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A dilatometric and small-angle X-ray scattering study of the electrochemical activation of mesophase pitch-derived carbon in non-aqueous electrolyte solution

机译:非水电解质溶液中中间相沥青衍生碳电化学活化的膨胀和小角X射线散射研究

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摘要

The electrochemical activation of certain pitch-derived carbons has been proposed as a promising route towards obtaining high-capacitance electrodes for electrochemical double-layer capacitors. In the present work, the mechanism of electrochemical activation of a graphitizable carbon after calcination and KOH-activation was studied by nitrogen adsorption, electrochemical dilatometry and in situ small-angle X-ray scattering (SAXS). During electrochemical activation, a large capacitance gain from 1 to 121 F/g (at 0 V in a 1 mol/L solution of Et4NBF4 in propylene carbonate) was accompanied by a significant irreversible swelling of the electrode by 24 (6) for activation in the negative (positive) potential range, respectively. In situ SAXS provided clear evidence for the insertion of ions into the latent microporosity of the carbon during electrochemical activation. Thus, the mechanism of electrochemical activation of weakly activated graphitizable carbon is not strictly due to ion intercalation between parallel graphene sheets.
机译:某些沥青衍生碳的电化学活化被认为是获得电化学双电层电容器高电容电极的有前途的途径。本工作通过氮气吸附、电化学膨胀法和原位小角X射线散射(SAXS)研究了煅烧和KOH活化后石墨化碳的电化学活化机理。在电化学活化过程中,从1到121 F/g(在1 mol/L碳酸丙烯酯中的Et4NBF4溶液中为0 V)的大电容增益伴随着电极的显着不可逆膨胀,分别在负(正)电位范围内活化24%(6%)。原位SAXS为在电化学活化过程中将离子插入碳的潜在微孔提供了明确的证据。因此,弱活化石墨烯碳的电化学活化机理并非严格归因于平行石墨烯片之间的离子插层。

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