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Carbon based double layer capacitors with aprotic electrolyte solutions: the possible role of intercalation/insertion processes

机译:带有非质子电解质溶液的碳基双层电容器:嵌入/插入过程的可能作用

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摘要

The extraordinary stability and cycle life performance of today's electrochemical double-layer capacitors (EDLCs) are generally ascribed to the fact that charge storage in activated carbon (AC) is based on pure double-layer charging. In contrast, Faradaic charge-transfer reactions like those occurring in batteries are often connected with dimensional changes, which can affect the cycle life of these storage devices. Here we report the charge-induced height change of an AC electrode in an aprotic electrolyte solution, 1 mol/l (C_2H_5)_4NBF_4 (TEABF_4) in acetonitrile. The results are compared with those obtained for a graphite electrode in the same electrolyte. For both electrodes, we observe an expansion/contraction of several percent for a potential window of ±2 V vs. the immersion potential (ip). For the EDLC electrode, significant expansion starts at about 1 V remote from the ip and hence is well within the normal EDLC operation range. For the graphite electrode, the height changes are unambiguously caused by intercalation/deintercalation of both anions and cations. The close analogies between the graphite and the EDLC electrode suggest that ion intercalation or insertion processes might play a major role for charge storage, self discharge, cyclability, and the voltage limitation of EDLCs.
机译:当今电化学双层电容器(EDLC)的非凡的稳定性和循环寿命性能通常归因于以下事实:活性炭(AC)中的电荷存储基于纯双层电荷。相反,法拉第电荷转移反应(如电池中发生的电荷转移反应)通常与尺寸变化相关,这会影响这些存储设备的循环寿命。在这里,我们报告了在非质子电解质溶液中,AC电极的电荷诱导高度变化,在乙腈中为1 mol / l(C_2H_5)_4NBF_4(TEABF_4)。将结果与在相同电解质中的石墨电极获得的结果进行比较。对于两个电极,对于±2 V的电势窗口与浸没电势(ip),我们观察到百分之几的膨胀/收缩。对于EDLC电极,明显的扩展始于距ip约1 V处,因此完全在正常EDLC操作范围内。对于石墨电极,高度变化明确地由阴离子和阳离子的嵌入/脱嵌引起。石墨和EDLC电极之间的相似之处表明,离子嵌入或插入过程可能对EDLC的电荷存储,自放电,可循环性和电压限制起主要作用。

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