TiO2/Bi4 Ti3 O12 hybrids have been widely prepared as promising photocatalysts for decomposing organic contaminations.However,the insufficient visible light absorption and low charge separation efficiency lead to thei...TiO2/Bi4 Ti3 O12 hybrids have been widely prepared as promising photocatalysts for decomposing organic contaminations.However,the insufficient visible light absorption and low charge separation efficiency lead to their poor photocatalytic activity.Herein,a robust methodology to construct novel TiO2/Bi4 Ti3 O12/MoS2 core/shell structures as visible light photocatalysts is presented.Homogeneous bismuth oxyiodide(BiOI) nanoplates were immobilized on electrospun TiO2 nanofiber surface by successive ionic layer adsorption and reaction(SILAR) method.TiO2/Bi4 Ti3 O12 core/shell nanofibers were conveniently prepared by partial conversion of TiO2 to high crystallized Bi4 Ti3 O12 shells through a solid-state reaction with BiOI nanoplates,which is accompanied with certain transition of TiO2 from anatase to rutile phase.Afterwards,MoS2 nanosheets with several layers thick were uniform decorated on the TiO2/Bi4 TiO3 O12 fiber surface resulting in TiO2/Bi4 Ti3 O12/MoS2 structures.Significant enhancement of visible light absorption and photo-generated charge separation of TiO2/Bi4 Ti3 O12 were achieved by introduction of MoS2.As a result,the optimized TiO2/Bi4 Ti3 O12/MoS2-2 presents 60% improvement for photodegrading RhB after 120 min irradiation under visible light and 3 times higher of apparent reaction rate constant in compared with the TiO2/Bi4 Ti3 O12.This synthetic method can also be used to establish other photocatalysts simply at low cost,therefore,is suitable for practical applications.展开更多
TiO2 nanostructures were fabricated by a reaction of Ti foils in H2O2 solution at mild temperature, Porous TiO2 nanostructurcs, well adhered to Ti foil surfaces, were formed at 80 ℃ in 10 rain, and then flower- like ...TiO2 nanostructures were fabricated by a reaction of Ti foils in H2O2 solution at mild temperature, Porous TiO2 nanostructurcs, well adhered to Ti foil surfaces, were formed at 80 ℃ in 10 rain, and then flower- like and rod nanostructures formed in succession after a longer reaction time. Samples prepared at 80 ℃ for 4 h arc amorphous, and anatase-dominated crystal phase emerged in the sample prepared for as long as 10 h. Almost pure anatase phase were obtained in TiO2 nanostructures by annealing the samples at a temperature of 300 ℃. Photoeatalysis of the TiO2 nanostructures was characterized by the degradation of RhB dye molecules in an aqueous solution exposed to ultraviolet light. Results show a 7 cm^2 annealed TiO2 flower-like nanostrueture having the degradation rate of RhB as fast as 29.8 times that of the dye solution exposed to ultraviolet light alone.展开更多
Hierarchically porous anatase Ti02 microspheres composited with carbonaceous species （TCS） have been successfully fabricated by a one-step template-free solvothermal method, combined with subsequent low temperature ...Hierarchically porous anatase Ti02 microspheres composited with carbonaceous species （TCS） have been successfully fabricated by a one-step template-free solvothermal method, combined with subsequent low temperature dried process. In this configuration, the TCS microspheres are constructed by the intercon- nected porous nanosheets, which are further assembled with abundant nanoparticles and carbonaceous species. Such composite microspheres possess a large specific surface area of 337 m2 g-l, uniform mesopores of 3.37 nm and high total pore volumes of 0.275 cm3 g-1. The materials exhibit the enhanced photocatalytic properties and stability for degradation of rhodamine B （RhB） under visible-light irradiation. The enhanced photocatalytic degradation performance may be ascribed to their abundant porous structure, large specific surface area and the unique assist-function of the carbonaceous species.展开更多
Fe-doped TiO2 was prepared by the sol gel method and characterized by X-ray diffraction. All the Fe-doped TiO2 were composed of an anatase crystal form. The activity of the Fe-doped TiO2 for the degradation of the ges...Fe-doped TiO2 was prepared by the sol gel method and characterized by X-ray diffraction. All the Fe-doped TiO2 were composed of an anatase crystal form. The activity of the Fe-doped TiO2 for the degradation of the gesaprim commercial herbicide (which contains atrazine as active compound and formulating agents) was studied by varying the iron content during UV (15 W), visible light and solar irradiations. The visible light came from commercial saving energy lamps (13, 15 and 20 Watts). The gesaprim degradation rate depended on the iron content in the photo catalyst. The Fe-doped TiO2 (0.5% by weight of TiO2) showed higher TOC removal under visible light and was more active than the undoped TiO2 photo catalyst under the light irradiation sources tested. Over 90% of chemical oxygen demand abatement was achieved with both UV and visible light but less time was required to decrease the chemical oxygen demand content by using the catalyst doped with iron at 0.5% under visible light. It was observed that the degradation of gesaprim increased by increasing the iron content in the catalyst under visible light.展开更多
Efficient solar light harvesting is essential for high-performance photocatalysts.Here,Rigorous CoupledWave Analysis(RCWA)computational method is used to investigate and optimize the optical absorption of TiO_(2)-BiVO...Efficient solar light harvesting is essential for high-performance photocatalysts.Here,Rigorous CoupledWave Analysis(RCWA)computational method is used to investigate and optimize the optical absorption of TiO_(2)-BiVO_(4) inverse opal(IO)structures under varying light incidence angles and pore-filling medium(air or water).Simulations were validated against experimental reflectance data.They revealed that small-pore IOs strongly absorb in the UV-C and UV-B regions due to the slow photon effect,making them ideal for sterilization and water disinfection.Medium-and large-pore IOs benefit from additional slow photon effect at the 2nd order photonic band gap,enhancing absorption across both UV and visible regions.Medium-pore IOs are suited for indoor air treatment and water purification,while large-pore IOs with the highest photon flux enhancement enable solar-driven photocatalysis such as outdoor pollutant removal and hydrogen production.For all tested IO designs,the absorbed photon flux exceeds that of equivalent planar slabs,highlighting the advantage of photonic structuring for sustainable photocatalytic applications.展开更多
