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A Novel Pentanary Metal Oxide Cathode with P2/O3 Biphasic Structure for High-Performance Sodium-Ion Batteries

机译:一种新型P2/O3双相结构的五氧化金属正极用于高性能钠离子电池

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摘要

The rapid capacity loss suffered by P2-type Mn-based layered oxide cathode materials, caused by deleterious high-voltage phase transformations and the dissolution of active materials, greatly limits their application in largescale sodium-ion battery installations. In this study, a novel P2/O3 biphasic cathode is developed using a multi-element (Fe, Mg, and Li) co-substitution strategy. The results of ex situ X-ray diffraction analyses and the absence of significant voltage plateaus in the charge-discharge profiles of cells featuring the proposed cathode indicate that deleterious phase transformations and concomitant lattice mismatch in the high-voltage region are effectively suppressed because of the topotactic intergrown structure of the resulting cathode. The optimized cathode also demonstrates improved structural stability and enhanced Na~+ diffusion kinetics, owing to the incorporation of stabilizing dopant pillars and suppressed metal-ion dissolution. Hence, the resulting Na half cell demonstrates a high initial capacity of 170.5 mA h g~(?1) at 0.1 C and excellent rate capability (106.6 mA h g~(?1) at 10 C). Furthermore, the resulting Na full cell, featuring a hard carbon anode, displays excellent cycling stability (72.1 capacity retention after 400 cycles), demonstrating its practical viability. This study presents the design and optimization of highperformance Mn-based cathodes.
机译:P2型锰基层状氧化物正极材料由于有害的高压相变和活性材料的溶解而遭受的快速容量损失,极大地限制了其在大规模钠离子电池装置中的应用。在这项研究中,使用多元素(Fe、Mg和Li)共取代策略开发了一种新型的P2/O3双相阴极。非原位X射线衍射分析结果表明,采用该阴极的电池的充放电曲线中没有明显的电压平台,这表明由于所得阴极的拓扑互生结构,高压区域的有害相变和伴随的晶格失配得到了有效抑制。优化后的正极还表现出更好的结构稳定性和增强的Na~+扩散动力学,这是由于稳定掺杂柱和抑制金属离子溶解。因此,所得的Na半电池在0.1 C下表现出170.5 mA h g~(?1)的高初始容量和优异的倍率能力(10 C时为106.6 mA h g~(?1))。此外,由此产生的Na全电池具有硬碳阳极,显示出出色的循环稳定性(400次循环后容量保持率为72.1%),证明了其实际可行性。本文介绍了高性能锰基正极的设计与优化。

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