A dendritic Cu/Cu2O structure with high curvature enables rapid and efficient reduction of carbon dioxide to C2 in an H-cell

IF 15.7 1区 化学 Q1 CHEMISTRY, APPLIED Chinese Journal of Catalysis Pub Date : 2024-08-01 DOI:10.1016/S1872-2067(24)60079-3
Lei shao, Bochen Hu, Jinhui Hao, Junjie Jin, Weidong Shi, Min Chen
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Abstract

Electrocatalytic reduction of CO2 (CO2RR) to multicarbon products is an efficient approach for addressing the energy crisis and achieving carbon neutrality. In H-cells, achieving high-current C2 products is challenging because of the inefficient mass transfer of the catalyst and the presence of the hydrogen evolution reaction (HER). In this study, dendritic Cu/Cu2O with abundant Cu0/Cu+ interfaces and numerous dendritic curves was synthesized in a CO2 atmosphere, resulting in the high selectivity and current density of the C2 products. Dendritic Cu/Cu2O achieved a C2 Faradaic efficiency of 69.8% and a C2 partial current density of 129.5 mA cm‒2 in an H-cell. Finite element simulations showed that a dendritic structure with a high curvature generates a strong electric field, leading to a localized CO2 concentration. Additionally, DRT analysis showed that a dendritic structure with a high curvature actively adsorbed the surrounding high concentration of CO2, enhancing the mass transfer rate and achieving a high current density. During the experiment, the impact of the electronic structure on the performance of the catalyst was investigated by varying the atomic ratio of Cu0/Cu+ on the catalyst surface, which resulted in improved ethylene selectivity. Under the optimal atomic ratio of Cu0/Cu+, the charge transfer resistance was minimized, and the desorption rate of the intermediates was low, favoring C2 generation. Density functional theory calculations indicated that the Cu0/Cu+ interfaces exhibited a lower Gibbs free energy for the rate-determining step, enhancing C2H4 formation. The Cu/Cu2O catalyst also exhibited a low Cu d-band center, which enhanced the adsorption stability of *CO on the surface and facilitated C2 formation. This observation explained the higher yield of C2 products at the Cu0/Cu+ interface than that of H2 under rapid mass transfer. The results of the net present value model showed that the H-cell holds promising industrial prospects, contingent upon it being a catalyst with both high selectivity and high current density. This approach of integrating the structure and composition provides new insights for advancing the CO2RR towards high-current C2 products.

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具有高曲率的树枝状 Cu/Cu2O 结构可在 H 细胞中快速高效地将二氧化碳还原为 C2
电催化还原二氧化碳(CO2RR)为多碳产品是解决能源危机和实现碳中和的有效方法。在氢电池中,由于催化剂的传质效率低以及氢进化反应(HER)的存在,实现大电流 C2 产物具有挑战性。本研究在二氧化碳气氛中合成了具有大量 Cu0/Cu+ 界面和无数树枝状曲线的树枝状 Cu/Cu2O,从而获得了高选择性和高电流密度的 C2 产物。树枝状 Cu/Cu2O 在 H 型电池中的 C2 法拉第效率达到 69.8%,C2 部分电流密度达到 129.5 mA cm-2。有限元模拟显示,具有高曲率的树枝状结构会产生强大的电场,导致局部二氧化碳浓度升高。此外,DRT 分析表明,高曲率树枝状结构能主动吸附周围高浓度的二氧化碳,从而提高传质速率并获得高电流密度。在实验过程中,通过改变催化剂表面 Cu0/Cu+ 的原子比,研究了电子结构对催化剂性能的影响,从而提高了乙烯选择性。在 Cu0/Cu+ 的最佳原子比下,电荷转移电阻最小,中间产物的解吸率低,有利于 C2 的生成。密度泛函理论计算表明,Cu0/Cu+界面在速率决定步骤中表现出较低的吉布斯自由能,从而促进了 C2H4 的生成。Cu/Cu2O 催化剂还表现出较低的 Cu d 带中心,这增强了*CO 在表面的吸附稳定性,促进了 C2 的生成。这一观察结果解释了在快速传质条件下,Cu0/Cu+界面上 C2 产物的产率高于 H2 产率的原因。净现值模型的结果表明,H-电池具有广阔的工业前景,这取决于它是一种具有高选择性和高电流密度的催化剂。这种将结构和组成相结合的方法为推动 CO2RR 向高电流 C2 产品发展提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Chinese Journal of Catalysis
Chinese Journal of Catalysis 工程技术-工程:化工
CiteScore
25.80
自引率
10.30%
发文量
235
审稿时长
1.2 months
期刊介绍: The journal covers a broad scope, encompassing new trends in catalysis for applications in energy production, environmental protection, and the preparation of materials, petroleum chemicals, and fine chemicals. It explores the scientific foundation for preparing and activating catalysts of commercial interest, emphasizing representative models.The focus includes spectroscopic methods for structural characterization, especially in situ techniques, as well as new theoretical methods with practical impact in catalysis and catalytic reactions.The journal delves into the relationship between homogeneous and heterogeneous catalysis and includes theoretical studies on the structure and reactivity of catalysts.Additionally, contributions on photocatalysis, biocatalysis, surface science, and catalysis-related chemical kinetics are welcomed.
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