TiO2 Nanocomposites Research Articles

Biocompatible PANI-Encapsulated Chemically Modified Nano-TiO2 Particles for Visible-Light Photocatalytic Applications.

Polyaniline (PANI) constitutes a very propitious conductive polymer utilized in several biomedical, as well as environmental applications, including tissue engineering, catalysis, and photocatalysis, due to its unique properties. In this study, nano-PANI/N-TiO2 and nano-PANI/Ag-TiO2 photocatalytic composites were fabricated via aniline's oxidative polymerization, while the Ag-and N-chemically modified TiO2 nanopowders were synthesized through the sol-gel approach. All produced materials were fully characterized. Through micro-Raman and FT-IR analysis, the co-existence of PANI and chemically modified TiO2 particles was confirmed, while via XRD analysis the composites' average crystallite size was determined as ≈20 nm. The semi-crystal structure of polyaniline exhibits higher photocatalytic efficiency compared to that of other less crystalline forms. The spherical-shaped developed materials are innovative, stable (zeta potential in the range from -26 to -37 mV), and cost-effective, characterized by enhanced photocatalytic efficiency under visible light (energy band gaps ≈ 2 eV), and synthesized with relatively simple methods, with the possibility of recycling and reusing them in potential future applications in industry, in wastewater treatment as well as in biomedicine. Thus, the PANI-encapsulated Ag and N chemically modified TiO2 nanocomposites exhibit high degradation efficiency towards Rhodamine B dye upon visible-light irradiation, presenting simultaneously high biocompatibility in different normal cell lines.

Physical and electrochemical properties of SnO2–TiO2 nanocomposites prepared with different surfactants

Physical and electrochemical properties of SnO2–TiO2 nanocomposites prepared with different surfactants

Using multi-criteria decision-making approach for material alternatives in TiO2/P(VDF-TrFE)/PDMS based hybrid nanogenerator as a wearable device

P(VDF-TrFE)/TiO2/PDMS-based hybrid nanogenerators with excellent piezoelectric performance are of particular interest for the development of sensors, wearable devices, and low-cost biomechanical energy harvesters. In this work, hybrid nanogenerator (HNG) is designed to enhance the energy output by integrating piezoelectric and triboelectric effects. P(VDF-TrFE)/TiO2 nanocomposites are synthesized using electrospinning to design hybrid nanogenerator for energy harvesting from a manual activity. The hybrid nanogenerator device generated 5.36 µA current across 10 MΩ resistor and 52 V electric voltage. An analysis of the effect of varying TiO2 on hybrid nanogenerators is reported here for the first time. The best material for biomechanical energy harvesting applications is selected using a multi-criteria decision-making (MCDM) based material selection and optimization technique TODIM, along with a sensitivity study. SA-4 type nanocomposite is the most suitable material as per the TODIM approach. This nanogenerator shows better performance than most nanogenerators designed with complex and sophisticated approaches.

Fabrication and synergistically enhanced photocatalytic activity of ternary kaolinite, TiO2, and Al2O3 (K65T30A5) nanocomposite for visible-light-induced degradation of methylene blue and remazol red dye

The ternary photocatalyst ((Al2Si2O5 (OH)4/TiO2/Al2O3) composites (where w/w = 65, 30, and 5 wt%) denoted K65T30A5 were successfully synthesized and examined for their efficiency in removing cationic (Methylene Blue, MB) and anionic (Remazol Red, RR) dye from aqueous medium under visible-light irradiation. A series of nanocomposites with varied wt% of kaolinite, TiO2, and Al2O3 were prepared through sonication followed by calcination at 600 °C. X-ray diffraction (XRD) analysis confirmed the crystallinity of the synthesized materials and established their average crystal size to be 83.87 nm. The morphological structure, composite molecule, and surface properties of the resulting K65T30A5 were characterized using FTIR, FE-SEM, and EDS analyses to confirm the successful fabrication of the nanocomposite. FTIR and EDS elemental mapping analyses confirmed the presence of Al, Si, Ti, and O elements in the nanocomposites. The composites exhibited photocatalytic behaviour across the UV–visible spectra, with values varying from the ultraviolet to the visible region with a sharp increase in reflectance at 510 nm. Near-complete degradation of MB (97.66 %) was achieved within 90 min at pH 9 and a 10 mg/L dye concentration, while RR removal reached 90.66 % within 120 min at pH 3.5 and the same dye concentration under visible light irradiation. The catalyst exhibited robust stability, retaining its efficiency by removing 85.09 % of MB and 80.21 % of RR dye after three reuse cycles. The composite catalyst discussed in this study emerges as a promising material for straightforward fabrication techniques, featuring a high percentage of kaolinite and proving to be a cost-effective solution for large-scale water and wastewater treatment processes.

