Decomposition Of Methylene Blue Research Articles

Unraveling the Impact of Adsorbed Molecules on Photocatalytic Processes: Advancements in Understanding Facet-Controlled Semiconductor Photocatalysts.

This work aims to demonstrate that the Fe2O3 nanocrystals' adsorptive and photocatalytic properties can be adjusted by exposing the crystal facets that are functionalized. To this end, cube- and disc-like structures were synthesized using a metal ion-mediated hydrothermal route. Thereafter, some of the samples were annealed at 500 °C for 3 h. Our paper combines the experimental part with theoretical calculations of the obtained materials' band edge positions. The results reveal that-aside from hematite-the as-synthesized discs also contain γ-FeOOH and β-Fe2O3 phases, which transform into α-Fe2O3 during annealing. The hydrodynamic diameter, zeta potential, and adsorption kinetics measurements show that the cube-like samples exhibit the highest affinity for cationic, whereas the discs have an affinity for anionic dye. Measurements of the wall zeta potential also reveal that annealing the discs modifies their surface state and ability to adsorb molecules. Photocatalytic tests show that the as-synthesized powders have better photocatalytic performance toward methylene blue decomposition than the annealed ones. The observed small changes in the concentration of the MO during illumination result from the energy band structure of the cube-like crystal orientation.

Bimetal Cu/Ni-BTC@SiO2 metal-organic framework as high performance photocatalyst for degradation of azo dyes under visible light irradiation

There has been significant attention on the efficient degradation of pollutants in wastewater using metal-organic frameworks (MOFs) photocatalytic methods over the past decade. Herein, we examined the elimination of two different types of water-contaminating dyes, specifically cationic dye methylene blue (MB) and anionic dye methyl orange (MO), through the application of bimetal Cu/Ni-BTC@SiO2 MOF as high performance photocatalyst. The bimetal Cu/Ni-BTC@SiO2 photocatalyst was synthesized and characterized by XRD, FTIR, SEM, TEM, TGA, BET, DRS, and VSM techniques. The examination of the impact of different operational factors on the elimination of pollutants involved a comprehensive analysis of variables including the photocatalyst type, initial pollutant concentration, quantity of photocatalyst, and pH levels. The highest removal efficiency for MO and MB dyes by the photocatalyst was found to be 98 and 71%, respectively, within 60 min. In the fifth reaction stage, degradation efficiency for MO and MB was 76 and 56% respectively. Kinetic investigations demonstrated that, in the context of the uptake of MB and MO dyes, the interparticle diffusion, and pseudo-second-order models emerged as possessing the most robust correlation coefficients with the experimental data, registering values of 0.988 and 0.961, respectively. The examination of isotherms reveals that the isotherm models proposed by BET, and Anderson (V) demonstrate the highest level of conformity with the empirical data for the decomposition of MB and MO dyes, correspondingly. The TOC levels decreased significantly from 51 to 14 and 47 to 3 mg/L for MB and MO dyes, indicating the effective mineralization process using Cu/Ni-BTC@SiO2.

A green approach to synthesis of Ag-doped CeO2 nanorods embedded reduced graphene oxide nanocomposite for excellent photocatalytic and antimicrobial activity

In this paper, the Ag-doped cerium oxide nanorods embedded reduced graphene oxide (Ag@CeO2/rGO) nanocomposite was synthesized via Punica Granatum leaf extract for for photocatalytic degradation of methylene blue (MB) and 4-nitrophenol (4-NP). The microstructural results confirmed the successful decoration of Ag-doped CeO2 nanorods on rGO matrix. The photocatalytic properties, including photocatalytic degradation, charge transfer kinetics and photocurrent generation, are systematically investigated using electrochemical impedance spectroscopy (EIS), photocurrent transient response (PCTR) and open circuit voltage decay (OCVD). The results of photocatalytic dye degradation measurements indicated that Ag@CeO2/rGO nanocomposite is more effective than pristine CeO2 to degrade the MB dye, and the degradation rate reached 100 % in 60 min. The decomposition of MB with Ag@CeO2/rGO nanostructure followed first-order reaction kinetics with a reaction rate constant (Ka) of 0.0198 min−1. The EIS and OCVD measurements revealed that the Ag doping and incorporation of rGO could suppress the recombination probability in CeO2 by the separation of photo-generated electron–hole pairs, which leads to the enhanced photocurrent generation and photocatalytic activity. The photocurrent density of Ag@CeO2/rGO, CeO2/rGO and pristine CeO2 are 215, 167.4 and 98.8 mAcm−2, respectively.

