Poly Acrylic Acid Research Articles

Enteric-coated cerium dioxide nanoparticles for effective inflammatory bowel disease treatment by regulating the redox balance and gut microbiome

Reactive oxygen species (ROS) play crucial roles in the pathogenesis of inflammatory bowel disease (IBD) by disrupting the mucosal barrier and subsequently leading to the dysregulation of the gut microbiome. Therefore, ROS scavengers present a promising and comprehensive strategy for the effective IBD treatment. In the current work, we explored the therapeutic potential of cerium dioxide (CeO2) nano-enzyme, which is well-known for their potent antioxidant properties and capability to mimic natural antioxidant enzymes in the regulation of oxidative stress. We developed a novel enteric-coated nanomedicine (CeO2@S100) aiming at improving the oral delivery efficacy of CeO2 in the complex gastrointestinal environment. CeO2@S100 is composed of a CeO2 nanoparticle core and a protective polyacrylic acid resin shell (Eudragit S100), ensuring targeted delivery of the core specifically at inflamed intestinal sites due to the negative surface charge. In vivo experiments revealed CeO2@S100 significantly alleviates the IBD by balancing oxidative stress and regulating gut microbiota in a dextran sulfate sodium-induced mouse colitis model. The uncomplicated synthesis of CeO2@S100 highlights its promise for clinical use, presenting an effective and safe approach to managing IBD.

Exploring the Origins of Association of Poly(acrylic acid) Polyelectrolyte with Lysozyme in Aqueous Environment through Molecular Simulations and Experiments.

This study provides a detailed picture of how a protein (lysozyme) complexes with a poly(acrylic acid) polyelectrolyte (PAA) in water at the atomic level using a combination of all-atom molecular dynamics simulations and experiments. The effect of PAA and temperature on the protein's structure is explored. The simulations reveal that a lysozyme's structure is relatively stable except from local conformational changes induced by the presence of PAA and temperature increase. The effect of a specific thermal treatment on the complexation process is investigated, revealing both structural and energetic changes. Certain types of secondary structures (i.e., α-helix) are found to undergo a partially irreversible shift upon thermal treatment, which aligns qualitatively with experimental observations. This uncovers the origins of thermally induced aggregation of lysozyme with PAA and points to new PAA/lysozyme bonds that are formed and potentially enhance the stability in the complexes. As the temperature changes, distinct amino acids are found to exhibit the closest proximity to PAA, resulting into different PAA/lysozyme interactions; consequently, a different complexation pathway is followed. Energy calculations reveal the dominant role of electrostatic interactions. This detailed information can be useful for designing new biopolymer/protein materials and understanding protein function under immobilization of polyelectrolytes and upon mild denaturation processes.

Self-healing, piezoresistive and temperature responsive behaviour of chitosan/polyacrylic acid dynamic hydrogels

Flexible electronics have introduced new challenges for efficient human–machine interactions. Hydrogels have emerged as prominent materials for electronic wearable applications due to their exceptional mechanical deformability and lightweight characteristics combined in some cases with conductive properties, and softness. Additionally, bio-interphases require multisensory response to stress, strain, temperature, and self-healing capacity. To mimic these properties, this work developed interpenetrated hydrogel networks composed of chitosan (CHI) and polyacrylic acid (PAA), combined with Fe (III) ions and varying amounts of NMBA (0–0.25 %), to achieve tailored conductivity (0.8–2.5 mS/cm), self-healing, self-standing and mechanical properties (E = 11.7–110 Pa and fracture strain = 64.9–1923 %) suitable for strain sensor applications. The results revealed a significant influence of the restrictive effect on the mobility of uncrosslinked chain segments, caused by Fe ions and NMBA, on the piezoresistance (GF 2.1–1.3) and self-healing capability of the gels.Interestingly, a transparent/turbid transition, driven by microphase separation that is characteristic of systems with high dynamic interactions, was encountered for the first time in these hydrogels. This transition was analyzed in relation to external temperature, water content, pH, and the influence of Fe ions and NMBA. The simultaneous sensitivity of these materials to temperature and pH, along with their piezoresistive and self-healing behaviour, can be highly valuable for multifunctional sensors in a wide range of applications.

Bulking up: the impact of polymer sterics on emulsion stability.