Improving the Performance of Titanium Oxide Nanocomposites as NO2 Gas Sensors for Optimum Sensitivity

In this study, we investigate the performance improvement of titanium oxide (TiO2) nanocomposites as NO2 gas sensors for optimum sensitivity. The TiO2 nanocomposites were synthesized using a solvothermal method and were modified with different dopants and additives to enhance their sensing properties. The sensing performance of the TiO2 nanocomposites was evaluated in terms of sensitivity, selectivity, response time, and recovery time. The synthesized nanocomposites were successfully characterized using AFM, FTIR, SEM-EDX and XRD techniques. The results showed that the addition of additives such as TiO2/GO, TiO2-Ag/GO and TiO2- Al2O3/GO: TiO2/GO significantly improved the sensing properties of the TiO2 nanocomposites. The Ag-doped TiO2 nanocomposites exhibited the highest sensitivity towards NO2 gas with a very low detection limit. The Al2O3-doped TiO2 nanocomposites showed good selectivity towards NO2 gas compared to other interfering gases and has led to increase in the surface area. In conclusion, the addition of additives and the optimization of the annealing temperature can significantly improve the sensing properties of TiO2 nanocomposites towards NO2 gas. The findings of this study can contribute to the development of highly sensitive and selective NO2 gas sensors for various applications such as environmental monitoring and industrial safety.

TiO2 Nanocomposite Coatings and Inactivation of Carbapenemase-Producing Klebsiella Pneumoniae Biofilm-Opportunities and Challenges.

The worldwide increase of multidrug-resistant Gram-negative bacteria is a global threat. The emergence and global spread of Klebsiella pneumoniae carbapenemase- (KPC-) producing Klebsiella pneumoniae represent a particular concern. This pathogen has increased resistance and abilities to persist in human reservoirs, in hospital environments, on medical devices, and to generate biofilms. Mortality related to this microorganism is high among immunosuppressed oncological patients and those with multiple hospitalizations and an extended stay in intensive care. There is a severe threat posed by the ability of biofilms to grow and resist antibiotics. Various nanotechnology-based strategies have been studied and developed to prevent and combat serious health problems caused by biofilm infections. The aim of this review was to evaluate the implications of nanotechnology in eradicating biofilms with KPC-producing Klebsiella pneumoniae, one of the bacteria most frequently associated with nosocomial infections in intensive care units, including in our department, and to highlight studies presenting the potential applicability of TiO2 nanocomposite materials in hospital practice. We also described the frequency of the presence of bacterial biofilms on medical surfaces, devices, and equipment. TiO2 nanocomposite coatings are one of the best long-term options for antimicrobial efficacy due to their biocompatibility, stability, corrosion resistance, and low cost; they find their applicability in hospital practice due to their critical antimicrobial role for surfaces and orthopedic and dental implants. The International Agency for Research on Cancer has recently classified titanium dioxide nanoparticles (TiO2 NPs) as possibly carcinogenic. Currently, there is an interest in the ecological, non-toxic synthesis of TiO2 nanoparticles via biological methods. Biogenic, non-toxic nanoparticles have remarkable properties due to their biocompatibility, stability, and size. Few studies have mentioned the use of nanoparticle-coated surfaces as antibiofilm agents. A literature review was performed to identify publications related to KPC-producing Klebsiella pneumoniae biofilms and antimicrobial TiO2 photocatalytic nanocomposite coatings. There are few reviews on the antibacterial and antibiofilm applications of TiO2 photocatalytic nanocomposite coatings. TiO2 nanoparticles demonstrated marked antibiofilm activity, but being nano in size, these nanoparticles can penetrate cell membranes and may initiate cellular toxicity and genotoxicity. Biogenic TiO2 nanoparticles obtained via green, ecological technology have less applicability but are actively investigated.

Effective development and utilization of SILAR-assisted TiO2 and CsPb2Br5 nanocomposites for photochemical and biological cleaning of environment

Recently, cesium lead halide perovskites such as CsPb2Br5 and CsPbBr3 have drawn the attention of researchers because of their unique optical, electronic, and chemical properties. To improve the photo and/or chemical performance of such CsPb2Br5 (termed as CPB hereafter), we have realized multiple facile routes for its combination with UV-active TiO2 nanoparticles. Resultantly developed binary nanocomposites of TiO2, CPB perovskites and TiO2/CPB-nanocomposite (TiO2/CPB-NC) offered a meaningful photochemical contrast between pseudo-successive ionic layer adsorption and reaction (p-SILAR) and electrostatic self-assembly methods for targeting photocatalytic degradation of toxic dyes under solar irradiation and resulted significant performance as reactant for oxygen evolution (OER) as revealed by extensive electrochemical impedance spectroscopy (EIS). In parallel to extensive material-based characterization using SEM, XRD, and UV Vis. etc, the study was further extended to the theoretical investigation of the structure of CsPb2Br5, and antibacterial activity against gram-positive and gram-negative bacteria namely Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus). RhB degradation of TiO2 increased from 13% to 58% by deposition of CPB, in parallel to 100% inhition zone growth.

Silver doped anatase nanocomposite: a novel photocatalyst with advanced activity under visible light for waste-water treatment

Anatase is a universal semiconductor photocatalyst; however, its wide band-gap energy limits its entire solar spectrum absorption to only 5%. Anatase could be activated in the visible region via nobel metal deposition. This study reports on the facile synthesis of colloidal mono-dispersed anatase nanoparticles of 5 nm particle size via hydrothermal synthesis. Nobel metals (Silver, Nickel) were deposited on colloidal anatase surface. The photocatalytic activities of Ag–TiO2, and Ni–TiO2 were investigated for the degradation of basic fuchsin dye. Ag–TiO2 nanocomposite demonstrated enhanced adsorption activity in dark, as well as superior photocatalytic. Ag–TiO2 nanocomposite demonstrated enhanced removal efficiency by 70.8% under visible irradiation to virgin anatase. Ag–TiO2 nanocomposite demonstrated enhanced oxygen-lattice with low binding energy using XPS analysis. Ag–TiO2 experienced band gap energy of 2.35 eV compared with 3.2 eV for virgin anatase; this feature could secure enhanced solar absorption. Ag–TiO2 demonstrated excellent photo-degradation efficiency of 88% with 0.3% H2O2 under visible light. Deposited silver could catalyze H2O2 decomposition and could promote free radical generation; Ag–TiO2 nanocomposite is a promising photocatalyst for wastewater treatment applications.

Synergistic effects of micronanobubbles and AC/Ag–TiO2 nanocomposites in photocatalytic process

The AC/Ag–TiO2 nanocomposites were prepared by sol-gel method using different concentrations of Ag. Comprehensive characterization of the crystalline structure, surface morphology, elemental composition, and optical properties of the AC/Ag–TiO2 photocatalysts was carried out using XRD, FTIR, SEM, EDX, TEM, and UV–vis DRS techniques. Consequently, a detailed investigation into the photocatalytic degradation of Indigo Carmine (IC) and Reactive Black 5 (RB5) dyes was conducted, thoroughly examining the involved photocatalytic mechanisms. The study revealed promising outcomes, particularly with the hybrid photocatalyst AC/0.5%Ag–TiO2, showcasing enhanced characteristics in both photooxidation and absorption processes, thereby boosting overall efficacy for IC (70.15%) and RB5 (69.9%). Remarkably, the introduction of small air bubbles significantly improved the removal efficiency of IC and RB5 dyes, achieving removal levels of 93.66% and 88.66%, respectively. The utilization of these micro-nanobubble systems (MNBs) resulted in notably higher first-order reaction constants compared to scenarios without MNBs, indicating the pivotal role of the photocatalyst in dye removal processes. Additionally, the photocatalyst showed unmatched efficacy in eliminating the pesticide carbaryl, attaining 100% removal with and without the presence of MNBs. Moreover, the AC/Ag–TiO2 photocatalyst exhibited significant inhibition of both gram-positive and gram-negative pathogenic bacteria, showcasing its capability to curb their growth even without MNB aeration. This underscores its potential for applications in environmental remediation and microbial control.

