In this work,a covalent organic framework(COF),which is constructed by the building blocks of[5,10,15,20-tetrakis(4-aminophenyl)porphinato]copper(Ⅱ)(CuTAPP)and p-benzaldehyde,is employed to integrate with TiO_(2) for...In this work,a covalent organic framework(COF),which is constructed by the building blocks of[5,10,15,20-tetrakis(4-aminophenyl)porphinato]copper(Ⅱ)(CuTAPP)and p-benzaldehyde,is employed to integrate with TiO_(2) for the purpose of establishing a Z-scheme hybrid.Within the system,isonicotinic acid performs the role of a bridge that connects the two components through a coordination bond.Further photocatalytic application reveals the hybrid framework is able to catalyze CO_(2) conversion under simulated solar light,resulting in CO production rate of 50.5 μmol g^(-1)·h^(-1),about 9.9 and 24.5 times that of COF and pristine TiO_(2),respectively.The ameliorated catalytic performance owes much to the por-phyrin block acting as photosensitizer that augments the light absorbance,and the establishment of Z-scheme system between the inorganic and orga nic comp on ents that enhances the separati on of the carriers.In addition,the chemical bridge also ensures a steady usage and stable charge delivery in the catalysis.Our study sheds light on the development of versatile approaches to covalently in corporate COFs with inorga nic semic on ductors.展开更多
Water splitting by photoelectrochemical(PEC)processes to convert solar energy into hydrogen energy using semiconductors is regarded as one of the most ideal methods to solve the current energy crisis and has attracted...Water splitting by photoelectrochemical(PEC)processes to convert solar energy into hydrogen energy using semiconductors is regarded as one of the most ideal methods to solve the current energy crisis and has attracted widespread attention.Herein,Co-based metal-organic framework(Co(bpdc)(H_(2)O)_(4)(CoMOF)nanosheets as passivation layers were in-situ constructed on the surface of Bi VO_(4)films through an uncomplicated hydrothermal method(Co-MOF/Bi VO_(4)).Under AM 1.5G illumination,synthesized CoMOF/BiVO_(4)electrode exhibited a 4-fold higher photocurrent than bare Bi VO_(4),measuring 6.0 m A/cm^(2)at 1.23 V vs.RHE in 1 mol/L potassium borate electrolyte(pH 9.5)solution.Moreover,the Co-MOF/BiVO_(4)film demonstrated a 96%charge separation efficiency,a result caused by an inhibited recombination rate of photogenerated electrons and holes by the addition of Co-MOF nanosheets.This work provides an idea for depositing inexpensive 2D Co-MOF nanosheets on the photoanode as an excellent passivation layer for solar fuel production.展开更多
As one of the highly effective methods to prepare catalysts for photocatalytic reduction of CO2 into valueadded chemicals,using metalloporphyrin as light-harvesting mixed ligand to modify metal-organic framework(MOF)i...As one of the highly effective methods to prepare catalysts for photocatalytic reduction of CO2 into valueadded chemicals,using metalloporphyrin as light-harvesting mixed ligand to modify metal-organic framework(MOF)is very valuable since it can greatly improve the prophyrin dispersibility and consequently inhibit its potential agglomeration.Herein,we employed a one-pot synthetic strategy to chemically immobilize Cu(II)tetra(4-carboxylphenyl)porphyrin(CuTCPP)into UiO-66 MOF structure through coordination mode.Meanwhile,in-situ growth of TiO2 nanoparticles onto the MOF is actualized with the generation of CuTCPP c UiO-66/TiO2(CTU/TiO2)composites.Under Xe lamp irradiation(λ>300 nm),the catalytic result presents that an optimal value of 31.32 μmol g^-1 h^-1 CO evolution amount,about 7 times higher than that of pure TiO2 was obtained through the photocatalysis.It is supposed owning to a consistent augment of light absorption derived from chemically implanted porphyrin derivative,which is simultaneously functioning with an efficacious separation of photo-induced carries given by the newly engendered composites between MOF and TiO2,an effective catalytic activity and approving recyclability of CTU/TiO2 can be achieved in the photocatalytic reduction of CO2 into CO.展开更多
