Effect of solvent on the emulsion and morphology of polyfluorene films: all-atom molecular dynamics approach.

The morphology of conjugated polymer thin films deposited by the resonant infrared matrix-assisted pulsed laser evaporation (RIR-MAPLE) process is related to the emulsion characteristics. However, a fundamental understanding of how and why the emulsion characteristics control the film properties and device performance is yet unclear. We performed all-atom molecular dynamics simulations of emulsions containing a mixture of polyfluorene (PFO) polymer, various primary solvents, secondary solvent, and water. The emulsion properties were then examined as a function of variable primary solvent and correlated with the morphology of deposited PFO thin films. The examination of the explicit interactions between all components of the emulsion indicated that using a primary solvent with a lower solubility-in-water and a higher non-bonded interaction energy ratio, between the solvent, polymer, and water in the emulsion recipe, produced the best result with smoother and denser films. Additionally, our simulation results are consistent with the AFM experimental results, indicating that interactions driven by trichlorobenzene (TCB) primary solvent within the emulsion are responsible for high-quality, smooth, and continuous thin film surfaces. Overall, this study can support the choice of a suitable primary solvent and provides the computational framework for predictions of new recipes for polymeric emulsion systems.

Correlation of Emulsion Chemistry, Film Morphology, and Device Performance in Polyfluorene LEDs Deposited by RIR-MAPLE.

Thin films of polyfluorene (PFO) were deposited using emulsion-based resonant infrared, matrix-assisted pulsed laser evaporation (RIR-MAPLE). Here, it is shown that properly selected surfactant chemistry in the emulsion can increase crystalline ß phase (ß-PFO) content and consequently improve the color purity of light emission. To determine the impact of surfactant on the device performance of resulting films, blue light-emitting diodes (LEDs) with PFO as an active region were fabricated and compared. Molecular dynamics (MD) simulations were used to explain the physical and chemical changes in the emulsion properties as a function of the surfactant. The results indicate that the experimental film morphology and device performance are highly correlated to the emulsion droplet micelle structure and interaction energy among PFO, primary solvent, and water obtained from MD simulations. While the champion device performance was lower than other reported devices (luminous flux ∼0.0206 lm, brightness ∼725.58 cd/m2, luminous efficacy ∼0.0548 lm/W, and luminous efficiency ∼0.174 cd/A), deep blue emission with good color purity (CIE chromaticity diagram coordinate of (0.177,0.141)) was achieved for low operating voltages around 3 V. Furthermore, a much higher ß-phase content of 21% was achieved in annealed films (without the pinholes typically found in ß-PFO deposited by other techniques) by using sodium dodecyl sulfate (SDS) as the surfactant.

Emulsion-Based RIR-MAPLE Deposition of Conjugated Polymers: Primary Solvent Effect and Its Implications on Organic Solar Cell Performance.

Emulsion-based, resonant infrared matrix-assisted pulsed laser evaporation (RIR-MAPLE) has been demonstrated as an alternative technique to deposit conjugated polymer films for photovoltaic applications; yet, a fundamental understanding of how the emulsion target characteristics translate into film properties and solar cell performance is unclear. Such understanding is crucial to enable the rational improvement of organic solar cell (OSC) efficiency and to realize the expected advantages of emulsion-based RIR-MAPLE for OSC fabrication. In this paper, the effect of the primary solvent used in the emulsion target is studied, both experimentally and theoretically, and it is found to determine the conjugated polymer cluster size in the emulsion as well as surface roughness and internal morphology of resulting polymer films. By using a primary solvent with low solubility-in-water and low vapor pressure, the surface roughness of deposited P3HT and PCPDTBT polymer films was reduced to 10 nm, and the efficiency of P3HT:PC61BM OSCs was increased to 3.2% (∼100 times higher compared to the first MAPLE OSC demonstration [ Caricato , A. P. ; Appl. Phys. Lett. 2012 , 100 , 073306 ]). This work unveils the mechanism of polymer film formation using emulsion-based RIR-MAPLE and provides insight and direction to determine the best ways to take advantage of the emulsion target approach to control film properties for different applications.

Antimicrobial and bacteria-releasing multifunctional surfaces: oligo (p-phenylene-ethynylene)/poly (N-isopropylacrylamide) films deposited by RIR-MAPLE.

Antimicrobial oligo (p-phenylene-ethynylene) (OPE) films have previously been demonstrated to show effective ultraviolet A (UVA) light-induced biocidal activity; however, a serious problem arises from the accumulation of dead bacteria and debris on the films that limits their effectiveness and application. In this work, we address this challenge by incorporating thermally-responsive poly (N-isopropylacrylamide) (PNIPAAm), which provides on-demand bacteria-releasing functionality. Multifunctional surfaces comprising blended films of OPE and PNIPAAm were deposited on substrates by resonant infrared, matrix-assisted pulsed laser evaporation (RIR-MAPLE) using a sequential co-deposition mode. In this way, RIR-MAPLE enabled the deposition of multifunctional films with surface properties and film functionality that can be tailored, precisely and systematically, by controlling the chemical composition of the deposited film. The surface properties of these films were characterized by UV-visible (UV-vis) absorbance spectroscopy, X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), and water contact angle measurements. The interactions between bacteria and the deposited films were tested using two model bacteria: Escherichia coli K12 (Gram-negative) and Staphylococcus epidermidis (Gram-positive). The antimicrobial and bacteria-release properties of the blended films were controlled by varying the OPE/PNIPAAm ratio in the RIR-MAPLE emulsion target, providing an easy way to optimize the multifunctional surface. The OPE/PNIPAAm blended films with optimized composition killed a majority of attached E. coli bacteria at 37 °C and under UVA exposure, and the dead bacteria were then removed from the films simply by rinsing with water at 25 °C.

Antimicrobial oligo(p-phenylene-ethynylene) film deposited by resonant infrared matrix-assisted pulsed laser evaporation.

The antimicrobial oligomer, oligo(p-phenylene-ethynylene) (OPE), was deposited as thin films by resonant infrared matrix-assisted pulsed laser evaporation (RIR-MAPLE) on solid substrates and exhibited light-induced biocidal activity. The biocidal activity of OPE thin films deposited by spin-coating and drop-casting was also investigated for comparison. Enhanced bacterial attachment and biocidal efficiency of the film deposited by RIR-MAPLE were observed and attributed to nanoscale surface topography of the thin film.

RIR-MAPLE deposition of multifunctional films combining biocidal and fouling release properties.

Multifunctional films with both antimicrobial activity and fouling-release ability based on a biocidal quaternary ammonium salt (QAS) and thermo-responsive poly(N-isopropylacrylamide) (PNIPAAm) were deposited on substrates using resonant infrared, matrix-assisted pulsed laser evaporation (RIR-MAPLE). The surface properties of these films were characterized by X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FTIR) spectroscopy, atomic force microscopy (AFM), and water contact angle measurements. The biocidal and release properties of the films were tested against Escherichia coli K12 and Staphylococcus epidermidis. At 37 °C, the deposited film facilitated bacterial attachment and killed a majority of attached bacteria. Decrease of the temperature to 25 °C promoted the hydration and at least partial dissolution of PNIPAAm, leading to bacterial detachment from the film. To enhance the retention of PNIPAAm on the substrate, a small amount of (3-aminopropyl)triethoxysilane (APTES) was incorporated as a stabilizer, resulting in a ternary film with biocidal activity and bacterial-release ability after several attach-kill-release cycles. The simplicity and universality of RIR-MAPLE to form films on a wide range of substrata make it a promising technique to deposit multifunctional films to actively mitigate bacterial biofouling.