Department of Chemistry - Ångström Laboratory, Physical Chemistry, Uppsala University , Box 523, SE 75120 Uppsala, Sweden.
Department of Chemistry - Ångström Laboratory, Structural Chemistry, Uppsala University , Box 538, SE 75120 Uppsala, Sweden.
ACS Nano. 2017 Mar 28;11(3):2823-2834. doi: 10.1021/acsnano.6b07916. Epub 2017 Mar 6.
Organometallic halide perovskites (OMHPs) have recently emerged as a promising class of materials in photovoltaic technology. Here, we present an in-depth investigation of the physics in these systems by measuring the photoinduced absorption (PIA) in OMHPs as a function of materials composition, excitation wavelength, and modulation frequency. We report a photoinduced Stark effect that depends on the excitation wavelength and on the dipole strength of the monovalent cations in the A position of the ABX perovskite. The results presented are corroborated by density functional theory calculations and provide fundamental information about the photoinduced local electric field change under blue and red excitation as well as insights into the mechanism of light-induced ion displacement in OMHPs. For optimized perovskite solar cell devices beyond 19% efficiency, we show that excess thermalization energy of blue photons plays a role in overcoming the activation energy for ion diffusion.
金属卤化物钙钛矿(OMHPs)最近在光伏技术中作为一类很有前途的材料出现。在这里,我们通过测量 OMHPs 中光致吸收(PIA)作为材料组成、激发波长和调制频率的函数,对这些系统中的物理现象进行了深入研究。我们报告了一个光致斯塔克效应,它取决于激发波长和 A 位的单价阳离子的偶极强度。提出的结果得到了密度泛函理论计算的支持,并提供了关于蓝、红激发下光致局部电场变化的基本信息,以及对 OMHPs 中光致离子位移机制的深入了解。对于超过 19%效率的优化钙钛矿太阳能电池器件,我们表明,蓝光子的过剩热化能在克服离子扩散的活化能方面起着作用。