| Literature DB >> 35088540 |
Fei Yuan1,2, Di Zhang1, Zhaojin Li1, Huilan Sun1, Qiyao Yu3, Qiujun Wang1, Jianguo Zhang3, Yusheng Wu2, Kai Xi4, Bo Wang1.
Abstract
Pore-structure design with increased ion-diffusion ability is usually regarded as an effective strategy to improve K-storage performance in hard carbon (HC). However, the relationship between porous structure and K+ migration behavior remains unclear and requires further exploration. Herein, a series of chemically activated hard carbon spheres (denoted as AHCSs) with controllable micro/mesopores structure are successfully synthesized to explore intercorrelation between micro/mesopores and K migration behavior. The experimental results indicate AHCSs have two different K+ storage ways, that is, adsorption behavior at high potential region and intercalation process at low potential region. These behaviors are closely related to the pores structure evolution: the micropores afford extra active sites for efficient K-ions adsorption, and therefore positive correlation between micropores and adsorption-contributed capacity is confirmed; the mesopores permit more K-ions intercalation/deintercalation by offering adequate pathways, and as a result positive correlations between mesopores and intercalation-contributed capacity as well as initial Coulombic efficiency are revealed. All these together contribute to achieving excellent reversible capacity, and exceptional rate capability with an ultra-long cycle lifespan in PIBs, and simultaneously exhibit a high energy density as well as considerable cycling stability for potassium-ion full cells. These results promote a fundamental understanding of K+ migration behaviors in hard carbon.Entities:
Keywords: anodes; hard carbons; micro/mesopores; potassium ion batteries; potassium migration behavior
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Year: 2022 PMID: 35088540 DOI: 10.1002/smll.202107113
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281