The study of strong metal-support interaction enhanced PdZn alloy nanocatalysts for methanol steam reforming

被引:3
|
作者
Wang, Huimin [1 ]
Fang, Zhaolin [1 ]
Wang, Yaxin [1 ]
Meng, Kong [1 ]
Sun, Shaorui [1 ,2 ]
机构
[1] Beijing Univ Technol, Coll Mat Sci & Engn, Beijing Key Lab Green Catalysis & Separat, Beijing 100124, Peoples R China
[2] Beijing Univ Technol, Coll Mat Sci & Engn, Beijing 100124, Peoples R China
基金
中国国家自然科学基金;
关键词
Methanol steam reforming; Ethylene glycol reduction; PdZn alloys; Strong metal-support interaction; Hydrogen production; HYDROGEN-PRODUCTION; PD/ZNO CATALYSTS; PERFORMANCE; 1ST-PRINCIPLES; NANOPARTICLES; PARTICLES; CO2; NI;
D O I
10.1016/j.jallcom.2024.174006
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
Methanol steam reforming faces a significant challenge due to CO formation, which can lead to poisoning of fuel cell electrodes. This study introduces a series of Pd/ZnO catalysts prepared by ethylene glycol reduction, exhibiting remarkable selectivity in methanol steam reforming (MSR). The majority of palladium species exist in the form of PdZn alloy, attributed to the dual reduction process. This process, along with the generation of zinc vacancies and oxygen vacancies, enhances the interaction between the metal-carrier, promoting the formation of PdZn alloy, significantly improving CO2 selectivity and catalytic activity. Even at a high temperature of 400 degrees C, the active phase remains stable. After 5 hours of MSR, the 3% Pd/ZnO-300 H-2 catalyst achieves a hydrogen production rate of 1628.0 mmol<middle dot>g(cat)(-1)<middle dot>h(-1), with methanol conversion stabilized at 94%, CO2 selectivity reaching 97.7%, and CO content as low as 0.5%. These results outperform recent studies on hydrogen production. Furthermore, DFT calculations elucidate the complete reaction pathway (111) on PdZn. This study provides initial insights into the influence of metal-carrier interaction on the formation of PdZn alloy, suggesting a new direction for palladium-based catalysts in methanol steam reforming.
引用
收藏
页数:10
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