Separating Bulk and Surface Contributions to Electronic Excited State Processes in Hybrid Mixed Perovskite Thin Films via Multimodal All-Optical Imaging

被引:20
作者
Simpson, Mary Jane [1 ]
Doughty, Benjamin [1 ]
Das, Sanjib [2 ]
Xiao, Kai [3 ]
Ma, Ying-Zhong [1 ]
机构
[1] Oak Ridge Natl Lab, Chem Sci Div, Oak Ridge, TN 37831 USA
[2] Univ Tennessee, Dept Elect Engn & Comp Sci, Knoxville, TN 37996 USA
[3] Oak Ridge Natl Lab, Ctr Nanophase Mat Sci, Oak Ridge, TN 37831 USA
关键词
LEAD HALIDE PEROVSKITES; CARRIER LIFETIME; CHARGE-TRANSPORT; EFFICIENCY;
D O I
10.1021/acs.jpclett.7b01368
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
A comprehensive understanding of electronic excited-state phenomena underlying the impressive performance of solution-processed hybrid halide perovskite solar cells requires access to both spatially resolved electronic processes and corresponding sample morphological characteristics. Here, we demonstrate an all-optical multimodal imaging approach that enables us to obtain both electronic excited-state and morphological information on a single optical microscope platform with simultaneous high temporal and spatial resolution. Specifically, images were acquired for the same region of interest in thin films of chloride containing mixed lead halide perovskites (CH3NH3PbI3-xClx) using femtosecond transient absorption, time-integrated photoluminescence, confocal reflectance, and transmission microscopies. Comprehensive image analysis revealed the presence of surface- and bulk-dominated contributions to the various images, which describe either spatially dependent electronic excited-state properties or morphological variations across the probed region of the thin films. These results show that PL probes effectively the species near or at the film surface.
引用
收藏
页码:3299 / 3305
页数:7
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