Stable Ni nanocrystals on porous single-crystalline MgO particles for enhanced dry reforming activity and durability of CH4/CO2

被引:2
作者
Zhang, Suning [1 ,2 ]
Cheng, Fangyuan [1 ,2 ,3 ]
Xie, Kui [1 ,2 ,3 ]
机构
[1] Fuzhou Univ, Coll Chem, Fuzhou 350108, Fujian, Peoples R China
[2] Chinese Acad Sci, Key Lab Design & Assembly Funct Nanostruct, Fujian Inst Res Struct Matter, Fuzhou 350002, Peoples R China
[3] Fujian Sci Technol Innovat Lab Optoelect Informat, Fuzhou 350108, Fujian, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
COKING RESISTANCE; NI/ZRO2; CATALYST; NI/MGO CATALYSTS; SUPPORTED NI; METHANE DRM; ZRO2; NANOPARTICLES; PERFORMANCE; DEPOSITION; FE;
D O I
10.1039/d3cy01560b
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
Dry reforming of methane (DRM) has garnered significant interest due to its potential for the efficient conversion of the greenhouse gases CH4 and CO2 into valuable chemical compounds, offering substantial economic prospects. However, DRM operations need to be carried out at high temperatures, so the resultant sintering of catalysts and carbon deposition remain as challenging issues. Here, we grow porous single crystalline (PSC) MgO particles using solid-solid phase transformation and stabilized Ni nanocrystals on the surface, creating an active metal oxide interface to evaluate the efficacy of the catalyst. The results reveal that the conversion rates of CH4 and CO2 are similar to 95% and similar to 96% at 700 degrees C, respectively. Despite continuous operation for 150 hours at 700 degrees C, the catalyst still exhibits good activity and durability. The well-defined Ni-MgO interface activates C-H bonds at reduced temperatures, contributing to enhanced catalytic activity and resistance to carbon deposition in DRM reactions. This work could offer a novel method for the growth of PSC oxide particles and provide strategies for stable catalyst designs.
引用
收藏
页码:681 / 688
页数:8
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