From Atomic-Level Synthesis to Device-Scale Reactors: A Multiscale Approach to Water Electrolysis

电解水 电解 催化作用 电催化剂 表征(材料科学) 纳米技术 分解水 制氢 耐久性 贵金属 工艺工程 电化学 电解质 材料科学 表面工程 化学 电极 工程类 物理化学 生物化学 光催化 复合材料
作者
Xiangbowen Du,Menghui Qi,Yong Wang
出处
期刊:Accounts of Chemical Research [American Chemical Society]
卷期号:57 (9): 1298-1309 被引量:40
标识
DOI:10.1021/acs.accounts.4c00029
摘要

Conspectus The development of an advanced energy conversion system for water electrolysis with high efficiency and durability is of great significance for a hydrogen-powered society. This progress relies on the fabrication of electrocatalysts with superior electrochemical performance. Despite decades of advancements in exploring high-performance noble and non-noble metal electrocatalysts, several challenges persist at both the micro- and macrolevels in the field of water electrolysis. At the microlevel, which encompasses electrocatalyst synthesis and characterization, design strategies for high-performance electrocatalysts have primarily focused on interface chemical engineering. However, comprehensive understanding and investigation of interface chemical engineering across various length scales, from micrometers to atomic scales, are still lacking. This deficiency hampers the rational design of catalysts with optimal performance. Under harsh reaction conditions, such as high bias potential and highly acidic or alkaline media, the surface of catalyst materials is susceptible to undergoing “reconstruction”, deviating from what is observed through ex situ characterization techniques postsynthesis. Conventional ex situ characterization methods do not provide an accurate depiction of the catalyst’s structural evolution during the electrocatalytic reaction, hindering the exploration of the catalytic mechanism. At the macrolevel, pertaining to catalysis-performance evaluation systems and devices, traditional laboratory settings employ a conventional three-electrode or two-electrode system to assess the catalytic performance of electrocatalysts. However, this approach does not accurately simulate hydrogen production under realistic industrial conditions, such as elevated temperatures (60–70 °C), high current densities exceeding 0.5 A cm –2, and flowing electrolytes. To address this limitation, it is crucial to develop testing equipment and methodologies that replicate the actual industrial conditions. In this Account, we propose a multiscale research framework for water electrolysis, spanning from microscale synthesis to macroscale scaled reactor design. Our approach focuses on the design and evaluation of high-performance HER/OER (hydrogen evolution reaction/oxygen evolution reaction) electrocatalysts, incorporating the following strategies: Leveraging principles of interface chemical engineering across various length scales (micrometers, nanometers, and atoms) enables the design of catalyst materials that enhance both activity and durability. This approach provides a comprehensive understanding of the intricate interplay between the catalyst structure and activity, implementing in situ / operando characterization techniques to monitor dynamic interfacial reactions and surface reconstruction processes. This facilitates a profound exploration of catalytic reaction mechanisms, offering insights into the catalyst’s structural evolution during the electrocatalytic reaction. We construct a laboratory-scale membrane electrode assembly (MEA) electrochemical reactor capable of operating at high current densities (>1 A cm –2 ) to evaluate the electrocatalytic performance under simulated industrial conditions. This ensures objective and authentic assessments of the catalyst application potential. Throughout the following sections, we illustrate the application of interface chemical engineering on different length scales in designing diverse electrocatalyst materials. We rely on in situ characterization techniques to gain a profound understanding of the mechanisms behind the HER and OER. Additionally, we describe the development of both acidic and alkaline MEA electrochemical reactors to enhance the precision of electrocatalytic performance evaluation. Finally, we provide a concise overview of the challenges and opportunities in this field.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Eric完成签到,获得积分20
刚刚
fjhsg25发布了新的文献求助10
刚刚
蓝天的应助被庄户采纳,获得10
1秒前
2秒前
芒果个冉冉完成签到,获得积分10
2秒前
科研通AI6.2的应助被泪西瓜采纳,获得10
2秒前
SciGPT的应助被lily采纳,获得10
2秒前
小电驴完成签到,获得积分10
3秒前
4秒前
陈辰晨发布了新的文献求助10
4秒前
笙凯完成签到,获得积分10
5秒前
下文献的蜉蝣完成签到,获得积分10
5秒前
5秒前
刘真焊发布了新的文献求助10
5秒前
6秒前
生活没有星期八完成签到,获得积分10
6秒前
7秒前
luyue9406完成签到,获得积分10
8秒前
SciGPT的应助被yi417采纳,获得10
8秒前
9秒前
sujiaoziemo完成签到,获得积分10
10秒前
hao发布了新的文献求助10
10秒前
11秒前
披萨不懂馕的心完成签到,获得积分10
11秒前
11秒前
七月流火重新开启了li的文献应助
13秒前
冯冯发布了新的文献求助10
14秒前
14秒前
14秒前
酷波er的应助被铁锤牛马版采纳,获得10
14秒前
粥粥粥发布了新的文献求助10
15秒前
Wellbeing发布了新的文献求助10
15秒前
丘比特的应助被专一的鼠标采纳,获得10
15秒前
17秒前
fofo完成签到,获得积分10
18秒前
chen发布了新的文献求助10
18秒前
thv发布了新的文献求助10
19秒前
20秒前
20秒前
20秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Rosenblum, Global Change Biology 800
自動車の空力技術 800
Organizational Behavior 510
Management and the Arts 510
Geschichtliche Grundbegriffe (GGB), Band 5: Pro–Soz 300
Die Religion in Geschichte und Gegenwart (RGG), 4. Auflage, Band 7: R–S 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 计算机科学 化学工程 工程类 有机化学 物理 复合材料 生物化学 内科学 细胞生物学 基因 遗传学 免疫学 冶金 光电子学 癌症研究
热门帖子
关注 科研通微信公众号,转发送积分 7790525
求助须知:如何正确求助?哪些是违规求助? 9328130
关于积分的说明 20421103
捐赠科研通 7380152
什么是DOI,文献DOI怎么找? 3323122
关于科研通互助平台的介绍 2470964
邀请新用户注册赠送积分活动 2339989