The growing global demand for sustainable solutions to address energy and environmental challenges has spurred significant interest in catalytic technologies.Piezocatalysis has emerged as a sustainable technology for ...The growing global demand for sustainable solutions to address energy and environmental challenges has spurred significant interest in catalytic technologies.Piezocatalysis has emerged as a sustainable technology for environmental remediation and energy conversion because of its unique characteristics of harvesting mechanical energy into electrochemical energy.Versatile BiFeO_(3)(BFO)stands out among a range of piezocatalysts for its distinctive integration of piezoelectric,multiferroic,and optical properties.This review critically examines piezocatalytic mechanisms,including energy band theory,screening charge effects,and displacement current theory,revealing the intricate roles of internal charges,screening charges,and piezoelectric electrons in driving catalytic reactions.Furthermore,the evolution of BFO-based piezocatalysis is systematically reviewed,emphasizing its structural characteristics,representative synthesis methods,performance optimization strategies,and diverse applications,such as organic pollutant degradation,H_(2) production,H_(2)O_(2)generation,CO_(2)reduction,and sterilization.In particular,the underestimated ferroelectric polarization effect of BFO on CO_(2)reduction is critically analyzed and elaborated.This review identifies critical challenges and outlines future research directions to advance high-efficiency BFO-based piezocatalytic systems.Overall,this comprehensive analysis underscores the potential of BFO in piezocatalysis,bridging materials engineering with practical applications and offering insights into future advancements.展开更多
This review provides an insightful and comprehensive exploration of the emerging 2D material borophene,both pristine and modified,emphasizing its unique attributes and potential for sustainable applications.Borophene...This review provides an insightful and comprehensive exploration of the emerging 2D material borophene,both pristine and modified,emphasizing its unique attributes and potential for sustainable applications.Borophene’s distinctive properties include its anisotropic crystal structures that contribute to its exceptional mechanical and electronic properties.The material exhibits superior electrical and thermal conductivity,surpassing many other 2D materials.Borophene’s unique atomic spin arrangements further diversify its potential application for magnetism.Surface and interface engineering,through doping,functionalization,and synthesis of hybridized and nanocomposite borophene-based systems,is crucial for tailoring borophene’s properties to specific applications.This review aims to address this knowledge gap through a comprehensive and critical analysis of different synthetic and functionalisation methods,to enhance surface reactivity by increasing active sites through doping and surface modifications.These approaches optimize diffusion pathways improving accessibility for catalytic reactions,and tailor the electronic density to tune the optical and electronic behavior.Key applications explored include energy systems(batteries,supercapacitors,and hydrogen storage),catalysis for hydrogen and oxygen evolution reactions,sensors,and optoelectronics for advanced photonic devices.The key to all these applications relies on strategies to introduce heteroatoms for tuning electronic and catalytic properties,employ chemical modifications to enhance stability and leverage borophene’s conductivity and reactivity for advanced photonics.Finally,the review addresses challenges and proposes solutions such as encapsulation,functionalization,and integration with composites to mitigate oxidation sensitivity and overcome scalability barriers,enabling sustainable,commercial-scale applications.展开更多
With the rapid advancement of computing and information technology at the turn of the 21st century,the power of data collection and processing has multiplied tremendously.Based on this a game-changing advancement,scie...With the rapid advancement of computing and information technology at the turn of the 21st century,the power of data collection and processing has multiplied tremendously.Based on this a game-changing advancement,science is at the advent of the “fourth paradigm”of massive data plus artificial intelligence,in which the efficiency of scientific research is continuously improved,research time is shortened,and research cost is reduced[1].展开更多
This study presents a facile and rapid method for synthesizing novel Layered Double Hydroxide(LDH)nanoflakes,exploring their application as a photocatalyst,and investigating the influence of condensed phosphates'g...This study presents a facile and rapid method for synthesizing novel Layered Double Hydroxide(LDH)nanoflakes,exploring their application as a photocatalyst,and investigating the influence of condensed phosphates'geometric linearity on their photocatalytic properties.Herein,the Mg O film,obtained by plasma electrolysis of AZ31 Mg alloys,was modified by growing an LDH film,which was further functionalized using cyclic sodium hexametaphosphate(CP)and linear sodium tripolyphosphate(LP).CP acted as an enhancer for flake spacing within the LDH structure,while LP changed flake dispersion and orientation.Consequently,CP@LDH demonstrated exceptional efficiency in heterogeneous photocatalysis,effectively degrading organic dyes like Methylene blue(MB),Congo red(CR),and Methyl orange(MO).The unique cyclic structure of CP likely enhances surface reactions and improves the catalyst's interaction with dye molecules.Furthermore,the condensed phosphate structure contributes to a higher surface area and reactivity in CP@LDH,leading to its superior photocatalytic performance compared to LP@LDH.Specifically,LP@LDH demonstrated notable degradation efficiencies of 93.02%,92.89%,and 88.81%for MB,MO,and CR respectively,over a 40 min duration.The highest degradation efficiencies were observed in the case of the CP@LDH sample,reporting 99.99%for MB,98.88%for CR,and 99.70%for MO.This underscores the potential of CP@LDH as a highly effective photocatalyst for organic dye degradation,offering promising prospects for environmental remediation and water detoxification applications.展开更多
The hybridization of metal-organic framework(MOF)with inorganic layers would lead to the discovery of novel hybrid materials that can provide a compelling strategy for enhancing its photocatalytic and electrochemical ...The hybridization of metal-organic framework(MOF)with inorganic layers would lead to the discovery of novel hybrid materials that can provide a compelling strategy for enhancing its photocatalytic and electrochemical response.In the present study,a highly efficient multifunctional hybrid material was developed by exploiting the defective layer formed on AZ31 Mg alloy through plasma electrolytic oxidation(PEO)as a nucleation and growth site for Co-MOF.The concentrations of the organic linker 2-Methylimidazole(2,MIm)and cobalt nitrate as a source of Co^(2+) ions were varied to control the growth of the obtained Co-MOF.Lower concentrations of the 2,MIm ligand favored the formation of leaf-like MOF structures through an anisotropic,two-dimensional growth,while higher concentrations led to rapid,isotropic nucleation and the creation of polyhedral Co-MOF structures.The sample characterized by polyhedral Co-MOF structures exhibited superior electrochemical stability,with the lowest corrosion current density(3.11×10^(-9) A/cm^(2))and the highest top layer resistance(2.34×10^(6)Ωcm^(2)),and demonstrated outstanding photocatalytic efficiency,achieving a remarkable 99.98%degradation of methylene blue,an organic pollutant,in model wastewater.To assess the active adsorption sites of the Co-MOF,density functional theory(DFT)was utilized.This study explores the changes in morphologies of the coatings of Co-MOF with the change of solution concentration to form coatings with enhanced properties on the metallic substrate,which could establish the groundwork for the development of next-generation multifunctional frameworks with diverse applications.展开更多
