Photocatalytic Effect Research Articles

Bi-ZFO/BMO-Vo Z-scheme heterojunction photocatalysis-PMS bidirectionally enhanced coupling system for environmental remediation

Given the urgency of organic pollutant removal and the low efficiency of advanced oxidation processes (AOPs), a novel Bi-ZFO/BMO-Vo photocatalyst was fabricated via the solvothermal method. A coupling system was constructed to combine photocatalysis with peroxymonosulfate (PMS) oxidation processes, which synergistically degrade organic pollutants. Bi-ZFO/BMO-Vo exhibited excellent photocatalytic performance, which could remove 100 % RhB in 110 min and degrade 100 % MG in 70 min, and 88 % H-TC in 50 min. The excellent catalytic performance of Bi-ZFO/BMO-Vo was not only attributed to the synergistic effect of PMS activation and photocatalysis, but also attributed to the SPR effect of Bi nanoparticles, electron capture of oxygen vacancies, and intense contact of Bi-ZFO/BMO-Vo heterojunctions. The active species capture experiments and EPR tests indicated that 1O2, SO4–·, ·OH, and O2–· worked together for the RhB removal. The degradation intermediates of RhB were identified by LC-MS. Based on the experimental results, the band structure and Z-scheme charge transfer mechanism were proposed. Toxicity evaluation indicated that Bi-ZFO/BMO-Vo-Vis/PMS could significantly reduce RhB toxicity. This efficient and stable catalyst is expected to be used in organic wastewater degradation and practical applications.

The Synthesis of Ag/TiO2 via the DC Magnetron Sputtering Method and Its Application in the Photocatalytic Degradation of Methyl Orange in Na2SO4 Solution

TiO2 and TiO2 films modified with Ag (Ag/TiO2) were prepared via the DC magnetron sputtering method and the degree of modification was controlled via the sputtering power and time of Ag. The microstructures and properties of these films were characterized using field emission scanning electron microscopy, X-ray diffractometry, ultraviolet–visible diffuse reflectance spectrometry, atomic force microscopy, and X-ray photoelectron spectroscopy (XPS). The results show that the prepared films have an anatase structure. Compared with pure TiO2, Ag deposition can improve the utilization of light. The three-dimensional images of Ag/TiO2 clearly show that with the increase in Ag sputtering power and sputtering time, Ag particles on the surface of the film gradually increase, and the structure of the film is relatively dense. The photocatalytic effect of Ag/TiO2 films is the best when the Ag sputtering power is 5 W and the sputtering time is 50 s. Under high-pressure mercury lamp irradiation, the photocatalytic degradation rate of methyl orange (MO) in pure MO solution with Ag/TiO2-5 W-50 s can reach 100% within 55 min, whereas that in MO-Na2SO4 mixed solution can reach 99.55% within 65 min. The results suggest that the presence of Na2SO4 in MO solution can inhibit the degradation of MO using Ag/TiO2, the result of XPS suggests that Na2SO4 accelerates the oxidation of Ag, which may lead to an increase in the recombination rate of photogenerated electron–hole pairs and a decrease in the degradation rate. During the process of recycling photocatalysts, the degradation rate of MO was apparently reduced. A possible reason is that the Ag particles have been oxidized and products of photocatalytic degradation are on the surface of the photocatalyst. The photocatalytic degradation mechanism was studied.

Enhancing performance of SnS2 based self-powered photodetector and photocatalyst by Na incorporation

