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首页> 外文期刊>Advanced Functional Materials >Faster Activation and Slower Capacity/Voltage Fading: A Bifunctional Urea Treatment on Lithium-Rich Cathode Materials
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Faster Activation and Slower Capacity/Voltage Fading: A Bifunctional Urea Treatment on Lithium-Rich Cathode Materials

机译:更快的活化和更慢的容量/电压衰减:富锂阴极材料上的双功能尿素处理

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摘要

Li-rich layered oxides are promising cathode materials for next-generation Li-ion batteries because of their extraordinary specific capacity. However, the activation process of the key active component Li2MnO3 in Li-rich materials is kinetically slow, and the complex phase transformation with electrode/electrolyte side reactions causes fast capacity/voltage fading. Herein, a simple thermal treatment strategy is reported to simultaneously tackle these challenges. The introduction of a urea thermal treatment on Li-rich material Li1.87Mn0.94Ni0.19O3 leads to oxygen deficiencies and partially reduced Mn ions on the oxide surface for activating the Li-rich phase. In situ synchrotron study confirms that the urea-treated cathode shows much faster Li extraction from both Li and transition metal layers with less oxygen evolution upon charging than that of untreated counterparts. Moreover, the decomposition products of urea during thermal treatment subsequently deposit on the surface of cathode material, leading to a unique passivation layer against side reactions between electrode and electrolyte. Soft X-ray absorption spectroscopy reveals the structural evolution mechanism with a significantly suppressed dissolution of Mn species over cycling measurement. The urea-treated Li1.87Mn0.94Ni0.19O3 shows accelerated activation kinetics to reach high capacity of 270 mA h g(-1) and demonstrates excellent capacity retention of 98.49% over 300 cycles with slower voltage decay.
机译:富含锂的层状氧化物因其非凡的比容量而成为下一代锂离子电池的有希望的正极材料。但是,富含锂的材料中关键活性成分Li2MnO3的活化过程在动力学上很慢,并且伴随电极/电解质副反应的复杂相变会导致快速的容量/电压衰减。在此,据报道,一种简单的热处理策略可以同时解决这些挑战。在富锂材料Li1.87Mn0.94Ni0.19O3上引入尿素热处理会导致氧缺乏,并在氧化物表面上部分还原了Mn离子,从而激活了富锂相。原位同步加速器研究证实,经尿素处理的阴极显示出从锂和过渡金属层中提取锂的速度要快得多,带电时放出的氧气比未处理的阴极要少。而且,在热处理期间尿素的分解产物随后沉积在阴极材料的表面上,从而导致独特的钝化层,以防止电极和电解质之间的副反应。软X射线吸收光谱揭示了结构演化机理,并在循环测量中显着抑制了Mn的溶解。尿素处理的Li1.87Mn0.94Ni0.19O3表现出加速的活化动力学,可达到270 mA h g(-1)的高容量,并在300个循环中表现出出色的容量保持率98.49%,电压衰减更慢。

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