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Correlation between capacitances of porous carbons in acidic and aprotic EDLC electrolytes

机译:酸性和非质子EDLC电解质中多孔碳电容之间的相关性

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摘要

A study based on a total of 41 nanoporous carbons shows that there exists a good correlation between the limiting gravimetric capacitances o at low current densities (1 mA cm ) measured in aprotic (1 M (CH)NBF in acetonitrile) and in acidic (2 M aqueous HSO) electrolytes. The comparison of the surface-related capacitances (F m ) of well characterized samples with the amount of thermodesorbed CO suggests a strong contribution of CO generating surface groups to charge storage in the acidic electrolyte, but a negligible contribution in the aprotic medium. It also appears that the decrease of the capacitance with current density is similar in both electrolytes. This confirms that the average micropore width and the CO generating surface groups are the main factors which limit the ionic mobility in both electrolytes.
机译:基于总共41种纳米多孔碳的研究表明,在质子惰性(1 M(CH)NBF在乙腈中)和酸性(2中,在低电流密度(1 mA cm)下测得的极限重量电容o之间存在良好的相关性M HSO水溶液)。表征良好的样品的表面相关电容(F m)与热解吸的CO量的比较表明,产生CO的表面基团对酸性电解质中电荷存储的贡献很大,但在非质子介质中的贡献可忽略不计。还似乎在两种电解质中电容随电流密度的减小是相似的。这证实了平均微孔宽度和产生CO的表面基团是限制两种电解质中离子迁移率的主要因素。

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