过电位
材料科学
塔菲尔方程
分解水
化学工程
析氧
碳纳米纤维
无定形碳
碳纤维
无定形固体
催化作用
无机化学
电化学
纳米技术
碳纳米管
化学
电极
光催化
结晶学
复合材料
物理化学
有机化学
工程类
复合数
作者
Aleena Tahir,Tanveer ul Haq,Faryal Aftab,Muhammad Zaheer,Hatïce Duran,Katrin Kirchhoff,Ingo Lieberwirth,S. Arshad
标识
DOI:10.1021/acsanm.2c04344
摘要
Nickel-based chalcogenides have recently gained considerable interest due to their potential as efficient electrocatalysts for overall water splitting. For example, nickel sulfide (NiSx) with suitable chemisorption energy for both oxygen- and hydrogen-containing intermediates can catalyze both half-cell reactions. Here, we report the synthesis of Ni3S2 nanostructures of ∼8 nm mean size, anchored over electrospun N-doped carbon nanofibers using microwave synthesis. Careful optimization of the process parameters enabled the structural synthesis of three different types of Ni3S2 (mostly amorphous, partially crystalline, and mostly crystalline) over carbon nanofibers. Scanning and high-resolution transmission electron microscopy, powder X-ray diffraction, and X-ray photoelectron spectroscopy were used to characterize the catalysts and electrochemical performance evaluated in an alkaline medium. The partially crystalline phase of Ni3S2 supported over carbon nanofibers was the best-performing catalyst for the oxygen evolution reaction (OER) due to its high electrochemically active surface area, N-doping of carbon, presence of a crystalline and amorphous mixed phase, and high conductivity of the carbon support which resulted in a low overpotential of 270 mV for the OER with a Tafel slope of only 51 mV/dec and a low charge transfer resistance of 1.08 Ω. Moreover, the catalyst was stable and yielded more than 95% Faradaic efficiency in both the oxygen evolution and hydrogen evolution reactions.
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