S/N co-doped hierarchical porous carbon from lignite as high-performance anode for potassium-ion batteries
Because of their lower prices and exceptional physicochemical features, hard carbon materials have received a lot of interest in potassium ion batteries (PIBs). However, the slow K+ transport kinetics and significant volume expansion make the use of carbonaceous materials in PIBs anodes difficult. H...
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Veröffentlicht in: | Journal of energy storage 2023-12, Vol.74, p.109486, Article 109486 |
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Sprache: | eng |
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Zusammenfassung: | Because of their lower prices and exceptional physicochemical features, hard carbon materials have received a lot of interest in potassium ion batteries (PIBs). However, the slow K+ transport kinetics and significant volume expansion make the use of carbonaceous materials in PIBs anodes difficult. Here, S/N co-doped hierarchical porous carbon composites are designed as anodes for PIBs using lignite as raw material. The S/N co-doped carbon composites produced feature a hierarchical porous structure, which ensures structural resilience and speeds up ion/electronic transport. S/N co-doping in the carbon matrix not only creates an abundance of defects and active sites for K+, but it also increases the distance between layers, allowing for more accessible K+ intercalation/deintercalation. As a result, when used as anodes for PIBs, the obtained S/N co-doped hierarchical porous carbon composites have a large reversible capacity of 347.5 mAh g−1 after 100 cycles at 0.1 A g−1 with a capacity retention of up to 94 %, as well as excellent long cycle stability of 136 mAh g−1 after 1500 cycles at 1.0 A g−1.
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•S,N co-doped hierarchical porous C (SN@LC) is designed as PIBs anode from lignite.•Porous structure ensures structural resilience and speeds up ion/electronic transport.•S,N co-doping in C matrix creates an abundance of defects and active sites for K+.•S,N co-doping expands interlayer distance for facile K+ intercalation/deintercalation.•SN@LC anode delivers high capacity, superior rate capability and good cycle stability. |
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ISSN: | 2352-152X 2352-1538 |
DOI: | 10.1016/j.est.2023.109486 |