Encapsulation of hydrophobic active ingredients is critical for targeted drug delivery as water-insoluble drugs dominate the pharmaceutical marketplace. We previously demonstrated hexadecane-in-water emulsions stabilized with a pH-tunable polymer, poly(acrylic acid) (PAA), via a steric layer preventing particle aggregation. Using vibrational sum frequency scattering spectroscopy (VSFSS), here we probe the influence of steric hindrance on emulsion colloidal stability by tailoring the molecular weight of PAA and by adding an additional methyl group to the polymer backbone via poly(methacrylic acid) (PMAA) at pH 2, 4, and 6. At low polymer molecular weight (2 and 10 kDa), PAA adsorption is entropy driven and akin to surfactant-mediated stabilization. With 450 kDa PAA, the longer polymer chain emphasizes enthalpically favored polymer-oil interactions to initially coat the surface, and forms layers at increasing molecular weight (1000 and 4000 kDa). PMAA exhibits better oil-solubility than PAA at low concentrations but cannot accommodate the steric hindrance at higher concentrations leading to disorder. Finally, we connect our molecular-level understanding of PAA ordering with temperature-dependent dynamic light scattering experiments and observe that emulsions coated with PAA at pH 2 and 4 maintain colloidal stability from 0-90 °C, making PAA a promising polymer for hydrophobic drug delivery.

First biological response on polyAcrylic Acid UV-grafted PDMS surface: Towards medical application

Several biomedical devices and implants are made with Poly(dimethyl siloxane) (PDMS) or include it. Its biocompatibility, transparency, thermal stability and low cost are some of the properties that made PDMS suitable for biomedical applications. However, some properties such as its hydrophobic character can lead to complications owing to bacteria adhesion for instance. For breast implant, which is implanted for a long-time, an enhanced surface integration can be needed to avoid bacterial biofilm formation and degeneration. In microfluidic systems or for catheters, the biofouling phenomena must be avoided. Surface covalent functionalization with bioactive polymers is an attractive strategy to fight these issues. This study deals with poly(acrylic) acid UV-grafting on PDMS surfaces. After chemical and mechanical characterizations, this work has focused on biological response occurring on the functionalized material. The results show slowdown fibroblasts proliferation. Investigation around protein (BSA, fibronectin, fibrinogen) adhesion, made possible to approach surface mechanism understanding. FTIR and water contact angle analysis highlighted the different protein affinity towards surface. These results provide clues about protein orientation on the surface, in order to adapt the surface functionalization to target a specific application.

A Self-Healing and Sweat-Chargeable Hydrogel Electrolyte for All-in-One Flexible Supercapacitors.

Flexible solid-state supercapacitors (SCs) with hydrogel as an electrolyte and separator combine the advantages of wearability and energy storage and exhibit a broad application prospect in wearable energy textiles. However, irreversible electrolyte damage and unstable electrode-electrolyte interfaces during mechanical deformations remain bottlenecks in realizing truly wearable applications. Herein, poly(acrylic acid) (PAA)-Fe hydrogels were prepared through a simple thermal polymerization strategy. The dynamic reversible metal coordination bonds between Fe3+ and carboxylic acids confers the hydrogels with excellent self-healing properties. As expected, the prepared hydrogels exhibited superior mechanical strength (tensile stress of 45.80 kPa), ionic conductivity (0.076 S cm-1), and self-healing properties. Subsequently, the SCs were constructed using composite hydrogel electrodes (MnO2@CC embedded in the PAA-Fe hydrogels) as symmetrical electrodes (marked as MSCs). The reversible metal coordination bonds between composite hydrogel electrodes formed an ultrastable electrode/electrolyte interface in the all-in-one MSCs, thus revealing excellent mechanical durability. The all-in-one MSCs delivered a remarkable specific capacitance (30.98 F g-1 at 0.2 A g-1), excellent cyclic stability (87.24% after 5000 cycles), outstanding mechanical deformation stability, and impressive electrochemical output stability after self-healing (capacitance retention of 85.34% after five cycles of cutting/self-healing). It is noteworthy that the all-in-one MSCs employed NaCl as an electrolyte, which can be obtained from human sweat. As a proof of the self-charged concept, the all-in-one MSCs can be reused in sweat, whose capacitance was maintained at 90.05% of the initial state after three repetitions. This work is expected to shine light into the design of all-in-one and fabric-based SCs and the development of wearable energy textiles.

Impact of Binder Content and Type on the Electrochemical Performance of Silicon Anode Materials.