This paper studies the antimicrobial activity of selected engineering materials surfaces at room and chill temperatures. The antimicrobial effects of selected materials surfaces were evaluated by dropping the test pie...This paper studies the antimicrobial activity of selected engineering materials surfaces at room and chill temperatures. The antimicrobial effects of selected materials surfaces were evaluated by dropping the test pieces into prepared cultures of Bacillus spp, Escherichia coli, and Staphylococcus aereus isolated from fruits, animal feaces and natural environment respectively. Bacteria count obtained after 0, 30, 60, 90, 120, 180, 240 and 300 minutes at room temperature and chill condition was taken and compared with their initial count. The amount of live bacteria drops by several orders of magnitude, to zero, on metallic copper and brass within 30 to 300 minutes in both room and chill conditions. In contrast, no reduction is seen in the number of colonies of live bacteria on plastics, ceramic and stainless steel in both room and chill conditions. These results suggest that the selection of metallic copper and brass for touch surfaces in hospitals, surfaces exposed to fruit processing and household utensils can materially assist in reducing bacterial contamination, which should lead to a reduction in the transmission of infectious organisms.展开更多
Herein,cure characteristics,morphology,and mechanical properties of natural rubber filled with activated carbon-based materials were investigated.Carbon-based materials were prepared from bagasse,coffee grounds and pi...Herein,cure characteristics,morphology,and mechanical properties of natural rubber filled with activated carbon-based materials were investigated.Carbon-based materials were prepared from bagasse,coffee grounds and pineapple crowns by the pyrolysis method at temperatures in the range of 300℃.As-synthesized carbon materials were characterized by optical microscopy(OM),scanning electron microscopy(SEM),and Fourier-transform infrared spectroscopy(FTIR)to analyze size distribution,morphology,and functional groups,respectively.OM and SEM analysis revealed that particles,flakes,and a small quantity of fiber-like carbon were obtained using bagasse and pineapple crown as raw materials,while honeycomb-like carbon materials can be derived from coffee grounds.To investigate the mechanical properties,natural rubber was filled with carbon black and as-synthesized carbon materials by the internal mixing and compression molding process.Transmission electron microscopy(TEM)was utilized to characterize the dispersion of carbon materials in the rubber matrix.The results of tensile testing showed that the natural rubber mixed with as-synthesized carbon materials from pineapple crowns exhibited 54%and 74%improvement in the ultimate tensile strength and Young’s modulus,respectively,compared with natural rubber without filled carbon materials.The enhancement in mechanical properties by activated carbon materials derived from pineapple crowns can be attributed to the flake-and fiber-like structures and good dispersion of carbon materials in the rubber matrix.In addition,it is higher than that of rubber mixed with carbon black.The results demonstrated that as-synthesized carbon materials from pineapple crowns have the potential materials to substitute carbon black in the rubber compound industry.展开更多
As battery technology evolves and demand for efficient energy storage solutions,aqueous zinc ion batteries(AZIBs)have garnered significant attention due to their safety and environmental benefits.However,the stability...As battery technology evolves and demand for efficient energy storage solutions,aqueous zinc ion batteries(AZIBs)have garnered significant attention due to their safety and environmental benefits.However,the stability of cathode materials under high-voltage conditions remains a critical challenge in improving its energy density.This review systematically explores the failure mechanisms of high-voltage cathode materials in AZIBs,including hydrogen evolution reaction,phase transformation and dissolution phenomena.To address these challenges,we propose a range of advanced strategies aimed at improving the stability of cathode materials.These strategies include surface coating and doping techniques designed to fortify the surface properties and structure integrity of the cathode materials under high-voltage conditions.Additionally,we emphasize the importance of designing antioxidant electrolytes,with a focus on understanding and optimizing electrolyte decomposition mechanisms.The review also highlights the significance of modifying conductive agents and employing innovative separators to further enhance the stability of AZIBs.By integrating these cutting-edge approaches,this review anticipates substantial advancements in the stability of high-voltage cathode materials,paving the way for the broader application and development of AZIBs in energy storage.展开更多
In lithium-sulfur batteries(LSBs),the limited utilization of sulfur and the sluggish kinetics of redox reaction significantly hinder their electrochemical performance,especially under high rates and high sulfur loadin...In lithium-sulfur batteries(LSBs),the limited utilization of sulfur and the sluggish kinetics of redox reaction significantly hinder their electrochemical performance,especially under high rates and high sulfur loadings.Here,we propose a novel separator structure with an interlayer composed of a vermiculite nanosheet combined with Ketjen Black(VMT@KB)for LSBs,facilitating efficient adsorption and rapid catalytic conversion toward lithium polysulfides(LiPSs).The VMT@KB nanosheets with an electrical double-layer structure and electronic conductivity are obtained through a high-temperature peeling process and Li^(+)exchange treatment in LiCl solution,followed by a mechanical combination process with KB.The results demonstrate that incorporating VMT@KB as an interlayer on a conventional separator enhances the conductivity and limits the LiPSs in the cathode region.The Li-S cell with VMT@KB interlayer shows satisfactory cycle and rate performance,especially in high sulfur loading.It exhibits a remarkable initial discharge capacity of 1225 mAh g^(-1)at 0.5 C and maintains a capacity of 816 mAh g^(-1)after 500 cycles.Besides,the discharge capacity remains 462 mAh g^(-1)even at 6 C.Moreover,the cell with high sulfur loading(8.2 mg cm^(-2))enables stable cycling for 100 cycles at 0.1 C with a discharge capacity of over1000 mAh g^(-1).展开更多
To guarantee the efficient and high-value reutilization of waste concrete from construction waste,the waste concrete was mechanically ground,and three degrees of fineness recycled concrete powder(RCP)were obtained by ...To guarantee the efficient and high-value reutilization of waste concrete from construction waste,the waste concrete was mechanically ground,and three degrees of fineness recycled concrete powder(RCP)were obtained by different grinding time.By analyzing the particle characteristics of RCP with different fineness,the filling-densification effect of cement-RCP cementitious material system was quantitatively investigated based on Andreasen,Fuller,and Aim-Goff models.In addition,the macroscopic mechanical properties of cement paste mixed with RCP were studied,and the influencing mechanisms of RCP on the microstructure of cement paste was revealed.Macroscopic research results show that the particle fineness of RCP after grinding is smaller than that of cement.When the RCP replaces 0%to 20%cement,the packing density based on the Aim-Goff model increases with the increase of RCP content,whereas the macro-mechanical properties first improve and then degrade with the increase of RCP content.Microscopic results show that at 5%RCP content,beneficial hydration products such as C-S-H and beneficial pore increase in cement-RCP paste;while at>15%content,beneficial products decrease and harmful substances such as Ca(OH)_(2)and harmful pore increases.These research findings suggest that the incorporation of RCP can make the cementitious system denser,and the appropriate RCP content can improve the macro-and microscopic properties of cement-based materials.展开更多
