In this study,melamine and cyanuric acid were used as precursors to form supramolecular crystals via hydrogen-bond-assisted self-assembly followed by hydrothermal treatment.Subsequent high-temperature calcination yiel...In this study,melamine and cyanuric acid were used as precursors to form supramolecular crystals via hydrogen-bond-assisted self-assembly followed by hydrothermal treatment.Subsequent high-temperature calcination yielded a novel brush-like three-dimensional carbon nitride.The brush-like 3D architecture was found to expose more accessible active sites,markedly accelerate electron transfer,and suppress the recombination of photogenerated charge carriers.The resulting superoxide(O_(2)^(-·))and hydroxyl(·OH)radicals generated via electron reduction were identified as the key reactive species in the photocatalytic process.Moreover,the surface of the brush-like structure is enriched with nitrogen vacancies,which enhance the catalyst’s ability to harvest visible light.The photocatalytic performance of the brush-like CNS-650 catalyst was evaluated for rhodamine B(RhB)degradation.Under red-light irradiation(660 nm),its degradation rate was 7.4 times higher than that of bulk CN.This work provides valuable insights into the design and application of efficient metal-free 3D photocatalysts.展开更多
Heterogeneous metal-catalyzed chemical conversions with a recyclable catalyst are very ideal and challenging for sustainable organic synthesis.A new bipyridyl-Mo(IV)-carbon nitride(CN-K/Mo-Bpy)was prepared by supporti...Heterogeneous metal-catalyzed chemical conversions with a recyclable catalyst are very ideal and challenging for sustainable organic synthesis.A new bipyridyl-Mo(IV)-carbon nitride(CN-K/Mo-Bpy)was prepared by supporting molybdenum complex on C_(3)N_(4)-K and characterized by FT-IR,XRD,SEM,XPS and ICP-OES.Heterogeneous CN–Mo-Bpy catalyst can be applied to the direct amination of nitroarenes and arylboronic acid,thus constructing various valuable diarylamines in high to excellent yields with a wide substrate scope and good functional group tolerance.It is worth noting that this heterogeneous catalyst has high chemical stability and can be recycled for at least five times without reducing its activity.展开更多
Graphitic carbon nitride(g-C_(3)N_(4)),known for its green and abundant nature and composed of carbon and nitrogen in a two-dimensional structure,has emerged as a significant area of interest across various discipline...Graphitic carbon nitride(g-C_(3)N_(4)),known for its green and abundant nature and composed of carbon and nitrogen in a two-dimensional structure,has emerged as a significant area of interest across various disciplines,particularly in energy conversion and storage.Its recent demonstrations of high potential in supercapacitor applications mark it as a promising alternative to graphene within the realm of materials science.Numerous favorable features,such as chemical and thermal stability,abundant nitrogen content,eco-friendly attributes,and gentle conditions for synthesis,are shown.This review summarizes recent advancements in the use of g-C_(3)N_(4)and its composites as electrodes for supercapacitors,highlighting the advantages and issues associated with g-C_(3)N_(4)in these applications.This emphasizes situations where the composition of g-C_(3)N_(4)with other materials,such as metal oxides,metal chalcogenides,carbon materials,and conducting polymers,overcomes its limitations,leading to composite materials with improved functionalities.This review discusses the challenges that still need to be addressed and the possible future roles of g-C_(3)N_(4)in the research of advanced supercapacitor technology,such as battery-hybrid supercapacitors,flexible supercapacitors,and photo-supercapacitors.展开更多
Photocatalytic conversion of CO_(2) is pivotal for mitigating the global greenhouse effect and fostering sustainable energy development.Nowadays,polymeric carbon nitride(PCN)has gained widespread application in CO_(2)...Photocatalytic conversion of CO_(2) is pivotal for mitigating the global greenhouse effect and fostering sustainable energy development.Nowadays,polymeric carbon nitride(PCN)has gained widespread application in CO_(2) solar reduction due to its excellent visible light response,suitable conduction band position,and good cost-effectiveness.However,the amorphous nature and low conductivity of PCN limit its photocatalytic efficiency by leading to low carrier concentrations and facile electron–hole recombination during photocatalysis.Addressing this bottleneck,in this study,potassium-doped PCN(KPCN)/copper(Ⅱ)-complexed bipyridine hydroxyquinoline carboxylic acid(Cu(Ⅱ)(bpy)(H_(2)hqc))composite catalysts were synthesized through a multistep microwave heating process.In the composite,the formation of an S-scheme junction facilitates the enrichment of more negative electrons on the conduction band of KPCN via intermolecular electron–hole recombination between Cu(Ⅱ)(bpy)(H_(2)hqc)(CuPyQc)and KPCN,thereby promoting efficient photoreduction of CO_(2) to CO.Microwave heating enhances the amidation reaction between these two components,achieving the immobilization of homogeneous molecular catalysts and forming amidation chemical bonds that serve as key channels for the S-scheme charge transfer.This work not only presents a new PCN-based catalytic system for CO_(2) reduction applications,but also offers a novel microwave-practical approach for immobilizing homogeneous catalysts.展开更多
Exploration of stable metal single-site supported porous graphitic carbon nitride(PCN)nanostructures and the development of maximum atom utilization for enhanced photocatalytic oxidation of antibiotics remains a chall...Exploration of stable metal single-site supported porous graphitic carbon nitride(PCN)nanostructures and the development of maximum atom utilization for enhanced photocatalytic oxidation of antibiotics remains a challenge in current research.This work proposed a one-step thermal copolymerization to obtain Cu(Ⅰ)doping porous carbon nitride(CUCN)through a spontaneously reducing atmosphere by urea in a covered crucible.The obtained CUCN had crumpled ultrathin nanosheets and mesoporous structures,which possessed higher specific surface areas than PCN.From X-ray absorption near edge structure(XANES)and Fourier transform extended X-ray absorption fine structure(FT-EXAFS)spectra analysis,the Cu doping existed in the oxidation state of Cu(Ⅰ)as single atoms anchored on the 2D layers of CN through two N neighbors,thereby facilitating efficient pathways for the transfer of photoexcited charge carriers.Furthermore,the photoluminescence(PL)spectra,electrochemical impedance spectra(EIS)and transient photocurrent response test proved the improved separation and transfer of photoexcited charge carriers for Cu(Ⅰ)introduction.Consequently,the photocatalytic activity of CUCN was much better than that of PCN for antibiotics norfloxacin(NOR),with 4.7-fold higher degradation reaction rate constants.From species-trapping experiments and density function theory(DFT)calculations,the Cu single atoms in Cu-N_(2)served as catalytic sites that could accelerate charge transfer and facilitate the adsorption of molecular oxygen to produce active species.The stable Cu(Ⅰ)embedded in the layer structure led to the excellent recycling test and remained stable after four runs of degradation and even thermal regenerated treatment.The degradation paths of NOR by CUCN under visible light were also demonstrated.Our work sheds light on a sustainable and practical approach for achieving stable metal single-atom doping and enhancing photocatalytic degradation of aqueous pollutants.展开更多
