Surface Functionalization Research Articles

Innovative TiO2 Photocatalysts: Advances and Strategies for Enhanced Hydrogen Evolution Efficiency

As a photocatalyst, titanium dioxide (TiO2) has attracted a lot of interest because of its remarkable qualities, including stability, affordability, and environmental friendliness. The latest developments in TiO2-based photocatalysts are examined in this thorough overview, along with cutting-edge methods for increasing their effectiveness in a range of photocatalytic applications. The article discusses developments in TiO2 modifications, such as surface functionalization, heterostructure, and doping, to increase charge separation, broaden the range of light absorption, and boost catalytic performance in general. Additionally, new methods for creating TiO2 and how they affect photocatalytic activity are covered. The paper highlights the diverse possibilities of TiO2-based photocatalysts in tackling modern issues by outlining applications ranging from solar fuel production to environmental remediation.

Carbon-based nanocomposites for sensing applications-a review

Abstract Carbon-based nanomaterials exhibit unique morphological and physical properties. When used as fillers in various matrices such as polymers, they can provide enhanced electrical, thermal and mechanical characteristics. The emerging field of sensing technologies has witnessed remarkable advancements, resulting from the integration of carbon-based nanocomposites. This paper presents a comprehensive review of the latest developments in key carbon-based nanocomposite sensors. First, the unique properties of carbon nanomaterials are reviewed covering the full dimensional spectrum, followed by main synthesis routes addressing critical aspects such as morphology, surface functionalization, and doping strategies. Later, the synergistic effects arising from the combination of carbon nanomaterials with other components, such as polymers, are explored in detail, emphasizing the role of percolation levels in the overall sensing performance. The different sensing applications presented in this review cover a broad range, including strain, temperature, gas and biosensing. The mechanisms and principles governing the sensing capabilities of carbon-based nanocomposites are provided, shedding light on the interactions between analytes and nanocomposite surfaces. A critical analysis of current challenges and prospects is also presented, outlining potential avenues for further research and innovation. Finally, this review aims to serve as a valuable resource for researchers interested in carbon-based nanocomposites and their evolving role in advancing sensing technologies.

Synthesis and Biomedical Applications of Covalent Organic Frameworks for Disease Diagnosis and Therapy

Covalent organic frameworks (COFs) have emerged as a distinguished class of porous materials. Owing to their ability to be constructed through covalent bonds involving light elements, such as hydrogen, boron, carbon, nitrogen, and oxygen, COFs offer greater stability and lower cytotoxicity than metal organic frameworks do, addressing critical limitations in in vivo applications. Their unique attributes, such as high surface area, customizable pore sizes, and versatile surface functionalities, make them ideal for various biomedical applications. This review aims to provide an overview of the recent advancements in modern COFs for biomedical uses. First, a variety of methods for the synthesis of COFs are outlined, which ensures their suitability for medical use. Next, we delve into innovative biomedical applications, emphasizing their role in disease diagnostics and therapies. Finally, challenges, such as clinical translation, biocompatibility, and controlled drug release, are critically discussed, providing comprehensive insight into the potential of COFs in revolutionizing biomedical technologies. Overall, this review offers a comprehensive overview of COFs' capabilities and future prospects in enhancing biomedical technologies.

Covalent Surface Functionalization of Exfoliated MoS2 Nanosheets for Improved Electrocatalysis

Covalent Surface Functionalization of Exfoliated MoS₂ Nanosheets for Improved Electrocatalysis

Synthesis, Functionalization, and Biomedical Applications of Iron Oxide Nanoparticles (IONPs)

