Boosting reactivity of water-gas shift reaction by synergistic function over CeO2-x/CoO1-x/Co dual interfacial structures

被引:44
作者
Fu, Xin-Pu [1 ]
Wu, Cui-Ping [1 ]
Wang, Wei-Wei [1 ]
Jin, Zhao [1 ]
Liu, Jin-Cheng [2 ,3 ]
Ma, Chao [4 ]
Jia, Chun-Jiang [1 ]
机构
[1] Shandong Univ, Sch Chem & Chem Engn, Key Lab Special Aggregated Mat, Key Lab Colloid & Interface Chem, Jinan 250100, Peoples R China
[2] Nankai Univ, Sch Mat Sci & Engn, Ctr Rare Earth & Inorgan Funct Mat, Tianjin 300350, Peoples R China
[3] Nankai Univ, Natl Inst Adv Mat, Tianjin 300350, Peoples R China
[4] Hunan Univ, Coll Mat Sci & Engn, Changsha 410082, Peoples R China
基金
美国国家科学基金会;
关键词
METAL-SUPPORT INTERACTIONS; RAMAN-SPECTROSCOPY; CATALYST; CO; SITES; GOLD; OPTIMIZATION; CO/CEO2; ALKALI; CEOX;
D O I
10.1038/s41467-023-42577-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Dual-interfacial structure within catalysts is capable of mitigating the detrimentally completive adsorption during the catalysis process, but its construction strategy and mechanism understanding remain vastly lacking. Here, a highly active dual-interfaces of CeO2-x/CoO1-x/Co is constructed using the pronounced interfacial interaction from surrounding small CeO2-x islets, which shows high activity in catalyzing the water-gas shift reaction. Kinetic evidence and in-situ characterization results revealed that CeO2-x modulates the oxidized state of Co species and consequently generates the dual active CeO2-x/CoO1-x/Co interface during the WGS reaction. A synergistic redox mechanism comprised of independent contribution from dual functional interfaces, including CeO2-x/CoO1-x and CoO1-x/Co, is authenticated by experimental and theoretical results, where the CeO2-x/CoO1-x interface alleviates the CO poison effect, and the CoO1-x/Co interface promotes the H-2 formation. The results may provide guidance for fabricating dual-interfacial structures within catalysts and shed light on the mechanism over multi-component catalyst systems.
引用
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页数:11
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