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Triplet generation at the CdTe quantum dot/anthracene interface mediated by hot and thermalized electron exchange for enhanced production of singlet oxygen.
Chi, Zhen; Xu, Jia; Luo, Shida; Ran, Xia; Wang, Xiaojuan; Liu, Pingan; He, Yulu; Kuang, Yanmin; Guo, Lijun.
Afiliação
  • Chi Z; School of Physics and Electronics, Academy for Advanced Interdisciplinary Studies, International Joint Research Laboratory of New Energy Materials and Devices of Henan Province, Henan University, Kaifeng 475004, China. henulpa@163.com.
  • Xu J; School of Physics and Electronics, Academy for Advanced Interdisciplinary Studies, International Joint Research Laboratory of New Energy Materials and Devices of Henan Province, Henan University, Kaifeng 475004, China. henulpa@163.com.
  • Luo S; School of Physics and Electronics, Academy for Advanced Interdisciplinary Studies, International Joint Research Laboratory of New Energy Materials and Devices of Henan Province, Henan University, Kaifeng 475004, China. henulpa@163.com.
  • Ran X; School of Physics and Electronics, Academy for Advanced Interdisciplinary Studies, International Joint Research Laboratory of New Energy Materials and Devices of Henan Province, Henan University, Kaifeng 475004, China. henulpa@163.com.
  • Wang X; School of Physics and Electronics, Academy for Advanced Interdisciplinary Studies, International Joint Research Laboratory of New Energy Materials and Devices of Henan Province, Henan University, Kaifeng 475004, China. henulpa@163.com.
  • Liu P; School of Physics and Electronics, Academy for Advanced Interdisciplinary Studies, International Joint Research Laboratory of New Energy Materials and Devices of Henan Province, Henan University, Kaifeng 475004, China. henulpa@163.com.
  • He Y; School of Physics and Electronics, Academy for Advanced Interdisciplinary Studies, International Joint Research Laboratory of New Energy Materials and Devices of Henan Province, Henan University, Kaifeng 475004, China. henulpa@163.com.
  • Kuang Y; School of Physics and Electronics, Academy for Advanced Interdisciplinary Studies, International Joint Research Laboratory of New Energy Materials and Devices of Henan Province, Henan University, Kaifeng 475004, China. henulpa@163.com.
  • Guo L; School of Physics and Electronics, Academy for Advanced Interdisciplinary Studies, International Joint Research Laboratory of New Energy Materials and Devices of Henan Province, Henan University, Kaifeng 475004, China. henulpa@163.com.
Phys Chem Chem Phys ; 25(12): 8913-8920, 2023 Mar 22.
Article em En | MEDLINE | ID: mdl-36916640
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.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article