Doped Titanium Dioxide Research Articles

Enhanced Water Pollutant Removal Using Titanium Doped Nickel Ferrite via Photocatalytic Degradation.

Enhanced Water Pollutant Removal Using Titanium Doped Nickel Ferrite via Photocatalytic Degradation.

The Morphological and Structural Properties of Chromium (Cr)-doped Titanium Dioxide (TiO2) Nanoparticles prepared via Sol–gel Method at Various Concentrations

The Morphological and Structural Properties of Chromium (Cr)-doped Titanium Dioxide (TiO2) Nanoparticles prepared via Sol–gel Method at Various Concentrations

Elastic mechanical thermodynamic and thermoelectric properties of pristine and titanium doped Mg2Si: a density functional theory study

Herein, we report a systematic investigation of the effect of Titanium doping on the structural, elastic, mechanical, thermodynamic, and thermoelectric (TE) dynamics of Mg2Si Compounds using first-principle investigation. The present study has been carried out using the full potential linearized augmented plane wave method as implemented inWien2kcode undermBJexchange potentials. The investigations revealed that Mg2-xTixSi compounds have structural stability with cubic phase (Fm-3msymmetry) and possess degenerate semiconducting nature. The analysis of elastic constants revealed mechanical stability of the investigated compounds following Born criteria. Thermodynamic investigations have been carried out in the temperature range of 100-1500 K at zero pressure and the quantities like heat capacity, Debye temperature, Grüneisen constant, and thermal expansion coefficient have been critically analyzed. Lastly, the TE performance of Mg2-xTixSi compounds has been predicted by estimating the thermopower (S2σ) and TE figure of merit (zT) in the temperature range of 300-1500 K. The predicted value ofzTmaxfor Mg2-xTixSi compound is 0.67 at 800 K forx= 0.25 titanium content, suggesting materials promising application for TE energy harvesting and mechanical devices.

SnO2QDs: Photophysical properties, photocatalytic activity, mineralization financial cost and recycling process during industrial effluent treatment

This study investigates the synthesis, characterization, and photocatalytic performance of pure and titanium-doped tin dioxide quantum dots (SnO2QDs) prepared via a sonochemical method. The structural and morphological properties were thoroughly examined using XRD, FTIR, SEM-EDX, HRTEM, UV-DRS, and BET surface area analysis. XRD confirmed the formation of tetragonal SnO2 with high phase purity and average crystallite sizes of 2.95 nm for SnO2QD1 (calcined at 270 °C) and 8.36 nm for SnO2QD2 (calcined at 480 °C). Titanium doping was achieved without altering the SnO2 crystalline structure, as evidenced by FTIR spectra showing characteristic vibrational modes and hydroxyl groups. HRTEM images revealed spherical nanoparticles with diameters of 3.2 nm for SnO2QD1 and 9.7 nm for SnO2QD2, supported by SAED patterns confirming their polycrystalline nature. The photocatalytic efficiency was evaluated through the degradation of Reactive Yellow 145 dye under Xenon lamp irradiation. SnO2QD1 exhibited superior photocatalytic activity with a rate constant (k) of 6.94 × 10−3 s−1, achieving 80 % dye degradation in 105 min, compared to SnO2QD2 with a k of 4.50 × 10−3 s−1 and 83 % degradation in 120 min. Titanium doping further enhanced the photocatalytic performance, with SnO2QDT1 (1 % Ti) showing a k of 9.89 × 10−3 s−1 and 80 % degradation in just 90 min, three times more efficient than SnO2QDT2 (9 % Ti). BET analysis indicated a significant reduction in surface area with increased calcination temperature, from 154 m2/g for SnO2QD1 to 86 m2/g for SnO2QD2. The bandgap energies, determined via UV-DRS, were 3.30 eV for SnO2QD1 and 3.34 eV for SnO2QD2, slightly reduced in Ti-doped samples, enhancing visible light absorption. The SnO2QDs demonstrated excellent recyclability, maintaining photocatalytic activity over eight reuse cycles. Economic analysis based on Saudi Arabian electricity tariffs highlighted the cost-effectiveness of SnO2QD1, offering a 5.2 % reduction in energy consumption compared to SnO2QD2. These findings position SnO2QDs as highly efficient and sustainable photocatalysts for industrial wastewater treatment applications.

