催化作用
烧结
氧化物
异质结
材料科学
溶解
化学工程
过渡金属
纳米技术
化学
冶金
有机化学
光电子学
工程类
作者
Hao Chen,Kecheng Jie,Charl J. Jafta,Zhenzhen Yang,Siyu Yao,Miaomiao Liu,Zihao Zhang,Jixing Liu,Miaofang Chi,Jie Fu,Sheng Dai
标识
DOI:10.1016/j.apcatb.2020.119155
摘要
Designing high-performance catalysts that can stabilize catalytic active sites against sintering to deactivation at temperature higher than 900 °C is significant but challenging. Here we report a new strategy to obtain a transition metal oxide catalyst with high temperature stability for CO oxidation. This is achieved through a synergistic interfacial interaction at the interface of a heterostructure between high–entropy oxides (HEO, high temperature stability) and CuCeOx (catalytic site). The catalytic site (CuCeOx) for CO oxidation is realized by dissolving an amount of Cu species in HEO into CeO2 via an entropy–driven mechanochemical process. In situ XRD and HAADF–STEM have confirmed the high temperature stability of the heterostructure CuCeOx–HEO, which can remain its CO oxidation catalytic activity at elevated temperatures. It should be expected that this innovative will offer the potential to the synthesis of catalysts with high temperature stability in industry.
科研通智能强力驱动
Strongly Powered by AbleSci AI