Although manganese-based oxide is regarded as a promising cathode material for zincion hybrid supercapacitors(ZHSCs),its practical application is hindered by slow zinc ion diffusion and the instability of MnO_(2).To o...Although manganese-based oxide is regarded as a promising cathode material for zincion hybrid supercapacitors(ZHSCs),its practical application is hindered by slow zinc ion diffusion and the instability of MnO_(2).To overcome this obstacle,a δ-MnO_(2)/MXene heterostructure was created using a simple one-step process under gentle condition.The ZHSC was assembled using this heterostructure as the cathode,activated carbon(AC)as the anode and 2 mol·L−1 ZnSO_(4) as the electrolyte.The resultingδ-MnO_(2)/MXene//ZnSO4//AC ZHSC shows a maximum specific capacitance of 97.4 F·g^(−1) and an energy density of 32.27 Wh·kg^(−1) at the best cathode-to-anode mass ratio.Ex situ characterizations reveal the reversible energy storage mechanism combing Zn^(2+)insertion/extraction in the cathode,ion adsorption and desorption on the anode surface,and partial reversible formation and dissolution of Zn_(4)SO_(4)(OH)_(6)·5H_(2)O(ZHS)components on both electrodes.Adding of Mn^(2+)to the electrolyte reduced Mn dissolution,improving the ZHSC’s specific capacitance and energy density to 140.4 F·g^(−1) and 49.36 Wh·kg^(−1),respectively,while also enhancing its rate performance and cyclability.The improved electrochemical reaction kinetics was verified through various tests.The results suggest that the δ-MnO_(2)/MXene heterostructure has great potential as a high-performance cathode material for ZHSCs.展开更多
Solution-processed Cu(In,Ga)Se_(2)(CIGS) solar cells suffer from serious carrier recombination and power conversion efficiency(PCE) loss because of the poor film properties and easy formation of defects.Herein, we pro...Solution-processed Cu(In,Ga)Se_(2)(CIGS) solar cells suffer from serious carrier recombination and power conversion efficiency(PCE) loss because of the poor film properties and easy formation of defects.Herein, we propose Ag&Se co-selenization strategy to enhance the crystallization and passivate harmful defects of the CIGS films. The formation of Ag-Se phase during the selenization process enables the formation of large grains and suppresses the deep level defects. It is found that Ag doping can enlarge the depletion region width, lower the Urbach energy and prolong the carrier lifetime. As a result, a champion solution-processed CIGS solar cell presents a high efficiency of 16.48% with the highly improved opencircuit voltage(VOC) of 662 m V and fill factor(FF) of 75.8%. This work provides an efficient strategy to prepare high quality solution-processed CIGS films for high-performance CIGS solar cells.展开更多
The crisis of excessive increase in CO_(2)emissions has quickly become a serious issue and requires low-cost and bio-compatible solutions.The employee of membrane technology for CO_(2)gas separation has garnered signi...The crisis of excessive increase in CO_(2)emissions has quickly become a serious issue and requires low-cost and bio-compatible solutions.The employee of membrane technology for CO_(2)gas separation has garnered significant interest among researchers.However,this method encounters challenges related to selectivity and permeability.Therefore,modifying and reinforcing the polymer membranes to improve gas separation performance seems essential.Among the various methods for polymer membrane modification,modification with magnesium-based fillers to prepare a mixed matrix membrane(MMM)is considered an efficient method.Owing to magnesium metal's low weight,low density,high strength,and good selectivity,magnesium-based materials(Mg-based materials)have more porosity,higher available surface area,more adsorption sites,lighter weight,and more gas absorption tendency than other fillers,which makes them an attractive choice for the preparation of gas separation MMMs.This research deals with the introduction of Mg-based materials,various methods of synthesis of Mg-based materials,different methods of introducing Mg-based materials into the membrane matrix,and their effect on the performance of MMMs in CO_(2)gas separation applications.Therefore,this review can provide researchers with light horizons in using the high potential of Mg-based materials as efficient fillers in MMMs to achieve excellent permeability and selectivity and generally improve their performance in CO_(2)gas separation applications.展开更多
Accurate determination and rapid degradation of organic pollutants are essential works in environmental improvement.Herein,the CuCo_(2)S_(4)@Co_(3)O_(4) heterojunction with fascinating 2D-on-3D hierarchical nanoflower...Accurate determination and rapid degradation of organic pollutants are essential works in environmental improvement.Herein,the CuCo_(2)S_(4)@Co_(3)O_(4) heterojunction with fascinating 2D-on-3D hierarchical nanoflowers architecture and highly distributed interface sites were successfully synthesized by CuCo-LDH topological transformation combine with in situ exterior sulfurization strategy.The 2D-on-3D nanoflowers architecture could improve light harvesting ability,provide large surface area,open channels and abundant edge sites.In particular,the intensive M-O-S-M heterojunction interface not only promote the photoexcited charge shuttling but provide abundant interface sites to enhance catalytic activity.As expected,the photocatalytic degradation rate of diclofenac sodium(DCF)on CuCo_(2)S_(4)@Co_(3)O_(4) was approximately 100%within 30 min under 300 W mercury lamp,which was 1.28 times and 1.45 times higher than that of CuCo-LDH and CuCo_(2)O_(4).The degradation rate for real samples weremore than 80%,themineralization rate was 90%,and the biological toxicity of degradation products decreased significantly.Furthermore,a novel photoelectrochemistry(PEC)sensorwith CuCo_(2)S_(4)@Co_(3)O_(4) as a photoanodewas successfully constructed for directly sensing DCF,showing a wide linear range and satisfactory detection limit.The results indicate that the CuCo_(2)S_(4)@Co_(3)O_(4) possess dual-functional peculiarity,hold vast potential for sensing and degradation environmental pollutants in wastewater.展开更多
Zinc-ion hybrid capacitors (ZIHCs) have received increasing attention as energy storage devices owing to their low cost,high safety,and environmental friendliness.However,their progress has been hampered by low energy...Zinc-ion hybrid capacitors (ZIHCs) have received increasing attention as energy storage devices owing to their low cost,high safety,and environmental friendliness.However,their progress has been hampered by low energy and power density,as well as unsatisfactory long-cycle stability,mainly due to the lack of suitable electrode materials.In this context,we have developed manganese single atoms implanted in nitrogen-doped porous carbon nanosheets (MnSAs/NCNs) using a metal salt template method as cathodes for ZIHCs.The metal salt serves a dual purpose in the synthesis process:It facilitates the uniform dispersion of Mn atoms within the carbon matrix and acts as an activating agent to create the porous structure.When applied in ZIHCs,the MnSAs/NCNs electrode demonstrates exceptional performance,including a high capacity of 203 m Ah g^(-1),an energy density of 138 Wh kg^(-1)at 68 W kg^(-1),and excellent cycle stability with 91%retention over 10,000 cycles.Theoretical calculations indicate that the introduced Mn atoms modulate the local charge distribution of carbon materials,thereby improving the electrochemical property.This work demonstrates the significant potential of carbon materials with metal atoms in zinc-ion hybrid capacitors,not only in enhancing electrochemical performance but also in providing new insights and methods for developing high-performance energy storage devices.展开更多