Binders are crucial for stabilizing the cycling performance of silicon (Si) materials by preventing Si particle pulverization during lithiation and delithiation. Poly(acrylic acid) (PAA) and carboxymethyl cellulose (CMC) are the two most studied binders for Si electrodes, with PAA being an elastic polymer and CMC a rigid polymer. Starting with the elastic PAA, in this work the impact of binder content on the cycling performance of Si electrodes is studied. It is found that regardless of Si particle size, there is an optimal binder content between 20 % and 25 % for the cycling stability of Si electrodes. On the other hand, the rigid CMC binder results in lower capacity and faster capacity fading for Si electrodes compared with the elastic PAA. AC-impedance analysis reveals that the lower capacity is due to higher grain boundary resistance (Rgb) in CMC-coated electrodes, leading to high charge-transfer resistance (Rct) and increased polarization. This high polarization triggers premature termination during the discharging process (i. e., the lithiation) of Li/Si cells, underutilizing the Si active material. Additionally, the rapid capacity fading of CMC-coated electrodes is attributed to the rigid binder's inferior ability to prevent Si particle pulverization.

In situ multilevel covalent crosslinking binder with high ionic conductivity for high-performance Si anodes

Silicon (Si) anode has emerged as a promising material for high-energy-density lithium-ion batteries (LIBs), thanks to its high theoretical capacity. However, the commercial application of Si anodes is hindered by inadequate cycling performance and poor interfacial stability, stemming from unfavorable stress conditions. In this study, a multiple crosslinking binder with high ionic conductivity is proposed combining high mechanical strength and high adhesion to current collector and active Si particles by coupling poly(acrylic acid), polyvinyl alcohol, and polyethylene glycol. The designed polymer binder not only efficiently dissipates the inner stress with its multiple crosslinked networks, but also establishes a fast lithium-ion conduction pathway to facilitate the electrode reaction kinetic. The resultant Si anode using the designed binder exhibits significantly improved cycling stability and superior rate performance. This work presents a straightforward yet highly effective method to alleviate the detrimental stress incurred by high-capacity anodes in high-energy LIBs.

A comprehensive investigation of cholesteric liquid crystal interpenetrating polymer networks for metal ion sensor technology

This study outlines the fabrication process of a photonic polymer cholesteric liquid crystal (PCLC) engineered for dynamic response to external stimuli. The methodological framework includes the precise templating of PCLC onto an interpenetrating polymer network (IPN) following selective UV crosslinking and the careful removal of nonreactive mesogens. The sensor component of the PCLC film is composed of poly(acrylic acid) hydrogel. A key aspect of the process involves the formation of micro-holes through acetone treatment to enhance sensitivity. Additionally, functionalization with potassium hydroxide (KOH) improves the detection of calcium ions (Ca2+) by disrupting hydrogen bonds and facilitating the formation of potassium carboxylate salt. Combining the inherent properties of PCLC with the hydrogel’s responsiveness to metal ions results in a sophisticated sensor designed to detect Ca2+ ions through the modulation of PCLC pitch, creating distinct transmission bands. The manuscript provides a detailed quantitative analysis of stimulus-induced changes in PCLC wavelength, using measured spectra to refine and optimize process conditions. The resulting PCLC sensor demonstrates exceptional sensitivity (9.30 nm/mM) within the 1–15 mM Ca2+ ion concentration range, along with excellent specificity. This cost-effective, user-friendly, and colorimetric sensing modality holds significant promise for various applications in analytical chemistry.

Nanoceria-induced variations in leaf anatomy and cell wall composition drive the increase in mesophyll conductance of salt-stressed cotton leaves

Nanomaterials as an emerging tool are being used to improve plant's net photosynthetic rate (AN) when suffering salt stress, but the underlying mechanisms remain unclear. To clarify this, a hydroponic experiment was conducted to study the effects of polyacrylic acid coated nanoceria (PNC) on the AN of salt-stressed cotton and related intrinsic mechanisms. Results showed that the PNC-induced AN enhancement of salt-stressed leaves was strongly facilitated by the mesophyll conductance to CO2 (gm). Further analysis showed that the PNC-induced improvement of gm was related to the increased chloroplast surface area exposed to intercellular airspaces, which was attribute to the increased mesophyll surface area exposed to intercellular airspaces and chloroplast number due to the increased K+ content and decreased reactive oxygen species level in salt-stressed leaves. Interestingly, our results also showed that PNC-induced variations in cell wall composition of salt-stressed cotton leaves strongly influenced gm, especially, hemicellulose and pectin. Moreover, the proportion of pectin in cell wall composition played a more important role in determining gm. Our study demonstrated for the first time that nanoceria, through alterations to anatomical traits and cell wall composition, drove gm enhancement, which ultimately increased AN of salt-stressed leaves.

