水煤气变换反应
材料科学
催化作用
串联
化学工程
铜
纳米技术
冶金
复合材料
有机化学
工程类
化学
作者
Zheng Jian Li,Mingzhi Wang,Yanyan Jia,Ruian Du,Tan Li,Yanping Zheng,Mingshu Chen,Yongcai Qiu,Keyou Yan,Weiwei Zhao,Pei Wang,Geoffrey I. N. Waterhouse,Sheng Dai,Yun Zhao,Guangxu Chen
标识
DOI:10.1021/acsami.3c06386
摘要
Metal-oxide interfaces on Cu-based catalysts play very important roles in the low-temperature water-gas shift reaction (LT-WGSR). However, developing catalysts with abundant, active, and robust Cu-metal oxide interfaces under LT-WGSR conditions remains challenging. Herein, we report the successful development of an inverse copper-ceria catalyst (Cu@CeO2), which exhibited very high efficiency for the LT-WGSR. At a reaction temperature of 250 °C, the LT-WGSR activity of the Cu@CeO2 catalyst was about three times higher than that of a pristine Cu catalyst without CeO2. Comprehensive quasi-in situ structural characterizations indicated that the Cu@CeO2 catalyst was rich in CeO2/Cu2O/Cu tandem interfaces. Reaction kinetics studies and density functional theory (DFT) calculations revealed that the Cu+/Cu0 interfaces were the active sites for the LT-WGSR, while adjacent CeO2 nanoparticles play a key role in activating H2O and stabilizing the Cu+/Cu0 interfaces. Our study highlights the role of the CeO2/Cu2O/Cu tandem interface in regulating catalyst activity and stability, thus contributing to the development of improved Cu-based catalysts for the LT-WGSR.
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