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封装在碳化壳聚糖中的SnS作为钾离子电池电极材料的实验与计算分析

Experimental and computational analysis of SnS encapsulated into carbonized chitosan as electrode material for potassium ion batteries.

作者信息

Nowak Andrzej P, Rokicińska Anna, Wang Zhilong, Prześniak-Welenc Marta, Zarach Zuzanna, Tao Kehao, Roda Daria, Szkoda Mariusz, Trzciński Konrad, Li Jinjin, Kuśtrowski Piotr

机构信息

Faculty of Chemistry, Gdańsk University of Technology, Narutowicza 11/12, 80-233, Gdańsk, Poland.

Advanced Materials Center, Gdańsk University of Technology, Narutowicza 11/12, 80-233, Gdańsk, Poland.

出版信息

Sci Rep. 2024 Dec 28;14(1):31212. doi: 10.1038/s41598-024-82588-0.

DOI:10.1038/s41598-024-82588-0
PMID:39732909
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11682189/
Abstract

Tin sulphide compounds (SnS, x = 1, 2) are potential anode materials for potassium-ion batteries (PIBs) due to their characteristic layered structure, high theoretical capacity, non-toxicity and low production cost. However, they suffer from significant volume changes resulting in poor performance of such anodes. In this work incorporation of SnS into the carbon structure was expected to overcome these disadvantages. Two SnS-based electrode materials encapsulated into chitosan, as a natural carbon source, are fabricated by two different synthesis routes: (a) solvothermal, and (b) solvothermal followed by pyrolysis. The results indicate that the synthesis route is a crucial factor affecting the composition and electrochemical performance of the negative electrode. The electrode material, exhibiting a high reversible capacity (304 mAh/g at 50 mA/g), and good rate capability (128 mAh/g at 1000 mA/g for 500 cycles) is produced by the solvothermal method. The relationship between specific capacity and synthesis procedure is analyzed using the results obtained from XRD, XPS. Additionally, density functional theory is employed to provide deeper insights into the underlying mechanisms governing the electrochemical performance of the SnS@C electrode materials.

摘要

硫化锡化合物(SnS,x = 1, 2)因其独特的层状结构、高理论容量、无毒且生产成本低,是钾离子电池(PIB)潜在的负极材料。然而,它们会发生显著的体积变化,导致此类负极性能不佳。在这项工作中,将SnS掺入碳结构有望克服这些缺点。通过两种不同的合成路线制备了两种封装在壳聚糖(一种天然碳源)中的SnS基电极材料:(a)溶剂热法,以及(b)溶剂热法后再进行热解。结果表明,合成路线是影响负极组成和电化学性能的关键因素。通过溶剂热法制备的电极材料具有高可逆容量(50 mA/g时为304 mAh/g)和良好的倍率性能(1000 mA/g下循环500次时为128 mAh/g)。利用XRD、XPS获得的结果分析了比容量与合成过程之间的关系。此外,采用密度泛函理论更深入地了解控制SnS@C电极材料电化学性能的潜在机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dd6/11682189/309dc4c6dbcb/41598_2024_82588_Fig8_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dd6/11682189/309dc4c6dbcb/41598_2024_82588_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dd6/11682189/ae55d0fe8122/41598_2024_82588_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dd6/11682189/554174f274a7/41598_2024_82588_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dd6/11682189/9f7025d5813b/41598_2024_82588_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dd6/11682189/3ca18affbf77/41598_2024_82588_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dd6/11682189/ebc415e912c4/41598_2024_82588_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dd6/11682189/309dc4c6dbcb/41598_2024_82588_Fig8_HTML.jpg

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本文引用的文献

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