4.8 Article

Approaching Superior Potassium Storage of Carbonaceous Anode Through a Combined Strategy of Carbon Hybridization and Sulfur Doping

期刊

ENERGY & ENVIRONMENTAL MATERIALS
卷 5, 期 3, 页码 944-953

出版社

WILEY
DOI: 10.1002/eem2.12217

关键词

carbonaceous anode; graphene; hollow carbon spindles; potassium-ion batteries; sulfur doping

资金

  1. National Natural Science Foundation of China [61935017, 21701174, 21771182]
  2. Synergetic Innovation Center for Organic Electronics and Information Displays, Projects of International Cooperation and Exchanges NSFC [51811530018]
  3. Youth Innovation Promotion Association CAS
  4. FJNU

向作者/读者索取更多资源

Carbonaceous materials show promise as anode candidates for potassium-ion batteries due to their high conductivity, stable properties, and abundant resources. A superior carbonaceous anode was developed in this study through a combined strategy of carbon hybridization and heteroatom doping, resulting in high capacity and superior rate capability. The use of graphene/amorphous carbon interface and sulfur doping played a key role in enhancing the electronic structure and ion adsorption/transport properties of the composite, leading to its excellent performance.
Carbonaceous materials are promising anode candidates for potassium-ion batteries (PIBs) given its high conductivity, stable property, and abundant resource, while its practical implementation is still hampered by its limited capacity and inferior rate behavior. Herein, we report a superior carbonaceous anode through a combined strategy of carbon hybridization and heteroatom doping. In this composite, hollow carbon spindles (HCS) were anchored on the surface of graphene (G) followed with sulfur doping treatment, aiming to integrate the high conductivity of graphene, the good structure stability of HCS, and the S doping-induced ample active sites. As a PIB anode, the S-G@HCS composite can display high capacity (301 mA h g(-1) at 0.1 A g(-1) after 500 cycles) and long-term cyclability up to 1800 cycles at 2 A g(-1). Impressively, it can deliver an outstanding rate capacity of 215 mA h g(-1) at 10 A g(-1), which is superior to most carbon anodes as-reported so far for PIBs. Experimental and theoretical analysis manifests that the construction of graphene/amorphous carbon interface as well as S doping enables the regulation of electronic structure and ion adsorption/transportation properties of carbonaceous material, thus accounting for the high capacity and superior rate capability of S-G@HCS composite.

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