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Mg^(2+)-driven triphasic reaction breaking kinetic barriers:Toward ultra-stable and ultrafast sodium-ion polyanionic cathodes
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作者 Yiran Yang Wei Zhang +12 位作者 Yanjiang Zhang Shuting Sun Wei Wang Shan Jin Chen Liu Tianning Lin Xinying Xu Zhixin Liu Hua Huo Meng Chen Jinlong Wang Ruhong Li Changsong Dai 《Journal of Energy Chemistry》 2025年第11期176-185,I0006,共11页
Sodium-ion batteries are promising candidates for next-generation large-scale energy storage owing to their abundance and low cost.Biphasic intercalation reactions,constrained by kinetic limitations and structural ins... Sodium-ion batteries are promising candidates for next-generation large-scale energy storage owing to their abundance and low cost.Biphasic intercalation reactions,constrained by kinetic limitations and structural instability,fundamentally restrict the rate capability and cycle life of sodium ion batteries.However,precise regulation of these reactions to enhance kinetics remains challenging.Here,we propose a strategy of atomic-scale phase engineering to activate the metastable state and achieve a three-phase reaction through precise Mg^(2+)doping at V sites in Na_(3)V_(2)(PO_(4))_(3).The Mg^(2+)occupancy promotes the exchange between Na1 and Na2 sites,thereby stabilizing a Na_(2)V_(2)(PO_(4))_(3) intermediate.First-principles calculations indicate that Mg^(2+)occupation facilitates charge redistribution by weakening Na-O electrostatic interaction,stabilizing the formation of Na_(2)V_(2)(PO_(4))_(3)phase.The optimized cathode exhibits ultrahigh capacity retention(84.5%after 5000 cycles at 3.51 A g^(-1)),supports ultrafast charging within 120 s,and exceptional rate capability(96.2 mAh g^(-1)at 4.68 A g^(-1)).This work establishes a universal route to unlock hidden reaction pathways by redefining the role of dopants in phase transition control. 展开更多
关键词 na_(3)V_(2)(PO_(4))_(3) naSICON Mg^(2+)regulation na+mobility Metastable phase
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