化学
脱氢
蒸汽重整
甲醇
格式化
电子转移
接口(物质)
化学工程
可持续能源
氧化还原
氢
转移加氢
能量转换
制氢
催化作用
锌
原位
活动站点
纳米技术
多相催化
氢燃料
光化学
电子效应
对偶(语法数字)
协同催化
水煤气变换反应
反应中间体
作者
Diru Liu,Mengyuan Zhang,Lin Zhao,Guangyan Xu,Hong He
摘要
Methanol steam reforming (MSR) is a promising technology for in situ hydrogen production, while the mechanistic role of zinc in the widely used Cu/ZnO/Al 2 O 3 catalyst remains ambiguous. Electronic metal–support interactions (EMSIs) are generally applied for modulating active sites in such heterogeneous catalysts, offering opportunities to optimize energy conversion processes. Here, we revealed that a dynamic EMSI between Cu and ZnO enhances catalytic performance by constructing ZnO x /Cu interfaces, facilitating bidirectional electron transfer between ZnO x and Cu. The electron transfer from ZnO x to Cu mitigates overoxidation of Cu 0 to Cu + during water activation, thereby improving water activation efficiency, while the electron transfer back to ZnO x accelerates the reduction of Cu + back to Cu 0, promoting dehydrogenation of reactive formate at the ZnO x /Cu interface, the rate-determining step at low temperatures. Thus, we establish a dual role for the EMSI-induced ZnO x /Cu interface in stabilizing active intermediates and facilitating redox cycling. These findings provide insights into the precise regulation of catalytic active sites via EMSI engineering, offering guidance for high-efficiency catalysts design for sustainable energy conversion.
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