The evolutionarily conserved mitogen-activated protein kinase(MAPK)cascades relay extracellular signals into cells,triggering a variety of cellular responses.We previously revealed NtMPK4 as a positive regulator of ni...The evolutionarily conserved mitogen-activated protein kinase(MAPK)cascades relay extracellular signals into cells,triggering a variety of cellular responses.We previously revealed NtMPK4 as a positive regulator of nicotine biosynthesis;however,its upstream regulation remains unclear.Here,we characterized a MAPK cascade,comprising NtMEKK1b,NtMPKK2a,and NtMPK4,that promotes nicotine biosynthesis.This signaling module transduces external cues,including jasmonate and pathogen elicitors such as flg22,into post-translational modifications that enhance transcriptional activity and pathway gene expression.NtMPKK2a physically interacts with and phosphorylates NtMPK4 in vivo,confirming its role as an upstream kinase.RNAi-mediated silencing of NtMPKK2a significantly reduced the expression of nicotine pathway genes and decreased nicotine accumulation,whereas induced-overexpression of NtMPKK2a upregulated nicotine pathway genes and increased nicotine contents in tobacco hairy roots.Overexpression of NtMPKK2a in tobacco cells enhanced the transactivation activity of a NIC2-locus Ethylene Response Factor NtERF221 on Putrescine N-methyltransferase(NtPMT)promotor,further supporting its role in promoting nicotine biosynthesis.Furthermore,we identified NtMEKK1b,a tobacco MEKK that interacts with NtMAPKK2a in yeast cells.Knock-down of NtMEKK1b in transgenic tobacco plants attenuated the expression of nicotine pathway genes and reduced nicotine contents,whereas induced-overexpression of NtMEKK1b upregulated gene expression and nicotine accumulation.Our findings uncover a previously uncharacterized MAPK cascade module,NtMEKK1b-NtMPKK2a-NtMPK4,that regulates nicotine biosynthesis,highlighting the importance of posttranslational regulation in nicotine biosynthesis.展开更多
The dissolution behaviors of lime,limestone,and core–shell structured lime,as well as their effects on dephosphorization behavior were studied.The results show that the slow dissolution of lime in converter slag is m...The dissolution behaviors of lime,limestone,and core–shell structured lime,as well as their effects on dephosphorization behavior were studied.The results show that the slow dissolution of lime in converter slag is mainly attributed to the calcium silicate layer at the lime/slag interface.CO_(2)generated by CaCO_(3)decomposition can destroy the calcium silicate layer,and thus accelerates the dissolution of limestone and core–shell structured lime.However,in the initial stage,a large amount of CO_(2)emission generated by limestone decomposition results in the poor contact between molten slag and limestone,and the dissolution rate is slower in the test of limestone than that of lime.For core–shell structured lime,the initial dissolution rate is not affected due to the lime surface,and is accelerated by the appropriate CO_(2)emission.Rapid CaO pickup in molten slag by fast dissolution of the lime sample can remarkably accelerate the dephosphorization reaction.Because of the fastest dissolution rate,the core–shell structured lime slagging mode shows the most promising prospects for the efficient dephosphorization.展开更多
To enhance the visible light response of titanium dioxide(TiO_(2)),titanium carbide(TiC)nanoparticles(NPs)were thermally treated in carbon powder,effectively overcoming the challenges associated with conventional dopi...To enhance the visible light response of titanium dioxide(TiO_(2)),titanium carbide(TiC)nanoparticles(NPs)were thermally treated in carbon powder,effectively overcoming the challenges associated with conventional doping methods.During the treatment,a TiO_(2)thin shell with oxygen vacancies(OVs)formed around the TiC NPs,creating a shell-core structure S-scheme photocatalyst.Transmission electron microscopy(TEM)and ultraviolet-visible(UV-vis)spectroscopy confirmed the successful formation of the TiO_(2)shell.By optimizing the shell thickness,the TiO_(2)-TiC shell-core structure achieved an ideal shell-core ratio,resulting in strong visible light absorption(400-800 nm),and the degradation rate constant of Rhodamine B(RhB)of sample cHT500 reached 0.0687 min^(−1),which is 20.8times higher than that of pristine TiO_(2)(0.0033 min^(−1))under visible-light irradiation.In addition,cytocompatibility tests showed that sample cHT500 exhibits favorable cell viability,which is comparable to that of TiO_(2)nanoparticles,and thus remarkably mitigates the poor biocompatibility inherent to TiC,making them promising candidates for biomedical and photocatalytic applications.展开更多
Curing temperature significantly affects the pozzolanic reaction kinetics of phosphorous slag(PS),thereby governing the early-age(7 d)hydration behavior of PS composite binders at 20,30,and 60℃.The Krstulovic-Dabic k...Curing temperature significantly affects the pozzolanic reaction kinetics of phosphorous slag(PS),thereby governing the early-age(7 d)hydration behavior of PS composite binders at 20,30,and 60℃.The Krstulovic-Dabic kinetic model was applied to identify three characteristic processes:nucleation and growth(NG),phase boundary interaction(I),and diffusion(D).Control mixtures containing inert quartz powder with comparable particle size distributions were prepared for comparison.Pore characteristics of hardened PS pastes at different temperatures were analyzed via mercury intrusion porosimetry,while hydration products were characterized using X-ray diffraction(XRD)and thermogravimetric analysis(TG-DTG).The experimental results indicate that the retarding effect of PS on early cement hydration outweighs its accelerating effect,attributed to the combined influence of nucleation and dilution,with retardation decreasing as temperature increases.PS exhibits early reactivity and continuously consumes calcium hydroxide through the pozzolanic reaction,as evidenced by stable phase assemblages accompanied by reduced CH content in XRD and TG-DTG analyses.At 20℃,increasing PS content maintains the NG→I→D mechanism but slows reaction rates across all stages.Elevated temperatures significantly accelerate the NG process,shifting the dominant mechanism from NG toward D.Simultaneously,enhanced PS reactivity contributes to a refined pore structure and improved compressive strength.展开更多
