Dual intercalation of inorganics–organics for synergistically tuning the layer spacing of V2O5·nH2O to boost Zn2+ storage for aqueous zinc-ion batteries

插层(化学) 层状结构 聚苯胺 电化学 材料科学 无机化学 化学工程 阴极 水溶液 化学 电极 工程类 聚合物 有机化学 冶金 复合材料 物理化学 聚合
作者
Ziyi Feng,Yifu Zhang,Yunfeng Zhao,Jingjing Sun,Yanyan Liu,Hanmei Jiang,Miao Cui,Tao Hu,Changgong Meng
出处
期刊:Nanoscale [The Royal Society of Chemistry]
卷期号:14 (24): 8776-8788 被引量:44
标识
DOI:10.1039/d2nr02122f
摘要

Possessing a 2D zinc-ion transport channel, layered vanadium oxides have become good candidates as cathode materials for aqueous rechargeable zinc-ion batteries (ARZIBs). Tuning the lamellar structure of vanadium oxides to enhance their zinc-ion storage is a great challenge. In the present study, we proposed and investigated a "co-intercalation mechanism" in which Mg2+ and polyaniline (PANI) were simultaneously intercalated into the layers of hydrated V2O5 (MgVOH/PANI) by a one-step hydrothermal method. Inorganic-organic co-intercalation could tune the layer spacing of VOH, and this combination played a synergistic role in enhancing the zinc-ion storage in MgVOH/PANI. It showed an extremely large layer spacing of 14.2 Å, specific capacity of up to 412 mA h g-1 at 0.1 A g-1, and the capacity retention rate could reach 98% after 1000 cycles. PANI itself has a zinc-storage capacity, and Mg2+ intercalated with PANI can improve the conductivity of the material and enhance its stability. Further first-principles calculations clearly revealed the structural changes and improved electrochemical performance of vanadium oxides. This method of inorganic and organic co-regulation of the VOH structure opens a new strategy for tuning the lamellar structure of layered materials to boost their electrochemical performances.
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