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通过大气压等离子体诱导接枝聚合进行无机表面纳米结构化

Inorganic surface nanostructuring by atmospheric pressure plasma-induced graft polymerization.

作者信息

Lewis Gregory T, Nowling Gregory R, Hicks Robert F, Cohen Yoram

机构信息

Department of Chemical and Biomolecular Engineering, University of California, Los Angeles, California 90095-1592, USA.

出版信息

Langmuir. 2007 Oct 9;23(21):10756-64. doi: 10.1021/la700577p. Epub 2007 Sep 8.

Abstract

Surface graft polymerization of 1-vinyl-2-pyrrolidone onto a silicon surface was accomplished by atmospheric pressure (AP) hydrogen plasma surface activation followed by graft polymerization in both N-methyl-2-pyrrolidone (NMP) and in an NMP/water solvent mixture. The formation of initiation sites was controlled by the plasma exposure period, radio frequency (rf) power, and adsorbed surface water. The surface number density of active sites was critically dependent on the presence of adsorbed surface water with a maximum observed at approximately a monolayer surface water coverage. The surface topology and morphology of the grafted polymer layer depended on the solvent mixture composition, initial monomer concentration, reaction temperature, and reaction time. Grafted polymer surfaces prepared in pure NMP resulted in a polymer feature spacing of as low as 5-10 nm (average feature diameter of about 17 nm), an rms surface roughness range of 0.18-0.72 nm, and a maximum grafted polymer layer thickness of 5.5 nm. Graft polymerization in an NMP/water solvent mixture, however, resulted in polymer feature sizes that increased up to a maximum average feature diameter of about 90 nm at [NMP] = 60% (v/v) with polymer feature spacing in the range of 10-50 nm. The surface topology of the polymer-modified silicon surfaces grafted in an NMP/water solvent mixture exhibited a bimodal feature height distribution. In constrast, graft polymerization in pure NMP resulted in a narrow feature height distribution of smaller-diameter surface features with smaller surface spacing. The results demonstrated that, with the present approach, the topology of the grafted polymer surface was tunable by adjusting the NMP/water ratio. The present surface graft polymerization method, which is carried out under AP conditions, is particularly advantageous for polymer surface structuring via radical polymerization and can, in principle, be scaled to large surfaces.

摘要

通过常压(AP)氢等离子体表面活化,随后在N-甲基-2-吡咯烷酮(NMP)以及NMP/水溶剂混合物中进行接枝聚合,实现了1-乙烯基-2-吡咯烷酮在硅表面的表面接枝聚合。引发位点的形成受等离子体暴露时间、射频(rf)功率和吸附的表面水控制。活性位点的表面数密度严重依赖于吸附的表面水的存在,在大约单层表面水覆盖时观察到最大值。接枝聚合物层的表面拓扑结构和形态取决于溶剂混合物组成、初始单体浓度、反应温度和反应时间。在纯NMP中制备的接枝聚合物表面导致聚合物特征间距低至5-10 nm(平均特征直径约为17 nm),均方根表面粗糙度范围为0.18-0.72 nm,最大接枝聚合物层厚度为5.5 nm。然而,在NMP/水溶剂混合物中进行接枝聚合,在[NMP]=60%(v/v)时,聚合物特征尺寸增大,最大平均特征直径约为90 nm,聚合物特征间距在10-50 nm范围内。在NMP/水溶剂混合物中接枝的聚合物改性硅表面的表面拓扑结构呈现双峰特征高度分布。相比之下,在纯NMP中进行接枝聚合导致较小直径表面特征的窄特征高度分布和较小的表面间距。结果表明,采用本方法,通过调节NMP/水比例可调节接枝聚合物表面的拓扑结构。本表面接枝聚合方法在常压条件下进行,对于通过自由基聚合进行聚合物表面结构化特别有利,原则上可扩展到大面积表面。

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