Light Responsive Photocatalyst Research Articles

Low-temperature hydrothermal self-assembly synthesis of ZnIn2S4/chitosan-graphene aerogels for enhanced aqueous pollutants removal

A novel visible-light-responsive ZnIn2S4/chitosan graphene aerogel (ZCGA) was prepared using a low-temperature hydrothermal self-assembly method for the adsorption and degradation of tetracycline. Infrared spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS) indicated interactions between ZnIn2S4 and chitosan graphene aerogel (CGA). Under the irradiation of a 500 W xenon lamp, ZCGA exhibited excellent adsorption and photocatalytic degradation performance for tetracycline, with a removal rate exceeding 90 % within 180 min. This significant performance improvement is attributed to the high carrier transport properties of CGA, which greatly enhanced the activity of the photocatalytic reaction and also showed high efficiency in removing other types of organic pollutants. Radical trapping experiments further confirmed that the superoxide anion (·O2−) is the main active species in the photocatalytic process. In addition, the monolithic aerogel has good recyclability and mechanical stability. This study not only demonstrates the great potential of ZCGA in the field of photocatalysis but also provides new ideas for designing efficient, recyclable, and visible light-responsive photocatalysts.

Fabrication of sulfur doped exfoliated gCN photocatalyst for enhanced visible light degradation of pernicious organic pollutants and their photocatalytic antibacterial activity

The synthesis of sulfur-doped exfoliated graphitic carbon nitride (S-gCN) photocatalyst was achieved by the implementation of a two-step calcination technique. The XRD results revealed that all the fabricated photocatalytic materials were crystalline in nature. The inclusion of 5% sulfur in gCN led to a conspicuous escalation in the surface area of photocatalyst, rising from 10.294 to 61.185 m2g⁻1. Morphological scrutiny of the samples using FE-SEM revealed that pristine gCN exhibited tightly stacked small nanosheets, whereas inclusion of sulfur and exfoliation resulted in generation of loosely distributed large nanosheet. Furthermore, the inclusion of sulfur also induced a shift in the energy band gap (Eg) from 2.81 eV to 2.63 eV, making it felicitous for investigation as proficient visible light photocatalyst. Additionally, the photoluminescence photo-induced charge carrier recombination behavior revealed a reduced peak intensity for 5% S-gCN compared to other synthesized compositions. This observation can be directly linked to the minimized electron-hole pairs recombination during photocatalysis, underscoring its superior photocatalytic performance. Our findings revealed that the 5% S-gCN photocatalyst exhibit the most promising attributes, it degraded Tetracycline drug, Chlorpyrifos pesticide and Eriochrome Black T dye under visible light irradiation almost ∼4 times more efficiently than pristine gCN. Additionally, exceptional visible light photocatalytic antibacterial efficacy was also perceived by 5% S-gCN against S. aureus bacteria. Overall, the present research sheds light on how doping and exfoliation interact to modify the structure and catalytic properties of gCN, paving the way for the development of outstanding performance, visible light-responsive efficient photocatalysts for environmental restoration.

Hybrid manufacturing process for the synthesis of doped TiO2 nanoparticles and optimization to determine an efficient photocatalyst

The hybrid sol-gel method was used to synthesize the transition metals (Cu and Ag) doped TiO2 nanoparticles for achieving enhanced visible light response photocatalysts. Different characterization techniques such as UV–Visible, FESEM, EDS, and TEM were carried out to characterize prepared nanocomposites. The synthesized Cu/TiO2 and Ag/TiO2 photocatalysts exhibit redshifts with improved light absorption capacity compared with pure TiO2. Scanning electron microscopic images show almost spherical morphology with relatively uniform sizes. Photocatalytic degradation of Methylene Blue (MB) and hydrogen production were carried out to estimate the photocatalytic efficiency of synthesized photocatalysts. As a result of increased charge separation efficiency and higher visible light absorption for photoexcitation, the photocatalytic response of the modified photocatalyst was elevated. In this study, the significant factors like initial pH, nitrate concentration, and dopant were identified. These factors were investigated in terms of hydrogen generation as a response to the successful optimization for the determination of the most efficient photocatalyst. In addition, in this work, density functional theory was used to simulate metals (Cu/Ag) doped TiO2 to learn more about the impact of doping on the structural, electrical, and photocatalytic properties of TiO2. Ag/TiO2 nanocomposite prepared via nitrate precursor concentration of 0.9 M and operated at an initial pH value of 4 exhibits maximum hydrogen generation capacity.

