材料科学
双锰矿
插层(化学)
阴极
锰
电化学
水溶液
化学工程
离子
X射线光电子能谱
储能
无机化学
电极
冶金
氧化锰
化学
有机化学
功率(物理)
物理化学
工程类
物理
量子力学
作者
Fengyang Jing,Yanan Liu,Yaru Shang,Chade Lv,Liangliang Xu,Jian Pei,Jian Liu,Gang Chen,Chunshuang Yan
标识
DOI:10.1016/j.ensm.2022.04.008
摘要
Rechargeable aqueous zinc-ion batteries (ZIBs) emerge as promising candidates for grid-scale storage due to the low cost of zinc and high safety. However, aqueous ZIBs still remain the grand challenges in the poor Zn2+ transport kinetics and the structural instability of the cathode materials during Zn2+ intercalation/deintercalation. In this work, we rationally introduce Mg ion and K ion into birnessite-type manganese oxide (K0.16Mg0.06Mn2O4·1.4H2O) by one-step hydrothermal method. The intercalation of dual ions guarantees accelerated Zn2+ diffusion and excellent structural stability. Such an elegant structure delivers an ultrahigh reversible capacity of 400 mAh g-1 at 0.1 A g-1 and outstanding cycling stability (capacity retention of 94% after 1000 cycles at 500 mA g-1). With the aid of ex-situ XRD, SEM and XPS, the zinc-ion storage mechanism is explored to uncover the origin of superior electrochemical performance. This study opens up the possibilities for designing high-power ZIBs and makes a step forward to the practical application of Zn-MnO2 batteries.
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