Charge carrier chemistry in methylammonium lead iodide

被引:35
|
作者
Senocrate, Alessandro [1 ,2 ]
Yang, Tae-Youl [1 ,3 ]
Gregori, Giuliano [1 ]
Kim, Gee Yeong [1 ]
Graetzel, Michael [1 ,2 ]
Maier, Joachim [1 ]
机构
[1] Max Planck Inst Solid State Res, Heisenbergstr 1, D-70569 Stuttgart, Germany
[2] Swiss Fed Inst Technol EPFL, Dept Chem & Chem Engn, CH-1015 Lausanne, Switzerland
[3] Korean Res Inst Chem Technol, 141 Gajeong Ro, Daejeon, South Korea
关键词
Ion migration; Perovskite solar cells; Methylammonium lead iodide; Ionic charge carriers; Electronic charge carriers; PHASE-TRANSITIONS; DEFECT CHEMISTRY; BOUNDARY-LAYERS; ION CONDUCTION; SOLID-STATE; HYSTERESIS; TRANSPORT; MIGRATION; PEROVSKITES; DIFFUSION;
D O I
10.1016/j.ssi.2018.03.029
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Both electronic and ionic transport properties are key issues in the performance of perovskite solar cells. In order to understand the electrical behavior of organic-inorganic halide perovskites, and the possibilities to influence them, the elucidation of their equilibrium charge carrier chemistry as a function of stoichiometry and dopant concentration is a necessary and fundamental prerequisite. We provide here insight into the point defect chemistry of methylammonium lead iodide, whereby the decisive carriers are identified and their concentrations discussed as a function of stoichiometry (iodine partial pressure) and dopant content (oxygen partial pressure or Na addition). The experimental results indicate how ionic conductivity, which can be attributed to iodine vacancies, and electronic conductivity, which can be attributed to electron holes (or conduction electrons under reducing conditions), can be significantly and systematically altered by such treatments. Experimental results are discussed in the context of simple defect chemical models.
引用
收藏
页码:69 / 74
页数:6
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