共聚物
材料科学
纳米尺度
模板
聚苯乙烯
聚合物
甲基丙烯酸甲酯
纳米技术
纳米结构
甲基丙烯酸酯
化学工程
高分子化学
复合材料
工程类
作者
Qing Peng,Yu‐Chih Tseng,Seth B. Darling,Jeffrey W. Elam
出处
期刊:ACS Nano
[American Chemical Society]
日期:2011-05-05
卷期号:5 (6): 4600-4606
被引量:271
摘要
Sequential infiltration synthesis (SIS), combining stepwise molecular assembly reactions with self-assembled block copolymer (BCP) substrates, provides a new strategy to pattern nanoscopic materials in a controllable way. The selective reaction of a metal precursor with one of the pristine BCP domains is the key step in the SIS process. Here we present a straightforward strategy to selectively modify self-assembled polystyrene-block-poly(methyl methacrylate) (PS-b-PMMA) BCP thin films to enable the SIS of a variety of materials including SiO(2), ZnO, and W. The selective and controlled interaction of trimethyl aluminum with carbonyl groups in the PMMA polymer domains generates Al-CH(3)/Al-OH sites inside the BCP scaffold which can seed the subsequent growth of a diverse range of materials without requiring complex block copolymer design and synthesis.
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