Australian Centre for Advanced Photovoltaics (ACAP), School of Photovoltaic and Renewable Energy Engineering, University of New South Wales , Sydney, New South Wales 2052, Australia.
ACS Appl Mater Interfaces. 2016 Mar 2;8(8):5351-7. doi: 10.1021/acsami.5b12376. Epub 2016 Feb 19.
Here, we investigate photoluminescence (PL) and time-resolved photoluminescence (TRPL) in CH3NH3PbBr3 perovskite under continuous illumination, using optical and electro-optical techniques. Under continuous excitation at constant intensity, PL intensity and PL decay (carrier recombination) exhibit excitation intensity dependent reductions in the time scale of seconds to minutes. The enhanced nonradiative recombination is ascribed to light activated negative ions and their accumulation which exhibit a slow dynamics in a time scale of seconds to minutes. The observed result suggests that the organic-inorganic hybrid perovskite is a mixed electronic-ionic semiconductor. The key findings in this work suggest that ions are photoactivated or electro-activated and their accumulation at localized sites can result in a change of carrier dynamics. The findings are therefore useful for the understanding of instability of perovskite solar cells and shed light on the necessary strategies for performance improvement.
在这里,我们使用光学和电光技术研究了 CH3NH3PbBr3 钙钛矿在连续光照下的光致发光(PL)和时间分辨光致发光(TRPL)。在恒定强度的连续激发下,PL 强度和 PL 衰减(载流子复合)在秒到分钟的时间尺度上表现出与激发强度相关的降低。增强的非辐射复合归因于光激活的负离子及其积累,它们在秒到分钟的时间尺度上表现出缓慢的动力学。观察到的结果表明,有机-无机杂化钙钛矿是一种混合电子-离子半导体。这项工作的主要发现表明,离子是光激活或电激活的,它们在局部位置的积累可能导致载流子动力学的变化。因此,这些发现有助于理解钙钛矿太阳能电池的不稳定性,并为提高性能提供了必要的策略。