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Investigation of PF_6~- and TFSI~- anion intercalation into graphitized carbon blacks and its influence on high voltage lithium ion batteries

机译:PF_6〜-和TFSI〜-阴离子嵌入石墨化炭黑中的研究及其对高压锂离子电池的影响

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Graphitized carbon blacks have shown a more promising electrochemical performance than the. non-treated ones when being applied in small amounts as conductive additives in composite cathode electrodes for lithium ion batteries, due to the absence of surface functional groups which contribute to detrimental side-reactions with the electrolyte. Here, we report that at high potentials of >4.5 V vs. Li/Li~+, graphitic structures in carbon black can provide host sites for the partially reversible intercalation of electrolyte salt anions. This process is in analogy to the charge reaction of graphite positive electrodes in dual-ion cells. A standard furnace carbon black with small graphitic structural units, as well as slightly and highly graphitized carbon blacks, were characterized and analyzed with regard to anion intercalation. A LiPF6 containing organic solvent based electrolyte as well as a state-of-the-art ionic liquid based electrolyte composed of LiTFSI in PYR14TFSI were applied. The intercalation of both PF_6~- and TFSI~- could be confirmed by cyclic voltammetry in electrodes made of carbon blacks. When exposed to high potentials, carbon blacks experienced strong activation in the 1st cycle, which promotes the perception for anion intercalation, and thus increases the anion intercalation capacity in the following cycles. The specific capacity from anion intercalation was evaluated by constant current charge-discharge cycling. The obtained capacity was proportional to the graphitization degree. As anion intercalation might be accompanied by decomposition reactions of the electrolyte, e.g., by co-intercalation of solvent molecules, it could induce the decomposition of the electrolyte inside the carbon and thus degradation of the carbon black graphitic structure. In order to avoid side reactions from surface groups and from anion intercalation, the thermal treatment of carbon blacks must be optimized.
机译:石墨化的炭黑已显示出比其更有前途的电化学性能。当未将其作为导电添加剂少量应用到锂离子电池的复合阴极中时,由于没有表面官能团,这些未处理的未处理的表面官能团会导致与电解质的有害副反应。在此,我们报道,在相对于Li / Li〜+的> 4.5 V的高电位下,炭黑中的石墨结构可以为电解质盐阴离子的部分可逆嵌入提供宿主位点。该过程类似于双离子电池中石墨正极的充电反应。对具有小石墨结构单元的标准熔炉炭黑以及轻度和高度石墨化的炭黑进行了表征,并进行了阴离子插值分析。施加了包含有机溶剂基电解质的LiPF6以及由PYR14TFSI中的LiTFSI组成的最新离子液体基电解质。 PF_6〜-和TFSI_-的插入可以通过循环伏安法在炭黑制成的电极中确定。当暴露于高电位下时,炭黑在第一个循环中经历了强烈的活化,这促进了对阴离子插层的感知,因此在随后的循环中增加了阴离子插层的能力。通过恒定电流充放电循环来评估阴离子嵌入的比容量。所获得的容量与石墨化程度成正比。由于阴离子的嵌入可能伴随着电解质的分解反应,例如,溶剂分子的共嵌入,因此它可能引起碳内部电解质的分解,进而导致炭黑石墨结构的降解。为了避免表面基团和阴离子插层的副反应,必须优化炭黑的热处理。

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