Simultaneous integration of rich oxygen vacancies(OVs)and twin crystals in a photocatalyst can not only significantly enhance the near-infrared(NIR)light response but also greatly improve the photocharge separation an...Simultaneous integration of rich oxygen vacancies(OVs)and twin crystals in a photocatalyst can not only significantly enhance the near-infrared(NIR)light response but also greatly improve the photocharge separation and transfer efficiency owing to the induced high electrical conductivity and strong built-in electric field.However,thus far,there has been a lack of a model catalyst containing both twin crystals and OVs.Herein,we develop a simple wet chemical strategy for synthesizing of unprecedented NIR light-responsive OVs-rich Cu_(2)O black nanoparticles with high-density of twin crystals(denoted as black twinned Cu_(2)O).As expected,the black twinned Cu_(2)O exhibits higher visible-NIR and NIR light-driven photodegradation of tetracycline(TC)solution than the counterparts.Significantly,the mechanism insight into twin-dependent photocatalysis in NIR light-responsive Cu_(2)O black nanocrystals with rich OVs is uncovered in depth by density functional theory(DFT)calculations and a series of experimental evidence.Expectantly,this work would be beneficial for the scientific researchers currently focusing on the NIR light-responsive photocatalysis and twin engineering of photocatalysts.展开更多
As efficient water treatment agents, a novel series of rectorite-based ZnO and TiO2 hybrid composites（REC/ZnO/TiO2） were synthesized and characterized in this study. Effects of experimental parameters including TiO2...As efficient water treatment agents, a novel series of rectorite-based ZnO and TiO2 hybrid composites（REC/ZnO/TiO2） were synthesized and characterized in this study. Effects of experimental parameters including TiO2 mass ratio, solution p H and catalyst dosage on the removal of methyl blue（MB） were also conducted. The presence of a little mass ratio（2%-6%） of TiO2 highly promoted the photoactivity of REC/ZnO/TiO2 in removal of MB dye from aqueous solution, in which ZnO and REC played a role of photocatalyst and adsorbent. The promotion effects of TiO2 may result from the accelerated separation of electron-hole on ZnO. The observed kinetic constant for the degradation of MB over REC/ZnO and REC/ZnO/TiO2 were 0.015 and 0.038 min^（-1）, respectively. The degradation kinetics of MB dye, which followed the Langmuir–Hinshelwood model, had a reaction constant of 0.17 mg/（L min）. The decrease of removal ratio of MB after five repetitive experiments was small, indicating REC/ZnO/TiO2 has great potential as an effective and stable catalyst.展开更多
Photocatalyst CoPcS/TiO2 was prepared by sol-gel method. Composite CoPcS/TiO2/K2Ti4O9 was prepared by dipping. It was incandesced at various temperatures and modification effect was compared. The results showed that o...Photocatalyst CoPcS/TiO2 was prepared by sol-gel method. Composite CoPcS/TiO2/K2Ti4O9 was prepared by dipping. It was incandesced at various temperatures and modification effect was compared. The results showed that optical absorption of sample incandesce at 423K occurred significant red-shift. Light absorption width extended from ultraviolet region to visible region, especially there was an intensive absorption between 600 nm and 680 nm. X-ray diffraction spectrogram showed that TiO2 in sample still maintained anatase crystal form. Under the illumination of visible light, photocatalysis degradation experiment was taken with Eosin B as simulated pollutants. Decoloration rate of Eosin B was much improved. The rate can reach 80% in 300 minutes.展开更多
The mass production and widespread use of Pharmaceuticals and Personal Care Products(PPCPs)have posed a serious threat to the water environment and public health.In this work,a green metal-based Metal Organic Framewor...The mass production and widespread use of Pharmaceuticals and Personal Care Products(PPCPs)have posed a serious threat to the water environment and public health.In this work,a green metal-based Metal Organic Framework(MOF)Bi-NH_(2)-BDC was prepared and characterized,and the adsorption characteristics of Bi-NH_(2)-BDCwere investigated with typical PPCPs-diclofenac sodium(DCF).It was found that DCF mainly covered the adsorbent surface as a single molecular layer,the adsorption reaction was a spontaneous,entropyincreasing exothermic process and the adsorption mechanisms between Bi-NH_(2)-BDC and DCF were hydrogen bonding,π-πinteractions and electrostatic interactions.In addition,Bi-NH_(2)-BDC also had considerable photocatalytic properties,and its application in adsor-bent desorption treatment effectively solved the problem of secondary pollution,achieving a green and sustainable adsorption desorption cycle.展开更多
The production of renewable methanol(CH_(3)OH)via the photocatalytic hydrogenation of CO_(2) is an ideal method to ameliorate energy shortages and mitigate CO_(2) emissions:however,the highly selective synthesis of me...The production of renewable methanol(CH_(3)OH)via the photocatalytic hydrogenation of CO_(2) is an ideal method to ameliorate energy shortages and mitigate CO_(2) emissions:however,the highly selective synthesis of methanol at atmospheric pressure remains challenging owing to the competing reverse water-gas shift(RWGS)reaction.Herein,we present a novel approach for the synthesis of CH_(3)OH via photocatalytic CO_(2) hydrogenation using a catalyst featuring highly dispersed Au nanoparticles loaded on oxygen vacancy(OV)-rich molybdenum dioxide(MoO_(2)),resulting in a remarkable selectivity of 43.78%.The active sites in the Au/MoO_(2) catalyst are high-density Au-oxygen vacancies,which synergistically promote the tandem methanol synthesis via an initial RWGS reaction and subsequent CO hydrogenation.This work provides comprehensive insights into the design of metal-vacancy synergistic sites for the highly selective photocatalytic hydrogenation of CO_(2) to CH_(3)OH.展开更多
Herein,a simple and effective outer-surface interactions assisted supramolecular hierarchical assembly has been first exploited to uniformly distribute tungstosilicic acid(TSA)inside the porous structure of cucurbit[1...Herein,a simple and effective outer-surface interactions assisted supramolecular hierarchical assembly has been first exploited to uniformly distribute tungstosilicic acid(TSA)inside the porous structure of cucurbit[10]uril-based single-layer 2D supramolecular-organic-frameworks(Q[10]-SOFs)in water.Importantly,the 2D Q[10]-SOFs can further serve as light harvesting antenna,achieving fast energy transfer to the embedded redox-active TSA upon photoexcitation,resulting in efficient visible light-driven selective oxidation of benzyl alcohols into the corresponding aldehydes in high yield at room temperature.Further studies revealed that the integrated of 2D Q[10]-SOFs and TSA played a key role in the catalytic process,due to the presence of a novel stepwise electron transfer route in the single-layer hybrid 2D structures.展开更多
