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可扩展合成封装在氮掺杂碳基质中的三维多孔锗作为锂离子电池的超长循环寿命阳极。

Scalable synthesis of 3D porous germanium encapsulated in nitrogen-doped carbon matrix as an ultra-long-cycle life anode for lithium-ion batteries.

作者信息

Liu Xianyu, Wang Yanting, Liu Zheng, Wei Huijuan, Ma Mingguang, Xue Rui, Zhang Qianliang, Li Shengying

机构信息

School of Chemistry and Chemical Engineering, Institute of Urban Ecology and Environment, Nanomaterials Laboratory, Lanzhou City University, Lanzhou, Gansu 730070, The People's Republic of China.

Key Laboratory of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, and State Key Laboratory of Crystal Materials, Shandong University, Jinan, Shandong 250100, The People's Republic of China.

出版信息

Dalton Trans. 2021 Oct 5;50(38):13476-13482. doi: 10.1039/d1dt00797a.

DOI:10.1039/d1dt00797a
PMID:34492669
Abstract

Germanium-based materials attract more interest as anodes for lithium-ion batteries, stemming from their physical and chemical advantages. However, these materials inevitably undergo capacity attenuation caused by significant volumetric variation in repeated electrochemical processes. Herein, we designed 3D porous Ge/N-doped carbon nanocomposites by the encapsulation of 3D porous Ge in a nitrogen-doped carbon matrix (denoted as 3D porous Ge/NC). The 3D porous structure can accommodate the volume change during alloying/dealloying processes and improve the penetration of the electrolyte. Furthermore, the doping of N in the carbon framework could introduce more defects and active sites, which can also contribute to electron transportation and lithium-ion diffusion. The half-cell test found that at a current density of 1 C (1 C = 1600 mA h g), the specific capacity stabilized at 917.9 mA h g after 800 cycles; and the specific capacity remained at 542.4 mA h g at 10 C. When assembled into a 3D porous Ge/NC//LiFePO full cell, the specific capacity was stabilized at 101.3 mA h g for 100 cycles at a current density of 1 C (1 C = 170 mA h g), and the cycle specific capacity was maintained at 72.6 mA h g at a high current density of 5 C. This work develops a low-cost, scalable and simple strategy to improve the electrochemical performance of these alloying type anode materials with huge volume change in the energy storage area.

摘要

锗基材料作为锂离子电池的负极材料受到了更多关注,这源于它们的物理和化学优势。然而,这些材料在反复的电化学过程中不可避免地会因显著的体积变化而导致容量衰减。在此,我们通过将三维多孔锗封装在氮掺杂碳基体中(记为三维多孔Ge/NC)设计了三维多孔Ge/N掺杂碳纳米复合材料。三维多孔结构可以适应合金化/脱合金化过程中的体积变化,并改善电解质的渗透。此外,在碳骨架中掺杂氮可以引入更多的缺陷和活性位点,这也有助于电子传输和锂离子扩散。半电池测试发现,在1 C(1 C = 1600 mA h g)的电流密度下,800次循环后比容量稳定在917.9 mA h g;在10 C时比容量保持在542.4 mA h g。当组装成三维多孔Ge/NC//LiFePO全电池时,在1 C(1 C = 170 mA h g)的电流密度下,100次循环后比容量稳定在101.3 mA h g,在5 C的高电流密度下循环比容量保持在72.6 mA h g。这项工作开发了一种低成本、可扩展且简单的策略,以改善储能领域中这些具有巨大体积变化的合金型负极材料的电化学性能。

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