A Novel Study on Antioxidant Activity and Catalytic Reduction of Methylene Blue using ZnO Nanoparticles Synthesized via the Middle Part of Walnut Shell (Juglans regia) Extract

Abstract: The synthesized ZnO nanoparticles were characterized using UV-Vis spectroscopy, SEM, XRD, FTIR, and TEM analysis. The catalytic activity of the prepared green catalyst ZnO nanoparticles was also investigated in the dye methylene blue (MB) decomposition. The catalytic decomposition reaction completed within 20 minutes, demonstrating the excellent catalytic properties of ZnO nanoparticles in reducing MB. This research describes the green synthesis of ZnO nanoparticles using an extract of the middle part of a walnut shell (Juglans regia). The antioxidant activities (radical capture capacity) of the synthesized ZnO nanoparticles were evaluated by the 2,2-diphenyl-1-picrylhydrazyl hydrate (DPPH) assay at different ZnO nanoparticle concentrations, and the radical capture activity was achieved at IC50 = 146.32 μg / mL. The radical capture activity was achieved at IC50 = 146.32 μg / mL. The biosynthesis of ZnO nanoparticles was caused by hydroxide precipitation at room temperature after calcination at 450°C.

The Properties and Activity of TiO2-based Nanorods as an Anti-Fouling Agent and a Photocatalyst

The properties and activity of TiO2-based nanorods as an antifouling agent and a photocatalyst for the catalytic degradation of methylene blue (MB) have been investigated. A modification of TiO2 with SiO2 was first carried out to enlarge the surface area. In order to enhance the TiO­2 photo response to the visible light region, a further modification of TiO2-SiO2 (TS) composites with polyaniline (PANI) was also conducted. The nanorod TiO2 exhibited an anatase structure based on the diffraction patterns. The TEM images showed that some TiO2 molecules were attached around SiO2 with a random orientation. The TiO2-SiO2-PANI (TS-PANI) exhibited the largest specific surface area (SBET) of about 256.85 m2/g. The profile on the AFM images of the composites showed that the nano-roughness of the coatings was confirmed. The photocatalytic activity was evaluated through the decomposition of MB both on the powder and the coated composites. The photocatalytic activity on the coatings was verified due to further application as anti-fouling coatings involving photocatalytic mechanism. The decomposition of MB using TS-PANI powder and TS-PANI coating composites was 89.5% and 90.2 %, respectively, with the irradiation time on the coatings was 20 min longer. The anti-fouling activity through the photocatalytic mechanism and nano-roughness surface was confirmed by the inhibition of barnacle growth on the teakwood surface immersed for two months in the sea.

Mixed Metal Oxide W-TiO2 Nanopowder for Environmental Process: Synergy of Adsorption and Photocatalysis.

A mixed metal oxide W-TiO2 nanopowder photocatalyst was prepared by using the sol-gel method with a broad range of elemental compositions x = CW/(CW + CTi), including TiO2 and WO3. The material was structurally characterized and evaluated in adsorption and photocatalytic processes by testing its removal capacity of a representative pollutant methylene blue (MB) in aqueous solutions and under UV-A and sunlight illuminations. The nanopowders appeared to be more effective adsorbents than pure TiO2 and WO3 materials, showing a maximum at 15 mol% W, which was set as the tungsten solubility limit in anatase titania. At the same time, the photocatalytic decomposition of MB peaked at 2 mol% W. The examination of different compositions showed that the most effective MB removal took place at 15 mol% W, which was attributed to the combined action of adsorption and heterogeneous photocatalysis. Moreover, MB decomposition under sunlight was stronger than under UV-A, suggesting photocatalyst activation by visible light. The pollutant removal efficiency of the material with 15 mol% W was enhanced by a factor of ~10 compared to pure TiO2 at the beginning of the process, which shows its high potential for use in depollution processes in emergency cases of a great pollutant leak. As a result, a Wx=0.15-TiO2 catalyst could be of high interest for wastewater purification in industrial plants.