Sn and S are environmentally friendly elements that are abundant in nature. The SnS2 compound formed with these elements has intrinsic n-type electrical conductivity and a direct forbidden band gap of ∼2.2 eV. Therefore, it is a very promising compound for visible light optoelectronic applications. In this study, SnS2thin films were coated on p-Si substrates and pn heterojunction structures were obtained. By adding certain amounts of Na element to SnS2, the photosensitivity of the heterojunction devices increased tremendously and reached a high value of 3.2 × 104 under zero bias condition. It was observed that the prepared devices had excellent speeds and stability with rise and decay times of as low as 28 m s and 23 m s. Moreover, the devices were found to be sensitive to visible light even at ultra-low light intensity of ∼0.3 μW/cm2. Furthermore, the responsivity and specific detectivity values of the prepared photodetectors reach very high values of 11 A/W and 8.4 × 1013 Jones at this low light intensity. The NEP value drops to a low level of 2.7 × 10−15 WHz −1/2. In addition, the photocatalytic properties of Na-doped and undoped SnS2 compound were also examined under visible LED light. Compared to undoped samples, photocatalytic efficiency increased by ∼42 % in Na-doped SnS2 thin films. The findings clearly reveal that Na improves both photodetector device performance and the photocatalytic effect of the SnS2 semiconductor.

A photothermal assisted zinc-air battery cathode based on pyroelectric and photocatalytic effect

Zinc–air battery as one of the new generations of battery system, its theoretical specific energy is as high as 1086 Wh kg−1, specific capacity up to 820 mAh/g, and zinc has the advantages of environmental friendliness, resource abundance, low cost and good safety, so it has attracted much attention. However, due to its slow reaction kinetic process, zinc–air battery will produce a large charging overpotential usually up to 2 V, it is far beyond the theoretical voltage of 1.65 V, so reducing the overpotential of zinc–air batteries is extremely necessary, and the most common way to solve this problem is to use excellent catalyst cathode to improve the oxygen reduction and oxygen evolution kinetics of zinc–air batteries. So we developed a new photothermal assisted zinc–air battery system with Hollow carbon nanosphere@poly (vinylidene fluoride-trifluoroethylene-chlorofluoroethylene)@CdS(HCN@PVTC@CdS) photocathode, the pyroelectric and photocatalysis effect can effectively promote the reaction kinetics and reduce the reaction overpotential. With the pyroelectric and photocatalysis synergistic effect, the zinc–air has displayed a high discharge potential of 1.33 V and a low charging potential of 1.5 V with good cycle stability. This multi-assist technology with built-in electric and light fields paves the way for the development of high-performance zinc–air batteries and other energy storage systems.

Enhancing the Production of Eco-Friendly Silk Fabrics through the Application of Nonthermal Plasma Wettability Techniques.

The combination of the effects of nonthermal plasma using atmospheric pressure of plasma jet and the photocatalytic effects of titanium dioxide nanoparticles was used to study the plasma flow modes, electrical characteristics, nonthermal characteristics, antimicrobial measurements, and surface modifications. Using different wettabilities of argon discharges in a laminar flow: (i) wet I, wettability with 2.4 slm argon mixture with oxygen ratio O2, equivalent to 15 mslm (Ar/O2), and (ii) wet II, wettability (Ar/O2) mixture combined with titanium dioxide, to accelerate the inactivation process on the nonwoven fabric surface. For wet 0, wet I, and wet II discharges, the average rate of heat transfer to the nonwoven silk fabric increased significantly. Specifically, it goes from 104.6 to 118.6 and then to 241.7 mW, respectively. The kinetic deactivation rate of Escherichia coli increases starting at 0.20, then going up to 0.32, and finally reaching 0.57 min-1. The increased wettability of the TiO2 photocatalyst results in an enhanced bactericidal rate, which is caused by both the heat impact from the nonthermal jet and potentially photocatalytic disinfection, leading to the generation of active species. The mechanical parameters owing to different wettabilities and plasma interactions with the fabric membrane were tested for the treated samples, such as stiffness, ultimate yield strength, tensile strength, strain, hardening, elongation, resilience, and toughness.

