卤化物
碘化物
溴化物
光致发光
超快激光光谱学
化学
量子产额
辐照
离子
相(物质)
激发态
吸收(声学)
光化学
钙钛矿(结构)
分析化学(期刊)
化学物理
材料科学
光谱学
无机化学
结晶学
光电子学
原子物理学
光学
物理
复合材料
量子力学
有机化学
核物理学
色谱法
荧光
作者
Seog Joon Yoon,Sergiu Draguta,Joseph S. Manser,Onise Sharia,William F. Schneider,Masaru Kuno,Prashant V. Kamat
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2016-06-22
卷期号:1 (1): 290-296
被引量:305
标识
DOI:10.1021/acsenergylett.6b00158
摘要
Mixed halide lead perovskites (e.g., CH3NH3PbBrxI3–x) undergo phase segregation creating iodide-rich and bromide-rich domains when subjected to visible irradiation. This intriguing aspect of halide ion movement in mixed halide films is now being tracked through excited-state behavior using emission and transient absorption spectroscopy tools. These transient experiments have allowed us to establish the time scale with which such separation occurs under laser irradiation (405 nm, 25 mW/cm2 to 1.7 W/cm2) as well as dark recovery. While the phase separation occurs with a rate constant of 0.1–0.3 s–1, the recovery occurs over a time period of several minutes to an hour. The relative photoluminescence quantum yield observed for Br-rich regions (em. max 530 nm) is nearly 2 orders of magnitude lower than that of I-rich regions (em. max 760 nm) and arises from the fact that I-rich regions serve as sinks for photogenerated charge carriers. Understanding such cascading charge transfer to localized sites could further enable the design of gradient halide structures in mixed halide systems.
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