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首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Sodium Storage and Pseudocapacitive Charge in Textured Li4Ti5O_(12) Thin Films
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Sodium Storage and Pseudocapacitive Charge in Textured Li4Ti5O_(12) Thin Films

机译:Li4Ti5O_(12)薄膜中的钠存储和伪电容电荷

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Phase transformation reactions including alloying or conversion ones have often been utilized recently to improve the capacity performance of Na-ion battery anodes. However, they tend to induce larger volume change and more sluggish Na-ion transport at multiphase solid interfaces than for Li-ion batteries, leading to inefficiency of mixed conductive networks and thus degradation of reversibility, polarization, or rate performance. In this work, we use a structurally stable Li4Ti5O_(12) spinel thin film as insertion-type model material to investigate its intrinsic Na-ion transport kinetics and coupled pseudocapacitive charging. It is found that the latter effect is remarkably activated by the nanocrystalline microstructure full of defect-rich surface, which can simultaneously promote Na-ion and electron accessibility to the surface/subsurface. It is proposed that the extra pseudocapacitive charge storage is a potential solution to the high-capacity and high-rate insertion anodes without tradeoff of serious phase transformation or structural collapse. Therefore, a highly reversible charge capacity of 225 mAh g~(-1) (exceeding the theoretical value 175 mAh g~(-1) based on insertion reaction) at 1C is achievable.
机译:近来经常使用包括合金化或转化反应的相变反应来改善Na离子电池负极的容量性能。然而,与锂离子电池相比,它们倾向于在多相固体界面上引起更大的体积变化和更缓慢的钠离子传输,从而导致混合导电网络效率低下,从而导致可逆性,极化或速率性能下降。在这项工作中,我们使用结构稳定的Li4Ti5O_(12)尖晶石薄膜作为插入型模型材料来研究其固有的Na离子传输动力学和耦合的伪电容充电。发现后一种效应被充满缺陷丰富的表面的纳米晶体微结构显着激活,其可以同时促进钠离子和电子对表面/次表面的可及性。提出了额外的伪电容电荷存储是对高容量和高速率插入阳极的潜在解决方案,而无需权衡严重的相变或结构崩溃。因此,在1℃下可获得225mAh g〜(-1)的高度可逆充电容量(超过基于插入反应的理论值175mAh g〜(-1))。

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