Liu Congcong, Lu Qiongqiong, Qu Jiang, Feng Wen, Thomas Alexander, Li Yuxi, Martinez Ignacio G Gonzalez, Pan Cunliang, Mikhailova Daria
Leibniz Institute for Solid State and Materials Research (IFW) Dresden e.V., Helmholtzstraße 20, 01069, Dresden, Germany.
Institute of Materials, Henan Key Laboratory of Advanced Conductor Materials, Henan Academy of Sciences, Zhengzhou, Henan, 450046, China.
Small. 2024 Aug;20(31):e2311253. doi: 10.1002/smll.202311253. Epub 2024 Mar 8.
A highly viable alternative to lithium-ion batteries for stationary electrochemical energy-storage systems is the potassium dual-ion hybrid capacitor (PIHC), especially toward fast-charging capability. However, the sluggish reaction kinetics of negative electrode materials seriously impedes their practical implementation. In this paper, a new negative electrode Bi@RPC (Nano-bismuth confined in nitrogen- and oxygen-doped carbon with rationally designed pores, evidenced by advanced characterization) is developed, leading to a remarkable electrochemical performance. PIHCs building with the active carbon YP50F positive electrode result in a high operation voltage (0.1-4 V), and remarkably well-retained energy density at a high-power density (11107 W kg at 98 Wh kg). After 5000 cycles the proposed PHICs still show a superior capacity retention of 92.6%. Moreover, a reversible mechanism of "absorption-alloying" of the Bi@RPC nanocomposite is revealed by operando synchrotron X-ray diffraction and Raman spectroscopy. With the synergistic potassium ions storage mechanism arising from the presence of well-structured pores and nano-sized bismuth, the Bi@RPC electrode exhibits an astonishingly rapid kinetics and high energy density. The results demonstrate that PIHCs with Bi@RPC-based negative electrode is the promising option for simultaneously high-capacity and fast-charging energy storage devices.
对于固定式电化学储能系统而言,钾双离子混合电容器(PIHC)是锂离子电池极具可行性的替代方案,尤其在快充能力方面。然而,负极材料缓慢的反应动力学严重阻碍了它们的实际应用。本文开发了一种新型负极Bi@RPC(纳米铋被限制在具有合理设计孔隙的氮氧掺杂碳中,先进表征证明),从而实现了卓越的电化学性能。采用活性炭YP50F作为正极构建的PIHC具有高工作电压(0.1 - 4V),并且在高功率密度下(98Wh kg时为11107W kg)能显著保持能量密度。经过5000次循环后,所提出的PHIC仍表现出92.6%的优异容量保持率。此外,通过同步辐射X射线衍射和拉曼光谱原位揭示了Bi@RPC纳米复合材料的“吸收 - 合金化”可逆机制。由于结构良好的孔隙和纳米尺寸铋的协同作用,Bi@RPC电极展现出惊人的快速动力学和高能量密度。结果表明,基于Bi@RPC负极的PIHC是同时实现高容量和快速充电储能设备的有前景选择。