Porous carbon microspheres assembled by defective nitrogen and sulfur co-doped nanosheets as anode materials for lithium-/sodium-ion batteries

IF 6.8 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Science China Materials Pub Date : 2024-09-10 DOI:10.1007/s40843-024-3041-3
Yutian Chen  (, ), Jie You  (, ), Xiaoran Zhao  (, ), Mai Li  (, ), Xiaolei Han  (, ), Hui Liu  (, ), Hongran Sun  (, ), Xiaojun Wang  (, ), Huifang Li  (, ), Peng Wang  (, ), Zhiming Liu  (, )
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Abstract

Carbon-based anode materials are widely used in various battery energy storage systems due to their low cost, wide source, high conductivity and easy morphology control. However, current commercially available anode materials as active materials for lithium-/sodium-ion batteries generally suffer from large volume changes and poor rate performance. In response, we synthesized defect-rich N, S co-doped two dimensional (2D) nanosheet-assembled porous carbon microspheres (N, S-PCS) via simple hydrothermal, carbonization and etching process based on the principle of Schiff base reaction. The N, S-PCS structure is thus constructed by removing Fe7S8 nanoparticles from the carbon skeleton to form porous microspheres with N, S doping. Therefore, the micromorphology characteristic, pore structure and electro-conductivity of carbon materials are effectively optimized via heteroatom doping and surface engineering. As expected, the prepared N, S-PCS electrodes exhibit excellent electrochemical performance in both lithium-ion and sodium-ion batteries. For lithium-ion batteries, it achieves reversible capacities of 1045 and 237 mAh g−1 at 0.1 and 20 A g−1, respectively. For sodium-ion batteries, it shows good cycling stability with a capacity of 157 mAh g−1 after 500 cycles at 1 A g−1. Experimental and theoretical calculation results confirm that the N, S co-doping strategies help to improve the structural stability, shorten the ion diffusion paths, and promote the reaction kinetics, thus achieving excellent electrochemical performance. This work is instructive for the practical application of nonmetal doping functionalized porous carbon structures for metal-ion batteries.

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由缺陷氮和硫共掺杂纳米片组装而成的多孔碳微球作为锂离子/钠离子电池的负极材料
碳基负极材料具有成本低、来源广、电导率高、形态易控制等特点,被广泛应用于各种电池储能系统中。然而,目前市面上作为锂离子/钠离子电池活性材料的负极材料普遍存在体积变化大、速率性能差的问题。为此,我们根据希夫碱反应原理,通过简单的水热、碳化和刻蚀工艺合成了富含缺陷的 N、S 共掺杂二维(2D)纳米片组装多孔碳微球(N,S-PCS)。因此,N、S-PCS 结构是通过从碳骨架中去除 Fe7S8 纳米颗粒,形成掺杂 N、S 的多孔微球。因此,通过杂原子掺杂和表面工程,碳材料的微观形貌特征、孔隙结构和导电性能得到了有效优化。正如预期的那样,制备的 N、S-PCS 电极在锂离子电池和钠离子电池中均表现出优异的电化学性能。对于锂离子电池,在 0.1 和 20 A g-1 的条件下,其可逆容量分别达到 1045 和 237 mAh g-1。对于钠离子电池,它显示出良好的循环稳定性,在 1 A g-1 下循环 500 次后,容量为 157 mAh g-1。实验和理论计算结果证实,N、S 共掺杂策略有助于提高结构稳定性、缩短离子扩散路径和促进反应动力学,从而实现优异的电化学性能。这项工作对金属离子电池非金属掺杂功能化多孔碳结构的实际应用具有指导意义。
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来源期刊
Science China Materials
Science China Materials Materials Science-General Materials Science
CiteScore
11.40
自引率
7.40%
发文量
949
期刊介绍: Science China Materials (SCM) is a globally peer-reviewed journal that covers all facets of materials science. It is supervised by the Chinese Academy of Sciences and co-sponsored by the Chinese Academy of Sciences and the National Natural Science Foundation of China. The journal is jointly published monthly in both printed and electronic forms by Science China Press and Springer. The aim of SCM is to encourage communication of high-quality, innovative research results at the cutting-edge interface of materials science with chemistry, physics, biology, and engineering. It focuses on breakthroughs from around the world and aims to become a world-leading academic journal for materials science.
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