铜
催化作用
纳米颗粒
化学吸附
材料科学
碳纤维
化学计量学
化学工程
X射线光电子能谱
无机化学
化学
纳米技术
有机化学
冶金
复合材料
复合数
工程类
作者
Liuye Mo,Sibudjing Kawi
摘要
Ultrasmall copper nanoparticles (1.6 nm) on silica catalysts were successfully prepared via an in situ self-assembled core–shell precursor route. XRD, SEM-EDS and chemisorption results showed that only fatty acids with carbon chain length > 2 carbon atoms could effectively promote the dispersion of copper on silica. XPS results showed that non-stoichiometric copper butyrate was formed when butyric acid was used as a capping agent, and this non-stoichiometric compound of copper butyrate self-assembles into a shell structure outside the core of copper nitrate species. The in situ self-assembled core–shell structure could effectively prevent the copper particles from agglomeration. The catalytic performances of as-prepared 10% Cu/SiO2 catalysts enhanced with fatty acids with carbon chain length > 2 carbon atoms exhibited good activities for water–gas shift reaction due to the high proportion of defect sites, highly dispersed Cu particles and/or isolated Cu atom sites.
科研通智能强力驱动
Strongly Powered by AbleSci AI