Ultra-stable trimetallic phosphide heterostructure with regulated electronic structure for overall water splitting at high current densities

磷化物 异质结 磷化铟 材料科学 光电子学 电流(流体) 电子结构 分解水 磷化镓 化学 结晶学 电气工程 金属 冶金 计算化学 光催化 工程类 砷化镓 催化作用 生物化学
作者
Daorui Wang,Xinruo Luo,Yuxiang Shang,Yuanyuan Wang,Haonan Zhang,Shuo Wang,Chenmeng Cui,Sungsik Lee,Shijie Hao,Ying Yang
出处
期刊:Journal of Power Sources [Elsevier BV]
卷期号:614: 234986-234986 被引量:3
标识
DOI:10.1016/j.jpowsour.2024.234986
摘要

Developing ultra-stable electrocatalysts for highly efficient overall water splitting at high current density (HCD) is critical for renewable hydrogen/oxygen production in the industry. However, the most active electrocatalysts for large current-driven water splitting are seriously handicapped by insufficient electrical contact kinetics due to the intensive bubble overflow. Herein, we demonstrate the ultra-stable trimetallic phosphides of NiFeP/NiCoP catalysts on a hydrophilic Ni foam skeleton via a corrosion-hydrothermal-phosphating strategy. The optimized NiFeP/NiCoP catalyst stabilizes for 600 h at −1 A cm −2 for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in alkaline solution, and it only needs low overpotentials of 237 and 314 mV to drive HER and OER at 1 A cm −2 , respectively. As expected, the optimized NiFeP/NiCoP electrode maintains 1000 h at 0.5 A cm −2 for water splitting, ranking among the top performers among reported catalysts. Such excellent performance could be attributed to the fast electron transfer for electrochemical reactions , the electron-deficient Fe/Ni sites contribute to forming robust metal oxyhydroxide during OER, and electron-rich Co sites facilitate H adsorption during HER. The findings present a highly promising candidate for ultra-stable non-noble metal electrocatalysts , offering a viable option for hydrogen/oxygen supply for fuel cells and metal-air batteries . The composition-balanced NiFeP/NiCoP electrodes stabilize for HER and OER over 600 h with a current density up to 1 A cm −2 . The electron-deficient Fe/Ni and electron-rich Co sites contribute to achieving this remarkable catalytic stability. The NiFeP/NiCoP-10 (+) || NiFeP/NiCoP-10 (−) electrode pairs present recorded stability with a long-lasting period of 1000 h at 0.5 A cm −2 for driving water splitting. • Corrosion-hydrothermal-phosphating yields NiFeP/NiCoP catalysts on Ni foam. • Optimized NiFeP/NiCoP endures 1000 h of water splitting at 0.5A cm −2 . • Trimetallic NiFeP/NiCoP displays fast electron transfer capability. • High-valence Ni/Fe sites in NiFeP/NiCoP boost the surface reconstruction for OER. • Low-valence states of Co sites in NiFeP/NiCoP favor H adsorption for HER.
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
潺潺流水完成签到,获得积分10
刚刚
1秒前
1秒前
1秒前
1秒前
1秒前
1秒前
爆米花应助长命百岁采纳,获得10
2秒前
MozzieMiao应助9527采纳,获得10
2秒前
888关闭了888文献求助
3秒前
申燕婷发布了新的文献求助10
4秒前
李爱国应助贵月采纳,获得10
4秒前
5秒前
5秒前
5秒前
落雁沙完成签到,获得积分10
5秒前
5秒前
6秒前
6秒前
mx完成签到,获得积分20
6秒前
zishuqio完成签到,获得积分10
6秒前
斩妖凉完成签到,获得积分10
7秒前
7秒前
7秒前
虚化发布了新的文献求助10
7秒前
7秒前
MozzieMiao应助Bob采纳,获得10
8秒前
汉堡包应助科研通管家采纳,获得10
8秒前
鑫问发布了新的文献求助10
8秒前
xzh应助科研通管家采纳,获得10
8秒前
8秒前
李健应助科研通管家采纳,获得10
8秒前
FashionBoy应助科研通管家采纳,获得10
8秒前
大模型应助科研通管家采纳,获得10
8秒前
eweawe发布了新的文献求助10
8秒前
8秒前
深情安青应助科研通管家采纳,获得10
8秒前
肉卷发布了新的文献求助10
8秒前
研友_85YNe8应助科研通管家采纳,获得10
8秒前
传奇3应助科研通管家采纳,获得10
9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
48V Low-voltage Power Distribution Network (PDN) Architecture Industry Report, 2024 800
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 700
Matrix Methods in Data Mining and Pattern Recognition Second Edition 610
适配Micro-LED色转换的高兼容性量子点负性光刻胶制备与工艺研究 500
Direct and Iterative Linear System Solvers 500
Vander's Renal Physiology第10版 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7308762
求助须知:如何正确求助?哪些是违规求助? 8926174
关于积分的说明 18916893
捐赠科研通 6971132
什么是DOI,文献DOI怎么找? 3212834
关于科研通互助平台的介绍 2381358
邀请新用户注册赠送积分活动 2190616