Issue 12, 2023

Triplet generation at the CdTe quantum dot/anthracene interface mediated by hot and thermalized electron exchange for enhanced production of singlet oxygen

Abstract

Triplet energy transfer (TET) from semiconductor quantum dots (QDs) to molecular triplets has potential applications in photon up-conversion and singlet oxygen generation. Here, we have constructed a complex consisting of CdTe QDs as the donor and 9-anthracenecarboxylic acid (ACA) as the triplet acceptor, and studied the TET pathways and enhanced singlet oxygen generation properties. The results from steady-state and time-resolved spectroscopy demonstrate efficient TET with a total efficiency of over 80% from photoexcited CdTe QDs to ACA. Dynamical analysis clearly indicates two distinctive TET channels – hot electron exchange and thermalized electron exchange – mediating the TET process in the CdTe QDs–ACA complex. The TET efficiencies from hot electron exchange at high energetic levels and thermalized electron exchange on the lowest exciton state can reach ∼27% and ∼85%, respectively, following 530 nm excitation. This efficient TET endows the CdTe QDs–ACA complex with a good capability of generating singlet oxygen species with a yield of up to ∼59%. These findings contribute further insights to the mechanisms of interfacial TET processes and are significant in designing efficient TET systems based on semiconductor nanoparticles and triplet molecules.

Graphical abstract: Triplet generation at the CdTe quantum dot/anthracene interface mediated by hot and thermalized electron exchange for enhanced production of singlet oxygen

Supplementary files

Article information

Article type
Paper
Submitted
03 Jan 2023
Accepted
28 Feb 2023
First published
04 Mar 2023

Phys. Chem. Chem. Phys., 2023,25, 8913-8920

Triplet generation at the CdTe quantum dot/anthracene interface mediated by hot and thermalized electron exchange for enhanced production of singlet oxygen

Z. Chi, J. Xu, S. Luo, X. Ran, X. Wang, P. Liu, Y. He, Y. Kuang and L. Guo, Phys. Chem. Chem. Phys., 2023, 25, 8913 DOI: 10.1039/D3CP00021D

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