Research Progress on Electrocatalytic Oxidation of Olefins: From Catalytic Mechanism Studies to Reactor Design

IF 8.9 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Chemical record Pub Date : 2026-09-22 Epub Date: 2026-06-21 DOI:10.1002/tcr.70199
Zhiyu Hu, Yu Chen, Yitong Lin, Shaohua Chai, Yingtang Zhou, Shunli Li
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引用次数: 0

Abstract

Ethylene oxide and propylene oxide are important chemical intermediates, yet their conventional industrial production routes are associated with high energy consumption and significant carbon intensity. Electrocatalytic oxidation powered by renewable electricity offers a promising low-carbon approach for the selective conversion of light olefins under mild conditions. This review systematically summarizes the latest advances in the electrocatalytic conversion of ethylene and propylene into epoxides and diols. Particular emphasis is placed on two major mechanistic pathways: direct oxidation via active oxygen species and indirect oxidation mediated by halogen species, including chlorine- and bromine-based routes. Within this framework, state-of-the-art catalyst design strategies and the underlying reaction mechanisms are critically analyzed. The development of olefin epoxidation reaction engineering is also reviewed, with a focus on optimizing key practical performance metrics, such as current density, Faradaic efficiency, and long-term operational stability. Furthermore, we describe the electrolyzers involved in the olefin oxidation process, which hold promise for achieving industrial-scale applications. Finally, a forward-looking perspective is presented on the major challenges and future directions in this field, including the design of highly stable electrocatalysts, deeper mechanistic understanding, seamless integration with renewable electricity systems, the construction of tandem reaction platforms, and the large-scale implementation of advanced reactor architectures.

烯烃电催化氧化研究进展:从催化机理研究到反应器设计。
环氧乙烷和环氧丙烷是重要的化学中间体,但其传统的工业生产路线与高能耗和高碳强度有关。由可再生电力驱动的电催化氧化为轻烯烃在温和条件下的选择性转化提供了一种有前途的低碳方法。本文系统地综述了乙烯和丙烯电催化转化成环氧化物和二醇的最新进展。特别强调两种主要的机制途径:通过活性氧的直接氧化和由卤素介导的间接氧化,包括氯和溴基途径。在这个框架内,最先进的催化剂设计策略和潜在的反应机制进行了批判性的分析。综述了烯烃环氧化反应工程的发展,重点介绍了电流密度、法拉第效率和长期运行稳定性等关键实用性能指标的优化。此外,我们描述了涉及烯烃氧化过程的电解槽,有望实现工业规模的应用。最后,展望了该领域的主要挑战和未来发展方向,包括高稳定性电催化剂的设计、对机理的深入理解、与可再生电力系统的无缝集成、串联反应平台的建设以及先进反应器架构的大规模实施。
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
Chemical record
Chemical record 化学-化学综合
CiteScore
11.00
自引率
3.00%
发文量
188
审稿时长
>12 weeks
期刊介绍: The Chemical Record (TCR) is a "highlights" journal publishing timely and critical overviews of new developments at the cutting edge of chemistry of interest to a wide audience of chemists (2013 journal impact factor: 5.577). The scope of published reviews includes all areas related to physical chemistry, analytical chemistry, inorganic chemistry, organic chemistry, polymer chemistry, materials chemistry, bioorganic chemistry, biochemistry, biotechnology and medicinal chemistry as well as interdisciplinary fields. TCR provides carefully selected highlight papers by leading researchers that introduce the author''s own experimental and theoretical results in a framework designed to establish perspectives with earlier and contemporary work and provide a critical review of the present state of the subject. The articles are intended to present concise evaluations of current trends in chemistry research to help chemists gain useful insights into fields outside their specialization and provide experts with summaries of recent key developments.
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