The structural changes in the CaO-SiO_(2)-Al_(2)O_(3)-MgO slag system with varying CaO contents were investigated through molecular dynamics(MD)simulations,and its effect on the dissolution behavior of alumina inclusi...The structural changes in the CaO-SiO_(2)-Al_(2)O_(3)-MgO slag system with varying CaO contents were investigated through molecular dynamics(MD)simulations,and its effect on the dissolution behavior of alumina inclusions was characterized by the Kullback-Leibler(KL)divergence.The slag structure analysis revealed that the[AlO]tetrahedral structure was the primary network structure in the slag.With increasing the CaO content,the non-bridge oxygen(NBO)content in the slag structure increases,and the bridge oxygen(BO)content decreases,thereby reducing the complexity of the slag network structure.Raman spectroscopy detection verifies the results of the MD simulations.The results indicated that the dissolution rate of alumina inclusions accelerates with increasing the CaO content in the slag,owing to the reduced complexity of the slag network structure and the enhanced interatomic interactions.The simulation results for the dissolution of alumina inclusions were consistent with theoretical calculations based on the slag inclusion capacity and the dimensionless dissolution rate of inclusions.Radial distribution function analysis demonstrated that the interaction between atoms in the slag system and alumina inclusions strengthens,increasing the dissolution rate of alumina inclusions.The[AlO_(6)]octahedral structure of the alumina inclusions is disrupted,forming BO structures,which in turn enhances the complexity of the slag network structure,slowing the dissolution rate of alumina inclusions.In contrast,the slag system with a higher CaO content has a relatively simpler network structure,promoting faster alumina inclusion dissolution.展开更多
Conversion-type electrode materials hold significant promise for potassium-ion batteries(PIBs)due to their high theoretical capacities,yet their practical deployment is hindered by sluggish kinetics and irreversible s...Conversion-type electrode materials hold significant promise for potassium-ion batteries(PIBs)due to their high theoretical capacities,yet their practical deployment is hindered by sluggish kinetics and irreversible structural degradation.To overcome these limitations,we propose a rationally engineered nanoreactor architecture that stabilizes defect-rich MoS_(2)via interlayer incorporation of a carbon monolayer,followed by encapsulation within a nitrogen-doped carbon shell,forming a MoSSe@NC heterostructure.This tailored structure synergistically accelerates both K^(+)diffusion kinetics and electron transfer,enabling unprecedented rate performance(107 mAh g^(-1)at 10 Ag^(-1))and ultralong cyclability(86.5%capacity retention after 1200 cycles at 3 A g^(-1)).Mechanistic insights reveal a distinctive“adsorption-conversion”pathway,where sulfur vacancies on exposed S-Mo-S basal planes act as preferential K^(+)adsorption sites,effectively suppressing parasitic phase transitions during intercalation.In situ X-ray diffraction and transmission electron microscopy corroborate the structural reversibility of the conversion reaction,with the carbon matrix dynamically accommodating strain while preserving electrode integrity.This work not only advances the understanding of defect-driven interfacial chemistry in conversion-type materials but also provides a versatile strategy for designing high-performance anodes in next-generation PIBs through heterostructure engineering.展开更多
Ammonium-ion hybrid supercapacitors(A-HSCs)have emerged as promising candidates for next-generation energy storage owing to their inherent safety and environmental sustainability.Hexagonal tungsten oxide(h-WO_(3)),wit...Ammonium-ion hybrid supercapacitors(A-HSCs)have emerged as promising candidates for next-generation energy storage owing to their inherent safety and environmental sustainability.Hexagonal tungsten oxide(h-WO_(3)),with its well-defined tunnel structure,holds great promise as a negative electrode material for NH^(4+)storage.However,its practical application is hindered by structural instability and poor intrinsic electrical conductivity.To address these challenges,a dual-regulation strategy is proposed,integrating molybdenum(Mo)doping and NH^(4+)pre-intercalation to concurrently optimize the tunnel structure and electronic environment of h-WO_(3)(Mo-NWO).Comprehensive experimental and theoretical analyses reveal that Mo doping narrows the bandgap of WO_(3)and reduces the diffusion energy barrier,thereby accelerating NH^(4+)adsorption and diffusion.Simultaneously,NH^(4+)pre-intercalation stabilizes the tunnel framework via hydrogen bonding,ensuring structural reversibility.As expected,the Mo-NWO/AC electrode achieves a high areal capacitance of 13.6 F cm^(−2)at 5 mA cm^(−2)and retains 80.14%of its capacitance after 5000 cycles,demonstrating exceptional rate capability and cycling stability.Moreover,the assembled Mn_(3)O_(4)//Mo-NWO/AC device delivers a high energy density of 3.41 mWh cm^(−2)and outstanding long-term stability(85.75%retention after 12,000 cycles).This work provides a viable strategy for designing high-performance NH^(4+)storage materials and advances the development of sustainable energy storage systems.展开更多
To assess the effectiveness of vaccination in contaminated environments,this study introduces a modeling framework that encompasses two transmission routes,namely direct human-to-human contact and indirect human-to-en...To assess the effectiveness of vaccination in contaminated environments,this study introduces a modeling framework that encompasses two transmission routes,namely direct human-to-human contact and indirect human-to-environment contact,as well as the implementation of new M72/AS01_(E)vaccine.Motivated by this,a coupled age-structured tuberculosis(TB)model is proposed.Its well-posedness requirement is verified using the integrated semigroup theory.Furthermore,this study presents a comprehensive analysis of threshold dynamics associated with the proposed model.Specifically,the global stability of the disease-free and positive steady states is demonstrated by employing Lyapunov functionals.Lastly,the effects of the vaccination with M72/AS01_(E)and contaminated environments on TB control are numerically simulated.Experimental results indicate that high concentrations of Mycobacterium tuberculosis in contaminated environments may somewhat impede TB control efforts,but that large-scale deployment of new vaccine could significantly reduce the prevalence of TB.展开更多
Designing materials with both structural load-bearing capacity and broadband electromagnetic(EM)wave absorption properties remains a significant challenge.In this work,SiOC/SiC/SiO_(2)composite with gyroid structures ...Designing materials with both structural load-bearing capacity and broadband electromagnetic(EM)wave absorption properties remains a significant challenge.In this work,SiOC/SiC/SiO_(2)composite with gyroid structures were prepared through digital light processing(DLP)3D printing,polymer-derived ceramics(PDCs),chemical vapor infiltration(CVI),and oxidation technologies.The incorporation of the CVISiC phase effectively increases the dissipation capability,while the synergistic interaction between the gyroid structure and SiO_(2)phase significantly improves impedance matching performance.The SiOC/SiC/SiO_(2)composite achieved a minimum reflection loss(RL min)of-62.2 d B at 4.3 mm,and the effective absorption bandwidth(EAB)covered the X-band,with a thickness range of 4.1 mm-4.65 mm.The CST simulation results explain the broadband and low-frequency absorption characteristics,with an EAB of 8.4 GHz(9.6-18 GHz)and an RL min of-21.5 dB at 5 GHz.The excellent EM wave attenuation performance is associated primarily with polarization loss,conduction loss,the gyroid structure's enhancement of multiple reflections and scattering of EM waves,and the resonance effect between the structural units.The SiOC/SiC/SiO_(2)composite also demonstrated strong mechanical properties,with a maximum compressive failure strength of 31.6 MPa in the height direction.This work opens novel prospects for the development of multifunctional structural wave-absorbing materials suitable for broadband microwave absorption and load-bearing properties.展开更多
With the rapid advancement of optoelectronic technology,high-performance photodetectors are increasingly in demand in fields such as environmental monitoring,optical communication,and defense systems,where ultraviolet...With the rapid advancement of optoelectronic technology,high-performance photodetectors are increasingly in demand in fields such as environmental monitoring,optical communication,and defense systems,where ultraviolet detection is critical.However,conventional semiconductor materials suffer from limited UV-visible detection capabilities owing to their narrow bandgaps and high dark currents.To address these challenges,wide-bandgap semiconductors have emerged as promising alternatives.Here,we fabricated a horizontally structured n–n heterojunction photodetector by growingβ-Ga_(2)O_(3) on Si–GaN via plasma-enhanced chemical vapor deposition.The device exhibits a self-powered photocurrent of 3.5 nA at zero bias,enabled by the photovoltaic effect of the space charge region.Under 254-nm and 365-nm illumination,it exhibits rectification behavior,achieving a responsivity of 0.475 m A/W(0 V,220??W/cm~2 at 254 nm)and 257.6 mA/W(-5 V),respectively.Notably,the photodetector demonstrates a high photocurrent-to-dark current ratio of 10~5 under-5-V bias,highlighting its potential for self-powered and high-performance UV detection applications.展开更多
The large volume expansion and rapid capacity attenuation of tin-based electrodes are the main factors limiting their commercial application.The reasonable design of electrode material structure is particularly import...The large volume expansion and rapid capacity attenuation of tin-based electrodes are the main factors limiting their commercial application.The reasonable design of electrode material structure is particularly important for improving its electrochemical performance.Herein,phosphorus-modified graphene encapsulated Sn_(6)O_(4)(OH)_(4)nanoparticles composite(P-Sn_(6)O_(4)(OH)_(4)@RGO)with crystalline-amorphous heterostructure has been successfully designed and prepared.The design of crystalline-amorphous structure has largely enhanced the active sites,and the construction of a graphene encapsulation structure has greatly alleviated volume expansion.Notably,P-Sn_(6)O_(4)(OH)_(4)@RGO obtained an excellent high-rate longterm cycling performance for lithium-ion batteries anode,reaching a high specific capacity of 970 m Ah/g at 1.0 A/g after 1450 cycles.This work demonstrates that restructuring the electrode material's structure and phase through phosphorus modification can effectively improve the electrochemical performance of tin-based electrode materials.展开更多
Currently,the Al_(2)O_(3)content in the high-alumina slag systems within blast furnaces is generally limited to 16wt%–18.5wt%,making it challenging to overcome this limitation.Unlike most studies that concentrated on...Currently,the Al_(2)O_(3)content in the high-alumina slag systems within blast furnaces is generally limited to 16wt%–18.5wt%,making it challenging to overcome this limitation.Unlike most studies that concentrated on managing the MgO/Al_(2)O_(3)ratio or basicity,this paper explored the effect of equimolar substitution of MgO for CaO on the viscosity and structure of a high-alumina CaO-MgO-Al_(2)O_(3)-SiO_(2)slag system,providing theoretical guidance and data to facilitate the application of high-alumina ores.The results revealed that the viscosity first decreased and then increased with higher MgO substitution,reaching a minimum at 15mol%MgO concentration.Fourier transform infrared spectroscopy(FTIR)results found that the depths of the troughs representing[SiO_(4)]tetrahedra,[AlO_(4)]tetrahedra,and Si-O-Al bending became progressively deeper with increased MgO substitution.Deconvolution of the Raman spectra showed that the average number of bridging oxygens per Si atom and the X_(Q^(3))/X_(Q^(2))(X_(Q^(i))is the molar fraction of Q^(i) unit,and i is the number of bridging oxygens in a[SiO_(4)]tetrahedral unit)ratio increased from 2.30 and 1.02 to 2.52 and 2.14,respectively,indicating a progressive polymerization of the silicate structure.X-ray photoelectron spectroscopy(XPS)results highlighted that non-bridging oxygen content decreased from 77.97mol% to 63.41mol% with increasing MgO concentration,whereas bridging oxygen and free oxygen contents increased.Structural analysis demonstrated a gradual increase in the polymerization degree of the tetrahedral structure with the increase in MgO substitution.However,bond strength is another important factor affecting the slag viscosity.The occurrence of a viscosity minimum can be attributed to the complex evolution of bond strengths of non-bridging oxygens generated during depolymerization of the[SiO_(4)]and[AlO_(4)]tetrahedral structures by CaO and MgO.展开更多