Removal and photocatalytic degradation of methylene blue on ZrO2 thin films modified with Anderson-Polioxometalates (Cr3+, Co3+, Cu2+): An experimental and theoretical study

In this work, several ZrO2 thin films modified with Anderson-type polyoxomolybdates (POMs) with general formula (NH4)6-n[XMo6O24H6]-6+n where X = Co3+, Cr3+ and, Cu2+ were prepared. Thin films were characterized through SEM and EDX assay, UV–Vis diffuse reflectance and Fourier Transform Infrared (FTIR) assay. The optical bandgap of ZrO2 thin films was determined to be 3.25 eV, while the modified thin films showed a red shift in the optical activity compared with bare ZrO2 thin films. Methylene Blue (MB) adsorption studies showed that Freundlich isotherm describes properly the experimental data for modified-ZrO2 thin films. Besides, the kinetic results showed the MB adsorption of modified-ZrO2 thin films was superior to bare ZrO2 thin film. The adsorption rate values (K2) of the pseudo-second order model follow these trend ZrO2/CrPOM > ZrO2/CoPOM > ZrO2/CuPOM > ZrO2. The photocatalytic activity of the thin films for MB decomposition under UV and Visible irradiation was studied. Among all the catalysts, the ZrO2 thin films showed the lowest photocatalytic degradation rate kap value (kap = 1.5 × 10−3 min−1), while the best result was obtained for ZrO2/CrPOM thin films (kap = 5.7 × 10−3 min−1) under UV irradiation. Besides, this was the only catalyst efficiently active in MB degradation under visible irradiation, these materials reach 10.4 % after 100 min under visible irradiation. Finally, chemical calculations supported the observed results, by means of TDDFT, EDA analysis, Fukui function and periodic DFT calculations.

Visible light-induced photocatalytic degradation of methylene blue dye using pure phase bismuth ferrite nanoparticles

The degradation of organic dyes in wastewater has become a significant environmental issue, requiring the development of degradation technologies that are both effective and environmentally friendly. The present study employed the sol-gel approach to synthesize nanoparticles of phase pure bismuth ferrite (BiFeO3). The nanoparticles were assessed for their ability to efficiently degrade methylene blue (MB) dye, especially under visible light irradiation. The X-ray diffractogram (XRD) confirmed the formation of BiFeO3 nanoparticles, with an average crystallite size of 48 nm. The material's band gap, with a value of 1.84 eV, demonstrates its capacity to effectively absorb light, including wavelengths within the visible spectrum. Scanning electron microscopy (SEM) was used to identify porous aggregated particles. Both Raman and Fourier transform infrared spectroscopy (FTIR) confirm the successful synthesis of pure BiFeO3 in the desired phase. The BiFeO3 photocatalyst exhibited a significant surface area and isotherms of type IV, a characteristic typically observed in mesoporous materials, as determined by the Brunauer-Emmett-Teller (BET) analysis. The efficacy of BiFeO3 nanoparticles in facilitating the decomposition of MB in a water-based solution was evaluated by visible light photocatalysis. An efficiency degradation of 98.49 % was recorded for MB within 2 h.

Synthesis of porous TiO2 and Fe-doped TiO2 films for photocatalysis by a cooling enhanced plasma electrolytic oxidation approach

Porous TiO2 films are widely used in photocatalysis for pollutant remediation and synthetic chemistry applications, and the homogeneity and stability of the films are important parameters. Here, we show that porous TiO2 and Fe-doped TiO2 (Fe-TiO2) films on Ti foils with homogeneous structure and well-controlled doping can be synthesized by a cooling enhanced plasma electrolytic oxidation (CPEO) method. The anatase content within pristine TiO2 films and the concentration of Fe dopant in Fe-TiO2 films can be manipulated by simply adjusting the synthetic parameters, leading to an optimum photocatalytic performance under both UV and visible light irradiation for the decomposition of methylene blue.

Syzygium cumini-mediated synthesis of rGO/Ag-Au nanostructures: Efficient catalysts for rapid degradation of organic dyes

