Surface Modification Approach Research Articles

Optimizing electrochemical power generation: Harnessing synergies and surface innovation in NiTe-modified MOF nanoarchitectures

Metal-organic frameworks (MOFs) are considered potential electrocatalysts due to their high specific surface area (SSA) and the facilitation of efficient synergistic interactions. In this work, we have implemented a simple and cost-effective surface modification approach to design an efficient electrocatalyst for energy-conversion technologies, specifically water splitting. This work focuses on engineering a novel NiTe functionalized MOF structure wherein NiTe within the MOF channels is the core material, intricately intertwined with highly dispersed Ni particles enveloped by Ni MOF. This fusion of MOFs and NiTe within a designed configuration produces an efficient electrocatalyst with synergistic and surface interface effects and demonstrates bifunctional activity for water splitting. Among the prepared catalysts, one of the resulting catalysts (named Ni MOF/Ni/Ni10Te8) exhibits a low overpotential of 99 mV for the hydrogen evolution reaction (HER) and 180 mV for the oxygen evolution reaction (OER), both benchmarked against RHE @10 mA cm−2. This performance remains steady, with a stability of 99 % after 15 h of continuous operation. Furthermore, the Ni MOF/Ni/Ni10Te8 catalyst also operates in seawater electrocatalysis, requiring a low overpotential of 440 mV at 10 mA cm−2 to produce 70 mL of hydrogen and 34 mL of oxygen. Equally noteworthy are the Faradaic efficiencies achieved, with hydrogen production at 95.7 % and oxygen production at 92.9 %. Developing efficient and economically viable electrocatalysts like the Ni MOF/Ni/NiTe catalyst will advance a cleaner and more sustainable future.

Construction of sustainable and highly efficient fire-protective nanocoatings based on polydopamine and phosphorylated cellulose for flexible polyurethane foam

Layer-by-layer (LBL) self-assembly is an effective strategy for constructing fire-resistant coatings on flexible polyurethane foam (FPUF), while the efficiency of fire-resistant coatings remains limited. Therefore, this study proposes an in situ flame retardancy modification combined with LBL self-assembly technology to enhance the efficiency of flame retardant coatings for FPUF. Initially, polydopamine (PDA) and polyethyleneimine (PEI) were employed to modify the FPUF skeleton, thereby augmenting the adhesion on the surface of the skeleton network. Then, the self-assembly of MXene and phosphorylated cellulose nanofibers (PCNFs) via the LBL technique on the foam skeleton network formed a novel, sustainable, and efficient flame retardant system. The final fire-protective coatings comprising PDA/PEI and MXenes/PCNF effectively prevented the collapse of the foam structure and suppressed the melt dripping of the FPUF during combustion. The peak heat release rate, the peak CO production rate and peak CO2 production rate were reduced by 68.6 %, 61.1 %, and 68.4 % only by applying a 10-bilayer coating. In addition, the smoke release rate and total smoke production were reduced by 83.3 % and 57.7 %, respectively. This work offers a surface modification approach for constructing highly efficient flame retardant coatings for flammable polymeric materials.

Facile preparation of zwitterionic core-shell nanogels for dual-functional coatings: Combining antifouling and antibacterial features in silicon implant model surface modification

To develop surface-coating technology for fabricating functionalized biomedical implant and overcome implant-associated bacterial infections, this study presented an innovative antifouling and antibacterial dual-functional nanogel coating methodology for engineering silicon-based biomedical implants/biochips. Firstly, zwitterionic core-shell PAA@(GMA/SBMA) nanogels were designed and prepared via reflux-precipitation polymerization and were characterized through NMR, FTIR, DLS, AFM and TEM. The nanogels exhibited uniform and spherical morphology, salt-ion responsiveness, and high lysozyme loading capability. Subsequently, the PAA@(GMA/SBMA) nanogels were covalently grafted onto the surface of silicon wafers, via an epoxy-amine ring-opening reaction, to prepare nanogel-coated silicon wafers (Si@nanogels). A comprehensive array of characterization techniques, including SEM-EDS, contact angle measurements, and XPS, validated the effective nanogel-coating. These coatings demonstrated notable resistance to protein adsorption, highlighting their robust antifouling properties. Upon loading with the antibacterial agent lysozyme, the nanogel coating displayed remarkable antibacterial efficacy against both Gram-negative (E. coli) and Grampositive (S. aureus) bacteria and effectively inhibited biofilm formation. Furthermore, the nanogel coatings exhibited good biocompatibility and dynamic stability, thus facilitating the surface-mediated adhesion and growth of fibroblast 3T3 cells. Significantly, this work provided a facile, economic and efficient surface modification approach to fabricate nanogel-coated antifouling/antibacterial dual-functional biomedical implant model towards potential clinical applications.

