Novel silicon nanoparticles-based carbonized polypyrrole nanotube composites as anode materials for Li-ion batteries

阳极 材料科学 聚吡咯 碳化 碳纳米管 电化学 纳米颗粒 锂(药物) 化学工程 纳米技术 复合材料 电导率 电极 聚合物 扫描电子显微镜 化学 物理化学 内分泌学 工程类 医学 聚合
作者
Gabriela Soukupová,Martin Jindra,Tomáš Lapka,Zuzana Živcová Vlčková,Marcela Dendisová,Ján Prokeš,Otakar Frank,Fatima Hassouna
出处
期刊:Journal of Power Sources [Elsevier]
卷期号:593: 233976-233976 被引量:7
标识
DOI:10.1016/j.jpowsour.2023.233976
摘要

The development of elastic nanostructured Si-based anodes holds promise for advancing lithium-ion batteries due to the high theoretical specific capacity exhibited by Si. Combining nanostructured Si with C proves to be a successful strategy in addressing the challenges tied to the substantial volume expansion of Si during lithiation. In this work, a novel Si-based anode is fashioned through a simple and universal strategy, integrating Si nanoparticles with 1D nano-carbonaceous fillers (CPPy-NT) featuring nanotubular morphology and N atoms, and a water-based binder (poly(acrylic acid)). CPPy-NT are derived by carbonizing pre-synthesized polypyrrole nanotubes (PPy-NT). A clear correlation is established among the carbonization temperature for CPPy-NT preparation, N content in CPPy-NT, electrical conductivity, and the electrochemical performance of the ensuing Si/CPPy-NT anode. For comparative analysis, the electrochemical properties of the Si-based anode employing Super P (commercial carbon black) or PPy-NT are contrasted with those of Si/CPPy-NT. Notably, the Si/CPPy-NT anode with CPPy-NT bearing the highest amount of graphitic N sites exhibits a substantial improvement in initial charge capacity (approximately 2200 mAh g−1) and enhanced cycling stability. These findings underscore the potential to elevate the electrochemical activity of the C filler by carefully optimizing morphology, conductivity, and the incorporation of an appropriate amount of graphitic N.

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