材料科学
纳米颗粒
共聚物
原子转移自由基聚合
模板
纳米技术
聚合物
光掩模
聚合
纳米结构
基质(水族馆)
抵抗
复合材料
海洋学
地质学
图层(电子)
作者
Yijie Liu,Jianping Peng,Yutong Chen,Mei Liu,Wen Tang,Zihao Guo,Kan Yue
出处
期刊:Giant
[Elsevier BV]
日期:2021-09-02
卷期号:8: 100076-100076
被引量:49
标识
DOI:10.1016/j.giant.2021.100076
摘要
Precisely controlling the spatial organization of inorganic nanoparticles is essential for many applications, such as sensing, catalytic, and optical/electronic systems. Here, we describe a general and robust strategy to fabricate arbitrary quasi-two-dimensional (quasi-2D) nanoparticle assembly structures with tunable size and thickness on a substrate by using block copolymer brushes as the templates. To achieve this, patterned amphiphilic block copolymer brushes were first grown via light-mediated surface-initiated atom transfer radical polymerization. The hydrophilic polymer blocks could interact and enrich the inorganic precursors, and thus accelerate the in-situ growth of nanoparticles within the patterned hydrophilic polymer domains. In our method, the block copolymer template could strictly limit the vertical growth of quasi-2D nanoparticle assemblies to achieve thickness control in the nanometer scale. By changing the design of the photomask and experimental conditions for the light-mediated polymerization, quasi-2D inorganic nanoparticle assemblies with controllable shape and dimension can be feasibly obtained. Moreover, this method is also generally applicable to prepare various patterned inorganic nanoparticle assemblies with different compositions.
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