阳极
材料科学
电解质
钠
电池(电)
化学工程
甲酸钠
金属
电极
无机化学
冶金
化学
功率(物理)
物理
物理化学
量子力学
工程类
作者
Chaozhi Wang,Ying Zheng,Zhe‐Ning Chen,Rongrong Zhang,Wei He,Kaixuan Li,Sen Yan,Jingqin Cui,Xiaoliang Fang,Jiawei Yan,Gang Xu,Dong‐Liang Peng,Bin Ren,Nanfeng Zheng
标识
DOI:10.1002/aenm.202204125
摘要
Abstract Sodium metal batteries (NMBs) have attracted increasing attention as next‐generation rechargeable batteries. How to improve their cycling stability and safety under limited sodium excess conditions, ideally zero sodium excess (i.e., anode‐free architecture), is highly desired yet remains challenging. Herein, it is demonstrated that sodium formate (HCOONa), one component of the solid electrolyte interphase (SEI) naturally formed on sodium metal anode, is a promising candidate for designing high‐performance artificial SEI layers, which can suppress the sodium dendrite formation and reduce the side reactions between sodium and the electrolyte. Profiting from the HCOONa interface, the Na|Na 3 V 2 (PO 4 ) 3 battery with a high mass loading of Na 3 V 2 (PO 4 ) 3 (10 mg cm −2 ) exhibits a superior cycling stability with an ultralow decay rate of 0.004% per cycle over 800 cycles. More impressively, a single molecular layer of HCOONa in situ formed on commercial copper current collector helps to extend the lifespan of the anode‐free Cu|Na 3 V 2 (PO 4 ) 3 battery to 400 cycles with 88.2% capacity relation, representing the longest cycle lifetime reported in anode‐free NMBs.
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