卤化物
离子
材料科学
钙钛矿(结构)
化学物理
电迁移率
离子键合
电子迁移率
金属
电极
分析化学(期刊)
电场
离子运输机
无机化学
光电子学
电流(流体)
航程(航空)
不稳定性
电流密度
暗电流
化学
联轴节(管道)
离子流
场效应晶体管
离子电导率
电阻率和电导率
串联
溴化物
锡
凝聚态物理
作者
Marisé García‐Batlle,Sarah Deumel,Judith E. Huerdler,Sandro F. Tedde,Osbel Almora,Germà García-Belmonte
标识
DOI:10.1002/adpr.202200136
摘要
Ion transport properties in metal halide perovskite still constitute a subject of intense research because of the evident connection between mobile defects and device performance and operation degradation. In the case of X‐ray detectors, dark current level and instability are regarded to be connected to the ion migration upon bias application. Two compositions (MAPbBr 3 and MAPbI 3 ) and structures (single‐ and microcrystalline) are checked by the analysis of long‐term dark current evolution. Electronic current increases with time before reaching a steady‐state value within a response time (from 10 4 down to 10 s) that strongly depends on the applied bias. A coupling between electronic transport and ion kinetics exists that ultimately establishes the time scale of electronic current. Effective ion mobility is extracted for a range of applied electric field ξ . While ion mobility results field‐independent in the case of MAPbI 3 , a clear field enhancement is observed for MAPbBr 3 (), irrespective of the crystallinity. Both perovskite compounds present effective ion mobility in the range of ≈ 10 −7 –10 −6 cm −2 V −1 s −1 , in accordance with previous analyses. The ξ ‐dependence of the ion mobility is related to the lower ionic concentration of the bromide compound. Slower migrating defect drift is suppressed in the case of MAPbBr 3 , in opposition to that observed here for MAPbI 3 .
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