4.8 Article

Sarp Kaya - Koc? University Tu?pras? Energy Center (KUTEM), Department of Chemistry, Koc? University, 34450 Istanbul, Turkey; ? orcid.org/0000-0002-2591-5843

期刊

CHEMISTRY OF MATERIALS
卷 34, 期 5, 页码 2313-2320

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemmater.1c04137

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资金

  1. Ministry of Science and Technology of China [2017YFA0204904]
  2. Swedish Research Council (VR)
  3. Knut och Alice Wallenbergs stiftelse
  4. STINT Joint China-Sweden Mobility program
  5. Ragnar Holm foundation
  6. Trygger's foundation
  7. Swedish Research Council [2018-07152]
  8. Swedish Governmental Agency for Innovation Systems [2018-04969]
  9. Formas [2019-02496]

向作者/读者索取更多资源

This study presents the synthesis and characterization of a new type of Co1Cu hybrid single-atom catalyst (SAC) on a Cu2O(111) support. The Co1Cu hybrid SACs are found to stabilize the active sites of the Cu2O catalyst and improve its stability under reaction conditions.
Single-atom catalysts (SACs) consist of a low coverage of isolated metal atoms dispersed on a metal substrate, called single-atom alloys (SAAs), or alternatively single metal atoms coordinated to oxygen atoms on an oxide support. We present the synthesis of a new type of Co1Cu SAC centers on a Cu2O(111) support by means of a site-selective atomic layer deposition technique. Isolated metallic Co atoms selectively coordinate to the native oxygen vacancy sites (Cu sites) of the reconstructed Cu2O(111) surface, forming a Co1Cu SAA with no direct Co- Ox bonds. The centers, here referred to as Co1Cu hybrid SACs, are found to stabilize the active Cu+ sites of the low-cost Cu2O catalyst that otherwise is prone to deactivation under reaction conditions. The stability of the Cu2O(111) surface was investigated by synchrotron radiation-based ambient-pressure X-ray photoelectron spectroscopy under reducing CO environment. The structure and reduction reaction are modeled by density functional theory calculations, in good agreement with experimental results.

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