Chemical-Free Stable and Multifunctional Electro-Based System for Treatment of Pesticides from Aqueous Solution

The usage of pesticides has become a common practice in modern agricultural systems to meet the growing demand for food production. However, the uncontrolled use of such chemicals results in the deterioration of natural ecosystems and living beings. Thus, herein, a hybrid treatment system performing the combined functions of electro- and photo Fenton was designed to treat aqueous pesticide solution. The anode was comprised of metal oxide-based electrode (MOx), whereas the cathode was comprised of N-doped carbon electrode (N-C). Both the electrodes consist of light-responsive photocatalysts, which facilitates the removal of pollutants by generating reactive radical species such as OH• and O2 •-. The application of external anodic bias helps to improve the photocatalytic activity by preventing the recombination of electron-hole pairs. In addition, N-C on the cathode helps to catalyze the reduction of O2 to H2O2, which further reacts with Fe2+ in the system to initiate the Fenton reaction. The hybrid reactor was further optimized to study the underlying mechanisms by varying the experimental conditions such as pH, current density, electrolyte concentration, and external H2O2 concentration.Moreover, scavenging tests were performed using methanol and tertbutyl alcohol to identify the predominant radical species responsible for removing pollutants from the aqueous solution. Also, the reusability test showed that the prepared electrodes were stable for more than three successive cycles, thus offering sustainability. In general, the present study demonstrates the potential of hybrid treatment units for environmental applications and acts as a stepping stone for future endeavors in material synthesis and sustainable treatment solutions.

Designing and synthesis of perovskite nanocrystals: a promising wide-spectrum solar light-responsive photocatalyst and lead ion sensor.

Perovskites are an emerging material with a variety of applications, ranging from their solar light conversion capability to their sensing efficiency. In current study, perovskite nanocrystals (PNCs) were designed using theoretical density functional theory (DFT) analysis. Moreover, the theoretically designed PNCs were fabricated and confirmed by various characterization techniques. The calculated optical bandgap from UV-Vis and fluorescence spectra were 2.15 and 2.05eV, respectively. The average crystallite size of PNCs calculated from Scherrer equation was 15.18nm, and point of zero charge (PZC) was obtained at pH 8. The maximum eosin B (EB) removal efficiency by PNCs was 99.56% at optimized conditions following first-order kinetics with 0.98 R2 value. The goodness of the response surface methodology (RSM) model was confirmed from analysis of variance (ANOVA), with the experimental F value (named after Ronald Fisher) of 194.66 being greater than the critical F value F0.05, 14, 14 = 2.48 and a lack of fit value of 0.0587. The Stern-Volmer equation with a larger Ksv value of for Pb2+ suggests its greater sensitivity for Pb2+ among the different metals tested.

Facile construction of copper-doped metal organic framework as a novel visible light-responsive photocatalyst for contaminant degradation

