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Defect-induced efficient dry reforming of methane over two-dimensional Ni/h-boron nitride nanosheet catalysts
被引:129
|作者:
Cao, Yang
[1
]
Maitarad, Phornphimon
[1
]
Gao, Min
[2
,3
]
Taketsugu, Tetsuya
[2
,3
]
Li, Hongrui
[1
]
Yan, Tingting
[1
]
Shi, Liyi
[1
]
Zhang, Dengsong
[1
]
机构:
[1] Shanghai Univ, Dept Chem, Res Ctr Nano Sci & Technol, Shanghai 200444, Peoples R China
[2] Hokkaido Univ, Dept Chem, Fac Sci, Sapporo, Hokkaido 0600810, Japan
[3] Kyoto Univ, Elements Strategy Initiat Catalysts & Batteries, Kyoto 6158245, Japan
基金:
中国国家自然科学基金;
关键词:
Dry reforming of methane;
Catalysts;
Boron nitride;
Density functional calculations;
GRAPHITIC CARBON NITRIDE;
OXIDATIVE DEHYDROGENATION;
NANOPARTICLES;
COKING;
OXYGEN;
PERFORMANCE;
STABILITY;
STORAGE;
DESIGN;
ROUTE;
D O I:
10.1016/j.apcatb.2018.07.001
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:
Efficient enhancement of catalytic stability and coke-resistance is a crucial aspect for dry reforming of methane. Here, we report Ni nanoparticles embedded on vacancy defects of hexagonal boron nitride nanosheets (Ni/h-BNNS) can optimize catalytic performance by taming two-dimensional (2D) interfacial electronic effects. Experimental results and density functional theory calculations indicate that surface engineering on defects of Ni/h-BNNS catalyst can strongly influence metal-support interaction via electron donor/acceptor mechanisms and favor the adsorption and catalytic activation of CH4 and CO2. The Ni/h-BNNS catalyst exhibits superior catalytic performance during a 120 h durability test. Furthermore, in situ techniques further reveal possible recovery mechanism of the active Ni sites, identifying the enhanced catalytic activities of the Ni/h-BNNS catalyst. This work highlights promotional mechanism of defect-modified interface and should be equally applicable for design of thermochemically stable catalysts.
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页码:51 / 60
页数:10
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