The metal complex 5-（4-aminophenyl）-10,15,20-triphenylporphyrin copper （CuAPTPP） was covalently linked on the surface of TiO2 microspheres by using toluene disocyanate （TDI） as a bridging bond unit. The hydroxyl...The metal complex 5-（4-aminophenyl）-10,15,20-triphenylporphyrin copper （CuAPTPP） was covalently linked on the surface of TiO2 microspheres by using toluene disocyanate （TDI） as a bridging bond unit. The hydroxyl group （-OH） of TiO2 microspheres surface and the amino group （-NH2） of CuAPTPP reacted respectively with the active -NCO groups of TDI to form a surface conjugated microsphere CuAPTPP-TDI-TiO2 that was confirmed by FT-IR spectra. The CuAPTPP-TDI-TiO2 microspheres were characterized with UV-visible, elemental analysis, XRD, SEM, and UV-Vis diffuse reflectance spectra. The effect of amounts of linked TDI on the performance of photocatalytic microspheres was discussed, and the optimal molar ratio of TDI：TiO2 was established. The photocatalytic activity of CuAPTPP- TDI-TiO2 was evaluated using the photocatalytic degradation of methylene blue （MB） under visible-light irradiation. The results showed that, TDI, as a bond unit, was used to form a steady chemical brigdging bond linking CuAPTPP and the surface of TiO2 microspheres, and the prepared catalyst exhibited higher photocatalytic activity under visible-light irradiation for MB degradation. The degradation rate of 20 mg/L MB could reach 98.7% under Xe- lamp （150 W） irradiation in 120 rain. The degradation of MB followed the first-order reaction model under visible light irradiation, and the rate constant of 5.1× 10^-2 min-1 and the half- life of 11.3 min were achieved. And the new photocatalyst can be recycled for 4 times, remaining 90.0% MB degradation rate.展开更多
Lattice‐doping and surface decoration are prospective routes to improve the visible‐light photocatalytic ability of TiO2,but the two techniques are difficult to combine into one preparation process because they are ...Lattice‐doping and surface decoration are prospective routes to improve the visible‐light photocatalytic ability of TiO2,but the two techniques are difficult to combine into one preparation process because they are usually conducted under different conditions,which limits the efficiency of TiO2 modification.In this study,TiO2 was successfully modified by simultaneous lattice‐doping and surface decoration,and the visible‐light photocatalytic capacity was largely improved.Upon comparing the method reported here with previous ones,the most significant difference is that Fe(II)‐phenanthroline was first used as the co‐precursor of the introduced elements of C,N,and Fe.These three elements were simultaneously introduced to TiO2 at high levels by this co‐precursor method.The as‐synthesized photocatalysts were systemically investigated and analyzed by several characterization methods such as XRD,FT‐IR,XPS,Raman spectroscopy,EPR,UV‐Vis DRS,photoluminescence spectra,photocurrent,electrochemical impedance spectra,TEM,and HRTEM.The photocatalytic degradation of 4‐NP under visible‐light irradiation was used to evaluate the photocatalytic activity of the photocatalysts.Based on the experimental data,a probable mechanism for the photocatalytic degradation by the photocatalysts is proposed.This is a novel method of using one source to simultaneously introduce metal and non‐metal elements to TiO2 at high levels,which may provide a new way to prepare highly effective TiO2 photocatalysts.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
Tailoring the microstructure of pristine TiO2 is essential to narrow its band gap and prolong the charge lifetime. In particular, strategies involving fluorine have been used successfully to tune the surface chemistry...Tailoring the microstructure of pristine TiO2 is essential to narrow its band gap and prolong the charge lifetime. In particular, strategies involving fluorine have been used successfully to tune the surface chemistry, electronic structure, and morphology of TiO2 photocatalysts to improve their photocatalytic activity based on the strong complexation between fluoride ions and TiO2 and the high electronegativity of fluorine. In this review, we summarize the strategies involving fluorine to establish highly efficient TiO2 photocatalytic systems or fabricate highly efficient TiO2 photocatalysts. The main fluorine effects(i.e. the effects of fluorine on photocatalysis) include the following four aspects:(1) Surface effects of fluoride on TiO2 photocatalysis,(2) effects of fluorine doping on TiO2 photocatalysis,(3) fluoride-mediated tailoring of the morphology of TiO2 photocatalysts, and(4) the effects of fluorine on non-TiO2 photocatalysis. Additionally, the unique applications of these fluorine effects in photocatalysis, including selective degradation of pollutants, selective oxidation of chemicals, water-splitting to produce H2, reduction of CO2 to produce solar fuels, and improvement of the thermostability of TiO2 photocatalysts, are reviewed.展开更多