Graphitic carbon nitride(g-C_(3)N_(4))exhibits great mechanical as well as thermal characteristics,making it a valuable ma-terial for use in photoelectric conversion devices,an accelerator for synthesis of organic com...Graphitic carbon nitride(g-C_(3)N_(4))exhibits great mechanical as well as thermal characteristics,making it a valuable ma-terial for use in photoelectric conversion devices,an accelerator for synthesis of organic compounds,an electrolyte for fuel cell applications or power sources,and a hydrogen storage substance and a fluorescence detector.It is fabricated using dif-ferent methods,and there is a variety of morphologies and nanostructures such as zero to three dimensions that have been designed for different purposes.Ther e are many reports about g-C_(3)N_(4) in recent years,but a comprehensive review which covers nanostructure dimensions and their properties are missing.This review paper aims to give basic and comprehensive understanding of the photocatalytic and electrocatalytic usages of g-C_(3)N_(4).It highlights the recent progress of g-C_(3)N_(4) nano-structure designing by covering synthesis methods,dimensions,morphologies,applications and properties.Along with the summary,we will also discuss the challenges and prospects.Scientists,investigators,and engineers looking at g-C_(3)N_(4) nanostructures for a variety of applications might find our review paper to be a useful resource.展开更多
Elemental doping is an effective strategy for tuning the band structure of graphite carbon nitride(CN)to enhance its photocatalytic performance.In this study,sodium(Na)and oxygen(O)co-doped carbon nitride(Na/O-CN_(x),...Elemental doping is an effective strategy for tuning the band structure of graphite carbon nitride(CN)to enhance its photocatalytic performance.In this study,sodium(Na)and oxygen(O)co-doped carbon nitride(Na/O-CN_(x),x=1.0,2.0,3.0,4.0)was synthesized via solid-phase reaction of sodium citrate(NaCA)and pure CN powder in the Teflon-sealed autoclave under air conditions at 180℃.Surface area of Na/O-CN_(3.0) is measured to be 18.8 m^(2)/g,increasing by 60.7%compared to that of pure CN(11.7 m^(2)/g).Bandgap energy of Na/O-CN_(3.0) is determined to be 2.68 eV,marginally lower than that of pure CN(2.70 eV),thereby enhancing its capacity for sunlight absorption.Meanwhile,the incorporation of Na and O atoms into Na/O-CN_(x) is found to effectively reduce recombination rates of photogenerated electron-hole pairs.As a result,Na/O-CN_(x) samples exhibit markedly enhanced photocatalytic hydrogen evolution activity under visible light irradiation.Notably,the optimal Na/O-CN_(3.0) sample achieves a photocatalytic hydrogen production rate of 103.2μmol·g^(–1)·h^(–1),which is 8.2 times greater than that of pure CN(11.2μmol·g^(–1)·h^(–1)).Furthermore,a series of Na/O-CN_(x)-yO_(2)(y=0,20%,40%,60%,80%,100%)samples were prepared by modulating the oxygen content within reaction atmosphere.The catalytic performance evaluations reveal that the incorporation of both Na and O atoms in Na/O-CN_(3.0) enhances photocatalytic activity.This study also introduces novel methodologies for synthesis of metal atom-doped CN materials at lower temperature,highlighting the synergistic effect of Na and O atoms in photocatalytic hydrogen production of Na/O-CN_(x) samples.展开更多
Integrating photocatalysis technology with peroxymonosulfate oxidation possesses huge potential for degrading stubborn pollutant.Herein,a porous ultra-thin carbon nitride with C-defect O-doping and advanced n-π^(∗)tr...Integrating photocatalysis technology with peroxymonosulfate oxidation possesses huge potential for degrading stubborn pollutant.Herein,a porous ultra-thin carbon nitride with C-defect O-doping and advanced n-π^(∗)transition was customized by one-pot thermalinduced polymerization of molten urea assisted with paraformaldehyde.Via visible-light coupling peroxymonosulfate activation,the DCN-100 can completely photodegrade 2,4-dichlorophenol,and rate constant is 136.6 and 37.9 times that of CN and DCN-100 without peroxymonosulfate.The light-absorption of DCN-100 surpasses 550 nm,specific surface area rises from 45.03 to 98.58m^(2)/g,and charge behaviors are significantly improved.The effects of paraformaldehyde amount,PMS dosage,pH,2,4-dichlorophenol concentration,different water-body,wavelength and recycling times on photodegradation performance were explored in detail.Via capture experiments,ESR,LC-MS,Fukui-function,TEXT toxicity assessment and DFT theoretical calculation,themain active substances,degradation pathway,intermediate toxicity and enhanced activity mechanism of DCN-100 were clarified.The research provides a cost-effective,high-efficiency and environmental-friendly photocatalysts to activate peroxymonosulfate for water remediating.展开更多
The huge carrier transfer resistance caused by large-sized"nitrogen pot"severely limits the photocatalytic performance of carbon nitride(CN).This study aims to explore the selection principle of metal ion br...The huge carrier transfer resistance caused by large-sized"nitrogen pot"severely limits the photocatalytic performance of carbon nitride(CN).This study aims to explore the selection principle of metal ion bridges for constructing dual carrier-transfer channels to delivery carriers to respectively active sites using photodegradation of phenol as the model reaction.Density functional theory(DFT)calculation was used to optimize the structure model of nitrogen vacancies(Nv,provide active sites for reduction of O_(2) and oxidation of phenol)and metal ions(Fe^(3+),Co^(2+),Ni^(2+)or Cu^(2+))co-modified CN,and screen metal ion bridges based on the three parameters including bonding state of metal ion and"nitrogen pot",electrostatic potential(ESP)distribution around the active sites,and three-electron bond length.Both calculation results and activity data show that Fe^(3+),Co^(2+)and Ni^(2+)can construct dual carrier-transfer channels to promote the degradation of phenol while Cu^(2+)cannot Ny and Fe^(3+)co-modified CN(Fe/N_(v)-CN)showed the best catalytic performance among various catalysts and was used as the model catalyst for the detailed characterization to verify the calculation results.This work provides not only the novel strategy for constructing dual carrier-transfer channels in CN,but also the crucial basis for computer simulation as a prediction tool of catalyst structure design rationality.展开更多
The rapid emergence of drug-resistant bacterial strains undermines the efficacy of conventional antibiotics,necessitating the development of alternative therapies.Antimicrobial photodynamic therapy(PDT)is a promising ...The rapid emergence of drug-resistant bacterial strains undermines the efficacy of conventional antibiotics,necessitating the development of alternative therapies.Antimicrobial photodynamic therapy(PDT)is a promising approach,but its effectiveness is often limited by the suboptimal photocatalytic activity of photosensitizers.In this study,we introduce a novel photoresponsive carbon-based antibacterial agent,Ce6/g-C_(3)N_(4),which combines the photocatalytic properties of graphite-phase carbon nitride(g-C_(3)N_(4))with the photodynamic attributes of chlorin e6(Ce6).This agent,with an average particle size of 250.7 nm,demonstrates significantly enhanced photocatalytic activity.Additionally,the strong affinity of Ce6/g-C_(3)N_(4)for bacteria and efficient delivery of Ce6 result in an inhibition rate exceeding 99%against Gram-positive bacteria and excellent biofilm eradication under light irradiation.In vivo experiments reveal that Ce6/gC_(3)N_(4)effectively inhibits bacterial growth on wounds,and promotes wound healing post-light treatment,while maintaining good biocompatibility.Overall,the Ce6/g-C_(3)N_(4)antibacterial agent synergizes photodynamic and photocatalytic mechanisms,offering a new avenue for the photo-mediated,multi-strategic treatment of bacterial infections and wound healing.展开更多
The photocatalytic hydrogen peroxide(H_(2)O_(2))production by graphitic carbon nitride is a sustainable and environment-benign alternative approach of conventional anthraquinone autoxidation technology,but it is great...The photocatalytic hydrogen peroxide(H_(2)O_(2))production by graphitic carbon nitride is a sustainable and environment-benign alternative approach of conventional anthraquinone autoxidation technology,but it is great challenges to promote two-electron O_(2)reduction and water oxidation.Herein,we present the well-dispersed graphitic carbon nitride quantum dots decorated with cyano groups(Na-CNQD and K-CNQD)by thermal polymerization of melamine in the presence of metal fluoride.The quantum confinement and edge effect have endowed the photocatalysts with rich active sites,wide light absorption range and the inhibited charge recombination.The cyano moieties function as O_(2)reduction centers to accept the photogenerated electrons and facilitate their rapid transfer to O_(2)molecules.This process enables the selective two-electron reduction of O_(2),leading to the production of H_(2)O_(2).Concurrently,the valence band holes on the heptazine moiety oxidize water into H_(2)O_(2).These synergistic effects promote photocatalytic H_(2)O_(2)production from O_(2)and H_(2)O without the need for additional photosensitizers,organic scavengers and co-catalysts.In contrast,pristine carbon nitride nanosheets remain inactive under the same conditions.This study offers new strategies for rational design of carbon-based materials for solar-to-chemical energy conversion.展开更多
The photocatalytic oxidation of methane to methanol using molecule oxygen directly is an attractive catalytic reaction,but designing catalysts to avoid over-oxidation remains a significant challenge.Herein,Cu single-a...The photocatalytic oxidation of methane to methanol using molecule oxygen directly is an attractive catalytic reaction,but designing catalysts to avoid over-oxidation remains a significant challenge.Herein,Cu single-atom anchored on the defective carbon nitride structure(Cu SA/Def-CN)is designed for selective photocatalytic oxidation of methane into methanol using O_(2) under mild conditions.The Cu SA/Def-CN catalyst exhibits a high methanol selectivity of 92.8%under optimized conditions.Mechanistic studies reveal a synergistic effect between Def-CN and Cu SA,where Def-CN is responsible for the in-situ generation of hydrogen peroxide,which is subsequently decomposed by the Cu SA sites to produce·OH radicals that play a key role in the rate-determining step of methane activation to form methanol.Additionally,the presence of Cu SA not only enhances the electron-hole separation efficiency and improves the transfer of the photo-generated charges,but also increases the number of active sites for methane adsorption and activation.These insights provide valuable guidance for designing efficient catalysts for the highly selective photocatalytic oxidation of methane to methanol.展开更多
The development of innovative and sustainable catalytic strategies for organic synthesis is a pivotal aspect of advancing material science and chemical engineering.This research presents a new catalytic method for the...The development of innovative and sustainable catalytic strategies for organic synthesis is a pivotal aspect of advancing material science and chemical engineering.This research presents a new catalytic method for the aminoacylation of N-sulfonyl ketimines by utilizing a potassium-doped graphite-like carbon nitride(g-C_(3)N_(4))framework.This method not only enhances the catalytic efficiency and broadens the light absorption spectrum of g-C_(3)N_(4)but also significantly reduces the recombination rate of electronhole pairs,thereby increasing the reaction yield and selectivity.Importantly,our approach facilitates the synthesis of aminoacylated N-heterocycles,expanding the applicability of potassium-modified g-C_(3)N_(4)in photocatalytic organic synthesis.A notable accomplishment of this study is the unprecedented generation of carbamoyl radicals via heterogeneous photocatalysis,which can be easily recycled after reaction.This advancement highlights the capability of potassium-doped g-C_(3)N_(4)(namely K-CN)as an advanced heterogeneous photocatalyst for the formation of complex organic compounds.展开更多
Solar-driven photocatalytic overall water splitting(POWS)has emerged as a sustainable pathway for hydrogen production,yet faces intrinsic challenges in developing robust catalysts that balance efficiency,stability,and...Solar-driven photocatalytic overall water splitting(POWS)has emerged as a sustainable pathway for hydrogen production,yet faces intrinsic challenges in developing robust catalysts that balance efficiency,stability,and cost-effectiveness.Polymeric carbon nitride(PCN)represents as a promising metal-free photocatalyst for hydrogen production due to the merits of unique electronic structure and exceptional thermal stability.Nevertheless,limited by rapid charge recombination and insufficient oxidative capability,little success has been achieved on pristine PCN photocatalyst in POWS.In this context,recent advances have demonstrated multi-dimensional modification strategies for improving POWS performance.Based on the fundamental principles of photocatalysis,this review discusses the advantages and challenges of PCN-based photocatalysts in POWS systems.With critical evaluation on one-step excitation systems and Z-scheme two-step excitation systems,modification strategies including crystallinity engineering,supramolecular precursor design,cocatalyst modulation,and construction of PCN-based heterojunctions and homojunctions were highlighted by introducing representative advances in POWS application over the past five years.Future perspectives for PCN-based photocatalysts are proposed,aiming to provide new insights for the design of advanced photocatalytic system for efficient POWS.展开更多
Graphitic carbon nitride(g-C_(3)N_(4))has garnered significant attention due to its remarkable advantages such as lightweight,exceptional chemical stability and defect-rich surface.Nevertheless,its inadequate electric...Graphitic carbon nitride(g-C_(3)N_(4))has garnered significant attention due to its remarkable advantages such as lightweight,exceptional chemical stability and defect-rich surface.Nevertheless,its inadequate electrical conductivity and impedance matching hindered the practical implementation in the electromagnetic wave absorption(EMWA)field.To address these challenges,we developed a composites system of carbon spheres/g-C_(3)N_(4)(CCN)through a supramolecular self-assembly strategy,subsequently integrated with reduced graphene oxide(RGO)via a water bath method.Systematic investigation revealed that the EMWA performance of CCN/RGO composites exhibited a distinct dependence(a trend of first increasing and then decreasing)on RGO content.Especially,when the mass ratio of RGO to CCN was 20%,the CCN/RGO composite brought a minimum reflection loss value of-45.40 dB at 13.44 GHz and a broad effective absorbing bandwidth of 6.32 GHz at 2.19 mm.First-principles calculations based on density functional theory suggested that the constructed heterostructure effectively facilitated electron mobility and charge redistribution,boosting both conductive loss and polarization loss mechanisms.The exceptional absorption performance was ascribed to the synergistic effects of conductive loss,relaxation loss,and suitable impedance matching.As a results,this work provided a rational design strategy for high-performance g-C_(3)N_(4)-based EMWA materials.展开更多
