Effective Photocatalytic Degradation Research Articles

Enhanced photocatalytic degradation and synergistic effects of Tin-Doped zinc oxide nanoparticles for environmental remediation

Using zinc acetate and sodium hydroxide as starting reagents, zinc oxide nanoparticles (NPs) were constructed using a co-precipitation process. Various metal elements were incorporated into the nanocomposites. The synthesized samples underwent calcination at different temperatures for a duration of 2 h. Characterization of the samples was conducted employing XRD, SEM, EDS, and PIXE analysis. SEM imagery revealed diverse morphological alterations of ZnO after doping. The whole width at half the maximum of the XRD peaks, which indicates sizes in the nano range, was used to calculate the average crystallite sizes of the samples using Debye-Scherer’s formula. EDS analysis confirmed the production of highly pure ZnO nanostructures via this method. The synthesized bimetallic and tri-metallic NPs were utilized for the degradation of hazardous organic dyes, with the degradation process monitored using UV–visible spectroscopy. This study underscores the significance of doped ZnO NPs as effective agents for biodegradation.

Chemical bath assisted construction of CuO/BiVO4 p-n heterojunction photocatalyst for visible light driven rapid removal of MB and Cr(VI)

Nowadays, uncontrolled discharge of industrial wastes containing organic dyes, drugs, as well as heavy metals into the water bodies presents serious pollution of thereby posing threat to the environment. Hence, there is a need to adopt a targeted approach to tackle the matter of water pollution. A method photocatalytic elimination of pollutants using semiconducting materials is a captivating approach. In this study, we report simple chemical bath assisted synthesis of CuO/BiVO4 (CuBi) p-n heterojunction photocatalyst for effective photocatalytic degradation of pollutants. Physico-chemical characteristics of the CuBi composite and its individual counterparts were assessed by XRD, SEM, TEM, BET, XPS and UV–visible spectrophotometry. The CuO mico-planks, BiVO4 nanodots and CuBi composite were utilized for the photocatalytic breakdown of MB dye and Cr(VI) reduction. The CuBi p-n heterojunction demonstrated superior efficiency in degrading MB (99 % within 120 minutes) and reducing Cr (VI) (94 % within 45 minutes) when compared with its bare counterparts. Furthermore, repeating recycle studies for MB degradation and Cr(VI) reduction showed minimal loss in performance even after consecutive five cycles on the trot verified the strong photo-stability and reusability of our CuBi composite.

Novel Synthesis of MnO2-SiC Fiber-TiO2 Ternary Composite and Effective Photocatalytic Degradation with Standard Dyes

Novel Synthesis of MnO2-SiC Fiber-TiO2 Ternary Composite and Effective Photocatalytic Degradation with Standard Dyes

2D‐MXene composite systems for effective photocatalytic degradation of pharmaceutical compounds

<scp>2D</scp>‐<scp>MXene</scp> composite systems for effective photocatalytic degradation of pharmaceutical compounds

Green synthesis of biomass-derived carbon quantum dots for photocatalytic degradation of methylene blue.

Water pollution, significantly influenced by the discharge of synthetic dyes from industries, such as textiles, poses a persistent global threat to human health. Among these dyes, methylene blue, particularly prevalent in the textile sector, exacerbates this issue. This study introduces an innovative approach to mitigate water pollution through the synthesis of nanomaterials using biomass-derived carbon quantum dots (CQDs) from grape pomace and watermelon peel. Utilizing the hydrothermal method at temperatures between 80 and 160 °C over periods ranging from 1 to 24 h, CQDs were successfully synthesized. A comprehensive characterization of the CQDs was performed using UV-visible spectroscopy, Fourier-transform infrared spectroscopy, dynamic light scattering, Raman spectroscopy, and luminescence spectroscopy, confirming their high quality. The photocatalytic activity of the CQDs in degrading methylene blue was evaluated under both sunlight and incandescent light irradiation, with measurements taken at 20 min intervals over a 2 h period. The CQDs, with sizes ranging from 1-10 nm, demonstrated notable optical properties, including upconversion and down-conversion luminescence. The results revealed effective photocatalytic degradation of methylene blue under sunlight, highlighting the potential for scalable production of these cost-effective catalytic nanomaterials for synthetic dye degradation.

