期刊
JOURNAL OF ALLOYS AND COMPOUNDS
卷 937, 期 -, 页码 -出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2022.168474
关键词
Porous network; Phosphotungstic acid; Anode materials; Lithium-ion battery
Polyoxometalates (POM) have versatile properties, and here we report the synthesis of a novel 3D porous network of ultrathin V6O13-POM nanosheets on carbon cloth (V6O13-POM//CC) for energy storage. The use of phosphotungstic acid as an inorganic ligand assists in the formation and control of the morphology of V6O13-POM composites, increasing the specific surface area and active sites. The V6O13-POM//CC anode material demonstrates high reversible capacity and stability in lithium-ion batteries, showing potential for commercial applications.
Polyoxometalates (POM) have a wide range of applications in electrochemistry, catalysis, and energy storage due to their variable structure and nature. Here, we designed a novel 3D porous network of ultrathin V6O13- POM nanosheets on carbon cloth (V6O13-POM//CC) for the first time by one-pot hydrothermal method with the help of phosphotungstic acid. Serving as inorganic ligands, the anions of phosphotungstic acid co-ordinate with V cations, facilitating the assembly of nanoclusters and guiding to control of the morphology of V6O13-POM composites, which increases the specific surface area and multiple active sites for the re-action of lithium ions batteries (LIBs). Furthermore, the synergistic effect of V6O13 and POM improves the stability of the structure and increases the capacity of the electrode in LIBs. V6O13-POM//CC as an anode material exhibited a high reversible capacity of 2.03 mAh cm-2 at a high current density of 2 mA cm-2 after 120 cycles. To illustrate the generality of the synthesis strategy, we also obtained MoO3-POM//CC via a similar method. By using V6O13-POM//CC and MoO3-POM//CC as the anode materials, LIBs exhibited high reversible areal specific capacity and excellent cycling stability which are expected to achieve commercial applications.(c) 2022 Elsevier B.V. All rights reserved.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据