Effects of doping of Sm, Y, Ce and La on crystal structure, phase and photocatalytic performance of TiO2 powders prepared by sol-gel method

In the present work, pure and 1 mol% samarium (Sm), yttrium(Y), lanthanum (La), cerium (Ce)-doped titanium dioxide (TiO2) powders were prepared by sol-gel method. Taking Methylene blue (MB) dye as degradation targets the photodegradation performance of the photocatalysts was studied. XRD spectra confirmed that the doping of rare earth elements (RE) could inhibit the transformation of TiO2 from anatase to rutile crystal at high temperature of 800 °C. XPS analyzed the chemical state of the elements in the powder. Characterization such as SEM and TEM found that the doping of the RE elements made the severely agglomerated particles become dispersed and refined, increased the specific surface area, and reduced the optical bandgap. Simulated visible light degradation results of MB showed that the degradation efficiency was significantly improved by doping of the RE elements, and the best efficiency is 88 % for Sm-doped TiO2 powder samples.

H2S gas sensing based on CuNi MOFs derivative with TiO2 quantum dot decoration applied for meat freshness detection

As food safety issues have been widely revealed and exposed, the pursuit of food for people has shifted from food and clothing to fresh and healthy. Currently, there are many detection systems for detecting meat freshness on the market. However, most of the problems still exist are that they cannot be monitored in real time, cannot guarantee traceless monitoring, and the cost is high. To solve these problems, this work has built a portable meat freshness detection system based on copper oxide (CuO)/nickel oxide (NiO) doped titanium oxide (TiO2) quantum dot composites and added real-time monitoring and remote monitoring and finally packaged it into an intelligent food box. Real-time monitoring of the freshness of meat can be carried out in a specific range regardless of the space. Hydrogen sulfide (H2S) has always been an essential indicator of meat decay. Therefore, in this paper, an H2S gas sensor based on CuO/NiO doped TiO2 quantum dot composites material is designed and fabricated, which can effectively and quickly identify H2S. The gas sensor exhibits excellent gas sensing characteristics for H2S with a detection limit of 100 parts per billion (ppb) and has excellent selectivity and repeatability, which because of the presence of p-p type heterojunctions in CuO/NiO. In addition, the feasibility of the system and material for analyzing the meat deterioration process is demonstrated through the test of different meat samples. It is firmly believed that this new type of sensor mentioned in this paper can make contribution to food quality monitoring.

Nonlinear optical studies of Bismuth-doped Titanium di-oxide colloids achieved by femtosecond Z-Scan technique

In this paper, we explored the nonlinear optical (NLO) properties of Bismuth (Bi) doped titanium dioxide (TiO2) nanoparticle (NP) colloids in ethanol, with laser pulses of duration ∼ 150 femtoseconds (fs). The Bi-doped TiO2 NPs were synthesized via the chemical route, sol-gel method. The increased photo response of TiO2 upon doping it with metals has become a burning issue to extend the applications of metal-doped TiO2 NPs as integral parts in solar cells, catalysts, phototherapy, etc. The bandgap of anatase TiO2 NPs was observed to be reduced to 2.89 eV upon doping Bi. The modified band structure of the Bi-doped TiO2 NPs demonstrates novel chemical, mechanical, and optical properties. NLO studies were conducted on Bismuth-doped TiO2 NPs submerged in ethanol employing femtosecond laser input pulses with incoming wavelengths 700, 750, 800, 850, 900, and 950 nm. It has been detected that open aperture (OA) studies performed at an input peak intensity of 100 MW/cm2 on Bi-doped TiO2 NPs in ethanol were exhibiting complex NLO behavior, i.e., reverse saturable absorption (RSA) in saturable absorption (SA) and SA in RSA with mostly effective two-photon absorption (1 + 1) coefficients. Particularly, at ∼800 nm, the behavior observed was so complex, i.e., RSA in SA in RSA in SA, with an effective 3 PA (2 + 1) co-efficient (γ) ∼6.5 × 10−24 m3/W2. The closed aperture (CA) studies at ∼37 MW/cm2 exhibited self-defocusing effects, i.e., an intensity-dependent refractive index (n2) with a negative signature.