Zeolite catalysts,such as H-mordenite(H-MOR),are readily deactivated by coke deposition in carbonylation reactions.Pyridine modification of H-MOR can improve its stability but can lead to an undesirable loss in cataly...Zeolite catalysts,such as H-mordenite(H-MOR),are readily deactivated by coke deposition in carbonylation reactions.Pyridine modification of H-MOR can improve its stability but can lead to an undesirable loss in catalytic activity.Herein,we report the intrinsic impact of the pyridine adsorption behavior on H-MOR and the spacial hindrance of the zeolite frameworks on dimethyl ether(DME)carbonylation at a molecular level.We discovered that acid sites at O2 positions,located on common walls of eight-membered ring(8-MR)side pockets and 12-MR channels,were active in DME carbonylation,but were unfortunately poisoned during pyridine modification.Density functional theory calculations revealed that the pyridine-poisoned acid sites at the O2 positions could be easily regenerated due to the spacial hindrance of the zeolite frameworks.Accordingly,they can be facilely regenerated by proper thermal treatment,which induces 60%promotion in the catalytic activity along with a high stability.Our findings demonstrate the determining role of O2 positions in H-MOR for DME carbonylation and provide a new avenue for the rational design of other efficient zeolite-relevant catalytic systems.展开更多
The construction of S‐scheme heterojunction photocatalysts has been regarded as an effective avenue to facilitate the conversion of solar energy to fuel.However,there are still considerable challenges with regard to ...The construction of S‐scheme heterojunction photocatalysts has been regarded as an effective avenue to facilitate the conversion of solar energy to fuel.However,there are still considerable challenges with regard to efficient charge transfer,the abundance of catalytic sites,and extended light absorption.Herein,an S‐scheme heterojunction of 2D/2D zinc porphyrin‐based metal‐organic frameworks/BiVO_(4)nanosheets(Zn‐MOF/BVON)was fabricated for efficient photocatalytic CO_(2)conversion.The optimal one shows a 22‐fold photoactivity enhancement when compared to the previously reported BiVO4 nanoflake(ca.15 nm),and even exhibits~2‐time improvement than the traditional g‐C3N4/BiVO4 heterojunction.The excellent photoactivities are ascribed to the strengthened S‐scheme charge transfer and separation,promoted CO_(2)activation by the well‐dispersed metal nodes Zn_(2)(COO)_(4)in the Zn‐MOF,and extended visible light response range based on the results of the electrochemical reduction,electron paramagnetic resonance,and in‐situ diffuse reflectance infrared Fourier transform spectroscopy.The dimension‐matched Zn‐MOF/BVON S‐scheme heterojunction endowed with highly efficient charge separation and abundant catalytic active sites contributed to the superior CO2 conversion.This study offers a facile strategy for constructing S‐scheme heterojunctions involving porphyrin‐based MOFs for solar fuel production.展开更多
Splitting water into hydrogen and oxygen by dye-sensitized photoelectrochemical cell(DSPEC)is a promising approach to solar fuels production.In this study,a series of pyridine derivatives as surface additives were mod...Splitting water into hydrogen and oxygen by dye-sensitized photoelectrochemical cell(DSPEC)is a promising approach to solar fuels production.In this study,a series of pyridine derivatives as surface additives were modified on a molecular chromophore and water oxidation catalyst co-loaded TiO_(2)photoanode,TiO_(2)|RuP,1(RuP=Ru(4,4′-(PO3H2)2-2,2′-bipyridine)(2,2′-bipyridine)2,1=Ru(bda)(L)2,(bda=2,2′-bipyridine-6,6′-dicarboxylate,L=10-(pyridin-4-yloxy)decyl)phosphonic acid).The addition of pyridine additives was found to result in up to 42%increase in photocurrent.Under simulated sun-light irradiation,TiO_(2)|RuP,1,P1(P1=4-Hydroxypyridine)produced a photocurrent density of 1 mA/cm2 at a bias of 0.4 V vs.NHE in acetate buffer.Moreover,the observed photocurrents are correlated with the electron-donating ability of the substituent groups on pyridine ring.Transient absorption measurements and electrochemical impedance spectroscopy revealed that surface-bound pyridine can effectively retard the back-electron transfer from the TiO_(2)conduction band to the oxidized dye,which is a major process responsible for energy loss in DSPECs.展开更多