The stability and electrocatalytic efficiency of transition metal oxides for water splitting is determined by geometric and electronic structure,especially under high current densities.Herein,a newly designed lamella-...The stability and electrocatalytic efficiency of transition metal oxides for water splitting is determined by geometric and electronic structure,especially under high current densities.Herein,a newly designed lamella-heterostructured nanoporous CoFe/CoFe_(2)O_(4) and CeO_(2−x),in situ grown on nickel foam(NF),holds great promise as a high-efficient bifunctional electrocatalyst(named R-CoFe/Ce/NF)for water splitting.Experimental characterization verifies surface reconstruction from CoFe alloy/oxide to highly active CoFeOOH during in situ electrochemical polarization.By virtues of three-dimensional nanoporous architecture and abundant electroactive CoFeOOH/CeO_(2−x) heterostructure interfaces,the R-CoFe/Ce/NF electrode achieves low overpotentials for oxygen evolution(η_(10)=227 mV;η_(500)=450 mV)and hydrogen evolution(η_(10)=35 mV;η_(408)=560 mV)reactions with high normalized electrochemical active surface areas,respectively.Additionally,the alkaline full water splitting electrolyzer of R-CoFe/Ce/NF||R-CoFe/Ce/NF achieves a current density of 50 mA·cm^(−2) only at 1.75 V;the decline of activity is satisfactory after 100-h durability test at 300 mA·cm^(−2).Density functional theory also demonstrates that the electron can transfer from CeO_(2−x) by virtue of O atom to CoFeOOH at CoFeOOH/CeO_(2−x) heterointerfaces and enhancing the adsorption of reactant,thus optimizing electronic structure and Gibbs free energies for the improvement of the activity for water splitting.展开更多
The novel generation of clean energy has captured substantial public interest as the ecological environment deteriorates and fossil energy sources become depleted,with electrochemical catalysis deemed essential to the...The novel generation of clean energy has captured substantial public interest as the ecological environment deteriorates and fossil energy sources become depleted,with electrochemical catalysis deemed essential to the progress of clean energy technologies.Core-shell nanocomposite materials exhibit excellent chemical erosion resistance and effectively mitigate issues such as nanoparticle aggregation and sintering.Therefore,core-shell electrocatalysts demonstrate considerable advantages,such as enhanced activity and stability,making them widely applicable in electrocatalysis.This review offers an extensive summary of the latest advances,techniques,and applications of core-shell noble metal-based catalysts in electrocatalysis,encompassing a diverse range of synthesis techniques and strategies designed to fine-tune electrocatalytic performance.The article presents techniques such as seed-mediated growth,electrodeposition,template synthesis,and self-assembly and further delves into control strategies for enhancing electrocatalytic performance via case studies,examining electronic and geometric effects,with the former broken down into strain and ligand effects.Next,the article focuses on the remarkable progress achieved by noble metal-based core-shell structures in enhancing the efficiency of key electrocatalytic reactions,such as the hydrogen evolution reaction(HER),oxygen evolution reaction(OER),oxygen reduction reaction(ORR),and carbon dioxide reduction reaction(CO_(2)RR).Finally,the primary challenges and future prospects in this field are discussed,offering insight that will inform further research and development efforts.The primary objective of this review is to illuminate the design and construction of novel core-shell noble metal-based catalysts for energy storage and conversion technologies.展开更多
Advanced chemical engineering for simultaneous modulation of nanomaterial morphology, defects, interfaces, and structure to enhance electromagnetic and microwave absorption (MA) performance. However, accurately distin...Advanced chemical engineering for simultaneous modulation of nanomaterial morphology, defects, interfaces, and structure to enhance electromagnetic and microwave absorption (MA) performance. However, accurately distinguishing the MA contributions of different scale factors and tuning the optimal combined effects remains a formidable challenge. This study employs a synergistic approach combining template protection etching and vacuum annealing to construct a controlled system of micrometer-sized cavities and amorphous carbon matrices in metal-organic framework (MOF) derivatives. The results demonstrate that the spatial effects introduced by the hollow structure enhance dielectric loss but significantly weaken impedance matching. By increasing the proportion of amorphous carbon, the balance between electromagnetic loss and impedance matching can be effectively maintained. Importantly, in a suitable graphitization environment, the presence of oxygen vacancies in amorphous carbon can induce significant polarization to compensate for the reduced conductivity loss due to the absence of sp2 carbon. Through the synergistic effects of morphology and composition, the samples exhibit a broader absorption bandwidth (6.28 GHz) and stronger reflection loss (−61.64 dB) compared to the original MOF. In conclusion, this study aims to elucidate the multiscale impacts of macroscopic micro-nano structure and microscopic defect engineering, providing valuable insights for future research in this field.展开更多
From the perspective of revealing the theoretical foundation in structural protection and impact resistance,an elaborate discussion was provided on the room-and hightemperature deformation behaviors of novel B2-struct...From the perspective of revealing the theoretical foundation in structural protection and impact resistance,an elaborate discussion was provided on the room-and hightemperature deformation behaviors of novel B2-structured Al_(0.5)NbTi_(3)VZr_(0.5)lightweight high-entropy alloy(LHEA),which provided a kind of potential structural material in application to lightweight high-temperature instruments.展开更多
基金supported partially by the Kentucky Tobacco Research and Development Center(KTRDC),University of Kentucky.
