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电泳沉积在三维多孔集流体上的黑磷用于调节锂成核以制备无枝晶锂金属负极

Electrophoretic Deposited Black Phosphorus on 3D Porous Current Collectors to Regulate Li Nucleation for Dendrite-Free Lithium Metal Anodes.

作者信息

Wang Yuan, Sang Hong-Qian, Zhang Wenqi, Qi Yuyang, He Rong-Xiang, Chen Bolei, Sun Weiwei, Zhao Xing-Zhong, Fu Dejun, Liu Yumin

机构信息

School of Physics and Technology, Key Laboratory of Artificial Micro/Nano Structures, Ministry of Education, Wuhan University, Wuhan 430072, China.

Institute for Interdisciplinary Research (IIR), Key Laboratory of Optoelectronic Chemical Materials and Devices, Ministry of Education, Jianghan University, Wuhan 430056, China.

出版信息

ACS Appl Mater Interfaces. 2020 Nov 18;12(46):51563-51572. doi: 10.1021/acsami.0c16430. Epub 2020 Nov 4.

Abstract

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 LiTiO or LiFePO 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.

摘要

锂金属被认为是下一代高能量密度可充电锂电池非常理想的阳极材料。然而,不规则的锂枝晶形成和无限的相对体积变化阻碍了锂金属阳极的商业应用。在此,首次报道了通过电泳沉积法将黑磷(BP)沉积在商用泡沫铜(BP@泡沫铜)上以调控锂的成核过程。第一性原理计算表明,BP独特的二维(2D)结构有利于锂的嵌入和扩散。与在裸泡沫铜上随机的锂成核和生长相比,锂离子更倾向于被限制在BP层中,这在锂沉积的早期诱导了均匀的锂成核,并引导了随后在BP@泡沫铜上的锂横向生长。此外,泡沫铜的三维(3D)多孔导电框架进一步减轻了体积变化并分散了电流密度。由于这些优点,与裸泡沫铜相比BP@泡沫铜表现出显著提高的库仑效率和循环稳定性。在与LiTiO或LiFePO阴极配对组成的全电池配置中,BP@泡沫铜也提升了电池性能。这项工作为开发用于实现无枝晶锂金属阳极材料的BP及其他精细二维材料提供了新的见解。

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