (~280 meV) of the dominant hole traps remains similar with and without surface passivation.
科研通智能强力驱动
Strongly Powered by AbleSci AI