文摘The evolutionarily conserved mitogen-activated protein kinase(MAPK)cascades relay extracellular signals into cells,triggering a variety of cellular responses.We previously revealed NtMPK4 as a positive regulator of nicotine biosynthesis;however,its upstream regulation remains unclear.Here,we characterized a MAPK cascade,comprising NtMEKK1b,NtMPKK2a,and NtMPK4,that promotes nicotine biosynthesis.This signaling module transduces external cues,including jasmonate and pathogen elicitors such as flg22,into post-translational modifications that enhance transcriptional activity and pathway gene expression.NtMPKK2a physically interacts with and phosphorylates NtMPK4 in vivo,confirming its role as an upstream kinase.RNAi-mediated silencing of NtMPKK2a significantly reduced the expression of nicotine pathway genes and decreased nicotine accumulation,whereas induced-overexpression of NtMPKK2a upregulated nicotine pathway genes and increased nicotine contents in tobacco hairy roots.Overexpression of NtMPKK2a in tobacco cells enhanced the transactivation activity of a NIC2-locus Ethylene Response Factor NtERF221 on Putrescine N-methyltransferase(NtPMT)promotor,further supporting its role in promoting nicotine biosynthesis.Furthermore,we identified NtMEKK1b,a tobacco MEKK that interacts with NtMAPKK2a in yeast cells.Knock-down of NtMEKK1b in transgenic tobacco plants attenuated the expression of nicotine pathway genes and reduced nicotine contents,whereas induced-overexpression of NtMEKK1b upregulated gene expression and nicotine accumulation.Our findings uncover a previously uncharacterized MAPK cascade module,NtMEKK1b-NtMPKK2a-NtMPK4,that regulates nicotine biosynthesis,highlighting the importance of posttranslational regulation in nicotine biosynthesis.
基金gratefully acknowledge the support from National Natural Science Foundation of China(Nos.52274305,52374309 and 52004189)Project of Hubei Provincial Department of Science and Technology(No.2022BAA021)+2 种基金China Postdoctoral Science Foundation(Nos.2023T160210 and 2022M721109)Young Elite Scientists Sponsorship Program by CAST(No.2022QNRC001)Open Foundation of Key Laboratory for Ferrous Metallurgy and Resources Utilization of Ministry of Education(FMRUlab-25-05).
文摘The dissolution behaviors of lime,limestone,and core–shell structured lime,as well as their effects on dephosphorization behavior were studied.The results show that the slow dissolution of lime in converter slag is mainly attributed to the calcium silicate layer at the lime/slag interface.CO_(2)generated by CaCO_(3)decomposition can destroy the calcium silicate layer,and thus accelerates the dissolution of limestone and core–shell structured lime.However,in the initial stage,a large amount of CO_(2)emission generated by limestone decomposition results in the poor contact between molten slag and limestone,and the dissolution rate is slower in the test of limestone than that of lime.For core–shell structured lime,the initial dissolution rate is not affected due to the lime surface,and is accelerated by the appropriate CO_(2)emission.Rapid CaO pickup in molten slag by fast dissolution of the lime sample can remarkably accelerate the dephosphorization reaction.Because of the fastest dissolution rate,the core–shell structured lime slagging mode shows the most promising prospects for the efficient dephosphorization.
基金supported by the Inoue Enryo Memorial Grant of Toyo University(2023No.63)the He’nan Provincial Natural Science Foundation,China(No.252300420433)the Leading goose research and development plan of Zhejiang,China(No.2023C02039).
文摘To enhance the visible light response of titanium dioxide(TiO_(2)),titanium carbide(TiC)nanoparticles(NPs)were thermally treated in carbon powder,effectively overcoming the challenges associated with conventional doping methods.During the treatment,a TiO_(2)thin shell with oxygen vacancies(OVs)formed around the TiC NPs,creating a shell-core structure S-scheme photocatalyst.Transmission electron microscopy(TEM)and ultraviolet-visible(UV-vis)spectroscopy confirmed the successful formation of the TiO_(2)shell.By optimizing the shell thickness,the TiO_(2)-TiC shell-core structure achieved an ideal shell-core ratio,resulting in strong visible light absorption(400-800 nm),and the degradation rate constant of Rhodamine B(RhB)of sample cHT500 reached 0.0687 min^(−1),which is 20.8times higher than that of pristine TiO_(2)(0.0033 min^(−1))under visible-light irradiation.In addition,cytocompatibility tests showed that sample cHT500 exhibits favorable cell viability,which is comparable to that of TiO_(2)nanoparticles,and thus remarkably mitigates the poor biocompatibility inherent to TiC,making them promising candidates for biomedical and photocatalytic applications.
基金Funded by the Sichuan Province Science and Technology Support Program(No.2025YFNZH0022)the Chengdu Municipal Science and Technology Program(No.2025-YF11-00003-HZ)。
文摘Curing temperature significantly affects the pozzolanic reaction kinetics of phosphorous slag(PS),thereby governing the early-age(7 d)hydration behavior of PS composite binders at 20,30,and 60℃.The Krstulovic-Dabic kinetic model was applied to identify three characteristic processes:nucleation and growth(NG),phase boundary interaction(I),and diffusion(D).Control mixtures containing inert quartz powder with comparable particle size distributions were prepared for comparison.Pore characteristics of hardened PS pastes at different temperatures were analyzed via mercury intrusion porosimetry,while hydration products were characterized using X-ray diffraction(XRD)and thermogravimetric analysis(TG-DTG).The experimental results indicate that the retarding effect of PS on early cement hydration outweighs its accelerating effect,attributed to the combined influence of nucleation and dilution,with retardation decreasing as temperature increases.PS exhibits early reactivity and continuously consumes calcium hydroxide through the pozzolanic reaction,as evidenced by stable phase assemblages accompanied by reduced CH content in XRD and TG-DTG analyses.At 20℃,increasing PS content maintains the NG→I→D mechanism but slows reaction rates across all stages.Elevated temperatures significantly accelerate the NG process,shifting the dominant mechanism from NG toward D.Simultaneously,enhanced PS reactivity contributes to a refined pore structure and improved compressive strength.
基金supported by Special Funding Projects for Local Science and Technology Development guided by the Central Committee(No.YDZJSX2022C028)the Fundamental Research Program of Shanxi Province(Nos.20210302123218 and 202203021211187)+4 种基金Innovation and Entrepreneurship Training Program for College Students in Shanxi Province(202210109006)the National Natural Science Foundation(52474367)the Key Research and Development for University-Local Government Collaboration of Lvliang City(2024XDHZ01)the Scientific and Technological Innovation Programs of Higher Education Institutions in Shanxi(2025Q022)the Foundation of State Key Laboratory of Advanced Metallurgy,USTB(K22-10).
