Novel graphitic carbon nitride(g-C_(3)N_(4))nanosheet/Bi_(5)O_(7)Br/NH_(2)-MIL-88B(Fe)photocatalysts(denoted as GCN-NSh/Bi_(5)O_(7)Br/FeMOF,in which MOF is metal–organic framework)with double S-scheme heterojunctions...Novel graphitic carbon nitride(g-C_(3)N_(4))nanosheet/Bi_(5)O_(7)Br/NH_(2)-MIL-88B(Fe)photocatalysts(denoted as GCN-NSh/Bi_(5)O_(7)Br/FeMOF,in which MOF is metal–organic framework)with double S-scheme heterojunctions were synthesized by a facile solvothermal route.The resultant materials were examined by X-ray photoelectron spectrometer(XPS),X-ray diffraction(XRD),scanning electron microscopy(SEM),energy dispersive X-ray spectroscopy(EDX),transmission electron microscopy(TEM),high-resolution transmission electron microscopy(HRTEM),photoluminescence spectroscopy(PL),Fourier transform infrared spectroscopy(FT-IR),UV-Vis diffuse reflection spectroscopy(UV-vis DRS),photocurrent density,electrochemical impedance spectroscopy(EIS),and Brunauer–Emmett–Teller(BET)analyses.After the integration of Fe-MOF with GCN-NSh/Bi_(5)O_(7)Br,the removal constant of tetracycline over the optimal GCN-NSh/Bi_(5)O_(7)Br/Fe-MOF(15wt%)nanocomposite was promoted 33 times compared with that of the pristine GCN.The GCN-NSh/Bi_(5)O_(7)Br/Fe-MOF(15wt%)nanocomposite showed superior photoactivity to azithromycin,metronidazole,and cephalexin removal that was 36.4,20.2,and 14.6 times higher than that of pure GCN,respectively.Radical quenching tests showed that·O_(2)-and h+mainly contributed to the elimination reaction.In addition,the nanocomposite maintained excellent activity after 4 successive cycles.Based on the developed n–n heterojunctions among n-GCN-NSh,n-Bi_(5)O_(7)Br,and n-Fe-MOF semiconductors,the double S-scheme charge transfer mechanism was proposed for the destruction of the selected antibiotics.展开更多
Two-dimensional carbon nitride(2 D-C_(3) N_(4))nanosheets are promising materials in photocatalytic water splitting,but still suffer from easy agglomeration and fast photogene rated electron-hole pairs recombination.T...Two-dimensional carbon nitride(2 D-C_(3) N_(4))nanosheets are promising materials in photocatalytic water splitting,but still suffer from easy agglomeration and fast photogene rated electron-hole pairs recombination.To tackle this issue,herein,a hierarchical Nb_(2) O_(5)/2 D-C_(3) N_(4) heterostructure is precisely constructed and the built-in electric field between Nb_(2)O_(5) and 2 D-C_(3) N_(4) can provide the driving force to separate/transfer the charge carriers efficiently.Moreover,the strongly Lewis acidic Nb_(2)O_(5) can adsorb TEOA molecules on its surface at locally high concentrations to facilitate the oxidation reaction kinetics under irradiation,resulting in efficient photogene rated electrons-holes separation and exceptional photocatalytic hydrogen evolution.As expected,the champion Nb_(2)O_(5)/2 D-C_(3)N_(4) heterostructure achieves an exceptional H2 evolution rate of 31.6 mmol g^(-1) h^(-1),which is 213.6 times and 4.3 times higher than that of pristine Nb_(2)O_(5) and2 D-C_(3)N_(4),respectively.Moreover,the champion heterostructure possesses a high apparent quantum efficiency(AQE)of 45.08%atλ=405 nm and superior cycling stability.Furthermore,a possible photocatalytic mechanism of the energy band alignment at the hetero-interface is proposed based on the systematical characterizations accompanied by density functional theory(DFT)calculations.This work paves the way for the precise construction of a high-quality heterostructured photocatalyst with efficient charge separation to boost hydrogen production.展开更多