ABSTRACT Metal–organic frameworks (MOFs) with photocatalytic activity have garnered significant attentions in environmental remediation. Herein, copper-doped zeolitic imidazolate framework-7 (Cu-doped ZIF-7) was synthesized rapidly and easily using a microwave-assisted technique. Various analytical and spectroscopic methods were employed to access the framework, morphology, light absorption, photo-electrochemical and photocatalytic performance of the synthesized materials. Compared to ZIF-7, Cu/ZIF-7 (molar ratio of Cu2+ to Zn2+ is 1:1) demonstrates superior visible light absorption ability, narrower band gap, enhanced charge separation capability, and reduced electron–hole recombination performance. Under visible light irradiation, Cu/ZIF-7 serves as a Fenton-like catalyst and demonstrates exceptional activity for contaminant degradation, while virgin ZIF-7 remains inactive. With the addition of 9.8 mmol H2O2 and exposure to visible light for 30 min, 10 mg of Cu/ZIF-7 can completely decompose RhB solution (10 mg/L, 50 mL). The synergistic effect of the Cu/ZIF-7/H2O2/visible light system is attributed to visible light photocatalysis and Fenton-like reactions. Cu/ZIF-7 demonstrates excellent catalytic performance stability, with only a slight decrease in degradation efficiency from an initial 97.0% to 95.4% over four cycles. Additionally, spin-trapping ESR measurements and active species trapping experiments revealed that h+ and ·OH occupied a significant position for Rhodamine B (RhB) degradation. Degradation intermediate products of Rhodamine B have been identified using UPLC-MS, and the degradation pathways have been proposed and discussed. This work offers a facile and efficient technique for developing MOF-based visible light photocatalysts for water purification.

Highly efficient Bi2Fe4O9-ZnIn2S4 Z-scheme heterojunction for piezo-photocatalytic overall water splitting under near-infrared light up to 1200 nm

Photocatalytic overall water splitting is considered as a sustainable and appealing strategy to solve the issues of energy supply and conversion. However, a critical hurdle to applying photocatalytic overall water splitting is the restricted light absorption and sluggish mobility of light-induced charge carriers in catalysts. Herein, a near-infrared light-responsive Bi2Fe4O9-ZnIn2S4 Z-scheme piezoelectric photocatalyst with a Fe-S bonded interface is constructed. This ingenious design synergistically utilizes the advantages of the Z-scheme, strong coupling interfaces, and piezoelectric field. The Bi2Fe4O9-ZnIn2S4 Z-scheme heterojunction significantly suppresses photogenerated carriers' recombine and extends photocatalytic response to the infrared light region, achieving highly efficient piezo-photocatalytic activity. Consequently, the optimized Bi2Fe4O9-ZnIn2S4 heterojunction displays an unprecedented piezo-photocatalytic H2 and O2 generation rate of 1862 and 927 μmol h−1 g−1 under sunlight illumination. This rate is approximately 4.9 and 10.0 times greater than that of photocatalysis and piezocatalysis alone. This study lays novel groundwork for developing future heterojunctions for photocatalytic water splitting.

The Development of Visible-Light Organic Photocatalysts for Atom Transfer Radical Polymerization via Conjugation Extension.

This work aimed to develop organic photocatalysts (PCs) that could mediate organocatalytic atom transfer radical polymerization (O-ATRP) under visible light. Through the core-modification of known chromophoric structures and ring-locking to reach a conjugation extension, annulated N-aryl benzo[kl]acridines were identified as effective visible light-responsive photocatalysts. The corresponding selenium-doped structure showed excellent performance in the O-ATRP of methacrylates, which could afford polymer products with controlled molecular weights and low dispersities under the irradiation of visible light at a 100 ppm catalyst loading.

Single−atom Co anchored on covalent organic framework for remarkable photocatalytic hydrogen evolution efficiency

Single-atom catalysts (SACs) have attracted extensive attention because of their high atomic utilization and superior catalytic activity. Herein, single-atom Co has anchored on the β-ketoenamine-linked covalent organic framework (Tp-Tta COF) pores and used for remarkable photocatalytic hydrogen(H2) production under Ultraviolet–Visible light (UV–Vis light) irradiation. The single-atom Co is visualized by the aberration-corrected high-angle annular dark-field scanning transmission electron microscopy (AC HAADF-STEM), and the C3–Co–N1 coordination structure is demonstrated by X-ray absorption fine structure (XAFS) measurements. The modified Co0.4-SAC/Tp-Tta COF shows a high photocatalytic H2 production of 1798.5 μmol g−1 h−1 and the Apparent quantum yield(AQY) is 3.02% at 420 nm. The improvement of the activity and stability of the photocatalyst is mainly attributed to the incorporation of Co single-atom that boosts the separation efficiency of photogenerated electron-hole pair and provides well-dispersed active sites. This study provides valuable insights into the development of UV–Vis light-responsive photocatalysts at the atomic level.

Earthworm excrete derived-enzyme enriched SnO2/g-C3N4 nanocomposite for near complete decomposition of toxic dye molecules

Enzymes derived from earthworm (Eudrilus eugeniae) excretes (vermiwash) were used as supporting bio-catalysts with SnO2/g-C3N4 nanocomposites for photocatalytic dye degradation of toxic organic dyes. The results were compared to those of the composite partners SnO2 and g-C3N4. The enzyme supported nanocomposite has superior photocatalytic efficiency of 95 %, 93 %, 83 % and 97 % against the test dyes Methylene Blue (MB), Malachite Green (MG), Methyl Orange (MO) and Rose Bengal (RB) whereas the partners SnO2 (62 %, 81 %, 36 % & 73 %) and g-C3N4 (76 %, 84 %, 80 % & 89 %) exhibited lower efficiencies. The enzymes phosphatase, amylase, urease and protease present in the synthesized nanocomposite play supporting role as co-catalyst in enhancing the photocatalytic ability of the nanocomposite. The mechanism involving the charge carrier recombination delay due to the formation of g-C3N4 sheets beneath the SnO2 particles is illustrated. The partnering mechanism with g-C3N4 having lower bandgap (2.8 eV) leads to a reduction in the bandgap from 3.5 eV for SnO2 to 2.6 eV for the nanocomposite making the nanocomposite as visible light responsive photocatalyst. The XRD, FTIR, SEM-EDX, UV–vis–NIR, XPS and DFT results support the discussion on photocatalytic mechanism. The near complete dye degradation is confirmed by phenotypic test on earthworm (Eudrilus eugeniae).

Influence of substrate temperature on the structural, morphological, and photoelectric properties of Bi2WO6 thin films deposited by magnetron sputtering

The effect of substrate temperature (Ts) increasing from RT (room temperature) to 600 °C on the structural, morphological, optical and photoelectrochemical properties of BixWO6 (1.98≤x ≤ 2.84) thin films deposited by RF magnetron sputtering has been investigated by various techniques including XRD, EDS, SEM, AFM, XPS, UV–vis DRS, PL and EIS. AFM and EDS show that as Ts increases, the Bi/W atomic ratio gradually decreases; the amorphous BixWO6 thin films grown under 300 °C had a very smooth surface with an RRMS value in the range of 0.5–0.8 nm. However, as the substrate temperature increases from 400 to 600 °C, for the crystalline BiWO6 thin films the RRMS value increases to a range of 18.3–30.5 nm and there is a transition of the crystalline orientation from {131} to {200} as confirmed by XRD. The films grown at Ts = 600 °C exhibit some favorable properties such as a Bi/W ratio close to 2:1, lattice expansion relaxation, low Eg and excellent photoelectric reproducibility which is about 3–29 times higher than that of other films grown at low Ts (300–500 °C). PL and EIS analysis as well as photoelectrochemical test results demonstrated the enhanced separation efficiency of photogenerated electron-hole pairs and charge transfer for the stoichiometric and well-crystallized BixWO6 thin films, showing their good potential for practical applications such as visible light responsive photocatalyst or photoelectrode.

