Regulating the location of metal promoters in CuFe-based catalysts for enhanced CO2 hydrogenation to higher alcohols

被引:0
作者
Fan, Qixin [1 ,2 ]
Liu, Na [1 ]
Zhao, Jingming [1 ,2 ]
Yu, Yang [1 ,2 ]
Sun, Yannan [1 ,2 ]
Han, Yu [1 ,2 ]
Zhang, Jixin [1 ,3 ]
Wang, Amin [4 ]
Ge, Qingjie [1 ,3 ]
Wei, Jian [1 ,3 ]
Sun, Jian [1 ,3 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, Dalian 116023, Liaoning, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Liaoning Binhai Lab, Dalian 116023, Liaoning, Peoples R China
[4] Yulin Univ, Yulin Engn Technol Res Ctr Low Metamorph Coal Mild, Yulin 719000, Shaanxi, Peoples R China
来源
JOURNAL OF ENERGY CHEMISTRY | 2025年 / 107卷
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
CO2; hydrogenation; CuFe bimetallic catalyst; Metal modification; Higher alcohols; Amorphous iron carbide; SELECTIVE HYDROGENATION; CARBON-DIOXIDE; TRANSFORMATION; ETHANOL; CONVERSION; METHANOL; OXIDE;
D O I
10.1016/j.jechem.2025.03.046
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Regulating the location of the metal promoters plays a vital role in catalyst structure and its catalytic behavior during CO2 hydrogenation to higher alcohols. Herein, we selected the metal promoters with a precipitation pH similar to that of Cu2+ or Fe3+ to prepare a series of CuFe-based catalysts. Characterization results show that doping Al or Cr promoter, located with the Fe phase, suppressed the excessive carburization of the Fe phase and maintained an optimal proportion between Fe3O4 and amorphous iron carbide (FeCx), thus exhibiting superior catalytic activity and stability. In contrast, doping Zn or In promoter, located with the Cu phase, underwent a deeper carburization and formed more crystalline FeCx, showing an inferior performance. The CuFeCr catalyst achieved the highest space-time yield of 330 mg g cat1 h-1 for higher alcohols among these catalysts. This study provides a novel strategy for optimizing the structure of the active phases for CO2 hydrogenation. (c) 2025 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
引用
收藏
页码:31 / 43
页数:13
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