Surface Modification Research Articles

Tailoring surface engineering with expanded precursor libraries via rapid mussel-inspired chemistry.

Mussel-inspired coating is a substrate-independent surface modification technology. However, its application is limited by time-consuming, tailoring specific functions require tedious secondary reaction. To overcome those drawbacks, a strategy for the rapid fabrication of diverse coatings by expanding the library of precursors using oxidation coupled with polyamine was proposed. Based on DFT simulations of the reaction pathways, a method was developed to achieve rapid deposition of coatings by coupling oxidation and polyamines, which simultaneously accelerated the oxidation of precursors and polymer chain growth. The feasibility and generalizability of the strategy was validated by the rapid coating of 10 catechol derivatives and polyamines on various substrates. The surface properties of the substrates such as functional group densities, Zeta potential and contact angles can be easily tuned. The tailored surface engineering application of the strategy was demonstrated by the heavy metal adsorbents and superwetting materials prepared through the delicate combination of different building blocks. Our strategy was flexible in terms of diverse surface engineering design which greatly enriched the connotation of mussel-inspired technique.

Surface charge engineering for structural control of colloidal silica rod-decorated silica particles and their flexible integration into magnetic core–multishell structures

In this study, the effect of surface modification and the resulting surface charge of colloidal silica seeds on the growth of silica rods during an emulsion droplet-based process is investigated. Through electrostatic interactions between negatively charged poly(vinylpyrrolidone) (PVP) and seed surfaces, significant PVP adsorption occurs as the seed surfaces are modified with positively charged cationic substances and then aged with PVP. This surface charge-enhanced PVP adsorption promotes the anchoring of water emulsion droplets, serving as the starting point for the growth of silica rods on the seed surfaces and leading to a high yield of silica rod-decorated particles during emulsion droplet-based growth. The surface properties, including surface charge and hydrophobicity, can be further modified by applying different cationic modifiers, which influence the morphology, structural architecture, and yield of the final product. We further demonstrated the versatility of this approach by successfully generating silica rod-decorated magnetic core (Fe3O4)–multishell (silica/polystyrene/titania) particles. The findings of this study highlight the critical role of surface charge engineering in controlling the structure and morphology of silica rod-decorated silica particles as well as their integration into complex multicomponent systems.

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.

Hybrid Double-Sided Tape with Asymmetrical Adhesion and Burst Pressure Tolerance for Abdominal Injury Treatment.

Patients with open abdominal (OA) wounds have a mortality risk of up to 30%, and the resulting disabilities would have profound effects on patients. Here, we present a novel double-sided adhesive tape developed for the management of OA wounds. The tape features an asymmetrical structure and employs an acellular dermal matrix (ADM) with asymmetric wettability as a scaffold. It is constructed by integrating a tissue-adhesive hydrogel composed of polydopamine (pDA), quaternary ammonium chitosan (QCS), and acrylic acid cross-linking onto the bottom side of the ADM. Following surface modification with pDA, the ADM would exhibit characteristics resistant to bacterial adhesion. Furthermore, the presence of a developed hydrogel ensures that the tape not only possesses tissue adhesiveness and noninvasive peelability but also effectively mitigates damage caused by oxidative stress. Besides, the ADM inherits the strength of the skin, imparting high burst pressure tolerance to the tape. Based on these remarkable attributes, we demonstrate that this double-sided (D-S) tape facilitates the repair of OA wounds, mitigates damage to exposed intestinal tubes, and reduces the risk of intestinal fistulae and complications. Additionally, the D-S tape is equally applicable to treating other abdominal injuries, such as gastric perforations. It effectively seals the perforation, promotes injury repair, and prevents the formation of postoperative adhesions. These notable features indicate that the presented double-sided tape holds significant potential value in the biomedical field.

Woven polyester vascular stent-grafts with surface modification of chitosan/heparin

Woven polyester vascular stent-grafts with surface modification of chitosan/heparin

Synchronously enhancing thermal conductivity and dielectric properties in epoxy composites via incorporation of functionalized boron nitride.