One‐pot immobilization of formate dehydrogenase on silica nanoparticles based on catechol chemistry with or without polyethyleneimine

AbstractConverting carbon dioxide into formic acid with formate dehydrogenase (FDH) as a catalyst is a gentle and eco‐friendly process that not only conserves energy and reduces emissions but transforms waste into valuable resource. Enzyme immobilization is a common strategy for improving the stability and recyclability of enzyme, however, the procedures are usually complicated that include surface modification and binding reactions in order to form reliable linkages. Co‐deposition of polydopamine (PDA) with polyethyleneimine (PEI) is a popular surface modification approach in versatile fields, but their co‐deposition with enzymes is rarely reported. Herein, one‐pot immobilization of FDH on SiO2 nanoparticles based on catechol chemistry was attempted for the first time with or without PEI, and the resultant immobilized enzymes, FDH/PDA/PEI‐SiO2 and FDH/PDA‐SiO2, were characterized, and the effects of the composition and deposition conditions on the catalytic performance were investigated. FDH/PDA‐SiO2 exhibited a higher apparent specific activity than FDH/PDA/PEI‐SiO2, which was separately 0.167 and 0.136 mM/h/mg. The activity recovery rate was 464% and 378% of that of free enzyme. After 5 cycles, their relative activity was 82.3% and 87.4%. This research is significant in presenting a simple and high‐efficient one‐pot immobilization method that can be extended to other kinds of enzymes.

Aluminum Carboxylate Modification Enabled Efficient and Stable Perovskite-Polystyrene Thin Films for Light-Emitting Applications.

Lead halide perovskite nanocrystals (PNCs) have demonstrated great potential in emerging display technologies. However, the practical application of PNCs is hindered by the inherent instability of their ionic surface. Here, we proposed a surface modification approach to enhance the stability of CsPbBr3 PNCs by postsynthetic treatment with aluminum phenylbutyrate (Al(PA)3). Our study reveals that Al(PA)3 displaces ammonium ligands and binds tightly on surface halide, providing excellent air and moisture resistance while preserving a high quantum efficiency of 81.6%. The modified PNCs maintain a constant photoluminescence intensity under continuous UV light illumination for 500 h. Additionally, the Al(PA)3 ligand is compatible with styrene, enabling homogeneous dispersion of PNCs in polystyrene matrices to form bright and uniform PNC-PS thin films. We demonstrated the application of the composite films for display backlighting, which exhibits a wide color gamut of 125% NTSC. The result highlights the potential of AlPA-modified PNCs in light-emitting and other optoelectronic devices.

Preparations and Thermal Properties of PDMS-AlN-Al2O3 Composites through the Incorporation of Poly(Catechol-Amine)-Modified Boron Nitride Nanotubes