This article systematically reviewed the applications of single-atom catalysts(SACs)in the domain of photocatalytic reactions,with a particular emphasis on the indispensable role of H_(2)O in these processes.SACs,due ...This article systematically reviewed the applications of single-atom catalysts(SACs)in the domain of photocatalytic reactions,with a particular emphasis on the indispensable role of H_(2)O in these processes.SACs,due to their distinct active sites and superior catalytic efficacy,found their applications in the fields of energy conversion and environmental protection.The review elaborated on the potential carriers,preparation methods,and characterization techniques for single-atom photocatalysts.Subsequently,the article provided an in-depth explanation of the crucial role of H_(2)O in photocatalytic reactions,serving as an important green solvent and an oxygen/proton source.The adsorption of water could also change the surface energy structure and charge distribution of the photocatalyst.Conversely,the presence of H_(2)O might also inhibit the target reaction.Additionally,the distinct roles of water in both liquid and gas phases were discussed.Furthermore,the review systematically summarized the applications of single-atom photocatalysts in H_(2)generation,CO_(2)reduction,N2fixation,H_(2)O_(2)production,and environmentalremediation.It delved into the mechanisms by which water molecules participated in photocatalytic processes and their interactions with competing pathways,thereby revealing the complexity and critical importance of water in photocatalytic reactions.Finally,the article discusses the opportunities and challenges of SACs in photocatalytic reactions with H_(2)O.This article provides a comprehensive perspective for understanding the role of SACs in waterinvolved photocatalytic reactions.展开更多
Water purification systems based on transition metal dichalcogenides face significant challenges,including lack of reactivity under dark conditions,scarcity of catalytically active sites,and rapid recombination of pho...Water purification systems based on transition metal dichalcogenides face significant challenges,including lack of reactivity under dark conditions,scarcity of catalytically active sites,and rapid recombination of photogenerated charge carriers.Simultaneously increasing the number of active sites and improving charge separation efficiency has proven difficult.In this study,we present a novel approach combining molybdenum(Mo) monoatomic doping and size engineering to produce a series of Mo-ReS_(2) quantum dots(MR QDs) with controllable dimensions.High-resolution structural characterization,first-principle calculations,and piezo force microscopy reveal that Mo monoatomic doping enhances the lattice asymmetry,thereby improving the piezoelectric properties.The resulting piezoelectric polarization and the generated built-in electric field significantly improve charge separation efficiency,leading to optimized photocatalytic performance.Additionally,the doping strategy increases the number of active sites and improves the adsorption of intermediate radicals,substantially boosting photo-sterilization efficiency.Our results demonstrate the elimination of 99.95% of Escherichia coli and 100.00% of Staphylococcus aureus within 30 min.Furthermore,we developed a self-purification system simulating water drainage,utilizing low-frequency water streams to trigger the piezoelectric behavior of MR QDs,achieving piezoelectric synergistic photodegradation.This innovative approach provides a more environmentally friendly and economical method for water self-purification,paving the way for advanced water treatment technologies.展开更多
Peroxymonosulfate(PMS)is commonly used in advanced oxidation processes to degrade organic pollutants in wastewater.In this work,to obtain better PMS activation efficiency,Bi_(4)O_(5)Br_(2)/BCZT(BBT)piezoelectric photo...Peroxymonosulfate(PMS)is commonly used in advanced oxidation processes to degrade organic pollutants in wastewater.In this work,to obtain better PMS activation efficiency,Bi_(4)O_(5)Br_(2)/BCZT(BBT)piezoelectric photocatalyst was designed.Abundant active radicals produced by BBT under visible light irradiation and ultrasonic vibration were used to activate PMS,thereby achieving rapid degradation of high concentration pollutants.With the introduction of BCZT,the catalyst has a strong internal electric field and three-dimensional lamellar structure,which promotes the separation and transfer of electrons and holes.It is worth noting that under optimal reaction conditions,the degradation rate of ARB reached 93%by BBT15 within 10 min.The catalytic experiment combined with the piezoelectric performance test results revealed the key role of piezoelectric photocatalytic reaction in PMS activation.This provides an important prospect for PMS to effectively deal with the degradation of high concentrations of organic pollutants.展开更多
The rational design and construction of heterojunction structure is an effective strategy to improve the photocatalytic performance.Herein,a series of BiOBr nanosheets-immobilized TiO2/Ti3C2Tx MXene hybrid materials w...The rational design and construction of heterojunction structure is an effective strategy to improve the photocatalytic performance.Herein,a series of BiOBr nanosheets-immobilized TiO2/Ti3C2Tx MXene hybrid materials with heterojunction structure were synthesized by a facial one-step hydrothermal method.The ternary composites show outstanding performance as photocatalysts for the degradation of rhodamine B due to the optimized synergetic effects of BiOBr,TiO2 and Ti3C2Tx.The improved photocatalytic performance is remarkably attributed to the construction of a heterojunction between TiO2 and BiOBr due to their well-matching of energy band position,which can enhance the absorption for visible light and promote the transfer of photo-generated charge carriers.Moreover,Ti3C2Tx acts as an electron trap to further accelerate the separation of photo-generated electrons and holes.展开更多
Photocatalysis,harnessing abundant solar energy,presents a sustainable strategy to address the dual chal-lenges of fossil fuel depletion and environmental degradation.Among the emerging materials for photo-catalytic a...Photocatalysis,harnessing abundant solar energy,presents a sustainable strategy to address the dual chal-lenges of fossil fuel depletion and environmental degradation.Among the emerging materials for photo-catalytic applications,reticular framework materials,including metal-organic frameworks(MOFs),cova-lent organic frameworks(COFs),and hydrogen-bonded organic frameworks(HOFs),have attracted signif-icant attention due to their high surface area,tunable architectures,and versatile chemical compositions.These properties enable efficient light harvesting and charge separation,making them promising candi-dates for various photocatalytic processes.This review systematically explores recent advancements in the synthesis and structural properties of MOFs,COFs,and HOFs,elucidating the complex mechanisms governing solar-driven photocatalysis and comparing their performance with a particular focus on their applications in CO_(2)reduction,H_(2)generation,H_(2)O_(2)production,N_(2)fixation,and pollutant degradation.Key strategies for enhancing photocatalytic performance,including structural modifications,bandgap en-gineering,defect engineering,hybridization,and heterojunction formation,are critically analyzed.A com-parative evaluation of reticular framework materials against traditional semiconductors is provided,con-sidering factors such as efficiency,cost,and long-term stability.Furthermore,this review highlights the challenges related to stability and scalability,along with key achievements and barriers to practical im-plementation.This work offers possible insights to overcome existing limitations and improve efficiency.Ultimately,this comprehensive assessment highlights the pivotal role of reticular frameworks in advanc-ing sustainable energy solutions and provides a roadmap for future research and innovation in this rapidly evolving field.展开更多
