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Oxygen vacancy of Pt/CeO2 enabled low-temperature hydrogen generation from methanol and water
被引:15
|作者:
Guo, Qing
[1
]
Wang, You
[1
]
Li, Wenbin
[1
]
Zou, Yong
[1
]
Zhang, Sai
[1
,2
]
机构:
[1] Northwestern Polytech Univ, Sch Chem & Chem Engn, Xian 710072, Peoples R China
[2] Northwestern Polytech Univ Shenzhen, Res & Dev Inst, Shenzhen 518057, Peoples R China
基金:
中国国家自然科学基金;
关键词:
H (2) generation;
Aqueous-phase reforming of methanol;
Low temperatures;
Oxygen vacancy;
Pt;
METAL-SUPPORT INTERACTION;
SELECTIVE HYDROGENATION;
CATALYSTS;
DEHYDROGENATION;
GAS;
SPILLOVER;
EFFICIENT;
COMPLEX;
H-2;
D O I:
10.1016/j.jcat.2024.115309
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:
Aqueous-phase reforming of methanol (APRM) represents an alternative approach to achieve a sustainable hydrogen generation and safe storage. Nonetheless, the limitations imposed by the high operating temperatures of heterogeneous catalysts serve as a bottleneck for the widespread adoption of this system. Herein, we demonstrated that the Pt nanoparticles supported on porous nanorods of CeO2 with abundant oxygen vacancies (Pt/PN-CeO2) enabled the efficient H-2 generation through low-temperature (<60 degrees C) APRM reaction. The presence of oxygen vacancies on PN-CeO2 could enhance the electronic density of supported Pt nanoparticles through strong metal-support interaction, thereby promoting the activation of methanol. Meanwhile, the oxygen vacancies could further promote the H2O activation. Consequently, the interface between Pt and PN-CeO2 enabled efficient H-2 generation at 60 degrees C with a TOF values of 173.5 h(-1) and suppress CO generation. This finding provides a promising pathway towards the low-temperature APRM reaction.
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页数:7
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