阳极
电解质
材料科学
电化学
锂(药物)
溶解
硝酸铈
枝晶(数学)
铈
化学工程
电池(电)
金属
剥离(纤维)
无机化学
电极
化学
复合材料
冶金
物理化学
功率(物理)
内分泌学
工程类
物理
医学
量子力学
数学
几何学
作者
Mouzhi Huang,Ting Hu,Yiteng Zhang,Ze Zhang,Ji Yu,Zhenyu Yang
标识
DOI:10.1021/acsami.1c25151
摘要
Lithium (Li) metal is considered to be the most promising anode due to the ultrahigh capacity and extremely low electrochemical potential. The tricky thing is that the growth of dendritic Li brings huge safety hazards to Li metal batteries. Herein, we demonstrate cerium nitrate as a multifunctional electrolyte additive to form a stable solid electrolyte interface on the metallic Li anode surface for durable Li-S batteries. The presence of Ce3+ helps to modulate the electroplating/stripping of Li and inhibits the growth of dendritic Li. An excellent cycle life exceeding 1400 h at the current density of 1 mA cm-2 can be realized in symmetric Li||Li cells. In addition, the in situ formed robust solid-electrolyte interface (SEI) layer containing cerium sulfide on the Li anode surface conduces to weaken the reducibility of Li and regulate the electrochemical dissolution/deposition reaction on the Li anode. Surprisingly, by virtue of cerium nitrate additive with a low concentration of 0.03 M, the Li-S batteries can afford a capacity of 553 mA h g-1 at 5 C and a long cycle life at 1 C with a high capacity retention of 70.4%. Therefore, this study provides a novel idea to realize a uniform and dendrite-free Li anode for practical Li-S batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI