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Cited by 297

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Stabilizing ultrasmall Au clusters for enhanced photoredox catalysis

Open access
Weng, Bo, Lu, Kang-Qiang, Tang, Zichao, Chen, Hao Ming, Xu, Yi-Jun·2018·Nature Communications

Abstract

Recently, loading ligand-protected gold (Au) clusters as visible light photosensitizers onto various supports for photoredox catalysis has attracted considerable attention. However, the efficient control of long-term photostability of Au clusters on the metal-support interface remains challenging. Herein, we report a simple and efficient method for enhancing the photostability of glutathione-protected Au clusters (Au GSH clusters) loaded on the surface of SiO 2 sphere by utilizing multifunctional branched poly-ethylenimine (BPEI) as a surface charge modifying, reducing and stabilizing agent. The sequential coating of thickness controlled TiO 2 shells can further significantly improve the photocatalytic efficiency, while such structurally designed core-shell SiO 2-Au GSH clusters-BPEI@TiO 2 composites maintain high photostability during longtime light illumination conditions. This joint strategy via interfacial modification and composition engineering provides a facile guideline for stabilizing ultrasmall Au clusters and rational design of Au clusters-based composites with improved activity toward targeting applications in photoredox catalysis.

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Metadata

Authors
Weng, B., Lu, K.-Q., Tang, Z., Chen, H. M., & Xu, Y.-J.
Venue
Nature Communications
Published
2018-04-18
Volume
9
Issue
1
Pages
1543-1543
ISSN
2041-1723 (ISSN-L)
OpenAlex
W2799851888
Cited by
297
References
1
FWCI
12.83
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Stabilizing ultrasmall Au clusters for enhanced photoredox catalysis. https://app.cochat.ai/papers/10.1038/s41467-018-04020-2
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Weng, B., Lu, K.-Q., Tang, Z., Chen, H. M., & Xu, Y.-J. (2018). Stabilizing ultrasmall Au clusters for enhanced photoredox catalysis. Nature Communications. https://doi.org/10.1038/s41467-018-04020-2

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