Defect-mediated optical properties of Fe-substituted TiO2 nanoparticles

Here, sol–gel derived Fe–TiO₂ anatase nanoparticles with varying concentrations of Ti_(1–x)Fe_xO₂ (x = 0%, 1%, 5%, 10%) were prepared. The structural, morphological, and optical properties of prepared samples were studied. X-ray diffraction (XRD) patterns show the formation of pure anatase phase. The mean crystallite size of Fe–TiO₂ decreases with increase in the concentration of Fe. Fourier transform infrared spectroscopy (FTIR) spectra confirmed the presence of Ti–O vibrational band for all the samples. In Raman spectrum, peak broadening and red shifting linked with Eg ∼144 cm^–1 divulge the Fe substitution at Ti sites into host lattice structure. Photoluminescence (PL) spectra verified nine peaks related to near band-edge emission and various defect states. The UV–vis diffuse reflectance spectra represent redshift and reduction in the bandgap energy. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) investigations show that the size of the grains decreases with increase in Fe doping concentration. The study shows that Fe-doped TiO₂ anatase phase nanoparticles are suitable for photocatalytic activity and solar cell applications.     

Preparation and characterization of TiO2 photocatalysts by Fe doping together with Au deposition for the degradation of organic pollutants

Fe³⁺ doped TiO₂ deposited with Au (Au/Fe–TiO₂) was successfully prepared with an attempt to extend light absorption of TiO₂ into the visible region and reduce the rapid recombination of electrons and holes. The samples were characterized by X-ray diffraction (XRD), N₂ physical adsorption, Raman spectroscopy, atomic absorption flame emission spectroscopy (AAS), UV–vis diffuse reflectance spectroscopy, X-ray photoelectron spectroscopy (XPS), and photoluminescence (PL) spectra. The photocatalytic activities of the samples were evaluated for the degradation of 2,4-chlorophenol in aqueous solutions under visible light (λ > 420 nm) and UV light irradiation. The results of XRD, XPS and high-resolution transmission electron microscopy (HRTEM) analysis indicated that Fe³⁺ substituted for Ti⁴⁺ in the lattice of TiO₂, Au existed as Au⁰ on the surface of the photocatalyst and the mean particle size of Au was 8 nm. Diffuse reflectance measurements showed an extension of light absorption into the visible region for Au/Fe–TiO₂, and PL analysis indicated that the electron–hole recombination rate has been effectively inhibited when Au deposited on the surface of Fe-doped TiO₂. Compared with Fe doped TiO₂ sample and Au deposited TiO₂ sample, the Au/Fe–TiO₂ photocatalyst exhibited excellent visible light and UV light activity and the synergistic effects of Fe³⁺ and Au was responsible for improving the photocatalytic activity.     

Synthesis of visible light-active nanostructured TiOx (x < 2) photocatalysts in a flame aerosol reactor

Titanium dioxide is a wide band gap (3.2 eV) semiconductor which is photo-active when irradiated with UV light. For wider scale use of TiO₂ as a photocatalyst, its activity needs to be extended to the visible light region (constituting 45% of total incident solar energy). A diffusion flame aerosol reactor (FLAR) with an oxygen lean environment in the particle formation zone has been used to synthesize oxygen deficient titanium suboxide (TiO_x with x < 2) nanoparticles. Using a standard-based electron energy loss spectroscopy (EELS) technique, the non-stoichiometry (x in TiO_x) in the flame synthesized particles has been quantified with high accuracy (uncertainty less than 3%). Under an oxygen lean environment in the particle formation zone, the non-stoichiometry in the TiO_x particles is a function of the flame temperature. The value of x in the flame synthesized TiO_x nanoparticles is in the range of 1.88 < x < 1.94. Diffuse reflectance spectra confirmed that the oxygen deficient TiO_x particles absorbed visible light. Visible light activity of the TiO_x particles is demonstrated by photocatalytic degradation of methyl orange solution under visible light illumination.     

