Yuanguo Xu

Preparation of sphere-like g-C3N4/BiOI photocatalysts via a reactable ionic liquid for visible-light-driven photocatalytic degradation of pollutants

Novel sphere-like g-C3N4/BiOI composite photocatalysts were prepared by a one-pot EG-assisted solvothermal process in the presence of reactable ionic liquid 1-butyl-3-methylimidazolium iodine ([Bmim]I). The nanostructured heterojunction was formed with g-C3N4 covering the surface of BiOI microspheres uniformly. Multiple techniques were applied to investigate the structure, morphology and photocatalytic properties of as-prepared samples. During the reactive process, the ionic liquid acted as solvent, reactant, template and dispersing agent at the same time, leading to g-C3N4 being uniformly dispersed on the sphere-like BiOI surface. Three different types of dyes rhodamine B (RhB), methylene blue (MB), methyl orange (MO) were chosen as model pollutants to evaluate the photocatalytic activity of g-C3N4/BiOI composite. The as-prepared g-C3N4/BiOI composite exhibited much higher photocatalytic activity than the pure BiOI. At the same time, colourless endocrine disrupting chemical bisphenol A (BPA) and phenols 4-chlorophenol (4-CP) were chosen to further evaluate the photocatalytic activity of g-C3N4/BiOI composite. The g-C3N4/BiOI composite also exhibited much higher photocatalytic activity than the pure BiOI, which showed a broad spectrum of photocatalytic degradation activities. The results indicated that the formed heterojunction of g-C3N4 covers the BiOI microspheres contributed to improved electron–hole separation and enhancement in photocatalytic activity. A photocatalytic mechanism of g-C3N4/BiOI composites is also proposed.

Exfoliated graphene-like carbon nitride in organic solvents: enhanced photocatalytic activity and highly selective and sensitive sensor for the detection of trace amounts of Cu2+

Due to their unprecedented electronic, surface and optical properties, the atomic-thick graphene-like materials have aroused great interest. Compared with the bulk counterparts, the graphene-like material can not only enhance the internal properties, but also gives rise to new promising properties. Herein, the graphene-like carbon nitride (graphene-like C3N4) was synthesized via liquid exfoliation from the bulk graphitic carbon nitride (g-C3N4) in 1,3-butanediol (1,3-BUT) for the first time. And the graphene-like C3N4 was characterized by X-ray diffraction (XRD), atomic force microscopy (AFM), transmission electron microscopy (TEM), thermogravimetric analysis (TG), and X-ray photoelectron spectroscopy (XPS). The obtained graphene-like C3N4 exhibited a two-dimensional thin-layer structure with about 3–6 atoms thickness, a high specific surface area of 32.54 m2 g−1, increased photocurrent responses, improved electron transport ability and enhanced photocatalytic activity. The photocatalytic reaction for the organic dye methylene blue (MB) by the graphene-like C3N4 followed first-order kinetics. Moreover, the graphene-like C3N4 exhibited a higher apparent rate of 0.1262 min−1, which was 3.1 times higher than that of the bulk g-C3N4 (0.0409 min−1). The enhanced photocatalytic reaction was due to a high specific surface area and a larger bandgap (by 0.14 eV). The yield of the graphene-like C3N4 was up to ∼0.35 mg mL−1. Moreover, the graphene-like C3N4 had a new property that it could be used as the sensor for trace amounts of Cu2+ determination, so the graphene-like C3N4 is a new but promising candidate for heavy metal ions (Cu2+) determination in water environment. Photoelectrochemical selective sensing of trace amounts of Cu2+ was also discussed.

Facile fabrication of the visible-light-driven Bi2WO6/BiOBr composite with enhanced photocatalytic activity

Novel Bi2WO6/BiOBr composite photocatalysts were prepared by a one-pot EG-assisted solvothermal process in the presence of reactable ionic liquid 1-hexadecyl-3-methylimidazolium bromide ([C16mim]Br). Multiple techniques, such as X-ray diffraction (XRD), X-ray photoemission spectroscopy (XPS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectrometry (EDS), Fourier transform infrared spectroscopy (FT-IR), UV-vis diffuse reflection spectroscopy (DRS), photoluminescence (PL), photocurrent and electrochemical impedance spectroscopy (EIS) were applied to investigate the structures, morphology and photocatalytic properties of as-prepared samples. Compared with bare Bi2WO6 and BiOBr, the Bi2WO6/BiOBr composites exhibited significantly enhanced photocatalytic activity for rhodamine B (RhB) degradation under visible light irradiation. The 50 at% Bi2WO6/BiOBr showed the highest photocatalytic activity under visible light irradiation, which was about 26.6 times and 1.8 times than that of the bare Bi2WO6 and BiOBr, respectively. The Bi2WO6/BiOBr composites also exhibited enhanced photocatalytic activity for bisphenol A (BPA) and methylene blue (MB) degradation under visible light irradiation. The results of PL, photocurrent and EIS indicated that Bi2WO6 and BiOBr could combine well to form a heterojunction structure which facilitated electron–hole separation, and led to the increasing photocatalytic activity. On the basis of the experimental results and estimated energy band positions, the mechanism of enhanced photocatalytic activity was proposed.