The utilization of visible light for photocatalytic nitrogen fixation offers a sustainable and eco-friendly strategy for the production of ammonia.The present study focuses on the synthesis of a series of rare earth-d...The utilization of visible light for photocatalytic nitrogen fixation offers a sustainable and eco-friendly strategy for the production of ammonia.The present study focuses on the synthesis of a series of rare earth-doped carbon nitride composite ultraviolet-activated Ce-UiO-66 catalysts,denoted as RECNactMOF,for efficient nitrogen fixation.Rare earth doping modulates the band structure of carbon nitride,facilitating the formation of a type-I heterojunction with Ce-UiO-66 and promoting photocarrier generation at nitrogen fixation sites.Among these,Sm-doped SmCN-actMOF exhibits high visible-light absorption and efficient utilization of photocarriers,resulting in an apparent quantum efficiency(AQE)of 1.58%under 495 nm light irradiation.This study provides a pathway for enhancing the nitrogen fixation efficiency of photocatalysts through the incorporation of rare earth elements,and expanding the potential applications of rare earth materials in the field of photocatalysis.展开更多
Photocatalytic hydrogen peroxide(H_(2)O_(2))production has been considered as a promising strategy for H_(2)O_(2)synthesis due to its environmentally friendly.Among various photocatalysts,carbon nitride-based material...Photocatalytic hydrogen peroxide(H_(2)O_(2))production has been considered as a promising strategy for H_(2)O_(2)synthesis due to its environmentally friendly.Among various photocatalysts,carbon nitride-based materials are excellent candidates for H_(2)O_(2)production because of their excellent visible-light response,low cost and high stability.In this review,we summarize in detail the research progress on the photocatalytic production of H_(2)O_(2)by carbon nitride.First,we summarize the basic principles of photocatalysis and photocatalytic H_(2)O_(2)production.Second,the classification and modification methods of carbonnitride-based materials are discussed,including morphology modulation,noble metal loading,defect control,heterojunction regulation,molecular structure engineering and elemental doping.Finally,the different in-situ applications of H_(2)O_(2)via photosynthesis were discussed,including disinfection and antibiotic resistant genes degradation,organic pollutants degradation,medical applications and fine chemical synthesis.This review brings great promise for in-situ H_(2)O_(2)photosynthesis,which is expected to serve as a key component in future applications.展开更多
Photocatalytic H_(2) evolution from wastewater exhibits fascinating prospects in environment and energy fields.Here,we propose a novel 3D cross-linked g-C_(3)N_(4) network(SCN)assembling with 1D nanowires.This network...Photocatalytic H_(2) evolution from wastewater exhibits fascinating prospects in environment and energy fields.Here,we propose a novel 3D cross-linked g-C_(3)N_(4) network(SCN)assembling with 1D nanowires.This network structure endows SCN with abundant carbon defects,creating a defect energy level and shallow charge trapping centres,which significantly prolongs the photocarrier lifetime,suppresses their recombination and facilitates the mass transfer process during the dye photodegradation.Consequently,in photocatalytic H_(2) evolution coupled with Rhodamine B(RhB)photodegradation under visible light,the H_(2) production rate of SCN is 283μmol h^(-1)g^(-1),accompanying by 97%RhB photodegradation efficiency,much higher than UCN's 31μmol h^(-1)g^(-1)and 64%.In particular,AQY of SCN for H_(2) evolution from RhB solution reaches 23.7%at 380 nm.Furthermore,the calculated transition states demonstrate that the N1 site connected to the defect in SCN has a minimum Gibbs free energy ΔG(H^(*)),indicating that H~+undergoes an H^(+)→H^(*)→H_(2) evolution process.展开更多
The integration of selective oxidation of renewable biomass and its derivatives with hydrogen(H_(2))pro-duction holds significant potential for simultaneously yielding value-added chemicals and“green H_(2)”,contribu...The integration of selective oxidation of renewable biomass and its derivatives with hydrogen(H_(2))pro-duction holds significant potential for simultaneously yielding value-added chemicals and“green H_(2)”,contributing to addressing sustainability challenges.The S-scheme charge transfer mechanism enhances charge separation by maintaining strong redox potentials at both ends,facilitating both oxidation and reduction reactions.Herein,we synthesize a visible-light-responsive oxygen vacancy-rich In_(2)O_(3-x)/tubular carbon nitride(IO_(OV)/TCN)S-scheme heterojunction photocatalyst via electrostatic adherence for selec-tive 5-hydroxymethylfurfural(HMF)oxidation to 2,5-diformylfuran(DFF)and 2,5-furandicarboxylic acid(FDCA),alongside H_(2)production.Under anaerobic conditions and visible-light irradiation,the optimal IOOV/TCN-10 catalyst achieves an HMF conversion of 94.8%with a selectivity of 53.6%for DFF and FDCA,and a H_(2)yield of 754.05μmol g^(−1)in 3 h.The significantly improved photocatalytic activity results from enhanced visible-light absorption,reduced carrier recombination,and abundant catalytic active sites due to the synergistic effect of surface oxygen vacancies,the hollow nanotube-based architecture,and the S-scheme charge transfer mechanism.This work highlights the great potentials of S-scheme heterojunctions in biomass conversion for sustainable energy use and chemical production.展开更多
With the objectives of enhancing the stability,optical properties and visible-light photocatalytic activity of photocatalysts,we modified oxygen vacancy-rich zinc oxide（Vo-ZnO） with graphitic carbon nitride（g-C3N4...With the objectives of enhancing the stability,optical properties and visible-light photocatalytic activity of photocatalysts,we modified oxygen vacancy-rich zinc oxide（Vo-ZnO） with graphitic carbon nitride（g-C3N4）. The resulting g-C3N4/Vo-ZnO hybrid photocatalysts showed higher visible-light photocatalytic activity than pure Vo-ZnO and g-C3N4. The hybrid photocatalyst with a g-C3N4 content of 1 wt% exhibited the highest photocatalytic degradation activity under visible-light irradiation（λ≥ 400 nm）. In addition,the g-C3N4/Vo-ZnO photocatalyst was not deactivated after five cycles of methyl orange degradation,indicating that it is stable under light irradiation. Finally,a Z-scheme mechanism for the enhanced photocatalytic activity and stability of the g-C3N4/Vo-ZnO hybrid photocatalyst was proposed. The fast charge separation and transport within the g-C3N4/Vo-ZnO hybrid photocatalyst were attributed as the origins of its enhanced photocatalytic performance.展开更多
基金Supported by the National Natural Science Foundation of China(Grant 22578376,52374283)the Natural Science Foundation of Jiangsu Province(Grant BK20240332)。
文摘In this study,melamine and cyanuric acid were used as precursors to form supramolecular crystals via hydrogen-bond-assisted self-assembly followed by hydrothermal treatment.Subsequent high-temperature calcination yielded a novel brush-like three-dimensional carbon nitride.The brush-like 3D architecture was found to expose more accessible active sites,markedly accelerate electron transfer,and suppress the recombination of photogenerated charge carriers.The resulting superoxide(O_(2)^(-·))and hydroxyl(·OH)radicals generated via electron reduction were identified as the key reactive species in the photocatalytic process.Moreover,the surface of the brush-like structure is enriched with nitrogen vacancies,which enhance the catalyst’s ability to harvest visible light.The photocatalytic performance of the brush-like CNS-650 catalyst was evaluated for rhodamine B(RhB)degradation.Under red-light irradiation(660 nm),its degradation rate was 7.4 times higher than that of bulk CN.This work provides valuable insights into the design and application of efficient metal-free 3D photocatalysts.