A tough Janus poly(vinyl alcohol)-based hydrogel for wound closure and anti postoperative adhesion

Traditional adhesive hydrogels perform well in tissue adhesion but they fail to prevent postoperative tissue adhesion. To address this challenge, a biodegradable Janus adhesive hydrogel (J-AH) was designed and fabricated by the assembly of three different functional layers including anti-adhesive layer, reinforceable layer, and wet tissue adhesive layer. Each layer of J-AH serves a specific function: the top zwitterionic polymeric anti-adhesive layer shows superior resistance to cell/protein and tissue adhesion; the middle poly(vinyl alcohol)/tannic acid reinforceable matrix layer endows the hydrogel with good mechanical toughness of ∼2.700 MJ/m3; the bottom poly(acrylic acid)/polyethyleneimine adhesive layer imparts tough adhesion (∼382.93 J/m2 of interfacial toughness) to wet tissues. In the rat liver and femoral injury models, J-AH could firmly adhere to the bleeding tissues to seal the wounds and exhibit impressive hemostatic efficiency. Moreover, in the in vivo adhesion/anti-adhesion assay of J-AH between the defected cecum and peritoneal walls, the top anti-adhesive layer can effectively inhibit undesired postoperative abdominal adhesion and inflammatory reaction. Therefore, this research may present a new strategy for the design of advanced bio-absorbable Janus adhesive hydrogels with multi-functions including tissue adhesion, anti-postoperative adhesion and biodegradation. Statement of significanceDespite many adhesive hydrogels with tough tissue adhesion capability have been reported, their proclivity for undesired postoperative adhesion remains a serious problem. The postoperative adhesion may lead to major complications and even endanger the lives of patients. The injectable hydrogels can cover the irregular wound and suppress the formation of postoperative adhesion. However, due to the lack of adhesive properties with tissue, it is difficult for the hydrogels to maintain on the wound surface, resulting in poor anti-postoperative adhesion effect. Herein, we design a Janus adhesive hydrogel (J-AH). J-AH integrates together robust wet tissue adhesion and anti-postoperative adhesion. Therefore, this research may present a new strategy for the design of advanced bio-absorbable Janus adhesive hydrogels.

Intense pulsed light-induced millisecond selective heat treatment for high-performance silicon anodes

Silicon, which is gaining prominence as a potential anode material, exhibits long-term cycle stability issues owing to volume changes during cycling. This study presents a meticulously designed Si anode that employs intense pulsed light (IPL) technology to simultaneously reduce carbon additives and construct an effective carbon quantum dot (CQD)-derived binder system. IPL, as a light-material interaction technique, offers a novel approach for selective heat treatment with remarkably short processing durations on the order of milliseconds. By comprehensively considering the geometric structure, optical characteristics, and thermal properties of each electrode component, heat transfer bridge (HTB) materials are introduced to ensure a homogeneous depth-directional heat treatment and to minimize binder decomposition in the IPL process. By employing HTB materials, the binder can reach a controlled target temperature for the condensation reaction between poly (acrylic acid) and the CQDs. Simultaneously, higher heat generation in the conductive carbon than in the binder leads to selective additional carbon reduction. This unique approach provides selective heat treatment, which cannot be achieved using conventional methods, resulting in a Si anode with excellent cyclic stability and rate capability. The versatility of the IPL technology is further demonstrated by applying it to relatively inexpensive Si microparticles.

Enabling Si‐Dominant Anodes: Influence of Neutralization Degree of Polyacrylic Acid on Low‐Cost Micron‐Sized Silicon Anode in High‐Energy Li‐Ion Full Cell

AbstractMicron‐sized silicon is a promising low‐cost, abundant material to increase the energy density of lithium‐ion batteries. Nevertheless, significant volume change and therefore excessive solid electrolyte interphase (SEI) growth lead to fast capacity fading. In this work, polyacrylic acid (PAA) with different neutralization degrees is used for the fabrication of Si anodes for practical applications. The electrochemical performance in full pouch cells reveals that the increase in neutralization degree of PAA up to 70 % enhances the overall performance by improved electrode properties, higher first cycle efficiency (FCE up to 78.1 % at C/3) and better capacity retention (85.4 % after 150 cycles at 1 C) over cycling, while with even higher neutralization degrees (such as 80 %) the performance declines. Since proper mixing of the slurry is another important factor, we optimized the mixing procedure by increasing the solid content of the slurry, which has shown positive influence on the electrochemical performance and electrode properties. To summarize, this work shows full cell 1 C cycling until capacity retention of 85 % after 150 cycles with pure Si microparticle anodes for 70 % neutralized PAA as well as increased C‐rate performance up to 5 C. Post‐mortem, less degradation on electrode and particle level is observed.

