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氧化石墨烯薄片与BF·THF的功能化机制及其对锂离子电池中锂离子相互作用的影响

Functionalization Mechanism of Reduced Graphene Oxide Flakes with BF·THF and Its Influence on Interaction with Li Ions in Lithium-Ion Batteries.

作者信息

Kaczmarek Łukasz, Balik Magdalena, Warga Tomasz, Acznik Ilona, Lota Katarzyna, Miszczak Sebastian, Sobczyk-Guzenda Anna, Kyzioł Karol, Zawadzki Piotr, Wosiak Agnieszka

机构信息

Institute of Materials Science and Engineering, Lodz University of Technology, Stefanowskiego 1/15, 90-924 Lodz, Poland.

Łukasiewicz Research Network-Institute of Non-Ferrous Metals Poznań Division, Forteczna 12, 61-362 Poznan, Poland.

出版信息

Materials (Basel). 2021 Feb 2;14(3):679. doi: 10.3390/ma14030679.

DOI:10.3390/ma14030679
PMID:33540630
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7867238/
Abstract

Doping of graphene and a controlled induction of disturbances in the graphene lattice allows the production of numerous active sites for lithium ions on the surface and edges of graphene nanolayers and improvement of the functionality of the material in lithium-ion batteries (LIBs). This work presents the process of introducing boron and fluorine atoms into the structure of the reduced graphene during hydrothermal reaction with boron fluoride tetrahydrofuran (BF·THF). The described process is a simple, one-step synthesis with little to no side products. The synthesized materials showed an irregular, porous structure, with an average pore size of 3.44-3.61 nm (total pore volume (BJH)) and a multi-layer structure and a developed specific surface area at the level of 586-660 m/g (analysis of specific surface Area (BET)). On the external surfaces, the occurrence of irregular particles with a size of 0.5 to 10 µm was observed, most probably the effect of doping the graphene structure and the formation of sp hybridization defects. The obtained materials show the ability to store electric charge due to the development of the specific surface area. Based on cyclic voltammetry, the tested material showed a capacity of 450-550 mAh/g (charged up to 2.5 V).

摘要

对石墨烯进行掺杂并在石墨烯晶格中可控地引入扰动,能够在石墨烯纳米层的表面和边缘产生大量锂离子活性位点,并改善材料在锂离子电池(LIBs)中的功能。本文介绍了在与四氢呋喃硼氟化物(BF·THF)进行水热反应过程中,将硼和氟原子引入还原石墨烯结构的过程。所描述的过程是一种简单的一步合成法,几乎没有副产物。合成材料呈现出不规则的多孔结构,平均孔径为3.44 - 3.61纳米(BJH总孔体积),具有多层结构,比表面积在586 - 660平方米/克(BET比表面积分析)。在材料外表面,观察到存在尺寸为0.5至10微米的不规则颗粒,这很可能是石墨烯结构掺杂和形成sp杂化缺陷的结果。由于比表面积的增大,所获得的材料显示出储存电荷的能力。基于循环伏安法,测试材料的容量为450 - 550毫安时/克(充电至2.5伏)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7400/7867238/f01bf5577f85/materials-14-00679-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7400/7867238/4e0a7ff13265/materials-14-00679-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7400/7867238/140df09c37c6/materials-14-00679-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7400/7867238/2a3ca94c0b20/materials-14-00679-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7400/7867238/fe7ce91b039a/materials-14-00679-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7400/7867238/e33f387d2ae3/materials-14-00679-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7400/7867238/635336554df5/materials-14-00679-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7400/7867238/f01bf5577f85/materials-14-00679-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7400/7867238/4e0a7ff13265/materials-14-00679-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7400/7867238/bf14f8625b1c/materials-14-00679-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7400/7867238/140df09c37c6/materials-14-00679-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7400/7867238/2a3ca94c0b20/materials-14-00679-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7400/7867238/fe7ce91b039a/materials-14-00679-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7400/7867238/e33f387d2ae3/materials-14-00679-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7400/7867238/635336554df5/materials-14-00679-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7400/7867238/f01bf5577f85/materials-14-00679-g008.jpg

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本文引用的文献

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Toward sustainable and systematic recycling of spent rechargeable batteries.迈向可持续且系统的可充电废旧电池回收。
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