催化作用
甲醇
尖晶石
氢
化学
氧化物
色散(光学)
无机化学
碳纤维
氧气
一氧化碳
材料科学
粒子(生态学)
化学工程
粒径
工业催化剂
多相催化
催化剂载体
制氢
功能(生物学)
合理设计
出处
期刊:
日期:2026-07-13
卷期号:249 (1): 103-109
标识
DOI:10.54254/2755-2721/2026.ad35226
摘要
CO₂ hydrogenation to methanol is an important route for reducing carbon emissions and utilizing hydrogen energy, and multiple catalytic systems have been developed. Among them, Cu-based catalysts remain an important class because of their low cost and substantial research foundation. This review focuses on structural regulation of Cu-based catalysts and discusses the effects of Cu particle size, the Cu⁰/Cu⁺ ratio, metal–support interfaces, oxygen vacancies, spinel supports, and alloying on reaction performance. The function of Cu-based catalysts is attributed mainly to multisite cooperation. Cu⁰ primarily supplies hydrogen species, whereas Cu⁺ and oxide interfaces more readily stabilize oxygenated intermediates. Excessive pursuit of Cu dispersion or defect concentration is not advisable. A more rational direction is to maintain moderate CO₂ adsorption, stable adjacent Cu⁰/Cu⁺ structures, and low interfacial deactivation during the reaction.
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