Direct seawater splitting has emerged as a popular and promising research direction for synthesising clean,green,non-polluting,and sustainable hydrogen energy without depending on high-purity water in the face of the ...Direct seawater splitting has emerged as a popular and promising research direction for synthesising clean,green,non-polluting,and sustainable hydrogen energy without depending on high-purity water in the face of the world’s shortage of fossil energy.However,efficient seawater splitting is hindered by slow kinetics caused by the ultra-low conductivity and the presence of bacteria,microorganisms,and stray ions in seawater.Additionally,producing hydrogen on an industrial scale is challenging due to the high production cost.The present review addresses these challenges from the catalyst point of view,namely,that designing catalysts with high catalytic activity and stability can directly affect the rate and effect of seawater splitting.From the ion transfer perspective,designing membranes can block harmful ions,improving the stability of seawater splitting.From the energy point of view,mixed seawater systems and self-powered systems also provide new and low-energy research systems for seawater splitting.Finally,ideas and directions for further research on direct seawater splitting in the future are pointed out,with the aim of achieving low-cost and high-efficiency hydrogen production.展开更多
Radiative cooling is a passive thermal management strategy that leverages the natural ability of materials to dissipate heat through infrared radiation.It has significant implications for energy efficiency,climate ada...Radiative cooling is a passive thermal management strategy that leverages the natural ability of materials to dissipate heat through infrared radiation.It has significant implications for energy efficiency,climate adaptation,and sustainable technology development,with applications in personal thermal management,building temperature regulation,and aerospace engineering.However,radiative cooling performance is susceptible to environmental aging and special environmental conditions,limiting its applicability in extreme environments.Herein,a critical review of extreme environmental radiative cooling is presented,focusing on enhancing environmental durability and cooling efficiency.This review first introduces the design principles of heat exchange channels,which are tailored based on the thermal flow equilibrium to optimize radiative cooling capacity in various extreme environments.Subsequently,recent advancements in radiative cooling materials and micronano structures that align with these principles are systematically discussed,with a focus on their implementation in terrestrial dwelling environments,terrestrial extreme environments,aeronautical environments,and space environments.Moreover,this review evaluates the cooling effects and anti-environmental abilities of extreme radiative cooling devices.Lastly,key challenges hindering the development of radiative cooling devices for extreme environmental applications are outlined,and potential strategies to overcome these limitations are proposed,aiming to prompt their future commercialization.展开更多
Mimicking the hierarchical structure of the skin is one of the most important strategies in skin tissue engineering.Monolayer wound dressings are usually not able to provide several functions at the same time and cann...Mimicking the hierarchical structure of the skin is one of the most important strategies in skin tissue engineering.Monolayer wound dressings are usually not able to provide several functions at the same time and cannot meet all clinical needs.In order to maximize therapeutic efficiency,herein,we fabricated a Tri-layer wound dressing,where the middle layer was fabricated via 3D-printing and composed of alginate,tragacanth and zinc oxide nanoparticles(ZnO NPs).Both upper and bottom layers were constructed using electrospinning technique;the upper layer was made of hydrophobic polycaprolactone to mimic epidermis,while the bottom layer consisted of Soluplus■ and insulin-like growth factor-1(IGF-1)to promote cell behavior.Swelling,water vapor permeability and tensile properties of the dressings were evaluated and the Tri-layer dressing exhibited impressive antibacterial activity and cell stimulation following by the release of ZnO NPs and IGF-1.Additionally,the Tri-layer dressing led to faster healing of full-thicknesswound in ratmodel compared to monolayer and Bilayer dressings.Overall,the evidence confirmed that the Trilayer wound dressing is extremely effective for full-thickness wound healing.展开更多
Unmanned combat aerial vehicles require lightweight,stealth-capable exhaust systems.However,traditional metallic nozzles increase radar detectability and reduce range,while advanced composites offer high performance b...Unmanned combat aerial vehicles require lightweight,stealth-capable exhaust systems.However,traditional metallic nozzles increase radar detectability and reduce range,while advanced composites offer high performance but are expensive.Therefore,to improve the operational range and survivability of unmanned combat aerial vehicles,a lightweight,high-temperature-resistant,oxidation-resistant,and low-observable composite exhaust nozzle is developed to replace conventional metallic straight-type nozzles.The nozzle features a double serpentine shape to reduce radar and infrared signatures and is manufactured as a monolithic structure using the filament winding process,accommodating the complex geometry and large size(length:1.8 m,width:0.8 m).The exhaust nozzle consists of a ceramic matrix composite made of silicon carbide fibers and a silicon oxycarbide matrix,which absorbs and scatters radio frequency signals while withstanding prolonged exposure to high-temperature(700℃)oxidizing environments typical of engine exhaust gases.The polysiloxane resin used to produce the silicon oxycarbide matrix poses significant challenges owing to its low tackiness and high viscosity variations depending on the presence of nanoparticles,making filament winding difficult.These challenges are addressed by optimizing resin viscosity and winding pattern design.As a result,the tensile strength of the composite specimens fabricated with the optimized viscosity increases by 228.03% before pyrolysis and 97.68%after pyrolysis,compared with that of the non-optimized specimens.In addition,the density and tensile strength of the composite processed via three cycles of polymer infiltration and pyrolysis increased by 13.08% and 80.37%,respectively,compared to those of the non-densified composite.High-temperature oxidation and flame tests demonstrate exceptional thermal and oxidative stability.Furthermore,when compared with carbon fiber-reinforced ceramic matrix composites,the developed composite exhibits a permittivity at least two levels lower and a reflection loss below7 dB within the frequency range of 9.3-10.9 GHz,underscoring its superior electromagnetic stealth performance.展开更多
The composition−property relationship of 18 quaternary high entropy diborides(HEBs)consisting of boron and IVB,VB and VIB transition metals(TM)was investigated using first-principles calculations.A valence electron co...The composition−property relationship of 18 quaternary high entropy diborides(HEBs)consisting of boron and IVB,VB and VIB transition metals(TM)was investigated using first-principles calculations.A valence electron concentration−relative electronegativity(VEC−REN)composite descriptor was developed to effectively predict the mechanical properties of HEBs.The results demonstrate that with a fixed VEC,the rise of the REN makes HEBs harder but more brittle when the electronegativity of doped TM atoms is lower than that of boron atoms.However,HEBs become softer and more ductile as REN increases if the doped TM atoms have higher electronegativity than boron atoms.The VEC−REN composite descriptor can accurately classify and predict the mechanical properties of HEBs with different components,which provides important theoretical guidance for the rapid design and development of novel high-entropy ceramic materials.展开更多
Electrocatalytic co-reduction of CO_(2)and nitrate offers an attractive and sustainable pathway for urea synthesis,as it enables the simultaneous valorization of nitrogenous waste and CO_(2)into value-added chemicals....Electrocatalytic co-reduction of CO_(2)and nitrate offers an attractive and sustainable pathway for urea synthesis,as it enables the simultaneous valorization of nitrogenous waste and CO_(2)into value-added chemicals.However,achieving ambient and high-performance urea electrosynthesis remains a persistent challenge,as it requires the simultaneous activation of CO_(2)and efficient H_(2)O dissociation to supply active^(*)H for^(*)NO x hydrogenation—ultimately forming key Cand N-containing intermediates necessary for effective C-N coupling.The stringent,sequential