基金support for this work by Hebei Education Department(No.JZX2024004)Central Guidance on Local Science and Technology Development Fund of Hebei Province(No.236Z1404G)+3 种基金the National Natural Science Foundation of China(Nos.22301060 and 21272053)China Postdoctoral Science Foundation(No.2023M730914)the Natural Science Foundation of Hebei Province(Biopharmaceutical Joint Fund No.B2022206008)Project of Science and Technology Department of Hebei Province(No.22567622H)。
文摘Heterogeneous metal-catalyzed chemical conversions with a recyclable catalyst are very ideal and challenging for sustainable organic synthesis.A new bipyridyl-Mo(IV)-carbon nitride(CN-K/Mo-Bpy)was prepared by supporting molybdenum complex on C_(3)N_(4)-K and characterized by FT-IR,XRD,SEM,XPS and ICP-OES.Heterogeneous CN–Mo-Bpy catalyst can be applied to the direct amination of nitroarenes and arylboronic acid,thus constructing various valuable diarylamines in high to excellent yields with a wide substrate scope and good functional group tolerance.It is worth noting that this heterogeneous catalyst has high chemical stability and can be recycled for at least five times without reducing its activity.
基金financial support of the TMA pai scholarship from the Manipal Institute of Technology,Manipal Academy of Higher Education,Manipal,in achieving this milestone。
文摘Graphitic carbon nitride(g-C_(3)N_(4)),known for its green and abundant nature and composed of carbon and nitrogen in a two-dimensional structure,has emerged as a significant area of interest across various disciplines,particularly in energy conversion and storage.Its recent demonstrations of high potential in supercapacitor applications mark it as a promising alternative to graphene within the realm of materials science.Numerous favorable features,such as chemical and thermal stability,abundant nitrogen content,eco-friendly attributes,and gentle conditions for synthesis,are shown.This review summarizes recent advancements in the use of g-C_(3)N_(4)and its composites as electrodes for supercapacitors,highlighting the advantages and issues associated with g-C_(3)N_(4)in these applications.This emphasizes situations where the composition of g-C_(3)N_(4)with other materials,such as metal oxides,metal chalcogenides,carbon materials,and conducting polymers,overcomes its limitations,leading to composite materials with improved functionalities.This review discusses the challenges that still need to be addressed and the possible future roles of g-C_(3)N_(4)in the research of advanced supercapacitor technology,such as battery-hybrid supercapacitors,flexible supercapacitors,and photo-supercapacitors.
基金supported by the National Natural Science Foundation of China(Nos.22106105 and 22201180)the Innovation Program of Shanghai Municipal Education Commission(No.2019-01-07-00-E00015)+2 种基金Shanghai Science and Technology Innovation Program(No.21DZ1206300)the Central Local Science and Technology Development Guidance Fund(No.YDZX20213100003002)Shanghai Science and Technology Commission Program(No.20060502200).
文摘Photocatalytic conversion of CO_(2) is pivotal for mitigating the global greenhouse effect and fostering sustainable energy development.Nowadays,polymeric carbon nitride(PCN)has gained widespread application in CO_(2) solar reduction due to its excellent visible light response,suitable conduction band position,and good cost-effectiveness.However,the amorphous nature and low conductivity of PCN limit its photocatalytic efficiency by leading to low carrier concentrations and facile electron–hole recombination during photocatalysis.Addressing this bottleneck,in this study,potassium-doped PCN(KPCN)/copper(Ⅱ)-complexed bipyridine hydroxyquinoline carboxylic acid(Cu(Ⅱ)(bpy)(H_(2)hqc))composite catalysts were synthesized through a multistep microwave heating process.In the composite,the formation of an S-scheme junction facilitates the enrichment of more negative electrons on the conduction band of KPCN via intermolecular electron–hole recombination between Cu(Ⅱ)(bpy)(H_(2)hqc)(CuPyQc)and KPCN,thereby promoting efficient photoreduction of CO_(2) to CO.Microwave heating enhances the amidation reaction between these two components,achieving the immobilization of homogeneous molecular catalysts and forming amidation chemical bonds that serve as key channels for the S-scheme charge transfer.This work not only presents a new PCN-based catalytic system for CO_(2) reduction applications,but also offers a novel microwave-practical approach for immobilizing homogeneous catalysts.
基金supported by the National Natural Science Foundation of China(Nos.52070103 and 22102102)Zhejiang Provincial Natural Science Foundation of China(Nos.LY21E090004 and LQ22B050004)+1 种基金Ningbo Public Welfare Science and Technology Program(No.2021S025)Ningbo Youth Leading Talent Project(No.2024QL038).
文摘Exploration of stable metal single-site supported porous graphitic carbon nitride(PCN)nanostructures and the development of maximum atom utilization for enhanced photocatalytic oxidation of antibiotics remains a challenge in current research.This work proposed a one-step thermal copolymerization to obtain Cu(Ⅰ)doping porous carbon nitride(CUCN)through a spontaneously reducing atmosphere by urea in a covered crucible.The obtained CUCN had crumpled ultrathin nanosheets and mesoporous structures,which possessed higher specific surface areas than PCN.From X-ray absorption near edge structure(XANES)and Fourier transform extended X-ray absorption fine structure(FT-EXAFS)spectra analysis,the Cu doping existed in the oxidation state of Cu(Ⅰ)as single atoms anchored on the 2D layers of CN through two N neighbors,thereby facilitating efficient pathways for the transfer of photoexcited charge carriers.Furthermore,the photoluminescence(PL)spectra,electrochemical impedance spectra(EIS)and transient photocurrent response test proved the improved separation and transfer of photoexcited charge carriers for Cu(Ⅰ)introduction.Consequently,the photocatalytic activity of CUCN was much better than that of PCN for antibiotics norfloxacin(NOR),with 4.7-fold higher degradation reaction rate constants.From species-trapping experiments and density function theory(DFT)calculations,the Cu single atoms in Cu-N_(2)served as catalytic sites that could accelerate charge transfer and facilitate the adsorption of molecular oxygen to produce active species.The stable Cu(Ⅰ)embedded in the layer structure led to the excellent recycling test and remained stable after four runs of degradation and even thermal regenerated treatment.The degradation paths of NOR by CUCN under visible light were also demonstrated.Our work sheds light on a sustainable and practical approach for achieving stable metal single-atom doping and enhancing photocatalytic degradation of aqueous pollutants.
