Nano-Intermetallic InNi3C0.5 Compound Discovered as a Superior Catalyst for CO2 Reutilization

被引:48
作者
Chen, Pengjing [1 ]
Zhao, Guofeng [2 ]
Shi, Xue-Rong [3 ,4 ]
Zhu, Jian [1 ]
Ding, Jia [1 ]
Lu, Yong [1 ,2 ]
机构
[1] East China Normal Univ, Shanghai Key Lab Green Chem & Chem Proc, Shanghai 200062, Peoples R China
[2] East China Normal Univ, Sch Chem & Mol Engn, Shanghai 200062, Peoples R China
[3] Shanghai Univ Engn Sci, Dept Mat Engn, Shanghai 201620, Peoples R China
[4] Univ Innsbruck, Inst Phys Chem, Innrain 80-82, Innsbruck, Austria
基金
中国国家自然科学基金;
关键词
GAS SHIFT REACTION; TOTAL-ENERGY CALCULATIONS; METHANOL SYNTHESIS; ENHANCED ACTIVITY; OXYGEN REDUCTION; SELECTIVE CO2; CONVERSION; CARBON; HYDROGENATION; METHANATION;
D O I
10.1016/j.isci.2019.07.006
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
CO2 circular economy is urgently calling for the effective large-scale CO2 reutilization technologies. The reverse water-gas shift (RWGS) reaction is the most techno-economically viable candidate for dealing with massive-volume CO2 via downstream mature Fischer-Tropsch and methanol syntheses, but the desired groundbreaking catalyst represents a grand challenge. Here, we report the discovery of a nano-intermetallic InNi3C0.5 catalyst, for example, being particularly active, selective, and stable for the RWGS reaction. The InNi3C0.5(111) surface is dominantly exposed and gifted with dual active sites (3Ni-In and 3Ni-C), which in synergy efficiently dissociate CO2 into CO star (on 3Ni-C) and O-star (on 3Ni-In). O-star can facilely react with 3Ni-C-offered H-star to form H2O. Interestingly, CO star is mainly desorbed at and above 400 degrees C, whereas alternatively hydrogenated to CH3OH highly selectively below 300 degrees C. Moreover, this nano-intermetallic can also fully hydrogenate CO-derived dimethyl oxalate to ethylene glycol (commodity chemical) with high selectivity (above 96%) and favorable stability.
引用
收藏
页码:315 / +
页数:50
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