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.
引用
收藏
页码:51 / 60
页数:10
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