Synergistic photocatalytic removal of moxifloxacin from aqueous solutions using ZnO-Fe3O4-chitosan composites

The escalating contamination of water bodies with antibiotic residues is an urgent environmental and public health issue. This study aimed to fabricate an innovative photocatalytic composite (CMZ) by combining chitosan, magnetic iron oxide (Fe3O4), and zinc oxide (ZnO) for efficiently removing antibiotic moxifloxacin (MFX) water. Comprehensive characterization of the fabricated CMZ was performed using various techniques such as X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), Raman spectroscopy, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), ultraviolet–visible diffuse reflectance spectroscopy (UV–Vis DRS), photoluminescence spectroscopy (PL) and nitrogen adsorption/desorption isotherm analysis. The synergistic incorporation of ZnO, Fe3O4, and chitosan in the CMZ composite altered the structural properties of ZnO and chitosan The band gap energy of CMZ was 2.58 eV, significantly boosting its photocatalytic effectiveness under visible light exposure. The CMZ composites exhibited a high efficiency in catalyzing MFX degradation in aqueous environments. The optimal conditions for MFX degradation were established, including a neutral pH level of 7, a 90 min exposure to irradiation, and employing 0.1 g of the CMZ catalyst. The degradation process obeyed closely to the first-order kinetic model. The CMZ material showed consistently high performance in degrading MFX across four consecutive reuse cycles, emphasizing its practical applicability for mitigating antibiotic pollution.

In situ synthesis of three-dimensional flower-like TiO2/WO3 heterojunction: Enhanced visible photocatalytic properties and theoretical calculations

The construction of heterojunction photocatalysts is an excellent strategy for treating wastewater. Herein, a three-dimensional nanoflower-like TiO2/WO3 heterojunction photocatalyst was synthesized in situ on the surface of pure Ti substrate by plasma electrolyte oxidation (PEO) combined with a subsequent process, and the abundant network topology and lattice defects improved the adsorption performance of the photocatalyst. The construction of Z-scheme heterojunction not only promotes the separation of photogenerated carriers, but also enhances the light absorption ability and greatly improves the photocatalytic performance of photocatalysts. Under the synergistic effect of adsorption and photocatalysis, the degradation rate of MB reached 86.2 % in 2 h, which was significantly higher than that of the single-component photocatalyst. Finally, the synthesis of TiO2/WO3 heterojunction photocatalysts by this process and the reaction mechanism of heterojunction photocatalysts for the degradation of organic dyes were illustrated by combining experiments and DFT calculations. In conclusion, this study opens up a new process for synthesizing Z-scheme heterojunction photocatalysts, which brings new insights for photocatalytic treatment of water pollution.

Functional modification of TC4 by Cu-containing titanium dioxide films

To improve the biological fouling and corrosion resistance of Ti6Al4V (TC4) in marine environments, copper-containing titanium dioxide (TiO2(Cu)) films were prepared by magnetron sputtering TiO2(Cu) powder targets. The morphologies of the films showed that they became rough and coarse from 1.6 nm of the TiO2 film to approximately 9 nm of the TiO2(Cu) films, which might be owing to the increase in the deposition rates from 1.33 to 2.08 nm/min. No diffraction orientations of the TiO2 and Cu phases were found compared to those of the TiO2(Cu) powder. Ti, O, and Cu were detected using X-ray photoelectron spectroscopy to confirm the composition of the films. The ratio of Cu2+ increased as the Cu content of the films increased, whereas that of Cu/Cu + scarcely changed. The TiO2 and TiO2(Cu) films exhibited photocatalytic effects and their photocatalytic intensities decreased as the Cu content increased. Hydrophobicity was enhanced by the addition of Cu to the film. The antibiological fouling effect of the TiO2(Cu) films remained unchanged as the Cu/Ti ratio varied. Compared with those of TC4, the corrosion current densities of the TiO2(Cu) films decreased by one order of magnitude and the corrosion potentials increased by 350 mV in artificial seawater, indicating that the corrosion resistance of TiO2(Cu)/TC4 was improved. Importantly, Cu was in abundance in the films for both antibiological and corrosion resistance functions owing to the saturated ratio of Cu/Cu+ irrespective of the Cu/Ti ratio in the films.