Synthesis and characterization of CeO2/g-C3N4 composites with enhanced visible-light photocatatalytic activity

Cerium dioxide/graphitic carbon nitride (CeO2/g-C3N4) visible-light-induced photocatalysts were successfully prepared by a simple mixing-calcination technique. The CeO2/g-C3N4 nanocomposites were characterized by thermogravimetric analysis (TG), powder X-ray diffraction (XRD), transmission electron microscopy (TEM), UV-vis diffuse reflection spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), photoluminescence (PL) and the photocurrent-time (PT) measurements. Photocatalytic activities of the prepared samples were examined by studying the degradation of methylene blue (MB) and 4-chlorophenol (4-CP) under visible light irradiation (>400 nm). The CeO2/g-C3N4 composites showed higher photocatalytic activity than that of CeO2 and g-C3N4. The optimum photoactivity of CeO2/g-C3N4 (13.0%) exhibited the highest photocatalytic activity in pollutant treatment and an enhanced photocurrent under visible light. These enhanced activities could be attributed to the synergetic effect between g-C3N4 and CeO2. The increasing photocatalytic activity mechanism was also discussed.

Construction of a 2D Graphene‐Like MoS2/C3N4 Heterojunction with Enhanced Visible‐Light Photocatalytic Activity and Photoelectrochemical Activity

A novel graphene-like MoS2 /C3N4 (GL-MoS2/C3N4) composite photocatalyst has been synthesized by a facile ethylene glycol (EG)-assisted solvothermal method. The structure and morphology of this GL-MoS2/C3N4 photocatalyst have been investigated by a wide range of characterization methods. The results showed that GL-MoS2 was uniformly distributed on the surface of GL-C3N4 forming a heterostructure. The obtained composite exhibited strong absorbing ability in the ultraviolet (UV) and visible regions. When irradiated with visible light, the composite photocatalyst showed high activity superior to those of the respective individual components GL-MoS2 and GL-C3N4 in the degradation of methyl orange. The enhanced photocatalytic activity of the composite may be attributed to the efficient separation of electron-hole pairs as a result of the matching band potentials between GL-MoS2 and GL-C3N4. Furthermore, a photocatalytic mechanism for the composite material has been proposed, and the photocatalytic reaction kinetics has been measured. Moreover, GL-MoS2/C3N4 could serve as a novel sensor for trace amounts of Cu(2+) since it exhibited good selectivity for Cu(2+) detection in water.

One-pot solvothermal synthesis of Cu-modified BiOCl via a Cu-containing ionic liquid and its visible-light photocatalytic properties

Novel visible-light-driven Cu-modified BiOCl uniform sphere-like materials have been successfully synthesized through a one-pot ethylene glycol (EG)-assisted solvothermal process in the presence of 1-octyl-3-methylimidazolium copper trichloride ([Omim]CuCl3). The Cu-modified BiOCl materials were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), energy dispersive X-ray spectrometry (EDS), Raman, photoluminescence (PL) and UV-vis diffuse reflectance spectroscopy (DRS). The results of the XRD, XPS, SEM, EDS, Raman analyses indicated that metal Cu was evenly distributed on the surface of the BiOCl microspheres in the form of Cu2+. During the reaction process, the metal-based ionic liquid acted as the solvent, the template, the Cl source and the Cu source at the same time. It is possible to tune the morphology of the Cu-modified BiOCl materials by varying the amount of ionic liquid used. In addition, the electrochemical and photocatalytic properties of the Cu-modified BiOCl materials were investigated. After the introduction of Cu2+, the photocurrent of the Cu-modified BiOCl materials was higher than that of the pure BiOCl. And the Cu-modified BiOCl materials exhibited higher photocatalytic activity for the degradation of methylene blue (MB) and bisphenol A (BPA) than that of pure BiOCl. The increased photocatalytic activity of the Cu-modified BiOCl materials was attributed to its large adsorption capacity, broad light absorption band and high separation efficiency of photo-generated electrons and holes. On the basis of these findings, the Cu-modified BiOCl materials showed great promise as photocatalysts for degrading organic pollutants and other applications.

