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Enhanced photoredox activity of CsPbBr3 nanocrystals by quantitative colloidal ligand exchange

Journal Article · · Journal of Chemical Physics
DOI:https://doi.org/10.1063/1.5129261· OSTI ID:1579639

Quantitative colloidal ligand exchange on lead-halide perovskite nanocrystals (NCs) has remained a challenge due to the dynamic passivation of amines and carboxylic acids and the instability of core lead-halide perovskite systems. Here in this paper, we present a facile colloidal ligand exchange process using cinnamate acid ligands to quantitatively displace native oleate ligands on CsPbBr3 NCs. The short cinnamate ligands lead to a 23-fold enhancement of the electron-donating ability of the CsPbBr3 NCs when benzoquinone is used as an electron acceptor. A significantly increased photoredox activity is also observed in a complete photocatalytic reaction: the α-alkylation of aldehydes. Our results provide a new strategy to tune the photoredox activity of halide perovskite NCs as well as the exploration of NC-ligand interactions.

Research Organization:
Energy Frontier Research Centers (EFRC) (United States). Center for Hybrid Organic-Inorganic Semiconductors for Energy (CHOISE); National Renewable Energy Laboratory (NREL), Golden, CO (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22)
Grant/Contract Number:
AC36-08GO28308
OSTI ID:
1579639
Alternate ID(s):
OSTI ID: 1575950
Report Number(s):
NREL/JA--5900-74931
Journal Information:
Journal of Chemical Physics, Journal Name: Journal of Chemical Physics Journal Issue: 20 Vol. 151; ISSN 0021-9606
Publisher:
American Institute of Physics (AIP)Copyright Statement
Country of Publication:
United States
Language:
English

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