Ceria-stabilized tetragonal zirconia(Ce-TZP)has become an interesting alternative for the widely used yttria-stabilized zirconia(Y-TZP),whereas efforts are needed to control its microstructure in order to im-prove the...Ceria-stabilized tetragonal zirconia(Ce-TZP)has become an interesting alternative for the widely used yttria-stabilized zirconia(Y-TZP),whereas efforts are needed to control its microstructure in order to im-prove the strength of Ce-TZP ceramics.In this work,CaO was used to co-dope Ce-TZP ceramics.More specifically,0.2-2.0 mol%Ca(NO_(3))_(3)·4H_(2)O precursor-based CaO was used to dope 10 mol%ceria-stabilized zirconia.Sintering was performed at 1300,1350,or 1400℃,which is lower than the temperatures commonly applied for zirconia ceramics.The microstructure and mechanical properties were investigated and correlated,revealing that 0.2 mol%CaO-doped CeO_(2)-stabilised zirconia sintered at 1350℃ exhibited a fully dense fine-grained tetragonal ZrO_(2) microstructure with high toughness(10.4 MPa m1/2)and biax-ial bending strength(1210±43 MPa),and a narrow strength distribution(weibull modulus of 32.5).1.5 and 2.0 mol% CaO-doping resulted in excellent biaxial bending strength but wider strength distribution and lower fracture resistance.The homogeneously distributed Ca(NO_(3))_(3)·4H_(2)O precursor prevented cubic zirconia-phase formation for CaO-doping up to 2.0 mol%.CaO-doped(≥0.2 mol%)10Ce-TZP sintered at 1350℃ also highly resisted hydrothermal degradation.Furthermore,CaO-doping enabled to make Ce-TZP ceramics as translucent as different commercially available 3Y-TZP ceramics,opening possibilities to use Ce-TZP for dental restorations.展开更多
High-performance lithium-ion batteries and sodium-ion batteries have been developed utilizing a hybrid anode material composed of zinc sulfide/sulfurized polyacrylonitrile.The in situ-generated zinc sulfide nanopartic...High-performance lithium-ion batteries and sodium-ion batteries have been developed utilizing a hybrid anode material composed of zinc sulfide/sulfurized polyacrylonitrile.The in situ-generated zinc sulfide nanoparticles serve as catalytic agents,significantly enhancing conductivity,shortening diffusion paths,and accelerating reaction kinetics.Simultaneously,the sulfurized polyacrylonitrile fibers form a three-dimensional matrix that not only provides a continuous network for rapid electron transfer but also prevents zinc sulfide nanoparticle aggregation and mitigates volume changes during charge-discharge cycles.Moreover,the heterointerface structure at the junction of zinc sulfide nanoparticles and the sulfurized polyacrylonitrile matrix increases the availability of active sites and facilitates both ion adsorption and electron transfer.As an anode material for lithium-ion batteries,the zinc sulfide/sulfurized polyacrylonitrile hybrid demonstrates a high reversible capacity of 1178 mAh g^(-1)after 100 cycles at a current density of 0.2 A g^(-1),maintaining a capacity of 788 mAh g^(-1)after 200 cycles at 1 A g^(-1).It also exhibits excellent sodium storage capabilities,retaining a capacity of 625 mAh g^(-1)after 150 cycles at 0.2 A g^(-1).Furthermore,ex-situ X-ray photoelectron spectroscopy,X-ray diffraction,7Li solid-state magic angle spinning nuclear magnetic resonance,and in situ Raman are employed to investigate the reaction mechanisms of the zinc sulfide/sulfurized polyacrylonitrile hybrid anode,providing valuable insights that pave the way for the advancement of hybrid anode materials in lithium-ion batteries and sodium-ion batteries.展开更多
Carbon quantum dots are a new type of fluorescent nanomaterials with broad applications in drug delivery,bioimaging,solar cells,and photocatalysis due to their unique biocompatibility,optical properties and easy funct...Carbon quantum dots are a new type of fluorescent nanomaterials with broad applications in drug delivery,bioimaging,solar cells,and photocatalysis due to their unique biocompatibility,optical properties and easy functionalization.In the meantime,because of its high carbon content,renewable nature,and environmental friendliness,lignin has drawn the attention of researchers as a desirable raw material for creating carbon quantum dots.Here we review the synthesis of carbon quantum dots from lignin,focusing on synthetic methods,properties,and applications in energy,and photocatalysis.Later,we propose some new development prospects from preparation methods,luminescence mechanism research,application,and commercial cost of lignin carbon quantum dots.Finally,based on this,the development prospects of this field are prospected and summarized.展开更多
Photocatalytic oxygen reduction for hydrogen peroxide(H_(2)O_(2))synthesis presents a green and costeffective production method.However,achieving highly selective H_(2)O_(2)synthesis remains challenging,necessitating ...Photocatalytic oxygen reduction for hydrogen peroxide(H_(2)O_(2))synthesis presents a green and costeffective production method.However,achieving highly selective H_(2)O_(2)synthesis remains challenging,necessitating precise control over free radical reaction pathways and minimizing undesirable oxidative by-products.Herein,we report for the visible light-driven simultaneous co-photocatalytic reduction of O2to H_(2)O_(2)and oxidation of biomass using the atomic rubidium-nitride modified carbon nitride(CNRb).The optimized CNRb catalyst demonstrates a record photoreduction rate of 8.01 mM h^(-1)for H_(2)O_(2)generation and photooxidation rate of 3.75 mM h^(-1)for furfuryl alcohol to furoic acid,achieving a remarkable solar-to-chemical conversion(SCC)efficiency of up to 2.27%.Experimental characterizations and DFT calculation disclosed that the introducing atomic Rb–N configurations allows for the high-selective generation of superoxide radicals while suppressing hydroxyl free radical formation.This is because the Rb–N serves as the new alternative site to perceive a stronger connection position for O2adsorption and reinforce the capability to extract protons,thereby triggering a high selective redox product formation.This study holds great potential in precisely regulating reactive radical processes at the atomic level,thereby paving the way for efficient synthesis of H_(2)O_(2)coupled with biomass valorization.展开更多
The development of cost-effective and high-efficiency catalysts for sustainable hydrogen production through electrocatalytic hydrogen evolution reaction(HER) is crucial yet remains challenging. In this work, we synthe...The development of cost-effective and high-efficiency catalysts for sustainable hydrogen production through electrocatalytic hydrogen evolution reaction(HER) is crucial yet remains challenging. In this work, we synthesized two types of bimetallic Pt Ni nanoparticles embedded in N-doped porous carbons derived from Ni-ABDC(5-aminoisophthalate) using both in-situ and ex-situ Pt inclusion methods. The in-situ Pt doping notably disrupted the effective growth of Ni-ABDC nanostrips owing to strong interactions between Pt and ABDC, resulting in an amorphous nanostructure. The optimized PtinNi-NC exhibited remarkable HER performance with a low overpotential of 29 mV at 10 mA/cm^(2), a Tafel slope of 47.4 mV/dec, and a current retention of 91.2% after 200 h in 1.0 mol/L KOH solution, surpassing the performance of Ni-NC, PtexNi-NC, and Pt/C. This research demonstrates the rational design and preparation of transition metal-based coordination polymer-derived metal-carbon nanomaterials with low Pt loading,emphasizing their considerable potential in energy conversion and storage technologies.展开更多
基金supported by the National Natural Science Foundation of China(Nos.52472122,52372106,and 52072092)the Natural Science Foundation of Heilongjiang Province(No.YQ2019E026)the Fundamental Research Funds for the Central Universities(No.2023FRFK03048).