Three new silica gel modified with calix[4]arene derivatives （p-tert-butyl-calix[4]arene （PC4）, calix[4]arene （C4） and calix[4]arene sulfonate （C4S）） have been prepared via modification of activated silica gel...Three new silica gel modified with calix[4]arene derivatives （p-tert-butyl-calix[4]arene （PC4）, calix[4]arene （C4） and calix[4]arene sulfonate （C4S）） have been prepared via modification of activated silica gel with toluene 2,4-di-iso-cyanate （TDI） as linker in tow step. The modified silica were characterized by fourier transform infrared spectroscopy （FT1R）, thermal analysis （TGA） and elemental analysis. The FTIR spectra and TGA analysis verified that the calix[4]arene derivates are covalent attached to the silica. Scanning electron microscope SEM and Brunauer-Emmett-Teller BET analysis have been done to get information about the sample＇s surface shape and area. SEM and BET analysis reveal that the modified silica are in the range of microporous adsorbent.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
Carbon-based perovskite solar cells have attracted much attention,due to their low cost,simple preparation process and high chemical stability.However,the devices exhibit low photoelectric conversion efficiency,owing ...Carbon-based perovskite solar cells have attracted much attention,due to their low cost,simple preparation process and high chemical stability.However,the devices exhibit low photoelectric conversion efficiency,owing to the presence of defects and interface impedance between the perovskite active layer and the contact interface.In order to minimize the interfacial defects and improve the charge transfer performance between the perovskite layer and the contact interface,cetyltrimethylammonium chloride(CTAC)was introduced into the lower interface of HTL-free carbon-based perovskite solar cells,because CTAC can be used as interface modification material to passivate the buried interface of perovskite and promote grain growth.It was found that CTAC can not only passivate the interface defects of perovskite,but also improve the crystalline quality of perovskite.As a result,the photovoltaic conversion efficiency of reaches 17.18%,which is 12.5%higher than that of the control group.After 20 days in air with 60%RH humidity,the cell can still maintain more than 90%of the initial efficiency,which provides a new strategy for interfacial passivation of perovskite solar cells.展开更多
Two-dimensional(2D)metal oxides and chalcogenides(MOs&MCs)have been regarded as a new class of promising electro-and photocatalysts for many important chemical reactions such as hydrogen evolution reaction,CO_(2) ...Two-dimensional(2D)metal oxides and chalcogenides(MOs&MCs)have been regarded as a new class of promising electro-and photocatalysts for many important chemical reactions such as hydrogen evolution reaction,CO_(2) reduction reaction and N2 reduction reaction in virtue of their outstanding physicochemical properties.However,pristine 2D MOs&MCs generally show the relatively poor catalytic performances due to the low electrical conductivity,few active sites and fast charge recombination.Therefore,considerable efforts have been devoted to engineering 2D MOs&MCs by rational structural design and chemical modification to further improve the catalytic activities.Herein,we comprehensively review the recent advances for engineering technologies of 2D MOs&MCs,which are mainly focused on the intercalation,doping,defects creation,facet design and compositing with functional materials.Meanwhile,the relationship between morphological,physicochemical,electronic,and optical properties of 2D MOs&MCs and their electro-and photocatalytic performances is also systematically discussed.Finally,we further give the prospect and challenge of the field and possible future research directions,aiming to inspire more research for achieving high-performance 2D MOs&MCs catalysts in energy storage and conversion fields.展开更多
基金ACKNOWLEDGMENTS This work was supported by the National Natural Science Foundation of China （No.21276208）, the Doctor Fundation of Education Ministry of China （No.20096118110008）, the Special Research Fund of Shaanxi Provincial Department of Education of China （No.12JK0606）, and the Research Fund for Excellent Doctoral Thesis of Xi＇an University of Technology （No.207-002J1304）.
