材料科学
阴极
快离子导体
碱金属
储能
化学工程
离子
氧化还原
金属
兴奋剂
电极
电解质
纳米技术
光电子学
物理化学
冶金
热力学
化学
物理
工程类
量子力学
功率(物理)
作者
Xing Shen,Han Miao,Yuefeng Su,Meng Wang,Feng Wu
出处
期刊:Nano Energy
[Elsevier]
日期:2023-06-25
卷期号:114: 108640-108640
被引量:7
标识
DOI:10.1016/j.nanoen.2023.108640
摘要
Na-ion batteries have been considered as promising candidates for future energy storage owing to Na availability and high-cost performance. However, their wide application is still hindered by poor rate capabilities, insufficient cycle lifespan and inferior variable-temperature performance. Here, we report an aliovalent-ion induced lattice regulation protocol with Li+, Na+, and K+ replacing V3+, which motivates the generation of electronic defects and expands the Na+ migration pathways. With the partial activation of V4+/V5+ redox, the prepared Na3V1.94K0.06(PO4)3 cathode exhibits capacity of 120.3 mAh g−1 at 0.1 C with remarkable capability (100.5 mAh g−1) and ultralong cycle stability (99.1 % capacity retention over 3000 cycles) at 20 C. Moreover, 96.9 % capacity retention after 200 cycles at 0.2 C for − 30 °C and discharge capacity of 127.8 mAh g−1 at 0.1 C for 55 °C were achieved for K+-substituted cathode. This work sheds lights on improving Na+ migration kinetics and clarifying the objective law for alkali metal ion doping in Na superionic conductor cathodes for wide-temperature batteries.
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