Fabrication Of Polymer Thin Films Research Articles

Assembly of Close-Packed Ferroelectric Polymer Nanowires via Interface-Epitaxy with ReS2.

The flexible, transparent, and low-weight nature of ferroelectric polymers makes them promising for wearable electronic and optical applications. To reach the full potential of the polarization-enabled device functionalities, large-scale fabrication of polymer thin films with well-controlled polar directions is called for, which remains a central challenge. The widely exploited Langmuir-Blodgett, spin-coating, and electrospinning methods only yield polymorphous or polycrystalline films, where the net polarization is compromised. Here, an easily scalable approach is reported to achieve poly(vinylidene fluoride-trifluoroethylene) P(VDF-TrFE) thin films composed of close-packed crystalline nanowires via interface-epitaxy with 1T'-ReS2 . Upon controlled thermal treatment, uniform P(VDF-TrFE) films restructure into about 10 and 35 nm-wide (010)-oriented nanowires that are crystallographically aligned with the underlying ReS2 , as revealed by high-resolution transmission electron microscopy. Piezoresponse force microscopy studies confirm the out-of-plane polar axis of the nanowire films and reveal coercive voltages as low as 0.1 V. Reversing the polarization can induce a conductance switching ratio of >108 in bilayer ReS2 , over six orders of magnitude higher than that achieved by an untreated polymer gate. This study points to a cost-effective route to large-scale processing of high-performance ferroelectric polymer thin films for flexible energy-efficient nanoelectronics.

Functional polymer thin films designed for antifouling materials and biosensors

AbstractPolymer thin films offer a versatile and ubiquitous platform for a wide variety of real-world applications in biomedicine, nanotechnology, catalysis, photovoltaic devices, and energy conversion and storage. Depending on the chemical composition of the polymers and the associated microenvironment, the physicochemical properties (biocompatibility, stability, wettability, adhesion, morphology, surface free energy, and others) of polymer films can be tuned for a specific application through precisely controlled surface synthesis and the incorporation of desirable and responsive functional groups. In this short review, we first summarise the methods most commonly used for the fabrication of polymer thin films. Then we discuss how these polymer thin films can be used in a selection of biomedical applications in antifouling materials and biosensors. Some directions for the rational design of polymer thin films to achieve a specific function or application are also provided.

Matrix-assisted pulsed laser evaporation of chemoselective polymers

In this work, matrix-assisted pulsed laser evaporation was applied to achieve gentle deposition of polymer thin films onto surface acoustic wave resonators. Polyepichlorhydrin, polyisobutylene and polyethylenimine were deposited both onto rigid substrates e.g. Si wafers as well as surface acoustic wave devices using a Nd-YAG laser (266 nm, 355 nm, 10 Hz repetition rate). Morphological investigations (atomic force microscopy and optical microscopy) reveal continuous deposited polymer thin films, and in the case of polyethylenimine a very low surface roughness of 1.2 nm (measured on a 40×40 μm2 area). It was found that only for a narrow range of laser fluences (i.e. 0.1–0.3 J/cm2 in the case of polyisobutylene) the chemical structure of the deposited polymer thin layers resembles to the native polymer. In addition, in the case of polyisobutylene it was shown that the irradiation at 355-nm wavelength produces deviations in the chemical structure of the deposited polymer, as compared to its bulk structure. Following the morphological and structural characterization, only a set of well established conditions was used for polymer deposition on the sensor structures. The surface acoustic wave resonators have been tested using the Network Analyzer before and after polymer deposition. The polymer coated surface acoustic wave resonator responses have been measured upon exposure to various concentrations of dimethylmethylphosphonate analyte. All sensors coated with different polymer layers (polyethylenimine, polyisobutylene, and polyepichlorhydrin) show a clear response to the dimethylmethylphosphonate vapor. The strongest signal is obtained for polyisobutylene, followed by polyethylenimine and polyepichlorhydrin. The results obtained indicate that matrix-assisted pulsed laser evaporation is potentially useful for the fabrication of polymer thin films to be used in applications including microsensor industry.

Characterization of polymer thin films obtained by pulsed laser deposition

The development of laser techniques for the deposition of polymer and biomaterial thin films on solid surfaces in a controlled manner has attracted great attention during the last few years. Here we report the deposition of thin polymer films, namely Polyepichlorhydrin by pulsed laser deposition. Polyepichlorhydrin polymer was deposited on flat substrate (i.e. silicon) using an NdYAG laser (266 nm, 5 ns pulse duration and 10 Hz repetition rate). The obtained thin films have been characterized by atomic force microscopy, scanning electron microscopy, Fourier transform infrared spectroscopy and spectroscopic ellipsometry. It was found that for laser fluences up to 1.5 J/cm 2 the chemical structure of the deposited polyepichlorhydrin polymer thin layers resembles to the native polymer, whilst by increasing the laser fluence above 1.5 J/cm 2 the polyepichlorohydrin films present deviations from the bulk polymer. Morphological investigations (atomic force microscopy and scanning electron microscopy) reveal continuous polyepichlorhydrin thin films for a relatively narrow range of fluences (1–1.5 J/cm 2). The wavelength dependence of the refractive index and extinction coefficient was determined by ellipsometry studies which lead to new insights about the material. The obtained results indicate that pulsed laser deposition method is potentially useful for the fabrication of polymer thin films to be used in applications including electronics, microsensor or bioengineering industries.

Fabrication of polymer thin films with in-depth dye-dispersed structures by the vacuum spray method

We report the fabrication of polymer thin films with “in-depth” dye-dispersed structures using a vacuum spray method. Copper (II) 2,9,16,23-tetra- tert-butyl-29 H,31 H-phthalocyanine [( t-Bu) 4CuPc] and polycarbonate in chloroform solution were sprayed onto the substrate. The ( t-Bu) 4CuPc distribution was controlled precisely during thin film growth by varying its concentration in the solution. Uniform, bilayer, and gradient structures of ( t-Bu) 4CuPc dispersed in thin films were confirmed by high-angle annular dark field imaging on scanning transmission electron microscopy. The vacuum spray method has several advantages compared to the casting method, such as smaller dispersed dye-aggregates and lack of cavities due to air bubbles.

One-step fabrication of polymer thin films with lithographic bas-relief micro-pattern and self-organized micro-porous structure

One-step fabrication of polymer thin films with lithographic bas-relief micro-pattern and self-organized micro-porous structure

Fabrication of Polymer Thin Films and Arrays with Spatial and Topographical Controls

Fabrication of Polymer Thin Films and Arrays with Spatial and Topographical Controls