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 生物化学 催化作用
作者
Daorui Wang,Xinruo Luo,Yuxiang Shang,Zeyan Wang,Haonan Zhang,Shuo Wang,C.Y. Cui,Sungsik Lee,Shijie Hao,Ying Yang
出处
期刊:Journal of Power Sources [Elsevier]
卷期号:614: 234986-234986 被引量:1
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
更新
大幅提高文件上传限制,最高150M (2024-4-1)

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
打打应助野性的小懒虫采纳,获得10
刚刚
若E18完成签到,获得积分10
刚刚
刚刚
务实凡灵完成签到,获得积分10
1秒前
彭于晏应助Rita采纳,获得10
1秒前
1秒前
5秒前
leo发布了新的文献求助10
5秒前
凡`发布了新的文献求助10
5秒前
hygge完成签到,获得积分20
5秒前
5秒前
5秒前
李健的小迷弟应助666采纳,获得10
6秒前
6秒前
reflux应助匆匆赶路人采纳,获得10
6秒前
番茄番茄发布了新的文献求助10
6秒前
7秒前
郑159753发布了新的文献求助10
8秒前
东海虞明完成签到,获得积分10
8秒前
Ava应助chrissylaiiii采纳,获得10
9秒前
10秒前
zora发布了新的文献求助10
10秒前
10秒前
llll发布了新的文献求助10
11秒前
娃哈哈发布了新的文献求助10
11秒前
12秒前
周裕川发布了新的文献求助10
12秒前
红发完成签到,获得积分10
13秒前
15秒前
恐龙扛狼完成签到,获得积分10
15秒前
15秒前
15秒前
搜集达人应助李谢谢采纳,获得70
16秒前
16秒前
16秒前
kyt发布了新的文献求助10
17秒前
香蕉觅云应助abo采纳,获得10
18秒前
18秒前
角落滴发布了新的文献求助10
19秒前
19秒前
高分求助中
Evolution 2024
Experimental investigation of the mechanics of explosive welding by means of a liquid analogue 1060
Die Elektra-Partitur von Richard Strauss : ein Lehrbuch für die Technik der dramatischen Komposition 1000
CLSI EP47 Evaluation of Reagent Carryover Effects on Test Results, 1st Edition 600
大平正芳: 「戦後保守」とは何か 550
Sustainability in ’Tides Chemistry 500
Cathodoluminescence and its Application to Geoscience 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3008649
求助须知:如何正确求助?哪些是违规求助? 2667777
关于积分的说明 7237566
捐赠科研通 2305035
什么是DOI,文献DOI怎么找? 1222210
科研通“疑难数据库(出版商)”最低求助积分说明 595468
版权声明 593410