材料科学
成核
法拉第效率
枝晶(数学)
阳极
锂(药物)
金属锂
阴极
黑磷
集电器
电流(流体)
多孔性
磷
金属
金属泡沫
化学工程
电泳沉积
电流密度
无机化学
冶金
复合材料
电极
物理化学
化学
涂层
有机化学
几何学
数学
物理
量子力学
内分泌学
医学
工程类
作者
Yuan Wang,Hongqian Sang,Wenqi Zhang,Yongfeng Qi,Rongxiang He,Bolei Chen,Weiwei Sun,Xingzhong Zhao,Dejun Fu,Yumin Liu
标识
DOI:10.1021/acsami.0c16430
摘要
Li metal is considered a highly desirable anode for next-generation high-energy-density rechargeable lithium batteries. However, irregular Li dendrite formation and infinite relative volume changes prevent the commercial adoption of Li-metal anodes. Here, electrophoretic deposition of black phosphorus (BP) on commercial Cu foam (BP@Cu foam) is reported to regulate Li nucleation for the first time. First-principles calculations reveal that the unique two-dimensional (2D) structure of BP is beneficial to Li intercalation and propagation. Compared with the random Li nucleation and growth on bare Cu foam, Li ions are preferably confined into the BP layers, which induces uniform Li nucleation at the early stage of the Li deposition and guides the following lateral Li growth on BP@Cu foam. In addition, the three-dimensional (3D) porous and conductive framework of Cu foams further mitigate the volume change and dissipate the current density. Attributing to these merits, the BP@Cu foam exhibits significantly enhanced Coulombic efficiency and cycling stability compared with bare Cu foam. In the full-cell configuration paired with a Li4Ti5O12 or LiFePO4 cathode, the BP@Cu foam also boosts the battery performances. This work provides new insights into the development of BP and other elaborate 2D materials for achieving dendrite-free Li-metal anodes.
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