Iron oxide nanoparticles (IONPs) have garnered significant attention in biomedical applications due to their unique magnetic properties, biocompatibility, and versatility. This review comprehensively examines the synthesis methods, surface functionalization techniques, and diverse biomedical applications of IONPs. Various chemical and physical synthesis techniques, including coprecipitation, sol–gel processes, thermal decomposition, hydrothermal synthesis, and sonochemical routes, are discussed in detail, highlighting their advantages and limitations. Surface functionalization strategies, such as ligand exchange, encapsulation, and silanization, are explored to enhance the biocompatibility and functionality of IONPs. Special emphasis is placed on the role of IONPs in biosensing technologies, where their magnetic and optical properties enable significant advancements, including in surface-enhanced Raman scattering (SERS)-based biosensors, fluorescence biosensors, and field-effect transistor (FET) biosensors. The review explores how IONPs enhance sensitivity and selectivity in detecting biomolecules, demonstrating their potential for point-of-care diagnostics. Additionally, biomedical applications such as magnetic resonance imaging (MRI), targeted drug delivery, tissue engineering, and stem cell tracking are discussed. The challenges and future perspectives in the clinical translation of IONPs are also addressed, emphasizing the need for further research to optimize their properties and ensure safety and efficacy in medical applications. This review aims to provide a comprehensive understanding of the current state and future potential of IONPs in both biosensing and broader biomedical fields.

Surface Functionalized Plasmonic Sensors for Uric Acid Detection With Gold-Graphene Stacked Nanocomposites

Abstract This study presented a surface-functionalized sensor probe using 3-aminopropyltriethoxysilane (APTES) self-assembled monolayers on a Kretschmann-configured plasmonic platform. The probe featured stacked nanocomposites of gold (via sputtering) and graphene quantum dots (GQD, via spin-coating) for highly sensitive and accurate uric acid (UA) detection within the physiological ranges. Characterization encompassed the field emission scanning electron microscopy for detailed imaging, energy-dispersive X-ray spectroscopy for elemental analysis, and Fourier transform infrared spectroscopy for molecular identification. Surface functionalization increased sensor sensitivity by 60.64%, achieving 0.0221 °/(mg/dL) for the gold-GQD probe and 0.035 5 °/(mg/dL) for the gold-APTES-GQD probe, with linear correlation coefficients of 0.8249 and 0.8509, respectively. The highest sensitivity was 0.070 6 °/(mg/dL), with a linear correlation coefficient of 0.993 and a low limit of detection of 0.2 mg/dL. Furthermore, binding affinity increased dramatically, with the Langmuir constants of 14.29 µM−1 for the gold-GQD probe and 0.000 1 µM−1 for the gold-APTES-GQD probe, representing a 142 900-fold increase. The probe demonstrated notable reproducibility and repeatability with relative standard deviations of 0.166% and 0.013%, respectively, and exceptional temporal stability of 99.66%. These findings represented a transformative leap in plasmonic UA sensors, characterized by enhanced precision, reliability, sensitivity, and increased surface binding capacity, synergistically fostering unprecedented practicality.

Construction of a MoOx/MoS2 Heterojunction via the Surface Sulfurization of the Oxide and Its Photocurrent-Switching Characteristics in the Range of the Broadband Light Spectrum

In order to utilize the longer wavelength light, the surface sulfurization of MoO3 was carried out. The photocurrent responses to typical 650, 808, 980, and 1064 nm light sources with Au gap electrodes were investigated. The results showed that the surface S–O exchange of MoO3 improved the interfacial charge transfer in the range of the broadband light spectrum. The S and O can be exchanged on the surface of MoO3 nanosheets under the hydrothermal condition, leading to the formation of a surface MoOx/MoS2 heterojunction. The interfacial interaction between the MoO3 nanosheets and MoS2 easily generated free electrons and holes, and it effectively avoided the recombination of photogenerated carriers. Meanwhile, the surface S-doping of MoO3 also resulted in the generation of an oxygen vacancy and sulfur vacancy on MoO3−xS2−y. The plasmonic characteristics of MoO3−x contributed to the enhancement of the interfacial charge transfer by photoexcitation. Otherwise, even with zero bias applied, a good photoelectric signal was still obtained with polyimide film substrates and carbon electrodes. This indicates that the formation of the heterojunction generates a strong built-in electric field that drives the photogenerated carrier transport, which can be self-powered. This study provides a simple and low-cost method for the surface functionalization of some metal oxides with a wide bandgap.

