过电位
成核
阳极
电池(电)
沉积(地质)
材料科学
金属
电镀(地质)
电流密度
剥离(纤维)
化学工程
纳米技术
冶金
化学
电化学
热力学
复合材料
物理化学
电极
物理
古生物学
功率(物理)
有机化学
量子力学
沉积物
地球物理学
生物
工程类
作者
Long Yao,Shunlong Ju,Guanglin Xia,Dalin Sun,Xuebin Yu
标识
DOI:10.1021/acsenergylett.3c02160
摘要
Al batteries exhibit high crustal abundance and theoretical energy density, making them promising candidates as next-generation batteries. However, the poor Al plating/stripping at the Al anode severely limits their potential application. Herein, MXene-induced atomically dispersed MN4 sites (M = Co, Ni, Cu) containing axial O coordination (MN4O2) are demonstrated to show a synergistic effect of dynamic Al–O interactions to induce Al homogeneous deposition. As an example, the single-atomic Co modified Al anode exhibits negligible nucleation overpotential and a long plating lifespan even under unprecedented conditions (areal capacity of 10 mAh cm–2, current density of 40 mA cm–2). A practical 323 Wh kg–1 metal Al–S battery is well demonstrated under a 7 mg cm–2 high sulfur loading. These findings provide atomic-scale insights for the regulation of Al deposition and provide an avenue to stabilize the metal Al battery under practical high energy density conditions.
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