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Electrochemically induced crystalline-to-amorphization transformation in sodium samarium silicate solid electrolyte for long-lasting sodium metal batteries

Exploiting solid electrolyte (SE) materials with high ionic conductivity, good interfacial compatibility, and conformal contact with electrodes is essential for solid-state sodium metal batteries (SSBs). Here we report a crystalline Na(5)SmSi(4)O(12) SE which features high room-temperature ionic con...

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Detalles Bibliográficos
Autores principales: Sun, Ge, Lou, Chenjie, Yi, Boqian, Jia, Wanqing, Wei, Zhixuan, Yao, Shiyu, Lu, Ziheng, Chen, Gang, Shen, Zexiang, Tang, Mingxue, Du, Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10579357/
https://www.ncbi.nlm.nih.gov/pubmed/37845205
http://dx.doi.org/10.1038/s41467-023-42308-0
Descripción
Sumario:Exploiting solid electrolyte (SE) materials with high ionic conductivity, good interfacial compatibility, and conformal contact with electrodes is essential for solid-state sodium metal batteries (SSBs). Here we report a crystalline Na(5)SmSi(4)O(12) SE which features high room-temperature ionic conductivity of 2.9 × 10(−3) S cm(−1) and a low activation energy of 0.15 eV. All-solid-state symmetric cell with Na(5)SmSi(4)O(12) delivers excellent cycling life over 800 h at 0.15 mA h cm(−2) and a high critical current density of 1.4 mA cm(−2). Such excellent electrochemical performance is attributed to an electrochemically induced in-situ crystalline-to-amorphous (CTA) transformation propagating from the interface to the bulk during repeated deposition and stripping of sodium, which leads to faster ionic transport and superior interfacial properties. Impressively, the Na|Na(5)SmSi(4)O(12)|Na(3)V(2)(PO(4))(3) sodium metal batteries achieve a remarkable cycling performance over 4000 cycles (6 months) with no capacity loss. These results not only identify Na(5)SmSi(4)O(12) as a promising SE but also emphasize the potential of the CTA transition as a promising mechanism towards long-lasting SSBs.