Mesoporous Ru(Co, Ni)B bimetallic amorphous alloy for CO2 hydrogenation to formic acid

被引:7
作者
Zhao, Jingjing
Wang, Jiaqi
Bai, Yuan
Du, Haoran
Yang, Juanjuan
Yin, Bolin
Jiang, Bo [1 ]
Li, Hexing [1 ]
机构
[1] Shanghai Normal Univ, Coll Chem & Mat Sci, Shanghai Frontiers Sci Ctr Biomimet Catalysis, Chinese Educ Minist Key Lab, Shanghai 200234, Peoples R China
基金
中国国家自然科学基金;
关键词
Ru(Co; Ni)B bimetallic amorphous alloy catalysts; Mesoporous structure; Surfactant self-assembly; CO; 2; hydrogenation; HCOOH; SELECTIVE HYDROGENATION; CINNAMALDEHYDE HYDROGENATION; CATALYST; CONVERSION; NANOWIRES; ALCOHOL;
D O I
10.1016/j.jcou.2023.102528
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Amorphous metal alloy catalysts have attracted even-increasing attention owing to their high activity and selectivity. However, they are mainly prepared in ultrafine nanoparticles, which are easily gathered and challenging to separate. In this work, mesoporous Ru(Co, Ni)B bimetallic amorphous alloy catalysts with magnetic properties that can be easily recovered were synthesized via surfactant self-assembly. The as-prepared Ru1%CoB catalyst exhibited 578 & mu;mol/g/h production rate and 99% selectivity to HCOOH during liquid phase CO2 hydrogenation owing to the unique amorphous alloy structure corresponding to the well-distributed, coordinationunsaturated, electron-enriched and synergistic active sites, which promoted the adsorption, activation, dissociation, and surface reaction of CO2 and H2. Moreover, the mesoporous channels also promoted the diffusion and adsorption of CO2 and H2. Besides, the Ru1%CoB catalyst also displayed good durability in CO2 hydrogenation owing to the robust stability against the crystallization of amorphous alloy, the collapse of mesopores, and the leaching of active sites.
引用
收藏
页数:7
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