ZrxCo0.8−xNi0.2−xFe2O4-graphene nanocomposite for enhanced structural,dielectric and visible light photocatalytic applications

Zirconium doped nickel cobalt ferrite (Zr_xCo_0.8−xNi_0.2−xFe₂O₄) nanoparticles and Zr_xCo_0.8−xNi_0.2−xFe₂O₄-graphene nanocomposites were synthesized by a cheap and facile co-precipitation method. Annealing was done at 750 °C for 6.5 h. Spinel cubic structure of prepared nanoparticles was confirmed by X-ray powder diffraction (XRD) technique. Crystalline size of nanoparticles was observed in the range of 18–27 nm. Graphene was synthesized by Hummer's method. Formation of rGO was confirmed by UV-visible spectroscopy (UV-vis) and XRD. Zr_xCo_0.8−xNi_0.2−xFe₂O₄-graphene nanocomposites were prepared by ultra-sonication route. Grain size of nanoparticles and dispersion of nanoparticles between rGO layers was determined by Scanning electron microscopy (SEM). In application studies of nanoparticles and their nanocomposites, photocatalytic efficiency of nanoparticles under visible light irradiation was observed by degradation of methylene blue. Charge transfer resistance was measured by electrochemical impedance spectroscopy (EIS) and the variation in dc electrical resistivity was analyzed by room temperature current voltage characteristics (I-V). Dielectric constant was also evaluated in frequency range from 1 MHz to 3 GHz. All these investigations confirmed the possible utilization of these materials for a variety of applications such as visible light photocatalysis, high frequency devices fabrication etc.     

Synthesis,characterization and demonstration of self-cleaning TiO2 coatings on glass and glazed ceramic tiles

An effort was made not only to demonstrate the performance of the self-cleaning coatings on building materials such as ceramic glazed tiles and glass windows, but also to understand the fundamental issues that are still alive in the field of self-cleaning surfaces based on photocatalysis. Nano TiO₂ transparent thin films were generated by dip, spray and flow coating method. The present results indicate that the inconsistent results in the self-cleaning studies may be due to the effect of aggregation of model pollutant (methylene blue) dye on TiO₂ surface. The effect of aliovalent metal ion (Ni²⁺, Fe³⁺, Nb⁵⁺) doping on phase formation, polymorphic transition, visible light absorbance and optical transparency of TiO₂ film were investigated using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and UV visible absorption spectroscopy. The improved visible light activity of doped TiO₂ thin film was correlated to the Ti(Ni/Fe)O₃ phase formation, UV and visible light absorbance, variation in the optical energy band gap and the probable light scattering associated with grain size.     

Structural,spectral, dielectric and photocatalytic studies of Zr-Ni doped MnFe2O4 co-precipitated nanoparticles

In this study the Mn_1–2xZr_xFe_2−yNi_yO₄ nanoparticles fabricated by co-precipitation technique were investigated. Thermo-gravimetric analysis (TGA) exhibited the annealing temperature of the nanoparticles ~990 °C. Cubic spinel structure of Mn_1–2xZr_xFe_2−yNi_yO₄ nanoparticles was confirmed by X-ray diffraction (XRD) and Fourier transform infrared (FTIR) analysis. Crystallite size was calculated by XRD data and found in the range of 32–58 nm. Photocatalytic activity of Mn_0.92Zr_0.04Fe_1.88Ni_0.12O₄/graphene nanocomposites was tested by degrading methylene blue (MB) under visible light irradiation. The MB was almost completely degraded in the presence of Mn_0.92Zr_0.04Fe_1.88Ni_0.12O₄-graphene nanocomposites under visible light irradiation. Dielectric parameters were also investigated in the frequency range 1×10⁶–3×10⁹ Hz. An overall decrease in the values of dielectric constant, dielectric loss and tangent loss was observed on account of the substitution of Zr and Ni with Mn and Fe cations.     

