Control of metal-support interactions in heterogeneous catalysts to enhance activity and selectivity

被引:1780
作者
van Deelen, Tom W. [1 ]
Mejia, Carlos Hernandez [1 ]
de Jong, Krijn P. [1 ]
机构
[1] Univ Utrecht, Debye Inst Nanomat Sci, Inorgan Chem & Catalysis, Utrecht, Netherlands
基金
欧洲研究理事会;
关键词
CO OXIDATION; IN-SITU; OXIDE SUPPORT; NANOPARTICLES; HYDROGENATION; GOLD; AU; TEMPERATURE; REDUCTION; STABILITY;
D O I
10.1038/s41929-019-0364-x
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
Metal nanoparticles stabilized on a support material catalyse many major industrial reactions. Metal-support interactions in these nanomaterials can have a substantial influence on the catalysis, making metal-support interaction modulation one of the few tools able to enhance catalytic performance. This topic has received much attention in recent years, however, a systematic rationalization of the field is lacking due to the great diversity in catalysts, reactions and modification strategies. In this review, we cover and categorize the recent progress in metal-support interaction tuning strategies to enhance catalytic performance for various reactions. Furthermore, we quantify the productivity enhancements resulting from metal-support interaction control that have been achieved in C-1 chemistry in recent years. Our analysis shows that up to fifteen-fold productivity enhancement has been achieved, and that metal-support interaction is most impactful for metal nanoparticles smaller than four nanometres. These findings demonstrate the importance of metal-support interaction to improve performance in catalysis.
引用
收藏
页码:955 / 970
页数:16
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