4.7 Article

Room-temperature liquid metal synthesis of nanoporous copper-indium heterostructures for efficient carbon dioxide reduction to syngas

期刊

SCIENCE CHINA-MATERIALS
卷 65, 期 12, 页码 3504-3512

出版社

SCIENCE PRESS
DOI: 10.1007/s40843-022-2058-5

关键词

syngas; liquid metal; EGaIn; heterostructure; nanoporous metal

资金

  1. National Natural Science Foundation of China [51872116, 12034002]
  2. Project for Self-Innovation Capability Construction of Jilin Province Development and Reform Commission [2021C026]
  3. Program for JLU Science and Technology Innovative Research Team [JLUSTIRT-2017TD-09]
  4. Science and Technology Development Program of Jilin Province [20190201233JC]
  5. Fundamental Research Funds for the Central Universities

向作者/读者索取更多资源

In this paper, a self-supporting bimetallic porous heterogeneous indium/copper structure catalyst was synthesized and proven to exhibit excellent performance in the reduction of carbon dioxide to syngas. The ratio of H-2/CO can be adjusted by changing working potentials. The catalyst shows high stability and has two distinct active sites, Cu-delta and Cu-0, enabling the high-performance generation of CO and H-2.
Nanoporous metals show promising performances in electrochemical catalysis. In this paper, we report a self-supporting bimetallic porous heterogeneous indium/copper structure synthesized with a eutectic gallium-indium (EGaIn) material on a copper substrate. This nanoporous copper-indium heterostructure catalyst exhibits excellent performance in the reduction of carbon dioxide to syngas. The ratio of H-2/CO is tunable from 0.47 to 2.0 by changing working potentials. The catalyst is highly stable, showing 96% maintenance of the current density after a 70-h continuous test. Density functional theory calculations reveal that the indium/copper interface induces charge redistribution within the copper surface, leading to the formation of two distinct active sites, namely, Cu-delta and Cu-0, and enabling a high-performance generation of CO and H-2. This work provides a new strategy for obtaining self-supporting nanoporous metal electrode catalysts.

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