A Review of Visible Light Responsive Photocatalysts for Arsenic Remediation in Water

This review summarizes the progress over the last fifteen years in visible light reactive photocatalysts for environmental arsenic remediation. The design and performance of several materials including (1) doped and surface functionalized TiO2, (2) binary composites combining TiO2 with another semiconductor that absorbs visible light radiation or a metal (Pt), (3) ternary composites incorporating TiO2, a conductive polymer that can retard electron-hole recombination and an excellent adsorbent material for the removal of As(V), (4) tungsten, zinc, and bismuth oxides, (5) g-C3N4 based catalysts, and (6) M@AgCl core–shell structures. These results show that long reaction time remains a major challenge in achieving high As(III) oxidation.

Intensifying Photocatalytic Baeyer-Villiger Oxidation of Ketones with the Introduction of Ru Metalloligands and Bimetallic Units in POM@MOF.

The synthesis of visible light-responsive and efficient photocatalysts toward green Baeyer-Villiger oxidation organic synthesis is of extraordinary significance. In this work, we have synthesized two examples of visible light responsive crystalline polyoxometalate@metal-organic framework materials Ru-NiMo and Ru-CoMo by introducing Ru metalloligands and {CdM3O12} bimetallic units (M = Ni or Co). This is the first report of metalloligand-modified polyoxometalate@metal-organic framework materials with bimetallic nodes, and the materials form a three-dimensional framework directly through coordination bonds between {CdM3O12} bimetallic units and metalloligands. In particular, Ru-NiMo can achieve efficient photocatalytic conversion of cyclohexanone to ε-caprolactone in yields as high as 95.5% under visible light excitation in the range of λ > 400 nm, achieving a turnover number and turnover frequency of 955 and 440 h-1, respectively, which are the best known photocatalysts for Baeyer-Villiger oxidation, while apparent quantum yield measured at 485 nm is 4.4%. Moreover, Ru-NiMo exhibited excellent structural stability and recyclability, producing a 90.8% yield after five cycles of recycling.

Graphitic carbon nitride quantum dots seeding in MnTiO3 spheres: A novel visible light responsive photocatalyst with high interface charge transfer for antibiotic degradation

As a promising heterojunction photocatalyst, MnTiO3 was incorporated with graphitic carbon nitride quantum dots (CNQDs) by performing a simple thermal method. The optimal sample MnTiO3@CNQDs(III) could degrade 93.1% of tetracycline, which was about 5.56 times than that of the pristine perovskite. This could be due to high light absorption ability, an appropriate band structure, enhanced separation rate of the photoinduced carrier species and the nitrogen-rich oxygen species content of CNQDs structure. The photocatalytic efficiency remained 78.9% in the seven cycle tests, indicating a considerable stable behavior. The main active substances were superoxide and holes as well as hydroxyl radicals slightly mediated the reaction. At neutral condition, the photocatalyst showed its best activity. After 60 min, the removal efficiency reached 100% by adding PMS while in the presence of H2O2 the highest removal obtained for 90 min. Different wastewater environments held a slight impact on photocatalytic efficiency to reveal a good applicability in real-world environments. Thus, the study presented a novel heterostructured semiconductor that includes the synergistic effect between CNQDs and MnTiO3, contributing to high photocatalytic activity.

Ornamental kale-like ZnO nanostructure/CdS nanoparticle/MoS2 nanosheet ternary heterojunctions for efficient charge transfer and robust visible-light photocatalytic performance

Photocatalytic technology utilizing Z-scheme protocol offers a promising method for eliminating contaminants from water in the presence of visible light. In this work, by combining hydrothermal and chemical deposition methods, a new type of ornamental kale-like ZnO nanostructure/CdS nanoparticle/MoS2 nanosheet (ZCM) ternary photocatalyst was fabricated, which exhibits excellent visible light photocatalytic performance. A small amount of MoS2 nanosheets significantly improves the activity of the double Z-scheme ZCM photocatalyst. As compared to ZnO/CdS, the pseudo-first-order kinetic constant of the best ZCM sample for degradation of rhodamine B is 2.2 times higher. In light of free radical capture and PL results, a Z-scheme transport mechanism was revealed to increase the carrier separation rate and maintain strong redox stability. This study provides a solid basis for designing Z-scheme photocatalysts and developing a range of visible light-responsive photocatalysts.

