Bismuth-Catalyzed Electrochemical Carbon Dioxide Reduction to Formic Acid: Material Innovation and Reactor Design

IF 14 Q1 CHEMISTRY, MULTIDISCIPLINARY
Yuqing Luo, Junmei Chen, Na Han and Yanguang Li*, 
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引用次数: 0

Abstract

Electrochemical CO2 reduction reaction (eCO2RR) has gained increasing attention as a promising strategy to mitigate the negative impacts of CO2 emission while simultaneously producing valuable chemicals or fuels. By converting CO2 into energy-rich products using renewable electricity, eCO2RR provides a sustainable approach to reducing the carbon footprint and promoting a circular carbon economy. Among different reduction products, the formic acid (or formate) is particularly attractive due to its economic viability and diverse industrial applications, making it a key focus for both research and industrial adoption.

Bismuth (Bi)-based electrocatalysts have emerged as promising candidates for eCO2RR to formic acid, by virtue of their nontoxicity, low cost, high abundance and exceptional selectivity for the two-electron pathway. These characteristics allow Bi-based catalysts to effectively suppress competing reactions and maximize formic acid production. In this Account, we discuss our contributions, along with those of others, to advancing the field of Bi-based materials for formic acid/formate production, focusing on both the fundamental understanding of their unique catalytic properties and innovative strategies employed to enhance their performances.

One of our significant contributions lies in the development of advanced nanostructures that enhance the catalytic activity of Bi-based materials. By tailoring the size and morphology of Bi nanostructures, we have demonstrated improvements in active site density and reaction kinetics, leading to higher formic acid/formate selectivity and productivity. We have also explored the design of three-dimensional architectures, which provide enhanced mass transport and reduce diffusion limitations, thereby improving the overall efficiency of the catalytic process. Furthermore, works on defect engineering have revealed how modifying the electronic properties of Bi can optimize its binding affinity for key intermediates, significantly enhancing its catalytic performance.

In addition to material innovations, recent research has contributed to the advancement of reactor designs that enable efficient and scalable eCO2RR systems. We have optimized flow cells to ensure continuous operation with high mass transport efficiency, making them suitable for industrial production. Furthermore, studies on membrane electrode assemblies (MEAs) have integrated Bi-based catalysts into compact and energy-efficient systems, furthering enhancing the practical applicability of eCO2RR. Solid-electrolyte systems have also been explored to simplify system configurations, improve stability and enable the production of pure formic acid. These efforts reflect the commitment of the community to bridging the gap between laboratory-scale research and industrial-scale implementation.

Despite the significant progress achieved, challenges remain in fully realizing the potential of Bi-based eCO2RR technologies. Future efforts should focus on improving the long-term stability of catalysts, using advanced characterization techniques to gain deeper insights into reaction mechanisms, and further refining reactor configurations for large-scale applications. Addressing these challenges will be crucial to unlocking the full potential of Bi-based systems for sustainable chemical manufacturing.

Abstract Image

铋催化的电化学二氧化碳还原为甲酸:材料创新和反应器设计
电化学CO2还原反应(eCO2RR)作为一种有前景的策略,在减轻CO2排放的负面影响的同时生产有价值的化学品或燃料,越来越受到人们的关注。通过使用可再生电力将二氧化碳转化为富含能源的产品,eCO2RR为减少碳足迹和促进循环碳经济提供了一种可持续的方法。在不同的还原产品中,甲酸(或甲酸盐)因其经济可行性和多样化的工业应用而特别有吸引力,使其成为研究和工业应用的重点。铋(Bi)基电催化剂因其无毒、低成本、高丰度和对双电子途径的特殊选择性,已成为eCO2RR制甲酸的有前景的候选者。这些特性使铋基催化剂能够有效抑制竞争反应并最大限度地提高甲酸产量。在本账户中,我们讨论了我们和其他人对推进用于甲酸/甲酸盐生产的铋基材料领域的贡献,重点是对其独特催化性能的基本理解和提高其性能的创新策略。我们的重要贡献之一在于开发了先进的纳米结构,提高了铋基材料的催化活性。通过调整铋纳米结构的尺寸和形态,我们证明了活性位点密度和反应动力学的改善,从而提高了甲酸/甲酸盐的选择性和生产率。我们还探索了三维结构的设计,这些结构提供了增强的传质并减少了扩散限制,从而提高了催化过程的整体效率。此外,缺陷工程方面的工作揭示了如何通过改变铋的电子性质来优化其对关键中间体的结合亲和力,从而显著提高其催化性能。除了材料创新外,最近的研究还为反应堆设计的进步做出了贡献,使其能够实现高效和可扩展的eCO2RR系统。我们优化了流动池,以确保高质量运输效率的连续运行,使其适用于工业生产。此外,对膜电极组件(MEA)的研究已将铋基催化剂集成到紧凑且节能的系统中,进一步提高了eCO2RR的实用性。还探索了固体电解质系统,以简化系统配置,提高稳定性,并能够生产纯甲酸。这些努力反映了社区致力于弥合实验室规模的研究和工业规模的实施之间的差距。尽管取得了重大进展,但在充分发挥铋基eCO2RR技术的潜力方面仍存在挑战。未来的努力应侧重于提高催化剂的长期稳定性,使用先进的表征技术来更深入地了解反应机理,并进一步完善大规模应用的反应器配置。应对这些挑战对于释放铋基系统在可持续化学制造中的全部潜力至关重要。
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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CiteScore
17.70
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