阴极
电解质
阳极
插层(化学)
电池(电)
金属
储能
材料科学
电化学
化学工程
钾离子电池
无机化学
离子
化学
电极
钠离子电池
锂(药物)
法拉第效率
钠
电流密度
锂离子电池
冶金
有机化学
热力学
物理化学
功率(物理)
工程类
物理
量子力学
作者
Yujie Zhang,Jianian Gui,Ting Li,Zhongxue Chen,Shun‐an Cao,Fei Xu
标识
DOI:10.1016/j.cej.2020.125689
摘要
Na-ion batteries (SIBs) are considered as the most promising candidate for next-generation large-scale electrochemical energy storage. However, the design of such a rocking-chair battery has intrinsic defects. During the first charge process of a SIB, irreversible reduction occurs at the carboneous anode to form solid electrolyte interphase (SEI), which would inevitably consume precious Na resource in the Na-rich cathode and result in a considerable capacity loss. Such an issue has also long existed in LIBs and particularly complicated prelithiation procedures are indispensable in commercial LIB fabrications. In the present study, a novel Mg/Na hybrid battery design is introduced with a Na-intercalation cathode of Na2VTi(PO4)3, a metallic Mg anode and a Mg2+/Na+ dual-ion electrolyte. Such a Mg/Na hybrid battery works perfectly with Na+ intercalation/deintercalation at the Na2VTi(PO4)3 cathode and Mg deposition/dissolution at the Mg anode, providing a high capacity of 168 mAh g−1 and a superior cycleability for 1000 cycles. In contrast, the SIB based on hard carbon anode could hardly cycle due to the large irreversibility at the anode. The present work highlights a novel high-performance and reliable battery design strategy using well-developed Na-storage cathodes, which has high potential in future large-scale energy-storage applications.
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