Elucidating the Nature of the Cu(I) Active Site in CuO/TiO2 for Excellent Low-Temperature CO Oxidation

被引:69
作者
Fang, Yarong [1 ]
Chi, Xiao [3 ]
Li, Li [1 ]
Yang, Ji [1 ]
Liu, Shoujie [1 ]
Lu, Xingxu [2 ]
Xiao, Wen [4 ]
Wang, Liming [5 ]
Luo, Zhu [1 ]
Yang, Weiwei [1 ]
Hu, Siyu [1 ]
Xiong, Juxia [1 ]
Hoang, Son [1 ]
Deng, Hongtao [1 ]
Liu, Fudong [6 ]
Zhang, Lizhi [1 ]
Gao, Puxian [2 ]
Ding, Jun [4 ]
Guo, Yanbing [1 ]
机构
[1] Cent China Normal Univ, Inst Environm & Appl Chem, Coll Chem, Key Lab Pesticide & Chem Biol,Minist Educ, Wuhan 430079, Peoples R China
[2] Univ Connecticut, Dept Chem Mat & Biomol Engn, Inst Mat Sci, Storrs, CT 06269 USA
[3] Natl Univ Singapore, Singapore Synchrotron Light Source, Singapore 117603, Singapore
[4] Natl Univ Singapore, Dept Mat Sci & Engn, Singapore 117575, Singapore
[5] Chinese Acad Sci, CAS Key Lab Biomed Effects Nanomat & Nanosafety, Inst High Energy Phys, Dept Mat Sci & Engn, Beijing 100049, Peoples R China
[6] Univ Cent Florida, NanoSci Technol Ctr, Dept Civil Environm & Construct Engn, Catalysis Cluster Renewable Energy & Chem Transfo, Orlando, FL 32816 USA
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
Ti-doped CuO; Ti-O-Cu hybridization; stabilized Cu+; CO adsorption; activated O; CATALYTIC-ACTIVITY; MANGANESE OXIDE; HIGH-EFFICIENCY; SURFACE SITES; MIXED OXIDES; CU2+ SITES; COPPER; OXYGEN; EPR; REDUCTION;
D O I
10.1021/acsami.9b18264
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Stabilized Cu+ species have been widely considered as catalytic active sites in composite copper catalysts for catalytic reactions with industrial importance. However, few examples comprehensively explicated the origin of stabilized Cu+ in a low-cost and widely investigated CuO/TiO2 system. In this study, mass producible CuO/TiO2 catalysts with interface-stabilized Cu+ were prepared, which showed excellent low-temperature CO oxidation activity. A thorough characterization and theoretical calculations proved that the strong charge-transfer effect and Ti-O-Cu hybridization in Ti-doped CuO(111) at the CuO/TiO2 interface contributed to the formation and stabilization of Cu+ species. The CO molecule adsorbed on Cu+ and reacted directly with Ti doping-promoted active lattice oxygen via a Mars-van Krevelen mechanism, leading to the enhanced low-temperature activity.
引用
收藏
页码:7091 / 7101
页数:11
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