As one of the emerging nanomaterials, boron nitride nanotubes (BNNTs) provide promising opportunities for diverse applications due to their unique properties, such as high thermal conductivity, immense inertness, and high-temperature durability, while the instability of BNNTs due to their high surface induces agglomerates susceptible to the loss of their advantages. Therefore, the proper functionalization of BNNTs is crucial to highlight their fundamental characteristics. Herein, a simplistic low-cost approach of BNNT surface modification through catechol-polyamine (CAPA) interfacial polymerization is postulated to improve its dispersibility on the polymeric matrix. The modified BNNT was assimilated as a filler additive with AlN/Al2O3 filling materials in a PDMS polymeric matrix to prepare a thermal interface material (TIM). The resulting composite exhibits a heightened isotropic thermal conductivity of 8.10 W/mK, which is a ~47.27% increase compared to pristine composite 5.50 W/mK, and this can be ascribed to the improved BNNT dispersion forming interconnected phonon pathways and the thermal interface resistance reduction due to its augmented compatibility with the polymeric matrix. Moreover, the fabricated composite manifests a fire resistance improvement of ~10% in LOI relative to the neat composite sample, which can be correlated to the thermal stability shift in the TGA and DTA data. An enhancement in thermal permanence is stipulated due to a melting point (Tm) shift of ∼38.5 °C upon the integration of BNNT-CAPA. This improvement can be associated with the good distribution and adhesion of BNNT-CAPA in the polymeric matrix, integrated with its inherent thermal stability, good charring capability, and free radical scavenging effect due to the presence of CAPA on its surface. This study offers new insights into BNNT utilization and its corresponding incorporation into the polymeric matrix, which provides a prospective direction in the preparation of multifunctional materials for electric devices.

One Stone Two Birds: Anomalously Enhancing the Cross‐Plane and In‐Plane Heat Transfer in 2D/3D Heterostructures by Defects Engineering

AbstractThis study addresses a crucial challenge in two‐dimensional (2D) material‐based electronic devices—inefficient heat dissipation across the van der Waals (vdW) interface connecting the 2D material to its three‐dimensional (3D) substrate. The objective is to enhance the interfacial thermal conductance (ITC) of 2D/3D heterostructures without compromising the intrinsic thermal conductivities (κ) of 2D materials. Using 2D‐MoS2/3D‐GaN as an example, a novel strategy to enhance both the ITC across 2D/3D interface and κ of 2D material is proposed by introducing a controlled concentration (ρ) of vacancy defects to substrate's bottom surface. Molecular dynamics simulations demonstrate a notable 2.1‐fold higher ITC of MoS2/GaN at ρ = 4% compared to the no‐defective counterpart, along with an impressive 56% enhancement in κ of MoS2 compared to the conventional upper surface modification approaches. Phonon dynamics analysis attributes the ITC enhancement to increased phonon coupling between MoS2 and GaN, resulting from polarization conversion and hybridization of phonons at the defective surface. Spectral energy density analysis affirms that the improved κ of MoS2 directly results from the proposed strategy, effectively reducing phonon scattering at the interface. This work provides an effective approach for enhancing heat transfer in 2D/3D vdW heterostructures, promisingly advancing electronics’ heat dissipation.

Anti-fouling coating with ROS-Triggered On-Demand regulation of inflammation to favor tissue healing on vascular devices

Unhealthy vascular tissue healing after stenting is primarily triggered by endothelial dysfunction and excessive smooth muscle cell proliferation, which is induced and aggravated by local thrombosis and excessive inflammation. Excessive inflammatory response is closely related to elevated concentrations of reactive oxygen species (ROS). Here, an environment-friendly coating strategy termed “Anti-fouling plus” with inflammatory self-regulation ability was proposed. Upon this, membrane-mimicking copolymer MA(PCLA) served as the antifouling coating, effectively inhibiting coagulation and inflammation during the early stage of implantation. Furthermore, a ROS-responsive prodrug was drawn into the coating to promote tissue healing. A molecular prodrug of thioketal-bearing dexamethasone was engineered to be released in a controlled and responsive manner in response to externally high levels of ROS. The released dexamethasone exhibited highly effective anti-inflammation properties after implantation. The combination of ROS-responsive prodrug and membrane-mimicking antifouling interface strategy intelligently integrated inflammation responsiveness and regulation, which could mediate a gentle vascular microenvironment and thus promote vascular remodeling. In vivo stent implantation studies demonstrated that the proposed “Anti-fouling plus” coating effectively inhibited neointima hyperplasia, modulated the inflammatory response and promoted endothelialization, offering promising surface modification approaches for vascular stents.

