快离子导体
阳极
钠
电化学
材料科学
法拉第效率
阴极
电解质
储能
剥离(纤维)
金属
化学工程
化学
分析化学(期刊)
电极
冶金
色谱法
热力学
复合材料
物理化学
功率(物理)
物理
工程类
作者
Junxiong Wu,Cong Lin,Qinghua Liang,Guodong Zhou,Jiapeng Liu,Gemeng Liang,Man Wang,Baohua Li,Liang Hu,Francesco Ciucci,Qiang Liu,Guohua Chen,Xiaoliang Yu
出处
期刊:InfoMat
[Wiley]
日期:2022-01-23
卷期号:4 (4)
被引量:73
摘要
Abstract Rechargeable sodium metal batteries (SMBs) have emerged as promising alternatives to commercial Li‐ion batteries because of the natural abundance and low cost of sodium resources. However, the overuse of metallic sodium in conventional SMBs limits their energy densities and leads to severe safety concerns. Herein, we propose a sodium‐free‐anode SMB (SFA‐SMB) configuration consisting of a sodium‐rich Na superionic conductor‐structured cathode and a bare Al/C current collector to address the above challenges. Sodiated Na 3 V 2 (PO 4 ) 3 in the form of Na 5 V 2 (PO 4 ) 3 was investigated as a cathode to provide a stable and controllable sodium source in the SFA‐SMB. It provides not only remarkable Coulombic efficiencies of Na plating/stripping cycles but also a highly reversible three‐electron redox reaction within 1.0–3.8 V versus Na/Na + confirmed by structural/electrochemical measurements. Consequently, an ultrahigh energy density of 400 Wh kg −1 was achieved for the SFA‐SMB with fast Na storage kinetics and impressive capacity retention of 93% after 130 cycles. A narrowed voltage window (3.0–3.8 V vs. Na/Na + ) further increased the lifespan to over 300 cycles with a high retained specific energy of 320 Wh kg −1 . Therefore, the proposed SFA‐SMB configuration opens a new avenue for fabricating next‐generation batteries with high energy densities and long lifetimes. image
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