Tuning properties of binary functionalization of Sc2C MXenes for supercapacitor electrodes

Surface functionalization of two-dimensional (2D) materials like Sc2C MXenes offers a promising avenue for tailoring their properties for various applications. At the same time, significant research has focused on pure terminations involving oxygen (-O), fluorine (-F), or hydroxyl (-OH) groups. Binary surface functionalization still needs to be explored. Our work addresses this gap by investigating binary functionalized Sc2C monolayers, specifically Sc2CFN and Sc2COS. Using first-principles calculations, we explore the structural, electronic, and quantum capacitance (CQ) properties of pristine Sc2C and functionalized Sc2CFN and Sc2COS. The CQ measurements reveal distinctive electronic behaviour, with Sc2CFN and Sc2COS exhibiting indirect bandgaps of 0.90 and 1.48 eV, respectively. Introducing functional groups induces a metal-to-semiconductor transition, enhancing charge storage at the cathode and increasing the CQ to 371.64 and 341.23 μF/cm2 for Sc2CFN and Sc2COS, respectively. As far as energy applications are concerned, we also calculate the Shockley-Queisser (SQ) efficiency, which is a widely accepted quantity to get an estimate of the photovoltaic efficiency of 28.77 % for Sc2CFN and 32.97 % for Sc2COS materials. Additionally, we analyze the current-voltage (IV) characteristics, uncovering negative differential conductance (NDC) effects in Sc2COS, indicative of its potential for fast molecular switching applications. Our study provides valuable insights into the properties of binary functionalized Sc2C MXenes, paving the way for their utilization in energy storage and nanoelectronic devices.

Graphene‐based Supercapacitor Using Microemulsion Electrolyte

AbstractGraphene‐like material prepared by a facile combustion synthesis was investigated as an electrode material in a microemulsion electrolyte. Notably, a stable voltage window of 2.2–2.4 V was achieved, surpassing previous reports for aqueous‐based electrolytes on similar materials. The fabricated supercapacitor device exhibited a commendable specific capacitance values of 59 F g−1 at 0.1 A g−1 and 32 F g−1 at 5 A g−1, indicating its potential for high‐current applications. Mechanistic examination revealed that the charge storage primarily relies on electric double‐layer formation, with minor non‐capacitive contribution from electrode surface functionalities and the supporting electrolyte. Further analysis showed significant capacitive contributions of 85 % at 2.2 V and 67 % at 2.4 V, underscoring the dominance of the capacitive process. The fabricated supercapacitor's stability indicated a decrease as the non‐capacitive process intensified, suggesting that electrode surface functionalities predominantly contribute to cell deterioration at elevated potentials. These results highlight the potential efficacy of microemulsion electrolytes in energy storage applications.

A biomimetic approach towards a universal slippery liquid infused surface coating

One biomimetic approach to surface passivation involves a series of surface coatings based on the slick surfaces of carnivorous pitcher plants (Nepenthes), termed slippery liquid-infused porous surfaces (SLIPS). This study introduces a simplified method to produce SLIPS using a polydopamine (PDA) anchor layer, inspired by mussel adhesion. SLIPS layers were formed on cyclic olefin copolymer, silicon, and stainless steel substrates, by first growing a PDA film on each substrate. This was followed by a hydrophobic liquid anchor layer created by functionalizing the PDA film with a fluorinated thiol. Finally, perfluorodecalin was applied to the surface immediately prior to use. These biomimetic surface functionalization steps were confirmed by several complimentary surface analysis techniques. The wettability of each surface was probed with water contact angle measurements, while the chemical composition of the layer was determined by X-ray photoelectron spectroscopy. Finally, ordering of specific chemical groups within our PDA SLIPS layer was determined via sum frequency generation spectroscopy. The hemocompatibility of our new PDA-based SLIPS coating was then evaluated by tracking FXII activation, fibrin generation time, clot morphology, and platelet adhesion to the surface. This hemocompatibility work suggests that PDA SLIPS coatings slow or prevent clotting, but the observation of both FXII activation and the presence of adherent and activated platelets at the PDA SLIPS samples imply that this formulation of a SLIPS coating is not completely omniphobic.

