材料科学
聚二甲基硅氧烷
表面改性
弹性体
纳米
纳米技术
模数
无定形固体
基质(水族馆)
弹性模量
曲面(拓扑)
纳米尺度
复合材料
化学工程
结晶学
地质学
工程类
几何学
数学
海洋学
化学
作者
Laura O. Williams,Emmanuel K. Nava,Anni Shi,Tyler J. Roberts,Chelsea S. Davis,Shelley A. Claridge
标识
DOI:10.1021/acsami.2c22646
摘要
Control over the surface chemistry of elastomers such as polydimethylsiloxane (PDMS) is important for many applications. However, achieving nanostructured chemical control on amorphous material interfaces below the length scale of substrate heterogeneity is not straightforward, and can be particularly difficult to decouple from changes in network structure that are required for certain applications (e.g., variation of elastic modulus for cell culture). We have recently reported a new method for precisely structured surface functionalization of PDMS and other soft materials, which displays high densities of ligands directly on the material surface, maximizing steric accessibility. Here, we systematically examine structural factors in the PDMS components (e.g., base and cross-linker structures) that impact efficiency of the interfacial reaction that leads to surface functionalization. Applying this understanding, we demonstrate routes for generating equivalent nanometer-scale functional patterns on PDMS with elastic moduli from 0.013 to 1.4 MPa, establishing a foundation for use in applications such as cell culture.
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