Constructing a suitable heterojunction photocatalytic system from two photocatalytic materials is an efficient approach for designing extremely efficient photocatalysts for a broader range of environmental,medical,and...Constructing a suitable heterojunction photocatalytic system from two photocatalytic materials is an efficient approach for designing extremely efficient photocatalysts for a broader range of environmental,medical,and energy applications.Recently,the construction of a step-scheme heterostructure system(hereafter called the S-scheme)has received widespread attention in the photocatalytic field due to its ability to achieve efficient photogenerated carrier separation and obtain strong photo-redox ability.Herein,a novel S-scheme heterojunction system consisting of 2D O-doped g-C_(3)N_(4)(OCN)nanosheets and 3D N-doped Nb_(2)O_(5)/C(N-NBO/C)nanoflowers is constructed via ultrasonication and vigorous agitation technique followed by heat treatment for the photocatalytic degradation of Rhodamine B(RhB).Detailed characterization and decomposition behaviour of RhB showed that the fabricated material shows excellent photocatalytic efficiency and stability towards RhB photodegradation under visible-light illumination.The enhanced performance could be attributed to the following factors:fast charge transfer,highly-efficient charge separation,extended lifetime of photoinduced charge carriers,and the high redox capability of the photoinduced charges in the S-scheme system.Various trapping experiment conditions and electron paramagnetic resonance provide clear evidence of the S-scheme photogenerated charge transfer path,meanwhile,the RhB mineralization degradation pathway was also investigated using LC-MS.This study presents an approach to constructing Nb_(2)O_(5)-based S-scheme heterojunctions for photocatalytic applications.展开更多
The fabrication of heterojunction catalysts is an effective strategy to enhance charge separation efficiency,thus boosting the performance of photocatalysts.This work presents the synthesis and investigation of a nove...The fabrication of heterojunction catalysts is an effective strategy to enhance charge separation efficiency,thus boosting the performance of photocatalysts.This work presents the synthesis and investigation of a novel KNbO_(3)/Bi_(4)O_(5)Br_(2) heterostructure catalyst for photocatalytic N_(2)-to-NH_(3) conversion under light illumination.While morphology analysis revealed KNbO_(3) microcubes embedded within Bi_(4)O_(5)Br_(2) nanosheets,the composite exhibited no significant improvement in specific surface area or optical property compared to Bi_(4)O_(5)Br_(2) due to the relatively wide band gap and low surface area of KNbO_(3).The main contribution lies in the enhanced separation efficiency of photogenerated electrons and holes.Besides,the band structure analysis suggests that KNbO_(3) and Bi_(4)O_(5)Br_(2) exhibit suitable band potentials to form a type II heterojunction.Benefiting from the higher Fermi level of KNbO_(3) than Bi_(4)O_(5)Br_(2),the electron drift at the contact region thus occurs and leads to the formation of a built-in electric field with the direction from KNbO_(3) to Bi_(4)O_(5)Br_(2),accelerating electron migration and improving the operational efficiency of the photocatalysts.Consequently,the KNbO_(3)/Bi_(4)O_(5)Br_(2) catalyst shows an increased photoactivity,achieving an NH_(3) generation rate 1.78 and 1.58 times those of KNbO_(3) and Bi_(4)O_(5)Br_(2),respectively.This work may offer valuable insights for the design and synthesis of heterojunction composite photocatalysts.展开更多