文摘The structural changes in the CaO-SiO_(2)-Al_(2)O_(3)-MgO slag system with varying CaO contents were investigated through molecular dynamics(MD)simulations,and its effect on the dissolution behavior of alumina inclusions was characterized by the Kullback-Leibler(KL)divergence.The slag structure analysis revealed that the[AlO]tetrahedral structure was the primary network structure in the slag.With increasing the CaO content,the non-bridge oxygen(NBO)content in the slag structure increases,and the bridge oxygen(BO)content decreases,thereby reducing the complexity of the slag network structure.Raman spectroscopy detection verifies the results of the MD simulations.The results indicated that the dissolution rate of alumina inclusions accelerates with increasing the CaO content in the slag,owing to the reduced complexity of the slag network structure and the enhanced interatomic interactions.The simulation results for the dissolution of alumina inclusions were consistent with theoretical calculations based on the slag inclusion capacity and the dimensionless dissolution rate of inclusions.Radial distribution function analysis demonstrated that the interaction between atoms in the slag system and alumina inclusions strengthens,increasing the dissolution rate of alumina inclusions.The[AlO_(6)]octahedral structure of the alumina inclusions is disrupted,forming BO structures,which in turn enhances the complexity of the slag network structure,slowing the dissolution rate of alumina inclusions.In contrast,the slag system with a higher CaO content has a relatively simpler network structure,promoting faster alumina inclusion dissolution.
基金financially supported by the supported by Shandong Provincial Natural Science Foundation(ZR2024MB108)Taishan Young Scholar Program(tsqn202312312)Excellent Young Scholars of the Shandong Provincial Natural Science Foundation(Overseas)(2023HWYQ-112)。
文摘Conversion-type electrode materials hold significant promise for potassium-ion batteries(PIBs)due to their high theoretical capacities,yet their practical deployment is hindered by sluggish kinetics and irreversible structural degradation.To overcome these limitations,we propose a rationally engineered nanoreactor architecture that stabilizes defect-rich MoS_(2)via interlayer incorporation of a carbon monolayer,followed by encapsulation within a nitrogen-doped carbon shell,forming a MoSSe@NC heterostructure.This tailored structure synergistically accelerates both K^(+)diffusion kinetics and electron transfer,enabling unprecedented rate performance(107 mAh g^(-1)at 10 Ag^(-1))and ultralong cyclability(86.5%capacity retention after 1200 cycles at 3 A g^(-1)).Mechanistic insights reveal a distinctive“adsorption-conversion”pathway,where sulfur vacancies on exposed S-Mo-S basal planes act as preferential K^(+)adsorption sites,effectively suppressing parasitic phase transitions during intercalation.In situ X-ray diffraction and transmission electron microscopy corroborate the structural reversibility of the conversion reaction,with the carbon matrix dynamically accommodating strain while preserving electrode integrity.This work not only advances the understanding of defect-driven interfacial chemistry in conversion-type materials but also provides a versatile strategy for designing high-performance anodes in next-generation PIBs through heterostructure engineering.
基金supported by the National Natural Science Foundation of Guangxi Province(2024GXNSFBA010033)the Special Fund for Science and Technology Development of Guangxi(Grant No.AD25069078).
文摘Ammonium-ion hybrid supercapacitors(A-HSCs)have emerged as promising candidates for next-generation energy storage owing to their inherent safety and environmental sustainability.Hexagonal tungsten oxide(h-WO_(3)),with its well-defined tunnel structure,holds great promise as a negative electrode material for NH^(4+)storage.However,its practical application is hindered by structural instability and poor intrinsic electrical conductivity.To address these challenges,a dual-regulation strategy is proposed,integrating molybdenum(Mo)doping and NH^(4+)pre-intercalation to concurrently optimize the tunnel structure and electronic environment of h-WO_(3)(Mo-NWO).Comprehensive experimental and theoretical analyses reveal that Mo doping narrows the bandgap of WO_(3)and reduces the diffusion energy barrier,thereby accelerating NH^(4+)adsorption and diffusion.Simultaneously,NH^(4+)pre-intercalation stabilizes the tunnel framework via hydrogen bonding,ensuring structural reversibility.As expected,the Mo-NWO/AC electrode achieves a high areal capacitance of 13.6 F cm^(−2)at 5 mA cm^(−2)and retains 80.14%of its capacitance after 5000 cycles,demonstrating exceptional rate capability and cycling stability.Moreover,the assembled Mn_(3)O_(4)//Mo-NWO/AC device delivers a high energy density of 3.41 mWh cm^(−2)and outstanding long-term stability(85.75%retention after 12,000 cycles).This work provides a viable strategy for designing high-performance NH^(4+)storage materials and advances the development of sustainable energy storage systems.
文摘To assess the effectiveness of vaccination in contaminated environments,this study introduces a modeling framework that encompasses two transmission routes,namely direct human-to-human contact and indirect human-to-environment contact,as well as the implementation of new M72/AS01_(E)vaccine.Motivated by this,a coupled age-structured tuberculosis(TB)model is proposed.Its well-posedness requirement is verified using the integrated semigroup theory.Furthermore,this study presents a comprehensive analysis of threshold dynamics associated with the proposed model.Specifically,the global stability of the disease-free and positive steady states is demonstrated by employing Lyapunov functionals.Lastly,the effects of the vaccination with M72/AS01_(E)and contaminated environments on TB control are numerically simulated.Experimental results indicate that high concentrations of Mycobacterium tuberculosis in contaminated environments may somewhat impede TB control efforts,but that large-scale deployment of new vaccine could significantly reduce the prevalence of TB.
