Search

Developing eco-friendly strategies to produce green fuel has attracted continuous and extensive attention. In this study, a novel gas-templating method was developed to prepare 2D porous S-doped g-C3N4 photocatalyst through simultaneous pyrolysis of urea (main g-C3N4 precursor) and ammonium sulfate (sulfur source and structure promoter). Different content of ammonium sulfate was examined to find the optimal synthesis conditions and to investigate the property-governed activity. The physicochemical properties of the obtained photocatalysts were analyzed by X-ray diffraction (XRD), field emission-scanning electron microscopy (FE-SEM), scanning transmission electron microscopy (STEM), specific surface area (BET) measurement, ultraviolet-visible light diffuse reflectance spectroscopy (UV/vis DRS), X-ray photoelectron spectroscopy (XPS), photoluminescence (PL) spectroscopy and reversed double-beam photo-acoustic spectroscopy (RDB-PAS). The as-prepared S-doped g-C3N4 photocatalysts were applied for photocatalytic H-2 evolution under vis irradiation. The condition-dependent activity was probed to achieve the best photocatalytic performance. It was demonstrated that ammonium sulfate played a crucial role to achieve concurrently 2D morphology, controlled nanostructure, and S-doping of g-C3N4 in a one-pot process. The 2D nanoporous S-doped g-C3N4 of crumpled lamellar-like structure with large specific surface area (73.8 m(2) g(-1)) and improved electron-hole separation showed a remarkable H-2 generation rate, which was almost one order in magnitude higher than that of pristine g-C3N4. It has been found that though all properties are crucial for the overall photocatalytic performance, efficient doping is probably a key factor for high photocatalytic activity. Moreover, the photocatalysts exhibit significant stability during recycling. Accordingly, a significant potential of S-doped g-C3N4 has been revealed for practical use under natural solar radiation.

Developing eco-friendly strategies to produce green fuel has attracted continuous and extensive attention. In this study, a novel gas-templating method was developed to prepare 2D porous S-doped g-C3N4 photocatalyst through simultaneous pyrolysis of urea (main g-C3N4 precursor) and ammonium sulfate (sulfur source and structure promoter). Different content of ammonium sulfate was examined to find the optimal synthesis conditions and to investigate the property-governed activity. The physicochemical properties of the obtained photocatalysts were analyzed by X-ray diffraction (XRD), field emission-scanning electron microscopy (FE-SEM), scanning transmission electron microscopy (STEM), specific surface area (BET) measurement, ultraviolet-visible light diffuse reflectance spectroscopy (UV/vis DRS), X-ray photoelectron spectroscopy (XPS), photoluminescence (PL) spectroscopy and reversed double-beam photo-acoustic spectroscopy (RDB-PAS). The as-prepared S-doped g-C3N4 photocatalysts were applied for photocatalytic H-2 evolution under vis irradiation. The condition-dependent activity was probed to achieve the best photocatalytic performance. It was demonstrated that ammonium sulfate played a crucial role to achieve concurrently 2D morphology, controlled nanostructure, and S-doping of g-C3N4 in a one-pot process. The 2D nanoporous S-doped g-C3N4 of crumpled lamellar-like structure with large specific surface area (73.8 m(2) g(-1)) and improved electron-hole separation showed a remarkable H-2 generation rate, which was almost one order in magnitude higher than that of pristine g-C3N4. It has been found that though all properties are crucial for the overall photocatalytic performance, efficient doping is probably a key factor for high photocatalytic activity. Moreover, the photocatalysts exhibit significant stability during recycling. Accordingly, a significant potential of S-doped g-C3N4 has been revealed for practical use under natural solar radiation.