A universal polymer-assisted route to fabricate Zr-doped TiO2 nanocomposite: boosting reactive desulfurization

A universal polymer-assisted route to fabricate Zr-doped TiO2 nanocomposite: boosting reactive desulfurization

In-situ hydrothermal synthesis of MoS2 /TiO2 nanocomposites for enhanced and stable photocatalytic performance: Methylene blue degradation pathway and mechanism

BackgroundIn recent years, nanocomposite photocatalytic has become more and more attractive and important since it has a great potential to contribute to such wastewater treatment and environmental problems. Pollutant dyes such as methylene blue (MB) have utilizations in manufacturing, paper, medicine and textiles. In addition, creating a Z-scheme nanocomposite illustrates a fitting approach for improving the photocatalytic performance of photocatalysts. Mott-Schottky curves demonstrate that MoS2 and TiO2 are combined to form Z-scheme nanocomposite. MethodsNovel MoS2/TiO2 nanocomposite photocatalysts were well synthesized by a simple hydrothermal process. The photodegradation intermediate products of MB dye are also identified by liquid chromatography-mass spectrometry (LC-MS) and the possible degradation pathway is proposed. Ultimately, the potential photocatalytic pathway mechanism of nanocomposites was verified according to the LC-MS analysis and trapping experiments. Significant findingsThe construction of a Z-scheme nanocomposite is a crucial factor in improving the photocatalytic activity of heterojunction photocatalysts. MoS2/TiO2 nanocomposites had photocatalytic activity within 120 min irradiation to visible light and achieved 98.5 % of MB. A stable heterostructure has been effort designed using MoS2/TiO2 with improved electron and hole migration. The photodegradation performance for MoS2/TiO2 is 3.8 folds that the bare photocatalysts. This nano-heterojunction significantly suppresses the recombination rate of photoexcited charge carriers and enhances the operation of solar energy. The Z-scheme nano-heterojunctions offer a potential strategy for promoting the utilization of photocatalysts in waste environmental purification and clean water.

Improvement of the photoelectric dye sensitized solar cell performance using Fe/S–TiO2 nanoparticles as photoanode electrode

A sulfur nanoparticles-incorporated iron-doped titanium oxide (Fe/TiO2) with different ratio was successfully synthesized by photolysis method and utilized as effective photoanode in dye sensitized solar cell (DSSC) application with N719 dye. The photolysis method was contained the irradiation of the Fe, S and Ti mixture solution with 15 W source irradiation, and then calcined the formed precipitate. The DSSCs fabricated with Fe/S–TiO2 photoanode appeared an improved solar-to-electrical energy conversion efficiency of 6.46, which more than pure TiO2 (3.43) below full sunlight illumination (1.5 G). The impact of Fe content on the total efficiency was also inspected and the Fe content with 6% S–TiO2 was found 5 wt%. Due to the improved the efficiency of solar cell conversion of Fe/S–TiO2 nanocomposite, it should be deemed as a potential photoanode for DSSCs with high performance.

Photocatalytic persulfate activation by highly dispersed nano-TiO2 supported by silica for efficient carbamazepine degradation

A silica-loaded nano-TiO2 composite (A-SiO2/TiO2) was prepared by wet-grinding method, using industrial silica (A-SiO2) as the carrier. A-SiO2/TiO2 was used for photocatalytic activation of peroxymonosulfate (PMS) to degrade carbamazepine (CBZ). The A-SiO2/TiO2 containing 20 wt% nano-TiO2 resulted in the CBZ degradation efficiency of 94.83 % after 90 min simulated sunlight irradiation with the presence of PMS. The main reactive species during CBZ degradation in the system of photocatalytic PMS activation by A-SiO2/TiO2 were O2•−, •OH and SO4•−. Compared to nano-TiO2, A-SiO2/TiO2 exhibits enhanced dispersion, increased surface active sites and improved photo-generated carrier separation efficiency, which contributed to enhanced degradation performance.

A template-assisted method for synthesizing TiO2 nanoparticles and Ni/TiO2 nanocomposites for urea electrooxidation