Impact of titanium modification on the performance improvement and phase change mechanism of ZnSb thin film

Phase change memory has emerged as a promising option for neuro-inspired and data-intensive AI applications, attracting significant attention from the semiconductor field recently. The performance of the device relies on the phase change material, aiming for enhanced thermal stability along with low power consumption. Nanocomposite ZnSb thin films with titanium dopant were prepared and their crystallization properties and mechanisms were investigated. Compared to pure ZnSb material, the addition of titanium can significantly enhance the temperature of crystallization and the 10-year data retention ability, both of which surpassing 16 °C. The obvious enhancement in thermal stability may be ascribed to the ionic bond formation between titanium and antimony elements, as indicated by differential charge calculations. Also, phase change memory cells with a diameter of 190 nm were fabricated using standard CMOS technology. The Ti-doped ZnSb thin film demonstrates rapid crystallization and amorphization within 50 ns while consuming low power at approximately 1.5 × 10−10 J. The decrease in power consumption may stem from the increase in band gap energy and a decrease in electrical conductivity, as confirmed by first-principles calculations. Both experimental and theoretical results prove that titanium doping can remarkably improve the physical properties of ZnSb thin film, facilitating the exploration and design of novel phase change materials with high thermal stability, low power consumption, as well as fast switching speed.

Optimizing dye-sensitized solar cell efficiency through TiO2/CuS doping: effects of internal parameter variations

Dye-sensitized solar cells (DSSC) have attracted significant research interest due to their semi-transparency, ease of fabrication, cost-effectiveness, and environmental friendliness. This research focuses on enhancing dye-sensitized solar cells efficiency by doping titanium dioxide with copper sulfide and varying internal parameters such as concentration, thickness, and temperature. The primary issue addressed is the low electron mobility of titanium dioxide, which limits its performance as a photoanode. Using simulation methods, this study analyzed dye-sensitized solar cells performance under different doping conditions. The results showed that the highest efficiency of 8.18 % was achieved at a TiO2/CuS concentration of 0.3 %. The optimal photoanode thickness was approximately 3 μm, yielding an efficiency of 8.33 %. Temperature variations at room temperature (275 K, 300 K, and 325 K) resulted in efficiency values of 13.94 %, 15.06 %, and 16.18 %, respectively. These findings indicate that targeted doping and precise control of internal parameters can significantly enhance the performance of titanium dioxide-based dye-sensitized solar cells. The improved efficiency is attributed to enhanced electron mobility and better structural and morphological characteristics of the doped titanium dioxide photoanode. This research provides valuable insights into developing more efficient and sustainable dye-sensitized solar cells. The practical implications of these results are significant for advancing dye-sensitized solar cells as a viable alternative to conventional solar cells, contributing to the global effort to address the energy crisis by providing a cost-effective and environmentally friendly energy source.

Effects of Nd-doping on crystal phase, structure and photocatalytic performance of TiO2 powders prepared by sol-gel method

Abstract In this work, 0.3–2 mol% neodymium (Nd) doped titanium dioxide (TiO2) powder was prepared by sol–gel method. The XRD showed that the anatase phase occur for the Nd doped TiO2 powders, and the Nd doping suppressed the original rutile phase for the pure TiO2 powder. SEM and TEM revealed that Nd doping reduced the tendency of severe aggregation and increased the specific surface area compare with pure TiO2 powder, and the Gibbs free energy difference did not reach the critical value of the phase transition driving force, while the adjustment of the Ti-O bond length caused by the addition of Nd3+ impeded the transformation of TiO2 to rutile phase. The photocatalytic activity test results for Methylene blue show that the 0.5 mol% Nd doped TiO2 had the best photocatalytic activity with the degradation efficiency of 96.2%.