文摘The metal complex 5-（4-aminophenyl）-10,15,20-triphenylporphyrin copper （CuAPTPP） was covalently linked on the surface of TiO2 microspheres by using toluene disocyanate （TDI） as a bridging bond unit. The hydroxyl group （-OH） of TiO2 microspheres surface and the amino group （-NH2） of CuAPTPP reacted respectively with the active -NCO groups of TDI to form a surface conjugated microsphere CuAPTPP-TDI-TiO2 that was confirmed by FT-IR spectra. The CuAPTPP-TDI-TiO2 microspheres were characterized with UV-visible, elemental analysis, XRD, SEM, and UV-Vis diffuse reflectance spectra. The effect of amounts of linked TDI on the performance of photocatalytic microspheres was discussed, and the optimal molar ratio of TDI：TiO2 was established. The photocatalytic activity of CuAPTPP- TDI-TiO2 was evaluated using the photocatalytic degradation of methylene blue （MB） under visible-light irradiation. The results showed that, TDI, as a bond unit, was used to form a steady chemical brigdging bond linking CuAPTPP and the surface of TiO2 microspheres, and the prepared catalyst exhibited higher photocatalytic activity under visible-light irradiation for MB degradation. The degradation rate of 20 mg/L MB could reach 98.7% under Xe- lamp （150 W） irradiation in 120 rain. The degradation of MB followed the first-order reaction model under visible light irradiation, and the rate constant of 5.1× 10^-2 min-1 and the half- life of 11.3 min were achieved. And the new photocatalyst can be recycled for 4 times, remaining 90.0% MB degradation rate.
基金supported by the National Natural Science Foundation of China(51368044,51568051,51668046)the National Science Fund for Excellent Young Scholars(51422807)+6 种基金the Science and Technology Supporting Program of Jiangxi Province(20151BBG70018)the Natural Science Foundation of Jiangxi Province for Distinguished Young Scholars(20162BCB23041)the Science Foundation for Young Scientists of Jiangxi Province-Key Project(20171ACB21034)the Science and Technology Project of Jiangxi Provincial Education Department(GJJ160700)the Natural Science Foundation of Jiangxi Province(20161BAB216102)the Jiangxi Province Educational Reform Project(JXJG-16-8-7)the Nanchang Hangkong University Educational Reform Project(JY1604,JY1605,KCPY-1511)~~
文摘Lattice‐doping and surface decoration are prospective routes to improve the visible‐light photocatalytic ability of TiO2,but the two techniques are difficult to combine into one preparation process because they are usually conducted under different conditions,which limits the efficiency of TiO2 modification.In this study,TiO2 was successfully modified by simultaneous lattice‐doping and surface decoration,and the visible‐light photocatalytic capacity was largely improved.Upon comparing the method reported here with previous ones,the most significant difference is that Fe(II)‐phenanthroline was first used as the co‐precursor of the introduced elements of C,N,and Fe.These three elements were simultaneously introduced to TiO2 at high levels by this co‐precursor method.The as‐synthesized photocatalysts were systemically investigated and analyzed by several characterization methods such as XRD,FT‐IR,XPS,Raman spectroscopy,EPR,UV‐Vis DRS,photoluminescence spectra,photocurrent,electrochemical impedance spectra,TEM,and HRTEM.The photocatalytic degradation of 4‐NP under visible‐light irradiation was used to evaluate the photocatalytic activity of the photocatalysts.Based on the experimental data,a probable mechanism for the photocatalytic degradation by the photocatalysts is proposed.This is a novel method of using one source to simultaneously introduce metal and non‐metal elements to TiO2 at high levels,which may provide a new way to prepare highly effective TiO2 photocatalysts.
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.
