电解质
复合数
材料科学
电池(电)
离子电导率
阴极
准固态
化学工程
离子键合
复合材料
纳米技术
离子
化学
电极
热力学
工程类
物理
色素敏化染料
物理化学
功率(物理)
有机化学
作者
Yu Feng,Jingyi Liu,Zhixuan Wei,Shiyu Yao,Gang Chen,Fei Du
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-04-16
卷期号:64 (25): e202507247-e202507247
被引量:2
标识
DOI:10.1002/anie.202507247
摘要
Abstract All‐solid‐state sodium batteries (ASSSBs) have emerged as the promising candidates for large‐scale energy storage; however, they still face challenges related to ionic transport across multi‐scale interfaces, which leads to suboptimal battery performances. In this study, we propose a core‐shell structured composite electrolyte with Na 3 PS 4 sulfide solid electrolyte (SE) as the core and Na 2.25 Y 0.25 Zr 0.75 Cl 6 halide SE as the shell. This design strategy boosts high SE's oxidative stability (4.0 V), ionic conductivity (0.44 mS cm −1 ) and mechanical strength (Young's modulus of 9.19 GPa). These properties enable the composite SE to effectively mitigate the chemo‐mechanically‐induced multi‐interfacial contact losses at the cathode side. Additionally, the homogeneous full‐cell configuration, utilizing the core‐shell structured composite electrolyte as both catholyte and SE layer, demonstrates superior rate capability, achieving a discharge capacity of 76.4 mAh g⁻¹ at 2.0 C, significantly outperforming the conventional sandwich‐like designs. This work not only provides a novel design strategy for functional SE but also offers valuable insights into the chemo‐mechanical failure mechanism at multiscale interfaces of ASSSBs.
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