Controllable Graphene/MoS2 Heterointerfaces by Perpendicular Surface Functionalization.

Surface chemistry and interface interactions profoundly influence the properties of two-dimensional (2D) materials and heterostructures. Therefore, developing methods to precisely control surfaces and interfaces is crucial for harnessing the properties and functions of 2D materials and heterostructures. Here, we developed a facile approach to tuning the interface distance and properties of graphene/MoS2 heterostructures (G/MoS2) by varying the functional groups attached to the surface of graphene bottom layer. We systematically investigated how different functionalized graphene bottom layers affect the interlayer distance, coupling between the interlayers, and optical properties of resulting G/MoS2 heterostructures. Our findings indicate that both the size and electron-withdrawing/donating properties of functional groups are pivotal in regulating charge transport properties, with size playing a particularly decisive role. Our approach demonstrates an efficient and flexible pathway to regulate the interlayer spacing and charge transport, highlighting the potential of engineering interface chemistry in optimizing properties of van der Waals heterostructures.

Controllable Graphene/MoS2 Heterointerfaces by Perpendicular Surface Functionalization

Controllable Graphene/MoS2 Heterointerfaces by Perpendicular Surface Functionalization

7-axis synchronization-integrated on-the-fly laser texturing system of freeform surface: design and development

Abstract While laser surface texturing (LST) is a promising manufacturing technique for surface functionalization, simultaneously realizing high precision and high efficiency in the LST of complex curved surface is challenging, due to continuously varied geometries of laser-matter incidence. In the present work, we propose a novel manufacturing system of 7-axis on-the-fly LST for complex curved surface, based on the integrated synchronization of 5-axis linkage motion platform with 2-axis galvanometer. Specifically, the algorithm for decomposing spatial texture trajectory on curved surface into low-frequency and high-frequency parts is established, based on which the kinematic model of synchronized 7-axis system is developed to derive the motion of each axis in both 5-axis linkage motion platform and 2-axis galvanometer simultaneously. Subsequently, the synchronized 7-axis LST system is experimentally realized, including the setup of mechanical stages integrated with optical path, the configuration of numerical control unit, and the development of processing software. Finally, case study of 7-axis on-the-fly LST of freeform aluminum surface is performed, and the advantages in terms of processing efficiency and texturing accuracy over 5-axis linkage LST are demonstrated. The correlation of reduced following errors between mechanical stages with the promoted performance of curved surface texturing by the 7-axis on-the-fly LST is further analyzed. Current work provides a feasible solution for establishing the manufacturing system for high performance LST of complex curved surface.

Thrombin Immobilized Hemocompatible Radiopaque Polyurethane Microspheres for Topical Blood Coagulation.

Over the past decade, there has been growing interest in developing microspheres for embolization procedures. However, the lack of noninvasive monitoring of the embolic agents and the occurrence of reflux phenomenon leading to unintentional occlusions has raised concerns regarding their compatibility/suitability for embolization therapy. Here we report the development of specialty microspheres having intrinsic radiopacity and surface functionality to tackle the existing complications that pave the way for more advanced solutions. To achieve the above goal, an iodinated monomer, termed "IBHV," capable of imparting radiopacity and functionality, was synthesized and used as a chain extender to make radiopaque polyurethane. Microspheres with a smooth surface and an average diameter of 474 ± 73 μm were fabricated from this polyurethane. The microspheres obtained were noncytotoxic, had a permissible hemolysis rate, and showed better traceability on x-ray imaging. Subsequent immobilization of thrombin onto microspheres improved their hemostatic effect. This study demonstrated that immobilization of thrombin would lead to microspheres with unique traits of radiopacity and hemostatic properties, which will undoubtedly enhance embolization efficiency.

