Fang Yongjin, Liu Qi, Xiao Lifen, Ai Xinping, Yang Hanxi, Cao Yuliang
†Hubei Key Laboratory of Electrochemical Power Sources, College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China.
‡College of Chemistry, Central China Normal University, Wuhan 430079, China.
ACS Appl Mater Interfaces. 2015 Aug 19;7(32):17977-84. doi: 10.1021/acsami.5b04691. Epub 2015 Aug 5.
Olivine NaFePO4/C microsphere cathode is prepared by a facile aqueous electrochemical displacement method from LiFePO4/C precursor. The NaFePO4/C cathode shows a high discharge capacity of 111 mAh g(-1), excellent cycling stability with 90% capacity retention over 240 cycles at 0.1 C, and high rate capacity (46 mAh g(-1) at 2 C). The excellent electrochemical performance demonstrates that the aqueous electrochemical displacement method is an effective and promising way to prepare NaFePO4/C material for Na-based energy storage applications. Moreover, the Na2/3FePO4 intermediate is observed for the first time during the Na intercalation process through conventional electrochemical techniques, corroborating an identical two-step phase transition reaction both upon Na intercalation and deintercalation processes. The clarification of the electrochemical reaction mechanism of olivine NaFePO4 could inspire more attention on the investigation of this material for Na ion batteries.
橄榄石型NaFePO₄/C微球阴极是通过一种简便的水相电化学置换法由LiFePO₄/C前驱体制备而成。NaFePO₄/C阴极展现出111 mAh g⁻¹的高放电容量、在0.1 C下240次循环中具有90%容量保持率的优异循环稳定性以及高倍率容量(2 C时为46 mAh g⁻¹)。优异的电化学性能表明,水相电化学置换法是制备用于钠基储能应用的NaFePO₄/C材料的一种有效且有前景的方法。此外,通过传统电化学技术首次在钠嵌入过程中观察到Na₂/₃FePO₄中间体,证实了在钠嵌入和脱嵌过程中均存在相同的两步相变反应。橄榄石型NaFePO₄电化学反应机理的阐明可能会激发人们对这种钠离子电池材料研究的更多关注。