A review of modulation strategies for improving catalytic performance of transition metal phosphides for oxygen evolution reaction

过渡金属 双功能 催化作用 分解水 析氧 贵金属 材料科学 活动站点 纳米技术 化学工程 化学 物理化学 电化学 有机化学 光催化 工程类 电极
作者
Chen‐Jin Huang,Huimin Xu,Ting‐Yu Shuai,Qi‐Ni Zhan,Zhijie Zhang,Gao‐Ren Li
出处
期刊:Applied Catalysis B-environmental [Elsevier]
卷期号:325: 122313-122313 被引量:169
标识
DOI:10.1016/j.apcatb.2022.122313
摘要

Recently, researchers have focused on non-noble metal catalysts to replace noble metal catalysts for oxygen evolution reaction that is crucial for hydrogen production from water splitting. Among many metal-based compounds, transition metal phosphides (TMPs) often exhibit excellent HER catalytic performance due to the high electronegativity of P, which is favored by researchers. However, the OER catalytic performance of TMPs is not outstanding. Thus, improving its OER catalytic performance is crucial for the realization of excellent overall water-splitting bifunctional TMPs catalysts. In this review, we take TMPs as an example to analyze how to prepare highly active OER catalysts. Firstly, the evaluation criteria of OER reaction are introduced to compare the activity of catalysts. Then, from two aspects of improving the intrinsic activity of active sites and increasing the number of active sites/active surface area, we analyzed how to prepare highly active OER catalysts. For the former, it is often necessary to explore the method to make the OER potential close to the thermodynamic limit on the basis of understanding the OER mechanism. Therefore, we first summarized the widely recognized OER mechanism. Then, in order to improve the intrinsic activity of active sites, this paper expounds how to prepare efficient OER catalysts from four aspects: optimizing the adsorption and desorption of key intermediates, generating and optimizing vacancies in the catalyst, building multiple active sites, and promoting the formation of active phases. These four aspects are in line with the mechanism one by one; To increase the number of active sites/active surface area, strategies for constructing unique nanostructures and selecting special carriers were proposed. Finally, we propose key issues and challenges for future development in view of the shortcomings of each method.
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
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

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
kei完成签到,获得积分10
刚刚
kxy完成签到,获得积分10
刚刚
1秒前
linguo完成签到,获得积分10
1秒前
阳yang发布了新的文献求助10
1秒前
英吉利25发布了新的文献求助30
2秒前
Lady_Lola完成签到,获得积分10
2秒前
3秒前
Eternity2025应助漂亮的芒果采纳,获得10
3秒前
3秒前
3秒前
璃城完成签到 ,获得积分10
3秒前
zhangxasq发布了新的文献求助10
4秒前
4秒前
4秒前
4秒前
ccc发布了新的文献求助10
5秒前
zyl完成签到,获得积分10
5秒前
多走一步发布了新的文献求助10
5秒前
甜甜大炮发布了新的文献求助10
5秒前
6秒前
6秒前
悦耳芹菜完成签到,获得积分10
6秒前
6秒前
小房子完成签到,获得积分10
6秒前
qiang发布了新的文献求助10
7秒前
咪咪完成签到,获得积分10
7秒前
yu完成签到,获得积分10
7秒前
7秒前
8秒前
小娄完成签到,获得积分10
8秒前
8秒前
潮哈哈耶完成签到,获得积分10
9秒前
科研通AI6应助伍六柒采纳,获得10
9秒前
9秒前
清河剑客完成签到,获得积分10
9秒前
璃城关注了科研通微信公众号
9秒前
10秒前
炙热晓露完成签到,获得积分10
10秒前
丂枧完成签到,获得积分10
10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
The Complete Pro-Guide to the All-New Affinity Studio: The A-to-Z Master Manual: Master Vector, Pixel, & Layout Design: Advanced Techniques for Photo, Designer, and Publisher in the Unified Suite 1000
The International Law of the Sea (fourth edition) 800
Teacher Wellbeing: A Real Conversation for Teachers and Leaders 600
Synthesis and properties of compounds of the type A (III) B2 (VI) X4 (VI), A (III) B4 (V) X7 (VI), and A3 (III) B4 (V) X9 (VI) 500
Microbially Influenced Corrosion of Materials 500
Die Fliegen der Palaearktischen Region. Familie 64 g: Larvaevorinae (Tachininae). 1975 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 纳米技术 计算机科学 内科学 化学工程 复合材料 物理化学 基因 遗传学 催化作用 冶金 量子力学 光电子学
热门帖子
关注 科研通微信公众号,转发送积分 5402507
求助须知:如何正确求助?哪些是违规求助? 4521132
关于积分的说明 14084150
捐赠科研通 4435162
什么是DOI,文献DOI怎么找? 2434563
邀请新用户注册赠送积分活动 1426697
关于科研通互助平台的介绍 1405496