阴极
钠
能量密度
化学
储能
钒
补偿(心理学)
无机化学
氧化还原
化学能
工作(物理)
材料科学
能量(信号处理)
化学工程
纳米技术
杠杆
化学反应
磷酸盐
能量需求
比能量
作者
Mingli Xu,Tingcan Li,Zu Chang,Qian Zhang,Kai Shi,Kexin Liu,Luqi Zhou,Mingyuan Jiang,Xuanze Wang,Xiaoyu Ji,Xiaoliang Yu,Lei Li,Jun Qian
摘要
ABSTRACT Anode‐free sodium batteries (AFSBs) promise high energy density and low cost but are fundamentally constrained by severe active sodium loss, leading to rapid cell failure. Here, we propose a precise chemical presodiation strategy that unlocks the full 4e–/4Na + redox chemistry of vanadium phosphate cathodes by converting Na‐stoichiometric Na 3 V 2 (PO 4 ) 3 (Na 3 VP) into Na‐saturated Na 5 V 2 (PO 4 ) 3 (Na 5 VP). Through voltage‐controlled sodium compensation, chemically sodiated Na 5 VP serves as a versatile cathode platform for the flexible design of AFSBs tailored for either ultra‐high energy density or exceptional longevity. With two sodium compensations, the (Na 5 VP→Na 3 VP)||carbon‐coated Al (C@Al) delivers an exceptional 1000‐cycle lifespan with a decent energy density of 334 Wh kg −1 , markedly outperforming the Na 3 VP counterpart (305 Wh kg −1 and a 10‐cycle lifespan). Particularly, the (Na 5 VP→Na 4 VP)||C@Al cell with one sodium compensation achieves an ultra‐high energy density of 430 Wh kg −1 and a competitive lifespan of 630 cycles, representing a state‐of‐the‐art benchmark. This work establishes precise sodium compensation as a powerful lever for designing high‐performance and application‐specific AFSBs.
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