Direct Observation of Charge Collection at Nanometer-Scale Iodide-Rich Perovskites during Halide Exchange Reaction on CH3NH3PbBr3

• Published in: The journal of physical chemistry letters 2017-04, Vol.8 (8), p.1724-1728
• Main Authors: Karimata, Izuru, Kobori, Yasuhiro, Tachikawa, Takashi
• Format: Article
• Language: English
• ISSN: 1948-7185; 1948-7185
• DOI: 10.1021/acs.jpclett.7b00482

Organolead halide perovskites MAPbX3 (MA = CH3NH3 +, X = Cl–, Br–, or I–) are known to undergo reversible halide exchange reactions, enabling bandgap tuning over the visible light region. Using single-particle photoluminescence (PL) imaging for in situ observation, we have studied the structure-dependent charge dynamics during halide exchange with iodide ions on an MAPbBr3 crystal. In particular, we optically detected nanometer-scale iodide-rich domains (i.e., MAPbBrI2) and found that their lifetimes of several tens of milliseconds are limited by reaction with diffusing vacancies. Furthermore, it was discovered that these domains effectively collect the charge carriers from the bulk crystal, thus resulting in amplified spontaneous emission (ASE) under continuous-wave laser irradiation. Our findings will provide direction for development of perovskite heterostructures with enhanced charge utilization.