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钠离子电池纳米级V2O5/C复合正极材料中钠嵌入机制的研究

Investigation of the Na Intercalation Mechanism into Nanosized V2O5/C Composite Cathode Material for Na-Ion Batteries.

作者信息

Ali Ghulam, Lee Ji Hoon, Oh Si Hyoung, Cho Byung Won, Nam Kyung-Wan, Chung Kyung Yoon

机构信息

Center for Energy Convergence Research, Korea Institute of Science and Technology , Hwarang-ro 14-gil 5, Seongbuk-gu, Seoul 136-791, Republic of Korea.

Korea University of Science and Technology , 217 Gajeong-ro Yuseong-gu, Daejeon 305-333, Republic of Korea.

出版信息

ACS Appl Mater Interfaces. 2016 Mar 9;8(9):6032-9. doi: 10.1021/acsami.5b11954. Epub 2016 Feb 26.

Abstract

There is a significant interest to develop high-performance and cost-effective electrode materials for next-generation sodium ion batteries. Herein, we report a facile synthesis method for nanosized V2O5/C composite cathodes and their electrochemical performance as well as energy storage mechanism. The composite exhibits a discharge capacity of 255 mAh g(-1) at a current density of 0.05 C, which surpasses that of previously reported layered oxide materials. Furthermore, the electrode shows good rate capability; discharge capacity of 160 mAh g(-1) at a current density of 1 C. The reaction mechanism of V2O5 upon sodium insertion/extraction is investigated using ex situ X-ray diffraction (XRD) and synchrotron based near edge X-ray absorption fine structure (NEXAFS) spectroscopy. Ex situ XRD result of the fully discharged state reveals the appearance of NaV2O5 as a major phase with minor Na2V2O5 phase. Upon insertion of sodium into the array of parallel ladders of V2O5, it was confirmed that lattice parameter of c is increased by 9.09%, corresponding to the increase in the unit-cell volume of 9.2%. NEXAFS results suggest that the charge compensation during de/sodiation process accompanied by the reversible changes in the oxidation state of vanadium (V(4+) ↔ V(5+)).

摘要

开发用于下一代钠离子电池的高性能且经济高效的电极材料具有重大意义。在此,我们报告了一种用于纳米级V2O5/C复合阴极的简便合成方法及其电化学性能以及能量存储机制。该复合材料在0.05 C的电流密度下表现出255 mAh g(-1)的放电容量,超过了先前报道的层状氧化物材料。此外,该电极显示出良好的倍率性能;在1 C的电流密度下放电容量为160 mAh g(-1)。使用非原位X射线衍射(XRD)和基于同步加速器的近边X射线吸收精细结构(NEXAFS)光谱研究了V2O5在钠嵌入/脱嵌时的反应机理。完全放电状态的非原位XRD结果表明,主要相为NaV2O5,还有少量Na2V2O5相。当钠插入V2O5的平行梯状阵列中时,证实c轴晶格参数增加了9.09%,对应于晶胞体积增加9.2%。NEXAFS结果表明,在脱钠/嵌钠过程中的电荷补偿伴随着钒氧化态(V(4+) ↔ V(5+))的可逆变化。

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