甲醇
催化作用
纳米晶材料
密度泛函理论
材料科学
化学工程
反应机理
合金
化学
分子动力学
结构变化
机械化学
无机化学
多相催化
晶体结构
化学反应
纳米颗粒
结晶学
蒸汽重整
纳米晶
铜
格子(音乐)
物理化学
原位
工作(物理)
活动站点
作者
Bing Li,Bin Lei,Xiao Liu,Yizhen Zhao,Ziyi Zhao,Yanping Sui,Pengyi Tang,Xize Liu,Jiahe Li,Jian‐Gong Ma,Donghai Mei,Peng Cheng
摘要
ABSTRACT Unraveling the active sites of Cu/Zn catalysts for CO 2 hydrogenation to methanol continues to pose a fundamental challenge, especially in clarifying the precise role of Zn promoters. Previous studies have predominantly emphasized the chemical state of Zn, while often neglecting accompanying structural changes in the Cu host. Here, we report the first direct observation of lattice expansion in nanocrystalline Cu within a bulk Zn/Cu single‐atom alloy—a geometric distortion that elevates the d ‐band center of Cu and increases interatomic Cu distances. As evidenced by combined in situ experiments and density functional theory (DFT) calculations, these structural modifications promote the activation of both H 2 and CO 2 , steering the reaction toward the *HCOO pathway and substantially enhancing methanol production at notably low temperatures. Our findings deliver unprecedented insight into Zn's promotional mechanism and significantly advance the mechanistic understanding of Cu/Zn catalysts for methanol synthesis.
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