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首页> 外文期刊>Carbon: An International Journal Sponsored by the American Carbon Society >Surface modification of graphitized carbonaceous materials by electropolymerization of thiophene and their effects on electrochemical properties
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Surface modification of graphitized carbonaceous materials by electropolymerization of thiophene and their effects on electrochemical properties

机译:噻吩的电聚合作用对石墨化含碳材料进行表面改性及其对电化学性能的影响

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Highly oriented pyrolytic graphite (HOPG) and graphitized carbonaceous thin films prepared by plasma-assisted chemical vapor deposition (PACVD) were surface-modified by electropolymerization of thiophene. The electrochemical properties of the carbonaceous materials were studied by cyclic voltammetry and ac impedance spectroscopy. Irreversible cathodic current of the carbonaceous materials above 0.5 V (vs. Li/Li+) in the cyclic voltammograms significantly decreased by electropolymerization of thiophene, indicating that electropolymerization of thiophene suppress the decomposition of electrolytes on the carbonaceous materials. On the Nyquist plots, a semi-circle due to surface film resistance was observed, and the value significantly decreased at around 1.5 V. At potentials below 0.9 V, another semi-circle appeared in the middle to lower frequency region, which was assigned to the charge transfer resistance due to lithium-ion transfer at the surface-modified carbon electrode/electrolyte interface. The charge-transfer resistances were dependent on electrode potentials. The activation energy for lithium-ion transfer through interface between the surface-modified HOPG electrode and electrolyte was evaluated, and the value was almost identical to that obtained for an untreated HOPG electrode. Based on these results, it is concluded that electropolymerization of thiophene played an important role not in the phase transfer kinetics of lithium-ion but in reduction of the electrolyte decomposition at a graphite electrode. (C) 2005 Published by Elsevier Ltd.
机译:通过噻吩的电聚合对通过等离子体辅助化学气相沉积(PACVD)制备的高取向热解石墨(HOPG)和石墨化碳质薄膜进行了表面改性。通过循环伏安法和交流阻抗谱研究了含碳材料的电化学性能。噻吩的电聚合可显着降低循环伏安图中0.5 V(vs. Li / Li +)以上含碳材料的不可逆阴极电流,表明噻吩的电聚合可抑制电解质在含碳材料上的分解。在Nyquist图上,观察到由于表面膜电阻引起的半圆形,该值在1.5 V左右显着下降。在低于0.9 V的电势下,另一个半圆形出现在中低频区域,这被指定为表面改性的碳电极/电解质界面处由于锂离子转移而引起的电荷转移阻力。电荷转移电阻取决于电极电势。评估了通过表面改性的HOPG电极和电解质之间的界面传递锂离子的活化能,该值几乎与未处理的HOPG电极的活化能相同。根据这些结果,可以得出结论,噻吩的电聚合在锂离子的相转移动力学中起着重要的作用,而不是在减少石墨电极上的电解质分解方面起着重要的作用。 (C)2005由Elsevier Ltd.发布

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