Microwave synthesized ternary BiOCl/BiOBr/Bi2O3 nanocomposite for enhanced degradation of organic contaminants under visible light exposure

BackgroundThis research addresses the urgent need for efficient water treatment methods to treat water pollution resulting from industrial activities and population growth. It focuses on developing semiconductor-based photo-catalysts with enhanced photocatalytic activity under visible light, aiming to contribute to pollution control and sustainable energy solutions. MethodsA novel layer-structured ternary BiOCl/BiOBr/Bi2O3 nanocomposite was successfully synthesized via a rapid, one-step microwave-assisted method. The unique layered structure of this heterojunction facilitated efficient migration and separation of photoinduced electron-hole pairs, essential for effective photocatalysis. Significant FindingsThe synthesized nanocomposite exhibited excellent photocatalytic performance, achieving complete degradation of 30 mg L−1 RhB, 98.0% efficiency for 10 mg L−1 TCH, and 83.0% efficiency for 10 mg L−1 MO. Furthermore, the photo-catalyst displayed remarkable photostability, retaining 99.7% efficiency even after seven cycles of RhB degradation. The study also revealed favorable conditions for RhB degradation, emphasizing the impact of high temperature and low pH media while demonstrating the catalyst's resilience to the presence of ions (NO3−, Cl−, SO42−, and NH4+). The study indicates that singlet oxygen (1O2) was predominant among the oxidizing species in photodegradation. This work introduces a highly efficient and stable ternary BiOCl/BiOBr/Bi2O3 nanocomposite as a promising solution for addressing water pollution issues and harnessing visible light for photocatalytic applications.

Fabrication of porous and defect-rich BiOI/MWCNTs photocatalyst by Ar plasma-etching for emerging pollutants degradation

Carbon material modification and defect engineering are indispensable for bolstering the photocatalytic effectiveness of bismuth halide oxide (BiOX). In this study, a novel porous and defect-rich Ar-CB-2 photocatalyst was synthesized for emerging pollutants degradation. Leveraging the interfacial coupling effect of multi-walled carbon nanotubes (MWCNTs), we expanded the absorption spectrum of BiOI nanosheets and significantly suppressed the recombination of charge carriers. Introducing defects via Argon (Ar) plasma-etching further bolstered the adsorption efficacy and electron transfer properties of photocatalyst. In comparison to the pristine BiOI and CB-2, the Ar-CB-2 photocatalyst demonstrated superior photodegradation efficiency, with the first-order reaction rates for the photodegradation of tetracycline (TC) and bisphenol A (BPA) increasing by 2.83 and 4.53 times, respectively. Further probe experiments revealed that the steady-state concentrations of ·O2− and 1O2 in the Ar-CB-2/light system were enhanced by a factor of 1.67 and 1.28 compared to CB-2/light system. This result confirmed that the porous and defect-rich structure of Ar-CB-2 inhibited electron-hole recombination and boosted photocatalyst-oxygen interaction, swiftly transforming O2 into active oxygen species, thus accelerating their production. Furthermore, the possible degradation pathways for TC and BPA in the Ar-CB-2/light system were predicted. Overall, these findings offered a groundbreaking approach to the development of highly effective photocatalysts, capable of swiftly breaking down emerging pollutants.

Development of 2D/2D h-MoO3/Ag/g-C3N4 heterojunction photocatalyst with enhanced photocatalytic performance for the detoxification of methylene blue and tetracycline under solar light illumination

