基于 MXene 的氧进化反应催化剂的研究进展

Electron Pub Date : 2023-12-30 DOI:10.1002/elt2.17
Jieli Chen, Xiaohong Gao, Jing Li, Zhenye Kang, Juan Bai, Tianjiao Wang, Yuliang Yuan, Chenghang You, Yu Chen, Bao Yu Xia, Xinlong Tian
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引用次数: 0

摘要

电化学水分离制氢被认为是减少使用化石燃料和将可再生电力储存在氢燃料中的最有前途的战略之一。然而,阳极氧进化过程仍然是一个瓶颈,因为要达到 10 mA cm-2 的电流密度,过电位高达约 300 mV。解决这一难题的关键在于开发具有最小过电位、长期稳定性和低成本的高效催化剂。作为一种新型二维材料,MXene 因其优越的导电性、出色的亲水性、高比表面积、多变的化学成分和易加工性等优点,已成为未来能源转换技术中一种引人关注的材料,使其成为氧进化催化剂层的潜在成分。本综述旨在总结和讨论以 MXene 为成分的氧进化催化剂的最新发展,重点介绍基于 MXene 的复合催化剂的合成和协同效应。在综述讨论的基础上,我们还就 MXene 基氧进化催化剂的电子相互作用、稳定性和结构演化提供了未来的研究方向。我们相信,在这一领域开展更广泛、更深入的研究,将加速发现高效的电化学氧进化催化剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Progress in MXene-based catalysts for oxygen evolution reaction

Progress in MXene-based catalysts for oxygen evolution reaction

Electrochemical water splitting for hydrogen generation is considered one of the most promising strategies for reducing the use of fossil fuels and storing renewable electricity in hydrogen fuel. However, the anodic oxygen evolution process remains a bottleneck due to the remarkably high overpotential of about 300 mV to achieve a current density of 10 mA cm−2. The key to solving this dilemma is the development of highly efficient catalysts with minimized overpotential, long-term stability, and low cost. As a new 2D material, MXene has emerged as an intriguing material for future energy conversion technology due to its benefits, including superior conductivity, excellent hydrophilic properties, high surface area, versatile chemical composition, and ease of processing, which make it a potential constituent of the oxygen evolution catalyst layer. This review aims to summarize and discuss the recent development of oxygen evolution catalysts using MXene as a component, emphasizing the synthesis and synergistic effect of MXene-based composite catalysts. Based on the discussions summarized in this review, we also provide future research directions regarding electronic interaction, stability, and structural evolution of MXene-based oxygen evolution catalysts. We believe that a broader and deeper research in this area could accelerate the discovery of efficient catalysts for electrochemical oxygen evolution.

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