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具有增强动力学性能的高度结晶普鲁士蓝用于高效钠存储

Highly Crystallized Prussian Blue with Enhanced Kinetics for Highly Efficient Sodium Storage.

作者信息

Qin Mingsheng, Ren Wenhao, Jiang Ruixuan, Li Qi, Yao Xuhui, Wang Shiqi, You Ya, Mai Liqiang

机构信息

State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070, Hubei, P.R. China.

School of Chemistry, Faculty of Science, The University of New South Wales, Sydney, New South Wales 2052, Australia.

出版信息

ACS Appl Mater Interfaces. 2021 Jan 27;13(3):3999-4007. doi: 10.1021/acsami.0c20067. Epub 2021 Jan 13.

Abstract

Prussian blue analogs (PBAs) featuring large interstitial voids and rigid structures are broadly recognized as promising cathode materials for sodium-ion batteries. Nevertheless, the conventionally prepared PBAs inevitably suffer from inferior crystallinity and lattice defects, leading to low specific capacity, poor rate capability, and unsatisfied long-term stability. As the Na migration within PBAs is directly dependent on the periodic lattice arrangement, it is of essential significance to improve the crystallinity of PBAs and hence ensure long-range lattice periodicity. Herein, a chemical inhibition strategy is developed to prepare a highly crystallized Prussian blue (NaFe[Fe(CN)]), which displays an outstanding rate performance (78 mAh g at 100 C) and long life-span properties (62% capacity retention after 2000 cycles) in sodium storage. Experimental results and kinetic analyses demonstrate the efficient electron transfer and smooth ion diffusion within the bulk phase of highly crystallized Prussian blue. Moreover, X-ray diffraction and Raman spectroscopy results demonstrate the robust crystalline framework and reversible phase transformation between cubic and rhombohedral within the charge-discharge process. This research provides an innovative way to optimize PBAs for advanced rechargeable batteries from the perspective of crystallinity.

摘要

具有大的间隙空隙和刚性结构的普鲁士蓝类似物(PBAs)被广泛认为是有前景的钠离子电池阴极材料。然而,传统制备的PBAs不可避免地存在结晶度差和晶格缺陷的问题,导致比容量低、倍率性能差和长期稳定性不理想。由于PBAs中的钠迁移直接依赖于周期性晶格排列,提高PBAs的结晶度并因此确保长程晶格周期性具有至关重要的意义。在此,开发了一种化学抑制策略来制备高度结晶的普鲁士蓝(NaFe[Fe(CN)]),其在钠存储中表现出出色的倍率性能(100 C时为78 mAh g)和长寿命特性(2000次循环后容量保持率为62%)。实验结果和动力学分析表明,在高度结晶的普鲁士蓝体相中存在高效的电子转移和平滑的离子扩散。此外,X射线衍射和拉曼光谱结果表明,在充放电过程中存在坚固的晶体框架以及立方相和菱面体相之间的可逆相变。本研究从结晶度的角度为优化用于先进可充电电池的PBAs提供了一种创新方法。

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