材料科学
三氧化钼
电化学
电极
插层(化学)
离子
钼
化学工程
阳极
阴极
纳米技术
储能
光电子学
无机化学
化学
冶金
功率(物理)
物理化学
热力学
工程类
物理
有机化学
作者
Minghao Yu,Hui Shao,Gang Wang,Fan Yang,Chaolun Liang,Patrick Rozier,Cai‐Zhuang Wang,Xihong Lu,Patrice Simon,Xinliang Feng
标识
DOI:10.1038/s41467-020-15216-w
摘要
Abstract Employing high-rate ion-intercalation electrodes represents a feasible way to mitigate the inherent trade-off between energy density and power density for electrochemical energy storage devices, but efficient approaches to boost the charge-storage kinetics of electrodes are still needed. Here, we demonstrate a water-incorporation strategy to expand the interlayer gap of α-MoO 3 , in which water molecules take the place of lattice oxygen of α-MoO 3 . Accordingly, the modified α-MoO 3 electrode exhibits theoretical-value-close specific capacity (963 C g −1 at 0.1 mV s −1 ), greatly improved rate capability (from 4.4% to 40.2% at 100 mV s −1 ) and boosted cycling stability (from 21 to 71% over 600 cycles). A fast-kinetics dual-ion-intercalation energy storage device is further assembled by combining the modified α-MoO 3 anode with an anion-intercalation graphite cathode, operating well over a wide discharge rate range. Our study sheds light on a promising design strategy of layered materials for high-kinetics charge storage.
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