甲脒
卤化物
离子电导率
钙钛矿(结构)
碘化物
金属
材料科学
离子键合
电导率
无机化学
金属卤化物
半导体
焓
介电谱
离子半径
化学物理
化学
物理化学
结晶学
热力学
离子
电解质
电化学
有机化学
物理
光电子学
电极
作者
Sandhya Tammireddy,Sebastian Reichert,Qingzhi An,Alexander D. Taylor,Ran Ji,Fabian Paulus,Yana Vaynzof,Carsten Deibel
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2021-12-16
卷期号:7 (1): 310-319
被引量:41
标识
DOI:10.1021/acsenergylett.1c02179
摘要
The properties of charged point defects in semiconductors such as metal halide perovskites play a critical role in the efficiency and stability of solar cells. Still, the formation and migration enthalpies as well as formation entropies of ionic defects in metal halide perovskites have not yet been determined experimentally. Through impedance spectroscopy, along with a quantification of the ionic defect properties, we demonstrate an approach to obtain ion migration and formation enthalpies as well as formation entropy changes in different metal halide perovskite thin films. We investigate lead-based perovskites that contain different cations (Cs, methylammonium (MA), and formamidinium (FA)) such as MAPbI3, CsPbI3, and a mixture of all Cs0.05(FA0.83MA0.17)0.95Pb(I0.9Br0.1)3. We assign the most dominant, common defect responsible for ion conductivity to iodide vacancy and compare its defect properties in terms of entropy and enthalpy changes in all measured perovskite compositions. Our approach is relevant for ionic conductors in general.
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