Wang Kai, Yang Mingxuan, Liu Qiming, Cao Shiyue, Wang Yilin, Hu Ting, Peng Ziyang
Key Laboratory of Artificial Micro- and Nano-structures of Ministry of Education, School of Physics and Technology, Wuhan University, Wuhan 430072, China; Duozhu Technology (Wuhan) Co., LTD, China.
Key Laboratory of Artificial Micro- and Nano-structures of Ministry of Education, School of Physics and Technology, Wuhan University, Wuhan 430072, China; Duozhu Technology (Wuhan) Co., LTD, China.
J Colloid Interface Sci. 2025 Jan 15;678(Pt C):346-358. doi: 10.1016/j.jcis.2024.09.070. Epub 2024 Sep 12.
In recent years, core-shell structured Prussian Blue Analogues (PBAs) have been considered as highly promising cathode materials for sodium-ion batteries. Reducing production costs and simplifying the preparation method for core-shell PBAs have also become crucial considerations. This paper presents a novel approach for the first time: by acid-treating the as-synthesized solution from a simple coprecipitation reaction, a high-crystallinity, sodium-rich Mn-doped iron hexacyanoferrate (Fe/MnHCF) shell material is self-grown on the surface of manganese hexacyanoferrate (MnHCF). This method significantly improves the electrochemical properties of the MnHCF material. The core-shell structured PBA exhibits excellent cycling performance (with a capacity retention of 95.5 % for 400 cycles at 1 A/g) and high rate performance (134.2mAh/g@10 mA/g, 95.2mAh/g@1 A/g). In this article, we explore the growth mechanism of the high-sodium content, high-crystallinity shell structure and introduce a green chelating agent that is better suited for the crystallization of Mn and Fe-type PBA systems. Our study demonstrates that Mn doping enhances the conductivity of the shell material. Meanwhile, the heterojunction structure of MnHCF@Fe/MnHCF conducive to charge separation and migration. This straightforward synthesis strategy offers a novel approach for fabricating high-performance core-shell structured Prussian Blue Analogue materials.
近年来,核壳结构的普鲁士蓝类似物(PBAs)被认为是极具潜力的钠离子电池正极材料。降低核壳PBAs的生产成本并简化其制备方法也成为了关键考量因素。本文首次提出了一种新颖的方法:通过对简单共沉淀反应合成的溶液进行酸处理,在六氰合铁酸锰(MnHCF)表面自生长出高结晶度、富钠的锰掺杂六氰合铁酸铁(Fe/MnHCF)壳层材料。该方法显著改善了MnHCF材料的电化学性能。这种核壳结构的PBA展现出优异的循环性能(在1 A/g下400次循环后容量保持率为95.5%)和高倍率性能(10 mA/g时为134.2mAh/g,1 A/g时为95.2mAh/g)。在本文中,我们探究了高钠含量、高结晶度壳层结构的生长机制,并引入了一种更适合Mn和Fe型PBA体系结晶的绿色螯合剂。我们的研究表明,Mn掺杂提高了壳层材料的导电性。同时,MnHCF@Fe/MnHCF的异质结结构有利于电荷分离和迁移。这种简单直接的合成策略为制备高性能核壳结构的普鲁士蓝类似物材料提供了一种新方法。