文摘Tailoring the microstructure of pristine TiO2 is essential to narrow its band gap and prolong the charge lifetime. In particular, strategies involving fluorine have been used successfully to tune the surface chemistry, electronic structure, and morphology of TiO2 photocatalysts to improve their photocatalytic activity based on the strong complexation between fluoride ions and TiO2 and the high electronegativity of fluorine. In this review, we summarize the strategies involving fluorine to establish highly efficient TiO2 photocatalytic systems or fabricate highly efficient TiO2 photocatalysts. The main fluorine effects(i.e. the effects of fluorine on photocatalysis) include the following four aspects:(1) Surface effects of fluoride on TiO2 photocatalysis,(2) effects of fluorine doping on TiO2 photocatalysis,(3) fluoride-mediated tailoring of the morphology of TiO2 photocatalysts, and(4) the effects of fluorine on non-TiO2 photocatalysis. Additionally, the unique applications of these fluorine effects in photocatalysis, including selective degradation of pollutants, selective oxidation of chemicals, water-splitting to produce H2, reduction of CO2 to produce solar fuels, and improvement of the thermostability of TiO2 photocatalysts, are reviewed.
基金supported by the National Natural Science Foundation of China(21476159,21676182)~~
文摘Zeolite catalysts,such as H-mordenite(H-MOR),are readily deactivated by coke deposition in carbonylation reactions.Pyridine modification of H-MOR can improve its stability but can lead to an undesirable loss in catalytic activity.Herein,we report the intrinsic impact of the pyridine adsorption behavior on H-MOR and the spacial hindrance of the zeolite frameworks on dimethyl ether(DME)carbonylation at a molecular level.We discovered that acid sites at O2 positions,located on common walls of eight-membered ring(8-MR)side pockets and 12-MR channels,were active in DME carbonylation,but were unfortunately poisoned during pyridine modification.Density functional theory calculations revealed that the pyridine-poisoned acid sites at the O2 positions could be easily regenerated due to the spacial hindrance of the zeolite frameworks.Accordingly,they can be facilely regenerated by proper thermal treatment,which induces 60%promotion in the catalytic activity along with a high stability.Our findings demonstrate the determining role of O2 positions in H-MOR for DME carbonylation and provide a new avenue for the rational design of other efficient zeolite-relevant catalytic systems.
文摘The construction of S‐scheme heterojunction photocatalysts has been regarded as an effective avenue to facilitate the conversion of solar energy to fuel.However,there are still considerable challenges with regard to efficient charge transfer,the abundance of catalytic sites,and extended light absorption.Herein,an S‐scheme heterojunction of 2D/2D zinc porphyrin‐based metal‐organic frameworks/BiVO_(4)nanosheets(Zn‐MOF/BVON)was fabricated for efficient photocatalytic CO_(2)conversion.The optimal one shows a 22‐fold photoactivity enhancement when compared to the previously reported BiVO4 nanoflake(ca.15 nm),and even exhibits~2‐time improvement than the traditional g‐C3N4/BiVO4 heterojunction.The excellent photoactivities are ascribed to the strengthened S‐scheme charge transfer and separation,promoted CO_(2)activation by the well‐dispersed metal nodes Zn_(2)(COO)_(4)in the Zn‐MOF,and extended visible light response range based on the results of the electrochemical reduction,electron paramagnetic resonance,and in‐situ diffuse reflectance infrared Fourier transform spectroscopy.The dimension‐matched Zn‐MOF/BVON S‐scheme heterojunction endowed with highly efficient charge separation and abundant catalytic active sites contributed to the superior CO2 conversion.This study offers a facile strategy for constructing S‐scheme heterojunctions involving porphyrin‐based MOFs for solar fuel production.
文摘Splitting water into hydrogen and oxygen by dye-sensitized photoelectrochemical cell(DSPEC)is a promising approach to solar fuels production.In this study,a series of pyridine derivatives as surface additives were modified on a molecular chromophore and water oxidation catalyst co-loaded TiO_(2)photoanode,TiO_(2)|RuP,1(RuP=Ru(4,4′-(PO3H2)2-2,2′-bipyridine)(2,2′-bipyridine)2,1=Ru(bda)(L)2,(bda=2,2′-bipyridine-6,6′-dicarboxylate,L=10-(pyridin-4-yloxy)decyl)phosphonic acid).The addition of pyridine additives was found to result in up to 42%increase in photocurrent.Under simulated sun-light irradiation,TiO_(2)|RuP,1,P1(P1=4-Hydroxypyridine)produced a photocurrent density of 1 mA/cm2 at a bias of 0.4 V vs.NHE in acetate buffer.Moreover,the observed photocurrents are correlated with the electron-donating ability of the substituent groups on pyridine ring.Transient absorption measurements and electrochemical impedance spectroscopy revealed that surface-bound pyridine can effectively retard the back-electron transfer from the TiO_(2)conduction band to the oxidized dye,which is a major process responsible for energy loss in DSPECs.