Ce-β-Bi_(2)O_(3)/AgI was prepared using solvothermal calcination and in-situ deposition methods.The introduction of Ce can inhibit the conversion of Bi_(2)O_(3)fromβtoαphase at high temperatures,promoting the forma...Ce-β-Bi_(2)O_(3)/AgI was prepared using solvothermal calcination and in-situ deposition methods.The introduction of Ce can inhibit the conversion of Bi_(2)O_(3)fromβtoαphase at high temperatures,promoting the formation of oxygen vacancies(OVs)in the photocatalyst.OVs can adsorb more dissolved oxygen to promote the formation rate of·O^(-)_(2).Moreover,the interaction between Ce-Bi_(2)O_(3)and AgI results in the formation of Z-scheme heterojunctions,which can broaden the light absorption region,facilitate photogenerated carrier separation and transfer and enhance the ability to produce more active oxygen species(ROS).The morphology,crystal,element distribution and photo-electric chemical properties of the Ce-Bi_(2)O_(3)/AgI were analyzed,and the result shows that the optimal ratio of Ce-Bi_(2)O_(3)/AgI photocatalyst achieves a removal rate of 88.63%(180 min)of tetracycline(TC)(20 mg/L)and 100%(120 min)of methyl orange(MO)(20 mg/L).This work clarified the photocatalytic degradation mechanism,providing a promising avenue for developing photocatalytic composites by rare earth metal doping in environme ntal remediation applications.展开更多
A series of TiO2/Bi2O3 heterojunction microfibers have been fabricated using cotton fibers as bio-templates, and characterized by XRD, SEM and UV-Vis techniques. Results reveal that Bi2O3 in the TiO2/Bi2O3 sample is a...A series of TiO2/Bi2O3 heterojunction microfibers have been fabricated using cotton fibers as bio-templates, and characterized by XRD, SEM and UV-Vis techniques. Results reveal that Bi2O3 in the TiO2/Bi2O3 sample is assigned to monoclinic and tetragonal mix-crystal phase. Fibers lengths can reach several micrometers and diameters range from 0.5 μm to 3 μm. Compared with pure TiO2 and Bi2O3, TiO2/Bi2O3 samples display better absorption in visible light region. Photocatalytic activity was evaluated by degradation of MB under visible light irradiation. TiO2/Bi2O3 microfibers exhibite much higher activity than pure TiO2 and Bi2O3, and 22.84%TiO2/Bi2O3 can achieve the decomposition of about 95%MB, which is attributed to synergistic effects of the strong visible-light absorption of TiO2/Bi2O3 microfibers and the heterojunction formed between TiO2 and Bi2O3.展开更多
We developed a novel approach for the preparation of N-doped TiO2 photocatalysts by calcining ammonium titanium oxalate at different temperatures. The structures of N-TiO2 were characterized by powder X-ray diffractio...We developed a novel approach for the preparation of N-doped TiO2 photocatalysts by calcining ammonium titanium oxalate at different temperatures. The structures of N-TiO2 were characterized by powder X-ray diffraction, infrared spectroscopy, thermogravimetric analysis, N2 adsorption-desorption isotherms, X-ray photoelectron spectroscopy, diffuse reflectance UV-Vis spectroscopy, and scanning electron microscope. The N-doped TiO2 photocatalysts calcined below 700 ℃ are the pure anatase phase but that calcined at 700 ℃ is a mixture of anatase and rutile phases. The doped N locates at the interstitial site of TiO2 which leads to the narrowing of bad gap of pure anatase N-TiO2. Among all photocatalysts, N-TiO2 photocatalysts calcined at 600 and 400 ℃ exhibit the best performance in the photodegradation of methyl orange under the UV light and all-wavelength light illuminations, respectively; however, because of the perfect crystallinity and the existence of anatase-rutile phase junctions, N-TiO2 photocatalyst calcined at 700 ℃ exhibits the highest specific photodegradation rate, i.e., the highest quantum yield, under both the UV light and all-wavelength light illuminations.展开更多
In this study,an acid-induced assembly strategy for a rutile TiO2 photocatalyst was proposed on the basis of the treatment of lamellar protonated titanate with a concentrated HNO3 solution.Nitrate groups were successf...In this study,an acid-induced assembly strategy for a rutile TiO2 photocatalyst was proposed on the basis of the treatment of lamellar protonated titanate with a concentrated HNO3 solution.Nitrate groups were successfully grafted onto a TiO2 surface and induced the assembly of rutile TiO2 nanorods into uniform spindle-like nanobundles.The resulting TiO2 product achieved a photocatalytic hydrogen evolution rate of 402.4μmol h^?1,which is 3.1 times higher than that of Degussa P25-TiO2.It was demonstrated that nitrate group grafting caused the rutile TiO2 surface to become negatively charged,which is favorable for trapping positive protons and improving charge carrier separation,thereby enhancing photocatalytic hydrogen production.Additionally,surface charges were crucial to structural stability based on electrostatic repulsion.This study not only developed a facile surface modification strategy for fabricating efficient H2 production photocatalysts but also identified an influence mechanism of inorganic acids different from that reported in the literature.展开更多
基金supported financially by the National Natural Science Foundation of China(Nos.21501140,21403165,51372197)the Outstanding Youth Science Fund of Xi’an University of Science and Technology(No.2019YQ2-06)the Key Innovation Team of Shaanxi Province(No.2014KCT-04)。
文摘TiO2/Bi4 Ti3 O12 hybrids have been widely prepared as promising photocatalysts for decomposing organic contaminations.However,the insufficient visible light absorption and low charge separation efficiency lead to their poor photocatalytic activity.Herein,a robust methodology to construct novel TiO2/Bi4 Ti3 O12/MoS2 core/shell structures as visible light photocatalysts is presented.Homogeneous bismuth oxyiodide(BiOI) nanoplates were immobilized on electrospun TiO2 nanofiber surface by successive ionic layer adsorption and reaction(SILAR) method.TiO2/Bi4 Ti3 O12 core/shell nanofibers were conveniently prepared by partial conversion of TiO2 to high crystallized Bi4 Ti3 O12 shells through a solid-state reaction with BiOI nanoplates,which is accompanied with certain transition of TiO2 from anatase to rutile phase.Afterwards,MoS2 nanosheets with several layers thick were uniform decorated on the TiO2/Bi4 TiO3 O12 fiber surface resulting in TiO2/Bi4 Ti3 O12/MoS2 structures.Significant enhancement of visible light absorption and photo-generated charge separation of TiO2/Bi4 Ti3 O12 were achieved by introduction of MoS2.As a result,the optimized TiO2/Bi4 Ti3 O12/MoS2-2 presents 60% improvement for photodegrading RhB after 120 min irradiation under visible light and 3 times higher of apparent reaction rate constant in compared with the TiO2/Bi4 Ti3 O12.This synthetic method can also be used to establish other photocatalysts simply at low cost,therefore,is suitable for practical applications.