BackgroundThe increasing human health risk caused by contamination of water by both natural and synthetic dye pollutants has become a crucial issue and poses an immense urge to find a sustainable approach for the removal of dye contaminants from wastewater. Photocatalysis performed in the presence of nanomaterials holds huge promise as an efficient and environmentally safe oxidation technology for organic dye removal from waste water. MethodsOur preparation methodology utilizes the extract derived from the endocarp of Syzygium cumini (SC) effects for concurrent reduction of GO and metal ions to form rGO/Ag-Au. The prepared rGO/Ag-Au nanostructures effectively breakdown organic dye pollutants like methylene blue (MB) and methyl orange (MO) dyes. Significant findingsA robust interaction between the rGO matrix and the Ag-Au nanoparticles was established by structural characterization, while morphological investigation displayed the nanoscale Ag-Au particles uniformly coated over the rGO sheet surface. The catalytic efficiency of the rGO/Ag-Au nanocomposite toward methylene blue (MB) and methyl orange (MO) chromophores decomposition was assessed with the aid of sodium borohydride (NaBH4). The decoration of well-spaced Ag-Au nanoparticles over the rGO sheet created firm catalytic active sites in the rGO/Ag-Au composite. With the improved catalytic active surface, the MB/MO dye was completely removed in a very short time of 2.5 to 5 min. The rGO/Ag-Au composite exhibited exceptional catalytic prowess in the disintegration of both dyes, leading to complete degradation. The remarkable efficacy in the dye degradation process can be attributed to the predominance of both electrostatic as well as π-π interactions between the nanocomposite and the dyes. As a result, the current study has developed an easy-to-use and green method for creating rGO/Ag-Au composites, offering a workable way to dispose of hazardous organic dyes in an affordable and efficient way.

The Photocatalytic Activity of the Bi2O3-B2O3-ZnO-TiO2 Glass Coating

Due to the low melting temperature, the glazes based on the Bi2O3-B2O3-ZnO system are used as coatings on the surface of industrial glass substrates. Moreover, the composition of these coatings does not contain PbO, meeting the optical and environmental properties requirements. In this study, TiO2 was used in the Bi2O3-B2O3-ZnO glaze system to improve its photocatalytic ability. This can be considered a four – component glass system Bi2O3-B2O3-ZnO-TiO2. The heating microscopy results show that the melting temperature of the glaze system is 606 °C. The Fourier transform infrared spectroscopy results show that the TiO2 polyhedra are located independently in the structure without participating in forming a glass network. Thanks to that, the photocatalytic properties of TiO2 are maintained. The X-ray diffraction patterns results show that the formed TiO2 nanocrystals are rutile and anatase crystals. The results of determining the band gap energy using UV-Vis show that the band gap energy of the base glaze system increases with the addition of TiO2. The methylene blue decomposition results also showed that the ability to decompose organic increased when TiO2 was added to the glaze coating. The characteristics such as melting temperature, microstructure, and photocatalytic capacity of Bi2O3-B2O3-ZnO-TiO2 white glazes (5 and 10 % weight of TiO2) also were indicated in this paper.

Boosted solar-driven photocatalysis: silver molybdate/reduced graphene oxide nanocomposites for methylene blue decomposition

Boosted solar-driven photocatalysis: silver molybdate/reduced graphene oxide nanocomposites for methylene blue decomposition

Efficient synthesis and characterization of novel BiVO4/ZnO/graphene composites to study enhanced photocatalytic activity for organic pollutant degradation

This study reports the efficient synthesis and thorough characterization of novel graphene doped BiVO4/ZnO nanocomposites. Among these doping percentages, 3% BVZO/G is optimized composite as it shows the highest photocatalytic performance i–e 98% and 95% among all the doping percentages. Under the visible light exposure λ⩾420nm , the decomposition of tetracycline (TC) and methylene blue has been studied to evaluate the photocatalytic activity of the prepared composites. The characterization techniques such as photoluminescence spectroscopy, UV visible (UV-Vis) spectroscopy, x-ray diffraction, scanning electron microscopy, and Fourier transform infrared have been used to investigate the optical, structural, morphological, and vibrational properties respectively. The findings of the research indicate that the doping of graphene resulted in enhanced absorption of visible light and efficient mitigation of charge carrier recombination. To check the stability of optimized photocatalyst, reusability test has been performed. Additionally, role of active species has been examined using different scavengers in trapping experiment. By understanding the composite material for the enhanced photocatalysis, the results of this research help to design a sustainable and efficient photocatalyst.

Electron structure and photocatalytic properties of (Na/K)VMoO6 nanosuspensions

Electron structure features of nanopowders with composition of (Na/K)VMoO6 have been investigated both experimentally and theoretically. The dispositions of valence edge and conduction band were determined experimentally for vacuum condition by X-ray photoelectron spectroscopy, UV–visible and impedance spectroscopy and evaluated theoretically for water solutions. The additional absorbance band in the band gap has been found for both compounds, which leads to electron conductivity at low-temperature range (250–350 °C). Nanopowders have been prepared by sol-gel method with further ground in the planetary mill. Prepared powders in water solution have formed nanosuspension with size's particle up to 100 nm for NaVMoO6 and 400 nm for KVMoO6, which is hardly sedimentated. The highly effective photocatalytic ability under visible light irradiation of the prepared compounds was observed using methylene blue decomposition process. The almost full methylene blue (20 mg/L) degradation is observed during 30 min for 10 mg of the photocatalysts. The investigation of possible dye degradation pathway has showed the high depth of decomposition.