Highly transparent inorganic superhydrophilic coatings with sustainable anti-fogging and mechanically robust underwater anti-oil-fouling capabilities

Inorganic coatings with high transparency and superhydrophilicity have attracted tremendous attention because of their potential applications in marine environment monitoring, and oily wastewater treatment. However, the transparency and superhydrophilicity are usually mutually exclusive. Herein, we present a new facile strategy for fabricating highly transparent and mechanically robust superhydrophilic inorganic coatings with outstanding anti-fogging ability and anti-oil-fouling performance for high-viscosity oils. In this strategy, amorphous calcium phosphate (ACP) coatings are mineralized on the surface of polydopamine and polyethylenimine (PDA/PEI) membranes under the synergistic effect of magnesium ions, citric acid, and poly(acrylic acid) at room temperature, forming an organic-inorganic composite structure with a uniform texture on various substrates. Owing to the strong hydration capacity of ACP, these coatings are highly efficient at preventing surface fogging and avoiding underwater crude oil fouling. Meanwhile, the ACP coating without grain boundaries or pores can reduce light scattering, thus maintaining the high transparency of the substrate. Moreover, the organic-inorganic composite structure endows the coatings with robust mechanical properties. This PDA/PEI-ACP mineralized coating can be deposited on various substrates, showing potential applications in underwater optical lenses, oily wastewater treatment, microfluidic devices, and other areas.

Construction of multiple interpenetrati ng network electric field-assisted healing hydrogel composite damage-resistant membrane

Inspired by the intrinsic self-healing ability of organisms, this study proposes to incorporate healing properties into separation membranes that are susceptible to physical damage during installation, operation, maintenance, and cleaning. The polyacrylic acid (PAA) hydrogel-modified layer was first obtained by in situ cross-linking and free radical polymerization in this research. After that, the construction of multiple interpenetrating three-dimensional (3D) network hydrogel-modified layers was realized via inserting amininated carbon nanotubes (CNTs-NH2) and Fe3+. Under the external effect of the electric field, the reversible dynamic linkage bonded in the conductive network constructed by CNTs-NH2 and Fe3+ benefited the rearrangement and diffusion of PAA molecular chains at the fractured interface. The dye separation performance of the composite membrane was restored to ca. 90 % of the initial level without affecting the dynamic operation after damage. The hydrogel-modified layer can be structurally stabilized for as long as 100 days. The Fe3+/CNTs-NH2/PAA/PES hydrogel composite membrane maintained a pure water flux of as high as 124.66 L m−2 h−1∙bar−1. This coating also exhibited excellent electrical conductivity (714.33 Ω/sq), mechanical strength (4.31 Mpa), repair, and screening capabilities. It provides a theoretical basis for achieving industrial scale-up and demonstrates good application prospects and empowerment potential.

Magnetic Silver Nanoparticles Stabilized by Superhydrophilic Polymer Brushes with Exceptional Kinetics and Catalysis.

Stimuli-responsive catalysts with exceptional kinetics and complete recoverability for efficient recyclability are essential in, for example, converting pollutants and hazardous organic compounds into less harmful chemicals. Here, we used a novel approach to stabilize silver nanoparticles (NPs) through magneto/hydro-responsive anionic polymer brushes that consist of poly (acrylic acid) (PAA) moieties at the amine functional groups of chitosan. Two types of responsive catalyst systems with variable silver loading (wt.%) of high and low (PAAgCHI/Fe3O4/Ag (H, L)) were prepared. The catalytic activity was evaluated by monitoring the reduction of organic dye compounds, 4-nitrophenol and methyl orange in the presence of NaBH4. The high dispersity and hydrophilic nature of the catalyst provided exceptional kinetics for dye reduction that surpassed previously reported nanocatalysts for organic dye reduction. Dynamic light scattering (DLS) measurements were carried out to study the colloidal stability of the nanocatalysts. The hybrid materials not only showed enhanced colloidal stability due to electrostatic repulsion among adjacent polymer brushes but also offered more rapid kinetics when compared with as-prepared Ag nanoparticles (AgNPs), which results from super-hydrophilicity and easy accumulation/diffusion of dye species within polymer brushes. Such remarkable kinetics, biodegradability, biocompatibility, low cost and facile magnetic recoverability of the Ag nanocatalysts reported here contribute to their ranking among the top catalyst systems reported in the literature. It was observed that the apparent catalytic rate constant for the reduction of methyl orange dye was enhanced, PAAgCHI/Fe3O4/Ag (H) ca. 35-fold and PAAgCHI/Fe3O4/Ag (L) ca. 23-fold, when compared against the as prepared AgNPs. Finally, the regeneration and recyclability of the nanocatalyst systems were studied over 15 consecutive cycles. It was demonstrated that the nanomaterials display excellent recyclability without a notable loss in catalytic activity.