基金supported by the National Natural Science Foundation of China(No.10574122 and No.60376008).
文摘TiO2 nanostructures were fabricated by a reaction of Ti foils in H2O2 solution at mild temperature, Porous TiO2 nanostructurcs, well adhered to Ti foil surfaces, were formed at 80 ℃ in 10 rain, and then flower- like and rod nanostructures formed in succession after a longer reaction time. Samples prepared at 80 ℃ for 4 h arc amorphous, and anatase-dominated crystal phase emerged in the sample prepared for as long as 10 h. Almost pure anatase phase were obtained in TiO2 nanostructures by annealing the samples at a temperature of 300 ℃. Photoeatalysis of the TiO2 nanostructures was characterized by the degradation of RhB dye molecules in an aqueous solution exposed to ultraviolet light. Results show a 7 cm^2 annealed TiO2 flower-like nanostrueture having the degradation rate of RhB as fast as 29.8 times that of the dye solution exposed to ultraviolet light alone.
基金financially supported by the National Natural Science Foundation of China(Nos.61271126,21547012 and 21305033)the Program for Innovative Research Team in University(No.IRT-1237)+2 种基金the Program for Science and Technology Project of Heilongjiang province(Nos.B201414 and B2015008)the Heilongjiang Educational Department(No.2013TD002,2011CJHB006,12531506)the Youth Foundation of Harbin(No.2015QQQXJ047)
文摘Hierarchically porous anatase Ti02 microspheres composited with carbonaceous species （TCS） have been successfully fabricated by a one-step template-free solvothermal method, combined with subsequent low temperature dried process. In this configuration, the TCS microspheres are constructed by the intercon- nected porous nanosheets, which are further assembled with abundant nanoparticles and carbonaceous species. Such composite microspheres possess a large specific surface area of 337 m2 g-l, uniform mesopores of 3.37 nm and high total pore volumes of 0.275 cm3 g-1. The materials exhibit the enhanced photocatalytic properties and stability for degradation of rhodamine B （RhB） under visible-light irradiation. The enhanced photocatalytic degradation performance may be ascribed to their abundant porous structure, large specific surface area and the unique assist-function of the carbonaceous species.
文摘Fe-doped TiO2 was prepared by the sol gel method and characterized by X-ray diffraction. All the Fe-doped TiO2 were composed of an anatase crystal form. The activity of the Fe-doped TiO2 for the degradation of the gesaprim commercial herbicide (which contains atrazine as active compound and formulating agents) was studied by varying the iron content during UV (15 W), visible light and solar irradiations. The visible light came from commercial saving energy lamps (13, 15 and 20 Watts). The gesaprim degradation rate depended on the iron content in the photo catalyst. The Fe-doped TiO2 (0.5% by weight of TiO2) showed higher TOC removal under visible light and was more active than the undoped TiO2 photo catalyst under the light irradiation sources tested. Over 90% of chemical oxygen demand abatement was achieved with both UV and visible light but less time was required to decrease the chemical oxygen demand content by using the catalyst doped with iron at 0.5% under visible light. It was observed that the degradation of gesaprim increased by increasing the iron content in the catalyst under visible light.
基金supported by the FNRS-FRFC,the Walloon Region,and the University of Namur(Conventions No.2.5020.11,GEQ U.G006.15,1610468,RW/GEQ2016 et U.G011.22)funding from the European Union’s Horizon 2020 research and innovation program under the Marie Sklodowska Curie grant agreement n°101034383。
文摘Efficient solar light harvesting is essential for high-performance photocatalysts.Here,Rigorous CoupledWave Analysis(RCWA)computational method is used to investigate and optimize the optical absorption of TiO_(2)-BiVO_(4) inverse opal(IO)structures under varying light incidence angles and pore-filling medium(air or water).Simulations were validated against experimental reflectance data.They revealed that small-pore IOs strongly absorb in the UV-C and UV-B regions due to the slow photon effect,making them ideal for sterilization and water disinfection.Medium-and large-pore IOs benefit from additional slow photon effect at the 2nd order photonic band gap,enhancing absorption across both UV and visible regions.Medium-pore IOs are suited for indoor air treatment and water purification,while large-pore IOs with the highest photon flux enhancement enable solar-driven photocatalysis such as outdoor pollutant removal and hydrogen production.For all tested IO designs,the absorbed photon flux exceeds that of equivalent planar slabs,highlighting the advantage of photonic structuring for sustainable photocatalytic applications.