In this study, direct thermal polycondensation, hydrothermal, and ultrasonic techniques were used to fabricate photocatalysts consisting of bare g-C3N4 (GCN), h-MoO3 (MoO3), MoO3/g-C3N4 (MGCN), and MoO3/Ag/g-C3N4 (MAGCN) composites. These methods were used to improve the photocatalytic effect, especially for environmental applications. The surface and chemical properties of the fabricated samples were investigated by XRD, FT-IR, FE-SEM, HR-TEM, UV-DRS, XPS, and PL analysis. Bare and composite photocatalysts were tested for photodegradation of the methylene blue (MB) dye and tetracycline (TC) antibiotic under solar irradiation. The MAGCN composite material exhibits remarkable efficiency in degrading 99% of MB dye and 90% of TC antibiotic within a time frame of 60 min when exposed to sunlight irradiation. The degradation rate constants (k) of MB and TC in the most active MAGCN photocatalyst were 11.02 and 7.03 times higher than those of pristine GCN, respectively. The scavenger reaction shows that the most important reactive species in the photocatalytic process are superoxide and photogenerated holes. The outstanding photocatalytic efficiency of the MAGCN catalyst was demonstrated by the fact that Ag nanoparticles act as mediators of fast charge transfer, resulting in higher absorption of sunlight, enhanced charge separation/transfer, and regeneration by MoO3 and GCN. The MAGCN photocatalyst exhibits remarkable activity, maintains its performance over six consecutive reaction cycles, and exhibits excellent stability and reusability. Intermediates were analyzed by GC-MS, and suitable degradation pathways were proposed. These results enable the development of an effective Z-scheme heterojunction photocatalyst and facilitate its wide application in the degradation of organic pollutants in wastewater.

La-doped Al2O3/g-C3N4 /agarose aerogel for removal of As(III) via simultaneous photocatalytic oxidation and adsorption

Attributing to its ubiquitous nature, arsenic (As) is frequently detected in various waterbodies across the globe, at concentrations often exceeding the permissible limits. In view of the acute and chronic toxicity of the arsenite species (As(III)), it is highly recommended to remove As(III) from aqueous matrices. Herein, we propose a agarose-based La-doped Al2O3/g-C3N4 (LAC) aerogel as a novel adsorptive photocatalyst for removal of As(III) via the synergistic effect of adsorption and photocatalysis. While g-C3N4 could transform As(III) to As(V) through photocatalytic oxidation, La-doped Al2O3 provided strong adsorption sites for the resulting As(V). Accordingly, the combination of adsorption and photocatalytic transformation of highly toxic As(III) into less toxic As(V), followed by subsequent adsorption of the latter can be considered as a promising technique to treat arsenic-contaminated water. The as-prepared aerogel was successfully characterized via a range of state-of-the-art microscopy, spectroscopy, and surface-specific analytical techniques. The optimized aerogel demonstrated a removal efficiency of 66.5% after 300 min of UV light irradiation. Furthermore, evaluating the effects of various reactive oxygen species via free-radical quenching experiments revealed that superoxide radicles (•O2−), singlet oxygen (1O2), and holes (h+) played a role key in the photocatalytic oxidation of As(III). More importantly, the LAC aerogel was structurally resilient and can be reused over multiple cycles, without any significant loss of the desired functionalities. Based on these deliberations, the integration of g-C3N4 with La-Al2O3 in the form of aerogel can be considered as a prospective strategy for the removal of arsenic from aqueous phase.

β-Ga2O3 nanostructures for photocatalytic degradation of red amaranth toxic dye

Beta gallium oxide (β-Ga2O3) microstructures composed of ∼50 nm nanoparticles were synthesized by the hydrothermal method. Using the Tauc plot method a value of ∼4.9 eV was obtained for the optical band gap of β-Ga2O3. TEM and XRD analyses revealed high crystallinity of the β-phase of gallium oxide nanostructures. Since there are few publications for the photocatalytic properties of β-Ga2O3 the obtained results contribute to better understanding of the photocatalytic effect of this material on toxic dye red amaranth. Moreover, it is shown that β-Ga2O3 is a very efficient photocatalyst leading to high percentage degradation of dyes for relatively short periods. For example, the degradation of red amaranth and rhodamine B toxic dyes under UV light irradiation reached 97% and 100% after 165 and 120 min, respectively.