SYNTHESIS STRUCTURAL AND MAGNETIC PROPERTIES OF TITANIUM DOPED MAGNESIUM ZINC FERRITE

Magnetic ceramics or ferrites are very well established group of magnetic materials which exhibits ferrimagnetism. It possess high electrical resistivity, low eddy current and dielectric loss which makes it superior than the other ordinary magnetic oxides that contain the ferric oxide (Fe₂O₃) as their basic magnetic compounds. The ceramic magnets are widely used in high frequency transformer application. [(Mg, Mn, F12o4)] spinels are used in square-loop application. Ceramic materials found application in nuclear physics. In nuclear reactors ceramics are used as core components. The studies include the preparation and analysis of Titanium doped Magnesium zinc ferrite. Here, Titanium doped magnesium zinc ferrite nanoparticles (NPS) were synthesized using solid state reaction method. Titanium doping can enhance the magnetic properties of magnesium zinc ferrite in several ways these can contribute to improved magnetic properties , such as increased magnetic moment, saturation magnetization, and magnetic ordering , making titanium – doped magnesium zinc ferrite a promising material for various applications including magnetic storage, sensors, and spintronics. According to the stoichiometric equation [Mg0.9Zn 0.1TixFe2-xO4] at different values of x, (x=0.1, 0.3) are synthesised. Calcination and sintering of the samples is made by high temperature PID controlled muffle furnace which can go up to 1000°C. The structural and magnetic properties are examined using XRD, FTIR and Curie temperature analysis. From the XRD analysis it revels the phase structure and lattice parameters of the samples. XRD analysis gives maximum intensity of (h k l) values as (3 1 1) in both cases. It also reveals that no secondary phases are produced during growth. That means the specimens FCC stacking. FTIR analysis of the samples done using Fourier transformer infrared spectroscopy. From this analysis it revels the detailed atomic structure and bonding of the samples. The bands obtained reveal spinal ferrite structure. Curie temperature of the specimens is determined by Curie temperature apparatus for the study of magnetic properties of the specimens.

First-principles study on the adsorption of gas molecules on Fe, Ti-Doped silicene

In this study, we employ first-principles calculations to investigate the geometric and electronic properties of intrinsic silicene and silicene doped with metal elements Fe and Ti. We analyze the adsorption performance of five gas molecules (CO, SO2, H2S, CH4 and H2CO) on the surfaces of these two materials. For each gas molecule, we determine the optimal adsorption site and calculate parameters such as adsorption distance, adsorption energy, charge transfer, recovery time, and density of states to understand the adsorption mechanism. Our study reveals that the adsorption affinity of the selected gas molecules on intrinsic silicene is relatively weak. The distance between the gas molecules and the intrinsic silicene surface is relatively large, and no stable chemical bonds are formed between them. In contrast, Fe and Ti-doped silicene exhibit relatively higher stability, with the adsorption energies of the gas molecules on their surfaces increasing obviously. The Titanium doping exerts a considerable influence on increasing the band gap and the adsorption energy of silicene compared with the intrinsic one, thus the whole structure is able to reveal semiconductors’ properties. In Ti-doped silicene structures, the band gap opens, exhibiting semiconductor properties, and the adsorption energies increase relative to intrinsic silicene. These results indicate that the doping of Fe and Ti atoms enhances the adsorption performance of silicene materials, providing theoretical reference for the gas sensing performance of Fe and Ti-doped silicene materials and the semiconductor performance of Ti-doped silicene.

Evolution of magnetization of Bi1-ySmyFe1-xTixO3 ceramics at the morphotropic phase boundary attested by multistep magnetization measurements, time aging and electric field

