催化作用
甲醇
合金
氧化物
材料科学
接口(物质)
化学工程
无机化学
物理化学
化学
冶金
有机化学
工程类
吸附
吉布斯等温线
作者
Biao Gao,Bin Yang,Kazuto Hatakeyama,Yifu Wang,Longtai Li,Shintaro Ida,Tatsumi Ishihara,Limin Guo
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2025-01-24
卷期号:15 (3): 2305-2314
被引量:31
标识
DOI:10.1021/acscatal.4c06851
摘要
CO 2 catalytic hydrogenation to methanol is promising for CO 2 utilization. In 2 O 3 -based catalysts are attracting much attention because of their high methanol selectivity. However, a low CO 2 conversion rate limits the overall methanol yield. Herein, we developed the interface of the CoIn 2 alloy and In 2 O 3 oxide as a CoIn 2 /In 2 O 3 catalyst and successfully achieved high performance for the hydrogenation of CO 2 to methanol. Experimental and theoretical results indicated that the alloy/oxide interface is stable during the reaction atmosphere; the high performance arising from the electronic interaction between CoIn 2 and In 2 O 3, which improves the electron density at the CoIn 2 interface, facilitates H 2 dissociation, CO 2 adsorption, and the hydrogenation of formate intermediates to methanol, which justifies the sustained high methanol selectivity and production rate. The optimized catalyst showed a methanol selectivity up to 74% and a high methanol space-time yield up to 0.69 g MeOH g cat –1 h –1 at 5.0 MPa, H 2 /CO 2 = 3:1, 300 °C and 36,000 mLg cat –1 h –1 .
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