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用SiO@PNiPAm核壳颗粒进行表面图案化

Surface Patterning with SiO@PNiPAm Core-Shell Particles.

作者信息

Tang Jo Sing Julia, Bader Romina Sigrid, Goerlitzer Eric S A, Wendisch Jan Fedja, Bourret Gilles Remi, Rey Marcel, Vogel Nicolas

机构信息

Institute of Particle Technology, Friedrich-Alexander University Erlangen-Nürnberg, Cauerstrasse 4, 91058 Erlangen, Germany.

Department of Chemistry and Physics of Materials, University of Salzburg, Jakob Haringer Strasse 2A, A-5020 Salzburg, Austria.

出版信息

ACS Omega. 2018 Sep 30;3(9):12089-12098. doi: 10.1021/acsomega.8b01985. Epub 2018 Sep 27.

Abstract

Colloidal lithography is a cost-efficient method to produce large-scale nanostructured arrays on surfaces. Typically, colloidal particles are assembled into hexagonal close-packed monolayers at liquid interfaces and deposited onto a solid substrate. Many applications, however, require non close-packed monolayers, which are more difficult to fabricate. Preassembly at the oil/water interface provides non close-packed colloidal assemblies but these are difficult to transfer to a solid substrate without compromising the ordering due to capillary forces acting upon drying. Alternatively, plasma etching can reduce a close-packed monolayer into a non close-packed arrangement, however, with limited interparticle distance and compromised particle shape. Here, we present a simple alternative approach toward non close-packed colloidal monolayers with tailored interparticle distance, high order, and retained spherical particle shape. We preassemble poly(-isopropylacrylamide)-silica (SiO@PNiPAm) core-shell particles at the air/water interface, transfer the interfacial spacer to a solid substrate, and use the polymer shell as a sacrificial layer that can be thermally removed to leave a non close-packed silica monolayer. The shell thickness, cross-linking density, and the phase behavior upon compression of these complex particles at the air/water interface provide parameters to precisely control the lattice spacing in these surface nanostructures. We achieve hexagonal non close-packed arrays of silica spheres with interparticle distances between 400 and 1280 nm, up to 8 times their diameter. The retained spherical shape is advantageous for surface nanostructuring, which we demonstrate by the fabrication of gold nanocrescent arrays via colloidal lithography and silicon nanopillar arrays via metal-assisted chemical etching.

摘要

胶体光刻是一种在表面制备大规模纳米结构阵列的经济高效方法。通常,胶体粒子在液体界面组装成六方密堆积单层,然后沉积到固体基板上。然而,许多应用需要非密堆积单层,而这种单层更难制备。在油/水界面进行预组装可提供非密堆积胶体组件,但由于干燥时的毛细作用力,这些组件在转移到固体基板时难以不影响其有序性。另外,等离子体蚀刻可将密堆积单层转变为非密堆积排列,然而,粒子间距离有限且粒子形状会受到影响。在此,我们提出一种简单的替代方法来制备具有定制粒子间距离、高阶性且保留球形粒子形状的非密堆积胶体单层。我们在空气/水界面预组装聚(N-异丙基丙烯酰胺)-二氧化硅(SiO@PNiPAm)核壳粒子,将界面间隔层转移到固体基板上,并将聚合物壳用作牺牲层,可通过热去除该层以留下非密堆积二氧化硅单层。这些复合粒子在空气/水界面压缩时的壳厚度、交联密度和相行为提供了精确控制这些表面纳米结构晶格间距的参数。我们实现了二氧化硅球的六方非密堆积阵列,粒子间距离在400至1280纳米之间,可达其直径的8倍。保留的球形形状有利于表面纳米结构化,我们通过胶体光刻制备金纳米新月阵列以及通过金属辅助化学蚀刻制备硅纳米柱阵列来证明这一点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9094/6646223/93d8cab2ebc6/ao-2018-019857_0007.jpg

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