Developing eco-friendly strategies to produce green fuel has attracted continuous and extensive attention. In this study, a novel gas-templating method was developed to prepare 2D porous S-doped g-C3N4 photocatalyst through simultaneous pyrolysis of urea (main g-C3N4 precursor) and ammonium sulfate (sulfur source and structure promoter). Different content of ammonium sulfate was examined to find the optimal synthesis conditions and to investigate the property-governed activity. The physicochemical properties of the obtained photocatalysts were analyzed by X-ray diffraction (XRD), field emission-scanning electron microscopy (FE-SEM), scanning transmission electron microscopy (STEM), specific surface area (BET) measurement, ultraviolet-visible light diffuse reflectance spectroscopy (UV/vis DRS), X-ray photoelectron spectroscopy (XPS), photoluminescence (PL) spectroscopy and reversed double-beam photo-acoustic spectroscopy (RDB-PAS). The as-prepared S-doped g-C3N4 photocatalysts were applied for photocatalytic H-2 evolution under vis irradiation. The condition-dependent activity was probed to achieve the best photocatalytic performance. It was demonstrated that ammonium sulfate played a crucial role to achieve concurrently 2D morphology, controlled nanostructure, and S-doping of g-C3N4 in a one-pot process. The 2D nanoporous S-doped g-C3N4 of crumpled lamellar-like structure with large specific surface area (73.8 m(2) g(-1)) and improved electron-hole separation showed a remarkable H-2 generation rate, which was almost one order in magnitude higher than that of pristine g-C3N4. It has been found that though all properties are crucial for the overall photocatalytic performance, efficient doping is probably a key factor for high photocatalytic activity. Moreover, the photocatalysts exhibit significant stability during recycling. Accordingly, a significant potential of S-doped g-C3N4 has been revealed for practical use under natural solar radiation.

The development of novel photocatalysts for efficient utilization of solar energy is highly essential for the most critical humanitarian challenges, i.e., energy and water crises as well as environmental pollution. Bismuth tungstate (Bi2WO6), an outstanding Aurivillius phase perovskite, has attracted intensive attention as a visiblelight-responsive photocatalyst because of its non-toxicity, low cost, and outstanding physicochemical characteristics, i.e., nonlinear dielectric susceptibility, ferroelectric piezoelectricity, pyroelectricity, catalytic behavior, modifiable morphology, strong oxidation power, and good photochemical stability. However, the photocatalytic activity of bare Bi2WO6 is restricted because of the inherent drawbacks such as poor light-harvesting efficiency, weak reduction potential, relatively low specific surface area, the fast recombination rate of photoinduced charge carriers, and thus poor quantum yields of photocatalytic reactions. Moreover, the impossibility of simultaneous strong redox ability (demanding wide bandgap) and high light-harvesting efficiency (requiring narrow bandgap) is considered as a big challenge for the practical application of Bi2WO6. Undeniably, the construction of Z-scheme photocatalytic systems is recommended strategy to overcome the above-mentioned disadvantages because of the efficient spatial separation of photogenerated charge carriers and the boosting the redox performance. This review summarizes the principles and recent developments on Z-scheme photocatalytic systems with special emphasis on the Bi2WO6-based photocatalysts, including the types, photocatalytic mechanisms and practical applications. Moreover, major differences between type-II heterojunction and Z-scheme photocatalyst have also been discussed. Additionally, the significant role of unique structures (e.g., core-shell and 2D/2D) for the improvement of photocatalytic activity of Z-scheme photocatalyst has been presented. Indeed, Bi2WO6-based Zscheme

Graphene, graphene oxide, reduced graphene oxide and their composites with various compounds/materials have high potential for substantial impact as cheap photocatalysts, which is essential to meet the demands of global activity, offering the advantage of utilizing “green” solar energy. Accordingly, graphene-based materials might help to reduce reliance on fossil fuel supplies and facile remediation routes to achieve clean environment and pure water. This review presents recent developments of graphene-based semiconductor photocatalysts, including novel composites with faceted particles, photonic crystals, and nanotubes/nanowires, where the enhancement of activity mechanism is associated with a synergistic effect resulting from the presence of graphene structure. Moreover, antimicrobial potential (highly needed these days), and facile recovery/reuse of photocatalysts by magnetic field have been addresses as very important issue for future commercialization. It is believed that graphene materials should be available soon in the market, especially because of constantly decreasing prices of graphene, vis response, excellent charge transfer ability, and thus high and broad photocatalytic activity against both organic pollutants and microorganisms.

Graphene, graphene oxide, reduced graphene oxide and their composites with various compounds/materials have high potential for substantial impact as cheap photocatalysts, which is essential to meet the demands of global activity, offering the advantage of utilizing “green” solar energy. Accordingly, graphene-based materials might help to reduce reliance on fossil fuel supplies and facile remediation routes to achieve clean environment and pure water. This review presents recent developments of graphene-based semiconductor photocatalysts, including novel composites with faceted particles, photonic crystals, and nanotubes/nanowires, where the enhancement of activity mechanism is associated with a synergistic effect resulting from the presence of graphene structure. Moreover, antimicrobial potential (highly needed these days), and facile recovery/reuse of photocatalysts by magnetic field have been addresses as very important issue for future commercialization. It is believed that graphene materials should be available soon in the market, especially because of constantly decreasing prices of graphene, vis response, excellent charge transfer ability, and thus high and broad photocatalytic activity against both organic pollutants and microorganisms.

