阴极
离子电导率
电化学
阳极
材料科学
钠
化学工程
离子键合
卤化物
电化学窗口
电导率
无定形固体
储能
工作(物理)
无机化学
电阻率和电导率
电池(电)
锂离子电池的纳米结构
活化能
高能
离子
电化学电池
化学稳定性
电极
化学
作者
Shashwat Singh,Mengyang Cui,Karthikeyen Natarajan Pugazhendhi,Gillian R. Goward,Linda F. Nazar
标识
DOI:10.1021/acsenergylett.5c03723
摘要
All-solid-state sodium batteries (ASSBs) are a potential cost-effective alternative to their lithium-ion analogues. However, their broad adoption requires catholytes that combine high ionic conductivity, good electrochemical stability, and mechanical deformability. Addressing these challenges, we report a new family of amorphous Zr-rich fluorochlorides, Na0.8Zr0.8Ta0.2Cl4.2-xF0.8+x (x = 0, 1) synthesized via a one-step mechanochemical route. These catholytes exhibit sodium-ion conductivities of ∼1 mS·cm–1 and low activation energies (∼322 meV), along with high oxidative stability up to 4.5 V vs. Na+/Na due to their dual-anion (Cl–/F–) oligomeric framework. ASSBs employing these halides coupled with Na3V2(PO4)3 cathodes deliver capacities of ∼100 mAh·g–1 with 90% retention over more than 300 cycles in a 2.5–4.1 V window due to suppressed interfacial side reactions. Pairing the optimal catholytes with a Na3V2(PO4)2O2F cathode enables cycling up to 4.4 V vs. Na+/Na, enhancing energy density. This work presents a general strategy to enhance the ionic conductivity and anodic stability of halide-based solid electrolytes.
科研通智能强力驱动
Strongly Powered by AbleSci AI