Stabilizing ultrasmall Au clusters for enhanced photoredox catalysis

被引:261
|
作者
Weng, Bo [1 ,2 ]
Lu, Kang-Qiang [1 ,2 ]
Tang, Zichao [3 ]
Chen, Hao Ming [4 ]
Xu, Yi-Jun [1 ,2 ]
机构
[1] Fuzhou Univ, State Key Lab Photocatalysis Energy & Environm, Coll Chem, Fuzhou 350116, Fujian, Peoples R China
[2] Fuzhou Univ, Coll Chem, New Campus, Fuzhou 350116, Fujian, Peoples R China
[3] Xiamen Univ, Coll Chem & Chem Engn, State Key Lab Phys Chem Solid Surfaces, Collaborat Innovat Ctr Chem Energy Mat, Xiamen 361005, Peoples R China
[4] Natl Taiwan Univ, Dept Chem, Taipei 106, Taiwan
来源
NATURE COMMUNICATIONS | 2018年 / 9卷
基金
中国国家自然科学基金;
关键词
EXCITED-STATE BEHAVIOR; GOLD CLUSTERS; PHOTOCATALYTIC ACTIVITY; METAL NANOCLUSTERS; RECENT PROGRESS; NANOPARTICLES; SIZE; TIO2; GRAPHENE; NANOCOMPOSITES;
D O I
10.1038/s41467-018-04020-2
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 SiO2 sphere by utilizing multifunctional branched poly-ethylenimine (BPEI) as a surface charge modifying, reducing and stabilizing agent. The sequential coating of thickness controlled TiO2 shells can further significantly improve the photocatalytic efficiency, while such structurally designed core-shell SiO2-Au GSH clusters-BPEI@TiO2 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.
引用
收藏
页数:11
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