Structural properties and photocatalytic activity of amorphous-crystalline TiO2 thin films

TiO2-coated glass plates were prepared by dip coating using TiO2 coating sol with a mixed amorphous and crystalline structure. These samples were dried at 100°C or calcined at 500°C, which were referred to as MT and CT, respectively. The TiO2 thin films on glass plates were characterized by X-ray diffraction, thermogravimetry-differential thermal analysis, X-ray photoelectron spectroscopy, Fourier transformed infrared spectroscopy, Brunauer-Emmett-Teller surface area measurement, scanning electron microscopy, and ultraviolet–visible diffuse reflectance spectra. The TiO2 thin films of MT samples had mixed amorphous and crystalline structures, while those of CT samples had only crystalline structures. The photocatalytic activity of the samples was investigated on the basis of methylene blue (MB) decomposition under ultraviolet and visible light irradiation. In the dark stabilization, MT samples had a higher MB adsorption capacity than CT samples. MT samples had a smaller amount of anatase TiO2 than CT samples, but both glass plate samples showed the same MB photocatalytic activity under ultraviolet light irradiation. We presumed that these results were because the amorphous-crystalline TiO2 thin films had a high specific surface area, so they had more adsorption and active sites. Under visible light irradiation, only the MT samples had photocatalytic activity, which can be attributed to their high visible light absorbance, which may be due to their peroxo groups, disordered structure, and larger specific surface area.

Pitch/Metal Oxide Composite Fibers via Electrospinning for Environmental Applications

This study investigates the synthesis and application of composite electrospun fibers incorporating coal tar pitch (CTP) and various nanomaterial additives, with a specific focus on their potential for eco-bio-applications. The research underscores the environmentally viable aspects of CTP following a thermal treatment process that eliminates volatile components and sulfur, rendering it amenable for fiber electrospinning and subsequent carbonization. Composite fibers were fabricated by integrating CTP with nanomaterials, including nickel oxide (NiO), titanium dioxide (TiO2), activated carbon (AC), and magnetite (Fe3O4). The C/NiO composite fibers exhibit notable acetone sensing capabilities, specifically displaying a rapid response time of 40.6 s to 100 ppm acetone at 220 °C. The C/TiO2 composite fibers exhibit a distinct “beads-on-a-string” structure and demonstrate a high efficiency of 96.13% in methylene blue decomposition, highlighting their potential for environmental remediation applications. Additionally, the C/AC composite fibers demonstrate effective adsorption properties, efficiently removing manganese (II) ions from aqueous solutions with an 88.62% efficiency, thereby suggesting their utility in water purification applications. This research employs an interdisciplinary approach by combining diverse methods, approaches, and materials, including the utilization of agricultural waste materials such as rice husks, to create composite materials with multifaceted applications. Beyond the immediate utility of the composite fibers, this study emphasizes the significance of deploying environmentally responsible materials and technologies to address pressing eco-bio-challenges.

Designing g-C3N4/ZnCo2O4 nanocoposite as a promising photocatalyst for photodegradation of MB under visible-light excitation: Response surface methodology (RSM) optimization and modeling

Creating a Z-scheme heterojunction system can enhance the efficiency of separating and transporting charge carriers responsible for degrading pollutants. Hence, in this study, ZnCo2O4 was combined with g-C3N4 through a straightforward approach to create a novel Z-scheme heterogeneous nanocomposite. Various techniques were employed to inspect the photocatalysts' crystallinity, morphology, chemical composition, functional groups, band structure, and electrochemical properties. The Photocatalytic degradation of methylene blue reveals that the catalytic activity of g-C3N4/ZnCo2O4 nanocomposite (414 × 10−4 min−1) is considerably greater than that of the individual building units (g-C3N4: 45.7 × 10−4 min−1 and ZnCo2O4 79.5 × 10−4 min−1). The impact of operational parameters such as photocatalyst dosage (mg), pH, and dye concentration (ppm) on the photodegradation ability of the nanocomposite g-C3N4/ZnCo2O4 was assessed and optimized based on response surface methodology and central composite design model. The highest level of degradation, reaching 99%, was gained in the optimal condition, including pH = 7, 90 mg of g-C3N4/ZnCo2O4 photocatalyst, and 5 ppm of MB. The photoluminescence and electrochemical impedance spectroscopy results revealed that the significant attenuation of the generated electron-hole pair recombination increased the nanocomposite photocatalytic performance. Also, extensive solar light absorption and adaptation of the band structures of the two semiconductors resulted in increased photocatalytic activity. The addition of scavengers to the photocatalytic test environment showed the importance of the contribution of each active species in the decomposition of methylene blue. The heterojunction photocatalytic system showed good reproducibility and reusability in the reaction solution.

