Correlating Microstructure and Activity for Polysulfide Reduction and Oxidation at WS2Electrocatalysts

多硫化物 氧化还原 电化学 扫描电子显微镜 催化作用 微观结构 法拉第效率 透射电子显微镜 化学工程 材料科学 化学 无机化学 电极 纳米技术 冶金 复合材料 有机化学 物理化学 工程类 电解质
作者
Ifan E. L. Stephens,Caterina Ducati,Derek J. Fray
出处
期刊:Journal of The Electrochemical Society [Institute of Physics]
卷期号:160 (6): A757-A768 被引量:25
标识
DOI:10.1149/2.027306jes
摘要

The polysulfide reduction and oxidation activity of WS2 electrocatalysts was studied. This was undertaken with a specific view to improve the efficiency of the polysulfide-bromine redox flow battery, for large scale energy storage. Using data from the literature, it is estimated that the catalysts would require exchange current densities of ∼0.7 to 1 mA cm−2 true microscopic surface area to enable them to become economically viable. The experiments were performed upon three different forms of WS2: platelet like particles of the 2H polytype of WS2 (2H-WS2), ball milled WS2 and inorganic fullerene-like WS2 (IF-WS2). The catalysts were characterized ex-situ using X-ray diffraction, scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray analysis and N2 gas adsorption methods. Electrochemical measurements were performed at 35°C, in aqueous solutions of 1.8 M Na2S2.47 and 1 M NaOH, simulating the operating conditions of a half-charged polysulfide-bromine redox flow battery. The catalyst activity increased in the following order: IF-WS2 < 2H-WS2 < ball milled WS2. We attempt to rationalize this trend on the basis of the morphological features observed ex-situ. The exchange current density of the ball milled WS2, at ∼0.012 mA cm−2, falls short of the estimated target by a factor of ∼60 to 70.
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