文摘The growing global demand for sustainable solutions to address energy and environmental challenges has spurred significant interest in catalytic technologies.Piezocatalysis has emerged as a sustainable technology for environmental remediation and energy conversion because of its unique characteristics of harvesting mechanical energy into electrochemical energy.Versatile BiFeO_(3)(BFO)stands out among a range of piezocatalysts for its distinctive integration of piezoelectric,multiferroic,and optical properties.This review critically examines piezocatalytic mechanisms,including energy band theory,screening charge effects,and displacement current theory,revealing the intricate roles of internal charges,screening charges,and piezoelectric electrons in driving catalytic reactions.Furthermore,the evolution of BFO-based piezocatalysis is systematically reviewed,emphasizing its structural characteristics,representative synthesis methods,performance optimization strategies,and diverse applications,such as organic pollutant degradation,H_(2) production,H_(2)O_(2)generation,CO_(2)reduction,and sterilization.In particular,the underestimated ferroelectric polarization effect of BFO on CO_(2)reduction is critically analyzed and elaborated.This review identifies critical challenges and outlines future research directions to advance high-efficiency BFO-based piezocatalytic systems.Overall,this comprehensive analysis underscores the potential of BFO in piezocatalysis,bridging materials engineering with practical applications and offering insights into future advancements.
基金the Engineering and Physical Sciences Research Council(EPSRC)for funding the researchUK India Education Research Initiative(UKIERI)for funding support.
文摘This review provides an insightful and comprehensive exploration of the emerging 2D material borophene,both pristine and modified,emphasizing its unique attributes and potential for sustainable applications.Borophene’s distinctive properties include its anisotropic crystal structures that contribute to its exceptional mechanical and electronic properties.The material exhibits superior electrical and thermal conductivity,surpassing many other 2D materials.Borophene’s unique atomic spin arrangements further diversify its potential application for magnetism.Surface and interface engineering,through doping,functionalization,and synthesis of hybridized and nanocomposite borophene-based systems,is crucial for tailoring borophene’s properties to specific applications.This review aims to address this knowledge gap through a comprehensive and critical analysis of different synthetic and functionalisation methods,to enhance surface reactivity by increasing active sites through doping and surface modifications.These approaches optimize diffusion pathways improving accessibility for catalytic reactions,and tailor the electronic density to tune the optical and electronic behavior.Key applications explored include energy systems(batteries,supercapacitors,and hydrogen storage),catalysis for hydrogen and oxygen evolution reactions,sensors,and optoelectronics for advanced photonic devices.The key to all these applications relies on strategies to introduce heteroatoms for tuning electronic and catalytic properties,employ chemical modifications to enhance stability and leverage borophene’s conductivity and reactivity for advanced photonics.Finally,the review addresses challenges and proposes solutions such as encapsulation,functionalization,and integration with composites to mitigate oxidation sensitivity and overcome scalability barriers,enabling sustainable,commercial-scale applications.
文摘With the rapid advancement of computing and information technology at the turn of the 21st century,the power of data collection and processing has multiplied tremendously.Based on this a game-changing advancement,science is at the advent of the “fourth paradigm”of massive data plus artificial intelligence,in which the efficiency of scientific research is continuously improved,research time is shortened,and research cost is reduced[1].
基金the National Research Foundation of Korea(NRF)funded by the Korean Government(MSIT)(No.2022R1A2C1006743)。
文摘This study presents a facile and rapid method for synthesizing novel Layered Double Hydroxide(LDH)nanoflakes,exploring their application as a photocatalyst,and investigating the influence of condensed phosphates'geometric linearity on their photocatalytic properties.Herein,the Mg O film,obtained by plasma electrolysis of AZ31 Mg alloys,was modified by growing an LDH film,which was further functionalized using cyclic sodium hexametaphosphate(CP)and linear sodium tripolyphosphate(LP).CP acted as an enhancer for flake spacing within the LDH structure,while LP changed flake dispersion and orientation.Consequently,CP@LDH demonstrated exceptional efficiency in heterogeneous photocatalysis,effectively degrading organic dyes like Methylene blue(MB),Congo red(CR),and Methyl orange(MO).The unique cyclic structure of CP likely enhances surface reactions and improves the catalyst's interaction with dye molecules.Furthermore,the condensed phosphate structure contributes to a higher surface area and reactivity in CP@LDH,leading to its superior photocatalytic performance compared to LP@LDH.Specifically,LP@LDH demonstrated notable degradation efficiencies of 93.02%,92.89%,and 88.81%for MB,MO,and CR respectively,over a 40 min duration.The highest degradation efficiencies were observed in the case of the CP@LDH sample,reporting 99.99%for MB,98.88%for CR,and 99.70%for MO.This underscores the potential of CP@LDH as a highly effective photocatalyst for organic dye degradation,offering promising prospects for environmental remediation and water detoxification applications.
基金supported by the National Research Foundation of Korea(NRF)funded by the Korean government(MSIT)(No.2022R1A2C1006743).
文摘The hybridization of metal-organic framework(MOF)with inorganic layers would lead to the discovery of novel hybrid materials that can provide a compelling strategy for enhancing its photocatalytic and electrochemical response.In the present study,a highly efficient multifunctional hybrid material was developed by exploiting the defective layer formed on AZ31 Mg alloy through plasma electrolytic oxidation(PEO)as a nucleation and growth site for Co-MOF.The concentrations of the organic linker 2-Methylimidazole(2,MIm)and cobalt nitrate as a source of Co^(2+) ions were varied to control the growth of the obtained Co-MOF.Lower concentrations of the 2,MIm ligand favored the formation of leaf-like MOF structures through an anisotropic,two-dimensional growth,while higher concentrations led to rapid,isotropic nucleation and the creation of polyhedral Co-MOF structures.The sample characterized by polyhedral Co-MOF structures exhibited superior electrochemical stability,with the lowest corrosion current density(3.11×10^(-9) A/cm^(2))and the highest top layer resistance(2.34×10^(6)Ωcm^(2)),and demonstrated outstanding photocatalytic efficiency,achieving a remarkable 99.98%degradation of methylene blue,an organic pollutant,in model wastewater.To assess the active adsorption sites of the Co-MOF,density functional theory(DFT)was utilized.This study explores the changes in morphologies of the coatings of Co-MOF with the change of solution concentration to form coatings with enhanced properties on the metallic substrate,which could establish the groundwork for the development of next-generation multifunctional frameworks with diverse applications.
文摘This paper studies the antimicrobial activity of selected engineering materials surfaces at room and chill temperatures. The antimicrobial effects of selected materials surfaces were evaluated by dropping the test pieces into prepared cultures of Bacillus spp, Escherichia coli, and Staphylococcus aereus isolated from fruits, animal feaces and natural environment respectively. Bacteria count obtained after 0, 30, 60, 90, 120, 180, 240 and 300 minutes at room temperature and chill condition was taken and compared with their initial count. The amount of live bacteria drops by several orders of magnitude, to zero, on metallic copper and brass within 30 to 300 minutes in both room and chill conditions. In contrast, no reduction is seen in the number of colonies of live bacteria on plastics, ceramic and stainless steel in both room and chill conditions. These results suggest that the selection of metallic copper and brass for touch surfaces in hospitals, surfaces exposed to fruit processing and household utensils can materially assist in reducing bacterial contamination, which should lead to a reduction in the transmission of infectious organisms.