nature of the reaction requirements continues to present substantial challenges for the rational design of advanced multifunctional catalysts.Herein,we report a creative two-in-one catalyst,bifunctional Pd-single-atom-modified Cu(Pd_(1)Cu)nanorods,to synergistically promote the adsorption and stepwise activation of dual species,that is,CO_(2)and H_(2)O,thereby effectively steering the reaction pathway toward the highly selective synthesis of urea.By integrating experimental evidence,in situ spectroscopy,and computational analyses,we clearly disclose that the atomically dispersed Pd sites kinetically favor the co-generation of^(*)CO and^(*)NH_(2)(via H_(2)O dissociation-driven proton transfer),thereby forming an optimal intermediate balance that facilitates urea synthesis.More importantly,the rationally designed Pd_(1)Cu leverages dual metal active sites to enhance C-N coupling via combined electronic and geometric effects,substantially lowering the reaction energy barrier and improving selectivity toward urea.展开更多
Extreme cold weather seriously harms human thermoregulatory system,necessitating high-performance insulating garments to maintain body temperature.However,as the core insulating layer,advanced fibrous materials always...Extreme cold weather seriously harms human thermoregulatory system,necessitating high-performance insulating garments to maintain body temperature.However,as the core insulating layer,advanced fibrous materials always struggle to balance mechanical properties and thermal insulation,resulting in their inability to meet the demands for both washing resistance and personal protection.Herein,inspired by the natural spring-like structures of cucumber tendrils,a superelastic and washable micro/nanofibrous sponge(MNFS)based on biomimetic helical fibers is directly prepared utilizing multiple-jet electrospinning technology for high-performance thermal insulation.By regulating the conductivity of polyvinylidene fluoride solution,multiple-jet ejection and multiple-stage whipping of jets are achieved,and further control of phase separation rates enables the rapid solidification of jets to form spring-like helical fibers,which are directly entangled to assemble MNFS.The resulting MNFS exhibits superelasticity that can withstand large tensile strain(200%),1000 cyclic tensile or compression deformations,and retain good resilience even in liquid nitrogen(-196℃).Furthermore,the MNFS shows efficient thermal insulation with low thermal conductivity(24.85 mW m^(-1)K^(-1)),close to the value of dry air,and remains structural stability even after cyclic washing.This work offers new possibilities for advanced fibrous sponges in transportation,environmental,and energy applications.展开更多
We are sorry for the mistakes of Affiliation,"a State Key Laboratory of Advanced Fiber Materials,Center for Advanced Low-Dimension Materials,Donghua University,Shanghai 201620,China"should be replaced by&quo...We are sorry for the mistakes of Affiliation,"a State Key Laboratory of Advanced Fiber Materials,Center for Advanced Low-Dimension Materials,Donghua University,Shanghai 201620,China"should be replaced by"a State Key Laboratory of Advanced Fiber Materials,Center for Advanced Low-Dimension Materials,College of Materials Science and Engineering,Donghua University,Shanghai 201620,China".We apologized for the inconvenience caused by this error.展开更多
CO_(2)utilization powered by sustainable energy offers a promising route to mitigate carbon emissions while producing value-added chemicals[1].Among these pathways,CO_(2)hydrogenation is especially attractive because ...CO_(2)utilization powered by sustainable energy offers a promising route to mitigate carbon emissions while producing value-added chemicals[1].Among these pathways,CO_(2)hydrogenation is especially attractive because it integrates renewable H 2 with carbon resources,which have achieved notable success in producing methanol,CO,etc.[2,3].展开更多
