阳极
电解质
法拉第效率
动力学
材料科学
扩散
电化学
化学物理
化学工程
极化(电化学)
碳纤维
化学
纳米技术
热力学
电极
物理化学
物理
工程类
复合材料
复合数
量子力学
作者
X.-M. Tang,Fei Xie,Yaxiang Lu,Huican Mao,Zhao Chen,Hongyi Pan,Suting Weng,Yang Yang,Guangmao Li,Zhenyu Guo,Qiubo Guo,Feixiang Ding,Xueyan Hou,Yuqi Li,Xuefeng Wang,Maria‐Magdalena Titirici,Liquan Chen,Yuanjiang Pan,Yong‐Sheng Hu
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-02-26
卷期号:9 (3): 1158-1167
被引量:28
标识
DOI:10.1021/acsenergylett.4c00041
摘要
Minimizing the irreversibility during the first cycle in carbon anodes is crucial to the energy density and lifespan of Na-ion batteries (NIBs). However, the underlying mechanism of the irreversible capacity, especially combined with the kinetics and interface, is still incompletely understood. Herein, we discovered that poor kinetics and strong polarization will drive the Na+ residual at the interface as pseudo-dead Na to trigger electrolyte decomposition and form extra SEI, thus sacrificing the initial Coulombic efficiency (ICE). Manipulating defect concentration is, therefore, developed to improve the kinetics, reduce the diffusion barrier of Na+, and lower the Fermi energy of the anode to impede the pseudo-dead Na and extra SEI formation, thereby ensuring high ICE and even capacity. This study proposes a complementary view on the understanding of initial irreversibility and interface evolution influenced by Na+ kinetics, which provides guidance for defect chemistry and engineering for future design of carbon anodes toward high-performance NIBs.
科研通智能强力驱动
Strongly Powered by AbleSci AI