Bi1-ySmyFe1-xTixO3 ceramics with compositions at the rhombohedral- orthorhombic morphotropic phase boundary (y = 0.1, 0.12, 0 ≤ x ≤ 0.1) were prepared by solid state reaction method. Analysis of the crystal structure of the compounds based on the results of laboratory and synchrotron X-ray diffraction measurements as well as Raman spectroscopy experiments revealed a coexistence of the rhombohedral phase (SG R3c) and the anti-polar orthorhombic phase (SG Pbam) in the compounds Bi0.88Sm0.12Fe1-xTixO3 with 0 ≤ x ≤ 0.1; the compounds Bi0.9Sm0.10Fe1-xTixO3 are characterized by the mixed structural state for the concentration range 0 ≤ x ≤ 0.06 and by the single phase rhombohedral state within 0.06 < x ≤ 0.1. Room temperature magnetization measurements demonstrate a gradual increase of remanent magnetization with Ti content in the compounds of both systems up to the maximal value of MR ∼0.28 emu/g for compounds with x = 0.06 which is followed by a decrease in magnetization with further titanium doping. Temperature decrease leads to a reduction of remanent magnetization which is mainly caused by a partial recovery of spatially modulated spin structure occurred in the compounds of both systems. Time aging of the compounds for about ∼1 year leads to a drastic increase of MR, which is caused by a change in the structural phase ratio, homogeneity of the structural state and a contribution of unbounded spins demonstrated by low field measurements. Subjecting of the annealed compounds to external electric field of E ∼40 kV/cm leads to a decrease of magnetization associated with backward structural transformations and redistribution of the local structural defects in the compounds.

Doping of Porous Transport Layers to Optimize Electrical Contact Behaviour in PEM Water Electrolysis Cells

A high overall efficiency is crucial for large-scale polymer electrolyte membrane water electrolysers. Due to the harsh environment at the anode, a titanium oxide layer with high electrical resistivity passivates porous transport layers (PTL). A common used way to overcome this problem is noble metal coating (e.g. with platinum, gold or iridium). [1] For the very first time, we present a new and inexpensive way of maintaining the high conductivity of PTLs by doping the titanium surface that faces the catalyst layer. Sun et al. [2] modelled the conductivity of doped titanium oxide for different elements. With respect to their results and Koech et al. [3] we chose tin, niobium, antimony and yttrium as dopants. The implantation was carried out at the Ion Beam Center of the HZDR in Dresden, Germany. All doped PTLs displayed a lower cell voltage than the undoped reference as visible in figure 1a). While tin improves in the range of 2-3 % at a current density of 2A/cm², the other dopants best results reach values of over 4 % with niobium achieving the best performance with 4.4 % improvement (see figure 1b) for comparison). Figure 1c) shows the high frequency resistance (HFR) originating from impedance measurements. The observable improvement of up to 11.4% at 2A/cm² proves the fact that the advantage corresponds to a better contact resistance due to a lower resistance of the doped titanium oxide layer. The improvement in percent presents figure 1d).The measurement results show that doping can have a great impact on the contact resistance of titanium PTLs. These results open a new opportunity in the manipulation of porous transport layers for enhanced contact behaviour, where no experimental publications exist yet. Especially in comparison to noble metal coatings like iridium, doping has an enormous cost advantage when using non noble metals with the potential of lowering the overall electrolyser system costs while increasing its efficiency.[1] Liu, C., Shviro, M., Gago, A. S., Zaccarine, S. F., Bender, G., Gazdzicki, P., Morawietz, T., Biswas, I., Rasinski, M., Everwand, A., Schierholz, R., Pfeilsticker, J., Müller, M., Lopes, P. P., Eichel, R.-A., Pivovar, B., Pylypenko, S., Friedrich, K. A., Lehnert, W., Carmo, M., Exploring the Interface of Skin-Layered Titanium Fibers for Electrochemical Water Splitting. Adv. Energy Mater. 2021, 11, 2002926. https://doi.org/10.1002/aenm.202002926[2] Hu Sun, Zhu-tian Xu, Di Zhang. First-principles calculations to investigate doping effects on electrical conductivity and interfacial contact resistance of TiO2, Applied Surface Science, Volume 614, 2023, 156202, ISSN 0169-4332, https://doi.org/10.1016/j.apsusc.2022.156202.[3] Koech, R.K.; Ichwani, R.; Oyewole, D.; Kigozi, M.; Amune, D.; Sanni, D.M.; Adeniji, S.; Oyewole, K.; Bello, A.; Ntsoenzok, E.; et al. Tin Oxide Modified Titanium Dioxide as Electron Transport Layer in Formamidinium-Rich Perovskite Solar Cells. Energies 2021, 14, 7870. https://doi.org/10.3390/en14237870 Figure 1