Preparation of direct Z-scheme heterojunction la-doped Bi2WO6/CdS with enhanced visible light absorption and its photocatalytic degradation of antibiotics

In this paper, a novel direct Z-scheme heterojunction La-Bi2WO6/CdS composed of 3-dimensional flower-like Bi2WO6 and hexagonally stacked succulent CdS was successfully designed and synthesized. The morphology, optical properties, element valence and crystal structure of the catalysts were systematically characterized. When the dosage of LBC-40 was 1.0 g/L, the degradation rate of oxytetracycline (OTC, 20 mg/L, pH = 6) was 85.28 %, under low visible light illumination (65 W energy saving lamp) for 120 min and the reaction kinetic constant (0.01336 min−1) was 2.50 and 1.56 times that of pure Bi2WO6 and La-Bi2WO6, respectively. Moreover, La-Bi2WO6/CdS showed good photocatalytic activity for other single antibiotics, mixed antibiotics and antibiotics from different water sources. The photocatalytic activity only decreased by 7.69 % after 3 cycles. Furthermore, the possible photocatalytic degradation pathway and photocatalytic mechanism of OTC were proposed. The excellent photocatalytic performance of La-Bi2WO6/CdS is for that the doping of La3+ and the construction of direct Z-scheme heterojunction enhances the visible light absorption capacity and separation efficiency of photogenerated electron-hole pairs. This paper reports a new method, which can provide a reference for the design and development of visible light responsive photocatalysts with excellent photocatalytic properties.

Microwave-hydrothermal synthesis of F and Fe co-doped CeO2 photocatalysts for efficient removal of 2,4,6-TCP under visible light

In recent years, the massive use and migration of chlorine-containing organics into the environment potentially threaten the natural environment and human health. Advanced oxidation technology based on photocatalysts is a promising approach for the degradation of chlorine-containing organic pollutants, but the development of stable and efficient photocatalysts remains a challenge. In this study, a new visible light-responsive photocatalyst based on F and Fe co-doped CeO2 (FeFC) was synthesized by making full use of overall heating characteristic of microwaves. XRD, SEM-EDS, XPS, BET and DRS results showed that F and Fe was successfully co-doped into CeO2 with increased BET surface and narrowed band gap. The degradation experiments showed that the co-doping of F and Fe significantly enhanced the photocatalytic activity of CeO2 by enhancing visible light absorption and charge carriers separation. Moreover, CeO2 material with both F and Fe doping of 10 % (FeFC-10) showed the highest removal (99.8%) and de-chlorination (89%) rates of 2,4,6-TCP within 4h, which was 3.8 and 3.2 times higher than that of pure CeO2 prepared by microwave and muffle furnace, respectively. Free radical scavenging experiments and electron paramagnetic resonance (EPR) tests finally demonstrated that the h+ and ·OH were the active species that played a catalytic redox role in this reaction system. Furthermore, the degradation intermediates of 2,4,6-TCP were identified by LC-MS and the possible reaction pathways were suggested. In this paper, the photocatalyst (FeFC-10) synthesized by microwave-hydrothermal method could not only save time and energy, but also efficiently degrade 2,4,6-TCP, which could provide the theory and practice for protecting water environment contaminated by chlorine-containing organics through the synthesis of CeO2 based photocatalysts.

Visible-light responsive BiVO4 nanocompositions: Enhanced photocatalytic, electrical and optical performance through Ni and Ni/Co doping

