Si3N4-Assisted Densification Sintering of Na3Zr2Si2PO12 Ceramic Electrolyte toward Solid-State Sodium Metal Batteries

烧结 材料科学 电解质 陶瓷 固态 金属 冶金 化学工程 化学 电极 物理化学 工程类
作者
Wenwen Sun,Yang Li,Chen Sun,Zheng Sun,Haibo Jin,Yongjie Zhao
出处
期刊:Batteries [Multidisciplinary Digital Publishing Institute]
卷期号:10 (10): 359-359
标识
DOI:10.3390/batteries10100359
摘要

The solid-state metal battery with solid-state electrolytes has been considered the next generation of energy storage technology owing to its superior safety and high energy density. But, unfavorable ionic conductivity and interfacial problems make it difficult to widely use in practice. In this work, Si3N4 was rationally introduced into the NASICON matrix as a sintering aid, and the influence of Si3N4 on the crystal phase, microstructure, electrochemical and electrical performance of Na3Zr2Si2PO12 (NZSP) ceramic was systematically studied. The results demonstrate that the introduction of Si3N4 can effectively lower the densification sintering temperature of Na3Zr2Si2PO12 electrolyte and enhance the room temperature ionic conductivity of the NZSP to 3.82 × 10−4 S cm−1. In addition, since Si3N4 has a high thermal conductivity and can inhibit the transmission of electrons between the grains of the electrolyte matrix, it will effectively hinder the generation of sodium metal dendrites and relieve the concentration of the heat source. Moreover, owing to the desirable interface compatibility of the Na and NZSP-Si3N4 electrolyte, the Na/NZSP-1150-1%Si3N4/Na symmetric battery exhibits excellent stability, and the electrode/electrolyte interface still maintains good integrity even after long-term cycling. The assembled Na/NZSP-1150-1%Si3N4/Na3.5V0.5Mn0.5Fe0.5Ti0.5(PO4)3 cell manifests an initial specific capacity of 152.5 mA h g−1, together with an initial Coulombic efficiency of 99.8%. Furthermore, after 200 cycles, the battery displays a capacity retention rate of 82%.
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