Mn/Co bimetallic catalyst immobilized on N-doped biochar for enhanced photocatalytic degradation of sulfanilamide in water

Single-atom catalyst has shown promising effect in photocatalysis. In particular, the construction of bimetallic catalytic sites can address the limitations of single-metallic catalysts, such as clustering and slow electron transfer, which enhances electron transfer between active sites and promotes photocatalytic activity. In this paper, Mn and Co bimetallic catalyst (Mn/Co@N-biochar) was developed by using the electronegativity difference of the bimetallic sites on N-doped biochar to construct catalytically active sites to enhance electron transfer. XRD and HR-TEM characterization confirmed that metal atoms were evenly dispersed within the carbon layer without aggregation or clustering of metal particles. The catalytic efficiency of Mn/Co@N-biochar was assessed through sulfanilamide (SNM) degradation experiments, demonstrating a remarkable degradation rate of 99.3% and a mineralization rate of 49.0%. These values were 10.45 times and 13.24 times more than that for biochar, respectively, indicating that the loading of bimetals greatly improved the photocatalytic activity. Furthermore, the doping of N atoms adjusted the electronic structure of adjacent C atoms and activated the free-flowing π electrons on the biochar surface, creating solid anchoring sites that facilitated efficient electron circulation between Mn and Co atomic sites. The higher local electron density at the Co-N4 site compared to the Mn-N4, created electron transfer channels, where Mn atoms (catalytic site) facilitated the flow of electrons to Co atoms (active site). This could rapidly generate the primary active species (‧OH and ‧O2-) to degrade SNM. Additionally, the stability and applicability of bimetallic catalysts in real water systems were also confirmed, providing valuable insights for the construction of bimetallic biochar structures to degrade organic pollutants in water.

Sonication supported green modulation of Fe:MoO3/g-C3N4 heterojunction as solar light sensitive photocatalyst for dye degradation and photoelectrochemical water splitting

The concerns of dye in an aquatic system associated with acute toxicity and carcinogenicity, and the increase in demand for hydrogen production has led to a keen interest in advancing solar driven methodologies utilizing potent photocatalysts to address environmental concerns through sustainable remediation practices. In this pursuit, we synthesized a heterostructure comprised of Fe doped MoO3 (Fe:MoO3), anchored on g-C3N4 sheet as a photocatalyst denoted as Fe:MoO3/g-C3N4, employing a sonication supported green synthesis method with the aid of Murraya paniculata leaf extract. We explored structural, morphological, and surface characteristics using various analytical techniques, including X-Ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, UV–visible spectroscopy, Field emission scanning electron microscopy (FE-SEM) and High-resolution transmission electron microscopy (HR-TEM), X-Ray photoelectron spectroscopy, and BET for a comprehensive surface analysis. The outcomes highlighted the exquisitely oriented and interconnected arrangement of MoO3 nano rods ensconced within a piled layer of g-C3N4. The XRD patterns unveiled the coexistence of g-C3N4 and Fe:MoO3 within the heterojunction structure. FESEM and HRTEM image analysis of Fe:MoO3/g-C3N4 heterojunction reveals a g-C3N4 nanosheet wrapping the Fe:MoO3 nanoparticles with the formation of nanorods of MoO3 with an average thickness of 9.46 nm containing circular Fe nanoparticles with a mean diameter of 8.97 nm. This intricate configuration resulting in a decrease of the size of the nanoparticle caused by effective sonication-supported green modulation configuration facilitated an optimized charge flow, contributing to the elevated photo assisted catalytic performance of the heterojunction. The Fe:MoO3/g-C3N4 semiconductor heterojunction exhibited a considerable surface area and pore volume, inherently amplifying the sites of the activity on the surface and thereby enhancing photoactivity. As opposed to both g-C3N4 and the Fe:MoO3 nanoparticles, the Fe:MoO3/g-C3N4 semiconductor heterojunction showcased enhanced photocatalytic effectiveness in the degradation of dye Crystal violet (CV). Under optimized circumstances, the photo assisted degradation of dye CV by the semiconductor heterojunction adhered to pseudo-first-order kinetics. The active species responsible for the photo assisted degradation process is identified as •O2−. These findings not only emphasize the enhanced efficacy of the developed semiconductor heterojunction but also reveal its potential for addressing the environmental challenges posed by dye CV contamination through prolonged and efficient photocatalytic remediation practices. A marked improvement in both photo assisted catalytic and photoelectrochemical (PEC) water splitting activities under visible light exposure was showcased. The augmented performance of the Fe:MoO3/g-C3N4 semiconductor heterojunction in photodegradation and PEC water splitting activities can be attributed to the extended absorption of visible light. Additionally, the synergistic influence of g-C3N4, contributes positively to the separation of charges and expedites the transfer efficiency of photogenerated charge carriers. This synergy enhances the overall effectiveness of the nanoparticles in harnessing visible light for efficient water-related processes.

