通过硅氮共掺石墨烯上的 SiC4 和 SiN1C3 活性中心对界面进行电荷调制,提高锂离子和氖离子电池阳极的性能

IF 3.5 4区 化学 Q2 ELECTROCHEMISTRY ChemElectroChem Pub Date : 2024-09-03 DOI:10.1002/celc.202400401
Berkay Sungur, Edip Bayram, Ali İhsan Kömür
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引用次数: 0

摘要

石墨烯的异构体掺杂是开发高性能锂离子和钠离子电池阳极的有力方法。本研究通过合理的可扩展溶热工艺成功合成了硅氮共掺杂石墨烯(Si-N-GN)纳米结构。通过先进的电化学技术详细研究了 Si-N-GN 在 Na+ 和 Li+ 半电池中的性能,并从 Si-N-GN 表面特性、反应动力学和电极/界面相互作用等方面分析了所得结果。在电流密度为 0.5 A g-1 时,Si-N-GN 对 Li+ 显示出 540 mAh g-1 的优异容量,对 Li+ 和 Na+ 的速率能力也有所提高。重要的是,由于表面电子密度的重新分布和 Si-N-GN/SEI 的相互作用,容量随着循环次数的增加而增加,这一点得到了 DFT 的支持。
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Enhanced Performance for Li & Na Ion Battery Anodes by Charge Modulation of Interface Through SiC4 and SiN1C3 Active Centers on Silicon Nitrogen Co-Doped Graphene

Heteroatom doping of graphene is a powerful approach to develop high-performance Li and Na ion battery anodes. In this study, silicon-nitrogen co-doped graphene (Si−N−GN) nanostructures were successfully synthesized via a rational and scalable solvothermal process. The performances of Si−N−GN in Na+ and Li+ half-cells were investigated in detail by advanced electrochemical techniques and the obtained results were analyzed in terms of Si−N−GN surface properties, reaction kinetics, and electrode/interface interactions. Si−N−GN exhibited a superior capacity of 540 mAh g−1 at a current density of 0.5 A g−1 for Li+ and improved rate capability for both Li+ and Na+ which are linked with the increased interlayer spacing and enlarged graphene sheets upon Si-doping. Importantly, the capacity increased with the number of cycles owing to surface electron density redistribution and Si−N−GN/SEI interactions, supported by DFT.

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来源期刊
ChemElectroChem
ChemElectroChem ELECTROCHEMISTRY-
CiteScore
7.90
自引率
2.50%
发文量
515
审稿时长
1.2 months
期刊介绍: ChemElectroChem is aimed to become a top-ranking electrochemistry journal for primary research papers and critical secondary information from authors across the world. The journal covers the entire scope of pure and applied electrochemistry, the latter encompassing (among others) energy applications, electrochemistry at interfaces (including surfaces), photoelectrochemistry and bioelectrochemistry.
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