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Loading effect of a barium titanate artificial interface on high voltage capabilities at high charge and discharge rates

机译:钛酸钡人工界面在高充放电速率下对高电压性能的负载效应

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Cyclic characteristics of BaTiO3 (BT)-decorated LiCoO2 (LC), for use as an artificial solid electrolyte interface (SEI) were evaluated at high voltages. Within the standard voltage window (i.e., 3.3-4.2 V), the BT-decorated LC exhibited greater capacities for up to 80 cycles compared with both the Al2O3 (paraelectric)-decorated and bare LC SEIs. The discharge capacity retention after 80 cycles (compared with the initial value) was 86.0% for the BT-LC cathode. This is a significant improvement over both the bare LC that showed 19.9% retention and the Al2O3-LC that displayed 71.5% retention. Thereafter, the cyclic stabilities of the BT-LC and bare LC were compared within potential windows at cutoff voltages as high as 4.9 V. In this region, BT decoration yielded marked improvements in capacity retention after 50 cycles, up to a potential of 4.7V. The post-situ XRD analysis of the cathode sheets showed that BT decoration effectively stabilized the hexagonal crystal structure of the LC, H1, resulting in the said cyclic stability increase. These observations demonstrate that the use of BT in SEI allows a significant increase in working voltage while maintaining the chemical stability of the underlying LC matrix, a key advancement in the perpetual pursuit of ever higher cell energy densities. (C) 2017 The Japan Society of Applied Physics
机译:在高压下评估了用作人造固体电解质界面(SEI)的BaTiO3(BT)修饰的LiCoO2(LC)的循环特性。在标准电压窗口(即3.3-4.2 V)内,与用Al2O3(顺电)装饰的和裸LC SEI相比,用BT装饰的LC在最多80个循环中表现出更大的容量。 BT-LC阴极在80个循环后的放电容量保持率(与初始值相比)为86.0%。这相对于显示19.9%保留率的裸露LC和显示71.5%保留率的Al2O3-LC都是一个显着的改进。此后,在高达4.9 V的截止电压下,在电位窗口内比较了BT-LC和裸LC的循环稳定性。在该区域中,BT装饰经过50个循环后电容保持率显着提高,最高可达4.7V。 。阴极片的后位XRD分析表明,BT装饰有效地稳定了LC,H1的六方晶体结构,导致所述循环稳定性增加。这些观察结果表明,在SEI中使用BT可以显着提高工作电压,同时保持基础LC基质的化学稳定性,这是永久追求更高电池能量密度的一项关键进展。 (C)2017日本应用物理学会

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  • 来源
    《Japanese journal of applied physics》 |2017年第10s期|10PC01.1-10PC01.4|共4页
  • 作者单位

    Okayama Univ, Grad Sch Nat Sci & Technol, Okayama 7008530, Japan;

    Okayama Univ, Grad Sch Nat Sci & Technol, Okayama 7008530, Japan;

    Okayama Univ, Grad Sch Nat Sci & Technol, Okayama 7008530, Japan;

    Okayama Univ, Grad Sch Nat Sci & Technol, Okayama 7008530, Japan;

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