Surface-Engineered Cesium Lead Bromide Perovskite Nanocrystals for Enabling Photoreduction Activity.

In recent years, colloidal lead halide perovskite (LHP) nanocrystals (NCs) have exhibited such intriguing light absorption properties to be contemplated as promising candidates for photocatalytic conversions. However, for effective photocatalysis, the light harvesting system needs to be stable under the reaction conditions propaedeutic to a specific transformation. Unlike photoinduced oxidative reaction pathways, photoreductions with LHP NCs are challenging due to their scarce compatibility with common hole scavengers like amines and alcohols. In this contribution, it is investigated the potential of CsPbBr3 NCs protected by a suitably engineered bidentate ligand for the photoreduction of quinone species. Using an in situ approach for the construction of the passivating agent and a halide excess environment, quantum-confined nanocubes (average edge length = 6.0 ± 0.8 nm) are obtained with a low ligand density (1.73 ligand/nm2) at the NC surface. The bifunctional adhesion of the engineered ligand boosts the colloidal stability of the corresponding NCs, preserving their optical properties also in the presence of an amine excess. Despite their relatively short exciton lifetime (τAV = 3.7 ± 0.2 ns), these NCs show an efficient fluorescence quenching in the presence of the selected electron accepting quinones (1,4-naphthoquinone, 9,10-phenanthrenequinone, and 9,10-anthraquinone). All of these aspects demonstrate the suitability of the NCs for an efficient photoreduction of 1,4-naphthoquinone to 1,4-dihydroxynaphthalene in the presence of triethylamine as a hole scavenger. This chemical transformation is impracticable with conventionally passivated LHP NCs, thereby highlighting the potential of the surface functionalization in this class of nanomaterials for exploring new photoinduced reactivities.

NiS modified SrTiO3:Al bifunctional photocatalyst for H2 generation and cathodic protection

Developing low-cost and high-efficiency non-precious metal cocatalysts is the key to the practical application of photocatalysis technology. Here, nickel sulfide (NiS) nanoparticles were synthesized on the surface of strontium titanate (SrTiO3) via a hydrothermal method, identifying the optimal loading molar concentration of NiS as 10 %. The solar-to-hydrogen efficiency (STH) of 10%NiS/SrTiO3:Al was enhanced by 97 times compared to SrTiO3:Al and by 1.62 times compared to RhCrCoOx/SrTiO3:Al. This improvement is primarily attributed to the metallic-like properties of NiS, which enhance the photocatalyst's light absorption capacity and charge transfer capability. Additionally, the STH value of samples loaded with both NiS and RhCrCoOx reached 0.436 %, indicating a positive synergistic effect in photocatalysis between NiS and RhCrCoOx. Their photocathodic protection capability was also studied in simulated seawater conditions, showing a reduced self-corrosion potential (−0.31V) and a low interface charge impedance (5962 KΩ). This work reveals the potential of NiS as an alternative to precious metal cocatalysts, offering new possibilities for developing cost-effective and high-performance materials for photocatalytic water splitting and photocathodic protection.