Enhanced optical transmittance and energy-storage performance in NaNbO3-modified Bi0.5Na0.5TiO3 ceramics

Dielectric ceramics with both excellent energy storage and optical transmittance have attracted much attention in recent years. However, the transparent Pb-free energy-storage ceramics were rare reported. In this work, we prepared transparent relaxor ferroelectric ceramics (1 − x)Bi_0.5Na_0.5TiO₃–xNaNbO₃ (BNT–xNN) by conventional solid-state reaction method. We find the NN-doping can enhance the polarization and breakdown strength of BNT by suppressing the grain growth and restrained the reduction of Ti⁴⁺ to Ti³⁺. As a result, a high recoverable energy-storage density of 5.14 J/cm³ and its energy efficiency of 79.65% are achieved in BNT–0.5NN ceramic at 286 kV/cm. Furthermore, NN-doping can promote the densification to improve the optical transmittance of BNT, rising from ∼26% (x = 0.2) to ∼32% (x = 0.5) in the visible light region. These characteristics demonstrate the potential application of BNT–xNN as transparent energy-storage dielectric ceramics.     

Correlation between microstructure parameters and anti-cancer activity of the [Mn0.5Zn0.5](EuxNdxFe2-2x)O4 nanoferrites produced by modified sol-gel and ultrasonic methods

[Mn_0.5Zn_0.5](Eu_xNd_xFe_2-2x)O₄ ferrite nanoparticles (FNP) were obtained by ultrasonic (USM) and sol-gel (SGM) methods. It was observed that SGM allows us to produce nanoparticles with the average crystal size of 10–40 nm and the specific surface area of 5–7.5 × 10⁴ m²/g with a strong correlation between the chemical composition (x) and the crystal size distribution. At the same time using USM, we obtained nanoparticles with the average crystal size of 3–15 nm and the specific surface area of 1.5–1.7 × 10⁵ m²/g without a strong correlation between Eu/Nd concentration and the crystal size distribution. The specific surface area and average crystal size are the main factors determining the antiproliferative activity of FNP. The anti-cancer activity of FNP was investigated both on cancerous cells, human adenocarcinoma cells and human colorectal carcinoma cells. It was established that samples obtained using USM were more effective in producing cytotoxic effects on cancer cells. Thus, we confirm a strong correlation between the main microstructure parameters for [Mn_0.5Zn_0.5](Eu_xNd_xFe_2-2x)O₄ ferrite nanoparticles.     

Photocatalytic Nb2O5-doped TiO2 nanoparticles for glazed ceramic tiles

TiO₂ nanoparticles are currently used as coating for self-cleaning building products. In order to achieve high self-cleaning efficiency for outdoor applications, it is important that titania is present as anatase phase. Moreover, it is desirable that the particle sizes are in nano-range, so that a large enough surface area is available for enhanced catalytic performance. In this work, TiO₂ nanoparticles doped with 0–5 mol% Nb₂O₅ were synthesized by co-precipitation. Nb₂O₅ postponed the anatase to rutile transformation of TiO₂ by about 200 °C, such that after calcination at 700 °C, no rutile was detected for 5 mol% Nb₂O₅-doped TiO₂, while undoped TiO₂ presented 90 wt% of the rutile phase. A systematic decreasing on crystallite size and increasing on specific surface area of TiO₂ were observed with higher concentration of Nb₂O₅ dopant. Photocatalytic activity of anatase polymorph was measured by the decomposition rate of methylene blue under ultraviolet and daylight illumination and compared to commercial standard catalyst (P25). The results showed enhanced catalysis under UV and visible light for Nb₂O₅-doped TiO₂ as compared to pure TiO₂. In addition, 5 mol% Nb₂O₅-doped TiO₂ presented higher photocatalytic activity than P25 under visible light. The enhanced performance was attributed to surface chemistry change associated with a slight shift in the band gap.     

Iron-doped TiO2 nanotubes with high photocatalytic activity under visible light synthesized by an ultrasonic-assisted sol-hydrothermal method

A series of iron-doped anatase TiO₂ nanotubes (Fe/TiO₂ NTs) catalysts with iron concentrations ranging from 0.88 to 7.00 wt% were prepared by an ultrasonic-assisted sol-hydrothermal process. The structures and the properties of the fabricated Fe/TiO₂ NTs were characterized in detail and photocatalytic activity was examined using a reactive brilliant red X-3B aqueous solution as pollutant under visible light. The lengths of the NTs were determined to range from 20 nm to 100 nm. The incorporation of the iron ions (Fe³⁺) into the TiO₂ nanotubes shifted the photon absorbing zone from the ultraviolet (UV) to the visible wavelengths, reducing the band gap energy from 3.2 to 2.75 eV. The photocatalytic activity of the Fe/TiO₂ NTs was 2–4 times higher than the values measured for the pure TiO₂ nanotubes.     

Iridium,carbon and nitrogen multiple-doped TiO2 Nanoparticles with enhanced photocatalytic activity

The aim of this research is to enhance the photocatalytic activity of TiO₂ nanoparticles for the UV–visible light by multiple-doping with Iridium, carbon and nitrogen. The tridoped TiO₂ photocatalyst were prepared by wet chemical method, and characterized by X-ray diffraction, Raman spectroscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, ultraviolet-visible light diffuse reflection spectroscopy and room temperature photoluminescence spectroscopy. Besides, the photocatalytic H₂ evolution performance of Ir-C-N tridoped TiO₂ under UV–visible light irradiation was evaluated. It was found that Ir existed as Ir⁴⁺ by substituting Ti in the lattice of TiO₂; meanwhile, C and N were also incorporated into the surface of TiO₂ nanoparticles in interstitial mode. Meanwhile, Ir-C-N tridoping extended the absorption of TiO₂ into the visible light region and narrowed its band gap to ~3.0 eV, resulting in enhanced photocatalytic H₂ evolution under UV–visible light irradiation. This could be attributed to narrow band gap and proper electronic structure of TiO₂ after Ir-C-N tridoping.     

One-pot synthesis of bifunctionalized TiO<Subscript>2</Subscript> mesoporous photocatalyst with visible light response

A series of Fe-doped SH/TiO₂ mesoporous photocatalysts have been firstly prepared by one-pot method using P123 as structure-directing agent. This bifunctionalized mesoporous TiO₂ possesses perfect anatase crystal structure and high surface area. The surface area of Fe-doped SH/TiO₂ mesoporous material is 4 times higher than that of P25. Based on the EPR results, it was found that trivalent Fe ions exist at low spin state and substitutes a part of Ti⁴⁺ ions into TiO₂ lattice. Fe-dropping in TiO₂ extends the adsorption band side of the resulting material to about 600 nm. Much high photocatalytic activity in the degradation of phenanthrene was obtained on the bifunctionalized mesoporous TiO₂ under visible light irradiation (λ > 420 nm), which is 6 times higher than that of pristine mesoporous TiO₂. The enhancement in the photocatalytic activity of bifunctionalized TiO₂ is ascribed to the extended absorption to visible light and strong interaction between SH-groups and PHE molecules.     

Photocatalytic Degradation of Organic Dyes by a High Efficient TiO2-Based Catalysts Under Solar Light Irradiation

In this work, the Er³⁺:YAlO₃/Fe-doped TiO₂ composite, a high efficient TiO₂-based photocatalyst, was synthesized by ultrasonic dispersion and liquid boil methods. Among which, the Er³⁺:YAlO₃ is a kind of upconversion luminescence agent, which was prepared by nitrate-citric acid method. It can emit ultraviolet light under visible light excitation. The Er³⁺:YAlO₃/Fe-doped TiO₂ composite was characterized by X-ray diffraction and UV–vis spectral techniques. The degradation of Acid Red B dye was used to evaluate the photocatalytic activity of the Er³⁺:YAlO₃/Fe-doped TiO₂ composite under solar light irradiation. It was found that the photocatalytic activity of Er³⁺:YAlO₃/Fe-doped TiO₂ composite was much higher than that for the similar system with only Fe-doped TiO₂. And the influencing factors, such as Er³⁺:YAlO₃ content, irradiation time, initial concentration of Acid Red B, addition amount of Er³⁺:YAlO₃/Fe-doped TiO₂ and NaCl, on the photocatalytic degradation were also investigated. The Er³⁺:YAlO₃ as upconversion luminescence agent can elevate the photocatalytic activity of Fe-doped TiO₂ powder. Moreover, the Fe²⁺ ion can restrain the recombination of photogenerated electrons and holes. Thus, this Er³⁺:YAlO₃/Fe-doped TiO₂ composite is a useful material for the detoxification of wastewater because it can efficiently utilize solar light by converting visible light into ultraviolet light.     

A hybrid Ag/TiO2 nanoarray-based in situ charge transfer toward multi-functional active-platform

Designing an efficient heteronanostructure array for surface-enhanced Raman scattering (SERS) to enable ultrasensitive and reproducible detection of analytes and degrading organic contaminants provides new perspectives for chemical and biological detection at trace levels and environmental remediation. Here, we design and fabricate a heterostructure consisting of Ag nanoparticles (NPs) in-situ grown on high-density arrays of vertical TiO₂ nanorods (NRs) (denoted Ag/TiO₂ NRs). As a result, compared with pristine TiO₂ NRs, the as-obtained Ag/TiO₂ NR substrate possesses a SERS activity for detecting rhodamine 6G (R6G) with a detection limit as low as 10⁻¹² M and an enhancement factor up to 1.2 × 10¹⁰. In addition, the substrate exhibits the highest degradation rates of R6G of 82% under illumination with visible light and an excellent self-cleaning effect under UV-assisted light. Such remarkable enhanced efficacy of the binary Ag/TiO₂ NRs nanocomposites may be attributed to the i) appropriate band alignment based on the synergistic effect of Ag decorated on TiO₂ NRs; ii) a large adhesion area and the localized surface plasmon resonance (LSPR) of Ag; and iii) high-density and engineering hotspots in the active platform. These properties make the heterostructure Ag/TiO₂ NR platform promising candidate for detecting analytes and photocatalytic applications.     

Synthesis of Ni doped barium hexaferrite by microemulsion route to enhance the visible light-driven photocatalytic degradation of crystal violet dye

The pristine and Ni doped BaNi_xFe_12-xO₁₉ (x = 0.0, 0.2, 0.4, 0.6, 0.8, 1.0) NPs have been fabricated via facile microemulsion approach and the impact of dopants was explored based dielectric, optical, structural and the photocatalytic properties of BaNi_xFe_12-xO₁₉ nanoparticles. X-ray diffraction and Raman study confirmed the formation of regular hexagonal geometry with space group P6₃/mmc with crystallite size in 32–50 nm range. Functional groups were identified using FTIR analysis. The remanence (Pr), saturation polarization (Ps) and coercivity (Hc) was explored by P-E loop analysis and the value of Pr and Ps was enhanced with the concentration of dopant. According to PL spectra, highly doped materials had a higher charge separation (e^?- h⁺) and low recombination rate, which resulted in higher photocatalytic degradation activity of fabricated nanomaterials. The optical band gap was found to be 1.78 eV versus undoped (2.60 eV for pristine BaFe₁₂O₁₉). Due to polarizations, the dielectric loss, dielectric constant and tangent loss values were declined, while AC conductivity was enhanced. Photocatalytic performance of doped and undoped samples under visible right irradiation was studied for crystal violet dye. For 100 min exposure to visible light, the highly doped catalyst exhibits 97% degradation versus 60% in case of pristine this is attributed to efficient electron-hole pair separation. Furthermore, quenching effect of different scavengers indicated that hydroxyl radical had a main role, and e^? or h⁺ played a minimal role in CV dye degradation. The enhanced properties due to doping make BaNi_xFe_12-xO₁₉ a potential candidate for photocatalytic applications under visible light irradiation.     

DyCrxFe(1-x)O3 nanoparticles prepared by wet chemical technique for photocatalytic applications

DyCr_xFe_(1-x)O₃ (0 ≤ x ≥ 0.4) nanoparticles were prepared using facile chemical route. Structural and morphological evaluation was carried out using X-ray diffraction (XRD) and electron microscopy. Formation of orthorhombic DyFeO₃ nanoparticles was confirmed by XRD with crystallite size of 9–10 nm. FESEM images revealed nearly spherical morphology of the fabricated nanoparticles. Energy dispersive X-ray (EDX) technique was employed to confirm the presence of Dy, Cr, Fe and O elements in DyCr_xFe_(1-x)O₃ nanoparticles. FTIR studies illustrated the presence of characteristics stretching and bending vibrations. UV–visible spectroscopy was used to analyze the photocatalytic performance of the DyFeO₃ and Cr-substituted DyFeO₃ nanoparticles and optical band gap measurements. Photocatalytic activities of the prepared substituted and un-substituted DyFeO₃ nanoparticles were conducted using three different dyes. These dyes were (i) methyl orange, (ii) rhodamine B and (iii) methylene blue. Lower band gap and higher photocatalytic performance was observed for Cr-substituted DyFeO₃ nanoparticles with methylene blue dye.     

Ultrafine nano-TiO2 loaded on dendritic porous silica nanoparticles for robust transparent antifogging self-cleaning nanocoatings

Multifunctional nanocoatings with mechanical robustness, high transparence, antifogging and self-cleaning have attracted significant attention because of their wide applications in glass-related fields. However, it is still very difficult to construct this kind of multifunctional nanocoatings due to the requirement of their comprehensive structure parameters. In this work, we successfully fabricated robust transparent antifogging self-cleaning nanocoatings by employing dendritic porous silica nanoparticles (DPSNs) evenly loaded with 2–3 nm of small TiO₂ nanoparticles (NPs) as a building block. A series of DPSNs@X% TiO₂ nanocomposites with tunable weight ratios (X%) of TiO₂/DPSNs from 10% to 60% were firstly prepared by controlling the growth of TiO₂ on the heterogeneous interface of center-radial large pores of DPSNs, followed by calcination. Noteworthily, DPSNs@10% TiO₂ exhibited highest photocatalytic and antibacterial performance mainly due to uniform distribution of TiO₂ NPs, their small sizes of 2–3 nm and center-radial pore. Therefore, DPSNs@10% TiO₂ was chosen as an optimized building block and combined with acid-catalyzed silica sol (ACSS) to develop an excellent suspension for multifunctional nanocoatings. The obtained glass slide with the optimal nanocoating showed photocatalytic self-cleaning behavior, high transparence, hydrophilic (WCA = 6.2°) antifogging, and high mechanical robustness, which can withstand 4B tape adhesion test and 3H pencil scratching test. This work provides an important exploration for developing multifunctional nanocoatings.     

A novel TiO2 − xNx/BN composite photocatalyst: Synthesis,characterization and enhanced photocatalytic activity for Rhodamine B degradation under visible light

A novel TiO_2 − xN_x/BN composite photocatalyst was prepared via a facile method using melamine–boron acid adducts (M·2B) and tetrabutyl titanate as reactants. The morphological results confirmed that nitrogen-doped TiO₂ nanoparticles were uniformly coated on the surface of porous BN fibers. A red shift of absorption edge from 400 nm (pure TiO₂) to 520 nm (TiO_2 − xN_x/BN composites) was observed in their UV–Vis light absorption spectra. The TiO_2 − xN_x/BN photocatalysts exhibited enhanced photocatalytic activity for the degradation of Rhodamine B (RhB) and the highest photocatalytic degradation efficiency reached 97.8% under visible light irradiation for 40 min. The mechanism of enhanced photocatalytic activity was finally proposed.     

Effect of Ni2+ substitution on structural,magnetic, dielectric and optical properties of mixed spinel CoFe2O4 nanoparticles

Nanoparticles of Co_1−xNi_xFe₂O₄ with x=0.0, 0.10, 0.20, 0.30, 0.40 and 0.50 were synthesized by co-precipitation method. The structural analysis reveals the formation of single phase cubic spinel structure with a narrow size distribution between 13–17 nm. Transmission electron microscope images are in agreement with size of nanoparticles calculated from XRD. The field emission scanning electron microscope images confirmed the presence of nano-sized grains with porous morphology. The X-ray photoelectron spectroscopy analysis confirmed the presence of Fe²⁺ ions with Fe³⁺. Room temperature magnetic measurements showed the strong influence of Ni²⁺ doping on saturation magnetization and coercivity. The saturation magnetization decreases from 91 emu/gm to 44 emu/gm for x=0.0–0.50 samples. Lower magnetic moment of Ni²⁺ (2 µ_B) ions in comparison to that of Co²⁺ (3 µ_B) ions is responsible for this reduction. Similarly, overall coercivity decreased from 1010 Oe to 832 Oe for x=0.0–0.50 samples and depends on crystallite size. Cation distribution has been proposed from XRD analysis and magnetization data. Electron spin resonance spectra suggested the dominancy of superexchange interactions in Co_1−xNi_xFe₂O₄ samples. The optical analysis indicates that Co_1−xNi_xFe₂O₄ is an indirect band gap material and band gap increases with increasing Ni²⁺ concentration. Dispersion behavior with increasing frequency is observed for both dielectric constant and loss tangent. The conduction process predominantly takes place through grain boundary volume. Grain boundary resistance increases with Ni²⁺ ion concentration.     

Synergic effect of cation doping and phase composition on the photocatalytic performance of TiO2 under visible light

The synergic effect of cation doping and phase composition for the further improvement of the photocatalytic activity of TiO₂ under visible light is reported for the first time. Fe^3 + and Sn^4 + co-doped TiO₂ with optimized phase composition were synthesized through a simple soft-chemical solution method. The visible-light-driven photocatalytic activity of Fe^3 + and Sn^4 + co-doped TiO₂ was 5 times of that of Evonik P25 TiO₂ using degradation of methylene blue as model reaction. The synthesized photocatalysts were characterized by powder X-ray diffraction, UV–Vis diffuse reflectance spectroscopy, X-ray photoelectron spectroscopy, ¹¹⁹Sn Mössbauer spectroscopy, and X-ray absorption fine structure spectroscopy. It is indicated that Sn^4 + doping can facilitate the phase transition from anatase to rutile. The different ratios of anatase and rutile can be achieved by tuning the amount of Sn^4 + doped into the lattice. Furthermore, the doping of Sn^4 + into TiO₂ lattice can stabilize the phase composition when Fe^3 + is co-doped. In the Fe^3 + and Sn^4 + co-doped TiO₂, Sn^4 + is mainly used to tune and stabilize the phase composition of TiO₂ and Fe^3 + acts as a doping cation to narrow the band gap of TiO₂. Both band gap and phase composition of TiO₂ can be tuned effectively by the simultaneous introduction of Fe^3 + and Sn^4 +. The synergic effect of optimized phase composition (anatase/rutile = 25/75) and narrowed band gap should be the two main reasons for the promoted photocatalytic activity of TiO₂ under visible light.