Advancements in Tumor Diagnostics through Carbon Dot‐Assisted Photoacoustic Imaging

AbstractSerendipitously discovered, carbon dots (CDs) have attracted significant attention as a potential contrast agent for photoacoustic imaging (PAI) in the biomedical sector. CDs play an essential role in PAI, contributing significantly to the early detection of diseases and monitoring treatment progress, particularly in tumor imaging. This review emphasizes the role of CDs in the domain of PAI, highlighting their characteristics like biocompatibility, enhanced spatial resolution, optical absorption in the NIR region, and facile surface functionalization for tumor‐ targeted imaging. The study explores the use of CDs for enhancing spatial resolution in PAI for improved detection and visualization of tumors in organs such as the breast, cervical, liver, gastrointestinal, skin, cardiovascular system, nervous system, and others. Challenges associated with PAI, such as optimizing the signal‐to‐noise ratio and ensuring stability under physiological conditions, have also been discussed.

Unlocking the Trade-off Between Intrinsic and Interfacial Thermal Transport of Boron Nitride Nanosheets by Surface Functionalization for Advanced Thermal Interface Materials.

The increasing computing power of AI presents a major challenge for high-power chip solution and heat dissipation. Boron nitride nanosheet-based thermal interface materials (BNNS-based TIMs) exhibit excellent electrical insulation property, ensuring the secure and stable operation of chips. However, the efficiency of micro/nano interfacial thermal transport is limited, impeding further enhancements in the thermal conductivity (TC) of BNNS-based TIMs. Here, a strategy of surface functionalization is reported to unlock the trade-off between the intrinsic and interfacial thermal transport of BNNS within TIMs. These results suggest that the surface functionalization maintains the intrinsic high TC of BNNS while significantly increasing binding energy between micro/nano interfaces in BNNS-based TIMs, effectively reducing interfacial thermal resistance of BNNS joint interfaces and interfaces between BNNSs and the matrix by 50% and 26.1%, respectively. The BNNS-based TIMs exhibit excellent TC (≈21-25W/(m·K)) and ultralow Young's modulus, which can promote the development of flexible high-performance chip cooling technology in the AI industry.

Tailoring Carbon Nanostructure for Selective Guar Gum Conversion: Unveiling the Interplay between Structure and Surface Functionalities in Galactose and Mannose Production

Tailoring Carbon Nanostructure for Selective Guar Gum Conversion: Unveiling the Interplay between Structure and Surface Functionalities in Galactose and Mannose Production

MgAl-Layered Double Hydroxide-Coated Bio-Silica as an Adsorbent for Anionic Pollutants Removal: A Case Study of the Implementation of Sustainable Technologies