Effect of polyacrylic acid on the corrosion behavior of Alloy 690 in pressurized water reactor secondary water

The effect of polyacrylic acid (PAA) on the corrosion behavior of Alloy 690 in simulated pressurized water reactor secondary water was investigated. The duplex oxide film structure, consisting of a Ni-rich outer layer and a Cr-rich inner layer, was maintained regardless of PAA presence. PAA inhibited the growth of outer Ni-rich particles while promoting Cr enrichment in the inner layer and inducing its amorphization, both enhancing oxidation resistance. However, excess PAA (≥ 500 ppb) suppressed protective oxide formation during initial oxidation, leading to oxygen penetration into the matrix. A PAA concentration of around 250 ppb is considered optimal for steam generators, as it provides the benefits of PAA without adverse effects on the alloy.

Suppression of aerosol dispersion by highly viscoelastic poly(acrylic acid)- and poly(ethylene oxide)-based coolants during bone drilling

Bone drilling in neurosurgical, dental, and orthopedic procedures, combined with the use of coolants, generates a dispersion of bone particles, coolants, and blood aerosols in the air. This poses the threat of airborne transmission of infectious diseases between patients and medical practitioners. Highly viscoelastic polymeric poly(acrylic acid) (PAA) and poly(ethylene oxide) (PEO) solutions of various concentrations were used as coolants during bone drilling at different mass flow rates to suppress aerosol generation, thereby mitigating the threat of cross-infection. The results revealed that the PAA and PEO solutions provide less advection than water and a comparable cooling performance. However, excessive viscoelasticity of PEO causes the fluid to rise along the cutting burr (the Weissenberg effect), thereby reducing the cooling coverage area. In contrast, slightly lower viscoelasticity of PEO results in a high cooling coverage area. The cooling coverage area is smaller for the PAA at 20 ml/min because the corresponding PAA solution easily swirls or splashes away from the drilling location. However, at 80 ml/min, the supplied PAA solution sufficiently cools the drilling area, despite the loss through splashing. The numbers of atomized droplets of water and the PAA and PEO solutions were quantified and compared to investigate the degree of aerosol formation and dispersion. The solution with the strongest viscoelasticity most significantly suppressed aerosolization and produced the fewest dispersed aerosol droplets during bone drilling.

Experimental Study for Enhancement of Water Flow in Horizontal Pipelines by Using Nanoparticles of Zinc Oxide and Poly Acrylic Acid

Experimental Study for Enhancement of Water Flow in Horizontal Pipelines by Using Nanoparticles of Zinc Oxide and Poly Acrylic Acid

INITIATED CHEMICAL VAPOR DEPOSITION (iCVD) OF POLY(ACRYLIC ACID): A COMPARISON BETWEEN CONTINUOUS AND CLOSED-BATCH iCVD APPROACHES

In this study, poly(acrylic acid) (PAA) thin films were deposited on silicon wafer and glass surfaces by initiated chemical vapor deposition (iCVD) method using di-tert-butyl peroxide (TBPO) as the initiator and acrylic acid (AA) as the monomer. During iCVD, two different precursor feeding approaches, namely continuous and closed-batch, were employed. The effects of substrate temperature and the precursor feeding approaches on the deposition rates and surface morphology of the films were investigated. The highest deposition rates for the continuous and closed-batch iCVD approaches were found as 26.1 nm/min and 18.6 nm/min, respectively, at a substrate temperature of 15 °C. FTIR analysis of the films deposited by both approaches indicated high structural retention of the monomer during the polymerization. AFM results indicated that, PAA thin films possessed low RMS roughness values of 2.76 nm and 1.84 nm using continuous and closed-batch iCVD, respectively. Due to the slightly higher surface roughness of the film deposited under continuous iCVD, that film exhibited a lower water contact angle of 16.1° than the film deposited in closed-batch iCVD. In terms of monomer utilization ratio, closed-batch system was found to be more effective, which may help to minimize the carbon footprint of iCVD process.