The pronounced light sensitivity of BiVO4 has garnered significant attention, establishing it as a visible light-responsive photocatalyst. This study was focused on enhancing the optical, dielectric constant properties, and photocatalytic activity of BiVO4 compositions. By employing a modified combustion method, pure BiVO4, Ni-mono-doped (BiNi0.02V0.98VO4), and Ni/Co-bi-doped (BiCo0.02Ni0.02V0.96VO4) were synthesized. X-ray diffraction (XRD) analysis validated the formation of a monoclinic BiVO4 phase. The incorporation of Ni2+ and Co2+ ions into the BiVO4 lattice was supported by variations in the lattice parameters, volume expansion and increased average crystallite size. Morphological investigation via scanning electron microscopy (SEM-EDAX) confirmed the purity of the synthesized nanocompositions and unveiled distinctive rod-like and needle-like particle shapes in BiNi0.02Co0.02V0.96VO4, with an aspect ratio of 0.07–0.1, indicating potential benefits for efficient charge separation in photocatalysis. Optical examination highlighted redshifts in band gap energy (2.36 eV) due to both Ni and (Co, Ni) co-doping, leading to direct band gaps of 2.34 eV and 2.32 eV, respectively. High refractive index values exceeding 2.5, conducive to optical applications, were observed across all samples. Through Ni and Ni/Co doping process, a notable enhancement in conductivity emerged, particularly within the low-frequency domain. The co-doping of Ni and Co demonstrated elevated relative permittivity (εʹ) values exclusively within the low-frequency span, up to 100 Hz. In contrast, the Ni-mono-doping interestingly disclosed an enhancement in (εʹ) across all frequency ranges. Photocatalytic results demonstrated heightened degradation activity in doped samples, with the BiNi0.02Co0.02V0.96VO4, sample exhibiting the highest rate, achieving 88 % degradation efficiency in 180 min. This exceptional performance can be attributed to its visible-light-responsive band gap, increased electron-hole trapping sites, and distinct morphology.

Modulating Narrow Bandgap in a Diacetylene Functionalized Woven Covalent Organic Framework as a Visible Light Responsive Photocatalyst.

Woven covalent organic frameworks (COF) possess three dimensional frameworks with spatially isolated Cu(I) centers and have promising optoelectronic properties because of metal to ligand charge transfer (MLCT). However, despite their potential, woven COFs have not yet been investigated as photocatalysts. In this study, we developed a new woven COF, Cu-PhenBDA-COF, functionalized with diacetylene bonds. Cu-PhenBDA-COF was fully characterized, and the optoelectronic and photocatalytic properties were compared to previously reported Cu-COF-505. The diacetylene bonds of the linker positively impacted the optoelectronic properties of Cu-PhenBDA-COF and resulted in a narrower band gap and better charge separation efficiency. When the Cu(I) center was removed from both woven COFs, the absorption edge was blue shifted, resulting in a wider band gap, and there was a considerable decrease in the charge separation efficiency, underscoring the pivotal role of MLCT. This trend was reflected in the photocatalytic activity of the woven COFs toward the degradation of sulfamethoxazole in water, where the highest reaction rate constant (k app ) was recorded for the metallated diacetylene functionalized woven COF, Cu-PhenBDA-COF.

Degradation of multiple xanthates using highly efficient visible light-responsive BiOBr-TiO2 composite photocatalysts

BiOBr-TiO2 (BT) composite photocatalysts were synthesized by using a two-step method including hydrothermal synthesis and water-bath precipitation. The microstructural characterization analysis proved that high-crystallinity and high-purity binary BT materials were achieved without by-products. TiO2 nanoparticles with a diameter of approximately 15 nm were decorated on multi-layered BiOBr nanosheets. The results showed that BT had highly-improved adsorption capacity and photocatalytic efficiency in comparison to pristine BiOBr and TiO2. The reaction rate constant of the optimal BT-2 composite photocatalysts for the degradation of 20 mg/L sodium ethyl-xanthate could reach 0.06496 min−1, which was 2.7 and 40.3 times than pure BiOBr and TiO2, respectively. The free radical scavenger test demonstrated that photogenerated holes were the main active species in the photocatalytic degradation reaction process. A possible degradation pathway for SEX molecules was provided through the interaction of visible light and BT-2 photocatalyst. The as-prepared BT materials can be used as efficient photocatalysts to completely degrade various types of xanthates under visible light.