基金financially supported by National Natural Science Foundation of China(Grant Nos.12141203,52202083,W2421013)the Natural Science Foundation Project of Shaanxi Province(Grant No.2024JC-YBMS-450)+1 种基金the Sichuan Science and Technology Program(Grant No.2024YFHZ0265)the Open Project of High-end Equipment Advanced Materials and Manufacturing Technology Laboratory(Grant No.2023KFKT0005)。
文摘Designing materials with both structural load-bearing capacity and broadband electromagnetic(EM)wave absorption properties remains a significant challenge.In this work,SiOC/SiC/SiO_(2)composite with gyroid structures were prepared through digital light processing(DLP)3D printing,polymer-derived ceramics(PDCs),chemical vapor infiltration(CVI),and oxidation technologies.The incorporation of the CVISiC phase effectively increases the dissipation capability,while the synergistic interaction between the gyroid structure and SiO_(2)phase significantly improves impedance matching performance.The SiOC/SiC/SiO_(2)composite achieved a minimum reflection loss(RL min)of-62.2 d B at 4.3 mm,and the effective absorption bandwidth(EAB)covered the X-band,with a thickness range of 4.1 mm-4.65 mm.The CST simulation results explain the broadband and low-frequency absorption characteristics,with an EAB of 8.4 GHz(9.6-18 GHz)and an RL min of-21.5 dB at 5 GHz.The excellent EM wave attenuation performance is associated primarily with polarization loss,conduction loss,the gyroid structure's enhancement of multiple reflections and scattering of EM waves,and the resonance effect between the structural units.The SiOC/SiC/SiO_(2)composite also demonstrated strong mechanical properties,with a maximum compressive failure strength of 31.6 MPa in the height direction.This work opens novel prospects for the development of multifunctional structural wave-absorbing materials suitable for broadband microwave absorption and load-bearing properties.
基金Project supported by the Joints Fund of the National Natural Science Foundation of China(Grant No.U23A20349)the Young Scientists Fund of the National Natural Science Foundation of China(Grant Nos.62204126,62305171,62304113)。
文摘With the rapid advancement of optoelectronic technology,high-performance photodetectors are increasingly in demand in fields such as environmental monitoring,optical communication,and defense systems,where ultraviolet detection is critical.However,conventional semiconductor materials suffer from limited UV-visible detection capabilities owing to their narrow bandgaps and high dark currents.To address these challenges,wide-bandgap semiconductors have emerged as promising alternatives.Here,we fabricated a horizontally structured n–n heterojunction photodetector by growingβ-Ga_(2)O_(3) on Si–GaN via plasma-enhanced chemical vapor deposition.The device exhibits a self-powered photocurrent of 3.5 nA at zero bias,enabled by the photovoltaic effect of the space charge region.Under 254-nm and 365-nm illumination,it exhibits rectification behavior,achieving a responsivity of 0.475 m A/W(0 V,220??W/cm~2 at 254 nm)and 257.6 mA/W(-5 V),respectively.Notably,the photodetector demonstrates a high photocurrent-to-dark current ratio of 10~5 under-5-V bias,highlighting its potential for self-powered and high-performance UV detection applications.
基金supported by the Natural Science Foundation of Shandong Province(Nos.ZR2024QE450,ZR2024QB302 and ZR2024QB004)the Taishan Scholars and Young Experts Program of Shandong Province(No.tsqn202211249)Research Program of Qilu Institute of Technology(Nos.QIT 23TP019,QIT23TP010 and QIT24NN007)。
文摘The large volume expansion and rapid capacity attenuation of tin-based electrodes are the main factors limiting their commercial application.The reasonable design of electrode material structure is particularly important for improving its electrochemical performance.Herein,phosphorus-modified graphene encapsulated Sn_(6)O_(4)(OH)_(4)nanoparticles composite(P-Sn_(6)O_(4)(OH)_(4)@RGO)with crystalline-amorphous heterostructure has been successfully designed and prepared.The design of crystalline-amorphous structure has largely enhanced the active sites,and the construction of a graphene encapsulation structure has greatly alleviated volume expansion.Notably,P-Sn_(6)O_(4)(OH)_(4)@RGO obtained an excellent high-rate longterm cycling performance for lithium-ion batteries anode,reaching a high specific capacity of 970 m Ah/g at 1.0 A/g after 1450 cycles.This work demonstrates that restructuring the electrode material's structure and phase through phosphorus modification can effectively improve the electrochemical performance of tin-based electrode materials.
基金financially supported by the National Natural Science Foundation of China(Nos.52425408 and 52304345)the Fundamental Research Funds for the Central Universities,China(No.2023CDJXY-016)the Postdoctoral Science Foundation of Chongqing(No.CSTB2023NSCQ-BHX0174)。
文摘Currently,the Al_(2)O_(3)content in the high-alumina slag systems within blast furnaces is generally limited to 16wt%–18.5wt%,making it challenging to overcome this limitation.Unlike most studies that concentrated on managing the MgO/Al_(2)O_(3)ratio or basicity,this paper explored the effect of equimolar substitution of MgO for CaO on the viscosity and structure of a high-alumina CaO-MgO-Al_(2)O_(3)-SiO_(2)slag system,providing theoretical guidance and data to facilitate the application of high-alumina ores.The results revealed that the viscosity first decreased and then increased with higher MgO substitution,reaching a minimum at 15mol%MgO concentration.Fourier transform infrared spectroscopy(FTIR)results found that the depths of the troughs representing[SiO_(4)]tetrahedra,[AlO_(4)]tetrahedra,and Si-O-Al bending became progressively deeper with increased MgO substitution.Deconvolution of the Raman spectra showed that the average number of bridging oxygens per Si atom and the X_(Q^(3))/X_(Q^(2))(X_(Q^(i))is the molar fraction of Q^(i) unit,and i is the number of bridging oxygens in a[SiO_(4)]tetrahedral unit)ratio increased from 2.30 and 1.02 to 2.52 and 2.14,respectively,indicating a progressive polymerization of the silicate structure.X-ray photoelectron spectroscopy(XPS)results highlighted that non-bridging oxygen content decreased from 77.97mol% to 63.41mol% with increasing MgO concentration,whereas bridging oxygen and free oxygen contents increased.Structural analysis demonstrated a gradual increase in the polymerization degree of the tetrahedral structure with the increase in MgO substitution.However,bond strength is another important factor affecting the slag viscosity.The occurrence of a viscosity minimum can be attributed to the complex evolution of bond strengths of non-bridging oxygens generated during depolymerization of the[SiO_(4)]and[AlO_(4)]tetrahedral structures by CaO and MgO.