The exploration of electrocatalytic urea-assisted wastewater treatment as a method for sustainable energy generation presents a compelling approach within the domain of green chemistry. In this context, titanium dioxide (TiO2) and nickel-doped TiO2 (Ni@TiO2) nanocomposites were developed through an innovative organic template-assisted synthesis strategy. These were denoted as m-TiO2-org and Ni@m-TiO2-org, respectively, to create cost-effective and high-performance electrodes for urea electrooxidation in urea-based fuel cells. The structural and chemical properties of the fabricated m-TiO2-org and Ni@m-TiO2-org materials were meticulously analyzed using a suite of physicochemical characterization techniques, including Scanning Electron Microscopy (SEM), X-ray Diffraction (XRD), Thermogravimetric Analysis (TGA), and Energy-Dispersive X-ray Spectroscopy (EDX). These investigations revealed that both m-TiO2-org and Ni@m-TiO2-org materials predominantly consisted of irregular monolithic microparticles formed through the aggregation of spherical nanoparticles, with diameters ranging from 8.16 nm to 13.1 nm. Subsequent evaluations of these TiO2-based materials as electrocatalysts for urea electrooxidation demonstrated their efficacy, as evidenced by voltammetric and electrochemical impedance spectroscopy measurements. Notably, the Ni@m-TiO2-org variant exhibited enhanced electrochemical performance, attributed to the presence of Ni2+ sites. These sites facilitated electrochemical activation and the formation of active NiOOH sites, leading to a significant increase in the current density (0.78 mA/cm2 at 1.523 V vs. the Reversible Hydrogen Electrode (RHE)), as a fiftyfold enhancement compared to m-TiO2-org@Glassy Carbon Electrode (GCE) under similar conditions (3 M KOH containing 3 M urea), with a Tafel slope of 33 mV/decade. This research not only elucidates the potential of TiO2-based nanocomposites in the electrooxidation of urea but also heralds the development of innovative electrode materials for commercial electrochemical cells, marking a significant advancement in the field of electrocatalysis and sustainable energy technology.

G-C3N4/TiO2 nanocomposite coated with zinc oxide for selective photocatalytic degradation of nitrate in aquatic media

g-C3N4/TiO2 nanocomposite coated with zinc oxide for selective photocatalytic degradation of nitrate in aquatic media

Study and Characterization of Copper and Titanium Oxides Nanostructures for Some Molecular and Biological Applications

In this work, Copper and Titanium nanocomposites (NPs) were prepared by mixture exchange process with ratios (25, 50 and 75 % CuO-TiO2). The biological activity was studied, and it was found that the concentrations of 50 and 100 µg/mL of 50 and 75 % CuO-TiO2 were the best concentrations, Low concentrations of the nanoparticle mixture at 25 µg/mL also stimulated the growth of symbiotic bacteria. The mixture of nanoparticles was easier to prepare and more effective in inhibiting bacterial growth. biochemical test and PCR were performed to confirm the identity of the studied bacteria. While isolating the bacteria, a new type of bacteria was detected and registered in the Global Gen Bank under accession No. OP942239. Surface and structure properties have been studied using FESEM, EDS analysis, XRD and FTIR respectively. It can be seen that the size and diameter of the nanocomposite increase with the weight ratio of CuO-TiO2. The aggregated CuO-TiO2 nanostructures with different ratios were transformed gradually into a uniform spherical shape. The average size of the CuO/TiO2 composite was found to be about 32.122, 29.865 and 27.607 nm at 25, 50 and 75 % CuO-TiO2 respectively. While the mean sizes of CuO and TiO2 were 25.35 and 34.38 nm respectively. The crystalline size decreases after the ion exchange process, which could be due to the diffraction peaks being broad in all the samples of Copper Titanate at the surface. Subsequently, adding Copper particles to the TiO2 film can improve the performance of the material. HIGHLIGHTSThe nanostructure CuO-TiO2 was created through various loading ratios. These NPs’ efficiency was calculated using a number of techniques, including FTIR, X-ray diffraction, EDS spectra, and FESEM. The observations indicate that molecular transition parameters play an essential role in determining the size, shape, and functionality of CuO- TiO2 NPs. The sharp peaks observed in the composites indicated higher crystallinity in CuO. In addition, two types of NPs have shown promising effects in inhibiting NPs aggregation and enhancing biological effects but the potential of these NPs against different bacteria may differ. Thus, further research and testing is needed to assess its efficacy and human health and environmental impact before considering its use. In conclusion, copper and titanium NPs have their distinct advantages in bacterial inhibition, and the choice between them should be based on specific conditions and environmentally friendly factors. GRAPHICAL ABSTRACT

The Catalytic Role of Superparamagnetic Iron Oxide Nanoparticles as a Support Material for TiO2 and ZnO on Chlorpyrifos Photodegradation in an Aqueous Solution.