Construction of NaYF4:Yb,Er,Tb@NaYF4:Yb,Tb/NH2-MIL-88B(Fe) composite photocatalyst for effective photocatalytic degradation of antibiotics

Photocatalysis is an efficient and robust strategy to degrade the pollutant in the aqueous environment. However, the decomposition of antibiotics is still a perplexing problem due to the outstanding stability. To fabricate the heterogeneous photocatalyst upconversion nanoparticle (UCNPs)/metal–organic framework (MOFs) with the broadened solar light absorption, especially for the near-infrared (NIR) light, is a feasible pathway to accomplish the above goal. The heterogeneous photocatalyst, NaYF4:Yb,Er,Tb@NaYF4:Yb,Tb/NH2-MIL-88B(Fe) (ErTb@YYbTb/NMB), is firstly synthesized, in which the shell is coated along with the doped energy trapping ions to improve the upconversion efficiency. Under the simulated solar light, the degradation efficiency of ErTb@YYbTb/NMB reaches 76% for sulfamethoxazole (SMZ), 75% for ofloxacin (OFL), and 78% for norfloxacin (NOR). To elucidate the influence of energy trapping ions and coated shell, a series of UCNPs, NaYF4:Yb,Er (Er), NaYF4:Yb,Er,Tb (ErTb), NaYF4:Yb,Er,Tb@NaYF4:Yb (ErTb@YYb), and NaYF4:Yb,Er,Tb@NaYF4 (ErTb@Y) are also synthesized to compare with ErTb@YYbTb. The excellent performance of ErTb@YYbTb/NMB is attributed to the cooperation of covering the widened light spectrum, the enhanced upconversion emission intensity, and the feasible electron-hole separation, which are confirmed by the corresponding measurements including photoelectrochemical measurements, free radical and hole trapping experiments, and pump power dependence of upconversion emission intensities. Incorporation of UCNPs and MOFs to form the heterogeneous photocatalyst is a promising pathway to reach the ideal degradation goal for antibiotics.

Effects of TiO2 Nanoparticles Synthesized via Microwave Assistance on Adsorption and Photocatalytic Degradation of Ciprofloxacin.

In this study, the optimal microwave-assisted sol-gel synthesis parameters for achieving TiO2 nanoparticles with the highest specific surface area and photocatalytic activity were determined. Titanium isopropoxide was used as a precursor to prepare the sol (colloidal solution) of TiO2. Isopropanol was used as a solvent; acetylacetone was used as a complexation moderator; and nitric acid was used as a catalyst. Four samples of titanium dioxide were synthesized from the prepared colloidal solution in a microwave reactor at a temperature of 150 °C for 30 min and at a temperature of 200 °C for 10, 20, and 30 min. The phase composition of the TiO2 samples was determined by X-ray diffraction analysis (XRD) and Fourier-transform infrared spectroscopy (FTIR). Nitrogen adsorption/desorption isotherms were used to determine the specific surface area and pore size distributions using the Brunauer-Emmett-Teller (BET) method. The band-gap energy values of the TiO2 samples were determined by diffuse reflectance spectroscopy (DRS). The distribution of Ti and O in the TiO2 samples was determined by SEM-EDS analysis. The effects of adsorption and photocatalytic activity of the prepared TiO2 samples were evaluated by the degradation of ciprofloxacin (CIP) as an emerging organic pollutant (EOP) under UV-A light (365 nm). The results of the photocatalytic activity of the synthesized TiO2 nanoparticles were compared to the benchmark Degussa P25 TiO2. Kinetic parameters of adsorption and photocatalysis were determined and analyzed. It was found that crystalline TiO2 nanoparticles with the highest specific surface area, the lowest energy band gap, and the highest photocatalytic degradation were the samples synthesized at 200 °C for 10 min. The results indicate that CIP degradation by all TiO2 samples prepared at 200 °C show a synergistic effect of adsorption and photocatalytic degradation in the removal process.

Combined Effect of Adsorption and Photocatalytic Degradation Using Magnesium Oxide Nano-flowers for Tetracycline Removal