Silver decoration of Cr2O3 nanoparticles: Facile preparation of Cr2O3 nanoparticles and Ag–Cr2O3 nanocomposites and characterization of their antibacterial activity and ability to photocatalytically degrade organic wastes under visible light

An eco-friendly, single-step process was adopted for the preparation of Cr2O3 nanoparticles (CR-NPs), and different concentrations of Ag were doped into the CR-NPs through liquid impregnation to synthesize a series of Ag-CRNPs composites. In order to prevent agglomeration, chemical transformation, and weak adhesion of Ag to CR-NPs, a mechanical process of circular-motion grinding and high-temperature treatment in a sealed condition were used. Well-defined heterojunctions were successfully formed between Ag and CR-NPs. In comparison to the CR-NPs, the Ag-doped CR-NP composites exhibited excellent performance in photocatalytic and antibacterial applications. Under visible light (VL), the best-performing composite (2 %-Ag decorated CR-NPs) showed 96 %, 79 %, and 57 % decomposition of methylene blue, Congo red, and tetracycline, respectively, in 100 min, which was attributed to a synergetic effect in the composites. The rate constant of the photocatalytic reaction is 14 times higher than that of the reaction without a photocatalyst. The enhanced efficiency was attributed to a reduced bandgap, prolonged retention of photogenerated electron–hole pairs, an increased amount of active spots, and increased absorption of VL. Similarly, the best-performing composite exhibited excellent antibacterial activity against Escherichia coli and Staphylococcus aureus with zones of inhibition of 15.4 and 15.1 mm, respectively. The 2 %-Ag decorated CR-NPs were the most efficient and exhibited robust recyclability until the fifth cycle (≥90 %). The photocatalytic activity was primarily driven by reactive oxygen species, holes and hydroxyl radicals.

Methylene blue decomposition in visible light by CaTiO3/g-C3N4 nanorods produced by the methanol mixing method

In recent years, research on using photocatalysts for solar energy has attracted much attention. In this study, g-C3N4 nanorods and CaTiO3 nanocuboids were mixed with methanol to produce g-C3N4 nanorods by molten salt synthesis; CaTiO3 nanocuboids were prepared by hydrothermal synthesis. These two types of particles were then mixed by adding them to methanol and stirring. The methanol mixing method dispersed the aggregated g-C3N4 nanorods, allowing them to bind more closely to the CaTiO3 particles. Methylene blue degradation by visible light was used to evaluate the organic degradation of the mixed particles. The composite particles showed excellent degradation ability for the removal of methylene blue.

Dielectric Barrier Discharge Plasma Coupled with Cobalt Oxyhydroxide for Methylene Blue Degradation.

In this study, the coupled use of a double dielectric barrier discharge (DDBD) and CoOOH catalyst was investigated for the degradation of methylene blue (MB). The results indicated that the addition of CoOOH significantly promoted MB degradation performance compared to the DDBD system alone. In addition, both the removal rate and energy efficiency increased with an increase in CoOOH dosage and discharge voltage. After 30 min of discharge treatment in the coupled system (with CoOOH of 150 mg), the removal rate reached 97.10% when the discharge voltage was 12 kV, which was 1.92 times that in the single DDBD system. And when the discharge time was 10 min, the energy efficiency could reach 0.10 g (k·Wh)-1, which was 3.19 times better than the one in the single DDBD system. Furthermore, the addition of CoOOH could also significantly enhance the TOC and COD removal rates of MB. In the DDBD-coupled-with-CoOOH system, TOC and COD were 1.97 times and 1.99 times those of the single DDBD system after 20 min of discharge treatment with a discharge voltage of 12 kV and 100 mg of CoOOH. The main active substances detected in the coupled system indicated the conversion of the active species H2O2 and O3 into a more oxidizing ·OH was enhanced through the addition of a CoOOH catalyst, resulting in the more effective decomposition of MB and intermediate molecules.