The fabrication of efficient catalysts to reduce nitrogen(N_(2))to ammonia(NH3)is a significant challenge for artificial N_(2) fixation under mild conditions.In this work,we demonstrated that the simultaneous introduc...The fabrication of efficient catalysts to reduce nitrogen(N_(2))to ammonia(NH3)is a significant challenge for artificial N_(2) fixation under mild conditions.In this work,we demonstrated that the simultaneous introduction of oxygen vacancies(OVs)and Mo dopants into Bi_(5)O_(7)Br nanosheets can significantly increase the activity for photocatalytic N_(2) fixation.The 1 mol% Mo-doped Bi_(5)O_(7)Br nanosheets exhibited an optimal NH_(3) generation rate of 122.9μmol g^(-1) h^(-1) and durable stability,which is attributed to their optimized conduction band position,suitable absorption edge,large number of light-switchable OVs,and improved charge carrier separation.This work provides a promising approach to design photocatalysts with light-switchable OVs for N_(2) reduction to NH_(3) under mild conditions,highlighting the wide application scope of nanostructured BiOBr-based photocatalysts as effective N_(2) fixation systems.展开更多
Wet scrubbing combined with ozone oxidation has become a promising technology for simultaneous removal of SO_2 and NO_x in exhaust gas.In this paper,a new 20-species,76-step detailed kinetic mechanism was proposed bet...Wet scrubbing combined with ozone oxidation has become a promising technology for simultaneous removal of SO_2 and NO_x in exhaust gas.In this paper,a new 20-species,76-step detailed kinetic mechanism was proposed between O_3 and NO_x.The concentration of N_2O_5 was measured using an in-situ IR spectrometer.The numerical evaluation results kept good pace with both the public experiment results and our experiment results.Key reaction parameters for the generation of NO_2 and N_2O_5 during the NO ozonation process were investigated by a numerical simulation method.The effect of temperature on producing NO_2 was found to be negligible.To produce NO_2,the optimal residence time was1.25 sec and the molar ratio of O_3/NO about 1.For the generation of N_2O_5,the residence time should be about 8 sec while the temperature of the exhaust gas should be strictly controlled and the molar ratio of O_3/NO about 1.75.This study provided detailed investigations on the reaction parameters of ozonation of NO_x by a numerical simulation method,and the results obtained should be helpful for the design and optimization of ozone oxidation combined with the wet flue gas desulfurization methods（WFGD） method for the removal of NO_x.展开更多
A mild,efficient and eco-friendly process for the electrophilic nitration is described using N_2O_5 as a green nitrating agent in the presence of rare earth metal triflates[RE（OTf）_3]under mild conditions.
Comprehensive observations of the nocturnal atmospheric oxidation of NO_(3)and N_(2)O_(5)were conducted at a suburban site in Changzhou in the YRD using cavity ring-down spectroscopy(CRDS)from 27 May to 24 June,2019.H...Comprehensive observations of the nocturnal atmospheric oxidation of NO_(3)and N_(2)O_(5)were conducted at a suburban site in Changzhou in the YRD using cavity ring-down spectroscopy(CRDS)from 27 May to 24 June,2019.High concentrations of NO_(3)precursors were observed,and the nocturnal production rate of NO_(3)was determined to be 1.7±1.2 ppbv/hr.However,the nighttime NO_(3)and N_(2)O_(5)concentrations were relatively low,with maximum values of 17.7 and 304.7 pptv,respectively,illustrating the rapid loss ofNO_(3)andN_(2)O_(5).Itwas found that NO_(3)dominated the nighttime atmospheric oxidation,accounting for 50.7%,whileO3 andOH only contributed 34.1%and 15.2%,respectively.For the reactions of NO_(3)with volatile organic compounds(VOCs),styrenewas found to account for 60.3%,highlighting its dominant role in the NO_(3)reactivity.In general,the contributions of the reactions between NO_(3)and VOCs and the N_(2)O_(5)uptake to NO_(3)losswere found to be about 39.5%and 60.5%,respectively,indicating that N_(2)O_(5)uptake also played an important role in the loss of NO_(3)and N_(2)O_(5),especially under the high humidity conditions in China.The formation of nitrate at night mainly originated from N_(2)O_(5)uptake,and the maximum production rate of NO_(3)^(-)reached 6.5 ppbv/hr.The average NOx consumption rate via NO_(3)and N_(2)O_(5)chemistry was found to be 0.4 ppbv/h,accounting for 47.9%of the total NO_(x)removal.The predominant roles of NO_(3)and N_(2)O_(5)in nitrate formation and NO_(x)removal in the YRD region was highlighted in this study.展开更多