基金supported by the National Natural Science Foundation of China(NSFC Nos.52271228,52127802,52201279,52301288,52202298,and 22208262)the Natural Science Foundation of Shaanxi Province(No.2023-JC-ZD-21)+1 种基金the Key Research and Development Plan of Shaanxi Province(No.2023GXLH-046)the Science and Technology Project of Xi'an(No.2021SFGX0004)。
文摘Simultaneous integration of rich oxygen vacancies(OVs)and twin crystals in a photocatalyst can not only significantly enhance the near-infrared(NIR)light response but also greatly improve the photocharge separation and transfer efficiency owing to the induced high electrical conductivity and strong built-in electric field.However,thus far,there has been a lack of a model catalyst containing both twin crystals and OVs.Herein,we develop a simple wet chemical strategy for synthesizing of unprecedented NIR light-responsive OVs-rich Cu_(2)O black nanoparticles with high-density of twin crystals(denoted as black twinned Cu_(2)O).As expected,the black twinned Cu_(2)O exhibits higher visible-NIR and NIR light-driven photodegradation of tetracycline(TC)solution than the counterparts.Significantly,the mechanism insight into twin-dependent photocatalysis in NIR light-responsive Cu_(2)O black nanocrystals with rich OVs is uncovered in depth by density functional theory(DFT)calculations and a series of experimental evidence.Expectantly,this work would be beneficial for the scientific researchers currently focusing on the NIR light-responsive photocatalysis and twin engineering of photocatalysts.
基金Funded by the National High Technology Research and Development Program of China(No.2007AA06Z418)the National Natural Science Foundation of China(Nos.20577036,20777058,20977070)+2 种基金the National Natural Science Foundation of Hubei Province,China(No.2015CFA137)the Open Fund of Hubei Biomass-Resource Chemistry and Environmental Biotechnology Key Laboratory(Wuhan University)the Fund of Eco-environment Technology R&D and Service Center(Wuhan University)
文摘As efficient water treatment agents, a novel series of rectorite-based ZnO and TiO2 hybrid composites（REC/ZnO/TiO2） were synthesized and characterized in this study. Effects of experimental parameters including TiO2 mass ratio, solution p H and catalyst dosage on the removal of methyl blue（MB） were also conducted. The presence of a little mass ratio（2%-6%） of TiO2 highly promoted the photoactivity of REC/ZnO/TiO2 in removal of MB dye from aqueous solution, in which ZnO and REC played a role of photocatalyst and adsorbent. The promotion effects of TiO2 may result from the accelerated separation of electron-hole on ZnO. The observed kinetic constant for the degradation of MB over REC/ZnO and REC/ZnO/TiO2 were 0.015 and 0.038 min^（-1）, respectively. The degradation kinetics of MB dye, which followed the Langmuir–Hinshelwood model, had a reaction constant of 0.17 mg/（L min）. The decrease of removal ratio of MB after five repetitive experiments was small, indicating REC/ZnO/TiO2 has great potential as an effective and stable catalyst.
基金Acknowledgements： This project is supported by the fund of the Plan of Postgraduate Scientific Research Innovation of Jiangsu Province （No. CX07B_175z） and the Natural Science Foundation of Henan Province （No. 0624720029）.
文摘Photocatalyst CoPcS/TiO2 was prepared by sol-gel method. Composite CoPcS/TiO2/K2Ti4O9 was prepared by dipping. It was incandesced at various temperatures and modification effect was compared. The results showed that optical absorption of sample incandesce at 423K occurred significant red-shift. Light absorption width extended from ultraviolet region to visible region, especially there was an intensive absorption between 600 nm and 680 nm. X-ray diffraction spectrogram showed that TiO2 in sample still maintained anatase crystal form. Under the illumination of visible light, photocatalysis degradation experiment was taken with Eosin B as simulated pollutants. Decoloration rate of Eosin B was much improved. The rate can reach 80% in 300 minutes.
基金supported by Liaoning Revitalization Talents Program(No.XLYC1907173)the Science and Technology General Project of Liaoning Provincial Education Department(No.LJKMZ20221835)the National Natural Science Foundation of China(Nos.22006073 and 22205027).
文摘The mass production and widespread use of Pharmaceuticals and Personal Care Products(PPCPs)have posed a serious threat to the water environment and public health.In this work,a green metal-based Metal Organic Framework(MOF)Bi-NH_(2)-BDC was prepared and characterized,and the adsorption characteristics of Bi-NH_(2)-BDCwere investigated with typical PPCPs-diclofenac sodium(DCF).It was found that DCF mainly covered the adsorbent surface as a single molecular layer,the adsorption reaction was a spontaneous,entropyincreasing exothermic process and the adsorption mechanisms between Bi-NH_(2)-BDC and DCF were hydrogen bonding,π-πinteractions and electrostatic interactions.In addition,Bi-NH_(2)-BDC also had considerable photocatalytic properties,and its application in adsor-bent desorption treatment effectively solved the problem of secondary pollution,achieving a green and sustainable adsorption desorption cycle.
文摘The production of renewable methanol(CH_(3)OH)via the photocatalytic hydrogenation of CO_(2) is an ideal method to ameliorate energy shortages and mitigate CO_(2) emissions:however,the highly selective synthesis of methanol at atmospheric pressure remains challenging owing to the competing reverse water-gas shift(RWGS)reaction.Herein,we present a novel approach for the synthesis of CH_(3)OH via photocatalytic CO_(2) hydrogenation using a catalyst featuring highly dispersed Au nanoparticles loaded on oxygen vacancy(OV)-rich molybdenum dioxide(MoO_(2)),resulting in a remarkable selectivity of 43.78%.The active sites in the Au/MoO_(2) catalyst are high-density Au-oxygen vacancies,which synergistically promote the tandem methanol synthesis via an initial RWGS reaction and subsequent CO hydrogenation.This work provides comprehensive insights into the design of metal-vacancy synergistic sites for the highly selective photocatalytic hydrogenation of CO_(2) to CH_(3)OH.
基金supported by the National Natural Science Foundation of China(No.22271090)。
文摘Herein,a simple and effective outer-surface interactions assisted supramolecular hierarchical assembly has been first exploited to uniformly distribute tungstosilicic acid(TSA)inside the porous structure of cucurbit[10]uril-based single-layer 2D supramolecular-organic-frameworks(Q[10]-SOFs)in water.Importantly,the 2D Q[10]-SOFs can further serve as light harvesting antenna,achieving fast energy transfer to the embedded redox-active TSA upon photoexcitation,resulting in efficient visible light-driven selective oxidation of benzyl alcohols into the corresponding aldehydes in high yield at room temperature.Further studies revealed that the integrated of 2D Q[10]-SOFs and TSA played a key role in the catalytic process,due to the presence of a novel stepwise electron transfer route in the single-layer hybrid 2D structures.
