Synthesis of carbon spheres from glucose using the hydrothermal carbonization method for the fabrication of EDLCs

水热碳化 碳化 电容 化学工程 材料科学 电化学 结块 碳纤维 制作 介孔材料 电极 超级电容器 热液循环 产量(工程) 比表面积 纳米技术 形态学(生物学) 复合材料 化学 扫描电子显微镜 催化作用 有机化学 遗传学 替代医学 物理化学 病理 医学 工程类 复合数 生物
作者
E. Tovar-Martínez,C.E. Sánchez-Rodríguez,J. D. Sánchez-Vásquez,M. Reyes‐Reyes,R. López‐Sandoval
出处
期刊:Diamond and Related Materials [Elsevier]
卷期号:136: 110010-110010 被引量:15
标识
DOI:10.1016/j.diamond.2023.110010
摘要

Carbon spheres (CSs) from glucose were synthesized by the hydrothermal carbonization method. We explored the effect of glucose concentration used in the synthesis on the yield as well as on the morphology of the CSs, and how this affects their electrochemical capacitance. For the possible application of CSs in commercial electrical double-layer capacitors (EDLCs), it is necessary to synthesize them in large quantities. For this reason, one of the main goals of this work was to increase the amount of CSs synthesized by increasing the concentration of glucose used in the synthesis process, affecting their electrochemical properties as little as possible for its use in EDLCs. Two post-synthesis procedures were performed on the CSs: 1) heat treatment at 800 °C in an argon atmosphere and 2) sulfonation process with subsequent heat treatment. The morphology of the six synthesized samples was analyzed. All the synthesized samples have the characteristic of generating large agglomerates of CSs; some are interconnected and fused forming a three-dimensional network of microspheres and other irregular shapes. This agglomeration of CSs may appear to be a negative effect on the performance of the electrodes, due to the apparent reduction in specific surface area. However good electrochemical capacitance results are obtained, because this morphology favors the creation of mesopores and, therefore, a greater facility for the insertion of ions in charging and discharging processes. The electrodes of CSs with better performance showed a capacitance of 85 F g−1 at 50 mV s−1.

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