文摘Novel graphitic carbon nitride(g-C_(3)N_(4))nanosheet/Bi_(5)O_(7)Br/NH_(2)-MIL-88B(Fe)photocatalysts(denoted as GCN-NSh/Bi_(5)O_(7)Br/FeMOF,in which MOF is metal–organic framework)with double S-scheme heterojunctions were synthesized by a facile solvothermal route.The resultant materials were examined by X-ray photoelectron spectrometer(XPS),X-ray diffraction(XRD),scanning electron microscopy(SEM),energy dispersive X-ray spectroscopy(EDX),transmission electron microscopy(TEM),high-resolution transmission electron microscopy(HRTEM),photoluminescence spectroscopy(PL),Fourier transform infrared spectroscopy(FT-IR),UV-Vis diffuse reflection spectroscopy(UV-vis DRS),photocurrent density,electrochemical impedance spectroscopy(EIS),and Brunauer–Emmett–Teller(BET)analyses.After the integration of Fe-MOF with GCN-NSh/Bi_(5)O_(7)Br,the removal constant of tetracycline over the optimal GCN-NSh/Bi_(5)O_(7)Br/Fe-MOF(15wt%)nanocomposite was promoted 33 times compared with that of the pristine GCN.The GCN-NSh/Bi_(5)O_(7)Br/Fe-MOF(15wt%)nanocomposite showed superior photoactivity to azithromycin,metronidazole,and cephalexin removal that was 36.4,20.2,and 14.6 times higher than that of pure GCN,respectively.Radical quenching tests showed that·O_(2)-and h+mainly contributed to the elimination reaction.In addition,the nanocomposite maintained excellent activity after 4 successive cycles.Based on the developed n–n heterojunctions among n-GCN-NSh,n-Bi_(5)O_(7)Br,and n-Fe-MOF semiconductors,the double S-scheme charge transfer mechanism was proposed for the destruction of the selected antibiotics.
基金Finacial support from the Natural Science Foundation of Jiangsu Province(BK20170549,BK20180887)the National Natural Science Foundation of China(21706103,62004084)+3 种基金Guangdong Innovation Research Team for Higher Education(2017KCXTD030)the High-level Talents Project of Dongguan University of Technology(KCYKYQD2017017)the Young Talent Cultivation Plan of Jiangsu UniversityJiangsu Provincial Program for High-Level Innovative and Entrepreneurial Talents Introduction。
文摘Two-dimensional carbon nitride(2 D-C_(3) N_(4))nanosheets are promising materials in photocatalytic water splitting,but still suffer from easy agglomeration and fast photogene rated electron-hole pairs recombination.To tackle this issue,herein,a hierarchical Nb_(2) O_(5)/2 D-C_(3) N_(4) heterostructure is precisely constructed and the built-in electric field between Nb_(2)O_(5) and 2 D-C_(3) N_(4) can provide the driving force to separate/transfer the charge carriers efficiently.Moreover,the strongly Lewis acidic Nb_(2)O_(5) can adsorb TEOA molecules on its surface at locally high concentrations to facilitate the oxidation reaction kinetics under irradiation,resulting in efficient photogene rated electrons-holes separation and exceptional photocatalytic hydrogen evolution.As expected,the champion Nb_(2)O_(5)/2 D-C_(3)N_(4) heterostructure achieves an exceptional H2 evolution rate of 31.6 mmol g^(-1) h^(-1),which is 213.6 times and 4.3 times higher than that of pristine Nb_(2)O_(5) and2 D-C_(3)N_(4),respectively.Moreover,the champion heterostructure possesses a high apparent quantum efficiency(AQE)of 45.08%atλ=405 nm and superior cycling stability.Furthermore,a possible photocatalytic mechanism of the energy band alignment at the hetero-interface is proposed based on the systematical characterizations accompanied by density functional theory(DFT)calculations.This work paves the way for the precise construction of a high-quality heterostructured photocatalyst with efficient charge separation to boost hydrogen production.
