Hongzhi Wang, Xiangcheng Shen, Weiguo Zhang, Suwei Yao
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引用次数: 0
Abstract
The synthesis of low-cost transition metal bifunctional electrocatalysts that can replace noble metals is crucial for realizing high efficiency hydrogen production from industrial water splitting. Herein, a novel binder-free amorphous/crystalline NiFeS@Ni0.85Se bifunctional electrocatalyst material has been fabricated on nickel foam (NF) via a straightforward two-step electrodeposition method. The electrode features a unique structure in which NiFeS nanosheets of uniform size grow on Ni0.85Se microspheres, thus providing more active sites. It exhibits a minimal overpotential of 63 mV at 10 mA cm−2 for hydrogen evolution reaction (HER) and 311 mV at 100 mA cm−2 for oxygen evolution reaction (OER). Impressively, when assembled into an electrolytic cell, the electrocatalyst can reach 10 mA cm−2 at just 1.51 V and remains stable for 220 h. Additionally, at 1.68 V, the catalyst reaches 50 mA cm−2 and maintains stable operation for 140 h, demonstrating outstanding water splitting potential. This paper presents a composite material that combines the crystalline and amorphous states, allowing them to complement each other and jointly promote catalytic performance.
制备低成本的过渡金属双功能电催化剂替代贵金属是实现工业水裂解高效制氢的关键。本文采用两步电沉积法在泡沫镍(NF)上制备了一种新型无粘结剂的无定形/结晶NiFeS@Ni0.85Se双功能电催化剂材料。该电极具有独特的结构,在Ni0.85Se微球上生长均匀尺寸的NiFeS纳米片,从而提供更多的活性位点。析氢反应(HER)在10 mA cm−2时的最小过电位为63 mV,析氧反应(OER)在100 mA cm−2时的最小过电位为311 mV。令人印象深刻的是,当组装到电解槽中时,电催化剂在1.51 V的电压下可以达到10 mA cm - 2,并保持220小时的稳定运行。此外,在1.68 V的电压下,催化剂达到50 mA cm - 2,并保持140小时的稳定运行,表现出出色的水分解潜力。本文提出了一种结合晶态和非晶态的复合材料,使两者相辅相成,共同促进催化性能。
期刊介绍:
Covering major developments in the field of solid state chemistry and related areas such as ceramics and amorphous materials, the Journal of Solid State Chemistry features studies of chemical, structural, thermodynamic, electronic, magnetic, and optical properties and processes in solids.