成核
电解质
法拉第效率
钠
合金
阳极
材料科学
剥离(纤维)
扩散
钾
电化学
金属
相(物质)
电镀
冶金
化学
化学工程
分析化学(期刊)
纳米技术
物理化学
热力学
色谱法
复合材料
电极
有机化学
工程类
物理
图层(电子)
作者
Cheng Liu,Hongyi Chen,Wen-Tao Deng,Jun Chen,Ye Tian,Xu Gao,Xinglan Deng,Shouyi Yi,Shuo Li,Linghua Chen,Shuquan Liang,Jianmin Ma,Hongshuai Hou,Guoqiang Zou,Debbie S. Silvester,Xiaobo Ji
标识
DOI:10.1021/acs.jpclett.1c02248
摘要
The prospects of sodium (Na) metal batteries have been fatally plagued by interfacial Na dendrites, mainly affected by preferred nucleation on the metal anode and the steep gradient of Na ions in the electrolyte, leading to limited Coulombic efficiency and short lifespans. Herein, an electrochemically inert potassium-based Na–K alloy demonstrates a liquid alloying diffusion mechanism that enables dendrite-free Na anodes. The extremely small Na fluctuation and flexible Na–K bonds in the liquid alloy phase bring isotropic nucleation of Na upon electroplating/stripping, which is directly observed by in situ optical imaging. Spontaneously, serving as (de)sodiation buffer with faster electron/mass transportation, the liquid inertia also provides attenuated concentration distribution of Na. Significantly, a record capacity retention of approximately 100% is rendered when coupled with Na3V2(PO4)3 cathodes (ca. 2 mg cm–2) over 500 cycles at 10C, advancing the possibility of using liquid alloy for stable metal anodes beyond Na storage systems.
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