In this study,a graphitic carbon nitride(g-C_(3)N_(4))based ternary catalyst Cu O/Cu Fe_(2)O_(4)/gC_(3)N_(4)(CCCN)is successfully prepared thorough calcination method.After confirming the structure and composition of ...In this study,a graphitic carbon nitride(g-C_(3)N_(4))based ternary catalyst Cu O/Cu Fe_(2)O_(4)/gC_(3)N_(4)(CCCN)is successfully prepared thorough calcination method.After confirming the structure and composition of CCCN,the as-synthesized composites are utilized to activate persulfate(PS)for the degradation of organic contaminant.While using tetracycline hydrochloride(TC)as pollutant surrogate,the effects of initial p H,PS and catalyst concentration on the degradation rate are systematically studied.Under the optimized reaction condition,CCCN/PS is able to give 99%degradation extent and 74%chemical oxygen demand removal in assistance of simulated solar light,both of which are apparently greater than that of either Cu O/Cu Fe_(2)O_(4)and pristine g-C_(3)N_(4).The great improvement in degradation can be assignable to the effective separation of photoinduced carriers thanks to the integration between Cu O/Cu Fe_(2)O_(4)and g-C_(3)N_(4),as well as the increased reaction sites given by the g-C_(3)N_(4)substrate.Moreover,the scavenging trials imply that the major oxidative matters involved in the decomposition are hydroxyl radicals(·OH),superoxide radicals(·O_(2)^(-))and photo-induced holes(h^(+)).展开更多
The composite catalytic materials based on the mineral kaolinite are considered to be a potential approach for solving global energy scarcity and environmental pollution,which have excellent catalytic performance,low ...The composite catalytic materials based on the mineral kaolinite are considered to be a potential approach for solving global energy scarcity and environmental pollution,which have excellent catalytic performance,low cost and excellent chemical stability.However,pure kaolinite does not have visible light absorption ability and cannot be used as a potential photocatalytic material.Fortunately,the unique physical and chemical properties of kaolinite can be acted as a good semiconductor carrier.Herein,this paper firstly presents the mineralogical characteristics of kaolinite.Next,kaolinite-based photocatalysts(such as TiO_(2)/kaolinite,g-C_(3)N_(4)/kaolinite,g-C_(3)N_(4)/TiO_(2)/kaolinite,Zn O)are discussed in detail from the formation of heterostructures,synthesis-modification methods,photocatalytic mechanisms,and electron transfer pathways.Furthermore,the specific role of kaolinite in photocatalytic materials is summarized and discussed.In addition,the photocatalytic applications of kaolinite-based photocatalysts in the fields of water decomposition,pollutant degradation,bacterial disinfection are reviewed.However,the modification of kaolinite is hard,the manufacture of a large number of kaolinite-based photocatalysts is difficult,the cost of doping noble metals is expensive,and the utilization rate of visible light is low,which limits its application in industrial practice.Finally,this paper presents some perspectives on the future development of kaolinite-based photocatalysts.展开更多
Photoelectrochemical(PEC)water splitting is an effective strategy to convert solar energy into clean and renewable hydrogen energy.In order to carry out effective PEC conversion,researchers have conducted a lot of exp...Photoelectrochemical(PEC)water splitting is an effective strategy to convert solar energy into clean and renewable hydrogen energy.In order to carry out effective PEC conversion,researchers have conducted a lot of exploration and developed a variety of semiconductors suitable for PEC water splitting.Among them,metal oxides stand out due to their higher stability.Compared with traditional oxide semiconductors,ferrite-based photoelectrodes have the advantages of low cost,small band gap,and good stability.Interestingly,due to the unique characteristics of ferrite,most of them have various tunable features,which will be more conducive to the development of efficient PEC electrode.However,this complex metal oxide is also troubled by severe charge recombination and low carrier transport efficiency,resulting in lower conversion efficiency compared to theoretical value.Based on this,this article reviews the structure,preparation methods,characteristics and modification strategies of various common ferrites.In addition,we analyzed the future research direction of ferrite for PEC water splitting,and looked forward to the development of more efficient catalysts.展开更多
Photoelectrochemical(PEC)technology is considered to be a promising approach for solar-driven hydrogen production with zero emissions.Bismuth vanadate(BiVO_(4))is a kind of photocatalytic material with strong photoact...Photoelectrochemical(PEC)technology is considered to be a promising approach for solar-driven hydrogen production with zero emissions.Bismuth vanadate(BiVO_(4))is a kind of photocatalytic material with strong photoactivity in the visible light region and appropriate band gap for PEC water splitting.However,the solar-to-hydrogen efficiency(STH)of BiVO_(4)is far away from the 10%target needed for practical application due to its poor charge separation ability.Therefore,this review attempts to summarize the strategies for improving the photocurrent density and especially hydrogen production of BiVO_(4)materials through PEC techniques in the last three years,such as doping nonmetal and metal elements,depositing noble metals,constructing heterojunctions,coupling with carbon and metalorganic framework(MOF)materials to further enhance the PEC performance of BiVO_(4)photoanode.This review aims to serve as a general guideline to fabricate highly efficient BiVO_(4)-based materials for PEC water splitting.展开更多
A kind of CdS/Cd-BiOCl immobilized films photocatalyst was prepared.The optical and physicochemical properties of the CdS/Cd-BiOCl photocatalysts were analysed,and the detailed characterization revealed CdS/Cd-BiOCl f...A kind of CdS/Cd-BiOCl immobilized films photocatalyst was prepared.The optical and physicochemical properties of the CdS/Cd-BiOCl photocatalysts were analysed,and the detailed characterization revealed CdS/Cd-BiOCl films photocatalyst with good charge carrier separation effect.The reusabilities and photocatalytic properties of the samples were studied.The 15%Cd S/Cd-Bi OCl photocatalyst exhibited superior performance in photocatalytic degradation of tetracycline(TC)and favorable stability under visible light irradiation.As for the photodegradation rate of TC,15%CdS/Cd-BiOCl exhibited an excellent photodegradation activity,which is 4.06 and 9.53 times higher than that of Cd S/Cd and Bi OCl,respectively.The results showed that dominant active species are·O_(2)^(-)and·OH radicals during photodegradation.The charge transfer in Z-scheme CdS/Cd-BiOCl films photocatalyst could synchronously generate conduct band(CB)electrons in BiOCl and valence band(VB)holes in CdS,and metal Cd served as electron mediator.This work can be a reference for the design of film photocatalysts and new insight for photodegradating towards contaminants.展开更多
The construction of rich phase interfaces to increase active reaction area in hybrid materials is an excellent strategy to improve electrochemical performance.Under this guideline,MIL-101@OX-metal organic framework(MO...The construction of rich phase interfaces to increase active reaction area in hybrid materials is an excellent strategy to improve electrochemical performance.Under this guideline,MIL-101@OX-metal organic framework(MOF)is constructed by the"MOF on MOF"method,then converts to MIL-101@NiFe-layered double hydroxides(LDH)by in situ transformation in alkaline solution.MIL-101@NiFe-LDH shows excellent electrochemical water oxidation performance.It needs only an overpotential of 215 m V to drive10 m A/cm^(2)of oxygen evolution reaction(OER),which is less than that of NiFe-LDH,MIL-101.In addition,MIL-101@NiFe-LDH has the smallest Tafel slope(55.1 mV/dec)compared with Ni Fe-LDH(61.1 m V/dec),MIL-101(150.8 m V/dec).The excellent water oxidation activity is due to the high phase interfaces derived from high specific surface area of MOF.This work offers an alternative method for making MOF/LDH heterostructures with an optimized phase interfaces and provides new insights for OER.展开更多
Due to the involvement of four-electron transfer process at photoanode,water oxidation is the ratelimiting step in water splitting reaction.To settle this dilemma,ZnCo_(2)O_(4)nanoparticles are combined with BiVO_(4)t...Due to the involvement of four-electron transfer process at photoanode,water oxidation is the ratelimiting step in water splitting reaction.To settle this dilemma,ZnCo_(2)O_(4)nanoparticles are combined with BiVO_(4)to form a p-n ZnCo_(2)O_(4)/BiVO;heterojunction photoanode,which is proved by an input voltage-output current test.The built-in electric field formed within the heterojunction structure promotes the effective separation of electrons and holes.ZnCo_(2)O_(4)is also an effective water oxidation cocatalyst,since it could cause the holes entering the electrode/electrolyte interface rapidly for the subsequent water oxidation reaction.The photocurrent density of ZnCo_(2)O_(4)/BiVO_(4)composite photoanode reaches 3.0 mA/cm^(2) at 1.23 V vs.RHE in 0.5 mol/L sodium sulfate under AM 1.5 G simulated sunlight,about 2.1 times greater than that of BiVO_(4)(1.4 mA/cm^(2)).These results suggest the potential of ZnCo_(2)O_(4)nanoparticles for improving photoelectrochemical water splitting anode materials.展开更多
