Strong Metal-Support Interaction in Pd/CeO2 Promotes the Catalytic Activity of Ethyl Acetate Oxidation

被引:27
|
作者
Wen, Xinying [1 ]
Li, Wuchao [1 ]
Yan, Jiaxing [1 ]
Wang, Xiaojiao [1 ]
Ren, Enbo [1 ]
Shi, Zhuofan [1 ]
Li, Jun [2 ]
Ding, Xuegang [2 ]
Mo, Shengpeng [2 ]
Mo, Deqing [1 ]
机构
[1] Guilin Univ Elect Technol, Sch Life & Environm Sci, Guilin 541004, Peoples R China
[2] Guilin Univ Technol, Coll Environm Sci & Engn, Guilin 541004, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2022年 / 126卷 / 03期
基金
中国博士后科学基金;
关键词
OXYGEN VACANCIES; CO; PERFORMANCE; TOLUENE; CERIA; CEO2; COMBUSTION; INTERFACE; REDUCTION; MN;
D O I
10.1021/acs.jpcc.1c10421
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
To study the promoting effect of strong metal-support interactions (SMSIs) on the catalytic oxidation of ethyl acetate, a series of Pd/CeO2 catalysts with different CeO2 support morphologies of nanocubes (NC), spindles (SP), and nanospheres (NS) were prepared for the catalytic oxidation of ethyl acetate. The study indicated that the catalytic activity of Pd/CeO2 catalysts possessed a significant structure-activity relationship. A series of characterization results revealed that the SMSIs between Pd nanoparticles (NPs) and the CeO2 support optimized surface chemical states, promoted the formation of surface oxygen vacancies, activated the surface oxygen species, and improved the low-temperature reducibility. Among all of these catalysts, Pd/CeO2-SP exhibited the best catalytic activity for ethyl acetate oxidation (T-90 = 180 degrees C, WHSV = 60 000 mL g(-1) h(-1)), which was attributed to the SMSIs between Pd NPs and the CeO2-SP support.
引用
收藏
页码:1450 / 1461
页数:12
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