Pore structure regulation of hard carbon: Towards fast and high‐capacity sodium‐ion storage

[Display omitted] •Nanopore regulation strategy can improve the sodium storage capacity of hard carbon.•The relationship between nanopore and sodium storage capability was investigated.•Micropores hardly accommodate Na+ ions and hinder Na+ ion diffusion.•Mesopores facilitate Na+ ion intercalation an...

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Veröffentlicht in:Journal of colloid and interface science 2020-04, Vol.566, p.257-264
Hauptverfasser: Yang, Le, Hu, Mingxiang, Zhang, Hongwei, Yang, Wen, Lv, Ruitao
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container_title Journal of colloid and interface science
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creator Yang, Le
Hu, Mingxiang
Zhang, Hongwei
Yang, Wen
Lv, Ruitao
description [Display omitted] •Nanopore regulation strategy can improve the sodium storage capacity of hard carbon.•The relationship between nanopore and sodium storage capability was investigated.•Micropores hardly accommodate Na+ ions and hinder Na+ ion diffusion.•Mesopores facilitate Na+ ion intercalation and shorten the ion diffusion pathway. Hard carbon is regarded as one of the most promising anode material for sodium-ion batteries in virtue of the low cost and stable framework. However, the correlation between pore structures of hard carbon and sodium-ion storage is still ambiguous. In this work, based on precise control of pore-size distribution, the capacity, ion diffusion, and initial Coulombic efficiency were improved. Meanwhile, the relationship between pore structure and capacity was investigated. Our result indicates that the micropores hinder ion diffusion and hardly ever accommodate Na+ ions, while mesopores facilitate Na+ ion intercalation. Hard carbon with negligible micropores and abundant mesopores delivers a maximum capacity of 283.7 mAh g−1 at 20 mA g−1, which is 83% higher than that of micropore-rich one. Even after 320 cycles at 200 mA g−1, the capacity still remains 189.4 mAh g−1.
doi_str_mv 10.1016/j.jcis.2020.01.085
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Hard carbon is regarded as one of the most promising anode material for sodium-ion batteries in virtue of the low cost and stable framework. However, the correlation between pore structures of hard carbon and sodium-ion storage is still ambiguous. In this work, based on precise control of pore-size distribution, the capacity, ion diffusion, and initial Coulombic efficiency were improved. Meanwhile, the relationship between pore structure and capacity was investigated. Our result indicates that the micropores hinder ion diffusion and hardly ever accommodate Na+ ions, while mesopores facilitate Na+ ion intercalation. Hard carbon with negligible micropores and abundant mesopores delivers a maximum capacity of 283.7 mAh g−1 at 20 mA g−1, which is 83% higher than that of micropore-rich one. Even after 320 cycles at 200 mA g−1, the capacity still remains 189.4 mAh g−1.</description><identifier>ISSN: 0021-9797</identifier><identifier>EISSN: 1095-7103</identifier><identifier>DOI: 10.1016/j.jcis.2020.01.085</identifier><identifier>PMID: 32007737</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Anode ; Hard carbon ; Mesopore ; Micropore ; Pore-structure evolution ; Sodium-ion battery</subject><ispartof>Journal of colloid and interface science, 2020-04, Vol.566, p.257-264</ispartof><rights>2020 Elsevier Inc.</rights><rights>Copyright © 2020 Elsevier Inc. 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Hard carbon is regarded as one of the most promising anode material for sodium-ion batteries in virtue of the low cost and stable framework. However, the correlation between pore structures of hard carbon and sodium-ion storage is still ambiguous. In this work, based on precise control of pore-size distribution, the capacity, ion diffusion, and initial Coulombic efficiency were improved. Meanwhile, the relationship between pore structure and capacity was investigated. Our result indicates that the micropores hinder ion diffusion and hardly ever accommodate Na+ ions, while mesopores facilitate Na+ ion intercalation. Hard carbon with negligible micropores and abundant mesopores delivers a maximum capacity of 283.7 mAh g−1 at 20 mA g−1, which is 83% higher than that of micropore-rich one. 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subjects Anode
Hard carbon
Mesopore
Micropore
Pore-structure evolution
Sodium-ion battery
title Pore structure regulation of hard carbon: Towards fast and high‐capacity sodium‐ion storage
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