Cho Szu-Hao, Lewis Elizabeth A, Zacharia Nicole S, Vogt Bryan D
Department of Polymer Engineering, University of Akron, Akron, OH 44325, USA.
Department of Chemical Engineering, The Pennsylvania State University, University Park, PA 16802, USA.
Soft Matter. 2021 Dec 1;17(46):10527-10535. doi: 10.1039/d1sm01246k.
Layer-by-layer (LbL) assembly facilitates controlled coatings on a variety of surfaces with the ability to manipulate the composition through the thickness by selection of the complementary pairs. However, the characterization of these composition profiles tends to be destructive and requires significant compositional differences that can limit their utility. Here, we demonstrate the ability to non-destructively quantify the depth dependence of the allyl content associated with the selective incorporation of poly(sodium acrylate--allylacrylamide) (84 : 16 mol : mol) (allyl-PAA) in LbL films based on the assembly of poly(diallyldimethylammonium chloride) (PDAC)/poly(acrylic acid) (PAA) and PDAC/allyl-PAA. Although the atomic composition of the film is not dramatically influenced by the change between PAA and allyl-PAA, the absorption in the IR near 1645 cm by the allyl group provides sufficient optical contrast to distinguish the LbL components with spectroscopic ellipsometry. The use of IR spectroscopic ellipsometry can determine the thickness of layers that contain allyl-PAA and also gradients that develop due to re-arrangements during the LbL process. With multiple films fabricated simultaneously, the location of the gradient between the 1st and 2nd series of multilayers (, first PDAC/PAA bilayers and then PDAC/allyl-PAA bilayers) can be readily assessed. The results from a variety of different multilayer architectures indicate that the gradient is located within the thickness expected for the 1st deposited bilayer stack (PDAC/PAA or PDAC/allyl-PAA). These results are indicative of a dynamic dissolution-deposition process (in- and out- diffusion) during the fabrication of these LbL films. These results provide additional evidence into the mechanisms for exponential growth in LbL assemblies. The ability to quantify a gradient with the low contrast system examined indicates that spectroscopic IR ellipsometry should be able to non-destructively determine compositional gradients for most polymer films where such gradients exist.
逐层(LbL)组装有助于在各种表面上形成可控涂层,通过选择互补对能够在整个厚度范围内操纵组成。然而,这些组成分布的表征往往具有破坏性,并且需要显著的组成差异,这可能会限制它们的实用性。在此,我们展示了基于聚二烯丙基二甲基氯化铵(PDAC)/聚丙烯酸(PAA)和PDAC/聚(丙烯酸钠 - 烯丙基丙烯酰胺)(84 : 16摩尔 : 摩尔)(烯丙基 - PAA)的组装,无损量化LbL薄膜中与烯丙基 - PAA选择性掺入相关的烯丙基含量的深度依赖性的能力。尽管薄膜的原子组成不会因PAA和烯丙基 - PAA之间的变化而受到显著影响,但烯丙基在1645 cm附近的红外吸收提供了足够的光学对比度,以便通过光谱椭偏仪区分LbL组件。使用红外光谱椭偏仪可以确定包含烯丙基 - PAA的层的厚度以及由于LbL过程中的重新排列而形成的梯度。通过同时制备多个薄膜,可以很容易地评估第一系列和第二系列多层膜(首先是PDAC/PAA双层,然后是PDAC/烯丙基 - PAA双层)之间梯度的位置。来自各种不同多层结构的结果表明,该梯度位于第一沉积双层堆叠(PDAC/PAA或PDAC/烯丙基 - PAA)预期的厚度范围内。这些结果表明在这些LbL薄膜制备过程中存在动态溶解 - 沉积过程(内扩散和外扩散)。这些结果为LbL组装中指数增长的机制提供了额外的证据。在所研究的低对比度系统中量化梯度的能力表明,光谱红外椭偏仪应该能够无损地确定大多数存在此类梯度的聚合物薄膜的组成梯度。