基金M Tahir is funded by EU H2020 Marie Skłodows-ka-Curie Fellowship(1439425).
文摘Graphitic carbon nitride(g-C_(3)N_(4))exhibits great mechanical as well as thermal characteristics,making it a valuable ma-terial for use in photoelectric conversion devices,an accelerator for synthesis of organic compounds,an electrolyte for fuel cell applications or power sources,and a hydrogen storage substance and a fluorescence detector.It is fabricated using dif-ferent methods,and there is a variety of morphologies and nanostructures such as zero to three dimensions that have been designed for different purposes.Ther e are many reports about g-C_(3)N_(4) in recent years,but a comprehensive review which covers nanostructure dimensions and their properties are missing.This review paper aims to give basic and comprehensive understanding of the photocatalytic and electrocatalytic usages of g-C_(3)N_(4).It highlights the recent progress of g-C_(3)N_(4) nano-structure designing by covering synthesis methods,dimensions,morphologies,applications and properties.Along with the summary,we will also discuss the challenges and prospects.Scientists,investigators,and engineers looking at g-C_(3)N_(4) nanostructures for a variety of applications might find our review paper to be a useful resource.
基金National Natural Science Foundation of China(21806023)Natural Science Foundation of Hunan Province(2021JJ40199)+2 种基金Education Department Foundation of Hunan Province(20C0813)Hunan University of Science and Technology Fundamental Research FundsPostgraduate Scientific Research Innovation Project of Hunan Province(CX20240877)。
文摘Elemental doping is an effective strategy for tuning the band structure of graphite carbon nitride(CN)to enhance its photocatalytic performance.In this study,sodium(Na)and oxygen(O)co-doped carbon nitride(Na/O-CN_(x),x=1.0,2.0,3.0,4.0)was synthesized via solid-phase reaction of sodium citrate(NaCA)and pure CN powder in the Teflon-sealed autoclave under air conditions at 180℃.Surface area of Na/O-CN_(3.0) is measured to be 18.8 m^(2)/g,increasing by 60.7%compared to that of pure CN(11.7 m^(2)/g).Bandgap energy of Na/O-CN_(3.0) is determined to be 2.68 eV,marginally lower than that of pure CN(2.70 eV),thereby enhancing its capacity for sunlight absorption.Meanwhile,the incorporation of Na and O atoms into Na/O-CN_(x) is found to effectively reduce recombination rates of photogenerated electron-hole pairs.As a result,Na/O-CN_(x) samples exhibit markedly enhanced photocatalytic hydrogen evolution activity under visible light irradiation.Notably,the optimal Na/O-CN_(3.0) sample achieves a photocatalytic hydrogen production rate of 103.2μmol·g^(–1)·h^(–1),which is 8.2 times greater than that of pure CN(11.2μmol·g^(–1)·h^(–1)).Furthermore,a series of Na/O-CN_(x)-yO_(2)(y=0,20%,40%,60%,80%,100%)samples were prepared by modulating the oxygen content within reaction atmosphere.The catalytic performance evaluations reveal that the incorporation of both Na and O atoms in Na/O-CN_(3.0) enhances photocatalytic activity.This study also introduces novel methodologies for synthesis of metal atom-doped CN materials at lower temperature,highlighting the synergistic effect of Na and O atoms in photocatalytic hydrogen production of Na/O-CN_(x) samples.
基金supported by the Natural Science Foundation Project of Jilin Province(Nos.20230101297JC,YDZJ202201ZYTS347,YDZJ202101ZYTS073,20210101117JC,YDZJ202201ZYTS349,YDZJ202102CXJD049)the National Natural Science Foundation(22004047)+4 种基金China Postdoctoral Science Foundation(No.2023M731299)the Project of Jilin Province Development and Reform Commission(Nos.2023C032-5,2023C032-4,2023C032-2)the Project of Human Resources and Social Security Department of Jilin Province(No.2023337)the National College students’innovation and entrepreneurship training program(No.202310203008)the Project of Education Department of Jilin Province(Nos.JJKH20220429KJ,JJKH20210460KJ).
文摘Integrating photocatalysis technology with peroxymonosulfate oxidation possesses huge potential for degrading stubborn pollutant.Herein,a porous ultra-thin carbon nitride with C-defect O-doping and advanced n-π^(∗)transition was customized by one-pot thermalinduced polymerization of molten urea assisted with paraformaldehyde.Via visible-light coupling peroxymonosulfate activation,the DCN-100 can completely photodegrade 2,4-dichlorophenol,and rate constant is 136.6 and 37.9 times that of CN and DCN-100 without peroxymonosulfate.The light-absorption of DCN-100 surpasses 550 nm,specific surface area rises from 45.03 to 98.58m^(2)/g,and charge behaviors are significantly improved.The effects of paraformaldehyde amount,PMS dosage,pH,2,4-dichlorophenol concentration,different water-body,wavelength and recycling times on photodegradation performance were explored in detail.Via capture experiments,ESR,LC-MS,Fukui-function,TEXT toxicity assessment and DFT theoretical calculation,themain active substances,degradation pathway,intermediate toxicity and enhanced activity mechanism of DCN-100 were clarified.The research provides a cost-effective,high-efficiency and environmental-friendly photocatalysts to activate peroxymonosulfate for water remediating.
基金supported by the National Natural Science Foundation of China(82301052)China Postdoctoral Science Foundation(2023M732151)+3 种基金Shanxi Provincial Science and Technology Department(202303021212131)Health Commission of Shanxi Province(2022XM14)Shanxi Provincial Education Department(2022L165)Shanxi Medical University(XD2232)。
文摘The huge carrier transfer resistance caused by large-sized"nitrogen pot"severely limits the photocatalytic performance of carbon nitride(CN).This study aims to explore the selection principle of metal ion bridges for constructing dual carrier-transfer channels to delivery carriers to respectively active sites using photodegradation of phenol as the model reaction.Density functional theory(DFT)calculation was used to optimize the structure model of nitrogen vacancies(Nv,provide active sites for reduction of O_(2) and oxidation of phenol)and metal ions(Fe^(3+),Co^(2+),Ni^(2+)or Cu^(2+))co-modified CN,and screen metal ion bridges based on the three parameters including bonding state of metal ion and"nitrogen pot",electrostatic potential(ESP)distribution around the active sites,and three-electron bond length.Both calculation results and activity data show that Fe^(3+),Co^(2+)and Ni^(2+)can construct dual carrier-transfer channels to promote the degradation of phenol while Cu^(2+)cannot Ny and Fe^(3+)co-modified CN(Fe/N_(v)-CN)showed the best catalytic performance among various catalysts and was used as the model catalyst for the detailed characterization to verify the calculation results.This work provides not only the novel strategy for constructing dual carrier-transfer channels in CN,but also the crucial basis for computer simulation as a prediction tool of catalyst structure design rationality.
