材料科学
光致发光
电场
消灭
电介质
钙钛矿(结构)
猝灭(荧光)
微晶
斯塔克效应
重组
卤化物
凝聚态物理
离子
光电子学
原子物理学
分子物理学
荧光
光学
结晶学
物理
化学
无机化学
量子力学
基因
冶金
生物化学
作者
Ruiyun Chen,Jun Li,Alexander Dobrovolsky,Soranyel González‐Carrero,Marina Gerhard,Maria E. Messing,Vladimir S. Chirvony,Julia Pérez‐Prieto,Ivan G. Scheblykin
标识
DOI:10.1002/adom.201901642
摘要
Abstract Metal halide perovskites are promising optoelectronic materials. Their electronic properties however are rather unstable which is often assigned to ion migration. Ion migration can be readily influenced by an electric field (EF). Here, the response of photoluminescence (PL) of individual MAPbX 3 (MA = CH 3 NH 3 , X = I, Br) sub‐micrometer‐sized polycrystals to EF is studied. Alternating EF with frequency higher than 10 Hz is found to reversibly quench PL. It is proposed that an alternating EF when applied together with light increases ion migration. This leads to a shift in the equilibrium between creation and annihilation of defects toward higher concentration of nonradiative recombination centers. The PL quenching is found to increase with increasing frequency of the field. This can be rationalized by the frequency dependence of the dielectric constant, leading to stronger internal fields for high modulation frequencies compared to, e.g., a constant EF with the same external amplitude. PL quenching and enhancement observed under constant EF are hypothesized to be due to a reconfiguration of already existing nonradiative recombination centers situated on grain boundaries. The control of perovskite PL by alternating EF reported here can find applications in optoelectronic devices.
科研通智能强力驱动
Strongly Powered by AbleSci AI