Zelzer Mischa, Scurr David, Abdullah Badr, Urquhart Andrew J, Gadegaard Nikolaj, Bradley James W, Alexander Morgan R
Laboratory of Biophysics and Surface Analysis, School of Pharmacy, The University of Nottingham, University Park, Nottingham, NG7 2RD, UK.
J Phys Chem B. 2009 Jun 25;113(25):8487-94. doi: 10.1021/jp902137y.
Plasma species that form plasma polymer deposits readily penetrate through small openings and are therefore well suited to coat the interior of porous objects. Here, we show how the size of the cross section of square channels influences the penetration of active species from a hexane plasma and how it affects the formation of surface chemical gradients in the interior of these model pores. WCA mapping and ToF-SIMS imaging are used to visualize the plasma polymer deposit in the interior of the model pores and demonstrate that a strong dependence of the wettability gradient profile only exists up to a channel cross section of about 1 mm. XPS data allow us to calculate a deposition rate of plasma polymerized hexane (ppHex) at discrete positions on the surface and show that the deposition rate of ppHex is reduced by the presence of the mask up to a distance of 16 mm in advance of the channel opening. A strong dependence of the ppHex deposition rate on the cross-section of the channels is found within the first 2 mm in front of the pore opening. An estimation of the sheath thickness suggests that this effect can be attributed to the plasma sheath that perturbs the plasma in front of the pores. Plasma mass spectrometry allows us to identify the nature of the plasma species penetrating from the plasma through the pores and shows that no negatively charged ions are able to penetrate through the small channels. Neutral and positively charged species penetrate several millimeters down the channels and both species are therefore likely to contribute to the formation of the deposit on the sample. In addition, the formation of positively charged higher molecular mass hexane fragments is observed in the gas phase, demonstrating the likelihood of neutral-positive reactions in the plasma.
容易形成等离子体聚合物沉积物的等离子体物种能够轻易穿透小孔,因此非常适合涂覆多孔物体的内部。在此,我们展示了方形通道横截面的尺寸如何影响己烷等离子体中活性物种的渗透,以及它如何影响这些模型孔内部表面化学梯度的形成。水接触角(WCA)映射和飞行时间二次离子质谱(ToF-SIMS)成像用于可视化模型孔内部的等离子体聚合物沉积物,并证明仅在通道横截面约为1毫米之前,润湿性梯度分布存在强烈依赖性。X射线光电子能谱(XPS)数据使我们能够计算等离子体聚合己烷(ppHex)在表面离散位置的沉积速率,并表明在通道开口前方16毫米的距离内,掩膜的存在会降低ppHex的沉积速率。在孔开口前方的前2毫米内,发现ppHex沉积速率对通道横截面有强烈依赖性。鞘层厚度的估计表明,这种效应可归因于扰动孔前方等离子体的等离子体鞘层。等离子体质谱使我们能够识别从等离子体穿过孔渗透的等离子体物种的性质,并表明没有带负电荷的离子能够穿透小通道。中性和带正电荷的物种会沿着通道向下渗透几毫米,因此这两种物种都可能有助于在样品上形成沉积物。此外,在气相中观察到带正电荷的高分子量己烷碎片的形成,这表明等离子体中存在中性-正反应的可能性。