Investigation of Chemical Origin of White-Light Emission in Two-Dimensional (C4H9NH3)(2)PbBr4 via Infrared Nanoscopy
- Authors
- Park, Dae Young; An, Sung-Jin; Lee, Chanwoo; Duc Anh Nguyen; Lee, Kang-Nyeoung; Jeong, Mun Seok
- Issue Date
- Dec-2019
- Publisher
- American Chemical Society
- Citation
- Journal of Physical Chemistry Letters, v.10, no.24, pp.7942 - 7948
- Indexed
- SCIE
SCOPUS
- Journal Title
- Journal of Physical Chemistry Letters
- Volume
- 10
- Number
- 24
- Start Page
- 7942
- End Page
- 7948
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/146573
- DOI
- 10.1021/acs.jpclett.9b03328
- ISSN
- 1948-7185
- Abstract
- The broadband light emission in low-dimensional organic lead halide perovskites (OHPs) is a fascinating property for white light-emitting diodes (LEDs). However, unique emission has been observed in highly distorted low-dimensional OHPs such as (110) and (111) perovskites. Herein, we report the first observation of white-light emission under ambient (21 degrees C) conditions in a rectangular microsheet of (C4H9NH3)(2)PbBr4, a (100) perovskite. The origin of white-light emission in (C4H9NH3)(2)PbBr4 was revealed as defect-assisted radiative recombination via excitation power-dependent photoluminescence measurement. Additionally, the origin of the defect was confirmed to be organic cation vacancies formed by intercalated water molecules via infrared nanoscopy. This result can help to improve the performance of white LEDs using low-dimensional OHPs.
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