Chlorpyrifos (CP) is a globally used pesticide with acute toxicity. This work studied the photocatalytic degradation of CP using TiO2, ZnO nanoparticles, and nanocomposites of TiO2 and ZnO supported on SPIONs (SPION@SiO2@TiO2 and SPION@SiO2@ZnO). The nanocomposites were synthesized by multi-step incipient wetness impregnation. The effects of the initial pH, catalyst type, and dose were evaluated. The nanocomposites of SPION@SiO2@TiO2 and SPION@SiO2@ZnO showed higher CP photodegradation levels than free nanoparticles, reaching 95.6% and 82.3%, respectively, at pH 7. The findings indicate that iron oxide, as a support material for TiO2 and ZnO, extended absorption edges and delayed the electron-hole recombination of the nanocomposites, improving their photocatalytic efficiency. At the same time, these nanocomposites, especially SPION@SiO2@TiO2, showed efficient degradation of 3,5,6-trichloropyridinol (TCP), one of the final metabolites of CP. The stability and reuse of this nanocomposite were also evaluated, with 74.6% efficiency found after six cycles. Therefore, this nanomaterial represents an eco-friendly, reusable, and effective alternative for the degradation of chlorpyrifos in wastewater treatment.

A Critical Review of the Evaluation of Sio2-Incorporated Tio2 Nanocomposite for Photocatalytic Activity

A Critical Review of the Evaluation of Sio2-Incorporated Tio2 Nanocomposite for Photocatalytic Activity

Graphite/carbon-doped TiO2 nanocomposite synthesized by ultrasound for the degradation of diclofenac.

Graphite/C-doped TiO2 nanocomposite was synthesized at room temperature using a simple, impressive, and indirect sonication (20kHz) by the cup horn system. Tetrabutyltitanate as the precursor of titanium and graphite (G) as the carbon source was used in the preparation of nanocomposite as a photocatalyst. The molar ratio of G/TiO2 as a key parameter was investigated in the synthesis of G/C-doped TiO2. The obtained materials were widely characterized using XRD, SEM, TEM, FTIR, XPS, and UV-Vis diffuse reflectance techniques. The UV-Vis diffuse reflectance spectroscopy results showed that the edge of light absorption of nanocomposite was distinctly red-shifted to the visible area via carbon doping. The XPS outcomes acknowledged the existence of the C, Ti, and O in the photocatalyst. The composite showed an enhancement in the dissociation efficiency of photoinduced charge carriers through the doping process. The photocatalytic activity of the synthesized nanocomposite was checked with diclofenac (DCF) as a pharmaceutical contaminant. The results displayed that G/C-doped TiO2 represented better photocatalytic performance for DCF than TiO2. This was due to the excellent crystallization, intense absorption of visible light, and the impressive separation of photoinduced charge carriers. Various active species such as •OH, •O2¯, h+, and H2O2 play a role in the degradation of DFC. Therefore, different scavengers were used and the role of each one in degradation was investigated. According to the obtained results, •O2¯ radical showed a major role in the photocatalytic process. This work not only proposes a deep insight into the photosensitization-like mechanism by using G-based materials but also develops new photocatalysts for the removal of emerging organic pollutants from waters using sunlight as available cheap energy.

Emerald eco-synthesis: harnessing oleander for green silver nanoparticle production and advancing photocatalytic MB degradation with TiO2&CuO nanocomposite

The tertiary composite of TiO2/CuO @ Ag (TCA) were synthesized by the solid state method using different ratios of TiO2/CuO NCs and Ag NPs. The structural, morphological, and optical properties of nanocomposites were analyzed by scanning electron microscope, Transmission electron microscope, X-ray diffraction, Fourier transform infrared spectra, UV–Vis diffuse reflectance spectra (UV–Vis/DRS) and photoluminescence spectrophotometry. The results showed enhanced activity of TCA hybrid nano crystals in oxidizing MB in water under visible light irradiation compared to pure TiO2. The photocatalytic performance TCA samples increased with suitable Ag content. The results show that the photo degradation efficiency of the TiO2 compound improved from 13 to 85% in the presence of TiO2–CuO and to 98.87% in the presence of Ag containing TiO2–CuO, which is 7.6 times higher than that of TiO2. Optical characterization results show enhanced nanocomposite absorption in the visible region with long lifetimes between e/h+ at optimal TiO2–CuO/Ag (TCA2) ratio. Reusable experiments indicated that the prepared TCA NC photo catalysts were stable during MB photo degradation and had practical applications for environmental remediation.