4.8 Article

Tailoring the Electronic Metal-Support Interactions in Supported Atomically Dispersed Gold Catalysts for Efficient Fenton-like Reaction

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 60, Issue 26, Pages 14370-14375

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202103652

Keywords

active sites; atomically dispersed; electronic metal– support interactions; one-pot strategy; substitutional solid solution

Funding

  1. Natural Science Foundation of China [21705117, 21575115]
  2. Program for Chang Jiang Scholars and Innovative Research Team, Ministry of Education, China [IRT-16R61]
  3. Program of Gansu Provincial Higher Education Research Project [2017-D-01]
  4. Special fund project for the central government
  5. Special fund project for the central government to guide local science and technology development (2020)

Ask authors/readers for more resources

The development of a catalyst with an atomically dispersed metal-atom alloy structure has significantly improved the degradation efficiency of recalcitrant organic pollutants. This catalyst exhibits excellent durability and reliability, achieving significant degradation rates for rhodamine, phenol, and bisphenol A.
The atomically dispersed metal is expected as one of the most promising Fenton-like catalysts for the degradation of recalcitrant organic pollutants (ROPs) by the strong electronic metal-support interactions (EMSIs). Here, we develop an atomically dispersed metal-atom alloy made by guest Au atoms substitute host V atoms in the two-dimensional VO2(B) nanobelt support (Au/VO2) to activate Fenton-like oxidation for elimination of ROPs. The 2D nanobelt structure enlarges the exposure of atomically Au thus increasing the number of active sites to absorb more S2O82- ions. And the EMSIs regulate the charge density in Au atoms to present positive charge Au+, lowering the energy barrier of S2O82- decomposition to produce SO4.-. The Au/VO2 catalyst possesses excellent durable and reliable characteristics and exhibits record-breaking efficiency with TOF as high as 21.42 min(-1), 16.19 min(-1), and 80.89 min(-1) for rhodamine, phenol, and bisphenol A degradation, respectively.

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