Abstract
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.
Original language | English |
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Pages (from-to) | 3299-3305 |
Number of pages | 7 |
Journal | Journal of Physical Chemistry Letters |
Volume | 8 |
Issue number | 14 |
DOIs | |
State | Published - Jul 20 2017 |
Funding
Work by M.J.S., B.D., and Y.-Z. M. was supported by the U.S. Department of Energy, Office of Science, Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division. Perovskite sample preparation and characterization by S.D. and K.X. was conducted at the Center for Nanophase Materials Sciences (CNMS), which is a DOE Office of Science User Facility.
Funders | Funder number |
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U.S. Department of Energy | |
Office of Science | |
Basic Energy Sciences | |
Chemical Sciences, Geosciences, and Biosciences Division |