The serious surface charge recombination and fatigued photogenerated carriers transfer of the BiVO_(4)photoanode restrict its photoelectrochemical(PEC)water splitting performance.In this work,nickel fluoride(NiF_(2))i...The serious surface charge recombination and fatigued photogenerated carriers transfer of the BiVO_(4)photoanode restrict its photoelectrochemical(PEC)water splitting performance.In this work,nickel fluoride(NiF_(2))is applied to revamp pure BiVO_(4)photoanode by using a facile electrodeposition method.As a result,the asprepared NiF_(2)/BiVO_(4)photoanode increases the dramatic photocurrent density by approximately 180%compared with the pristine BiVO_(4)photoanode.Furthermore,the correlative photon-to-current conversion efficiency,the charge injection,and the separation efficiency,as well as the hydrogen generation of the composite photoanode have been memorably enhanced due to the synergy of NiF_(2)and BiVO_(4).This study may furnish a dependable guidance in fabricating the fluoride-based compound/semiconductor composite photoanode system.展开更多
基金supported by the National Natural Science Foundation of China(21663027,51262028,21261021)the Science and Technology Support Project of Gansu Province(1504GKCA027)+2 种基金the Program for the Young Innovative Talents of Longyuanthe Program for Innovative Research Team(NWNULKQN-15-2)the Undergraduate Academic Innovative Research Team of Northwest Normal University~~
基金financially supported by the National Natural Science Foundation of China (21663027 and 21808189)the Key Science and Technology Foundation of Gansu Province (20YF3GA021)+2 种基金the Innovation funding program of Universities of Gansu province (2020B-091)the Opening Project of Key Laboratory of Green Chemistry of Sichuan Institutes of Higher Education (LYJ18205)the Promotion Project of Young-Teacher Researchcapacity of Northwest Normal University (NWNU-LKQN-18-5).
文摘In this work,a covalent organic framework(COF),which is constructed by the building blocks of[5,10,15,20-tetrakis(4-aminophenyl)porphinato]copper(Ⅱ)(CuTAPP)and p-benzaldehyde,is employed to integrate with TiO_(2) for the purpose of establishing a Z-scheme hybrid.Within the system,isonicotinic acid performs the role of a bridge that connects the two components through a coordination bond.Further photocatalytic application reveals the hybrid framework is able to catalyze CO_(2) conversion under simulated solar light,resulting in CO production rate of 50.5 μmol g^(-1)·h^(-1),about 9.9 and 24.5 times that of COF and pristine TiO_(2),respectively.The ameliorated catalytic performance owes much to the por-phyrin block acting as photosensitizer that augments the light absorbance,and the establishment of Z-scheme system between the inorganic and orga nic comp on ents that enhances the separati on of the carriers.In addition,the chemical bridge also ensures a steady usage and stable charge delivery in the catalysis.Our study sheds light on the development of versatile approaches to covalently in corporate COFs with inorga nic semic on ductors.
基金financially supported by the National Natural Science Foundation of China(No.52173277)the Innovative Research Team for Science and Technology of Shaanxi Province(No.2022TD-04)+1 种基金the Fundamental Research Funds for the Central Universities of Chang’an University(Nos.300102299304,300102291403)the Natural Science Basic Research Fund of Shaanxi Province(No.2020JZ-20)。
文摘Water splitting by photoelectrochemical(PEC)processes to convert solar energy into hydrogen energy using semiconductors is regarded as one of the most ideal methods to solve the current energy crisis and has attracted widespread attention.Herein,Co-based metal-organic framework(Co(bpdc)(H_(2)O)_(4)(CoMOF)nanosheets as passivation layers were in-situ constructed on the surface of Bi VO_(4)films through an uncomplicated hydrothermal method(Co-MOF/Bi VO_(4)).Under AM 1.5G illumination,synthesized CoMOF/BiVO_(4)electrode exhibited a 4-fold higher photocurrent than bare Bi VO_(4),measuring 6.0 m A/cm^(2)at 1.23 V vs.RHE in 1 mol/L potassium borate electrolyte(pH 9.5)solution.Moreover,the Co-MOF/BiVO_(4)film demonstrated a 96%charge separation efficiency,a result caused by an inhibited recombination rate of photogenerated electrons and holes by the addition of Co-MOF nanosheets.This work provides an idea for depositing inexpensive 2D Co-MOF nanosheets on the photoanode as an excellent passivation layer for solar fuel production.
