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首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >N-Boronated polybenzimidazole for composite electrolyte design of highly ion conducting pseudo solid-state ion gel electrolytes with a high Li-transference number
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N-Boronated polybenzimidazole for composite electrolyte design of highly ion conducting pseudo solid-state ion gel electrolytes with a high Li-transference number

机译:具有高锂转移数的高离子传导伪固态离子凝胶电解质的复合电解质设计的N-硼酸化聚苯胺唑

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摘要

We prepared highly ion conducting polymer electrolytes with a high lithium transference number (t(Li+)) using organoborane-modified polybenzimidazole (B-PBI) and an ionic liquid (IL), 1-butyl-3-methylimidazolium bis(trifluoromethane-sulfonyl) imide (BMImTFSI). The structural characteristics of these electrolytes were examined by nuclear magnetic resonance and Fourier-transform infrared spectroscopy. Thermogravimetric analysis and dynamic viscosity measurements were used to investigate the thermal and rheological properties of the electrolytes. Unlike other solid polymer electrolyte systems, the addition of lithium salts was not required in the case of the electrolytes prepared in this study as the molecular designing already incorporates lithium. The amount of BMImTFSI (w/w%) affected the ion transport behaviour of the composite polymer electrolytes. The ionic conductivity of the electrolytes increased with an increase in the IL content. The electrolyte with B-PBI/BMImTFSI (w/w%) (25/75) showed the highest conductivity of 8.8 x 10(-3) S cm(-1) at 51 degrees C. It also showed the highest t(Li+) value of 0.63 at room temperature with a wider electrochemical potential window of 5.45 V. The composite electrolytes were employed in anodic half-cells (Si/electrolyte/Li), and they showed a high reversible capacity up to 1300 mA h g(-1) which was retained even at a high charging rate. Electrochemical impedance spectroscopy and dynamic electrochemical impedance spectroscopy were performed before and after the charge-discharge measurements to confirm the formation of a stable solid electrolyte interface with B-PBI/BMImTFSI (w/w%).
机译:我们高度制备离子具有高的锂迁移数导电聚合物电解质(T(Li +)的),使用的有机硼烷改性的聚苯并咪唑(B-PBI)和离子液体(IL),1-丁基-3-甲基咪唑鎓双(三氟甲烷磺酰基)酰亚胺(BMImTFSI)。这些电解质的结构特征由核磁共振检查和傅里叶变换红外光谱。热重分析和动态粘度测量被用来研究电解液的热和流变性能。不像其他的固体聚合物电解质系统,在本研究中制备的分子设计已经包含锂的电解质的情况下,不需要进行另外的锂盐。 BMImTFSI的量(w / w的%)的影响的复合聚合物电解质的离子迁移行为。电解质的离子导电性与增加的IL含量增加。与B-PBI / BMImTFSI(W / W%)(25/75)的电解质在51度显示出8.8×10(-3)S厘米(-1)导电率最高C.它还表现出最高的T(Li +的)在室温下用5.45 V.的复合电解质在阳极半电池(硅/电解质/锂)被雇用的更宽的电化学电势窗的0.63值,并且它们表现出高的可逆容量高达1300毫安汞柱(-1 ),其即使在高充电速率保持。电化学阻抗谱和动态电化学阻抗谱之前和充电 - 放电测量之后进行,以确认一个稳定的固体电解质界面的与B-PBI / BMImTFSI的形成(w / w的%)。

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    Japan Adv Inst Sci &

    Technol Energy &

    Environm Area Grad Sch Adv Sci &

    Technol 1-1 Asahidai Nomi Ishikawa 9231292 Japan;

    Japan Adv Inst Sci &

    Technol Energy &

    Environm Area Grad Sch Adv Sci &

    Technol 1-1 Asahidai Nomi Ishikawa 9231292 Japan;

    Japan Adv Inst Sci &

    Technol Energy &

    Environm Area Grad Sch Adv Sci &

    Technol 1-1 Asahidai Nomi Ishikawa 9231292 Japan;

    Japan Adv Inst Sci &

    Technol Energy &

    Environm Area Grad Sch Adv Sci &

    Technol 1-1 Asahidai Nomi Ishikawa 9231292 Japan;

    Japan Adv Inst Sci &

    Technol Energy &

    Environm Area Grad Sch Adv Sci &

    Technol 1-1 Asahidai Nomi Ishikawa 9231292 Japan;

    Japan Adv Inst Sci &

    Technol Energy &

    Environm Area Grad Sch Adv Sci &

    Technol 1-1 Asahidai Nomi Ishikawa 9231292 Japan;

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  • 正文语种 eng
  • 中图分类 工程材料学;
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