用于增强CO2电还原的工程晶/非晶界面。

Bingkun Li, Ziyi Zhong, Hao Li, Mingzhu Yue, Qingman Niu, Lu Liu, Wenfu Xie, Min Li, Mingfei Shao, Qiang Wang
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引用次数: 0

摘要

在碳中和的要求下,二氧化碳电还原成高价值的燃料和化学品,特别是甲酸,已成为一种有前途的方法。然而,在工业规模上实施它受到催化剂在高电流密度下的不稳定性和传统电解系统的过度能耗的阻碍。为了解决这些挑战,我们提出了一种非晶化策略来调节催化剂在操作条件下的重建。特别是,设计了一种无定形In基催化剂,InOx(OH)3-2x,在-800至-1000 mA cm-2下实现了98%的高法拉第效率,用于CO2电还原生成甲酸,同时保持100小时的稳定性。机理研究表明,InOx(OH)3-2x不是完全还原为金属In,而是部分还原为稳定的结晶/非晶In/In-OH界面,增强了对CO2和*OCHO中间体的吸附。为了提高电解系统的经济可行性,建立了CO2电还原-废塑料电氧化制甲酸酯系统。与传统电解系统相比,耦合系统能耗降低34.7%,甲酸酯产量提高49.7%,为CO2电还原提供了一种更节能、更经济的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Engineering Crystalline/Amorphous Interfaces for Enhanced CO2 Electroreduction.

In the request for carbon neutrality, CO2 electroreduction to high-value fuels and chemicals, particularly formic acid, has become as a promising approach. However, implementing it on an industrial scale is hindered by the catalyst instability under high current densities and the excessive energy consumption of conventional electrolysis systems. To tackle these challenges, we propose an amorphization strategy to regulate catalyst reconstruction under operational conditions. In particular, an amorphous In-based catalyst, InOx(OH)3-2x, was designed and achieved high Faradaic efficiencies of 98% at -800 to -1000 mA cm-2 for CO2 electroreduction to formate, while maintaining stability for 100 hours. Mechanistic studies show that InOx(OH)3-2x undergoes partial reduction to stable crystalline/amorphous In/In-OH interfaces instead of fully reducing to metallic In, enhancing the adsorption of CO2 and *OCHO intermediate. To improve the economic viability of electrolysis system, a CO2 electroreduction coupled with waste plastics electrooxidation system for formate production was constructed. Compared to conventional electrolysis system, the coupled system reduced energy consumption by 34.7% and increased formate production by 49.7%, offering a more energy-efficient and cost-effective approach to CO2 electroreduction.

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