Novel alkali intercalated and acid-exfoliated biochars with enhanced surface areas for contaminant adsorption applications

Cost-effective and eco-friendly adsorbents are essential in environmental engineering and biochar is a promising material from the perspective. A novel and efficient surface modification approach involving alkali intercalation and acid exfoliation was designed in this study to enhance the physicochemical properties of biochar. The alkali intercalation process utilizes potassium hydroxide (KOH), while acid exfoliation involves varying HNO3, H2SO4, and H3PO4 concentrations. A simple two-stage pyrolysis process was employed to facilitate the intercalation-exfoliation modification. The modified biochars were characterized using BET, SEM, XRD, etc., to understand physicochemical properties. To quantify the effectiveness of the modifications, adsorption of malachite green dye as a model moiety was investigated. Dye removal sorption rates exceeding 99 % were recorded in the case of the biochars modified through a two-step process using KOH and 0.1MH3PO4. Specifically, the highest contaminant removal of 99.9 % was recorded when 60 mg of the KOH-0.1MH3PO4 biochar was employed, which is significantly higher than unmodified biochar’s 45.41 % removal at a higher dosage of 100 mg. Moreover, the adsorption kinetics revealed that all the modified biochars attained the maximum removal concentrations (∼99 % removal) in a mere 300 min, indicating a tenfold improvement in adsorption rate from unmodified biochar's requirement of over 5000 min. The results achieved through this study provide a cost-effective, fast, and environment-friendly technology for enhancing the adsorption characteristics and performance of biochars toward contaminant removal.

Surface modification of the laser powder bed-fused Ti-Zr-Nb scaffolds by dynamic chemical etching and Ag nanoparticles decoration

Metallic lattice scaffolds are designed to mimic the architecture and mechanical properties of bone tissue and their surface compatibility is of primary importance. This study presents a novel surface modification protocol for metallic lattice scaffolds printed from a superelastic Ti-Zr-Nb alloy. This protocol consists of dynamic chemical etching (DCE) followed by silver nanoparticles (AgNP) decoration. DCE, using an 1HF + 3HNO3 + 12H2O23% based solution, was used to remove partially-fused particles from the surfaces of different as-built lattice structures (rhombic dodecahedron, sheet gyroid, and Voronoi polyhedra). Subsequently, an antibacterial coating was synthesized on the surface of the scaffolds by a controlled (20 min at a fixed volume flowrate of 500 mL/min) pumping of the functionalization solutions (NaBH4 (2 mg/mL) and AgNO3 (1 mg/mL)) through the porous structures. Following these treatments, the scaffolds' surfaces were found to be densely populated with Ag nanoparticles and their agglomerates, and manifested an excellent antibacterial effect (Ag ion release rate of 4–8 ppm) suppressing the growth of both E. coli and B. subtilis bacteria up to 99 %. The scaffold extracts showed no cytotoxicity and did not affect cell proliferation, indicating their safety for subsequent use as implants. A cytocompatibility assessment using MG-63 spheroids demonstrated good attachment, spreading, and active migration of cells on the scaffold surface (over 96 % of living cells), confirming their biotolerance. These findings suggest the promise of this surface modification approach for developing superelastic Ti-Zr-Nb scaffolds with superior antibacterial properties and biocompatibility, making them highly suitable for bone implant applications.

Fe-TiO2-x/TiO2 S-scheme homojunction for efficient photocatalytic CO2 reduction

CO2-to-high value-added chemicals via a photocatalytic route is of interest but strangled by the low efficiency. Herein, a novel Fe-TiO2-x/TiO2 S-scheme homojunction was designed and constructed by using a facile surface modification approach whereby oxygen vacancy (OV) and Fe introducing on the TiO2 nanorod surface. The as-synthesized Fe-TiO2-x/TiO2 S-scheme homojunction exhibits positive properties on promoting photocatalytic CO2 reduction: i) the nanorod structure provides numerous active sites and a radical charge transfer path; ii) the doped Fe and OV not only synergistically enhance light utilization but also promote CO2 adsorption; iii) the Fe-TiO2-x/TiO2 S-scheme homojunction benefits photoexcited charge separation and retains stronger redox capacity. Thanks to those good characters, the Fe-TiO2-x/TiO2 homojunction exhibits superior CO2 reduction performances with optimized CO/CH4 generation rates of 122/22 μmol g-1h−1 which exceed those of pure TiO2 by more than 9.4/7.3 folds and most currently reported catalytic systems. This manuscript develops a facile and universal approach to synthesize well-defined homojunction and may inspire the construction of other more high-efficiency photocatalysts toward CO2 reduction and beyond.

