阴极
材料科学
扩散
碱金属
动力学
化学工程
氧化物
离子
纳米技术
化学
物理化学
热力学
冶金
物理
有机化学
量子力学
工程类
作者
Bo Peng,Zihao Zhou,Jie Xu,Nazir Ahmad,Shunqin Zeng,Mingyu Cheng,Lianbo Ma,Yongtao Li,Genqiang Zhang
出处
期刊:ACS materials letters
[American Chemical Society]
日期:2023-07-24
卷期号:5 (8): 2233-2242
被引量:21
标识
DOI:10.1021/acsmaterialslett.3c00625
摘要
Layered transition metal oxides (LTMOs) have been identified as promising cathodes for alkali metal-ion batteries. However, their low-temperature performance is generally restricted by the sluggish ion diffusion kinetics within the LTMOs' host. Nanostructured materials have been developed to enhance ion diffusion kinetics but often significantly reduce the tap density. Herein, using NaCrO2 as a model cathode material, from the aspect of crystallography, we report a large-sized monocrystalline NaCrO2 with abundant Na+ active facets exposed by a straightforward acetate-assisted solid-state reaction, which addresses the dilemma between the volumetric energy density and ion diffusion kinetics and enables excellent low-temperature performance. Specifically, the synthesized NaCrO2 cathode showcases a high specific capacity of 94.7 mAh g–1 at a high rate of 20C under room temperature and displays good capacity retention of 97.2% after 100 cycles at 1C under −20 °C. Additionally, the full-cell device demonstrates a remarkable initial capacity of 113.0 mAh g–1 at a rate of 0.1C and exhibits excellent cyclic performance, retaining 84.2% of its capacity after 100 cycles at 0.2C under −10 °C. This study opens up new possibilities to design LTMOs with improved ion diffusion kinetics for alkali metal-ion batteries.
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