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Giant switchable photovoltaic effect in organometal trihalide perovskite devices
Author(s) -
Zhengguo Xiao,
Yongbo Yuan,
Yuchuan Shao,
Qi Wang,
Qingfeng Dong,
Cheng Bi,
Pankaj Sharma,
Alexei Gruverman,
Jinsong Huang
Publication year - 2014
Publication title -
nature materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 14.344
H-Index - 483
eISSN - 1476-4660
pISSN - 1476-1122
DOI - 10.1038/nmat4150
Subject(s) - trihalide , photocurrent , perovskite (structure) , materials science , optoelectronics , ferroelectricity , photovoltaics , poling , electric field , photovoltaic system , solar cell , perovskite solar cell , photovoltaic effect , dielectric , nanotechnology , chemistry , electrical engineering , inorganic chemistry , physics , quantum mechanics , halide , crystallography , engineering
Organolead trihalide perovskite (OTP) materials are emerging as naturally abundant materials for low-cost, solution-processed and highly efficient solar cells. Here, we show that, in OTP-based photovoltaic devices with vertical and lateral cell configurations, the photocurrent direction can be switched repeatedly by applying a small electric field of <1 V μm(-1). The switchable photocurrent, generally observed in devices based on ferroelectric materials, reached 20.1 mA cm(-2) under one sun illumination in OTP devices with a vertical architecture, which is four orders of magnitude larger than that measured in other ferroelectric photovoltaic devices. This field-switchable photovoltaic effect can be explained by the formation of reversible p-i-n structures induced by ion drift in the perovskite layer. The demonstration of switchable OTP photovoltaics and electric-field-manipulated doping paves the way for innovative solar cell designs and for the exploitation of OTP materials in electrically and optically readable memristors and circuits.

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