AbstractThe extensive use of antibiotics, including tetracycline (TC), has several negative impacts on ecosystems that need attention. In the present study, magnesium oxide nano-flowers (MgO NFs) were examined as an adsorbent and as a degradation photocatalyst for TC elimination. MgO NFs were characterized by XRD, UV-Vis, PL, SEM, TEM, and FTIR. Optimization of the removal process included varying the treatment time, initial pH, MgO NFs dosage, and testing with different initial TC concentrations. The highest removal efficiency (77.3%) was achieved for 50 mg/L TC using 0.6 g/L of MgO NFs at pH 9. Adsorption removal contributed to 26.0% of this removal, while 51.3% was attributed to photocatalytic removal. A one-way analysis of variance (ANOVA) revealed significant impacts of time, initial pH, MgO NFs dose, and initial TC concentrations on TC removal. Although adding different ions showed strong effects on TC adsorption on MgO NFs, those ions inhibited TC removal by about 5% after photocatalytic degradation. Adsorption data fitted well with the Langmuir isotherm and pseudo-second-order kinetic models, the adsorption process was monolayer on a homogenous surface based on chemical interactions. Based on the Langmuir-Hinshelwood model, t1/2 values ranged from 60.79 to 76.15 min for TC concentrations varying from 10 to 60 mg/L. Bacterial growth inhibition of Escherichia coli (ATCC 25,922) and Bacillus cereus (ATCC 33,019) were reduced after TC treatment. The study evidenced that using MgO NFs in photodegradation is an effective approach for TC removal from water bodies.

Size controlled synthesis of hydrous TiO2 spheres by a thiol structure directing agent and its application in photocatalysis and efficient DSSC cells

In this work, hydrated TiO2 spheres (HTS) of the submicron order have been developed. Normally, the group of amines, such as dodecylamine, hexadecylamine, methylamine, and NH3, had been the main structure-directing agents (SDAs) used in the sol–gel process to obtain monodisperse hydrated TiO2 spheres. Even though progress has been made in the synthesis of HTS, it is crucial to include new SDAs capable of synthesizing monodisperse HTS with improved or new properties for practical applications. In this work, for the first time we demonstrate that a thiol, 3-mercaptopropionic acid (MPA), can be used as an effective SDA to synthesize monodisperse hydrous TiO2 spheres with a controllable particle diameter between 150 to 950 nm. Experimental preparation parameters such as Ti concentration, [MPA]/[Ti] and [Water]/[Ti] molar ratio in the precursor solution (Titanium (IV) butoxide—MPA—ethanol—water) were thoroughly optimized to get both high yield and high monodispersity. Remarkably, a wide range in the [Water]/[Ti] molar ratio, 17 to 118, was achieved, which is much wider than the typical Rw range of the amines group of 2 to 16, thus giving more control for choosing the HTS final size. The controlled growth of hydrated TiO2 nanospheres was explained according to the LaMer and DVLO theory. To demonstrate the applicability of the HTS synthesized using MPA as SDA, the development of efficient dye-sensitized solar cells getting an energy conversion greater than 9% as well as of an effective photocatalytic degradation process of the analgesic acetaminophen under concentrated solar radiation was conducted.

Highly Effective Photocatalytic Degradation of Malachite Green Dye for Waste Water Treatment through 1T/2H MoS2 Nanoflower

Highly Effective Photocatalytic Degradation of Malachite Green Dye for Waste Water Treatment through 1T/2H MoS2 Nanoflower

Efficient photocatalytic degradation of profenofos by CuO-ZnO nanocomposite

Exposure to organophosphate pesticides, such as profenofos, poses a serious threat to humans and other living organisms and thus, it needs serious precaution measurements. Herein, we have developed bimetallic nanocomposite CuO-ZnO (2:1 ratio) with two band edges (1.60 eV and 3.1 eV) and two band potentials (1.373 eV and − 0.207 eV) as an appealing heterogeneous photocatalyst for the effective adsorption and photocatalytic degradation of profenofos at an ambient condition. The degradation process occurs rapidly, manifesting within a brief duration under light exposure. Notably, the CuO-ZnO) nanocomposite was directly subjected to the highest profenofos dose (1215 mg/L). Impressively, complete photocatalytic degradation (100 %) was achieved within just 80 min of exposure, emphasizing the efficacy of the photocatalytic process as a degradation/transformation pathway. Furthermore, a proposed degradation/transformation and mineralization pathway for the profenofos pesticide was delineated, based on results obtained from spectroscopic and chromatographic techniques. UV–visible spectrophotometric analysis tracked the degradation and transformation of profenofos (275.5 nm) to 2-chloro-3-bromo phenol (287.2 nm), while its mineralization was confirmed through NMR, ATR-IR, and GC–MS analysis. The explored catalytic activities, and degradation pathway intensely suggested that the hydroxyl radical (HO•) radicals are the central active degradation species produced through the “VB” pathway on the surface of CuO-ZnO nanocomposite.The kinetics models showed that the reaction predominantly follows second-order kinetics. Additionally, thermodynamic parameters, like enthalpy (ΔH), entropy (ΔS) and Gibbs free energy (ΔG) were evaluated, revealing the exothermic and spontaneous nature and of the reaction. Besides, CuO-ZnO nanocomposite possesses the optimal recyclability for up to seven rounds with nominal loss in the degradation efficacy and sustaining its structural features proving its robust nature towards the degradation of profenofos. Additionally, the environmental hazard posed by the profenofos pesticide, and its degradation products was assessed using the Estimation Program Interface (EPI) SuiteTM v.4.11, developed by the US Environmental Protection Agency. The estimation models affirmed that the degradation and transformation products exhibit relatively lower toxicity levels compared to profenofos.