基金supported by the Natural Science Foundation of the Jiangsu Higher Education Institutes of China(No.22KJB530006)Hainan Provincial Natural Science Foundation of China(No.824QN267)。
文摘The rapid emergence of drug-resistant bacterial strains undermines the efficacy of conventional antibiotics,necessitating the development of alternative therapies.Antimicrobial photodynamic therapy(PDT)is a promising approach,but its effectiveness is often limited by the suboptimal photocatalytic activity of photosensitizers.In this study,we introduce a novel photoresponsive carbon-based antibacterial agent,Ce6/g-C_(3)N_(4),which combines the photocatalytic properties of graphite-phase carbon nitride(g-C_(3)N_(4))with the photodynamic attributes of chlorin e6(Ce6).This agent,with an average particle size of 250.7 nm,demonstrates significantly enhanced photocatalytic activity.Additionally,the strong affinity of Ce6/g-C_(3)N_(4)for bacteria and efficient delivery of Ce6 result in an inhibition rate exceeding 99%against Gram-positive bacteria and excellent biofilm eradication under light irradiation.In vivo experiments reveal that Ce6/gC_(3)N_(4)effectively inhibits bacterial growth on wounds,and promotes wound healing post-light treatment,while maintaining good biocompatibility.Overall,the Ce6/g-C_(3)N_(4)antibacterial agent synergizes photodynamic and photocatalytic mechanisms,offering a new avenue for the photo-mediated,multi-strategic treatment of bacterial infections and wound healing.
基金supported by the National Natural Science Foundation of China(22361024 and 22471055)Natural Science Foundation of Jiangxi Province(20232ACB203001)+1 种基金Natural Science Foundation of Hebei Province(B2024202021,B2022202039)S&T Program of Hebei(236Z4308G)。
文摘The photocatalytic hydrogen peroxide(H_(2)O_(2))production by graphitic carbon nitride is a sustainable and environment-benign alternative approach of conventional anthraquinone autoxidation technology,but it is great challenges to promote two-electron O_(2)reduction and water oxidation.Herein,we present the well-dispersed graphitic carbon nitride quantum dots decorated with cyano groups(Na-CNQD and K-CNQD)by thermal polymerization of melamine in the presence of metal fluoride.The quantum confinement and edge effect have endowed the photocatalysts with rich active sites,wide light absorption range and the inhibited charge recombination.The cyano moieties function as O_(2)reduction centers to accept the photogenerated electrons and facilitate their rapid transfer to O_(2)molecules.This process enables the selective two-electron reduction of O_(2),leading to the production of H_(2)O_(2).Concurrently,the valence band holes on the heptazine moiety oxidize water into H_(2)O_(2).These synergistic effects promote photocatalytic H_(2)O_(2)production from O_(2)and H_(2)O without the need for additional photosensitizers,organic scavengers and co-catalysts.In contrast,pristine carbon nitride nanosheets remain inactive under the same conditions.This study offers new strategies for rational design of carbon-based materials for solar-to-chemical energy conversion.
文摘The photocatalytic oxidation of methane to methanol using molecule oxygen directly is an attractive catalytic reaction,but designing catalysts to avoid over-oxidation remains a significant challenge.Herein,Cu single-atom anchored on the defective carbon nitride structure(Cu SA/Def-CN)is designed for selective photocatalytic oxidation of methane into methanol using O_(2) under mild conditions.The Cu SA/Def-CN catalyst exhibits a high methanol selectivity of 92.8%under optimized conditions.Mechanistic studies reveal a synergistic effect between Def-CN and Cu SA,where Def-CN is responsible for the in-situ generation of hydrogen peroxide,which is subsequently decomposed by the Cu SA sites to produce·OH radicals that play a key role in the rate-determining step of methane activation to form methanol.Additionally,the presence of Cu SA not only enhances the electron-hole separation efficiency and improves the transfer of the photo-generated charges,but also increases the number of active sites for methane adsorption and activation.These insights provide valuable guidance for designing efficient catalysts for the highly selective photocatalytic oxidation of methane to methanol.
基金financial support from the National Natural Science Foundation of China(No.22171249)the Science&Technology Innovation Talents in Universities of Henan Province(No.23HASTIT003)。
文摘The development of innovative and sustainable catalytic strategies for organic synthesis is a pivotal aspect of advancing material science and chemical engineering.This research presents a new catalytic method for the aminoacylation of N-sulfonyl ketimines by utilizing a potassium-doped graphite-like carbon nitride(g-C_(3)N_(4))framework.This method not only enhances the catalytic efficiency and broadens the light absorption spectrum of g-C_(3)N_(4)but also significantly reduces the recombination rate of electronhole pairs,thereby increasing the reaction yield and selectivity.Importantly,our approach facilitates the synthesis of aminoacylated N-heterocycles,expanding the applicability of potassium-modified g-C_(3)N_(4)in photocatalytic organic synthesis.A notable accomplishment of this study is the unprecedented generation of carbamoyl radicals via heterogeneous photocatalysis,which can be easily recycled after reaction.This advancement highlights the capability of potassium-doped g-C_(3)N_(4)(namely K-CN)as an advanced heterogeneous photocatalyst for the formation of complex organic compounds.
基金the National Natural Science Foundation of China(Nos.52488201,52376209)the Fundamental Research Funds for the Central Universities.Zhenxiong Huang thanks the Key Project of Jiangxi Academy of Science(No.2022YYB05)the Science and Technology Innovation Project for Carbon Peak and Neutrality of Jiangxi Carbon Neutralization Research Center(2022JXST02).
文摘Solar-driven photocatalytic overall water splitting(POWS)has emerged as a sustainable pathway for hydrogen production,yet faces intrinsic challenges in developing robust catalysts that balance efficiency,stability,and cost-effectiveness.Polymeric carbon nitride(PCN)represents as a promising metal-free photocatalyst for hydrogen production due to the merits of unique electronic structure and exceptional thermal stability.Nevertheless,limited by rapid charge recombination and insufficient oxidative capability,little success has been achieved on pristine PCN photocatalyst in POWS.In this context,recent advances have demonstrated multi-dimensional modification strategies for improving POWS performance.Based on the fundamental principles of photocatalysis,this review discusses the advantages and challenges of PCN-based photocatalysts in POWS systems.With critical evaluation on one-step excitation systems and Z-scheme two-step excitation systems,modification strategies including crystallinity engineering,supramolecular precursor design,cocatalyst modulation,and construction of PCN-based heterojunctions and homojunctions were highlighted by introducing representative advances in POWS application over the past five years.Future perspectives for PCN-based photocatalysts are proposed,aiming to provide new insights for the design of advanced photocatalytic system for efficient POWS.
基金supported by the National Natural Science Foundation of China(No.52173267)the Key Laboratory of High Temperature Electromagnetic Materials and Structure of MOE(No.KB202402).