Polymer-like dielectrics with superb thermal conductivity as well as high dielectric properties hold great promise for the modern electronic field. Nevertheless, integrating these properties into a single material simultaneously remains problematic due to their mutually limited physical connotations. In this study, we developed high-quality thermally conductive epoxy composites with excellent dielectric properties. This was achieved by incorporating surface-functionalized microscale hexagonal boron nitride (BN) along with N-[3-(Trimethoxysilyl)propyl]ethylene diamine (DN) and N-[3-(Trimethoxysilyl)propyl]aniline (PN). In the resulting epoxy composite, microscale BN serves as the primary building block for establishing the thermally conductive network, while silica particles act as bridges to regulate heat transfer and reduce interfacial phonon-scattering. The prepared composites were thoroughly examined across various filler contents (ranging from 10 to 80 wt%). Among them, the DNBN/epoxy composite exhibited higher thermal conductivity (in-plane: 47.03 W m-1 K-1) at 60 wt% filler content compared to BN/epoxy (39.40 W m-1 K-1) and PNBN/epoxy (33 W m-1 K-1) composites. These results highlight the usefulness of surface modification of BN in improving compatibility between fillers and epoxy, ultimately reducing composite viscosity. Furthermore, the DNBN/epoxy composite at 60 wt% demonstrated superb dielectric constant (∼6.15) without compromising on dissipation loss (∼0.06). The strategy adopted in this study offers significant insights into designing dielectric thermally conductive composites with superior performance outcomes.

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.

Multimodal electrohydrodynamic jet printing-based microstructure-sensitized flexible pressure sensor

Surface modification with micro/nanostructures is a common approach for enhancing the performance of flexible pressure sensors. However, the current fabrication of the singular functionality of instruments and redundancy of processes increase the complexity of the sensor manufacturing process. In this study, we developed a multilayer microstructure-enhanced flexible capacitive pressure sensor based on the multimodal electrohydrodynamic jet (E-jet) printing technology. The experimental results demonstrate that the sensors incorporating the microstructure-sensitized electrode layer and the polyvinyl alcohol/graphene/polydimethylsiloxane dielectric layer exhibit the following characteristics: high sensitivity (0.3139 kPa−1/0–2 kPa), low limit of detection (∼100 mg), and stable performance even after 10,000 cycles. Moreover, microstructure-enhanced sensors have considerable potential for human behavior detection, such as detecting fluid flow, tracking muscle movements, and measuring pulse rates. Finally, microstructure-enhanced sensors fabricated using the E-jet printing method present a novel approach for designing sensitized structures in capacitive pressure sensors.

A Review on Investigating the Interactions between Nanoparticles and the Pulmonary Surfactant Monolayer with Coarse-Grained Molecular Dynamics Method.

Pulmonary drug delivery has garnered significant attention due to its targeted local lung action, minimal toxic side effects, and high drug utilization. However, the physicochemical properties of inhaled nanoparticles (NPs) used as drug carriers can influence their interactions with the pulmonary surfactant (PS) monolayer, potentially altering the fate of the NPs and impairing the biophysical function of the PS monolayer. Thus, the objective of this review is to summarize how the physicochemical properties of NPs affect their interactions with the PS monolayer. Initially, the definition and properties of NPs, as well as the composition and characteristics of the PS monolayer, are introduced. Subsequently, the coarse-grained molecular dynamics (CGMD) simulation method for studying the interactions between NPs and the PS monolayer is presented. Finally, the implications of the hydrophobicity, size, shape, surface charge, surface modification, and aggregation of NPs on their interactions with the PS monolayer and on the composition of biomolecular corona are discussed. In conclusion, gaining a deeper understanding of the effects of the physicochemical properties of NPs on their interactions with the PS monolayer will contribute to the development of safer and more effective nanomedicines for pulmonary drug delivery.

Using 2% PVPI topical solution for serial intravitreous injections and ocular surface findings: a case control study

BackgroundThe use of povidone-iodine for ocular surface asepsis is widespread for intravitreal injections. They became frequent procedures, leading to serial exposure of patients’ eyes to iodinated solutions. In this study, we investigate the changes in the ocular surface in patients submitted to repeated use of povidine for intravitreal injection of anti-VEGF asepsis, analyzing Ocular Surface Disease Index, non-invasive break up time, blinking quality, lipid layer, meniscus height and osmolarity.MethodsThis case-control study included 34 individuals (68 eyes), 14 males, 20 females aged 48 to 94. Inclusion criteria were individuals who received application of 2% povidone-iodine eyedrops for intravitreal injections treatment with the non-treated contralateral eye used as control. Ocular surface examinations were performed at a single occasion. A pre-intravitreal injection asepsis protocol with povidone-iodine was applied. All statistical analysis was performed using the STATA® 18.0 Software and a p-value = 0.05 was considered as the statistical significance value in all tests.ResultsThe median number of IVIs in treated eyes was 12 (range 6–20). The results in treated eyes compared with untreated eyes were respectively : median OSDI 16 (IQR 6–39) and 12.5 (IQR 8–39) (p = 0.380); mean NIBUT 10.30 (SD ± 2.62) and 10.78 (SD ± 2.92) ( s, p = 0.476); median blinking quality 100 (IQR 100) and 100 (IQR 100 ) (%, p = 0.188); median lipid layer 87 (IQR 77–90) and 86 (IQR 74–100) (nm, p = 0.451); median meniscus height 0.22 (IQR 0.19-0,31) and 0.24 (IQR 0.20–0.27) (mm, p = 0.862), median Meibomian gland atrophy 33 (IQR 24–45) and 31.5 (IQR 25–39) (%, p = 0.524); and mean osmolarity 306.6 (SD ± 21.13) and 313.8 (SD ± 29) (mOsm, p = 0.297). There was no statistically significant relationship between the repetitive use of 2% iodinated solution and signs or symptoms compatible with dry eye syndrome in this group of patients.ConclusionsThe findings suggest that 2% povidone iodine is a safe and efficacious agent for ocular surface antisepsis during intravitreal injections, not leading to substantial ocular surface modifications. This conclusion supports the continued use of povidone iodine in routine ophthalmic procedures without increased risk of inducing dry eye syndrome.

