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Enhanced Capacity and Rate Capability of Nitrogen/Oxygen Dual‐Doped Hard Carbon in Capacitive Potassium‐Ion Storage

Jinlin YangKey Laboratory of the Colloid and Interface Chemistry Ministry of Education and School of Chemistry and Chemical Engineering Shandong University Jinan 250100 P. R. ChinaZhicheng JuKey Laboratory of the Colloid and Interface Chemistry Ministry of Education and School of Chemistry and Chemical Engineering Shandong University Jinan 250100 P. R. ChinaYong JiangKey Laboratory of the Colloid and Interface Chemistry Ministry of Education and School of Chemistry and Chemical Engineering Shandong University Jinan 250100 P. R. ChinaZheng XingSchool of Materials Science and Engineering China University of Mining and Technology Xuzhou Jiangsu 221116 P. R. ChinaBaojuan XiKey Laboratory of the Colloid and Interface Chemistry Ministry of Education and School of Chemistry and Chemical Engineering Shandong University Jinan 250100 P. R. ChinaJinkui FengKey Laboratory for Liquid‐Solid Structural Evolution & Processing of Materials Ministry of Education, and School of Materials Science and Engineering Shandong University Jinan 250061 P. R. ChinaShenglin XiongKey Laboratory of the Colloid and Interface Chemistry Ministry of Education and School of Chemistry and Chemical Engineering Shandong University Jinan 250100 P. R. China
2017en
ABI

Аннотация

Abstract The intercalation of potassium ions into graphite is demonstrated to be feasible, while the electrochemical performance of potassium‐ion batteries (KIBs) remains unsatisfying. More effort is needed to improve the specific capacity while maintaining a superior rate capability. As an attempt, nitrogen/oxygen dual‐doped hierarchical porous hard carbon (NOHPHC) is introduced as the anode in KIBs by carbonizing and acidizing the NH 2 ‐MIL‐101(Al) precursor. Specifically, the NOHPHC electrode delivers high reversible capacities of 365 and 118 mA h g −1 at 25 and 3000 mA g −1 , respectively. The capacity retention reaches 69.5% at 1050 mA g −1 for 1100 cycles. The reasons for the enhanced electrochemical performance, such as the high capacity, good cycling stability, and superior rate capability, are analyzed qualitatively and quantitatively. Quantitative analysis reveals that mixed mechanisms, including capacitance and diffusion, account for the K‐ion storage, in which the capacitance plays a more important role. Specifically, the enhanced interlayer spacing (0.39 nm) enables the intercalation of large K ions, while the high specific surface area of ≈1030 m 2 g −1 and the dual‐heteroatom doping (N and O) are conducive to the reversible adsorption of K ions.

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