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用于非水镁电池的高容量、快速充电和长寿命镁/黑磷复合负极。

High-capacity, fast-charging and long-life magnesium/black phosphorous composite negative electrode for non-aqueous magnesium battery.

作者信息

Zhao Qiannan, Zhao Kaiqi, Han Gao-Feng, Huang Ming, Wang Ronghua, Wang Zhiqiao, Zhou Wang, Ma Yue, Liu Jilei, Wang Zhongting, Xu Chaohe, Huang Guangsheng, Wang Jingfeng, Pan Fusheng, Baek Jong-Beom

机构信息

National Engineering Research Center for Magnesium Alloys, Chongqing University, Chongqing, 400044, P.R. China.

School of Energy and Chemical Engineering, Center for Dimension-Controllable Organic Frameworks, Ulsan National Institute of Science and Technology (UNIST), Ulsan, 44919, South Korea.

出版信息

Nat Commun. 2024 Oct 7;15(1):8680. doi: 10.1038/s41467-024-52949-4.

Abstract

Secondary non-aqueous magnesium-based batteries are a promising candidate for post-lithium-ion battery technologies. However, the uneven Mg plating behavior at the negative electrode leads to high overpotential and short cycle life. Here, to circumvent these issues, we report the preparation of a magnesium/black phosphorus (Mg@BP) composite and its use as a negative electrode for non-aqueous magnesium-based batteries. Via in situ and ex situ physicochemical measurements, we demonstrate that Mg ions are initially intercalated in black phosphorus two-dimensional structures, forming chemically stable MgP intermediates. After the formation of the intermediates, Mg electrodeposition reaction became the predominant. When tested in the asymmetric coin cell configuration, the Mg@BP composite electrode allowed stable stripping/plating performances for 1600 h (800 cycles), a cumulative capacity of 3200 mAh cm, and a Coulombic efficiency of 99.98%. Assembly and testing of the Mg@BP | |nano-CuS coin cell enabled a discharge capacity of 398 mAh g and an average cell discharge potential of about 1.15 V at a specific current of 560 mA g with a low decay rate of 0.016% per cycle for 225 cycles at 25 °C.

摘要

二次非水镁基电池是锂离子电池技术之后很有前景的候选者。然而,负极上不均匀的镁镀层行为导致高过电位和短循环寿命。在此,为了规避这些问题,我们报道了镁/黑磷(Mg@BP)复合材料的制备及其作为非水镁基电池负极的应用。通过原位和非原位物理化学测量,我们证明镁离子最初嵌入黑磷二维结构中,形成化学稳定的MgP中间体。中间体形成后,镁电沉积反应成为主导。在不对称硬币电池配置中测试时,Mg@BP复合电极在1600小时(800次循环)内具有稳定的脱嵌/镀覆性能,累积容量为3200 mAh cm,库仑效率为99.98%。Mg@BP||纳米CuS硬币电池的组装和测试在25°C下以560 mA g的特定电流实现了398 mAh g的放电容量和约1.15 V的平均电池放电电位,在225次循环中每循环的低衰减率为0.016%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d48e/11458587/3d32690c1fa9/41467_2024_52949_Fig1_HTML.jpg

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