5- 羟甲基糠醛氧化辅助水分离电催化剂的调制策略

Tongxue Zhang, Shuai Liu, Fumin Wang, Wenxian Liu, Xinyuan He, Qian Liu, Xubin Zhang, Xijun Liu
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引用次数: 0

摘要

为解决能源短缺和环境问题,优先发展和使用可再生能源至关重要。利用可再生能源进行水电解是一种可持续的制氢方法。降低水电解的电位对于高效的清洁能源转换和储存至关重要。用热力学上更有利的 5-hydroxymethylfurfural (HMF) 氧化反应取代传统水电解制氢中的阳极氧进化反应,可以大大降低过电位,并产生有价值的产品 2,5-呋喃二甲酸。这一过程的关键在于开发有效的电催化剂,以最大限度地降低 HMF 电氧化-制氢系统的电位。因此,本综述全面介绍了影响 HMF 氧化辅助水分离电催化剂的电子和几何结构的调制策略。这些策略包括杂原子掺杂、缺陷投影、界面工程、结构设计和多金属协同作用。从结构特征、反应机理和电化学性能等多个角度对催化剂进行了评估。最后,提出了催化剂设计目前面临的挑战以及这一前景广阔领域的潜在发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modulation strategies of electrocatalysts for 5-hydroxymethylfurfural oxidation-assisted water splitting
To address energy shortages and environmental issues, prioritizing renewable energy development and usage is crucial. Employing renewable sources for water electrolysis offers a sustainable method for hydrogen generation. Reducing the water electrolysis potential is vital for efficient clean energy conversion and storage. Substituting the anodic oxygen evolution reaction in conventional hydrogen production from water electrolysis with the more thermodynamically favorable 5-hydroxymethylfurfural (HMF) oxidation reaction can greatly decrease overpotential and yield the valuable product 2,5-furan dicarboxylic acid. The key to this process is developing effective electrocatalysts to minimize the potential of the HMF electrooxidation-hydrogen production system. Therefore, this review provides a comprehensive introduction to the modulation strategies that affect the electronic and geometric structure of electrocatalysts for HMF oxidation-assisted water splitting. The strategies encompass heteroatom doping, defect projection, interface engineering, structural design, and multi-metal synergies. The catalysts are assessed from various angles, encompassing structural characterization, reaction mechanisms, and electrochemical performance. Finally, current challenges in the catalyst design and potential development of this promising field are proposed.
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