Graphene, graphene oxide, reduced graphene oxide and their composites with various compounds/materials have high potential for substantial impact as cheap photocatalysts, which is essential to meet the demands of global activity, offering the advantage of utilizing “green” solar energy. Accordingly, graphene-based materials might help to reduce reliance on fossil fuel supplies and facile remediation routes to achieve clean environment and pure water. This review presents recent developments of graphene-based semiconductor photocatalysts, including novel composites with faceted particles, photonic crystals, and nanotubes/nanowires, where the enhancement of activity mechanism is associated with a synergistic effect resulting from the presence of graphene structure. Moreover, antimicrobial potential (highly needed these days), and facile recovery/reuse of photocatalysts by magnetic field have been addresses as very important issue for future commercialization. It is believed that graphene materials should be available soon in the market, especially because of constantly decreasing prices of graphene, vis response, excellent charge transfer ability, and thus high and broad photocatalytic activity against both organic pollutants and microorganisms.

Titania photocatalysts have been intensively examined for both mechanism study and possible commercial applications for more than 30 years. Although various reports have already been published on titania, including comprehensive review papers, the morphology-governed activity, especially for novel nanostructures, has not been reviewed recently. Therefore, this paper presents novel, attractive, and prospective titania photocatalysts, including zero-, one-, two-, and three-dimensional titania structures. The 1D, 2D, and 3D titania structures have been mainly designed for possible applications, e.g., (i) continuous use without the necessity of particulate titania separation, (ii) efficient light harvesting (e.g., inverse opals), (iii) enhanced activity (fast charge carriers’ separation, e.g., 1D nanoplates and 2D nanotubes). It should be pointed out that these structures might be also useful for mechanism investigation, e.g., (i) 3D titania aerogels with gold either incorporated inside the 3D network or supported in the porosity, and (ii) titania mesocrystals with gold deposited either on basal or lateral surfaces, for the clarification of plasmonic photocatalysis. Moreover, 0D nanostructures of special composition and morphology, e.g., magnetic(core)–titania(shell), mixed-phase titania (anatase/rutile/brookite), and faceted titania NPs have been presented, due to their exceptional properties, including easy separation in the magnetic field, high activity, and mechanism clarification, respectively. Although anatase has been usually thought as the most active phase of titania, the co-existence of other crystalline phases accelerates the photocatalytic activity significantly, and thus mixed-phase titania (e.g., famous P25) exhibits high photocatalytic activity for both oxidation and reduction reactions. It is believed that this review might be useful for the architecture design of novel nanomaterials for broad and diverse applications, including environmental purificatio

In an endeavor to tackle environmental problems, the photodegradation of microcystin-LR (MC-LR), one of the most common and toxic cyanotoxins, produced by the cyanobacteria blooms, was examined using nanostructured TiO2 photocatalysts (anatase, brookite, anatase–brookite, and C/N/S co-modified anatase–brookite) under UV-A, solar and visible light irradiation. The tailoring of TiO2 properties to hinder the electron–hole recombination and improve MC-LR adsorption on TiO2 surface was achieved by altering the preparation pH value. The highest photocatalytic efficiency was 97% and 99% with degradation rate of 0.002 mmol L−1 min−1 and 0.0007 mmol L−1 min−1 under UV and solar irradiation, respectively, using a bare TiO2 photocatalyst prepared at pH 10 with anatase to brookite ratio of ca. 1:2.5. However, the bare TiO2 samples were hardly active under visible light irradiation (<25%) due to a large band gap. Upon UV, solar and vis irradiation, the complete MC-LR degradation (100%) was obtained in the presence of C/N/S co-modified TiO2 with a degradation rate constant of 0.26 min−1, 0.11 min−1 and 0.04 min−1, respectively. It was proposed that the remarkable activity of co-modified TiO2 might originate from its mixed-phase composition, mesoporous structure, and non-metal co-modification.