文摘Graphitic carbon nitride(g-C_(3)N_(4))has garnered significant attention due to its remarkable advantages such as lightweight,exceptional chemical stability and defect-rich surface.Nevertheless,its inadequate electrical conductivity and impedance matching hindered the practical implementation in the electromagnetic wave absorption(EMWA)field.To address these challenges,we developed a composites system of carbon spheres/g-C_(3)N_(4)(CCN)through a supramolecular self-assembly strategy,subsequently integrated with reduced graphene oxide(RGO)via a water bath method.Systematic investigation revealed that the EMWA performance of CCN/RGO composites exhibited a distinct dependence(a trend of first increasing and then decreasing)on RGO content.Especially,when the mass ratio of RGO to CCN was 20%,the CCN/RGO composite brought a minimum reflection loss value of-45.40 dB at 13.44 GHz and a broad effective absorbing bandwidth of 6.32 GHz at 2.19 mm.First-principles calculations based on density functional theory suggested that the constructed heterostructure effectively facilitated electron mobility and charge redistribution,boosting both conductive loss and polarization loss mechanisms.The exceptional absorption performance was ascribed to the synergistic effects of conductive loss,relaxation loss,and suitable impedance matching.As a results,this work provided a rational design strategy for high-performance g-C_(3)N_(4)-based EMWA materials.
基金Project supported by the National Natural Science Foundation of China(22102141)。
文摘The utilization of visible light for photocatalytic nitrogen fixation offers a sustainable and eco-friendly strategy for the production of ammonia.The present study focuses on the synthesis of a series of rare earth-doped carbon nitride composite ultraviolet-activated Ce-UiO-66 catalysts,denoted as RECNactMOF,for efficient nitrogen fixation.Rare earth doping modulates the band structure of carbon nitride,facilitating the formation of a type-I heterojunction with Ce-UiO-66 and promoting photocarrier generation at nitrogen fixation sites.Among these,Sm-doped SmCN-actMOF exhibits high visible-light absorption and efficient utilization of photocarriers,resulting in an apparent quantum efficiency(AQE)of 1.58%under 495 nm light irradiation.This study provides a pathway for enhancing the nitrogen fixation efficiency of photocatalysts through the incorporation of rare earth elements,and expanding the potential applications of rare earth materials in the field of photocatalysis.
基金supported by the National Key Research and Development Program of China(No.2023YFC3705901)。
文摘Photocatalytic hydrogen peroxide(H_(2)O_(2))production has been considered as a promising strategy for H_(2)O_(2)synthesis due to its environmentally friendly.Among various photocatalysts,carbon nitride-based materials are excellent candidates for H_(2)O_(2)production because of their excellent visible-light response,low cost and high stability.In this review,we summarize in detail the research progress on the photocatalytic production of H_(2)O_(2)by carbon nitride.First,we summarize the basic principles of photocatalysis and photocatalytic H_(2)O_(2)production.Second,the classification and modification methods of carbonnitride-based materials are discussed,including morphology modulation,noble metal loading,defect control,heterojunction regulation,molecular structure engineering and elemental doping.Finally,the different in-situ applications of H_(2)O_(2)via photosynthesis were discussed,including disinfection and antibiotic resistant genes degradation,organic pollutants degradation,medical applications and fine chemical synthesis.This review brings great promise for in-situ H_(2)O_(2)photosynthesis,which is expected to serve as a key component in future applications.
基金supported by the National Natural Science Foundation of China(No.22202033)National College Students Innovation and Entrepreneurship Training Program(No.202310347048)Zhejiang Provincial Training Programs of Innovation and Entrepreneurship for Undergraduates(No.S202310347032)。
文摘Photocatalytic H_(2) evolution from wastewater exhibits fascinating prospects in environment and energy fields.Here,we propose a novel 3D cross-linked g-C_(3)N_(4) network(SCN)assembling with 1D nanowires.This network structure endows SCN with abundant carbon defects,creating a defect energy level and shallow charge trapping centres,which significantly prolongs the photocarrier lifetime,suppresses their recombination and facilitates the mass transfer process during the dye photodegradation.Consequently,in photocatalytic H_(2) evolution coupled with Rhodamine B(RhB)photodegradation under visible light,the H_(2) production rate of SCN is 283μmol h^(-1)g^(-1),accompanying by 97%RhB photodegradation efficiency,much higher than UCN's 31μmol h^(-1)g^(-1)and 64%.In particular,AQY of SCN for H_(2) evolution from RhB solution reaches 23.7%at 380 nm.Furthermore,the calculated transition states demonstrate that the N1 site connected to the defect in SCN has a minimum Gibbs free energy ΔG(H^(*)),indicating that H~+undergoes an H^(+)→H^(*)→H_(2) evolution process.
基金financially supported by the Natural Science Foundation of China(Nos.21972058,22102064,and 22302080)Anhui Key Laboratory of Nanomaterials and Nanotechnology,the Major Science and Technology Projects in Anhui Province(No.202305a12020006).
文摘The integration of selective oxidation of renewable biomass and its derivatives with hydrogen(H_(2))pro-duction holds significant potential for simultaneously yielding value-added chemicals and“green H_(2)”,contributing to addressing sustainability challenges.The S-scheme charge transfer mechanism enhances charge separation by maintaining strong redox potentials at both ends,facilitating both oxidation and reduction reactions.Herein,we synthesize a visible-light-responsive oxygen vacancy-rich In_(2)O_(3-x)/tubular carbon nitride(IO_(OV)/TCN)S-scheme heterojunction photocatalyst via electrostatic adherence for selec-tive 5-hydroxymethylfurfural(HMF)oxidation to 2,5-diformylfuran(DFF)and 2,5-furandicarboxylic acid(FDCA),alongside H_(2)production.Under anaerobic conditions and visible-light irradiation,the optimal IOOV/TCN-10 catalyst achieves an HMF conversion of 94.8%with a selectivity of 53.6%for DFF and FDCA,and a H_(2)yield of 754.05μmol g^(−1)in 3 h.The significantly improved photocatalytic activity results from enhanced visible-light absorption,reduced carrier recombination,and abundant catalytic active sites due to the synergistic effect of surface oxygen vacancies,the hollow nanotube-based architecture,and the S-scheme charge transfer mechanism.This work highlights the great potentials of S-scheme heterojunctions in biomass conversion for sustainable energy use and chemical production.
基金supported by the National Basic Research Program of China(2011CB933700)the National Natural Science Foundation of China(21271165)~~
文摘With the objectives of enhancing the stability,optical properties and visible-light photocatalytic activity of photocatalysts,we modified oxygen vacancy-rich zinc oxide（Vo-ZnO） with graphitic carbon nitride（g-C3N4）. The resulting g-C3N4/Vo-ZnO hybrid photocatalysts showed higher visible-light photocatalytic activity than pure Vo-ZnO and g-C3N4. The hybrid photocatalyst with a g-C3N4 content of 1 wt% exhibited the highest photocatalytic degradation activity under visible-light irradiation（λ≥ 400 nm）. In addition,the g-C3N4/Vo-ZnO photocatalyst was not deactivated after five cycles of methyl orange degradation,indicating that it is stable under light irradiation. Finally,a Z-scheme mechanism for the enhanced photocatalytic activity and stability of the g-C3N4/Vo-ZnO hybrid photocatalyst was proposed. The fast charge separation and transport within the g-C3N4/Vo-ZnO hybrid photocatalyst were attributed as the origins of its enhanced photocatalytic performance.
