制备 LNMO 阴极材料时镍锰氧化物的形态演变和表面取向效应

IF 5.5 3区 材料科学 Q1 ELECTROCHEMISTRY Electrochimica Acta Pub Date : 2024-11-09 DOI:10.1016/j.electacta.2024.145330
Zhengqing Pei , Jiawei Wang , Haifeng Wang , Kexin Zheng , Qian Wang , Jiexin Zhou , Dehua Ma , Ju Lu , Fanghai Lu
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引用次数: 0

摘要

该研究探讨了 LNMO(LiNi0.5Mn1.5O4)的形态和表面取向随温度升高而发生的演变。结果表明,在初始煅烧温度为 750 ℃ 时,LNMO 呈球形多面体,具有 (111)、(110) 和 (100) 面,颗粒尺寸相对较小。随着温度的升高,颗粒尺寸增大,晶面数量减少,材料最终过渡到典型的尖晶石结构。值得注意的是,在 750°C 煅烧的 LNMO 材料具有很高的锂离子迁移率,以 2 C 的速率循环 500 次后,其容量仍能保持 81.24%。这种优异的性能归功于多个晶面的暴露、合适的粒度以及 Mn³⁺ 的存在,这些因素共同稳定了晶体结构,并为锂离子迁移提供了合适的途径。
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Morphological evolution and surface orientation effects of nickel manganese oxide in the preparation of LNMO cathode material
The study investigated the evolution of LNMO (LiNi0.5Mn1.5O4) morphology and surface orientation as a function of increasing temperature. The results show that at an initial calcination temperature of 750 °C, LNMO exhibits spherical polyhedral with (111), (110), and (100) facets and relatively small particle sizes. In response to increasing temperatures, the particle size increases, the number of crystal facets decreases, and the material ultimately transitions to a typical spinel structure. Notably, the LNMO material calcined at 750 °C demonstrates a high lithium-ion migration rate, retaining 81.24% of its capacity after 500 cycles at a 2 C rate. This exceptional performance is attributed to the exposure of multiple crystal facets, suitable particle size, and the presence of Mn³⁺, which collectively stabilize the crystal structure and provide suitable pathways for Li⁺ transport.
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来源期刊
Electrochimica Acta
Electrochimica Acta 工程技术-电化学
CiteScore
11.30
自引率
6.10%
发文量
1634
审稿时长
41 days
期刊介绍: Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.
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