PEGylation,the controlled covalent conjugation of polyethylene glycol to therapeutics,enhances therapeutic efficacy through optimized pharmacokinetics.However,to date no high-molecular-weight PEGylated small-molecule ...PEGylation,the controlled covalent conjugation of polyethylene glycol to therapeutics,enhances therapeutic efficacy through optimized pharmacokinetics.However,to date no high-molecular-weight PEGylated small-molecule prodrugs have received regulatory approval.This technological gap can be partially attributed to the exponential proliferation of metabolic intermediates resulting from multi-payload conjugation strategies,which introduces unprecedented analytical complexities in metabolite profiling and pharmacokinetic characterization.To address this challenge,we developed a liquid chromatography-triple-quadrupole/time-of-flight mass spectrometry platform for PEG20k-(irinotecan)3,a Phase III clinical candidate.Our methodology employs payload stoichiometry-based chromatographic resolution for clustering isomeric PEG species.Complementarily,diagnostic product ions at m/z 699.83,569.27,and 587.28 enable systematic differentiation between double-loaded,single-loaded,and released irinotecan payload.This approach successfully identifies eight metabolic clusters spanning from PEG-conjugates,cleaved PEG segments,and released small-molecule species.Its demonstrated capacity to deconvolute complex metabolic profiles—through payload-stoichiometry based chromatographic resolution coupled with diagnostic ion analysis—positions this workflow as an attractive tool for accelerating the development of PEGylated small-molecule therapeutics.展开更多
Tin-lead(Sn-Pb)halide perovskite single crystals combine narrow bandgaps,long carrier diffusion lengths,and low trap densities,positioning them as ideal candidates for near-infrared(NIR)optoelectronics.However,convent...Tin-lead(Sn-Pb)halide perovskite single crystals combine narrow bandgaps,long carrier diffusion lengths,and low trap densities,positioning them as ideal candidates for near-infrared(NIR)optoelectronics.However,conventional growth strategies rely on bulk crystallization at elevated temperatures,leading to uncontrolled nucleation,Sn^(2+)oxidation,and poor compatibility with planar integration.Here,we develop a coordination-engineered crystallization strategy that enables direct,lowtemperature growth of micrometer-thick Sn-Pb single-crystal thin films on device-compatible substrates.By modulating metal-solvent coordination strength using a low-donor number cosolvent system,we delineate a narrow processing window that stabilizes precursor speciation,lowers the nucleation barrier,and guides directional crystal growth under mild thermal conditions(<40℃).The resulting crystal films exhibit smooth morphology,high crystallinity,compositional uniformity,and ultralow trap densities(~3.98×10^(12)cm^(-3)).When integrated into NIR photodetectors,these films deliver high responsivity(0.51 A W^(-1)at 900 nm),specific detectivity up to 3.6×10^(12)Jones,fast response(~188μs),and>25,000 cycles of ambient operational stability.This approach establishes a scalable platform for redox-stable,low-temperature growth of Sn-Pb perovskite crystal films and expands the processing-structure-function landscape for next-generation infrared optoelectronics.展开更多
Lithium-oxygen(Li-O2)batteries are perceived as a promising breakthrough in sustainable electrochemical energy storage,utilizing ambient air as an energy source,eliminating the need for costly cathode materials,and of...Lithium-oxygen(Li-O2)batteries are perceived as a promising breakthrough in sustainable electrochemical energy storage,utilizing ambient air as an energy source,eliminating the need for costly cathode materials,and offering the highest theoretical energy density(~3.5 k Wh kg^(-1))among discussed candidates.Contributing to the poor cycle life of currently reported Li-O_(2)cells is singlet oxygen(1O_(2))formation,inducing parasitic reactions,degrading key components,and severely deteriorating cell performance.Here,we harness the chirality-induced spin selectivity effect of chiral cobalt oxide nanosheets(Co_(3)O_(4)NSs)as cathode materials to suppress 1O_(2)in Li-O_(2)batteries for the first time.Operando photoluminescence spectroscopy reveals a 3.7-fold and 3.23-fold reduction in 1O_(2)during discharge and charge,respectively,compared to conventional carbon paperbased cells,consistent with differential electrochemical mass spectrometry results,which indicate a near-theoretical charge-to-O_(2)ratio(2.04 e-/O_(2)).Density functional theory calculations demonstrate that chirality induces a peak shift near the Fermi level,enhancing Co 3d-O 2p hybridization,stabilizing reaction intermediates,and lowering activation barriers for Li_(2)O_(2)formation and decomposition.These findings establish a new strategy for improving the stability and energy efficiency of sustainable Li-O_(2)batteries,abridging the current gap to commercialization.展开更多
