Chen Xiaoxia, Muheiyati Haliya, Sun Xiuping, Zhou Pan, Wang Peican, Ding Xuyang, Qian Yitai, Xu Liqiang
Key Laboratory of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, State Key Laboratory of Crystal Materials Shandong University, Ji'nan, 250100, China.
The State Key Laboratory of Chemical Engineering, Department of Chemical Engineering, Tsinghua University, Beijing, 100084, China.
Small. 2022 Feb;18(5):e2104363. doi: 10.1002/smll.202104363. Epub 2021 Nov 25.
Potassium-ion batteries (PIBs) are deemed as one of the most promising energy storage systems due to their high energy density and low cost. However, their commercial application is far away from satisfactory because of limited suitable electrode materials. Herein, core-shell structured WSe @N-doped C nanotubes are rationally designed and synthesized via selenizing WO @ polypyrrole for the first time. The large interlayer spacing of WSe can facilitate the intercalation/deintercalation of K . Meanwhile, the core-shell structured nanotube provides favorable interior void space to accommodate the volume expansion of WSe during cycling. Thus, the obtained electrode exhibits superb electrochemical performance with a high capacity of 301.7 mAh g at 100 mA g over 120 cycles, and 122.1 mAh g can remain at 500 mA g even after 1300 cycles. Ex-situ X-ray diffraction analysis reveals the K-ion storage mechanism of WSe @N-doped C includes intercalation and conversion reaction. Density function theory (DFT) calculation demonstrates the reasonable diffusion pathway of K . In addition, the obtained WSe @N-doped C nanotubes have been used as anode material for lithium-ion batteries, which also show good rate performance and high cycle stability. Therefore, this work offers a new methodology for the ration design of new structure electrode materials with long cycle stability.
钾离子电池(PIBs)因其高能量密度和低成本而被视为最有前景的储能系统之一。然而,由于合适的电极材料有限,其商业应用远不能令人满意。在此,首次通过将WO@聚吡咯硒化,合理设计并合成了核壳结构的WSe@N掺杂C纳米管。WSe的大层间距可促进K的嵌入/脱出。同时,核壳结构的纳米管提供了有利的内部空隙空间,以适应WSe在循环过程中的体积膨胀。因此,所制备的电极表现出优异的电化学性能,在100 mA g下120次循环时容量高达301.7 mAh g,即使在500 mA g下循环1300次后仍有122.1 mAh g的容量。非原位X射线衍射分析揭示了WSe@N掺杂C的钾离子存储机制包括嵌入和转化反应。密度泛函理论(DFT)计算证明了K的合理扩散途径。此外,所制备的WSe@N掺杂C纳米管已被用作锂离子电池的负极材料,也表现出良好的倍率性能和高循环稳定性。因此,这项工作为合理设计具有长循环稳定性的新型结构电极材料提供了一种新方法。