CdS@CS/PVA inverse opal films as photocatalyst

We prepared CdS@CS/PVA inverse opal (IO) films by the colloidal photonic crystal (CPC) template method. The photonic structure of the CdS@CS/PVA IO films consists of three-dimensional periodic macropores interconnected by CS/PVA polymers. The as-prepared CdS@CS/PVA IO films were utilized as photocatalysts for the degradation of methylene blue dyes. The degradation rate of methylene blue by the CdS@CS/PVA IO film catalyst was 92%, while that of the CdS@CS/PVA film catalyst was 55% for 6 h. The photocatalytic degradation effect of the CdS@CS/PVA IO film catalyst on methylene blue is [Formula: see text]1.7 times higher than that of the CdS@CS/PVA film catalyst, which proves that the introduction of the inverse opal structure into the photocatalyst is beneficial to improve the efficiency of the photocatalyst for degrading dyes.

Synergistic adsorption and photocatalytic degradation of tetracycline using a Z-scheme kaolin/g-C3N4/MoO3 nanocomposite: A sustainable approach for water treatment

This research focuses on the synthesis and application of a novel kaolin-supported g-C3N4/MoO3 nanocomposite for the degradation of tetracycline, an important antibiotic contaminant in water systems. The nanocomposite was prepared through a facile and environmentally friendly approach, leveraging the adsorption and photocatalytic properties of kaolin, g-C3N4 and MoO3 nanoparticles, respectively. Comprehensive characterization of the nanocomposite was conducted using techniques such as X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR) and optical spectra. The surface parameters were studied using N2 adsorption-desorption isotherm. The elemental composition was studied using X-ray photoelectron spectroscopy. The efficiency of the developed nanocomposite in tetracycline degradation was evaluated and the results revealed an efficient tetracycline degradation exhibiting the synergistic effects of adsorption and photocatalytic degradation in the removal process. The tetracycline degradation was achieved in 60 min. Kinetic studies and thermodynamic analyses provided insights into the degradation mechanism, suggesting potential applications for the nanocomposite in wastewater treatment. Additionally, the recyclability and stability of the nanocomposite were investigated, demonstrating its potential for sustainable and long-term application in water treatment.

Low dose, high function: Visible light photocatalytic performance of in-situ sensitized Ti3+/Ov self-doped rutile TiO2-x nanorods with a small amount of ultrathin g-C3N4 nanosheets

Harnessing solar energy for photocatalytic sewage purification represents a significant strategy for addressing water pollution. This study focused on synthesizing ultrathin g-C3N4 nanosheets through ultrasonic refluxing g-C3N4 aggregates in a mixture of water and triethylamine. Subsequently, Ti3+/oxygen vacancy (Ov) self-doped rutile TiO2 (TiO2-x) nanorods were synthesized via an in-situ mixed solvothermal reaction. By sensitizing a minimal quantity of these ultrathin g-C3N4 nanosheets, a Z-scheme heterojunction with reduced rutile TiO2-x nanorods was achieved. Various analytical techniques were employed, including X-ray diffraction (XRD), Raman spectroscopy, Fourier transform infrared spectroscopy (FT-IR), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), ultraviolet–visible diffuse reflectance spectroscopy (UV–Vis DRS), and transient photocurrent analysis. These methods determined the phase, structure, morphology, and photoelectrochemical properties of the fabricated materials. The visible light photocatalytic performance was tested using rhodamine B, methyl orange, and Cr2O72- solutions as simulated pollutants and three distinct types of actual wastewater from a pharmaceutical factory as photocatalytic degradation object. The findings revealed that Ti3+/Ov self-doping significantly enhances the visible light responsiveness of rutile TiO2. The integration of minimal amounts of ultrathin g-C3N4 nanosheets with rutile TiO2-x nanorods, formed via an in-situ mixed solvothermal reaction, effectively promoted the separation of photogenerated electrons and holes, thereby increasing the photocatalytic efficiency. Interestingly, increasing the g-C3N4 content in the mixture led to an increase in the number of defects within TiO2-x and a reduction in crystallinity. Wastewater treatments yielded varied results: wastewater containing solely phenols underwent effective photocatalytic degradation, while samples with high salt content or complex compositions proved more challenging. This study demonstrated that the heterojunction formed by sensitizing rutile TiO2-x nanorods with a small amount of ultrathin g-C3N4 nanosheets retained remarkable photocatalytic activity. These findings offer valuable insights for the design of effective photocatalysts and their application in sewage treatment.

