Design of highly active cobalt catalysts for CO2 hydrogenation via the tailoring of surface orientation of nanostructures

被引:35
作者
Jimenez, Juan D. [1 ]
Wen, Cun [1 ]
Lauterbach, Jochen [1 ]
机构
[1] Univ South Carolina, Dept Chem Engn, Columbia, SC 29208 USA
基金
美国国家科学基金会;
关键词
FISCHER-TROPSCH SYNTHESIS; GROUP-VIII METALS; CARBON-DIOXIDE; NANOPARTICLE CATALYSTS; PARTICLE-SIZE; METHANATION; ADSORPTION; OXIDE; PROMOTION; SPECTROSCOPY;
D O I
10.1039/c9cy00402e
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
The synthesis of nanomaterials with well-controlled morphologies and surface orientations has opened new avenues towards increasing catalytic performance and understanding of fundamental catalytic pathways. Here, we illustrate how tailoring surface orientations of Co3O4 catalysts on the nanoscale results in control over catalytic performance via the preferential formation of active surface species during CO2 hydrogenation. This results in a significant increase in the methane yield on Co3O4 nanorods, as opposed to conventional nanoparticle catalysts, where Co3O4 nanorods inhibit the formation of formate spectator species via the preferential formation of bridged CO as an intermediate species. This design approach provides a new dimension for the development of next generation catalysts and opens new, more efficient strategies for the conversion of carbon dioxide into useful hydrocarbons.
引用
收藏
页码:1970 / 1978
页数:9
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