Tuning of fluorescence in titanium carbide MXene nanosheets with La3+ ion doping for the recognition of creatinine biomarker in biofluids

There is a strong correlation between the concentration of creatinine in human urine and the overall health of the kidneys. Therefore, there has been a persistent need for a rapid, and cost-effective quantitative method to assay creatinine levels in urine. Herein, green fluorescent La3+ doped titanium carbide nanosheets (La3+-doped Ti3C2 NSs) are fabricated via HF etching method by using Ti3AlC2 as MAX phase material and La(NO3)3 as a doping agent. As synthesized fluorescent La3+-doped Ti3C2 NSs are stable, showing green fluorescence under UV light. The as-synthesized La3+-doped Ti3C2 NSs act as a fluorescent sensor for the sensitive recognition of creatinine biomarker. The La3+-doped Ti3C2 NSs-based fluorescence method showed a fluorescence quenching at emission wavelength 518 nm towards creatinine with a linear range of 0.25–7.5 μM and detection limit of 63.44 nM. The paper strip based on La3+-doped Ti3C2 NSs was developed for the visual identification of creatinine. Furthermore, La3+-doped Ti3C2 NSs were used as probes for imaging of Saccharomyces cerevisiae cells. Also, the as-fabricated La3+-doped Ti3C2 NSs propose a quick response giving a cost-effective analytical strategy for the selective assay of creatinine in biofluids (plasma and urine).

Fine microstructure tuning via titanium doping in ultrahigh-nickel cathodes to enhance the reversibility of the H2/H3 phase transition and reduce micro-cracks

Due to increasing demands for electric vehicles with high energy density and low costs, ultrahigh-nickel LiNixCoyM1-x-yO2 (x≥0.9, M=Mn/Al) cathodes have attracted increasing attention. However, the preparation of ultrahigh-nickel cathode materials with satisfactory cycle stability remains challenging because of their structural and interface instability. In this study, the effects of Ti-doping on the performance of Li(Ni0.95Co0.05Mn0.01)1-xTixO2 (NCMT) were systematically investigated. Titanium doping enlarged the spacing between the lithium layers and increased the c/a ratio, thereby improving the structural stability of the cathode materials. In situ X-ray diffraction showed that the anisotropy change was significantly reduced after Ti doping. The reversibility of the H2/H3 transition was enhanced and the initiation of microcracks caused by the anisotropy change was restrained. Moreover, the emission structure induced by Ti doping effectively mitigated stress accumulation and restrained the propagation of microcracks. Therefore, the optimal NCMT cathode (with 1 mol.% of Ti doping) demonstrated an outstanding rate performance and cycle stability without capacity loss. Compared with the retentions of the pristine cathode without Ti doping (89.73 % in a coin cell and 51.16 % in a pouch cell), the NCMT cathode with 1 mol.% Ti maintained a capacity retention of 92.45 % in a coin cell after 100 cycles at 0.5 C and 70.49 % in a pouch cell after 1000 cycles at 1 C. This study provides an effective solution to realize stable cyclability without capacity loss in ultrahigh-nickel cathode materials.

Remarkable photodegradation breakdown cost, antimicrobial activity, photocatalytic efficiency, and recycling of SnO2 quantum dots throughout industrial hazardous pollutants treatment

