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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.
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