成核
过电位
法拉第效率
枝晶(数学)
材料科学
电解质
阳极
涂层
图层(电子)
化学工程
纳米技术
电极
化学
电化学
有机化学
工程类
物理化学
数学
几何学
作者
Rong Zhuang,Xiaoru Cai,Changzhen Qu,Shuyue He,Stefan Kaskel,Atef Y. Shenouda,Hongqiang Wang,Fei Xu
出处
期刊:Carbon
[Elsevier BV]
日期:2024-01-26
卷期号:221: 118862-118862
被引量:9
标识
DOI:10.1016/j.carbon.2024.118862
摘要
Sodium metal batteries are promising next-generation energy-dense rechargeable batteries but are severely obstructed by uneven Na nucleation and subsequent dendritic Na growth, leading to the use of highly excessive Na in anode. Herein, a molecular-designed fluorinated carbonaceous triazine-based network (F-CTN) has been employed as the seeding/hosting coating layer to realize high interface stability with limited-excess Na source. The well-defined F functionality acts as uniform sodiophilic sites, effectively reducing the nucleation barrier, suppressing the growth of Na dendrite, and meanwhile promoting the formation of robust solid electrolyte interphase. Accordingly, a low nucleation overpotential of 12 mV, a high average Coulombic efficiency of 99.5 % for 600 cycles in half cells, and long-term interfacial durability of 5000 h in symmetric cells are realized using the F-CTN coating layer, far exceeding the control sample without fluorination. Moreover, the symmetric cell demonstrates stable cycling of 3300 h under a high depth of discharge. Eventually, the proof-of-concept pouch cells deliver a robust lifespan of 500 cycles with negligible capacity fading and energy density of 253 Wh kg−1 under low negative to positive capacity ratio of 2.5, proving the viability of the fluorinated carbonaceous coating layer in the practical deployment of dendrite-free Na metal batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI