The Fabrication and Property Characterization of a Ho2YSbO7/Bi2MoO6 Heterojunction Photocatalyst and the Application of the Photodegradation of Diuron under Visible Light Irradiation.

A novel photocatalytic nanomaterial, Ho2YSbO7, was successfully synthesized for the first time using the solvothermal synthesis technique. In addition, a Ho2YSbO7/Bi2MoO6 heterojunction photocatalyst (HBHP) was prepared via the hydrothermal fabrication technique. Extensive characterizations of the synthesized samples were conducted using various instruments, such as an X-ray diffractometer, a Fourier transform infrared spectrometer, a Raman spectrometer, a UV-visible spectrophotometer, an X-ray photoelectron spectrometer, and a transmission electron microscope, as well as X-ray energy dispersive spectroscopy, photoluminescence spectroscopy, a photocurrent test, electrochemical impedance spectroscopy, ultraviolet photoelectron spectroscopy, and electron paramagnetic resonance. The photocatalytic activity of the HBHP was evaluated for the degradation of diuron (DRN) and the mineralization of total organic carbon (TOC) under visible light exposure for 152 min. Remarkable removal efficiencies were achieved, with 99.78% for DRN and 97.19% for TOC. Comparative analysis demonstrated that the HBHP exhibited markedly higher removal efficiencies for DRN compared to Ho2YSbO7, Bi2MoO6, or N-doped TiO2 photocatalyst, with removal efficiencies 1.13 times, 1.21 times, or 2.95 times higher, respectively. Similarly, the HBHP demonstrated significantly higher removal efficiencies for TOC compared to Ho2YSbO7, Bi2MoO6, or N-doped TiO2 photocatalyst, with removal efficiencies 1.17 times, 1.25 times, or 3.39 times higher, respectively. Furthermore, the HBHP demonstrated excellent stability and reusability. The mechanisms which could enhance the photocatalytic activity remarkably and the involvement of the major active species were comprehensively discussed, with superoxide radicals identified as the primary active species, followed by hydroxyl radicals and holes. The results of this study contribute to the advancement of efficient heterostructural materials and offer valuable insights into the development of sustainable remediation strategies for addressing DRN contamination.

Preparation and Property Characterization of Sm2EuSbO7/ZnBiSbO5 Heterojunction Photocatalyst for Photodegradation of Parathion Methyl under Visible Light Irradiation.

An unprecedented photocatalyst, Sm2EuSbO7, was successfully fabricated in this paper, through a high-temperature solid-state calcination method, which represented its first ever synthesis. Additionally, using the solvothermal method, the Sm2EuSbO7/ZnBiSbO5 heterojunction photocatalyst (SZHP) was fabricated, marking its debut in this study. XRD analysis confirmed that both Sm2EuSbO7 and ZnBiSbO5 exhibited pyrochlore-type crystal structures with a cubic lattice, belonging to the Fd3m space group. The crystal cell parameter was determined to be 10.5682 Å or 10.2943 Å for Sm2EuSbO7 or ZnBiSbO5, respectively. The band gap width measured for Sm2EuSbO7 or ZnBiSbO5 was 2.73 eV or 2.61 eV, respectively. Under visible light irradiation for 150 min (VLTI-150 min), SZHP exhibited remarkable photocatalytic activity, achieving 100% removal of parathion methyl (PM) concentration and 99.45% removal of total organic carbon (TOC) concentration. The kinetic constant (k) for PM degradation and visible light illumination treatment was determined to be 0.0206 min-1, with a similar constant k of 0.0202 min-1 observed for TOC degradation. Remarkably, SZHP exhibited superior PM removal rates compared with Sm2EuSbO7, ZnBiSbO5, or N-doped TiO2 photocatalyst, accompanied by removal rates 1.09 times, 1.20 times, or 2.38 times higher, respectively. Furthermore, the study investigated the oxidizing capability of free radicals through the use of trapping agents. The results showed that hydroxyl radicals had the strongest oxidative capability, followed by superoxide anions and holes. These findings provide a solid scientific foundation for future research and development of efficient heterojunction compound catalysts.

Preparation and Property Characterization of In2YSbO7/BiSnSbO6 Heterojunction Photocatalyst toward Photocatalytic Degradation of Indigo Carmine within Dye Wastewater under Visible-Light Irradiation.

In2YSbO7 and In2YSbO7/BiSnSbO6 heterojunction photocatalyst were prepared by a solvothermal method for the first time. The structural characteristics of In2YSbO7 had been represented. The outcomes showed that In2YSbO7 crystallized well and possessed pyrochlore constitution, a stable cubic crystal system and space group Fd3m. The lattice parameter of In2YSbO7 was discovered to be a = 11.102698 Å and the band gap energy of In2YSbO7 was discovered to be 2.68 eV, separately. After visible-light irradiation of 120 minutes (VLGI-120M), the removal rate (ROR) of indigo carmine (IC) reached 99.42% with In2YSbO7/BiSnSbO6 heterojunction (IBH) as a photocatalyst. The ROR of total organic carbon (TOC) reached 93.10% with IBH as a photocatalyst after VLGI-120M. Additionally, the dynamics constant k which was taken from the dynamic curve toward (DCT) IC density and VLGI time with IBH as a catalyst reached 0.02950 min-1. The dynamics constant k which came from the DCT TOC density and VLGI time with IBH as a photocatalyst reached 0.01783 min-1. The photocatalytic degradation of IC in dye wastewater (DW) with IBH as a photocatalyst under VLGI was in accordance with the first-order kinetic curves. IBH was used to degrade IC in DW for three cycles of experiments under VLGI, and the ROR of IC reached 98.74%, 96.89% and 94.88%, respectively, after VLGI-120M, indicating that IBH had high stability. Compared with superoxide anions or holes, hydroxyl radicals possessed the largest oxidative ability for removing IC in DW, as demonstrated by experiments with the addition of trapping agents. Lastly, the probable degradation mechanism and degradation pathway of IC were revealed in detail. The results showed that a visible-light-responsive heterojunction photocatalyst which possessed high catalytic activity and a photocatalytic reaction system which could effectively remove IC in DW were obtained. This work provided a fresh scientific research idea for improving the performance of a single catalyst.

Synthesis and Property Examination of Er2FeSbO7/BiTiSbO6 Heterojunction Composite Catalyst and Light-Catalyzed Retrogradation of Enrofloxacin in Pharmaceutical Waste Water under Visible Light Irradiation.

A new photocatalyst, Er2FeSbO7, was prepared by solid phase sintering using the high-temperature synthesis method for the first time in this paper. Er2FeSbO7/BiTiSbO6 heterojunction (EBH) catalyst was prepared by the solvent thermal method for the first time. Er2FeSbO7 compound crystallized in the pyrochlore-type architecture and cubelike crystal system; the interspace group of Er2FeSbO7 was Fd3m and the crystal cellular parameter a of Er2FeSbO7 was 10.179902 Å. The band gap (BDG) width of Er2FeSbO7 was 1.88 eV. After visible light irradiation of 150 minutes (VLGI-150min) with EBH as a photocatalyst, the removal rate (RR) of enrofloxacin (ENR) concentration was 99.16%, and the total organic carbon (TOC) concentration RR was 94.96%. The power mechanics invariable k toward ENR consistency and visible light irradiation (VLGI) time with EBH as a photocatalyzer attained 0.02296 min−1. The power mechanics invariable k which was involved with TOC attained 0.01535 min−1. The experimental results showed that the photocatalytic degradation (PCD) of ENR within pharmaceutical waste water with EBH as a photocatalyzer under VLGI was in keeping with the single-order reactivity power mechanics. The RR of ENR with EBH as a photocatalyzer was 1.151 times, 1.269 times or 2.524 times that with Er2FeSbO7 as a photocatalyst, BiTiSbO6 as a photocatalyst, or N-doping TiO2 (N-TO) as a photocatalyst after VLGI-150min. The photocatalytic activity, which ranged from high to low among above four photocatalysts, was as follows: EBHP > Er2FeSbO7 > BiTiSbO6 > N-TO. After VLGI-150min toward three periods of the project with EBH as a photocatalyst, the RR of ENR attained 98.00%, 96.76% and 95.60%. The results showed that the stability of EBH was very high. With appending trapping agent, it could be proved that the oxidative capability for degrading ENR, which ranged from strong to weak among three oxidic radicals, was as follows: superoxide anion > hydroxyl radicals (HRS) > holes. This work provides a scientific basis for the research and oriented leader development of efficient heterojunction catalysts.

Synthesis, Performance Measurement of Bi2SmSbO7/ZnBiYO4 Heterojunction Photocatalyst and Photocatalytic Degradation of Direct Orange within Dye Wastewater under Visible Light Irradiation.

Originally, the new catalyst Bi2SmSbO7 was synthesized by the hydrothermal synthesis method or by the solid-phase sintering method at a lofty temperature. A solvothermal method was utilized to prepare a Bi2SmSbO7/ZnBiYO4 heterojunction photocatalyst (BZHP). The crystal structure of Bi2SmSbO7 belonged to the pyrochlore structure and face-centered cubic crystal system by the space group of Fd3m. The cell parameter a was equivalent to 10.835(1) Å (Bi2SmSbO7). With Bi2SmSbO7/ZnBiYO4 heterojunction (BZH) as the photocatalyst, the removal rate (RR) of direct orange (DO) and the total organic carbon were 99.10% and 96.21% after visible light irradiation of 160 min (VLI-160M). The kinetic constant k toward DO concentration and visible light irradiation time (VLI) with BZH as photocatalyst reached 2.167 min−1. The kinetic constant k, which was concerned with total organic carbon, reached 0.047 min−1. The kinetic curve that came from DO degradation with BZH as a catalyst under VLI conformed to the second-order reaction kinetics. After VLI-160M, the photocatalytic degradation (PD) removal percentage of DO with BZH as the photocatalyst was 1.200 times, 1.268 times or 3.019 times that with Bi2SmSbO7 as the photocatalyst, ZnBiYO4 as the photocatalyst or with nitrogen-doped titanium dioxide as the photocatalyst. The photocatalytic activity (PA) was as following: BZH > Bi2SmSbO7 > ZnBiYO4 > nitrogen-doped titanium dioxide. After VLI-160M for three cycles of experiments with BZH as the photocatalyst, the RR of DO reached 98.03%, 96.73% and 95.43%, respectively, which meant that BZHP possessed high stability. By using the experiment of adding a trapping agent, the oxidative purifying capability for degradation of direct orange, which was in gradual depressed order, was as following: hydroxyl radical > superoxide anion > holes. Finally, the possible degradation pathway and degradation mechanism of DO were discussed systematically. A new high active heterojunction catalyst BZHP, which could efficiently remove toxic organic pollutants such as DO from dye wastewater after VLI, was obtained. Our research was meant to improve the photocatalytic property of the single photocatalyst.

First-Principles Density Functional Theory Study of Modified Germanene-Based Electrode Materials.

Germanene, with a wrinkled atomic layer structure and high specific surface area, showed high potential as an electrode material for supercapacitors. According to the first-principles calculation based on Density Functional Theory, the quantum capacitance of germanene could be significantly improved by introducing doping/co-doping, vacancy defects and multilayered structures. The quantum capacitance obtained enhancement as a result of the generation of localized states near the Dirac point and/or the movement of the Fermi level induced by doping and/or defects. In addition, it was found that the quantum capacitance enhanced monotonically with the increase of the defect concentration.

Synthesis of a GaOOH/ZnBiTaO5 heterojunction photocatalyst with enhanced photocatalytic performance toward enrofloxacin.

In this work, a GaOOH/ZnBiTaO5 heterojunction photocatalyst was synthesized innovatively and characterization techniques including XRD, SEM-EDS, XPS, FT-IR, PL and UV-Vis DRS were carried out to analyse the structural and morphological properties of the GaOOH/ZnBiTaO5 heterojunction photocatalyst. The GaOOH is dispersed on the surface of ZnBiTaO5 to form a heterojunction structure according to the SEM image. The band gaps of 10 wt%, 25 wt% and 50 wt% GaOOH/ZnBiTaO5 heterojunction photocatalysts were calculated to be 3.21 eV, 3.22 eV and 3.23 eV, respectively, which were between the band gaps of pure ZnBiTaO5 (3.19 eV) and pure GaOOH (4.76 eV). The photocatalytic performance of the GaOOH/ZnBiTaO5 heterojunction photocatalyst was investigated by degrading enrofloxacin under ultraviolet light. The results showed that the as-prepared 25 wt% GaOOH/ZnBiTaO5 presented optimal photocatalytic performance and could remove 58.27% of enrofloxacin in 60 min, which was higher than that of pure ZnBiTaO5 (53.7%) and pure GaOOH (35.4%). In addition, it was confirmed that ˙O2 -, h+ and ˙OH were all the active radicals during the degradation process. Finally, the possible degradation mechanism of enrofloxacin was discussed in detail. This work provided a viable strategy for improving the photocatalytic performance of wide band gap semiconductors.

Investigation into the synthesis conditions of CuMoO4 by an in situ method and its photocatalytic properties under visible light irradiation.

A kind of molybdenum and copper compound, CuMoO4, was prepared by a hydrothermal method. The construction and photocatalytic properties of CuMoO4 have been characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, transmission electron microscopy (TEM), UV-visible spectrometry and comprehensive thermal analysis. XRD analysis showed that samples which were synthesized under different hydrothermal time conditions were consistent, but the crystallinities of the samples were different. In another situation, disparate hydrothermal temperatures during the synthesis of CuMoO4 would lead to the appearance of different samples. The band gap of CuMoO4 was estimated to be 1.97 eV. It could be found from the results that CuMoO4 was an indirect band gap semiconductor by simulating its band structure. The photocatalytic activities of CuMoO4 were studied by means of monitoring the abilities of these compounds to degrade rhodamine B or 1H-benzotriazole in liquid media under visible light irradiation. Under different synthesis conditions, the hydrothermal time for obtaining the optimal degradation efficiency was 10 h, and the hydrothermal temperature was 180 °C. The results showed that CuMoO4 had excellent degradation performance for rhodamine B or 1H-benzotriazole. CuMoO4 showed excellent mineralization efficiency for rhodamine B compared with N-doped TiO2 based on the reduction of total organic carbon (TOC) during the photocatalytic process. The photocatalytic degradation rate of rhodamine B by CuMoO4 was 1.39 times that by N-doped TiO2, and the degradation rate of TOC by CuMoO4 was 1.53 times that by N-doped TiO2. Based on the intermediate products which were detected by liquid chromatography/mass spectrometry (LC/MS), the possible degradation pathway of rhodamine B was derived.

Structure and photocatalytic performance of rice husk-like Ba-doped GaOOH under light irradiation.

The effects of Ba-doping on the structure and photocatalytic performance of GaOOH were investigated for the first time in this paper. XRD, SEM, TEM, XPS, UPS, FT-IR, UV-Vis DRS, PL, BET and EPR characterizations were carried out to analyze the properties of Ba-doped GaOOH. The results showed that GaOOH crystallized well with the orthorhombic crystal system with space group Pbnm. The lattice parameters of GaOOH were found to be a = 4.509526 Å, b = 9.771034 Å and c = 2.969284 Å. The transition in the structural morphology of GaOOH before and after Ba-doping was observed in SEM pictures in which the morphology of GaOOH varied from wood-like to rice husk-like. At the same time, the specific surface area of 4 wt% Ba-doped GaOOH (21.5854 m2 g-1) was 3.42 times that of pure GaOOH (6.3047 m2 g-1). Ba-doping caused a red shift of the band gap according to UV-Vis DRS results. The enhanced defect states caused by Ba-doping was confirmed by PL results, which decreased the recombination rate of photogenerated electrons and photogenerated holes. Compared with pure GaOOH, when GaOOH with different Ba content was used as photocatalyst, the removal rate of enrofloxacin was increased by more than 20% only by illumination for 60 min. In addition, Ba-doped GaOOH had excellent stability and could be reused, which could reduce costs and increase the potential of its practical application.

Dispersed GaOOH rods loaded on the surface of ZnBiNbO5 particles with enhanced photocatalytic activity toward enrofloxacin.

A GaOOH/ZnBiNbO5 composite was constructed by loading dispersed GaOOH rods on the surface of ZnBiNbO5 particles and characterizations, including SEM-EDS, XRD, FT-IR spectroscopy, XPS, and UV-Vis DRS, were performed to analyze the morphology, structure and optical properties of the GaOOH/ZnBiNbO5 composite. The characterization results showed that ZnBiNbO5 was not destroyed by a high temperature and high pressure in the solvothermal process and that GaOOH was successfully dispersed on the surface of ZnBiNbO5. Simultaneously, there was a red-shift of the absorbance edge for GaOOH/ZnBiNbO5 compared with those of pure ZnBiNbO5 and pure GaOOH. The band gaps of ZnBiNbO5, GaOOH and GaOOH/ZnBiNbO5 were calculated to be 2.96 eV, 4.76 eV and 2.93 eV, respectively. The photocatalytic activity of GaOOH/ZnBiNbO5 was explored by degrading enrofloxacin under illumination. After ultraviolet light irradiation for 60 min, the removal rate of enrofloxacin with GaOOH/ZnBiNbO5 as a photocatalyst was 15.11% higher than that of pure ZnBiNbO5 and was 29.29% higher than that of pure GaOOH. In addition, the contribution of the free radicals in the photocatalytic process was confirmed to be ·O2 - > ·OH > h+. The construction of the GaOOH/ZnBiNbO5 composite improved the performance of the single ZnBiNbO5 photocatalyst and single GaOOH photocatalyst, thereby increasing their practical application potential.

Photophysical and Photocatalytic Properties of BiSnSbO6 under Visible Light Irradiation.

BiSnSbO6 with strong photocatalytic activity was first fabricated by a high-temperature, solid-state sintering method. The resulting BiSnSbO6 was characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), UV-vis diffuse reflectance spectroscopy (DRS) and X-ray photoelectron spectroscopy (XPS). The results showed that BiSnSbO6, with a pyrochlore structure and a cubic crystal system by a space group Fd3m, was well crystallized. The lattice parameter or the band gap of BiSnSbO6 was 10.234594 Šor 2.83 eV. Compared with N-doped TiO2, BiSnSbO6 showed higher photocatalytic activity in the degradation of benzotriazole and rhodamine B. The apparent first-order rate constant for BiSnSbO6 in the degradation of benzotriazole and rhodamine B was 0.0182 min-1 and 0.0147 min-1, respectively. On the basis of the scavenger experiment, during the photocatalytic process, the main active species were arranged in order of increasing photodegradation rate: •OH < •O2- < h⁺. The removal rate of benzotriazole or rhodamine B was approximately estimated to be 100% with BiSnSbO6 as a photocatalyst after 200 min visible-light irradiation. Plentiful CO2 produced by the experiment indicated that benzotriazole or rhodamine B was continuously mineralized during the photocatalytic process. Finally, the possible photodegradation pathways of benzotriazole and rhodamine B were deduced.

Synthesis, Structural Property, Photophysical Property, Photocatalytic Property of Novel ZnBiErO4 under Visible Light Irradiation.

A novel photocatalyst ZnBiErO4 was firstly synthesized by solid-state reaction method and its structural and photocatalytic properties were analyzed by scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy and UV-Vis diffuse reflectance. The results demonstrated that ZnBiErO4 crystallized with tetragonal crystal structure with space group I41/A. The lattice parameters for ZnBiErO4 were proved to be a = b = 10.255738 Å and c = 9.938888 Å. The band gap of ZnBiErO4 was estimated to be about 1.69 eV. Compared with nitrogen doped TiO2, ZnBiErO4 showed excellent photocatalytic activities for degrading methyl blue during visible light irradiation. The photocatalytic degradation of methyl blue with ZnBiErO4 or N-doped TiO2 as catalyst followed the first-order reaction kinetics. Moreover, the apparent first-order rate constant of ZnBiErO4 or N-doped TiO2 was 0.01607 min-1 or 0.00435 min-1. The reduction of total organic carbon, formation of inorganic products, such as SO42- and NO3- and the evolution of CO2 revealed the continuous mineralization of methyl blue during the photocatalytic process. ZnBiErO4 photocatalyst had great potential to purify textile industry wastewater.

Synthesis, Property Characterization and Photocatalytic Activity of the Polyaniline/BiYTi2O7 Polymer Composite.

A new polyaniline/BiYTi2O7 polymer composite was synthesized by chemical oxidation in-situ polymerization method for the first time. The effect of polyaniline doping on structural and catalytic properties of BiYTi2O7 was reported. The structural properties of novel polyaniline/BiYTi2O7 have been characterized by X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy and UV-Vis DRS. The results showed that BiYTi2O7 crystallized well with the pyrochlore-type structure, stable cubic crystal system by space group Fd3m. The lattice parameter or band gap energy of BiYTi2O7 was found to be a = 10.2132 Å or 2.349 eV, respectively. The novel polyaniline/BiYTi2O7 polymer composite possessed higher catalytic activity compared with BiYTi2O7 or nitrogen doped TiO2 for photocatalytic degradation of Azocarmine G under visible light irradiation. Additionally, the Azocarmine G removal efficiency was boosted from 3.0% for undoped BiYTi2O7 to 78.0% for the 10% polyaniline-modified BiYTi2O7, after only 60 min of reaction. After visible light irradiation for 330 min with polyaniline/BiYTi2O7 polymer composite as photocatalyst, complete removal and mineralization of Azocarmine G was observed. The photocatalytic degradation of Azocarmine G followed first-order reaction kinetics. Ultimately, the promoter action of H2O2 for photocatalytic degradation of AG with BiYTi2O7 as catalyst in the wastewater was discovered.

Property Characterization and Photocatalytic Activity Evaluation of BiGdO3 Nanoparticles under Visible Light Irradiation.

BiGdO3 nanoparticles were prepared by a solid-state reaction method and applied in photocatalytic degradation of dyes in this study. BiGdO3 was characterized by X-ray powder diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, Brunauer-Emmett-Teller, UV-Vis diffuse reflectance spectroscopy and transmission electron microscopy. The results showed that BiGdO3 crystallized well with the fluorite-type structure, a face-centered cubic crystal system and a space group Fm3m 225. The lattice parameter of BiGdO3 was 5.465 angstrom. The band gap of BiGdO3 was estimated to be 2.25 eV. BiGdO3 showed a strong optical absorption during the visible light region. Moreover, the photocatalytic activity of BiGdO3 was evaluated by photocatalytic degradation of direct dyes in aqueous solution under visible light irradiation. BiGdO3 demonstrated excellent photocatalytic activity in degrading Direct Orange 26 (DO-26) or Direct Red 23 (DR-23) under visible light irradiation. The photocatalytic degradation of DO-26 or DR-23 followed the first-order reaction kinetics, and the first-order rate constant was 0.0046 or 0.0023 min(-1) with BiGdO3 as catalyst. The degradation intermediates of DO-26 were observed and the possible photocatalytic degradation pathway of DO-26 under visible light irradiation was provided. The effect of various operational parameters on the photocatalytic activity and the stability of BiGdO3 particles were also discussed in detail. BiGdO3/(visible light) photocatalysis system was confirmed to be suitable for textile industry wastewater treatment.

The Structural, Photocatalytic Property Characterization and Enhanced Photocatalytic Activities of Novel Photocatalysts Bi2GaSbO7 and Bi2InSbO7 during Visible Light Irradiation.

In order to develop original and efficient visible light response photocatalysts for degrading organic pollutants in wastewater, new photocatalysts Bi2GaSbO7 and Bi2InSbO7 were firstly synthesized by a solid-state reaction method and their chemical, physical and structural properties were characterized. Bi2GaSbO7 and Bi2InSbO7 were crystallized with a pyrochlore-type structure and the lattice parameter of Bi2GaSbO7 or Bi2InSbO7 was 10.356497 Å or 10.666031 Å. The band gap of Bi2GaSbO7 or Bi2InSbO7 was estimated to be 2.59 eV or 2.54 eV. Compared with nitrogen doped TiO2, Bi2GaSbO7 and Bi2InSbO7, both showed excellent photocatalytic activities for degrading methylene blue during visible light irradiation due to their narrower band gaps and higher crystallization perfection. Bi2GaSbO7 showed higher catalytic activity compared with Bi2InSbO7. The photocatalytic degradation of methylene blue followed by the first-order reaction kinetics and the first-order rate constant was 0.01470 min-1, 0.00967 min-1 or 0.00259 min-1 with Bi2GaSbO7, Bi2InSbO7 or nitrogen doped TiO2 as a catalyst. The evolution of CO2 and the removal of total organic carbon were successfully measured and these results indicated continuous mineralization of methylene blue during the photocatalytic process. The possible degradation scheme and pathway of methylene blue was also analyzed. Bi2GaSbO7 and Bi2InSbO7 photocatalysts both had great potential to purify textile industry wastewater.

Synthesis, crystal structure, photodegradation kinetics and photocatalytic activity of novel photocatalyst ZnBiYO4.

ZnBiYO4 was synthesized by a solid-state reaction method for the first time. The structural and photocatalytic properties of ZnBiYO4 were characterized by X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy and UV-Vis diffuse reflectance. ZnBiYO4 crystallized with a tetragonal spinel structure with space group I41/A. The lattice parameters for ZnBiYO4 were a=b=11.176479Å and c=10.014323Å. The band gap of ZnBiYO4 was estimated to be 1.58eV. The photocatalytic activity of ZnBiYO4 was assessed by photodegradation of methyl orange under visible light irradiation. The results showed that ZnBiYO4 had higher catalytic activity compared with N-doped TiO2 under the same experimental conditions using visible light irradiation. The photocatalytic degradation of methyl orange with ZnBiYO4 or N-doped TiO2 as catalyst followed first-order reaction kinetics, and the first-order rate constant was 0.01575 and 0.00416 min(-1) for ZnBiYO4 and N-doped TiO2, respectively. After visible light irradiation for 220 min with ZnBiYO4 as catalyst, complete removal and mineralization of methyl orange were observed. The reduction of total organic carbon, formation of inorganic products, SO4(2-) and NO3-, and evolution of CO2 revealed the continuous mineralization of methyl orange during the photocatalytic process. The intermediate products were identified using liquid chromatography-mass spectrometry. The ZnBiYO4/(visible light) photocatalysis system was found to be suitable for textile industry wastewater treatment and could be used to solve other environmental chemical pollution problems.

Synthesis, characterization and photocatalytic activity of new photocatalyst ZnBiSbO4 under visible light irradiation.

In this paper, ZnBiSbO4 was synthesized by a solid-state reaction method for the first time. The structural and photocatalytic properties of ZnBiSbO4 had been characterized by X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy, Fourier-transform infrared spectroscopy, transmission electron microscope and UV-visible spectrometer. ZnBiSbO4 crystallized with a pyrochlore-type structure and a tetragonal crystal system. The band gap of ZnBiSbO4 was estimated to be 2.49 eV. The photocatalytic degradation of indigo carmine was realized under visible light irradiation with ZnBiSbO4 as a catalyst compared with nitrogen-doped TiO2 (N-TiO2) and CdBiYO4. The results showed that ZnBiSbO4 owned higher photocatalytic activity compared with N-TiO2 or CdBiYO4 for the photocatalytic degradation of indigo carmine under visible light irradiation. The reduction of the total organic carbon, the formation of inorganic products, SO4(2-) and NO3(-), and the evolution of CO2 revealed the continuous mineralization of indigo carmine during the photocatalytic process. One possible photocatalytic degradation pathway of indigo carmine was obtained. The phytotoxicity of the photocatalytic-treated indigo carmine (IC) wastewater was detected by examining its effect on seed germination and growth.

Photocatalytic Water Splitting for Hydrogen Production with Gd2MSbO7 (M = Fe, In, Y) Photocatalysts under Visible Light Irradiation.

Novel photocatalysts Gd2FeSbO7, Gd2InSbO7 and Gd2YSbO7 were synthesized by the solid state reaction method for the first time. A comparative study about the structural and photocatalytic properties of Gd2MSbO7 (M = Fe, In, Y) was reported. The results showed that Gd2FeSbO7, Gd2InSbO7 and Gd2YSbO7 crystallized with the pyrochlore-type structure, cubic crystal system and space group Fd3m. The lattice parameter a for Gd2FeSbO7, Gd2InSbO7 or Gd2YSbO7 was 10.276026 Å, 10.449546 Å or 10.653651 Å. The band gap of Gd2FeSbO7, Gd2InSbO7 or Gd2YSbO7 was estimated to be 2.151 eV, 2.897 eV or 2.396 eV. For the photocatalytic water-splitting reaction, H2 or O2 evolution was observed from pure water with Gd2FeSbO7, Gd2InSbO7 or Gd2YSbO7 as catalyst under visible light irradiation (wavelength > 420 nm). Moreover, H2 or O2 also spilt by using Gd2FeSbO7, Gd2InSbO7 or Gd2YSbO7 as catalyst from CH3OH/H2O or AgNO3/H2O solutions under visible light irradiation (λ > 420 nm). Gd2FeSbO7 showed the highest activity compared with Gd2InSbO7 or Gd2YSbO7. At the same time, Gd2InSbO7 showed higher activity compared with Gd2YSbO7. The photocatalytic activities were further improved under visible light irradiation with Gd2FeSbO7, Gd2InSbO7 or Gd2YSbO7 being loaded by Pt, NiO or RuO2. The effect of Pt was better than that of NiO or RuO2 for improving the photocatalytic activity of Gd2FeSbO7, Gd2InSbO7 or Gd2YSbO7.

Photophysical property and photocatalytic activity of new Gd(2)InSbO(7) and Gd(2)FeSbO(7) compounds under visible light irradiation.

Gd(2)InSbO(7) and Gd(2)FeSbO(7) were synthesized first, and their structural and photocatalytic properties were studied. The lattice parameters and the band gaps for Gd(2)InSbO(7) and Gd(2)FeSbO(7) were 10.449546 Å, 10.276026 Å, 2.897 eV and 2.151 eV. The photocatalytic degradation of rhodamine B was performed with Gd(2)InSbO(7) and Gd(2)FeSbO(7) under visible light irradiation. Gd(2)InSbO(7) and Gd(2)FeSbO(7) had higher catalytic activity compared with Bi(2)InTaO(7). Gd(2)FeSbO(7) exhibited higher catalytic activity than Gd(2)InSbO(7). The photocatalytic degradation of rhodamine B followed with the first-order reaction kinetics, and the first-order rate constant k was 0.01606, 0.02220 or 0.00329 min-1 with Gd(2)InSbO(7), Gd(2)FeSbO(7) or Bi(2)InTaO(7) as photocatalyst. Complete removal of rhodamine B was observed after visible light irradiation for 225 min or 260 min with Gd(2)FeSbO(7) or Gd(2)InSbO(7) as photocatalyst. The evolution of CO(2) was realized, and it indicated continuous mineralization of rhodamine B during the photocatalytic process. The possible photocatalytic degradation pathway of rhodamine B was proposed.

Synthesis, property characterization and photocatalytic activity of the novel composite polymer polyaniline/Bi2SnTiO7.

A novel polyaniline/Bi(2)SnTiO(7 )composite polymer was synthesized by chemical oxidation in-situ polymerization method and sol-gel method for the first time. The structural properties of novel polyaniline/Bi(2)SnTiO(7) have been characterized by X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy and X-ray spectrometry. The lattice parameter of Bi(2)SnTiO(7) was found to be a = 10.52582(8) Å. The photocatalytic degradation of methylene blue was realized under visible light irradiation with the novel polyaniline/Bi(2)SnTiO(7) as catalyst. The results showed that novel polyaniline/Bi(2)SnTiO(7 )possessed higher catalytic activity compared with Bi(2)InTaO(7) or pure TiO(2) or N-doped TiO(2) for photocatalytic degradation of methylene blue under visible light irradiation. The photocatalytic degradation of methylene blue with the novel polyaniline/Bi(2)SnTiO(7) or N-doped TiO(2) as catalyst followed first-order reaction kinetics, and the first-order rate constant was 0.01504 or 0.00333 min(-1). After visible light irradiation for 220 minutes with novel polyaniline/Bi(2)SnTiO(7 )as catalyst, complete removal and mineralization of methylene blue was observed. The reduction of the total organic carbon, the formation of inorganic products, SO(4)2- and NO(3-), and the evolution of CO(2) revealed the continuous mineralization of methylene blue during the photocatalytic process. The possible photocatalytic degradation pathway of methylene blue was obtained under visible light irradiation.