Effective photocatalytic degradation of antibiotic chloramphenicol and anionic direct violet 51 dye using g-C3N4 embedded NiO nanocomposite

Effective photocatalytic degradation of antibiotic chloramphenicol and anionic direct violet 51 dye using g-C3N4 embedded NiO nanocomposite

MXene/ZnS/chitosan-cellulose composite with Schottky heterostructure for efficient removal of anionic dyes by synergistic effect of adsorption and photocatalytic degradation

Nowadays, dye water pollution is becoming increasingly severe. Composite of MXene, ZnS, and chitosan-cellulose material (MX/ZnS/CC) was developed to remove anionic dyes through the synergistic effect of adsorption and photocatalytic degradation. MXene was introduced as the cocatalyst to form Schottky heterostructure with ZnS for improving the separation efficiency of photocarriers and photocatalytic performance. Chitosan-cellulose material mainly served as the dye adsorbent, while also could improve material stability and assist in generation of free radicals for dye degradation. The physics and chemistry properties of MX/ZnS/CC composite were systematically inspected through various characterizations. MX/ZnS/CC composite exhibited good adsorption ability to anionic dyes with adsorption capacity up to 1.29 g/g, and excellent synergistic effects of adsorption and photodegradation with synergistic removal capacity up to 5.63 g/g. MX/ZnS/CC composite performed higher synergistic removal ability and better optical and electrical properties than pure MXene, ZnS, chitosan-cellulose material, and MXene/ZnS. After compounding, the synergistic removal percentage of dyes increased by a maximum of 309 %. MX/ZnS/CC composite mainly adsorbs anionic dyes through electrostatic interactions and catalyzes the generation of •O2−, h+, and •OH to degrade dyes, which has been successfully used to remove anionic dyes from environmental water, achieving a 100 % removal of 50 mg/L dye.

Rational design of CdS-enwrapped polypyrrole nanoparticles for wastewater treatment: removal of hazardous pollutants in aqueous solutions.

The modern world requires a chemical industry that can run at low production costs while producing high-quality products with minimal environmental impact. The development of environmentally friendly, cost-effective, and efficient wastewater treatment materials remains a majorproblem for the sustainable approach. We prepared nanoscale cadmium sulfide (CdS)-enwrapped polypyrrole (PPy) polymer composites for degradation of organic pollutants. The prepared CdS@PPy nanocomposites were characterized by powder X-ray diffraction, scanning electron microscope (SEM), field emission scanning electron microscope (FESEM), Fourier transform infrared spectroscopy (FTIR), and ultraviolet-visible(UV) absorption spectroscopy, indicating proper intercalation between CdS and PPy. Consequently, the catalytic efficiency of the synthesized hybrid nanocomposites was analyzed through the degradation of methylene blue (MB) and rhodamine B (Rh B) under visible light irradiation. The measured degradation efficiency of the dye solutions under the photolysis process is about 18% and 23% for MB and Rh B dye, respectively. Furthermore, the recycle test result concludes that the CdS@PPy composite exhibits 91% and 89% of MB and Rh B dye degradation efficiency even at the 4th cycle, respectively. The positive synergistic impact of CdS and PPymay be the result of effective photocatalytic degradation of MB and RhB.

Construction of BiOCl/bismuth-based halide perovskite heterojunctions derived from the metal-organic framework CAU-17 for effective photocatalytic degradation