Microcystin-LR (MC-LR), a potent hepatotoxin produced by the cyanobacteria, is of increasing concern worldwide because of severe and persistent impacts on humans and animals by inhalation and consumption of contaminated waters and food. In this work, MC-LR was removed completely from aqueous solution using visible-light-active C/N-co-modified mesoporous anatase/brookite TiO 2 photocatalyst. The co-modified TiO 2 nanoparticles were synthesized by a one-pot hydrothermal process, and then calcined at different temperatures (300, 400, and 500 °C). All the obtained TiO 2 powders were analyzed by X-ray diffraction (XRD), Raman spectroscopy, transmission electron microscope (TEM), specific surface area (SSA) measurements, ultraviolet-visible diffuse reflectance spectra (UV-vis DRS), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FTIR) spectroscopy, and photoluminescence (PL) analysis. It was found that all samples contained mixed-phase TiO 2 (anatase and brookite), and the content of brookite decreased with an increase in calcination temperature, as well as the specific surface area and the content of non-metal elements. The effects of initial pH value, the TiO 2 content, and MC-LR concentration on the photocatalytic activity were also studied. It was found that the photocatalytic activity of the obtained TiO 2 photocatalysts declined with increasing temperature. The complete degradation (100%) of MC-LR (10 mg L -1 ) was observed within 3 h, using as-synthesized co-modified TiO 2 (0.4 g L -1 ) at pH 4 under visible light. Based on the obtained results, the mechanism of MC-LR degradation has been proposed. © 2019 by the authors.

In an endeavor to tackle environmental problems, the photodegradation of microcystin- LR (MC-LR), one of the most common and toxic cyanotoxins, produced by the cyanobacteria blooms, was examined using nanostructured TiO2 photocatalysts (anatase, brookite, anatase- brookite, and C/N/S co-modified anatase-brookite) under UV-A, solar and visible light irradiation. The tailoring of TiO2 properties to hinder the electron-hole recombination and improve MC-LR adsorption on TiO2 surface was achieved by altering the preparation pH value. The highest photocatalytic efficiency was 97% and 99% with degradation rate of 0.002 mmol L-1 min-1 and 0.0007 mmol L-1 min-1 under UV and solar irradiation, respectively, using a bare TiO2 photocatalyst prepared at pH 10 with anatase to brookite ratio of ca. 1:2.5. However, the bare TiO2 samples were hardly active under visible light irradiation (<25%) due to a large band gap. Upon UV, solar and vis irradiation, the complete MC-LR degradation (100%) was obtained in the presence of C/N/S comodified TiO2 with a degradation rate constant of 0.26 min-1, 0.11 min-1 and 0.04 min-1, respectively. It was proposed that the remarkable activity of co-modified TiO2 might originate from its mixedphase composition, mesoporous structure, and non-metal co-modification.

In an endeavor to tackle environmental problems, the photodegradation of microcystin-LR (MC-LR), one of the most common and toxic cyanotoxins, produced by the cyanobacteria blooms, was examined using nanostructured TiO2 photocatalysts (anatase, brookite, anatase–brookite, and C/N/S co-modified anatase–brookite) under UV-A, solar and visible light irradiation. The tailoring of TiO2 properties to hinder the electron–hole recombination and improve MC-LR adsorption on TiO2 surface was achieved by altering the preparation pH value. The highest photocatalytic efficiency was 97% and 99% with degradation rate of 0.002 mmol L−1 min−1 and 0.0007 mmol L−1 min−1 under UV and solar irradiation, respectively, using a bare TiO2 photocatalyst prepared at pH 10 with anatase to brookite ratio of ca. 1:2.5. However, the bare TiO2 samples were hardly active under visible light irradiation (<25%) due to a large band gap. Upon UV, solar and vis irradiation, the complete MC-LR degradation (100%) was obtained in the presence of C/N/S co-modified TiO2 with a degradation rate constant of 0.26 min−1, 0.11 min−1 and 0.04 min−1, respectively. It was proposed that the remarkable activity of co-modified TiO2 might originate from its mixed-phase composition, mesoporous structure, and non-metal co-modification.