基金financially supported by the National Natural Science Foundation of China (21663027, 21808189)the Science and Technology Support Project of Gansu Province (1504GKCA027)
文摘As one of the highly effective methods to prepare catalysts for photocatalytic reduction of CO2 into valueadded chemicals,using metalloporphyrin as light-harvesting mixed ligand to modify metal-organic framework(MOF)is very valuable since it can greatly improve the prophyrin dispersibility and consequently inhibit its potential agglomeration.Herein,we employed a one-pot synthetic strategy to chemically immobilize Cu(II)tetra(4-carboxylphenyl)porphyrin(CuTCPP)into UiO-66 MOF structure through coordination mode.Meanwhile,in-situ growth of TiO2 nanoparticles onto the MOF is actualized with the generation of CuTCPP c UiO-66/TiO2(CTU/TiO2)composites.Under Xe lamp irradiation(λ>300 nm),the catalytic result presents that an optimal value of 31.32 μmol g^-1 h^-1 CO evolution amount,about 7 times higher than that of pure TiO2 was obtained through the photocatalysis.It is supposed owning to a consistent augment of light absorption derived from chemically implanted porphyrin derivative,which is simultaneously functioning with an efficacious separation of photo-induced carries given by the newly engendered composites between MOF and TiO2,an effective catalytic activity and approving recyclability of CTU/TiO2 can be achieved in the photocatalytic reduction of CO2 into CO.
基金financially supported by the National Natural Science Foundation of China(Nos.21663027 and 21808189)the Key Science and Technology Foundation of Gansu Province(No.20YF3GA021)+2 种基金the Innovation funding program of Universities of Gansu province(No.2020B-091)the Opening Project of Key Laboratory of Green Chemistry of Sichuan Institutes of Higher Education(No.LYJ18205)the Promotion Project of Young-Teacher Research-capacity of Northwest Normal University(No.NWNU-LKQN-18-5)。
文摘In this study,a graphitic carbon nitride(g-C_(3)N_(4))based ternary catalyst Cu O/Cu Fe_(2)O_(4)/gC_(3)N_(4)(CCCN)is successfully prepared thorough calcination method.After confirming the structure and composition of CCCN,the as-synthesized composites are utilized to activate persulfate(PS)for the degradation of organic contaminant.While using tetracycline hydrochloride(TC)as pollutant surrogate,the effects of initial p H,PS and catalyst concentration on the degradation rate are systematically studied.Under the optimized reaction condition,CCCN/PS is able to give 99%degradation extent and 74%chemical oxygen demand removal in assistance of simulated solar light,both of which are apparently greater than that of either Cu O/Cu Fe_(2)O_(4)and pristine g-C_(3)N_(4).The great improvement in degradation can be assignable to the effective separation of photoinduced carriers thanks to the integration between Cu O/Cu Fe_(2)O_(4)and g-C_(3)N_(4),as well as the increased reaction sites given by the g-C_(3)N_(4)substrate.Moreover,the scavenging trials imply that the major oxidative matters involved in the decomposition are hydroxyl radicals(·OH),superoxide radicals(·O_(2)^(-))and photo-induced holes(h^(+)).