The adsorption efficiency of Cr(VI) and anionic textile dyes onto MgAl-layered double hydroxides (LDHs) and MgAl-LDH coated on bio-silica (b-SiO2) nanoparticles (MgAl-LDH@SiO2) derived from waste rice husks was studied in this work. The material was characterized using field-emission scanning electron microscopy (FE-SEM/EDS), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopic (XPS) techniques. The adsorption capacities of MgAl-LDH@SiO2 were increased by 12.2%, 11.7%, 10.6%, and 10.0% in the processes of Cr(VI), Acid Blue 225 (AB-225), Acid Violet 109 (AV-109), and Acid Green 40 (AG-40) dye removal versus MgAl-LDH. The obtained results indicated the contribution of b-SiO2 to the development of active surface functionalities of MgAl-LDH. A kinetic study indicated lower intraparticle diffusional transport resistance. Physisorption is the dominant mechanism for dye removal, while surface complexation dominates in the processes of Cr(VI) removal. The disposal of effluent water after five adsorption/desorption cycles was attained using enzymatic decolorization, photocatalytic degradation of the dyes, and chromate reduction, satisfying the prescribed national legislation. Under optimal conditions and using immobilized horseradish peroxidase (HRP), efficient decolorization of effluent solutions containing AB-225 and AV-109 dyes was achieved. Exhausted MgAl-LDH@SiO2 was processed by dissolution/precipitation of Mg and Al hydroxides, while residual silica was used as a reinforcing filler in polyester composites. The fire-proofing properties of composites with Mg and Al hydroxides were also improved, which provides a closed loop with zero waste generation. The development of wastewater treatment technologies and the production of potentially marketable composites led to the successful achievement of both low environmental impacts and circular economy implementation.

Clickable Plastic Surfaces with Controllable Azide Surface Density

AbstractThis study investigates the surface functionalization of plastic substrates through dip‐coating in azide‐functionalized polymer solutions, followed by a click reaction (i.e., strain‐promoted azide–alkyne cycloaddition). Acrylic, poly(ethylene terephthalate) (PET), and nylon substrates are dip‐coated with a series of polymers containing various azide groups grafted onto the poly(methyl methacrylate‐co‐hydroxyethyl methacrylate) backbone to examine structural effects on the surface density of clickable azide groups. X‐ray photoelectron spectroscopy and fluorescence spectroscopy confirm the subsequent click‐immobilization of cycloalkyne‐tagged fluorescein, which is quantified to calculate the surface density of clickable azide groups. Further investigations demonstrate that the surface density of azide groups can be controlled by manipulating the polymer ratio during dip‐coating, thus enabling the preparation of a linear surface gradient in terms of azide group density. Finally, the microcontact printing (µCP) method is employed to pattern the functionalized surfaces and quantify the functional molecules immobilized on the surface by µCP. This study highlights the adaptability of click chemistry and polymer coating techniques for the advanced functionalization of plastic surfaces for materials science and engineering applications.

Harnessing visible light for sustainable biodiesel production with Ni/Si/MgO photocatalyst

Sustainable energy sources frequently demonstrate greater reliability and resilience in comparison to conventional energy sources. Biodiesel, with its markedly reduced carbon footprint when compared to petroleum-based diesel fuel, owes this advantage to its production from renewable resources. Heterojunction photocatalysts have gained significant interest due to their immense promise in tackling environmental challenges. In this study, a highly efficient photocatalyst, Ni/Si/MgO, for biodiesel production under visible light irradiation was synthesized using a solid-phase reaction method with silica as the silicon source, along with Ni and MgO. The surface functionality of Ni/Si/MgO was crucial for achieving high efficiency of photocatalytic systems, as evident from XPS. The transesterification reaction on the Ni/Si/MgO photocatalyst proceeds by the formation of SiH and SiOH bonds over the catalyst. The photocatalytic activities of Ni/Si/MgO photocatalysts were higher than those of the Si/MgO nanoparticle when exposed to light. Achieving an optimal yield of 98 %, the biodiesel production was carried out under the following reaction conditions: A catalyst dosage of 2 % by weight was utilized, along with a methanol-to-oil molar ratio of 12:1, and the entire procedure was executed within a duration of 3.5 h. Plasmonic near-fields are speculated to be responsible for the increased transesterification activity along the Ni/Si/MgO interface. In order to carry out the transesterification reaction, electron-hole pairs are generated along the Ni/Si/MgO interface, where plasmonic near-fields are highly concentrated. This study contributes a significant perspective on mechanisms governing the process of efficient plasmonic photocatalysis responsive to visible light. These findings hold the potential to offer valuable guidance in the formulation and design of next-generation, high-performance photocatalysts.