Lin Jing, Daboss Sven, Blaimer Dominik, Kranz Christine
Institute of Analytical and Bioanalytical Chemistry, Ulm University, Albert-Einstein-Allee 11, 89081 Ulm, Germany.
Nanomaterials (Basel). 2019 Feb 11;9(2):242. doi: 10.3390/nano9020242.
Polydopamine (PDA) films are interesting as smart functional materials, and their controlled structured formation plays a significant role in a wide range of applications ranging from cell adhesion to sensing and catalysis. A pulsed deposition technique is reported for micro-structuring polydopamine films using scanning electrochemical microscopy (SECM) in direct mode. Thereby, precise and reproducible film thicknesses of the deposited spots could be achieved ranging from 5.9 +/- 0.48 nm (1 pulse cycle) to 75.4 nm +/- 2.5 nm for 90 pulse cycles. The obtained morphology is different in comparison to films deposited via cyclic voltammetry or films formed by autooxidation showing a cracked blister-like structure for high pulse cycle numbers. The obtained polydopamine spots were investigated in respect to their electrochemical properties using SECM approach curves. Quantitative kinetic data in dependence of the film thickness, the substrate potential, and the used redox species were obtained.
聚多巴胺(PDA)薄膜作为智能功能材料备受关注,其可控的结构化形成在从细胞黏附到传感和催化等广泛应用中发挥着重要作用。本文报道了一种脉冲沉积技术,该技术利用扫描电化学显微镜(SECM)的直接模式对聚多巴胺薄膜进行微结构化处理。由此,可实现沉积斑点精确且可重复的膜厚,范围从5.9±0.48纳米(1个脉冲周期)到90个脉冲周期时的75.4纳米±2.5纳米。与通过循环伏安法沉积的薄膜或自氧化形成的薄膜相比,所得形态有所不同,对于高脉冲周期数,呈现出裂纹水泡状结构。利用SECM方法曲线研究了所得聚多巴胺斑点的电化学性质。获得了依赖于膜厚、基底电位和所用氧化还原物种的定量动力学数据。