Carbon Monoliths with Hierarchical Porous Structure for All-Vanadium Redox Flow Batteries

氧化还原 循环伏安法 碳纤维 化学工程 热解 无机化学 材料科学 多孔性 溶解 电化学 化学 电极 复合材料 冶金 复合数 工程类 物理化学
作者
Jose F. Vivo‐Vilches,Blagoj Karakashov,Alain Celzard,Vanessa Fierro,Ranine El Hage,Nicolas Brosse,Anthony Dufour,Mathieu Etienne
出处
期刊:Batteries [Multidisciplinary Digital Publishing Institute]
卷期号:7 (3): 55-55 被引量:11
标识
DOI:10.3390/batteries7030055
摘要

Carbon monoliths were tested as electrodes for vanadium redox batteries. The materials were synthesised by a hard-templating route, employing sucrose as carbon precursor and sodium chloride crystals as the hard template. For the preparation process, both sucrose and sodium chloride were ball-milled together and molten into a paste which was hot-pressed to achieve polycondensation of sucrose into a hard monolith. The resultant material was pyrolysed in nitrogen at 750 °C, and then washed to remove the salt by dissolving it in water. Once the porosity was opened, a second pyrolysis step at 900 °C was performed for the complete conversion of the materials into carbon. The products were next characterised in terms of textural properties and composition. Changes in porosity, obtained by varying the proportions of sucrose to sodium chloride in the initial mixture, were correlated with the electrochemical performances of the samples, and a good agreement between capacitive response and microporosity was indeed observed highlighted by an increase in the cyclic voltammetry curve area when the SBET increased. In contrast, the reversibility of vanadium redox reactions measured as a function of the difference between reduction and oxidation potentials was correlated with the accessibility of the active vanadium species to the carbon surface, i.e., was correlated with the macroporosity. The latter was a critical parameter for understanding the differences of energy and voltage efficiencies among the materials, those with larger macropore volumes having the higher efficiencies.
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