In situ probing the origin of interfacial of Na metal anode

被引:47
作者
Ji, Yuchen [1 ]
Qiu, Jimin [1 ]
Zhao, Wenguang [1 ]
Liu, Tongchao [2 ]
Dong, Zihang [3 ]
Yang, Kai [4 ]
Zheng, Guorui [1 ]
Qian, Guoyu [1 ]
Yang, Ming [5 ]
Chen, Qindong [3 ]
Amine, Khalil [2 ]
Pan, Feng [1 ]
Yang, Luyi [1 ]
机构
[1] Peking Univ, Shenzhen Grad Sch, Sch Adv Mat, Shenzhen 518055, Peoples R China
[2] Argonne Natl Lab, Chem Sci & Engn Div, Argonne, IL 60439 USA
[3] Peking Univ, Shenzhen Grad Sch, Sch Environm & Energy, Shenzhen 518055, Peoples R China
[4] Univ Surrey, Adv Technol Inst, Dept Elect & Elect Engn, Guildford GU2 7XH, Surrey, England
[5] Shenzhen Univ, Coll Chem & Environm Engn, Shenzhen 518060, Peoples R China
关键词
SODIUM-ION BATTERIES; SOLID-ELECTROLYTE INTERPHASE; DEPOSITION;
D O I
10.1016/j.chempr.2023.06.002
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The unstable and fragile solid electrolyte interphase (SEI) has restricted the application of Na metal anodes. Despite numerous research efforts being put into understanding its chemical composition and physical properties, direct observation of its formation remains a challenge due to the lack of temporal and spatial resolution. Here, through combined in situ probing techniques, we exhibit two pivotal stages associated with SEI instability during the often -neglected formation process. It is revealed that Na metal that is not uniformly passivated at the initial (passivating) stage will trigger unrestricted electrolyte decomposition and homogeneous components distribution during the subsequent (growing) stage. SEI with homogenously distributed components is found to have higher solubility than that with a layered structure evolved from a compact passivation layer. Through demonstrating an SEI dissolution model that is closely related to its formation process and compositional distribution, this work sheds light on an uncharted territory of Na metal batteries.
引用
收藏
页码:2943 / 2955
页数:14
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