基金funded by Faculty of Engineering,Burapha University,grant number 003/2567.
文摘Herein,cure characteristics,morphology,and mechanical properties of natural rubber filled with activated carbon-based materials were investigated.Carbon-based materials were prepared from bagasse,coffee grounds and pineapple crowns by the pyrolysis method at temperatures in the range of 300℃.As-synthesized carbon materials were characterized by optical microscopy(OM),scanning electron microscopy(SEM),and Fourier-transform infrared spectroscopy(FTIR)to analyze size distribution,morphology,and functional groups,respectively.OM and SEM analysis revealed that particles,flakes,and a small quantity of fiber-like carbon were obtained using bagasse and pineapple crown as raw materials,while honeycomb-like carbon materials can be derived from coffee grounds.To investigate the mechanical properties,natural rubber was filled with carbon black and as-synthesized carbon materials by the internal mixing and compression molding process.Transmission electron microscopy(TEM)was utilized to characterize the dispersion of carbon materials in the rubber matrix.The results of tensile testing showed that the natural rubber mixed with as-synthesized carbon materials from pineapple crowns exhibited 54%and 74%improvement in the ultimate tensile strength and Young’s modulus,respectively,compared with natural rubber without filled carbon materials.The enhancement in mechanical properties by activated carbon materials derived from pineapple crowns can be attributed to the flake-and fiber-like structures and good dispersion of carbon materials in the rubber matrix.In addition,it is higher than that of rubber mixed with carbon black.The results demonstrated that as-synthesized carbon materials from pineapple crowns have the potential materials to substitute carbon black in the rubber compound industry.
基金supported by the Exchange Program of Highend Foreign Experts of Ministry of Science and Technology of People’s Republic of China(No.G2023041003L)the Natural Science Foundation of Shaanxi Provincial Department of Education(No.23JK0367)+1 种基金the Scientific Research Startup Program for Introduced Talents of Shaanxi University of Technology(Nos.SLGRCQD2208,SLGRCQD2306,SLGRCQD2133)Contaminated Soil Remediation and Resource Utilization Innovation Team at Shaanxi University of Technology。
文摘As battery technology evolves and demand for efficient energy storage solutions,aqueous zinc ion batteries(AZIBs)have garnered significant attention due to their safety and environmental benefits.However,the stability of cathode materials under high-voltage conditions remains a critical challenge in improving its energy density.This review systematically explores the failure mechanisms of high-voltage cathode materials in AZIBs,including hydrogen evolution reaction,phase transformation and dissolution phenomena.To address these challenges,we propose a range of advanced strategies aimed at improving the stability of cathode materials.These strategies include surface coating and doping techniques designed to fortify the surface properties and structure integrity of the cathode materials under high-voltage conditions.Additionally,we emphasize the importance of designing antioxidant electrolytes,with a focus on understanding and optimizing electrolyte decomposition mechanisms.The review also highlights the significance of modifying conductive agents and employing innovative separators to further enhance the stability of AZIBs.By integrating these cutting-edge approaches,this review anticipates substantial advancements in the stability of high-voltage cathode materials,paving the way for the broader application and development of AZIBs in energy storage.
基金financially supported by the National Natural Science Foundation of China(52172245)the Key Scientific and Technological Innovation Project of Shandong(2023CXGC010302)the Qingdao Flexible Materials Precision Die-cutting Technology Innovation Center。
文摘In lithium-sulfur batteries(LSBs),the limited utilization of sulfur and the sluggish kinetics of redox reaction significantly hinder their electrochemical performance,especially under high rates and high sulfur loadings.Here,we propose a novel separator structure with an interlayer composed of a vermiculite nanosheet combined with Ketjen Black(VMT@KB)for LSBs,facilitating efficient adsorption and rapid catalytic conversion toward lithium polysulfides(LiPSs).The VMT@KB nanosheets with an electrical double-layer structure and electronic conductivity are obtained through a high-temperature peeling process and Li^(+)exchange treatment in LiCl solution,followed by a mechanical combination process with KB.The results demonstrate that incorporating VMT@KB as an interlayer on a conventional separator enhances the conductivity and limits the LiPSs in the cathode region.The Li-S cell with VMT@KB interlayer shows satisfactory cycle and rate performance,especially in high sulfur loading.It exhibits a remarkable initial discharge capacity of 1225 mAh g^(-1)at 0.5 C and maintains a capacity of 816 mAh g^(-1)after 500 cycles.Besides,the discharge capacity remains 462 mAh g^(-1)even at 6 C.Moreover,the cell with high sulfur loading(8.2 mg cm^(-2))enables stable cycling for 100 cycles at 0.1 C with a discharge capacity of over1000 mAh g^(-1).
基金Funded by the National Natural Science Foundation of China Project(Nos.52108219 and U21A20150)the Lanzhou University of Technology Hongliu Outstanding Young Talent Program,China(No.04-062407)。
文摘To guarantee the efficient and high-value reutilization of waste concrete from construction waste,the waste concrete was mechanically ground,and three degrees of fineness recycled concrete powder(RCP)were obtained by different grinding time.By analyzing the particle characteristics of RCP with different fineness,the filling-densification effect of cement-RCP cementitious material system was quantitatively investigated based on Andreasen,Fuller,and Aim-Goff models.In addition,the macroscopic mechanical properties of cement paste mixed with RCP were studied,and the influencing mechanisms of RCP on the microstructure of cement paste was revealed.Macroscopic research results show that the particle fineness of RCP after grinding is smaller than that of cement.When the RCP replaces 0%to 20%cement,the packing density based on the Aim-Goff model increases with the increase of RCP content,whereas the macro-mechanical properties first improve and then degrade with the increase of RCP content.Microscopic results show that at 5%RCP content,beneficial hydration products such as C-S-H and beneficial pore increase in cement-RCP paste;while at>15%content,beneficial products decrease and harmful substances such as Ca(OH)_(2)and harmful pore increases.These research findings suggest that the incorporation of RCP can make the cementitious system denser,and the appropriate RCP content can improve the macro-and microscopic properties of cement-based materials.
基金supported by Natural Science Foundation of Ningxia Province,China(No.2023AAC05047)Special Project for the Central-Guided Local Science and Technology Development(No.2024FRD05062)+1 种基金Graduate Student Innovation Project of North Minzu University(No.YCX24102)Ningxia Science and Technology Innovation Team for Key Materials and Devices in High-Performance Secondary Batteries(No.2024CXTD003).
