Journal
JOURNAL OF PHYSICAL CHEMISTRY C
Volume 125, Issue 24, Pages 13696-13705Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.1c04335
Keywords
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Funding
- Natural Sciences and Engineering Research Council Canada (NSERC) [DG RGPIN-2018-06556, SPG STPGP-2016-493924, DG RGPIN-2020-06675]
- Canada Foundation of Innovation/Ontario Innovation Trust (CFI/OIT) [9040]
- University of Western Ontario
- NSERC-CGSM scholarship
- Ontario graduate scholarship
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The electrochemiluminescence (ECL) of Mn-doped CsPbCl3 perovskite quantum dot (MPQ) films was investigated for the first time, revealing the presence of two emission peaks, one from Mn2+ d-d transition and the other originating from surface states, differing from the frequently reported photoluminescence (PL) of MPQ. The study also found that the presence of the 660 nm peak in the ECL of undoped CsPbCl3 (UPQ) further supports the proposed surface-state emission scheme.
Electrochemiluminescence (ECL) of Mn-doped CsPbCl3 perovskite quantum dot (MPQ) films was investigated for the first time. The electrochemical properties of the perovskite quantum dots are probed by cyclic voltammetry and spooling ECL spectroscopy. It has been discovered that the ECL of the MPQ/benzoyl peroxide coreactant system proceeds through two channels: an energy transfer process from the band-edge exciton to Mn2+, producing emission centered at 595 nm from Mn2+ d-d transition, and a second emission peak centered at 660 nm, which is of a surface-state origin. This observation is drastically different from the frequently reported photoluminescence (PL) of MPQ which contains dual emission from the host and the dopant, respectively. ECL of the undoped CsPbCl3 (UPQ) was also investigated, and the presence of the 660 nm peak further supports our proposed surface-state emission scheme.
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