材料科学
阴极
分析化学(期刊)
电荷(物理)
超短脉冲
原子物理学
物理化学
化学
环境化学
激光器
光学
量子力学
物理
作者
Zhuangzhou Wang,Guijia Cui,Qinfeng Zheng,Xiangyu Ren,Qingheng Yang,Siqi Yuan,Xujin Bao,Chaojiu Shu,Yixiao Zhang,Linsen Li,Yu‐Shi He,Liwei Chen,Zhenqiang Ma,Xiao‐Zhen Liao
出处
期刊:Small
[Wiley]
日期:2023-02-01
卷期号:19 (17)
被引量:10
标识
DOI:10.1002/smll.202206987
摘要
Na4 MnV(PO4 )3 /C (NMVP) has been considered an attractive cathode for sodium-ion batteries with higher working voltage and lower cost than Na3 V2 (PO4 )3 /C. However, the poor intrinsic electronic conductivity and Jahn-Teller distortion caused by Mn3+ inhibit its practical application. In this work, the remarkable effects of Zr-substitution on prompting electronic and Na-ion conductivity and also structural stabilization are reported. The optimized Na3.9 Mn0.95 Zr0.05 V(PO4 )3 /C sample shows ultrafast charge-discharge capability with discharge capacities of 108.8, 103.1, 99.1, and 88.0 mAh g-1 at 0.2, 1, 20, and 50 C, respectively, which is the best result for cation substituted NMVP samples reported so far. This sample also shows excellent cycling stability with a capacity retention of 81.2% at 1 C after 500 cycles. XRD analyses confirm the introduction of Zr into the lattice structure which expands the lattice volume and facilitates the Na+ diffusion. First-principle calculation indicates that Zr modification reduces the band gap energy and leads to increased electronic conductivity. In situ XRD analyses confirm the same structure evolution mechanism of the Zr-modified sample as pristine NMVP, however the strong ZrO bond obviously stabilizes the structure framework that ensures long-term cycling stability.
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