Enhanced Hemocompatibility and Cytocompatibility of Stainless Steel.

The present study introduces an advanced surface modification approach combining electrochemical anodization and non-thermal plasma treatment, tailored for biomedical applications on stainless steel grade 316L (SS316L) surfaces. Nanopores with various diameters (100-300 nm) were synthesized with electrochemical anodization, and samples were further modified with non-thermal oxygen plasma. The surface properties of SS316L surfaces were examined by scanning electron microscopy, atomic force microscopy, X-ray photoemission spectroscopy, and Water contact angle measurements. It has been shown that a combination of electrochemical anodization and plasma treatment significantly alters the surface properties of SS316L and affects its interactions with blood platelets and human coronary cells. Optimal performance is attained on the anodized specimen featuring pores within the 150-300 nm diameter range, subjected to subsequent oxygen plasma treatment; the absence of platelet adhesion was observed. At the same time, the sample demonstrated good endothelialization and a reduction in smooth muscle cell adhesion compared to the untreated SS316L and the sample with smaller pores (100-150 nm). This novel surface modification strategy has significant implications for improving biocompatibility and performance of SS316L in biomedical applications.

Unlocking Heavy Metal Remediation Potential: A Review of Cellulose–Silica Composites

This comprehensive review explores recent advancements in heavy metal remediation techniques, focusing on the utilization of cellulose–silica composites and tailored surface modification techniques. We examine the synthesis strategies and properties of cellulose–silica adsorbents, highlighting their enhanced adsorption capacities and structural robustness for removing heavy metal pollutants from aqueous environments. The review investigates various surface modification approaches, including thiol functionalization, amino acid grafting, and silane coupling agents, for optimizing the surface chemistry and morphology of cellulose–silica composites. Mechanistic insights into the adsorption processes and kinetics of modified adsorbents are discussed, along with considerations for optimizing adsorption performance under different environmental conditions. This review provides valuable perspectives on the development of effective adsorbent materials for sustainable heavy metal remediation applications.

Pd nanocubes enclosed by {100} facets for activating electroless Cu deposition on liquid crystal polymer substrates with strong adhesion strength

In this study, we investigate the catalytic performance of palladium (Pd) nanocatalysts with different surface atomic structures for activating electroless copper (Cu) deposition on liquid crystal polymer (LCP) substrates. These nanocatalysts include Pd nanocubes featuring {100} facets of square atomic arrangement as their predominant surface structure and Pd spherical nanoparticles characterized by random atomic arrangements, synthesized using an aqueous method. Our electrochemical measurements reveal that the induction time for the growth of Cu films is significantly shorter when utilizing Pd nanocubes compared to Pd nanospheres. This shorter induction time signifies a quicker initiation of Cu growth, primarily due to the presence of Pd {100} facets. Furthermore, we also develop a surface modification approach involving a crosslinking reaction that utilizes the highly branched polyethylenimine and linear polyvinylpyrrolidone on the Pd nanocubes. This method not only facilitates the adsorption of Pd nanocubes onto the LCP substrates but also achieves a robust peel adhesion strength (630 gf/cm) of the resulting Cu films, exceeding the industrial adhesion goal of 500 gf/cm. Moreover, in-depth synchrotron X-ray photoelectron spectroscopy analysis provides valuable insights into the depth-dependent chemical changes within the Cu films and proves the removal of Cu oxides after the acid treatment.

Lipid-Based Nanoparticle Functionalization with Coiled-Coil Peptides for In Vitro and In Vivo Drug Delivery.

