Fanrong Chen , Ze-Cheng Yao , Zhen-Hua Lyu , Jiaju Fu , Xiaoling Zhang , Jin-Song Hu
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In addition, the unique p-block electron structure can suppress the competitive hydrogen evolution reaction and enhance the adsorption of ECR intermediates. Seeking to systematically understand the structure–activity relationship of PMC-based ECR catalysts, this review summarizes the recent advances in designing PMC electrocatalysts for CO<sub>2</sub> reduction based on the fundamental aspects of heterogeneous ECR process, including advanced strategies for optimizing the intrinsic activity and improving the loading density of catalytic sites, constructing highly stable catalysts, and tuning product selectivities. 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Seeking to systematically understand the structure–activity relationship of PMC-based ECR catalysts, this review summarizes the recent advances in designing PMC electrocatalysts for CO<sub>2</sub> reduction based on the fundamental aspects of heterogeneous ECR process, including advanced strategies for optimizing the intrinsic activity and improving the loading density of catalytic sites, constructing highly stable catalysts, and tuning product selectivities. 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引用次数: 0
摘要
电催化二氧化碳还原(ECR)将二氧化碳转化为高价值燃料和化学品,为实现可持续碳循环提供了一种前景广阔的转化技术。近年来,尽管人们在开发高效 ECR 催化剂方面做出了巨大努力,但在同时实现高活性和长耐久性方面仍然存在挑战。利用可调结构、可调组分和 M-Ch(M = Sn、In、Bi 等,Ch = S、Se、Te)共价键稳定金属中心的优势,基于对嵌段金属瑀(PMC)的电催化剂在将 CO2 转化为 CO 或甲酸盐方面显示出巨大的潜力。此外,独特的对嵌段电子结构还能抑制竞争性氢进化反应,并增强对 ECR 中间产物的吸附。为了系统地了解基于 PMC 的 ECR 催化剂的结构-活性关系,本综述总结了基于异相 ECR 过程基本方面设计用于 CO2 还原的 PMC 电催化剂的最新进展,包括优化催化位点的内在活性和提高负载密度、构建高稳定性催化剂以及调整产物选择性的先进策略。随后,我们概述了为实际应用开发高性能 PMC ECR 催化剂所面临的挑战和前景。
Recent advances in p-block metal chalcogenide electrocatalysts for high-efficiency CO2 reduction
Electrocatalytic CO2 reduction (ECR) to high-value fuels and chemicals offers a promising conversion technology for achieving sustainable carbon cycles. In recent years, although great efforts have been made to develop high-efficiency ECR catalysts, challenges remain in achieving high activity and long durability simultaneously. Taking advantage of the adjustable structure, tunable component, and the M–Ch (M = Sn, In, Bi, etc., Ch = S, Se, Te) covalent bonds stabilized metal centers, the p-block metal chalcogenides (PMC) based electrocatalysts have shown great potential in converting CO2 into CO or formates. In addition, the unique p-block electron structure can suppress the competitive hydrogen evolution reaction and enhance the adsorption of ECR intermediates. Seeking to systematically understand the structure–activity relationship of PMC-based ECR catalysts, this review summarizes the recent advances in designing PMC electrocatalysts for CO2 reduction based on the fundamental aspects of heterogeneous ECR process, including advanced strategies for optimizing the intrinsic activity and improving the loading density of catalytic sites, constructing highly stable catalysts, and tuning product selectivities. Subsequently, we outline the challenges and perspectives on developing high-performance PMC ECR catalysts for practical applications.