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在铜镓双金属催化剂上高效地将一氧化碳高转化率转化为多碳产物。

Energy-efficient CO conversion to multicarbon products at high rates on CuGa bimetallic catalyst.

作者信息

Chen Lei, Chen Junmei, Fu Weiwei, Chen Jiayi, Wang Di, Xiao Yukun, Xi Shibo, Ji Yongfei, Wang Lei

机构信息

Department of Chemical and Biomolecular Engineering, National University of Singapore, Singapore, Singapore.

Department of Chemistry, National University of Singapore, Singapore, Singapore.

出版信息

Nat Commun. 2024 Aug 15;15(1):7053. doi: 10.1038/s41467-024-51466-8.

Abstract

Electrocatalytic CO reduction to multi-carbon products is a promising approach for achieving carbon-neutral economies. However, the energy efficiency of these processes remains low, particularly at high current densities. Herein, we demonstrate that the low energy efficiencies are, in part, sometimes significantly, attributed to the high concentration overpotential resulting from the instability (i.e., flooding) of catalyst-layer during electrolysis. To tackle this challenge, we develop copper/gallium bimetallic catalysts with reduced activation energies for the formation of multi-carbon products. Consequently, the reduced activation overpotential allows us to achieve practical-relevant current densities for CO reduction at low cathodic potentials, ensuring good stability of the catalyst-layer and thereby minimizing the undesired concentration overpotential. The optimized bimetallic catalyst achieves over 50% cathodic energy efficiency for multi-carbon production at a high current density of over . Furthermore, we achieve current densities exceeding in a zero-gap membrane-electrode-assembly reactor, with a full-cell energy efficiency surpassing 30%.

摘要

电催化将CO还原为多碳产物是实现碳中和经济的一种很有前景的方法。然而,这些过程的能源效率仍然很低,特别是在高电流密度下。在此,我们证明低能源效率部分(有时是显著地)归因于电解过程中催化剂层不稳定性(即水淹)导致的高浓度过电位。为应对这一挑战,我们开发了具有降低的多碳产物形成活化能的铜/镓双金属催化剂。因此,降低的活化过电位使我们能够在低阴极电位下实现与实际相关的CO还原电流密度,确保催化剂层的良好稳定性,从而将不希望的浓度过电位降至最低。优化后的双金属催化剂在超过 的高电流密度下实现了超过50%的多碳产物阴极能源效率。此外,我们在零间隙膜电极组装反应器中实现了超过 的电流密度,全电池能源效率超过30%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da8f/11327302/91c81c77b8b6/41467_2024_51466_Fig1_HTML.jpg

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