嵌入镍-金属富勒烯(Nin@C60)作为CO可控C-C偶联的有效催化剂

IF 3.9 2区 化学 Q2 CHEMISTRY, PHYSICAL
Pengfei Liu , Mingqian Wang , Wanfei Hu , Xiaoying Feng , Xing Gao , Wei Qian , Qiang Wang , Junying Zhang
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引用次数: 0

摘要

CO的CC偶联在CO/CO2还原为C2+化合物中起着至关重要的作用。控制催化剂的活性和活性位点是实现可控CC耦合的有效方法。通过将金属掺杂到富勒烯中形成内嵌金属富勒烯(EMF),可以获得独特的催化活性。本文报道了嵌入镍-金属富勒烯(Nin@C60)作为一种高效催化剂,可以实现CO的可控CC偶联,从而促进C2产物的生成。结果表明,Nin簇嵌入C60形成Nin@C60在热力学上是可行的,电子结构分析表明,Nin簇可以通过电子转移激活C60。随后研究发现,C60和Nin@C60表面物理吸附的CO可通过可控的CC耦合直接形成O*C*CO中间体,具有极低的活化能垒(0.10 ~ 0.41 eV)。其中Ni6@C60的活化能势垒最低,为0.10 eV。这项工作为CC可控耦合和新型CO/CO2高效转化催化剂的设计提供了新的理论见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Embedded nickel-metallofullerenes (Nin@C60) as an effective catalyst for controlled C-C coupling of CO
The CC coupling of CO plays a crucial role in the reduction of CO/CO2 to C2+ compounds. Controlling the activity and active sites of the catalyst proves to be an effective method to achieve controllable CC coupling. By doping metals into fullerene to form endohedral metallofullerenes (EMF), a strategy emerges to achieve unique catalytic activity. Herein, we report that embedded nickel-metallofullerenes (Nin@C60) as an efficient catalyst can achieve controllable CC coupling of CO, thereby promoting the generation of C2 products. The results show that it is thermodynamically feasible for Nin clusters to embed into C60 to form Nin@C60, electronic structure analysis reveals that Nin clusters can activate C60 through electron transfer. Subsequently, research finds that the physically adsorbed CO on C60 and Nin@C60 surface can directly form O*C*CO intermediate through controllable CC coupling, with an extremely low activation energy barrier (0.10 ∼ 0.41 eV). Among them, Ni6@C60 has the lowest activation energy barrier, which is 0.10 eV. This work provides new theoretical insights into CC controllable coupling and the design of novel catalysts for efficient CO/CO2 conversion.
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来源期刊
Molecular Catalysis
Molecular Catalysis Chemical Engineering-Process Chemistry and Technology
CiteScore
6.90
自引率
10.90%
发文量
700
审稿时长
40 days
期刊介绍: Molecular Catalysis publishes full papers that are original, rigorous, and scholarly contributions examining the molecular and atomic aspects of catalytic activation and reaction mechanisms. The fields covered are: Heterogeneous catalysis including immobilized molecular catalysts Homogeneous catalysis including organocatalysis, organometallic catalysis and biocatalysis Photo- and electrochemistry Theoretical aspects of catalysis analyzed by computational methods
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