覆盖层
催化作用
金属
甲醇
氧化物
材料科学
纳米颗粒
化学工程
氧化还原
相(物质)
无机化学
纳米技术
化学
冶金
物理化学
有机化学
工程类
作者
Tongyuan Song,Rongtan Li,Jianyang Wang,Cui Dong,Xiaohui Feng,Yanxiao Ning,Rentao Mu,Qiang Fu
标识
DOI:10.1002/anie.202316888
摘要
Abstract Supported metal catalysts are widely used for chemical conversion, in which construction of high density metal‐oxide or oxide‐metal interface is an important means to improve their reaction performance. Here, Cu@ZnO x encapsulation structure has been in situ constructed through gas‐phase migration of Zn species from ZnO particles onto surface of Cu nanoparticles under CO 2 hydrogenation atmosphere at 450 °C. The gas‐phase deposition of Zn species onto the Cu surface and growth of ZnO x overlayer is self‐limited under the high temperature and redox gas (CO 2 /H 2 ) conditions. Accordingly, high density ZnO x ‐Cu interface sites can be effectively tailored to have an enhanced activity in CO 2 hydrogenation to methanol. This work reveals a new route for the construction of active oxide‐metal interface and classic strong metal‐support interaction state through gas‐phase migration of support species induced by high temperature redox reaction atmosphere.
科研通智能强力驱动
Strongly Powered by AbleSci AI