MXene/Ag3PO4 modified PVDF composite membranes for efficient interfacial evaporation and photodegradation

Solar-powered interface evaporation is considered a promising technology to obtain freshwater from non-potable water by using sustainable solar energy. However, research on combining the photocatalytic effect with solar interfacial evaporation technology to go for photothermal conversion materials with full solar spectrum utilization for photothermal and photodegradation capabilities is still scarce. Due to the unique optical properties of MXene, a novel MXene/Ag3PO4-based membrane with synergistic photothermal and photocatalytic effects was developed from the perspective of practical applications such as water purification, photodegradation of organic dyes and antibacterial properties. In this paper, polyvinylidene fluoride (PVDF) and carbon black (CB) were used as the substrate, calcium carbonate (CaCO3) and hydrochloric acid (HCl) were selected as the pore-forming agent for hydrophilic modification, and MXene/Ag3PO4 serves as the photocatalyst. The prepared composite polyvinylidene fluoride membrane (PCC-MXene/Ag3PO4) with Schottky junction, possesses a rich pore structure, abundant water molecule transport channels, high light absorption ability, and low thermal conductivity, which lead to a good performance in solar interface evaporation, photodegradation and antibacterial. The superhydrophobicity and floatability of the nanosponges in water enable them to continuously pump water, which greatly promotes the dissolution of salt accumulation. With the help of porous nanosponges, PCC-MXene/Ag3PO4 exhibits excellent evaporation stability and salt resistance under 1 kW m−2 solar irradiation, as well as photodegradation of organic dyes. In addition, the PCC-MXene/Ag3PO4 membrane has the properties of self-buoyancy, electrical conductivity, and superior flexibility. Therefore, considering the simple preparation method and fine performances, the PCC-MXene/Ag3PO4 mixed membrane has great application potential in the study of interface evaporation, photodegradation of organic dyes, and antibacterial properties.

Antimicrobial and Antiviral Nanofibers Halt Co-Infection Spread via Nuclease-Mimicry and Photocatalysis.

The escalating spread of drug-resistant bacteria and viruses is a grave concern for global health. Nucleic acids dominate the drug-resistance and transmission of pathogenic microbes. Here, imidazolium-type poly(ionic liquid)/porphyrin (PIL-P) based electrospun nanofibrous membrane and its cerium (IV) ion complex (PIL-P-Ce) are developed. The obtained PIL-P-Ce membrane exhibits high and stable efficiency in eradicating various microorganisms (bacteria, fungi, and viruses) and decomposing microbial antibiotic resistance genes and viral nucleic acids under light. The nuclease-mimetic and photocatalytic mechanisms of the PIL-P-Ce are elucidated. Co-infection wound models in mice with methicillin-resistant S. aureus and hepatitis B virus demonstrate that PIL-P-Ce integrate the triple effects of cationic polymer, photocatalysis, and nuclease-mimetic activities. As revealed by proteomic analysis, PIL-P-Ce shows minimal phototoxicity to normal tissues. Hence, PIL-P-Ce has potential as a "green" wound dressing to curb the spread of drug-resistant bacteria and viruses in clinical settings.

Light-assisted ethanol dry reforming over NiZnOx hollow microspheres with enhanced activity and stability

Light-assisted thermocatalytic dry reforming of ethanol (EDR) utilizing the synergistic effect of photocatalysis and thermocatalysis is regarded as a promising route to convert greenhouse gas CO2 into value-added chemicals. In this work, double-shell NiZnOx hollow microspheres (NiZnOx-M) were synthesized as light-harvesting catalyst to enhance EDR performance under mild conditions. The characterization results of UV–vis–NIR and Photoluminescence Spectroscopy (PL) indicated that the band gap energy of NiZnOx-M catalyst was narrower because of the smaller Ni nanoparticles, thereby broadening its optical response range especially in visible light. The strong absorbance of light could greatly improve the activation of ethanol/CO2 and the gasification of carbon. With light irradiation, light could induce the transfer of photogenerated electron from semiconductor ZnO to active metal Ni, reducing the reaction energy barrier. Hence, NiZnOx-M catalyst showed superior photothermal catalytic activity along with good resistance capacity to coke accumulation and aggregation of active metal. Ethanol conversion was ca.2 times those obtained over NiZnOx-C prepared by conventional precipitation method. No obvious deactivation occurred after 100 h tests. This work provides some guidance for the design of high-performance photothermal catalyst to achieve the photo-thermal-chemical conversion of the greenhouse gases.