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通过接枝含O/N官能团对以超微孔为主的碳进行改性以提高超级电容器性能。

Modification of ultra-micropore dominated carbon by O/N-containing functional groups grafted for enhanced supercapacitor performances.

作者信息

Ma Yan-Dong, Gao Jian-Fei, He Zheng-Hua, Kong Ling-Bin

机构信息

State Key Laboratory of Advanced Processing and Recycling of Non-ferrous Metals, Lanzhou University of Technology, Lanzhou 730050, P. R. China.

出版信息

Dalton Trans. 2021 Aug 4;50(30):10471-10481. doi: 10.1039/d1dt02017j.

Abstract

In our study, a simple method was employed to prepare ultra-micropore-dominated carbon materials with controllable pore size. A mass of heteroatoms was introduced by surface functional group grafting, resulting in enhanced electrochemical performance: the maximum specific capacity of 327.5 F g-1 was obtained at 0.5 A g-1 in 6 M KOH, while that of un-grafted original ultra-microporous carbon was only 188 F g-1, with long-term cycle stability (90.5% of the initial after 10 000 cycles), and excellent rate performance (over 82% at the current density from 0.5 A g-1 to 10 A g-1). The mechanism behind the improved performance was due to the presence of the introduced functional groups that improved the surface wettability of the material and provided additional redox active sites. Their synergistic effects promoted the enhanced electrochemical performance of the ultra-microporous carbon. This study provides a basis for the study of the energy storage mechanism of ultra-microporous carbon and the grafted modification of carbon materials with heteroatom-containing functional groups.

摘要

在我们的研究中,采用了一种简单的方法来制备孔径可控的以超微孔为主的碳材料。通过表面官能团接枝引入了大量杂原子,从而提高了电化学性能:在6 M KOH中,0.5 A g-1电流密度下的最大比电容为327.5 F g-1,而未接枝的原始超微孔碳仅为188 F g-1,具有长期循环稳定性(10000次循环后为初始值的90.5%),以及优异的倍率性能(在0.5 A g-1至10 A g-1的电流密度下超过82%)。性能提升背后的机制是由于引入的官能团改善了材料的表面润湿性并提供了额外的氧化还原活性位点。它们的协同作用促进了超微孔碳电化学性能的增强。本研究为超微孔碳储能机制的研究以及含杂原子官能团对碳材料的接枝改性提供了依据。

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