阴极
材料科学
电池(电)
钠离子电池
兴奋剂
相变
离子
储能
电导率
电压
高压
相(物质)
化学工程
纳米技术
分析化学(期刊)
电化学
光电子学
化学
电极
热力学
电气工程
有机化学
功率(物理)
物理
法拉第效率
工程类
物理化学
色谱法
作者
Li Zou,Jiang Zhong,Qiliang Wei,Yong Lin,Yijie Zhou,Yanqing Fu,Ruizhi Yu,Ping Gao,Hongbo Shu,Li Liu,Weiyou Yang,Xiukang Yang,Xianyou Wang
出处
期刊:Small
[Wiley]
日期:2024-03-15
卷期号:20 (32)
被引量:3
标识
DOI:10.1002/smll.202400315
摘要
Abstract Currently, a major target in the development of Na‐ion batteries is the concurrent attainment of high‐rate capacity and long cycling stability. Herein, an advanced Na‐ion battery with high‐rate capability and long cycle stability based on Li/Ti co‐doped P2‐type Na 0.67 Mn 0.67 Ni 0.33 O 2 , a host material with high‐voltage zero‐phase transition behavior and fast Na + migration/conductivity during dynamic de‐embedding process, is constructed. Experimental results and theoretical calculations reveal that the two‐element doping strategy promotes a mutually reinforcing effect, which greatly facilitates the transfer capability of Na + . The cation Ti 4+ doping is a dominant high voltage, significantly elevating the operation voltage to 4.4 V. Meanwhile, doping Li + shows the function in charge transfer, improving the rate performance and prolonging cycling lifespan. Consequently, the designed P2‐Na 0.75 Mn 0.54 Ni 0.27 Li 0.14 Ti 0.05 O 2 cathode material exhibits discharge capacities of 129, 104, and 85 mAh g − 1 under high voltage of 4.4 V at 1, 10, and 20 C, respectively. More importantly, the full‐cell delivers a high initial capacity of 198 mAh g −1 at 0.1 C (17.3 mA g −1 ) and a capacity retention of 73% at 5 C (865 mA g −1 ) after 1000 cycles, which is seldom witnessed in previous reports, emphasizing their potential applications in advanced energy storage.
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