基金the financial support provided by the Science and Technology Major Projects of Shanxi Province of China(No.20181101003)Special Funds for Basic Scientific Research of Central Colleges(No.300102299306,300102299304)。
文摘The composite catalytic materials based on the mineral kaolinite are considered to be a potential approach for solving global energy scarcity and environmental pollution,which have excellent catalytic performance,low cost and excellent chemical stability.However,pure kaolinite does not have visible light absorption ability and cannot be used as a potential photocatalytic material.Fortunately,the unique physical and chemical properties of kaolinite can be acted as a good semiconductor carrier.Herein,this paper firstly presents the mineralogical characteristics of kaolinite.Next,kaolinite-based photocatalysts(such as TiO_(2)/kaolinite,g-C_(3)N_(4)/kaolinite,g-C_(3)N_(4)/TiO_(2)/kaolinite,Zn O)are discussed in detail from the formation of heterostructures,synthesis-modification methods,photocatalytic mechanisms,and electron transfer pathways.Furthermore,the specific role of kaolinite in photocatalytic materials is summarized and discussed.In addition,the photocatalytic applications of kaolinite-based photocatalysts in the fields of water decomposition,pollutant degradation,bacterial disinfection are reviewed.However,the modification of kaolinite is hard,the manufacture of a large number of kaolinite-based photocatalysts is difficult,the cost of doping noble metals is expensive,and the utilization rate of visible light is low,which limits its application in industrial practice.Finally,this paper presents some perspectives on the future development of kaolinite-based photocatalysts.
基金This work was financially supported by the National Natural Science Foundation of China(21808189,52173277)National Natural Science Foundation of Gansu province(No.20JR5RA523)the Young Teachers’Research Ability Improvement Project of Northwest Normal University(NWNULKQN2020-01).
文摘Photoelectrochemical(PEC)water splitting is an effective strategy to convert solar energy into clean and renewable hydrogen energy.In order to carry out effective PEC conversion,researchers have conducted a lot of exploration and developed a variety of semiconductors suitable for PEC water splitting.Among them,metal oxides stand out due to their higher stability.Compared with traditional oxide semiconductors,ferrite-based photoelectrodes have the advantages of low cost,small band gap,and good stability.Interestingly,due to the unique characteristics of ferrite,most of them have various tunable features,which will be more conducive to the development of efficient PEC electrode.However,this complex metal oxide is also troubled by severe charge recombination and low carrier transport efficiency,resulting in lower conversion efficiency compared to theoretical value.Based on this,this article reviews the structure,preparation methods,characteristics and modification strategies of various common ferrites.In addition,we analyzed the future research direction of ferrite for PEC water splitting,and looked forward to the development of more efficient catalysts.
基金financially supported by the National Natural Science Foundation of China(Nos.21663027,21808189)the Fundamental Research Funds for the Central Universities of Chang’an University(No.300102299304)the Natural Science Basic Research Fund of Shaanxi Province(No.2020JZ20)。
文摘Photoelectrochemical(PEC)technology is considered to be a promising approach for solar-driven hydrogen production with zero emissions.Bismuth vanadate(BiVO_(4))is a kind of photocatalytic material with strong photoactivity in the visible light region and appropriate band gap for PEC water splitting.However,the solar-to-hydrogen efficiency(STH)of BiVO_(4)is far away from the 10%target needed for practical application due to its poor charge separation ability.Therefore,this review attempts to summarize the strategies for improving the photocurrent density and especially hydrogen production of BiVO_(4)materials through PEC techniques in the last three years,such as doping nonmetal and metal elements,depositing noble metals,constructing heterojunctions,coupling with carbon and metalorganic framework(MOF)materials to further enhance the PEC performance of BiVO_(4)photoanode.This review aims to serve as a general guideline to fabricate highly efficient BiVO_(4)-based materials for PEC water splitting.
基金supported by the National Natural Science Foundation of China(Nos.81573714,81603258,81773882and 21902125)Natural Science Basic Research Program of Shaanxi Provincial Education Department(No.20JK0607)+1 种基金Young Teacher Research Foundation of Shaanxi University of Chinese Medicine(No.2020GP33)Subject Innovation Team of Shaanxi University of Chinese Medicine(No.2019-YL10)。
文摘A kind of CdS/Cd-BiOCl immobilized films photocatalyst was prepared.The optical and physicochemical properties of the CdS/Cd-BiOCl photocatalysts were analysed,and the detailed characterization revealed CdS/Cd-BiOCl films photocatalyst with good charge carrier separation effect.The reusabilities and photocatalytic properties of the samples were studied.The 15%Cd S/Cd-Bi OCl photocatalyst exhibited superior performance in photocatalytic degradation of tetracycline(TC)and favorable stability under visible light irradiation.As for the photodegradation rate of TC,15%CdS/Cd-BiOCl exhibited an excellent photodegradation activity,which is 4.06 and 9.53 times higher than that of Cd S/Cd and Bi OCl,respectively.The results showed that dominant active species are·O_(2)^(-)and·OH radicals during photodegradation.The charge transfer in Z-scheme CdS/Cd-BiOCl films photocatalyst could synchronously generate conduct band(CB)electrons in BiOCl and valence band(VB)holes in CdS,and metal Cd served as electron mediator.This work can be a reference for the design of film photocatalysts and new insight for photodegradating towards contaminants.
