阳极
锂(药物)
材料科学
锗
纳米颗粒
兴奋剂
碳纤维
氮气
锌
金属
金属锂
无机化学
纳米技术
化学
电极
光电子学
冶金
复合数
有机化学
复合材料
物理化学
硅
内分泌学
医学
作者
Zhuo Wang,Xue Bai,Jiabao Dong,Kexin Zhang,Bin Zhao,Xiaoli Dong
标识
DOI:10.1002/batt.202400442
摘要
Abstract Germanium (Ge) is demonstrated to be prospective as a lithium‐ion battery anode material, yet the cycling stability is undermined by substantial volume fluctuations, restricting its viability for practical applications. Here, we present a facile Zn‐based metal−organic framework (MOF) engaged route to produce Ge nanoparticles in situ encapsulated in nitrogen‐doped mesoporous carbon (denoted as Ge@N‐C) as an anode material. This method uses a zinc‐triazolate MOF (MET‐6) and commercial GeO 2 as the hybrid carbon and Ge precursors. After a heating treatment, the Ge@N‐C composite is readily obtained along with the simultaneous thermal decomposition of MET‐6 and the reduction of GeO 2 . Benefiting from the mesoporous structure and high electrical conductivity of N−C, along with the strong interaction between Ge and N−C, the obtained Ge@N‐C electrode exhibits a significant reversible charge capacity of 1012.8 mAh g −1 after 150 cycles at 0.1 A g −1 , and excellent rate capability. Furthermore, a reversible charge capacity of 521.1 mAh g −1 can be maintained at 5.0 A g −1 after 1000 cycles.
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