For the delivery of drugs, different nanosized drug carriers (e.g., liposomes, lipid nanoparticles, and micelles) have been developed in order to treat diseases that afflict society. Frequently, these vehicles are formed by the self-assembly of small molecules to encapsulate the therapeutic cargo of interest. Over decades, nanoparticles have been optimized to make them more efficient and specific to fulfill tailor-made tasks, such as specific cell targeting or enhanced cellular uptake. In recent years, lipid-based nanoparticles in particular have taken center stage; however, off-targeting side effects and poor endosomal escape remain major challenges since therapies require high efficacy and acceptable toxicity.To overcome these issues, many different approaches have been explored to make drug delivery more specific, resulting in reduced side effects, to achieve an optimal therapeutic effect and a lower required dose. The fate of nanoparticles is largely dependent on size, shape, and surface charge. A common approach to designing drug carriers with targeting capability is surface modification. Different approaches to functionalize nanoparticles have been investigated since the attachment of targeting moieties plays a significant role in whether they can later interact with surface-exposed receptors of cells. To this end, various strategies have been used involving different classes of biomolecules, such as small molecules, nucleic acids, antibodies, aptamers, and peptides.Peptides in particular are often used since there are many receptors overexpressed in different specific cell types. Furthermore, peptides can be produced and modified at a low cost, enabling high therapeutic screening. Cell-penetrating peptides (CPPs) and cell-targeting peptides (CTPs) are frequently used for this purpose. Less studied in this context are fusogenic coiled-coil peptides. Lipid-based nanoparticles functionalized with these peptides are able to avoid the endolysosomal pathway; instead such particles can be taken up by membrane fusion, resulting in increased delivery of payload. Furthermore, they can be used for targeting cells/organs but are not directed at surface-exposed receptors. Instead, they recognize complementary peptide sequences, facilitating their uptake into cells.In this Account, we will discuss peptides as moieties for enhanced cytosolic delivery, targeted uptake, and how they can be attached to lipid-based nanoparticles to alter their properties. We will discuss the properties imparted to the particles by peptides, surface modification approaches, and recent examples showing the power of peptides for in vitro and in vivo drug delivery. The main focus will be on the functionalization of lipid-based nanoparticles by fusogenic coiled-coil peptides, highlighting the relevance of this concept for the development of future therapeutics.

Surface modification of PEEKs with cyclic peptides to support endothelialization and antithrombogenicity

Synthetic polymers are often utilized in the creation of vascular devices, and need to possess specific qualities to prevent thrombosis. Traditional strategies for this include surface modification of vascular devices through covalent attachment of substrates such as heparin, antiplatelet agents, thrombolytic agents, or hydrophilic polymers. One promising prosthetic material is polyether ether ketone (PEEK), which is utilized in various FDA-approved medical devices, including vascular and endovascular prostheses. We hypothesized that surface modification of biologically inert PEEK can help improve its endothelial cell affinity and reduce its thrombogenic potential. To evaluate this, we developed an effective surface-modification approach with unique cyclic peptides, such as CCHGGVRLYC and CCREDVC. We treated the PEEK surface with ammonia plasma, which introduced amine groups onto the PEEK surface. Subsequently, we were able to conjugate these peptides to the plasma-modified PEEKs. We observed that cyclic CCHGGVRLYC conjugated on prosthetic PEEK not only supported endothelialization, but minimized platelet adhesion and activation. This technology can be potentially applied for in vivo vascular and endovascular protheses to enhance their utility and patency.

On Antimicrobial Polymers: Development, Mechanism of Action, International Testing Procedures, and Applications.

The development of antimicrobial polymeric materials has evolved into one of the more promising methods for preventing the growth of microbes and mitigating the spread of infectious diseases in several applications including the health and food packaging sectors. The outbreak of global pandemics, and particularly the recent COVID-19 pandemic, further strengthen the importance of developing such solutions. This review paper presents a fundamental understanding of how antimicrobial polymers are developed, describes the possible surface modification approaches to render polymers with antimicrobial properties, highlights the potential mechanism of action against a range of microorganisms (bacterial, viral, and fungal), and details some of the international standard protocols and procedures to evaluate the antimicrobial properties of modified materials (such as plastics and textiles). In addition, this review paper discusses the toxicity of antimicrobial additives when used in healthcare and food packaging applications.