Uncovering kinesin dynamics in neurites with MINFLUX

Neurons grow neurites of several tens of micrometers in length, necessitating active transport from the cell body by motor proteins. By tracking fluorophores as minimally invasive labels, MINFLUX is able to quantify the motion of those proteins with nanometer/millisecond resolution. Here we study the substeps of a truncated kinesin-1 mutant in primary rat hippocampal neurons, which have so far been mainly observed on polymerized microtubules deposited onto glass coverslips. A gentle fixation protocol largely maintains the structure and surface modifications of the microtubules in the cell. By analyzing the time between the substeps, we identify the ATP-binding state of kinesin-1 and observe the associated rotation of the kinesin-1 head in neurites. We also observed kinesin-1 switching microtubules mid-walk, highlighting the potential of MINFLUX to study the details of active cellular transport.

Effect of Y2O3 Content on Microstructure and Wear Resistance of Laser Cladding Layer of Stellite-6 Alloy

Laser cladding technology is an effective surface modification technique. In order to prepare coating with excellent properties on the surface of the cold heading die punch, stellite-6 cladding coating with different proportions of Y2O3 was prepared on the surface of W6Mo5Cr4V2 high-speed steel using laser cladding technology in this paper. The effects of different Y2O3 contents on the macroscopic morphology, microstructure, phase analysis, microhardness, and tribological properties of the stellite-6 coatings were investigated. It was determined that the optimal Y2O3 content for the stellite-6 powder was 2%. The results showed that the coating with 2%Y2O3 had the least number of pores and cracks and exhibited good surface flatness when joined. The microstructure became finer and denser, composed mainly of branch, cellular, equiaxed, and columnar grains. The coating consisted mainly of γ-Co, Fe-Cr, and Co3Fe7 strengthening phases, indicating good metallurgical bonding between the coating and the substrate. The average microhardness reached 539 HV when 2%Y2O3 was added, a 15.2% increase compared with the unmodified multilayer coating. The friction coefficient of the clad layer was 0.356, a 21.8% improvement over the unmodified stellite-6 coating. The average worn area of the cross-section was 3398.35 μm2, a reduction of approximately 27.8% compared with the unmodified stellite-6 clad layer. The wear surface primarily exhibited abrasive wear, with fewer cavities and a smoother surface.

High-Performance Cobalt Chalcogenides for Oxygen Reduction Reaction

Abstract: The oxygen reduction reaction (ORR) is vital to numerous energy conversion technologies, such as fuel cells and metal-air batteries. Moreover, to enhance the overall efficacy and durability of these devices, it is crucial to develop catalysts that are both effective and economical. Among the many explored catalyst materials, cobalt chalcogenides have attracted considerable interest due to their unique properties and exceptional ORR performance. This review focuses on the synthesis methods, structural characteristics, and electrochemical performance of high-performance cobalt chalcogenides as catalysts for the ORR. In addition, the influence of various synthetic parameters on the catalytic activity and stability of cobalt chalcogenides is investigated. Also addressed are the effects of defects, doping, and surface modification on the ORR performance of cobalt chalcogenides. In addition, the use of cobalt chalcogenides in practical fuel cell devices is discussed, along with their outstanding performance as ORR catalysts in both acidic and alkaline environments. The durability and long-term stability of cobalt chalcogenides under severe operating conditions are evaluated, indicating their potential commercial applications. Finally, the field of cobalt chalcogenides for ORR challenges and prospects are outlined. This review proposes strategies for further enhancing their catalytic activity, selectivity, and durability, such as interface engineering and synergistic combinations with other catalyst materials. For researchers working on the development of next-generation ORR catalysts and the practical implementation of cobalt chalcogenides for sustainable energy applications, the insights garnered from this review are invaluable.