In the conducted research, a one-step hydrothermal synthesis of pure and titanium-doped tin dioxide quantum dots is elaborated upon, with a thorough analysis of their structural, optical, morphological, and photocatalytic properties undertaken using advanced analytical techniques. Through X-ray Diffraction XRD, the crystalline nature and phase purity of the tetragonal structures of SnDs were confirmed, with the crystallite sizes measured at 3.0 nm for SnD1 and 7.66 nm for SnD2, following treatments at 240 °C and 300 °C, respectively. The structural integrity of SnO2 was maintained despite titanium doping. FTIR spectroscopy verified the existence of specific vibrational modes indicative of surface hydroxyl groups. HRTEM images revealed the spherical morphology of particles, with diameters of 3.5 nm for SnD1 and 9.1 nm for SnD2. Optical band gaps, determined through UV-DRS, ranged from 3.33 eV in SnD1 to 3.47 eV in SnDTi2. The photocatalytic degradation of Congo Red dye under xenon lamp irradiation was quantitatively assessed; notably, SnD1 exhibited a 23 % higher rate constant compared to SnD2, attributed to its smaller particle size and a 31 % greater surface area. Doping with 4 % Ti in Sn0.96Ti0.04O2 more than doubled the degradation rate compared to a 6 % Ti doping in Sn0.94Ti0.06O2. Furthermore, the generation of hydroxyl radicals was significantly enhanced, showing an increase of approximately 220 % for SnD1 and 80 % for SnD2. The capability of these nanomaterials to reduce the chemical oxygen demand of industrial organic pollutants to within regulatory limits under solar irradiation was documented, with SnD1 maintaining its photocatalytic efficiency over seven cycles of reuse. In the photocatalytic degradation rate of Congo Red dye, which was 23 % higher for SnD1 compared to SnD2, and the threefold increase in the degradation rate for SnDTi1 compared to SnDTi2. An economic assessment, based on electricity tariffs in Saudi Arabia, highlighted the cost-effectiveness of SnD1, which ranged from 26.93 to 30.36 USD per breakdown cost of the photodegradation process, showing it to be less costly than SnD2. Conversely, SnDTi1 was found to be more economical than SnDTi2, with costs ranging from 26.67 to 33.09 USD. Collectively, the results emphasize the outstanding photocatalytic performance and cost-efficiency of SnDs, reinforcing their potential as sustainable solutions for the treatment of industrial wastewater. Additionally, the antibacterial efficacy of these materials against a range of bacteria, yeast, and fungi was investigated and substantiated.

Investigation on Deterioration of Allura Red Dye Under Visible Radiation by TiO2 Based Nanocomposite

This current study is to prepare and characterise a Cu-doped Titanium dioxide (TiO2) and Cu-doped Titanium dioxide with Tungsten (WO3) nanocomposite and its application for the deterioration of Allura Red (AR) Dye. After preparing the Cu- doped Titanium dioxide (TiO2) with WO3 and Cu-doped Titanium dioxide (TiO2) nanocomposites using wet chemical Sol-gel method over various soaking times, the XRD, BET, and Ultraviolet-visible spectroscopy were used to determine the properties of the synthesized Copper-doped Titanium dioxide and Copper-doped Titanium dioxide with Tungsten nanocomposites. When Tungsten was added to Cu-doped Titanium dioxide (TiO2), the X-Ray Diffraction showed that all of the composites' peaks shifted slightly in the direction of a higher diffraction angle. To evaluate surface area BET curve was used. The Copper-doped Titanium dioxide (TiO2)/Tungsten (WO3) nanocomposite gives a significant photocatalytic activity because of its increased surface area. High surface area (BET) and anatase phase development (XRD), which are the main contributors to effective photocatalytic activity, were identified by the work's results. XRD revealed that the synthesised materials were in the anatase phase. Compared to CDT, CTW-15, CTW-30, and CTW-60 nanocomposites, the surface area (BET) of the CTW-45 nanocomposite is larger at 128.79 m2/g. By examining the kinetics of reaction parameters such as dopant concentrations, pH, catalyst dose, and dye concentration, the catalysts were able to determine the ideal conditions for improved photocatalytic degradation of Allura Red dye. At pH 4, dye concentrations of 5 mg/L, and CTW-45 concentrations of 100 mg/L, the percentage of AR dye degradation was greater. The findings of this study can be used to develop efficient nanocomposites that remove Allura Red dye from wastewater.

Band structure study of pure and doped anatase titanium dioxide (TiO2) using first-principle-calculations: role of atomic mass of transition metal elements (TME) on band gap reduction

Band structure study of pure and doped anatase titanium dioxide (TiO2) using first-principle-calculations: role of atomic mass of transition metal elements (TME) on band gap reduction

Publisher Correction: Effect of the vanadium doped titanium oxide nanoparticles on ionic contribution in dielectric behaviour of a nematic liquid crystal

Publisher Correction: Effect of the vanadium doped titanium oxide nanoparticles on ionic contribution in dielectric behaviour of a nematic liquid crystal