The designed synthesis of an S-scheme heterojunction has possessed a great potential for improving photocatalytic wastewater treatment by demonstrating increased the photoredox capacity and improved the charge separation efficiency. Here, we introduce the fabrication of a heterojunction-based photocatalyst comprising bismuth oxychloride (BiOCl) and bismuth-based halide perovskite (BHP) nanosheets, derived from metal-organic frameworks (MOFs). Our composite photocatalyst is synthesized through a one-pot solvothermal strategy, where a halogenation process is applied to a bismuth-based metal-organic framework (CAU-17) as the precursor for bismuth sourcing. As a result, the rod-like structure of CAU-17 transforms into well-defined plate and nanosheet architectures after 4 and 8 h of solvothermal treatment, respectively. The modulation of the solvothermal reaction time facilitates the establishment of an S-scheme heterojunction, resulting in an increase in the photocatalytic degradation efficiency of rhodamine B (RhB) and sulfamethoxazole (SMX). The optimized BiOCl/BHP composite exhibits superior RhB and SMX degradation rates, achieving 99.8% degradation of RhB in 60 min and 75.1% degradation of SMX in 300 min. Also, the optimized BiOCl/BHP composite (CAU-17-st-8h sample) exhibited the highest rate constant (k = 3.48 × 10−3 min−1), nearly 6 times higher than that of the bare BHP in the photocatalytic degradation process of SMX. The enhanced photocatalytic efficiency can be endorsed to various factors: (i) the in-situ formation of two-components BiOCl/BHP photocatalyst, derived from CAU-17, effectively suppresses the aggregation of pristine BHP and BiOCl particles; (ii) the S-scheme heterostructure establishes a closely-knit interfacial connection, thereby facilitating efficient pathways for charge separation/transfer; and (iii) the BiOCl/BHP heterostructure enhances its capacity to absorb visible light. Our investigation establishes an effective strategy for constructing heterostructured photocatalysts, offering significant potential for application in photocatalytic wastewater treatment.

Modulating of Bi2MoO6-based photocatalyst through manipulation of reactant ratios for enhanced visible light photocatalytic activity

In this work, a novel photocatalyst, comprising of Bi2MoO6 and Bi2O2(OH)(NO3), was successfully synthesized by the one-pot hydrothermal method, thereby illuminating an innovative avenue for structure modulation of Bi2MoO6. The characterizations proved the facile attainability of controllable modifications in the microstructure and morphology of Bi2MoO6. The comprehensive appraisal of the synergistic adsorption-photocatalytic performances of the composites in the context of ciprofloxacin (CIP) was carried out. The findings presented compelling evidence that the amalgamation of Bi2MoO6/Bi2O2(OH)(NO3) exhibited an extraordinary adsorption capacity and photocatalytic activity when compared with the pristine Bi2MoO6 and Bi2O2(OH)(NO3). By virtue of its high surface area and pore volume, the optimized BMO/BON manifested a CIP adsorption capacity that surpassed that of Bi2MoO6 and Bi2O2(OH)(NO3) by approximately 2.4 and 11.2 times, respectively. Furthermore, through the concerted effects of adsorption and photocatalytic degradation, BMO/BON demonstrated an impressive CIP removal efficiency of 99.2 % following a mere 30 min of visible light exposure. The reaction rate constant was found to be approximately 0.124 min−1 for BMO/BON, surpassing that of Bi2MoO6 and Bi2O2(OH)(NO3). The augmentation in the photocatalytic activity of BMO/BON can be ascribed to its diminutive crystalline dimensions, large specific surface area, and narrowed bandgap. Thus, this investigation introduces a practical and ingenious strategy for the tuning of the Bi2MoO6 structure by manipulation of reactant ratios, showcasing significant implications in the realm of catalysis.

Nanotransfer Printing of Functional Nanomaterials on Electrospun Fibers for Wearable Healthcare Applications

AbstractWith the advancement of functional textile technology, there is a growing demand for functional enhancements in textiles from both industrial and societal perspectives. Recently, nanopattern transfer technology has emerged as a potential approach for fabricating functional textiles. However, conventional transfer methods have some limitations such as transfer difficulties on curved fiber surfaces, polymer residues, and delamination of transferred nanopatterns. In this study, an advanced nanopattern transfer method based on surface modification and thermoforming principles is applied to microscale electrospun fibers. This transfer method utilizes covalent bonding and mechanical interlocking between nanopatterns and the fibers without requiring extra adhesives. Various nanopatterns transferred electrospun fibers possess significant potential for diverse wearable healthcare applications. This work introduces two specific application scenarios in the field of wearable healthcare, both of which leverage the light: diagnostics and antimicrobials. Versatile textile with silver nanogap‐pattern detects glucose in sweat, diagnosing hypoglycemia and diabetes by shifting Raman peaks from 1071.0 to 1075.4 cm−1 for 0 to 150 µm glucose. Additionally, a bactericidal mask using visible light to induce the photocatalytic degradation effect of titanium dioxide and silver nanopatterns is developed. Bactericidal efficacy against Escherichia coli and Staphylococcus aureus is 99.9% due to photolysis from visible light irradiation.