沉积(地质)
锂(药物)
锂原子
Atom(片上系统)
材料科学
离子
纳米技术
化学
结晶学
计算机科学
嵌入式系统
古生物学
内分泌学
有机化学
生物
医学
电离
沉积物
作者
Xue Liang Li,Wei Ying Lieu,Liguang Wang,Dong Yan,Yifan Li,Tanmay Ghosh,Yuanjian Li,Jun Lu,Zhi Wei Seh,Hui Ying Yang
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-09-19
卷期号:9 (10): 4929-4938
被引量:11
标识
DOI:10.1021/acsenergylett.4c02190
摘要
Effective management of lithium (Li) metal nucleation and growth is critical for its practical application, yet a limited understanding of Li metal anode morphology has impeded progress. This study advances the comprehension of dense spherical Li deposition by linking atomic charge distributions to macroscopic phenomena. By introducing silver (Ag) single atoms into titanium (Ti) vacancies in MXene, we form a unique Ag–C composite that modulates charge distribution, thereby facilitating uniform, spherical Li deposition across the surface. This approach minimizes Ag consumption to below 1 wt % while achieving Li metal deposition capacities exceeding 40 mAh cm–2. Moreover, full cells incorporating MXene-AgSAs@Li anodes paired with LiFePO4 or sulfur cathodes exhibit a significantly enhanced cycling performance and high rate capabilities. These findings provide novel insights into the role of charge partitioning in Li metal deposition and the formation of dense, spherical Li arrays.
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