Cation-polymerized artificial SEI layer modified Li metal applied in soft-matter polymer electrolyte

Li metal batteries with polymer electrolyte are of great interest for next-generation batteries for high safety and high energy density. However, uneven deposition on the lithium metal surface can greatly affect battery life. Therefore, surface modification on the Li metal become necessary to achieve good performance. Herein, an artificial solid electrolyte interface (SEI) modified lithium metal anode is prepared using cation-polymerization process, as triggered by PF5 generated from CsPF6. As a result, the polarization voltage of Li||Li symmetric battery assembled with artificial SEI-modified Li metal anode was stable with a small over-potential of 25 mV after 3000 h at current density of 1.5 mA cm−2. Electrochemical performance of Li||NCM 622 (LiNi0.6Co0.2Mn0.2O2) full cell with soft-matter polymer electrolyte is significantly improved than bare Li-metal, the capacity retention is 75% after 120 cycles with N/P = 3:1 at a cut-off voltage of 4.3 V. Our work has shed lights on the commercialization of Li metal battery with polymer electrolyte.

Carbonated Beverage Chemistry for High-Voltage Battery Cathodes.

Advanced lithium-ion batteries utilize high upper cut-off voltages up to 4.8V versus lithium metal to reach extraordinary energy densities. Such a harsh environment challenges the cathode stability and requires the construction of robust cathode electrolyte interphases at their electrochemical interface. Inspired by carbonated beverages with supersaturated CO2, here, a surface modification strategy that produces effective passivation layer of low modulus from the weakest link, is proposed CO2 bubbles preferentially nucleate and grow at rough surfaces, which in oxide cathodes, are also the local regions offering fast degradation pathway. Metal ion exchange on carbonated layer assists the construction of highly elastic interface under the guidance of packing factor. This method enables surface reconstruction at both primary and secondary particle levels for various cathodes exemplified by high-voltage LiNi0.8Co0.1Mn0.1O2 (NCM811) and LiCoO2 (LCO). Remarkably, with ultra-high upper cut-off voltage of 4.8V versus Li+/Li, over 235 mAh g-1 discharge capacity, and over 900W h kg-1 discharge energy at cathode level, ≈90% capacity retention can be obtained for LiNi0.8Co0.1Mn0.1O2 over 100 cycles at 0.5 C with commercial carbonate electrolytes. This carbonated beverage chemistry is promising for constructing high-quality surface passivation in many extreme-condition applications beyond battery cathodes.

Experimental Investigation of the Impact of CO2 Injection Strategies on Rock Wettability Alteration for CCS Applications

Carbon capture and storage (CCS) has been recognized as a pivotal technology for mitigating climate change by reducing CO2 emissions. Storing CO2 in deep saline aquifers requires preserving the water-wet nature of the formation throughout the storage period, which is crucial for maintaining rock integrity and storage efficiency. However, the wettability of formations can change upon exposure to supercritical CO2 (scCO2), potentially compromising storage efficiency. Despite extensive studies on various factors influencing wettability alteration, a significant research gap remains in understanding the effects of different CO2 injection strategies on wettability in deep saline formations (DSFs). This study addresses this gap by investigating how three distinct CO2 injection strategies—continuous scCO2 injection (CCI), water alternating with scCO2 injection (WAG), and simultaneous water and scCO2 injection (SAI)—affect the wettability of gray Berea sandstone and Indiana limestone, both selected for their homogeneous properties relevant to CCS. Using a standardized sessile drop contact angle method before and after CO2 injection, along with core flooding to model the injection process at an injection pressure of 1500 psi and temperature of 100 °F with a confining pressure of 2500 psi, the results indicate a shift in wettability towards more CO2-wet conditions for both rock types under all strategies with changes in CA of 61.6–83.4° and 77.6–87.9° and 81.5–124.2° and 94.6–128.0° for sandstone and limestone, respectively. However, the degree of change varies depending on the injection strategy: sandstone exhibits a pronounced response to the CCI strategy, with up to a 77% increase in contact angle (CA), particularly after extended exposure. At the same time, WAG shows the least change, suggesting that water introduction slows surface modification. For limestone, the changes in CA ranged from 9% to 49% across strategies, with WAG and SAI being more effective in altering its wettability. This study underscores the importance of selecting suitable CO2 injection strategies based on rock type and wettability characteristics to maximize carbon storage efficiency. The findings offer valuable insights into the complex interactions of fluid–rock systems and a guide for enhancing the design and implementation of CCS technologies in various geological settings.

