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
关键词
-
资金
- Ministry of Science and Technology of China [2017YFA0204904]
- Swedish Research Council (VR)
- Knut och Alice Wallenbergs stiftelse
- STINT Joint China-Sweden Mobility program
- Ragnar Holm foundation
- Trygger's foundation
- Swedish Research Council [2018-07152]
- Swedish Governmental Agency for Innovation Systems [2018-04969]
- Formas [2019-02496]
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.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据