文摘Constructing a suitable heterojunction photocatalytic system from two photocatalytic materials is an efficient approach for designing extremely efficient photocatalysts for a broader range of environmental,medical,and energy applications.Recently,the construction of a step-scheme heterostructure system(hereafter called the S-scheme)has received widespread attention in the photocatalytic field due to its ability to achieve efficient photogenerated carrier separation and obtain strong photo-redox ability.Herein,a novel S-scheme heterojunction system consisting of 2D O-doped g-C_(3)N_(4)(OCN)nanosheets and 3D N-doped Nb_(2)O_(5)/C(N-NBO/C)nanoflowers is constructed via ultrasonication and vigorous agitation technique followed by heat treatment for the photocatalytic degradation of Rhodamine B(RhB).Detailed characterization and decomposition behaviour of RhB showed that the fabricated material shows excellent photocatalytic efficiency and stability towards RhB photodegradation under visible-light illumination.The enhanced performance could be attributed to the following factors:fast charge transfer,highly-efficient charge separation,extended lifetime of photoinduced charge carriers,and the high redox capability of the photoinduced charges in the S-scheme system.Various trapping experiment conditions and electron paramagnetic resonance provide clear evidence of the S-scheme photogenerated charge transfer path,meanwhile,the RhB mineralization degradation pathway was also investigated using LC-MS.This study presents an approach to constructing Nb_(2)O_(5)-based S-scheme heterojunctions for photocatalytic applications.
基金supported by the National Natural Science Foundation of China (Grant No.22172144)the Key Research and Development Program of Zhejiang Province (Grant No.2023C03148).
文摘The fabrication of heterojunction catalysts is an effective strategy to enhance charge separation efficiency,thus boosting the performance of photocatalysts.This work presents the synthesis and investigation of a novel KNbO_(3)/Bi_(4)O_(5)Br_(2) heterostructure catalyst for photocatalytic N_(2)-to-NH_(3) conversion under light illumination.While morphology analysis revealed KNbO_(3) microcubes embedded within Bi_(4)O_(5)Br_(2) nanosheets,the composite exhibited no significant improvement in specific surface area or optical property compared to Bi_(4)O_(5)Br_(2) due to the relatively wide band gap and low surface area of KNbO_(3).The main contribution lies in the enhanced separation efficiency of photogenerated electrons and holes.Besides,the band structure analysis suggests that KNbO_(3) and Bi_(4)O_(5)Br_(2) exhibit suitable band potentials to form a type II heterojunction.Benefiting from the higher Fermi level of KNbO_(3) than Bi_(4)O_(5)Br_(2),the electron drift at the contact region thus occurs and leads to the formation of a built-in electric field with the direction from KNbO_(3) to Bi_(4)O_(5)Br_(2),accelerating electron migration and improving the operational efficiency of the photocatalysts.Consequently,the KNbO_(3)/Bi_(4)O_(5)Br_(2) catalyst shows an increased photoactivity,achieving an NH_(3) generation rate 1.78 and 1.58 times those of KNbO_(3) and Bi_(4)O_(5)Br_(2),respectively.This work may offer valuable insights for the design and synthesis of heterojunction composite photocatalysts.
基金supported by Shanghai Pujiang Program(21PJ1400400)Shanghai Municipal Science and Technology Commission(22511103900)+1 种基金the Fundamental Research Funds for the Central Universities(2232023A-02)the National Natural Science Foundation of China(22173017).
文摘The fabrication of efficient catalysts to reduce nitrogen(N_(2))to ammonia(NH3)is a significant challenge for artificial N_(2) fixation under mild conditions.In this work,we demonstrated that the simultaneous introduction of oxygen vacancies(OVs)and Mo dopants into Bi_(5)O_(7)Br nanosheets can significantly increase the activity for photocatalytic N_(2) fixation.The 1 mol% Mo-doped Bi_(5)O_(7)Br nanosheets exhibited an optimal NH_(3) generation rate of 122.9μmol g^(-1) h^(-1) and durable stability,which is attributed to their optimized conduction band position,suitable absorption edge,large number of light-switchable OVs,and improved charge carrier separation.This work provides a promising approach to design photocatalysts with light-switchable OVs for N_(2) reduction to NH_(3) under mild conditions,highlighting the wide application scope of nanostructured BiOBr-based photocatalysts as effective N_(2) fixation systems.
