卤化物
三碘化物
材料科学
碘化物
钙钛矿(结构)
溴化物
电化学
兴奋剂
碘
无机化学
光电子学
分析化学(期刊)
化学工程
电极
色素敏化染料
化学
物理化学
电解质
有机化学
工程类
冶金
作者
Zhaojian Xu,Ross A. Kerner,Joseph J. Berry,Barry P. Rand
标识
DOI:10.1002/adfm.202203432
摘要
Abstract Owing to straightforward stoichiometry–bandgap tunability, mixed‐halide perovskites are ideal for many optoelectronic devices. However, unwanted halide segregation under operational conditions, including light illumination and voltage bias, restricts practical use. Additionally, the origin of voltage‐induced halide segregation is still unclear. Herein, a systematic voltage threshold study in mixed bromide/iodide perovskite devices is performed and leads to observation of three distinct voltage thresholds corresponding to the doping of the hole transport material (0.7 ± 0.1 V), halide segregation (0.95 ± 0.05 V), and degradation (1.15 ± 0.05 V) for an optically stable mixed‐halide perovskite composition with a low bromide content (10%). These empirical threshold voltages are minimally affected by composition until very Br‐rich compositions, which reveals the dominant role of iodide/triiodide/iodine electrochemistry in voltage‐induced Br/I phase separation and transport layer doping reactions in halide perovskite devices.
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