Efficient Photoinduced Living Polymerization Driven by Shortwave Infrared CuInSe<sub><b>2</b></sub>/CuInS<sub><b>2</b></sub> Quantum Dots

Shortwave infrared (SWIR) light-driven photoinduced electron/energy transfer reversible addition-fragmentation chain transfer (PET-RAFT) polymerization holds great promise for applications such as 3D printing and transdermal photopolymerization. However, efficient SWIR-active photocatalysts remain lacking. Herein, we report the use of lead-free CuInSe<sub>2</sub>/CuInS<sub>2</sub> core/shell quantum dots (QDs), with their absorption onset extending to 1100 nm, to drive efficient SWIR PET-RAFT polymerization. Time-resolved spectroscopy reveals that both band-edge and trap-state electrons can transfer to the RAFT agent. The relatively sluggish hole transfer, due to hole localization to copper states, can be accelerated by introducing amines as hole scavengers. The reaction exhibits well-defined characteristics of living polymerization and proceeds efficiently in the presence of a 3 mm biological tissue barrier under 1050 nm irradiation.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-09-02
DOI
https://doi.org/10.1021/jacs.5c11312
Citations
3
Primary Topic
Advanced Photocatalysis Techniques
Type
article
Field-Weighted Citation Impact
1.09
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article

Efficient Photoinduced Living Polymerization Driven by Shortwave Infrared CuInSe2/CuInS2 Quantum Dots

Cyrille Andre Boyer, Kaifeng Wu, Y. F. Lyu, Qun Zhang et al.
3 citations
Journal of the American Chemical Society
Advanced Photocatalysis Techniques
1.09
article

Efficient Photoinduced Living Polymerization Driven by Shortwave Infrared CuInSe2/CuInS2 Quantum Dots

Cyrille Andre Boyer, Kaifeng Wu, Y. F. Lyu, Qun Zhang, Jun Du
article en
3 citations

Abstract

Shortwave infrared (SWIR) light-driven photoinduced electron/energy transfer reversible addition-fragmentation chain transfer (PET-RAFT) polymerization holds great promise for applications such as 3D printing and transdermal photopolymerization. However, efficient SWIR-active photocatalysts remain lacking. Herein, we report the use of lead-free CuInSe<sub>2</sub>/CuInS<sub>2</sub> core/shell quantum dots (QDs), with their absorption onset extending to 1100 nm, to drive efficient SWIR PET-RAFT polymerization. Time-resolved spectroscopy reveals that both band-edge and trap-state electrons can transfer to the RAFT agent. The relatively sluggish hole transfer, due to hole localization to copper states, can be accelerated by introducing amines as hole scavengers. The reaction exhibits well-defined characteristics of living polymerization and proceeds efficiently in the presence of a 3 mm biological tissue barrier under 1050 nm irradiation.

Journal of the American Chemical SocietyVol. 147(40)
Dalian Institute of Chemical Physics (CN), Chinese Academy of Sciences (CN), UNSW Sydney (AU), University of Chinese Academy of Sciences (CN)
Openalex Percentile: Top 22%
Advanced Photocatalysis Techniques
1.09
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Efficient Photoinduced Living Polymerization Driven by Shortwave Infrared CuInSe<sub><b>2</b></sub>/CuInS<sub><b>2</b></sub> Quantum Dots — Cyrille Andre Boyer, Kaifeng Wu, et al. · Journal of the American Chemical Society (2025) | TGRS Research Map | TGRS