4.8 Article

Stabilizing ultrasmall Au clusters for enhanced photoredox catalysis

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NATURE COMMUNICATIONS
卷 9, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-018-04020-2

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资金

  1. National Natural Science Foundation of China [U1463204, 21173045]
  2. Award Program for Minjiang Scholar Professorship
  3. NSF of Fujian Province for Distinguished Young Investigator Rolling Grant [2017J07002]
  4. Independent Research Project of State Key Laboratory of Photocatalysis on Energy and Environment [2014A05]
  5. 1st Program of Fujian Province for Top Creative Young Talents
  6. Program for Returned High-Level Overseas Chinese Scholars of Fujian province
  7. Ministry of Science and Technology, Taiwan [MOST 106-2119-M-002-031]

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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.

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