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Investigating alternate binders: Impact on the performance of lithium titanate anode

机译:调查交替粘合剂:对钛酸锂阳极性能的影响

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Rechargeable Li-ion batteries although efficiently power small portable devices, implementation in electric vehicle mobility to assuage environmental concerns demand batteries possessing higher power densities and capacities while being compact and safer. Recent research is hence focused towards developing battery components that can sustain high charge-discharge rates while comprehensively addressing the safety issues. In our present research effort, attempts are made to investigate the role of different binders on the performance of nanostructured lithium titanate (LTO, Li_4Ti_5O_(12)) anodes in half-cell configuration against Li-metal. Commercial nano-LTO, Super-P and polyvinylidene fluoride (PVdF) are used as reference materials for comparative appraisal. An endeavor is made to showcase the feasibility of water soluble binders: sodium alginate (Na-alginate) and sodium carboxymethyl cellulose (Na-CMC) for greener processing of the electrodes and evaluate the effect on specific capacity, reversibility, charge retention and adaptability towards faster charging rate in the half-cells assembled. Binders provide sufficient adhesion interconnecting the active particles as well as maintain proper contact with the current collector, thus imparting electrode integrity over multiple charge-discharge cycles. This apart, binders are understood to influence the conductivity of electrodes, electrolyte wetting behavior, formation of solid-electrolyte interface (SEI) and the charge-transfer across interfaces. A lower interfacial resistance can promote higher specific capacity, increase energy density, improve reversibility, etc. while restricting capacity fade even at high C-rates; and the role of binders is found to contribute significantly. Comprehensive analysis of electrochemical impedance data collected at the end of each galvanostatic charge/discharge cycle provided crucial clues in understanding the charge transfer behavior for the electrodes fabricated with the binders.
机译:可充电锂离子电池虽然有效地动力小便携式设备,但在电动汽车移动中的实现,以缓和环境问题需要电池,在紧凑而更安全的同时需要具有更高功率密度和容量的电池。因此,最近的研究专注于开发能够维持高电荷 - 放电率的电池组件,同时全面解决安全问题。在我们目前的研究工作中,尝试探讨不同粘合剂对钛酸锂钛酸锂(LTO,Li_4Ti_5O_(12))阳极对LI-金属的阳极的作用。商业纳米LTO,超级P和聚偏二氟乙烯(PVDF)用作比较评价的参考材料。努力展示水溶性粘合剂的可行性:藻酸钠(Na-藻酸盐)和羧甲基纤维素(Na-CMC)的羧甲基纤维素(Na-CMC),用于更环保的电极加工,并评估对特定容量,可逆性,电荷保持和适应性的影响组装半电池中的更快充电率。粘合剂提供足够的粘合力,互连活性颗粒以及保持与集电器的适当接触,从而赋予多个充放电循环的电极完整性。除此之外,粘合剂应理解为影响电极的电导率,电解质润湿行为,固体电解质界面(SEI)的形成以及穿过界面的电荷转移。较低的界面抗性可以促进更高的比容量,增加能量密度,提高可逆性等,同时限制甚至在高C率下限制容量褪色;发现粘合剂的作用显着贡献。在每个镀锌电荷/放电循环结束时收集的电化学阻抗数据的综合分析为理解用粘合剂制造的电极的电荷转移行为提供了关键的线索。

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