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氟化协同调控Na2FePO4F正极晶格与界面以提升钠离子存储性能

Fluorination-enabled synergistic engineering of lattice and interface in Na2FePO4F cathode for enhanced sodium-ion storage

作者 Xi Zhou · Ze-Rong Deng · Lu-Lu Zhang · Biao-Yang Li · Hua-Bin Sun · Ya-Hao Li · Bo Yan · Xue-Lin Yang
期刊 Applied Physics Letters
出版日期 2026年2月
卷/期 第 128 卷 第 8 期
技术分类 储能系统技术
技术标签 电池管理系统BMS 储能变流器PCS 储能系统 用户侧储能
相关度评分 ★★★★ 4.0 / 5.0
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中文摘要

本文提出氟化协同工程策略,同步优化Na2FePO4F正极的晶格结构与界面特性:拓宽Na+迁移通道、强化Fe–F键、构建缺陷富集界面,显著提升钠离子扩散动力学、结构稳定性和界面电荷转移能力,实现优异倍率性能(5 C下80.2 mAh g⁻¹)和长循环稳定性(200次后容量保持率89.3%)。

English Abstract

The development of sodium-ion batteries is limited by the intrinsic kinetics and stability of cathode materials. Herein, we develop a synergistic engineering strategy for concurrently regulating the lattice structure and interfacial properties of Na2FePO4F cathode via a novel fluorination approach. This approach triggers a lattice reconstruction, widening Na+ migration channels and strengthening the Fe–F bond, thereby facilitating Na+ diffusion and enhancing framework stability. Simultaneously, this strategy promotes the formation of a defect-rich interface that accelerates interfacial charge transfer and enhances pseudocapacitive sodium storage. These synergistic effects achieve remarkable performance, including excellent rate capability (80.2 mAh g−1 at 5 C) and exceptional full-cell cyclability (89.3% capacity retention after 200 cycles at 1 C). This work provides a physical insight into the design of high-performance fluorinated electrodes through concurrent lattice and interface engineering.
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SunView 深度解读

该研究面向钠离子电池正极材料的本征改性,直接支撑阳光电源在新型电化学储能系统(如PowerTitan、ST系列PCS适配的钠电方案)中的材料兼容性升级与性能边界拓展。氟化协同设计可指导BMS对钠电SOC/SOH的高精度建模,并为PCS提供更宽温域、更高倍率的钠电接口参数依据。建议阳光电源在用户侧储能及电网侧储能产品线中开展钠电兼容性验证,并联合材料厂商推进氟化正极中试导入。