Cost-effective conversion of “stones” into high-performance capacitor carbon through a solid–solid inorganic chemical reaction

Abstract

Supercapacitors are highly sought after by the expanding new energy industry owing to their advantages of high power and long life. However, porous carbon, a crucial electrode material, is extremely expensive. As a result, the supercapacitor manufacturing industry has developed a strong demand for a new, low-cost method for synthesizing capacitor carbon. This study reports for the first time a novel method for producing high-performance capacitive carbon from ultra-low-cost raw materials CaCO3 (the primary stone component) and CaC2 (also referred to as electrical stone), which is accomplished via ball milling the two materials to facilitate a solid–solid inorganic chemical reaction. The specific surface area attained by this approach reaches 1000 m2 g−1 because of the template function of CaO generated in situ during the reaction, which is the highest value reported to date for CaC2-derived carbon. The as-prepared capacitive carbon performed well in both aqueous and organic electrolytes, with a coulombic efficiency of approximately 100%. It outperforms the commercial capacitive carbon YP50F, even when prepared on a kilogram scale. This advancement dramatically reduces the cost associated with the large-scale production of porous carbon for supercapacitors, thus establishing a long-term relationship between carbon neutrality and clean energy development.

Graphical abstract: Cost-effective conversion of “stones” into high-performance capacitor carbon through a solid–solid inorganic chemical reaction

Supplementary files

Article information

Article type
Research Article
Submitted
08 juil. 2024
Accepted
09 sept. 2024
First published
10 sept. 2024

Inorg. Chem. Front., 2024, Advance Article

Cost-effective conversion of “stones” into high-performance capacitor carbon through a solid–solid inorganic chemical reaction

Y. Bu, S. Wang, Y. Li, S. Tang, Q. Kang, Z. Zhu, H. Li, L. Pan and H. Liang, Inorg. Chem. Front., 2024, Advance Article , DOI: 10.1039/D4QI01715C

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