基金financially supported by Guangdong Basic and Applied Basic Research Foundation(No.2024A1515010976)Shenzhen Peacock Plan(No.20210802524B)+3 种基金the Postdoctoral Research Foundation of China(Nos.GZC20241085,GZC20230562,GZC20230564)China Postdoctoral Science Foundation(No.2024M760583)the National Natural Science Foundation of China(No.52402234)Shenzhen Key Laboratory of 2D Metamaterials for Information Technology
文摘This article systematically reviewed the applications of single-atom catalysts(SACs)in the domain of photocatalytic reactions,with a particular emphasis on the indispensable role of H_(2)O in these processes.SACs,due to their distinct active sites and superior catalytic efficacy,found their applications in the fields of energy conversion and environmental protection.The review elaborated on the potential carriers,preparation methods,and characterization techniques for single-atom photocatalysts.Subsequently,the article provided an in-depth explanation of the crucial role of H_(2)O in photocatalytic reactions,serving as an important green solvent and an oxygen/proton source.The adsorption of water could also change the surface energy structure and charge distribution of the photocatalyst.Conversely,the presence of H_(2)O might also inhibit the target reaction.Additionally,the distinct roles of water in both liquid and gas phases were discussed.Furthermore,the review systematically summarized the applications of single-atom photocatalysts in H_(2)generation,CO_(2)reduction,N2fixation,H_(2)O_(2)production,and environmentalremediation.It delved into the mechanisms by which water molecules participated in photocatalytic processes and their interactions with competing pathways,thereby revealing the complexity and critical importance of water in photocatalytic reactions.Finally,the article discusses the opportunities and challenges of SACs in photocatalytic reactions with H_(2)O.This article provides a comprehensive perspective for understanding the role of SACs in waterinvolved photocatalytic reactions.
基金financially supported by the National Natural Science Foundation of China (No.52071146)Guangdong Provincial Natural Science Foundation (No.2023A1515010989)the Science and Technology Projects in Guangzhou (No.202201000008)。
文摘Water purification systems based on transition metal dichalcogenides face significant challenges,including lack of reactivity under dark conditions,scarcity of catalytically active sites,and rapid recombination of photogenerated charge carriers.Simultaneously increasing the number of active sites and improving charge separation efficiency has proven difficult.In this study,we present a novel approach combining molybdenum(Mo) monoatomic doping and size engineering to produce a series of Mo-ReS_(2) quantum dots(MR QDs) with controllable dimensions.High-resolution structural characterization,first-principle calculations,and piezo force microscopy reveal that Mo monoatomic doping enhances the lattice asymmetry,thereby improving the piezoelectric properties.The resulting piezoelectric polarization and the generated built-in electric field significantly improve charge separation efficiency,leading to optimized photocatalytic performance.Additionally,the doping strategy increases the number of active sites and improves the adsorption of intermediate radicals,substantially boosting photo-sterilization efficiency.Our results demonstrate the elimination of 99.95% of Escherichia coli and 100.00% of Staphylococcus aureus within 30 min.Furthermore,we developed a self-purification system simulating water drainage,utilizing low-frequency water streams to trigger the piezoelectric behavior of MR QDs,achieving piezoelectric synergistic photodegradation.This innovative approach provides a more environmentally friendly and economical method for water self-purification,paving the way for advanced water treatment technologies.
基金financially supported by the National Natural Science Foundation of China(No.51302061)Natural Science Foundation of Hebei Province(No.E2020201021 and E2023201019)+4 种基金Industry-University-Research Cooperation Major Projects of Shijiazhuang(No.241130477A)Research Innovation Team of College of Chemistry and Environmental Science of Hebei University(No.hxkytd2102)Industry-University-research Cooperation Project of Colleges and Universities in Hebei Province(No.CXZX2025016)Hebei Province Innovation Capability Enhancement Plan Project(No.22567620H)Bintuan Science and Technology Program(Nos.2020DB002 and 2022DB009)。
文摘Peroxymonosulfate(PMS)is commonly used in advanced oxidation processes to degrade organic pollutants in wastewater.In this work,to obtain better PMS activation efficiency,Bi_(4)O_(5)Br_(2)/BCZT(BBT)piezoelectric photocatalyst was designed.Abundant active radicals produced by BBT under visible light irradiation and ultrasonic vibration were used to activate PMS,thereby achieving rapid degradation of high concentration pollutants.With the introduction of BCZT,the catalyst has a strong internal electric field and three-dimensional lamellar structure,which promotes the separation and transfer of electrons and holes.It is worth noting that under optimal reaction conditions,the degradation rate of ARB reached 93%by BBT15 within 10 min.The catalytic experiment combined with the piezoelectric performance test results revealed the key role of piezoelectric photocatalytic reaction in PMS activation.This provides an important prospect for PMS to effectively deal with the degradation of high concentrations of organic pollutants.
基金supported by the National Natural Science Foundation of China (Nos.51472186,51902232,51402221)the China Scholarship Council Fund (No.201708420210)。
文摘The rational design and construction of heterojunction structure is an effective strategy to improve the photocatalytic performance.Herein,a series of BiOBr nanosheets-immobilized TiO2/Ti3C2Tx MXene hybrid materials with heterojunction structure were synthesized by a facial one-step hydrothermal method.The ternary composites show outstanding performance as photocatalysts for the degradation of rhodamine B due to the optimized synergetic effects of BiOBr,TiO2 and Ti3C2Tx.The improved photocatalytic performance is remarkably attributed to the construction of a heterojunction between TiO2 and BiOBr due to their well-matching of energy band position,which can enhance the absorption for visible light and promote the transfer of photo-generated charge carriers.Moreover,Ti3C2Tx acts as an electron trap to further accelerate the separation of photo-generated electrons and holes.
基金financially supported by the National Natural Science Foundation of China(Nos.22350410391 and 22001094)the Research Initiation Fund Project from Zhejiang Sci-Tech University(No.23212072-Y).