文摘Although manganese-based oxide is regarded as a promising cathode material for zincion hybrid supercapacitors(ZHSCs),its practical application is hindered by slow zinc ion diffusion and the instability of MnO_(2).To overcome this obstacle,a δ-MnO_(2)/MXene heterostructure was created using a simple one-step process under gentle condition.The ZHSC was assembled using this heterostructure as the cathode,activated carbon(AC)as the anode and 2 mol·L−1 ZnSO_(4) as the electrolyte.The resultingδ-MnO_(2)/MXene//ZnSO4//AC ZHSC shows a maximum specific capacitance of 97.4 F·g^(−1) and an energy density of 32.27 Wh·kg^(−1) at the best cathode-to-anode mass ratio.Ex situ characterizations reveal the reversible energy storage mechanism combing Zn^(2+)insertion/extraction in the cathode,ion adsorption and desorption on the anode surface,and partial reversible formation and dissolution of Zn_(4)SO_(4)(OH)_(6)·5H_(2)O(ZHS)components on both electrodes.Adding of Mn^(2+)to the electrolyte reduced Mn dissolution,improving the ZHSC’s specific capacitance and energy density to 140.4 F·g^(−1) and 49.36 Wh·kg^(−1),respectively,while also enhancing its rate performance and cyclability.The improved electrochemical reaction kinetics was verified through various tests.The results suggest that the δ-MnO_(2)/MXene heterostructure has great potential as a high-performance cathode material for ZHSCs.
基金National Natural Science Foundation of China (62104061, 62074052, 61974173 and 52072327)。
文摘Solution-processed Cu(In,Ga)Se_(2)(CIGS) solar cells suffer from serious carrier recombination and power conversion efficiency(PCE) loss because of the poor film properties and easy formation of defects.Herein, we propose Ag&Se co-selenization strategy to enhance the crystallization and passivate harmful defects of the CIGS films. The formation of Ag-Se phase during the selenization process enables the formation of large grains and suppresses the deep level defects. It is found that Ag doping can enlarge the depletion region width, lower the Urbach energy and prolong the carrier lifetime. As a result, a champion solution-processed CIGS solar cell presents a high efficiency of 16.48% with the highly improved opencircuit voltage(VOC) of 662 m V and fill factor(FF) of 75.8%. This work provides an efficient strategy to prepare high quality solution-processed CIGS films for high-performance CIGS solar cells.
文摘The crisis of excessive increase in CO_(2)emissions has quickly become a serious issue and requires low-cost and bio-compatible solutions.The employee of membrane technology for CO_(2)gas separation has garnered significant interest among researchers.However,this method encounters challenges related to selectivity and permeability.Therefore,modifying and reinforcing the polymer membranes to improve gas separation performance seems essential.Among the various methods for polymer membrane modification,modification with magnesium-based fillers to prepare a mixed matrix membrane(MMM)is considered an efficient method.Owing to magnesium metal's low weight,low density,high strength,and good selectivity,magnesium-based materials(Mg-based materials)have more porosity,higher available surface area,more adsorption sites,lighter weight,and more gas absorption tendency than other fillers,which makes them an attractive choice for the preparation of gas separation MMMs.This research deals with the introduction of Mg-based materials,various methods of synthesis of Mg-based materials,different methods of introducing Mg-based materials into the membrane matrix,and their effect on the performance of MMMs in CO_(2)gas separation applications.Therefore,this review can provide researchers with light horizons in using the high potential of Mg-based materials as efficient fillers in MMMs to achieve excellent permeability and selectivity and generally improve their performance in CO_(2)gas separation applications.
基金supported by the National Nature Science Foundation Youth Program(No.22205027)Liaoning Province Science and Technology Department project(No.LQ2020014).
文摘Accurate determination and rapid degradation of organic pollutants are essential works in environmental improvement.Herein,the CuCo_(2)S_(4)@Co_(3)O_(4) heterojunction with fascinating 2D-on-3D hierarchical nanoflowers architecture and highly distributed interface sites were successfully synthesized by CuCo-LDH topological transformation combine with in situ exterior sulfurization strategy.The 2D-on-3D nanoflowers architecture could improve light harvesting ability,provide large surface area,open channels and abundant edge sites.In particular,the intensive M-O-S-M heterojunction interface not only promote the photoexcited charge shuttling but provide abundant interface sites to enhance catalytic activity.As expected,the photocatalytic degradation rate of diclofenac sodium(DCF)on CuCo_(2)S_(4)@Co_(3)O_(4) was approximately 100%within 30 min under 300 W mercury lamp,which was 1.28 times and 1.45 times higher than that of CuCo-LDH and CuCo_(2)O_(4).The degradation rate for real samples weremore than 80%,themineralization rate was 90%,and the biological toxicity of degradation products decreased significantly.Furthermore,a novel photoelectrochemistry(PEC)sensorwith CuCo_(2)S_(4)@Co_(3)O_(4) as a photoanodewas successfully constructed for directly sensing DCF,showing a wide linear range and satisfactory detection limit.The results indicate that the CuCo_(2)S_(4)@Co_(3)O_(4) possess dual-functional peculiarity,hold vast potential for sensing and degradation environmental pollutants in wastewater.
基金National Natural Science Foundation of China (No. 22179123)Taishan Scholar Program of Shandong Province,China (No. tsqn202211048)Fundamental Research Funds for the Central Universities (No.202262010)。
文摘Zinc-ion hybrid capacitors (ZIHCs) have received increasing attention as energy storage devices owing to their low cost,high safety,and environmental friendliness.However,their progress has been hampered by low energy and power density,as well as unsatisfactory long-cycle stability,mainly due to the lack of suitable electrode materials.In this context,we have developed manganese single atoms implanted in nitrogen-doped porous carbon nanosheets (MnSAs/NCNs) using a metal salt template method as cathodes for ZIHCs.The metal salt serves a dual purpose in the synthesis process:It facilitates the uniform dispersion of Mn atoms within the carbon matrix and acts as an activating agent to create the porous structure.When applied in ZIHCs,the MnSAs/NCNs electrode demonstrates exceptional performance,including a high capacity of 203 m Ah g^(-1),an energy density of 138 Wh kg^(-1)at 68 W kg^(-1),and excellent cycle stability with 91%retention over 10,000 cycles.Theoretical calculations indicate that the introduced Mn atoms modulate the local charge distribution of carbon materials,thereby improving the electrochemical property.This work demonstrates the significant potential of carbon materials with metal atoms in zinc-ion hybrid capacitors,not only in enhancing electrochemical performance but also in providing new insights and methods for developing high-performance energy storage devices.
基金the China Scholarship Council(CSC No.201806460096)for financial supportthe Scientific Research-Flanders(FWO-Vlaanderen)for her post-doctoral fellowships(grant Nos.12S8418N and 12S8421N)supported by the Research Fund of KU Leuven project No.C2-17-00402 and the Fund for Scientific Research-Flanders(FWO-Vlaanderen)(grant Nos.G.0431.10N and G.0959.20N).
文摘Ceria-stabilized tetragonal zirconia(Ce-TZP)has become an interesting alternative for the widely used yttria-stabilized zirconia(Y-TZP),whereas efforts are needed to control its microstructure in order to im-prove the strength of Ce-TZP ceramics.In this work,CaO was used to co-dope Ce-TZP ceramics.More specifically,0.2-2.0 mol%Ca(NO_(3))_(3)·4H_(2)O precursor-based CaO was used to dope 10 mol%ceria-stabilized zirconia.Sintering was performed at 1300,1350,or 1400℃,which is lower than the temperatures commonly applied for zirconia ceramics.The microstructure and mechanical properties were investigated and correlated,revealing that 0.2 mol%CaO-doped CeO_(2)-stabilised zirconia sintered at 1350℃ exhibited a fully dense fine-grained tetragonal ZrO_(2) microstructure with high toughness(10.4 MPa m1/2)and biax-ial bending strength(1210±43 MPa),and a narrow strength distribution(weibull modulus of 32.5).1.5 and 2.0 mol% CaO-doping resulted in excellent biaxial bending strength but wider strength distribution and lower fracture resistance.The homogeneously distributed Ca(NO_(3))_(3)·4H_(2)O precursor prevented cubic zirconia-phase formation for CaO-doping up to 2.0 mol%.CaO-doped(≥0.2 mol%)10Ce-TZP sintered at 1350℃ also highly resisted hydrothermal degradation.Furthermore,CaO-doping enabled to make Ce-TZP ceramics as translucent as different commercially available 3Y-TZP ceramics,opening possibilities to use Ce-TZP for dental restorations.
