Vanadium Carbide Nanoflakes as Catalysts for V3+/V2+ Redox Reactions

IF 5.5 3区 材料科学 Q1 ELECTROCHEMISTRY Electrochimica Acta Pub Date : 2024-11-22 DOI:10.1016/j.electacta.2024.145399
Jing Qi, Yunfeng Zhai, Keith Bethune, Jean St-Pierre
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Abstract

Vanadium carbide nanoflakes were synthesized and investigated as catalysts for V3+/V2+ redox reaction. This work explored a simple and environmentally friendly synthesis process that involved in situ carburization of a metal precursor and a carbon material as the carbon source and support. The structure, composition, morphology, and thermal stability of the vanadium carbide nanoflakes were characterized by X-ray diffraction, scanning electron microscopy/energy dispersive X-ray spectroscopy, transmission electron microscopy, and thermogravimetric analysis. Vanadium carbide supported on Vulcan XC72 carbon black showed a smaller particle size than that on graphite. Electrochemical properties of vanadium carbide nanoflakes toward the V3+/V2+ redox reaction were characterized by cyclic voltammetry and electrochemical impedance spectroscopy. The results show that vanadium carbide nanoflakes exhibited significantly enhanced catalytic activities and reversibility than graphite toward the V3+/V2+ redox reaction.

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碳化钒纳米片作为 V3+/V2+ 氧化还原反应的催化剂
合成了碳化钒纳米片,并将其作为 V3+/V2+ 氧化还原反应的催化剂进行了研究。这项工作探索了一种简单、环保的合成工艺,包括金属前驱体的原位渗碳和作为碳源和支撑的碳材料。通过 X 射线衍射、扫描电子显微镜/能量色散 X 射线光谱、透射电子显微镜和热重分析,对碳化钒纳米片的结构、成分、形态和热稳定性进行了表征。与石墨相比,支撑在 Vulcan XC72 炭黑上的碳化钒粒径更小。循环伏安法和电化学阻抗谱分析了纳米碳化钒在 V3+/V2+ 氧化还原反应中的电化学特性。结果表明,碳化钒纳米片对 V3+/V2+ 氧化还原反应的催化活性和可逆性明显高于石墨。
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来源期刊
Electrochimica Acta
Electrochimica Acta 工程技术-电化学
CiteScore
11.30
自引率
6.10%
发文量
1634
审稿时长
41 days
期刊介绍: Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.
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