基金sponsored by the National Natural Science Foundation of China(Nos.5210125 and 52375422)the Science Research Project of Hebei Education Department(No.BJK2023058)the Natural Science Foundation of Hebei Province(Nos.E2020208069,B2020208083 and E202320801).
文摘The stability and electrocatalytic efficiency of transition metal oxides for water splitting is determined by geometric and electronic structure,especially under high current densities.Herein,a newly designed lamella-heterostructured nanoporous CoFe/CoFe_(2)O_(4) and CeO_(2−x),in situ grown on nickel foam(NF),holds great promise as a high-efficient bifunctional electrocatalyst(named R-CoFe/Ce/NF)for water splitting.Experimental characterization verifies surface reconstruction from CoFe alloy/oxide to highly active CoFeOOH during in situ electrochemical polarization.By virtues of three-dimensional nanoporous architecture and abundant electroactive CoFeOOH/CeO_(2−x) heterostructure interfaces,the R-CoFe/Ce/NF electrode achieves low overpotentials for oxygen evolution(η_(10)=227 mV;η_(500)=450 mV)and hydrogen evolution(η_(10)=35 mV;η_(408)=560 mV)reactions with high normalized electrochemical active surface areas,respectively.Additionally,the alkaline full water splitting electrolyzer of R-CoFe/Ce/NF||R-CoFe/Ce/NF achieves a current density of 50 mA·cm^(−2) only at 1.75 V;the decline of activity is satisfactory after 100-h durability test at 300 mA·cm^(−2).Density functional theory also demonstrates that the electron can transfer from CeO_(2−x) by virtue of O atom to CoFeOOH at CoFeOOH/CeO_(2−x) heterointerfaces and enhancing the adsorption of reactant,thus optimizing electronic structure and Gibbs free energies for the improvement of the activity for water splitting.
基金financially supported by the National Natural Science Foundation of China(Nos.52001136,52171179 and 82371913)the Youth Innovation Team of Higher Education Institutions in Shandong Province(No.2023KJ105)Collaborative Innovation Center of Yellow River Basin Pharmaceutical Green Manufacturing and Engineering Equipment,University of Jinan,Jinan 250022,China,Jinan City University Integration Development Strategy Project(No.JNSX2023021).
文摘The novel generation of clean energy has captured substantial public interest as the ecological environment deteriorates and fossil energy sources become depleted,with electrochemical catalysis deemed essential to the progress of clean energy technologies.Core-shell nanocomposite materials exhibit excellent chemical erosion resistance and effectively mitigate issues such as nanoparticle aggregation and sintering.Therefore,core-shell electrocatalysts demonstrate considerable advantages,such as enhanced activity and stability,making them widely applicable in electrocatalysis.This review offers an extensive summary of the latest advances,techniques,and applications of core-shell noble metal-based catalysts in electrocatalysis,encompassing a diverse range of synthesis techniques and strategies designed to fine-tune electrocatalytic performance.The article presents techniques such as seed-mediated growth,electrodeposition,template synthesis,and self-assembly and further delves into control strategies for enhancing electrocatalytic performance via case studies,examining electronic and geometric effects,with the former broken down into strain and ligand effects.Next,the article focuses on the remarkable progress achieved by noble metal-based core-shell structures in enhancing the efficiency of key electrocatalytic reactions,such as the hydrogen evolution reaction(HER),oxygen evolution reaction(OER),oxygen reduction reaction(ORR),and carbon dioxide reduction reaction(CO_(2)RR).Finally,the primary challenges and future prospects in this field are discussed,offering insight that will inform further research and development efforts.The primary objective of this review is to illuminate the design and construction of novel core-shell noble metal-based catalysts for energy storage and conversion technologies.
基金supported by the National Natural Science Foundation of China(52172091,52172295)Defense Industrial Technology Development Program(JCKY2023605C002)+4 种基金Frontier Leading Technology Basic Research Major Project of Jiangsu Province(SBK2023050110)the National Key Laboratory on Electromagnetic Environmental Effects and Electro-optical Engineering(NO.61422062301)the Opening Project of Science and Technology on Reliability Physics and Application Technology of Electronic Component Laboratory(ZHD202305)the Opening Project of Jiangsu Key Laboratory of Advanced Structural Materials and Application Technology(ASMA202303)the Postgraduate Research&Practice Innovation Program of Jiangsu Province(KYCX23_0371).
文摘Advanced chemical engineering for simultaneous modulation of nanomaterial morphology, defects, interfaces, and structure to enhance electromagnetic and microwave absorption (MA) performance. However, accurately distinguishing the MA contributions of different scale factors and tuning the optimal combined effects remains a formidable challenge. This study employs a synergistic approach combining template protection etching and vacuum annealing to construct a controlled system of micrometer-sized cavities and amorphous carbon matrices in metal-organic framework (MOF) derivatives. The results demonstrate that the spatial effects introduced by the hollow structure enhance dielectric loss but significantly weaken impedance matching. By increasing the proportion of amorphous carbon, the balance between electromagnetic loss and impedance matching can be effectively maintained. Importantly, in a suitable graphitization environment, the presence of oxygen vacancies in amorphous carbon can induce significant polarization to compensate for the reduced conductivity loss due to the absence of sp2 carbon. Through the synergistic effects of morphology and composition, the samples exhibit a broader absorption bandwidth (6.28 GHz) and stronger reflection loss (−61.64 dB) compared to the original MOF. In conclusion, this study aims to elucidate the multiscale impacts of macroscopic micro-nano structure and microscopic defect engineering, providing valuable insights for future research in this field.
基金financially supported by the Science and Technology Innovation Fund Project of GRIMAT Engineering Institute Co.,Ltd.,China and the National Key R&D Program of China(No.2023YFB3710403)
文摘From the perspective of revealing the theoretical foundation in structural protection and impact resistance,an elaborate discussion was provided on the room-and hightemperature deformation behaviors of novel B2-structured Al_(0.5)NbTi_(3)VZr_(0.5)lightweight high-entropy alloy(LHEA),which provided a kind of potential structural material in application to lightweight high-temperature instruments.
