首页> 外文期刊>International journal of hydrogen energy >Effect of physical activation/surface functional groups on wettability and electrochemical performance of carbon/activated carbon aerogels based electrode materials for electrochemical capacitors
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Effect of physical activation/surface functional groups on wettability and electrochemical performance of carbon/activated carbon aerogels based electrode materials for electrochemical capacitors

机译:物理活化/表面官能团对电化学电容器电极材料碳/活性炭气凝胶润湿性和电化学性能的影响

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Polymeric carbon/activated carbon aerogels were synthesized through sol-gel polycondensation reaction followed by the carbonization at 800 degrees C under Argon (Ar) atmosphere and subsequent physical activation under CO2 environment at different temperatures with different degrees of burn-off. Significant increase in BET specific surface area (SSA) from 537 to 1775 m(2)g(-1) and pore volume from 0.24 to 0.94 cm(3)g(-1) was observed after physical activation while the pore size remained constant (around 2 nm). Morphological characterization of the carbon and activated carbons was conducted using X-ray diffraction (XRD) and Raman spectroscopy. Fourier-transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS) were used to investigate the effect of thermal treatment (surface cleaning) on the chemical composition of carbon samples.Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) were used to analyse the capacitive and resistive behaviour of non-activated/activated/and surface cleaned activated carbons employed as electroactive material in a two electrode symmetrical electrochemical capacitor (EC) cell with 6 M KOH solution used as the electrolyte.CV measurements showed improved specific capacitance (SC) of 197 Fg(-1) for activated carbon as compared to the SC of 136 Fg(-1) when non-activated carbon was used as electroactive material at a scan rate of 5 mVs(-1). Reduction in SC from 197 Fg(-1) to 163 Fg(-1) was witnessed after surface cleaning at elevated temperatures due to the reduction of surface oxygen function groups.The result of EIS measurements showed low internal resistance for all carbon samples indicating that the polymeric carbons possess a highly conductive three dimensional crosslinked structure. Because of their preferred properties such as controlled porosity, exceptionally high specific surface area, high conductivity and desirable capacitive behaviour, these materials have shown potential to be adopted as electrode materials in electrochemical capacitors. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:通过溶胶 - 凝胶缩聚反应合成聚合物碳/活性炭气凝胶,然后在氩气(Ar)气氛下在800℃下碳化,随后在不同温度下的CO 2环境下的物理活化,不同程度的烧坏。在物理活化后观察到从537至1775μm(2 )g(-1)和孔体积的BET比表面积(SSA)的显着增加,而孔径仍然是恒定的,在物理活化后观察到0.24至0.94cm(3 )g(-1)的孔体积。 (大约2纳米)。使用X射线衍射(XRD)和拉曼光谱进行碳和活性碳的形态学表征。傅里叶变换红外光谱(FTIR)和X射线光电子能谱(XPS)用于研究热处理(表面清洁)对碳样品化学成分的影响。环伏安法(CV)和电化学阻抗光谱(EIS)用于分析在两个电极对称电化学电容器(EC)电池中使用的非活化/活化/和表面清洁的活性碳的电容和电阻性能,其具有6M KOH溶液,用作电解质的电解质测量结果。显示出改善当非活性炭以5mV(-1)的扫描速率使用时,与136 FG(-1)的SC相比,197FG(-1)的特定电容(SC)为活性炭。由于表面氧函数组的降低,在升高的温度下,在高温下的表面清洁后,目睹了197fg(-1)至163fg(-1)的SC的减少。EIS测量结果表明所有碳样品的内阻低聚合物碳具有高导电的三维交联结构。由于它们优选的性质,例如受控孔隙率,特别高的表面积,高导电性和理想的电容性能,因此这些材料显示出电位作为电化学电容器中的电极材料。 (c)2018氢能源出版物LLC。 elsevier有限公司出版。保留所有权利。

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