Nanoflower-like K-birnessite cathode material for high-capacity aqueous Zn-ion battery

IF 2.6 4区 化学 Q3 CHEMISTRY, PHYSICAL
Ionics Pub Date : 2025-05-13 DOI:10.1007/s11581-025-06348-4
Yuxuan Xiao, Changxin Han, Ting Yin, Wenjing Zhou, Juan Chou, Yuhong Zheng, Fengyue Zhang, Juanjuan Cheng, Yun Ou, Longfei Liu
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Abstract

Aqueous zinc ion batteries (AZIBs) have become a research hotspot due to their advantages of low cost, high safety, and environmental friendliness. K-Birnessite (KxMnO2) has been proved to be a candidate cathode material. However, the low conductivity and capacity degradation issues of δ-MnO2 limit its application. In the study, KxMnO2 (x = 0.27 and 0.31) with a nanoflower structure to improve the specific capacity has been designed, and capacity deterioration related to the evolution of Zn4SO4(OH)6·xH2O was analyzed. The capacity of K0.27MnO2 and K0.31MnO2 were 401.8 and 412.4 mAh g−1 at 0.1 A g−1 in the initial cycle due to the large specific surface area provided by the nanoflower structure. After 100 cycles, the specific capacity of the K0.27MnO2 electrode was 156.8 mAh g−1 at 1.0 A g−1, with a capacity retention rate close to 80%. During cycling, Zn4SO4(OH)6·xH2O was formed on the surface of the KxMnO2 cathode and transformed from a thin slice to a cracked block, leading to slow ion transport. This work provides a perspective for high-performance cathode design in AZIBs.

高容量含水锌离子电池正极材料纳米花状钾铋酸盐
水锌离子电池以其成本低、安全性高、环境友好等优点成为研究热点。K-Birnessite (KxMnO2)已被证明是一种候选正极材料。然而,δ-MnO2的低电导率和容量退化问题限制了其应用。本研究设计了具有纳米花结构的KxMnO2 (x = 0.27和0.31),以提高比容量,并分析了Zn4SO4(OH)6·xH2O的演化与容量退化的关系。由于纳米花结构提供了较大的比表面积,k0.27和K0.31MnO2在0.1 A g−1时的初始循环容量分别为401.8和412.4 mAh g−1。循环100次后,K0.27MnO2电极在1.0 A g−1下的比容量为156.8 mAh g−1,容量保持率接近80%。在循环过程中,KxMnO2阴极表面形成Zn4SO4(OH)6·xH2O,并由薄片转变为裂纹块,导致离子传输缓慢。这项工作为azib的高性能阴极设计提供了前景。
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来源期刊
Ionics
Ionics 化学-电化学
CiteScore
5.30
自引率
7.10%
发文量
427
审稿时长
2.2 months
期刊介绍: Ionics is publishing original results in the fields of science and technology of ionic motion. This includes theoretical, experimental and practical work on electrolytes, electrode, ionic/electronic interfaces, ionic transport aspects of corrosion, galvanic cells, e.g. for thermodynamic and kinetic studies, batteries, fuel cells, sensors and electrochromics. Fast solid ionic conductors are presently providing new opportunities in view of several advantages, in addition to conventional liquid electrolytes.
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