Titania photocatalysts have been intensively examined for both mechanism study and possible commercial applications for more than 30 years. Although various reports have already been published on titania, including comprehensive review papers, the morphology-governed activity, especially for novel nanostructures, has not been reviewed recently. Therefore, this paper presents novel, attractive, and prospective titania photocatalysts, including zero-, one-, two-, and three-dimensional titania structures. The 1D, 2D, and 3D titania structures have been mainly designed for possible applications, e.g., (i) continuous use without the necessity of particulate titania separation, (ii) efficient light harvesting (e.g., inverse opals), (iii) enhanced activity (fast charge carriers’ separation, e.g., 1D nanoplates and 2D nanotubes). It should be pointed out that these structures might be also useful for mechanism investigation, e.g., (i) 3D titania aerogels with gold either incorporated inside the 3D network or supported in the porosity, and (ii) titania mesocrystals with gold deposited either on basal or lateral surfaces, for the clarification of plasmonic photocatalysis. Moreover, 0D nanostructures of special composition and morphology, e.g., magnetic(core)–titania(shell), mixed-phase titania (anatase/rutile/brookite), and faceted titania NPs have been presented, due to their exceptional properties, including easy separation in the magnetic field, high activity, and mechanism clarification, respectively. Although anatase has been usually thought as the most active phase of titania, the co-existence of other crystalline phases accelerates the photocatalytic activity significantly, and thus mixed-phase titania (e.g., famous P25) exhibits high photocatalytic activity for both oxidation and reduction reactions. It is believed that this review might be useful for the architecture design of novel nanomaterials for broad and diverse applications, including environmental purificatio

In an endeavor to tackle environmental problems, the photodegradation of microcystin-LR (MC-LR), one of the most common and toxic cyanotoxins, produced by the cyanobacteria blooms, was examined using nanostructured TiO2 photocatalysts (anatase, brookite, anatase–brookite, and C/N/S co-modified anatase–brookite) under UV-A, solar and visible light irradiation. The tailoring of TiO2 properties to hinder the electron–hole recombination and improve MC-LR adsorption on TiO2 surface was achieved by altering the preparation pH value. The highest photocatalytic efficiency was 97% and 99% with degradation rate of 0.002 mmol L−1 min−1 and 0.0007 mmol L−1 min−1 under UV and solar irradiation, respectively, using a bare TiO2 photocatalyst prepared at pH 10 with anatase to brookite ratio of ca. 1:2.5. However, the bare TiO2 samples were hardly active under visible light irradiation (<25%) due to a large band gap. Upon UV, solar and vis irradiation, the complete MC-LR degradation (100%) was obtained in the presence of C/N/S co-modified TiO2 with a degradation rate constant of 0.26 min−1, 0.11 min−1 and 0.04 min−1, respectively. It was proposed that the remarkable activity of co-modified TiO2 might originate from its mixed-phase composition, mesoporous structure, and non-metal co-modification.

Titania photocatalysts have been intensively examined for both mechanism study and possible commercial applications for more than 30 years. Although various reports have already been published on titania, including comprehensive review papers, the morphology-governed activity, especially for novel nanostructures, has not been reviewed recently. Therefore, this paper presents novel, attractive, and prospective titania photocatalysts, including zero-, one-, two-, and three-dimensional titania structures. The 1D, 2D, and 3D titania structures have been mainly designed for possible applications, e.g., (i) continuous use without the necessity of particulate titania separation, (ii) efficient light harvesting (e.g., inverse opals), (iii) enhanced activity (fast charge carriers’ separation, e.g., 1D nanoplates and 2D nanotubes). It should be pointed out that these structures might be also useful for mechanism investigation, e.g., (i) 3D titania aerogels with gold either incorporated inside the 3D network or supported in the porosity, and (ii) titania mesocrystals with gold deposited either on basal or lateral surfaces, for the clarification of plasmonic photocatalysis. Moreover, 0D nanostructures of special composition and morphology, e.g., magnetic(core)–titania(shell), mixed-phase titania (anatase/rutile/brookite), and faceted titania NPs have been presented, due to their exceptional properties, including easy separation in the magnetic field, high activity, and mechanism clarification, respectively. Although anatase has been usually thought as the most active phase of titania, the co-existence of other crystalline phases accelerates the photocatalytic activity significantly, and thus mixed-phase titania (e.g., famous P25) exhibits high photocatalytic activity for both oxidation and reduction reactions. It is believed that this review might be useful for the architecture design of novel nanomaterials for broad and diverse applications, including environmental purificatio