Comparison of surface modification and corrosion resistance of Ti6Al4V alloy using matcha tea extract-based silver and copper oxide nanoparticles

In this study, our aim was to investigate the application of green-synthesized silver nanoparticles (Ag NPs) and copper oxide nanoparticles (CuO NPs) for surface modification, specifically focusing on their influence on the corrosion properties of Ti6Al4V alloy. The green NPs were thoroughly characterized, and their role in enhancing the anticorrosive performance of Ti6Al4V was carefully evaluated. Various coating methods and drying temperatures were utilized to coat Ti6Al4V samples with the NPs, aiming to assess their impact on corrosion resistance. The electrochemical corrosion behavior was examined through electrochemical polarization tests in Ringer's bio-liquid. The study underscored the significant impact of coating type, coating method, and drying temperature (25 °C and 60 °C) in achieving favorable anticorrosive performance. Notably, samples oven-dried at both temperatures and coated with Ag NPs and CuO NPs using spray coating demonstrated the most effective substrate protection, achieving protection efficiencies of 97.37 % and 90.56 %, respectively. This outcome can be attributed to the unique spherical and homogeneously dispersed particulate structure of the NPs, effectively reducing microporosity. In summary, the combination of increased surface area and reduced microporosity resulting from the surface properties of the NPs underscores the potential of well-designed surface modification approaches in advancing the development of titanium-based implants for biomedical applications.

Dodecyl methacrylate (DM) dispersion-assisted surface modification approach for increasing crystallinity of coir fibers

Coir fiber crystallinity is crucial since it widens the range of possible uses for natural fiber. To increase the crystallinity of coir fiber, the study describes an easy-to-use, simple-to-implement method that is cost-effective, eco-friendly, and highly productive. With the help of dodecyl methacrylate disperson, hydrocarbon molecules of varying chain lengths are covalently attached to the surface of coir fibers, modulating their surface wettability. There are a few different long-chain hydrocarbon compounds employed, including n-butyl methacrylate, n-octyl acrylate, and dodecyl methacrylate (DM), but DM has shown to be the most effective. The degree of grafting yield alteration is determined gravimetrically. It has been found that grafting yields of 28–30 wt.% can be used to convert hydrophilic coir fibers into water repellent crystalline fibers (water contact angle 148°). A total of 15 nm of dispersion, a disperson rate of 2 nm/min, DM concentration of 20%, and water content of 10% are fixed as key reaction parameters. Thermal and mechanical analyses show no significant changes in the fiber structure during alteration. The grafting and changes in surface wettability are well supported by the surface morphology of pure and modified coir fiber, which can be seen using scanning electron microscopy.

Electrically Stimulated Dental Implants Triggers Soft‐Tissue Integration and Bactericidal Functions

AbstractModulating cellular functions at the dental implant‐tissue interface to augment integration and prevent bacterial ingress is crucial for achieving early stability and long‐term implant success. Nano‐engineering strategies, such as anodized titanium implants with titania (TiO2) nanotubes/nanopores, are emerging as a promising dental implant surface modification approach to enhance integration and prevent infection. Achieving on‐demand therapy through electrical stimulation therapy (EST, supply of voltage/current to local tissue) may be advantageous but has not been explored for dental implants. Further, anodized implants with TiO2 nanotubes/nanopores represent a semi‐conducting modification that can impede EST effectiveness. In this pioneering study, TiO2 nanopores are converted into conducting Ti nanopores to perform EST to achieve superior soft‐tissue integration and antibacterial efficacy. In‐depth surface characterizations are followed by assays investigating the effect of EST on cultured human salivary biofilm and gingival fibroblasts. Significant bactericidal efficacy is demonstrated for EST (1.5 V for 5 min per day) using Ti nanopores. Further, EST enhanced fibroblast proliferation and collagen secretion. In summary, EST applied to Ti nanoporous implants promotes soft‐tissue healing and antibacterial functions and is proposed as a next‐generation approach in implant dentistry to achieve on‐demand therapy.