基金supported by“regional innovation mega project”program through the Korea Innovation Foundation funded by Ministry of Science and ICT(Project Number:2023-DD-UP-0026)the Energy Technology Evaluation and Planning(KETEP)and the Ministry of Trade,Industry&Energy(MOTIE)(No.RS-2024-00509401,RS-2023-00217581)“Regional Innovation Strategy(RIS)”through the National Research Foundation of Korea(NRF)funded by the Ministry of Education(MOE)(2021RIS-001).
文摘High-performance lithium-ion batteries and sodium-ion batteries have been developed utilizing a hybrid anode material composed of zinc sulfide/sulfurized polyacrylonitrile.The in situ-generated zinc sulfide nanoparticles serve as catalytic agents,significantly enhancing conductivity,shortening diffusion paths,and accelerating reaction kinetics.Simultaneously,the sulfurized polyacrylonitrile fibers form a three-dimensional matrix that not only provides a continuous network for rapid electron transfer but also prevents zinc sulfide nanoparticle aggregation and mitigates volume changes during charge-discharge cycles.Moreover,the heterointerface structure at the junction of zinc sulfide nanoparticles and the sulfurized polyacrylonitrile matrix increases the availability of active sites and facilitates both ion adsorption and electron transfer.As an anode material for lithium-ion batteries,the zinc sulfide/sulfurized polyacrylonitrile hybrid demonstrates a high reversible capacity of 1178 mAh g^(-1)after 100 cycles at a current density of 0.2 A g^(-1),maintaining a capacity of 788 mAh g^(-1)after 200 cycles at 1 A g^(-1).It also exhibits excellent sodium storage capabilities,retaining a capacity of 625 mAh g^(-1)after 150 cycles at 0.2 A g^(-1).Furthermore,ex-situ X-ray photoelectron spectroscopy,X-ray diffraction,7Li solid-state magic angle spinning nuclear magnetic resonance,and in situ Raman are employed to investigate the reaction mechanisms of the zinc sulfide/sulfurized polyacrylonitrile hybrid anode,providing valuable insights that pave the way for the advancement of hybrid anode materials in lithium-ion batteries and sodium-ion batteries.
基金Sponsorship Program by CAST(2023QNRC001)University-Industry Collaborative Education Program(220901115200913,220901115201954)+2 种基金Hunan Provincial Natural Science Foundation of China(2022JJ40007)Jiangsu Agricultural Science and Technology Innovation Fund(CX(22)3047)the National Natural Science Foundation of China(32201491)。
文摘Carbon quantum dots are a new type of fluorescent nanomaterials with broad applications in drug delivery,bioimaging,solar cells,and photocatalysis due to their unique biocompatibility,optical properties and easy functionalization.In the meantime,because of its high carbon content,renewable nature,and environmental friendliness,lignin has drawn the attention of researchers as a desirable raw material for creating carbon quantum dots.Here we review the synthesis of carbon quantum dots from lignin,focusing on synthetic methods,properties,and applications in energy,and photocatalysis.Later,we propose some new development prospects from preparation methods,luminescence mechanism research,application,and commercial cost of lignin carbon quantum dots.Finally,based on this,the development prospects of this field are prospected and summarized.
基金National Natural Science Foundation of China(22309032,22109120,and 62104170)Guangdong Basic and Applied Basic Research Foundation(2022A1515011737)+2 种基金Science and Technology Program of Guangzhou(2023A04J1395)GDAS’Project of Science and Technology Development(2021GDASYL-20210102010)Zhejiang Provincial Natural Science Foundation of China(LY23F040001)。
文摘Photocatalytic oxygen reduction for hydrogen peroxide(H_(2)O_(2))synthesis presents a green and costeffective production method.However,achieving highly selective H_(2)O_(2)synthesis remains challenging,necessitating precise control over free radical reaction pathways and minimizing undesirable oxidative by-products.Herein,we report for the visible light-driven simultaneous co-photocatalytic reduction of O2to H_(2)O_(2)and oxidation of biomass using the atomic rubidium-nitride modified carbon nitride(CNRb).The optimized CNRb catalyst demonstrates a record photoreduction rate of 8.01 mM h^(-1)for H_(2)O_(2)generation and photooxidation rate of 3.75 mM h^(-1)for furfuryl alcohol to furoic acid,achieving a remarkable solar-to-chemical conversion(SCC)efficiency of up to 2.27%.Experimental characterizations and DFT calculation disclosed that the introducing atomic Rb–N configurations allows for the high-selective generation of superoxide radicals while suppressing hydroxyl free radical formation.This is because the Rb–N serves as the new alternative site to perceive a stronger connection position for O2adsorption and reinforce the capability to extract protons,thereby triggering a high selective redox product formation.This study holds great potential in precisely regulating reactive radical processes at the atomic level,thereby paving the way for efficient synthesis of H_(2)O_(2)coupled with biomass valorization.
基金financially supported by National Natural Science Foundation of China (No. 21601137)Basic Science and Technology Research Project of Wenzhou, Zhejiang Province (No. G20240038)+2 种基金the Special Basic Cooperative Research Programs of Yunnan Provincial Undergraduate Universities Association (Nos. 202101BA070001-031, 202101BA070001-042 and 202301BA070001-093)Yunnan Province Young and Middle-aged Academic and Technical Leaders Reserve Talent Project (No. 202105AC160060)Yunnan Province High-level Talent Training Support Program “Youth Top Talent” Project (2020)。
文摘The development of cost-effective and high-efficiency catalysts for sustainable hydrogen production through electrocatalytic hydrogen evolution reaction(HER) is crucial yet remains challenging. In this work, we synthesized two types of bimetallic Pt Ni nanoparticles embedded in N-doped porous carbons derived from Ni-ABDC(5-aminoisophthalate) using both in-situ and ex-situ Pt inclusion methods. The in-situ Pt doping notably disrupted the effective growth of Ni-ABDC nanostrips owing to strong interactions between Pt and ABDC, resulting in an amorphous nanostructure. The optimized PtinNi-NC exhibited remarkable HER performance with a low overpotential of 29 mV at 10 mA/cm^(2), a Tafel slope of 47.4 mV/dec, and a current retention of 91.2% after 200 h in 1.0 mol/L KOH solution, surpassing the performance of Ni-NC, PtexNi-NC, and Pt/C. This research demonstrates the rational design and preparation of transition metal-based coordination polymer-derived metal-carbon nanomaterials with low Pt loading,emphasizing their considerable potential in energy conversion and storage technologies.