文摘Photocatalysis,harnessing abundant solar energy,presents a sustainable strategy to address the dual chal-lenges of fossil fuel depletion and environmental degradation.Among the emerging materials for photo-catalytic applications,reticular framework materials,including metal-organic frameworks(MOFs),cova-lent organic frameworks(COFs),and hydrogen-bonded organic frameworks(HOFs),have attracted signif-icant attention due to their high surface area,tunable architectures,and versatile chemical compositions.These properties enable efficient light harvesting and charge separation,making them promising candi-dates for various photocatalytic processes.This review systematically explores recent advancements in the synthesis and structural properties of MOFs,COFs,and HOFs,elucidating the complex mechanisms governing solar-driven photocatalysis and comparing their performance with a particular focus on their applications in CO_(2)reduction,H_(2)generation,H_(2)O_(2)production,N_(2)fixation,and pollutant degradation.Key strategies for enhancing photocatalytic performance,including structural modifications,bandgap en-gineering,defect engineering,hybridization,and heterojunction formation,are critically analyzed.A com-parative evaluation of reticular framework materials against traditional semiconductors is provided,con-sidering factors such as efficiency,cost,and long-term stability.Furthermore,this review highlights the challenges related to stability and scalability,along with key achievements and barriers to practical im-plementation.This work offers possible insights to overcome existing limitations and improve efficiency.Ultimately,this comprehensive assessment highlights the pivotal role of reticular frameworks in advanc-ing sustainable energy solutions and provides a roadmap for future research and innovation in this rapidly evolving field.
基金Project supported by the National Natural Science Foundation of China(22106074)Tianjin Science and Technology Program(23YDTPJC00540,22YJDSS00060)。
文摘Ce-β-Bi_(2)O_(3)/AgI was prepared using solvothermal calcination and in-situ deposition methods.The introduction of Ce can inhibit the conversion of Bi_(2)O_(3)fromβtoαphase at high temperatures,promoting the formation of oxygen vacancies(OVs)in the photocatalyst.OVs can adsorb more dissolved oxygen to promote the formation rate of·O^(-)_(2).Moreover,the interaction between Ce-Bi_(2)O_(3)and AgI results in the formation of Z-scheme heterojunctions,which can broaden the light absorption region,facilitate photogenerated carrier separation and transfer and enhance the ability to produce more active oxygen species(ROS).The morphology,crystal,element distribution and photo-electric chemical properties of the Ce-Bi_(2)O_(3)/AgI were analyzed,and the result shows that the optimal ratio of Ce-Bi_(2)O_(3)/AgI photocatalyst achieves a removal rate of 88.63%(180 min)of tetracycline(TC)(20 mg/L)and 100%(120 min)of methyl orange(MO)(20 mg/L).This work clarified the photocatalytic degradation mechanism,providing a promising avenue for developing photocatalytic composites by rare earth metal doping in environme ntal remediation applications.
基金V. ACKNOWLEDGEMENTS This work was supported by the Scientific Research Program Funded by Shaanxi Provincial Education Department （No.2013JK0690）, and the Shaanxi Province Natural Science Foundation （No.2013JM2013）, the National Natural Science Foundation of China （No.21203160）, and the Special Research Fund of Xianyang Normal University （No. 11XSYK204）.
文摘A series of TiO2/Bi2O3 heterojunction microfibers have been fabricated using cotton fibers as bio-templates, and characterized by XRD, SEM and UV-Vis techniques. Results reveal that Bi2O3 in the TiO2/Bi2O3 sample is assigned to monoclinic and tetragonal mix-crystal phase. Fibers lengths can reach several micrometers and diameters range from 0.5 μm to 3 μm. Compared with pure TiO2 and Bi2O3, TiO2/Bi2O3 samples display better absorption in visible light region. Photocatalytic activity was evaluated by degradation of MB under visible light irradiation. TiO2/Bi2O3 microfibers exhibite much higher activity than pure TiO2 and Bi2O3, and 22.84%TiO2/Bi2O3 can achieve the decomposition of about 95%MB, which is attributed to synergistic effects of the strong visible-light absorption of TiO2/Bi2O3 microfibers and the heterojunction formed between TiO2 and Bi2O3.
基金ACKNOWLEDGMENTS This work was supported by the National Natural Science Foundation of China （No.20773113）, the Solar Energy Project of Chinese Academy of Sciences, the Ministry of Education program for PCSIRT （No.IRT0756）, and the Max Planck Gesellschaft of Chinese Academy of Sciences partner group.
文摘We developed a novel approach for the preparation of N-doped TiO2 photocatalysts by calcining ammonium titanium oxalate at different temperatures. The structures of N-TiO2 were characterized by powder X-ray diffraction, infrared spectroscopy, thermogravimetric analysis, N2 adsorption-desorption isotherms, X-ray photoelectron spectroscopy, diffuse reflectance UV-Vis spectroscopy, and scanning electron microscope. The N-doped TiO2 photocatalysts calcined below 700 ℃ are the pure anatase phase but that calcined at 700 ℃ is a mixture of anatase and rutile phases. The doped N locates at the interstitial site of TiO2 which leads to the narrowing of bad gap of pure anatase N-TiO2. Among all photocatalysts, N-TiO2 photocatalysts calcined at 600 and 400 ℃ exhibit the best performance in the photodegradation of methyl orange under the UV light and all-wavelength light illuminations, respectively; however, because of the perfect crystallinity and the existence of anatase-rutile phase junctions, N-TiO2 photocatalyst calcined at 700 ℃ exhibits the highest specific photodegradation rate, i.e., the highest quantum yield, under both the UV light and all-wavelength light illuminations.
基金supported by the National Natural Science Foundation of China (21771070, 21571071)the Fundamental Research Funds for the Central Universities (2018KFYYXJJ120, 2019KFYRCPY104)~~
文摘In this study,an acid-induced assembly strategy for a rutile TiO2 photocatalyst was proposed on the basis of the treatment of lamellar protonated titanate with a concentrated HNO3 solution.Nitrate groups were successfully grafted onto a TiO2 surface and induced the assembly of rutile TiO2 nanorods into uniform spindle-like nanobundles.The resulting TiO2 product achieved a photocatalytic hydrogen evolution rate of 402.4μmol h^?1,which is 3.1 times higher than that of Degussa P25-TiO2.It was demonstrated that nitrate group grafting caused the rutile TiO2 surface to become negatively charged,which is favorable for trapping positive protons and improving charge carrier separation,thereby enhancing photocatalytic hydrogen production.Additionally,surface charges were crucial to structural stability based on electrostatic repulsion.This study not only developed a facile surface modification strategy for fabricating efficient H2 production photocatalysts but also identified an influence mechanism of inorganic acids different from that reported in the literature.