文摘Three new silica gel modified with calix[4]arene derivatives （p-tert-butyl-calix[4]arene （PC4）, calix[4]arene （C4） and calix[4]arene sulfonate （C4S）） have been prepared via modification of activated silica gel with toluene 2,4-di-iso-cyanate （TDI） as linker in tow step. The modified silica were characterized by fourier transform infrared spectroscopy （FT1R）, thermal analysis （TGA） and elemental analysis. The FTIR spectra and TGA analysis verified that the calix[4]arene derivates are covalent attached to the silica. Scanning electron microscope SEM and Brunauer-Emmett-Teller BET analysis have been done to get information about the sample＇s surface shape and area. SEM and BET analysis reveal that the modified silica are in the range of microporous adsorbent.
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National Natural Science Foundation of China (52162028)Natural Science Foundation of Jiangxi Province (20232ACB204011,20224BAB204001)+3 种基金Education Department of Jiangxi Province (GJJ2201001)Jingdezhen Municipal Science and Technology Bureau (2023GY001-16,2023ZDGG001 and 20224SF005-08)Opening Project of National Engineering Research Center for Domestic&Building Ceramics (GCZX2301)State Key Laboratory of New Ceramics and Fine Processing in Tsinghua University (KF202309,KF202414)。
文摘Carbon-based perovskite solar cells have attracted much attention,due to their low cost,simple preparation process and high chemical stability.However,the devices exhibit low photoelectric conversion efficiency,owing to the presence of defects and interface impedance between the perovskite active layer and the contact interface.In order to minimize the interfacial defects and improve the charge transfer performance between the perovskite layer and the contact interface,cetyltrimethylammonium chloride(CTAC)was introduced into the lower interface of HTL-free carbon-based perovskite solar cells,because CTAC can be used as interface modification material to passivate the buried interface of perovskite and promote grain growth.It was found that CTAC can not only passivate the interface defects of perovskite,but also improve the crystalline quality of perovskite.As a result,the photovoltaic conversion efficiency of reaches 17.18%,which is 12.5%higher than that of the control group.After 20 days in air with 60%RH humidity,the cell can still maintain more than 90%of the initial efficiency,which provides a new strategy for interfacial passivation of perovskite solar cells.
基金Australian Research Council(ARC)for funding received under the ARC Discovery Project scheme(DP180102752)the financial support via the ARC DECRA scheme(DE160100715)+1 种基金the support from the Shuguang Program supported by Shanghai Education Development Foundation and Shanghai Municipal Education Commission(18SG035)State Key Laboratory for Modification of Chemical Fibers and Polymer Materials,Donghua University(KF2015)。
文摘Two-dimensional(2D)metal oxides and chalcogenides(MOs&MCs)have been regarded as a new class of promising electro-and photocatalysts for many important chemical reactions such as hydrogen evolution reaction,CO_(2) reduction reaction and N2 reduction reaction in virtue of their outstanding physicochemical properties.However,pristine 2D MOs&MCs generally show the relatively poor catalytic performances due to the low electrical conductivity,few active sites and fast charge recombination.Therefore,considerable efforts have been devoted to engineering 2D MOs&MCs by rational structural design and chemical modification to further improve the catalytic activities.Herein,we comprehensively review the recent advances for engineering technologies of 2D MOs&MCs,which are mainly focused on the intercalation,doping,defects creation,facet design and compositing with functional materials.Meanwhile,the relationship between morphological,physicochemical,electronic,and optical properties of 2D MOs&MCs and their electro-and photocatalytic performances is also systematically discussed.Finally,we further give the prospect and challenge of the field and possible future research directions,aiming to inspire more research for achieving high-performance 2D MOs&MCs catalysts in energy storage and conversion fields.
