Dynamic Active‐Hydrogen‐Buffering Interfaces Enable Fluctuation‐Resilient Selective Electrocatalytic Hydrogenation

IF 29.1 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Yan Du,Jian Shang,Zichao Xi,Jinxiao Wu,Longji Yuan,Huimin Yu,Huanyu Jin,Hui‐Ming Cheng
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引用次数: 0

Abstract

ABSTRACT Renewable‐electricity‐driven electrocatalysis is difficult to maintain under steady‐state operation because of the intermittent, variable, and stochastic nature of renewable power. This challenge is particularly critical for selective electrocatalytic hydrogenation (ECH), such as phenol‐to‐cyclohexanone conversion in acidic media, where fluctuating operation can induce transient accumulation of active hydrogen intermediates, compromising product selectivity and energy efficiency. In this study, we develop a dynamic active‐hydrogen‐buffering interface strategy to construct fluctuation‐resistant electrocatalysts using the short‐chain surfactant butyltrimethylammonium bromide (BTAB). Under simulated power fluctuations in a flow cell, the BTAB‐modified catalyst maintains near‐steady‐state performance, achieving 90.1% cyclohexanone selectivity and 83.6% Faradaic efficiency (FE), and outperforms the unmodified system by 1.69‐fold in cyclohexanone FE under more drastic fluctuations. Mechanistic studies reveal that the BTAB layer weakens the interfacial hydrogen‐bond network and attenuates Grotthuss‐type proton relay, thereby regulating proton flux and buffering active hydrogen accumulation during current fluctuations. This suppresses competing hydrogen evolution and overhydrogenation to cyclohexanol while preserving phenol hydrogenation kinetics. Combined with techno‐economic analysis, this work establishes active‐hydrogen buffering as an interfacial strategy for maintaining selective electrosynthesis under dynamic operating conditions.
动态活性-氢-缓冲界面实现波动弹性选择性电催化加氢
由于可再生电力的间歇性、可变性和随机性,可再生电力驱动的电催化难以在稳态运行下维持。这一挑战对于选择性电催化加氢(ECH)尤其关键,例如在酸性介质中苯酚到环己酮的转化,其中波动操作会导致活性氢中间体的短暂积累,从而影响产品的选择性和能源效率。在这项研究中,我们开发了一种动态活性氢缓冲界面策略,利用短链表面活性剂丁基三甲基溴化铵(BTAB)构建抗波动电催化剂。在模拟的流动电池功率波动下,BTAB修饰的催化剂保持了接近稳态的性能,达到90.1%的环己酮选择性和83.6%的法拉第效率(FE),在更剧烈的波动下,其环己酮FE比未修饰的体系高出1.69倍。机理研究表明,BTAB层削弱了界面氢键网络,减弱了Grotthuss型质子中继,从而调节了质子通量,缓冲了电流波动过程中活性氢的积累。这抑制了竞氢演化和过氢化到环己醇,同时保持了苯酚加氢动力学。结合技术经济分析,这项工作建立了活性氢缓冲作为在动态操作条件下保持选择性电合成的界面策略。
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
Advanced Materials
Advanced Materials 工程技术-材料科学:综合
CiteScore
43.00
自引率
4.10%
发文量
2182
审稿时长
2 months
期刊介绍: Advanced Materials, one of the world's most prestigious journals and the foundation of the Advanced portfolio, is the home of choice for best-in-class materials science for more than 30 years. Following this fast-growing and interdisciplinary field, we are considering and publishing the most important discoveries on any and all materials from materials scientists, chemists, physicists, engineers as well as health and life scientists and bringing you the latest results and trends in modern materials-related research every week.
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