基金financially supported by the National High Tech Research and Development Program(863)of China(No.2011AA060801)the Program for Zhejiang Leading Team of S&T Innovation(No.2013TD07)
文摘Wet scrubbing combined with ozone oxidation has become a promising technology for simultaneous removal of SO_2 and NO_x in exhaust gas.In this paper,a new 20-species,76-step detailed kinetic mechanism was proposed between O_3 and NO_x.The concentration of N_2O_5 was measured using an in-situ IR spectrometer.The numerical evaluation results kept good pace with both the public experiment results and our experiment results.Key reaction parameters for the generation of NO_2 and N_2O_5 during the NO ozonation process were investigated by a numerical simulation method.The effect of temperature on producing NO_2 was found to be negligible.To produce NO_2,the optimal residence time was1.25 sec and the molar ratio of O_3/NO about 1.For the generation of N_2O_5,the residence time should be about 8 sec while the temperature of the exhaust gas should be strictly controlled and the molar ratio of O_3/NO about 1.75.This study provided detailed investigations on the reaction parameters of ozonation of NO_x by a numerical simulation method,and the results obtained should be helpful for the design and optimization of ozone oxidation combined with the wet flue gas desulfurization methods（WFGD） method for the removal of NO_x.
基金the financial support from the National Nature Science Foundation of China Academy of Engineering Physics(No.10976014)Nature Science Foundation of Jiangsu Province(No.BK2011697)
文摘A mild,efficient and eco-friendly process for the electrophilic nitration is described using N_2O_5 as a green nitrating agent in the presence of rare earth metal triflates[RE（OTf）_3]under mild conditions.
基金supported by the National Natural Science Foundation of China(Nos.42030609,91644107,61905003,and U19A2044)the Natural Science Foundation of Anhui Province(No.2008085J20)+1 种基金the National Key Research and Development Program of China(No.2017YFC0209403)the Cultivating Project of Strategic Priority Research Program of Chinese Academy of Sciences(No.XDPB1901)
文摘Comprehensive observations of the nocturnal atmospheric oxidation of NO_(3)and N_(2)O_(5)were conducted at a suburban site in Changzhou in the YRD using cavity ring-down spectroscopy(CRDS)from 27 May to 24 June,2019.High concentrations of NO_(3)precursors were observed,and the nocturnal production rate of NO_(3)was determined to be 1.7±1.2 ppbv/hr.However,the nighttime NO_(3)and N_(2)O_(5)concentrations were relatively low,with maximum values of 17.7 and 304.7 pptv,respectively,illustrating the rapid loss ofNO_(3)andN_(2)O_(5).Itwas found that NO_(3)dominated the nighttime atmospheric oxidation,accounting for 50.7%,whileO3 andOH only contributed 34.1%and 15.2%,respectively.For the reactions of NO_(3)with volatile organic compounds(VOCs),styrenewas found to account for 60.3%,highlighting its dominant role in the NO_(3)reactivity.In general,the contributions of the reactions between NO_(3)and VOCs and the N_(2)O_(5)uptake to NO_(3)losswere found to be about 39.5%and 60.5%,respectively,indicating that N_(2)O_(5)uptake also played an important role in the loss of NO_(3)and N_(2)O_(5),especially under the high humidity conditions in China.The formation of nitrate at night mainly originated from N_(2)O_(5)uptake,and the maximum production rate of NO_(3)^(-)reached 6.5 ppbv/hr.The average NOx consumption rate via NO_(3)and N_(2)O_(5)chemistry was found to be 0.4 ppbv/h,accounting for 47.9%of the total NO_(x)removal.The predominant roles of NO_(3)and N_(2)O_(5)in nitrate formation and NO_(x)removal in the YRD region was highlighted in this study.