Ion-exchange preparation for visible-light-driven photocatalyst AgBr/Ag2CO3 and its photocatalytic activity

The AgBr/Ag2CO3 composite was synthesized by an ion-exchange reaction. The physical and chemical properties of the catalysts were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), energy dispersive spectrometry (EDS), transmission electron microscopy (TEM), diffuse-reflection spectra (DRS) and photocurrent techniques. The photocatalytic performance of the samples was evaluated by photocatalytic oxidation of methylene blue (MB) dye under visible-light irradiation. The XRD, SEM-EDS, TEM, and XPS analyses indicated that the heterojunction structure had been obtained. The results indicated that the AgBr/Ag2CO3 heterojunction had exhibited a much higher photocatalytic activity than the pure Ag2CO3. The enhancement of photocatalytic activity was related to the efficient separation of electron–hole pairs because of the stagger band potentials between AgBr and Ag2CO3.

High yield synthesis of nano-size g-C3N4 derivatives by a dissolve-regrowth method with enhanced photocatalytic ability

Nano-size g-C3N4 derivatives were fabricated by a simple dissolve-regrowth method in HNO3 solution followed by a calcination process. X-ray diffraction (XRD), Z-potential, elemental analysis and IR are used to investigate the structure, composition and the properties of the samples. Scanning electron microscopy (SEM) shows the average size of the nano-size g-C3N4 derivatives increases with increasing calcination temperature. Methyl orange (MO) dye was used as the target pollutant to investigate the photoactivity of the samples. The pure g-C3N4 can only degrade about 1.1% MO, while the g-C3N4 derivatives calcined at 300 °C can decompose about 31.9% of MO in 4 h. Besides, when a small amount of methylene blue (MB) solution was introduced, the g-C3N4–HNO3-300 can decompose about 75.8% in 4 h. The photoactivity of g-C3N4 was greatly enhanced after the modification process (especially with the assistance of MB). Additionally, this work supplied a simple method to modify materials with enhanced photoactivity. Finally, the possible reactive species and the possible mechanism were proposed based on Electron spin resonance (ESR) and XPS results.

Magnetic g-C3N4/NiFe2O4 hybrids with enhanced photocatalytic activity

Composite photocatalysts have attracted considerable attention in the exploration of both highly efficient and low cost materials. In this study, novel magnetic g-C3N4/NiFe2O4 photocatalysts were fabricated by a facile chemisorption method. X-ray diffraction (XRD), transmission electron microscopy (TEM), infrared spectroscopy (IR), UV-vis diffuse reflectance spectroscopy (DRS) and X-ray photoelectron spectroscopy (XPS) were utilized to analyze the structure and properties of samples, which indicated that NiFe2O4 had been integrated onto the surface of g-C3N4 successfully. The as-prepared 7.5% g-C3N4/NiFe2O4, with the best photocatalytic activity, can maintain high photocatalytic activity and stability after five runs in the presence of hydrogen peroxide under visible light irradiation. During the catalytic reaction, the synergistic effect between g-C3N4 and NiFe2O4 can accelerate photogenerated charge separation and facilitate the photo-Fenton process to get an enhanced photocatalytic activity. Moreover, the collection and recycling of photocatalyst was readily achieved owing to the distinctive magnetism of g-C3N4/NiFe2O4.

A core–shell structured magnetic Ag/AgBr@Fe2O3 composite with enhanced photocatalytic activity for organic pollutant degradation and antibacterium

A core–shell structured magnetic Ag/AgBr@Fe2O3 composite was synthesized through a facile solvothermal method. Powder X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and ultraviolet-visible absorption spectroscopy (UV-vis) were applied to characterize the structures and properties of the as-prepared samples. The results indicate that Fe2O3 was coated on the surface of Ag/AgBr and heterostructures were formed. Electrochemistry analysis and photoluminescence (PL) spectra analysis indicate that the introduction of Fe2O3 could improve electron and hole separation efficiency. The photocatalytic activity of the Ag/AgBr@Fe2O3 composites was evaluated by using organic dye methyl orange (MO), endocrine disrupting chemical bisphenol A (BPA) and Escherichia coli (E. coli) as the target pollutants. The as-prepared Ag/AgBr@Fe2O3 composites exhibited much higher photocatalytic activities than pure Ag/AgBr, which was attributed to the effective charge separation of the Ag/AgBr@Fe2O3 composite. In addition, the as-prepared Ag/AgBr@Fe2O3 composite has magnetic properties, therefore after the photocatalytic reaction, it can be quickly separated from solution by an extra magnetic field. Trapping experiments and ESR analysis indicate that the h+ and ˙O2− are the main active species for the photocatalytic degradation. A possible Z-scheme pathway photocatalytic mechanism was proposed.