多金属氧酸盐
阳极
超晶格
材料科学
离子
钠
电池(电)
无机化学
纳米技术
钠离子电池
化学工程
化学
功率(物理)
电极
光电子学
物理化学
有机化学
物理
法拉第效率
冶金
催化作用
量子力学
工程类
作者
Yunping Wu,Sheng Chen,Caihe Bai,Shuwen Niu,Wei Wei
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-12-05
卷期号:16 (12): 21431-21442
被引量:7
标识
DOI:10.1021/acsnano.2c09796
摘要
The use of polyoxometalate clusters (POMs) with multitudinous structures and surface properties as building blocks has sparked the development of cluster-assembled materials with many prospective applications. In comparison to classic molecules and assembly processes, control over the steric interactions and linkage of large POMs to achieve superlattices with multiple levels of organization remains a great challenge. This work presents a universal approach to modulate the spatial coordination behavior and configurations, and achieves a class of cluster superlattice architectures formed by linear alignment and two-dimensional arrangement of POM units. The formation mechanism is explained as a stepwise co-assembly pathway in which POMs can intervene and dictate a typical stripping-restacking combination mode with the lamellar mediator. These cluster superlattices with long-range POMs ordering impart distinct merits to their derivatives by sulfuration, for which we demonstrate the substantially promoted power and cycling life of these POM derivatives applied as sodium-ion battery anodes.
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