基金financially supported by the National Natural Science Foundation of China(No.21808189)the National Natural Science Foundation of Gansu(No.20JR5RA523)the Young Teachers’Research Ability Improvement Project of Northwest Normal University(NWNU-LKQN2020-01)。
文摘The construction of rich phase interfaces to increase active reaction area in hybrid materials is an excellent strategy to improve electrochemical performance.Under this guideline,MIL-101@OX-metal organic framework(MOF)is constructed by the"MOF on MOF"method,then converts to MIL-101@NiFe-layered double hydroxides(LDH)by in situ transformation in alkaline solution.MIL-101@NiFe-LDH shows excellent electrochemical water oxidation performance.It needs only an overpotential of 215 m V to drive10 m A/cm^(2)of oxygen evolution reaction(OER),which is less than that of NiFe-LDH,MIL-101.In addition,MIL-101@NiFe-LDH has the smallest Tafel slope(55.1 mV/dec)compared with Ni Fe-LDH(61.1 m V/dec),MIL-101(150.8 m V/dec).The excellent water oxidation activity is due to the high phase interfaces derived from high specific surface area of MOF.This work offers an alternative method for making MOF/LDH heterostructures with an optimized phase interfaces and provides new insights for OER.
基金financially supported by the National Natural Science Foundation of China (Nos. 21808189 and 21663027)Natural Science Basic Research Fund of Shaanxi Province (No.2020JZ20)Fundamental Research Funds for the Central Universities of Chang’an University (No. 300102299304)。
文摘Due to the involvement of four-electron transfer process at photoanode,water oxidation is the ratelimiting step in water splitting reaction.To settle this dilemma,ZnCo_(2)O_(4)nanoparticles are combined with BiVO_(4)to form a p-n ZnCo_(2)O_(4)/BiVO;heterojunction photoanode,which is proved by an input voltage-output current test.The built-in electric field formed within the heterojunction structure promotes the effective separation of electrons and holes.ZnCo_(2)O_(4)is also an effective water oxidation cocatalyst,since it could cause the holes entering the electrode/electrolyte interface rapidly for the subsequent water oxidation reaction.The photocurrent density of ZnCo_(2)O_(4)/BiVO_(4)composite photoanode reaches 3.0 mA/cm^(2) at 1.23 V vs.RHE in 0.5 mol/L sodium sulfate under AM 1.5 G simulated sunlight,about 2.1 times greater than that of BiVO_(4)(1.4 mA/cm^(2)).These results suggest the potential of ZnCo_(2)O_(4)nanoparticles for improving photoelectrochemical water splitting anode materials.
基金This work was financially supported by the National Key Research and Development Program of China(Grant No.2017YFC0602306)the National Natural Science Foundation of China(Grant No.21808189)National Natural Science Foundation of Gansu Province(Grant No.20JR5RA523).
文摘The serious surface charge recombination and fatigued photogenerated carriers transfer of the BiVO_(4)photoanode restrict its photoelectrochemical(PEC)water splitting performance.In this work,nickel fluoride(NiF_(2))is applied to revamp pure BiVO_(4)photoanode by using a facile electrodeposition method.As a result,the asprepared NiF_(2)/BiVO_(4)photoanode increases the dramatic photocurrent density by approximately 180%compared with the pristine BiVO_(4)photoanode.Furthermore,the correlative photon-to-current conversion efficiency,the charge injection,and the separation efficiency,as well as the hydrogen generation of the composite photoanode have been memorably enhanced due to the synergy of NiF_(2)and BiVO_(4).This study may furnish a dependable guidance in fabricating the fluoride-based compound/semiconductor composite photoanode system.
