碘化物
钙钛矿(结构)
卤化物
材料科学
钙钛矿太阳能电池
铅(地质)
太阳能电池
氯化铅
透射电子显微镜
无机化学
化学工程
化学物理
化学
纳米技术
结晶学
光电子学
氯化物
冶金
工程类
地貌学
地质学
作者
Byung‐wook Park,Nir Kedem,Michael Kulbak,Do Yoon Lee,Woon Seok Yang,Nam Joong Jeon,Jangwon Seo,Geonhwa Kim,Ki Jeong Kim,Tae Joo Shin,Gary Hodes,David Cahen,Sang Il Seok
标识
DOI:10.1038/s41467-018-05583-w
摘要
The presence of excess lead iodide in halide perovskites has been key for surpassing 20% photon-to-power conversion efficiency. To achieve even higher power conversion efficiencies, it is important to understand the role of remnant lead iodide in these perovskites. To that end, we explored the mechanism facilitating this effect by identifying the impact of excess lead iodide within the perovskite film on charge diffusion length, using electron-beam-induced current measurements, and on film formation properties, from grazing-incidence wide-angle X-ray scattering and high-resolution transmission electron microscopy. Based on our results, we propose that excess lead iodide in the perovskite precursors can reduce the halide vacancy concentration and lead to formation of azimuthal angle-oriented cubic α-perovskite crystals in-between 0° and 90°. We further identify a higher perovskite carrier concentration inside the nanostructured titanium dioxide layer than in the capping layer. These effects are consistent with enhanced lead iodide-rich perovskite solar cell performance and illustrate the role of lead iodide.
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