Recent 10-year development on surface modification of polymeric hollow fiber membranes via surface coating approach for gas separation: a review

Recent 10-year development on surface modification of polymeric hollow fiber membranes via surface coating approach for gas separation: a review

Catalyst-Enhancing Hydrothermal Carbonization of Biomass for Hydrochar and Liquid Fuel Production-A Review.

The research impact of catalysts on the hydrothermal carbonization (HTC) process remains an ongoing debate, especially regarding the quest to enhance biomass conversion into fuels and chemicals, which requires diverse catalysts to optimize bio-oil utilization. Comprehensive insights and standardized analytical methodologies are crucial for understanding HTC's potential benefits in terms of biomass conversion stages. This review seeks to understand how catalysts enhance the HTC of biomass for liquid fuel and hydrochar production, drawing from the following key sections: (a) catalyst types applied in HTC processes; (b) biochar functionality as a potential catalyst; (c) catalysts increasing the success of HTC process; and (d) catalyst's effect on the morphological and textural character of hydrochar. The performance of activated carbon would greatly increase via catalyst action, which would progress the degree of carbonization and surface modification, alongside key heteroatoms. As catalytic HTC technology advances, producing carbon materials for thermochemical activities will become more cost-effective, considering the ever-growing demands for high-performance thermochemical technologies.

Exclusion-zone water inside and outside of plant xylem vessels

The fourth phase of water has garnered increased attention within the scientific community due to its distinct properties that differentiate it from regular water. This unique state seems to arise potentially from a liquid crystalline structure, which has been observed near various hydrophilic surfaces to possess the capability of excluding microspheres. Consequently, it has been labeled as exclusion zone (EZ) water. When in contact with hydrophilic surfaces, water could exhibit the ability to form organized layers of EZ water. In this study, we investigated the quick buildup of EZ water exposed to xylem vessels of four vegetable plants: cabbage, celery, asparagus, and pumpkin. Among them, pumpkin vessels showed larger EZs, up to 240 ± 56 μm in width. The width of EZ water found near the xylem vessels of the other plants ranged from 133 ± 22 to 142 ± 20 μm. EZ water generally excludes a wide range of particles, including polystyrene microspheres with various surface modifications, as well as silica microspheres. This implies that the formation of EZ water is not an artificial result of using specific microsphere types but rather demonstrates EZ’s ability to exclude particles regardless of their composition. Inside single xylem vessels of the pumpkin, we could observe the dynamics of EZ buildup, growing from the inside edge of the vessel toward the center. The relationship between vessel diameter, vessel length, and salt concentration on EZ generation inside the xylem vessel was also explored. The results showed that EZ water can build up both inside and outside the xylem vessels. Our findings suggest that EZ generation inside xylem vessels is associated with water flow, likely driven by a proton gradient. Further research is warranted to elucidate the role of EZ water in the physiology of living plants, particularly considering the limitations of the current experiments conducted on cut-out xylem vessel samples.

Patterning of COC Polymers by Middle‐Energy Ion Beams for Selective Cell Adhesion in Microfluidic Devices

AbstractMicrofluidic devices play a crucial role in advanced cell biology applications, including cell separations, cultivations, migration and interaction studies, diagnostic devices, and organ‐on‐chips. One of the frequent purposes of such devices is the ability to selectively address the attachment of cells at defined locations on the surface. This study explores the application of middle‐energy carbon, oxygen, and nitrogen ions to locally modify the surface of cyclic olefin copolymer (COC) thermoplastic material, allowing selective cell growth on patterned polymer surfaces. The investigation considers ion element type, ion beam energy, and ion irradiation fluence, analyzing their influence on the modification effect. Characterization of the modified surfaces involves various surface‐analytical methods such as contact angle, energy dispersive spectroscopy (SEM‐EDX), atomic force microscopy (AFM), x‐ray photoelectron spectroscopy (XPS), rutherford backscattering spectrometry (RBS), and elastic recoil detection analysis (ERDA). The study extends to practical aspects, with a representative cancer cell line, MCF‐7, grown on the patterned surface to evaluate the degree of selective attachment. Additionally, the stability of the irradiated patterns is tested under elevated temperatures beyond the glass transition temperature (Tg), demonstrating the compatibility of the approach with hot embossing technology. The findings underscore the potential of ion beam treatment for COC in cell‐biology‐related applications, offering insights into surface modification techniques for enhanced functionality in microfluidic devices.