Strategies for achieving high-energy-density lithium-ion batteries include using high-capacity materials such as high-nickel NCM,increasing the active material content in the electrode by utilizing high-conductivity c...Strategies for achieving high-energy-density lithium-ion batteries include using high-capacity materials such as high-nickel NCM,increasing the active material content in the electrode by utilizing high-conductivity carbon nanotubes(CNT)conductive materials,and electrode thickening.However,these methods are still limited due to the limitation in the capacity of high-nickel NCM,aggregation of CNT conductive materials,and nonuniform material distribution of thick-film electrodes,which ultimately damage the mechanical and electrical integrity of the electrode,leading to a decrease in electrochemical performance.Here,we present an integrated binder-CNT composite dispersion solution to realize a high-solids-content(>77 wt%)slurry for high-mass-loading electrodes and to mitigate the migration of binder and conductive additives.Indeed,the approach reduces solvent usage by approximately 30%and ensures uniform conductive additive-binder domain distribution during electrode manufacturing,resulting in improved coating quality and adhesive strength for high-mass-loading electrodes(>12 mAh cm^(−2)).In terms of various electrode properties,the presented electrode showed low resistance and excellent electrochemical properties despite the low CNT contents of 0.6 wt%compared to the pristine-applied electrode with 0.85 wt%CNT contents.Moreover,our strategy enables faster drying,which increases the coating speed,thereby offering potential energy savings and supporting carbon neutrality in wet-based electrode manufacturing processes.展开更多
High calcium-fly ash(HCFA)collected from the Mae Moh electricity generating plant in Thailand was utilized as a raw material for ceramic production.The main compositions of HCFA characterized by X-ray fluorescence mai...High calcium-fly ash(HCFA)collected from the Mae Moh electricity generating plant in Thailand was utilized as a raw material for ceramic production.The main compositions of HCFA characterized by X-ray fluorescence mainly consisted of 28.55wt%SiO_(2),16.06wt%Al_(2)O_(3),23.40wt%CaO,and 17.03wt%Fe_(2)O_(3).Due to high proportion of calcareous and ferruginous contents,HCFA was used for replacing the potash feldspar in amounts of 10wt%-40wt%.The influence of substituting high-calcium fly ash(0-40wt%)and sintering temperatures(1000-1200℃)on physical,mechanical,and thermal properties of ceramic-based materials was investigated.The results showed that the in-corporation of HCFA in appropriate amounts could enhance the densification and the strength as well as reduce the thermal conductivity of ceramic samples.High proportion of calcareous and ferruginous constituents in fly ash promoted the vitrification behavior of ceramic samples.As a result,the densification was enhanced by liquid phase formation at optimum fly ash content and sintering temperature.In addition,these components also facilitated a more abundant mullite formation and consequently improved flexural strength of the ceramic samples.The op-timum ceramic properties were achieved with adding fly ash content between 10wt%-30wt%sintered at 1150-1200℃.At 1200℃,the max-imum flexural strength of ceramic-FA samples with adding fly ash 10wt%-30wt%(PSW-FA(10)-(30))was obtained in the range of 92.25-94.71 MPa when the water absorption reached almost zero(0.03%).In terms of thermal insulation materials,the increase in fly ash addi-tion had a positively effect on the thermal conductivity,due to the higher levels of porosity created by gas evolving from the inorganic decom-position reactions inside the ceramic-FA samples.The addition of 20wt%-40wt%high-calcium fly ash in ceramic samples sintered at 1150℃reduced the thermal conductivity to 14.78%-49.25%,while maintaining acceptable flexural strength values(~45.67-87.62 MPa).Based on these promising mechanical and thermal characteristics,it is feasible to utilize this high-calcium fly ash as an alternative raw material in clay compositions for manufacturing of ceramic tiles.展开更多
A two-dimensional(2 D)SnNb_(2)O_(6)/amino-functionalized graphene(En-RGO)nanocomposite with a representative 2 D-2 D architecture has been constructed by an easy self-assembly approach and firstly investigated as anod...A two-dimensional(2 D)SnNb_(2)O_(6)/amino-functionalized graphene(En-RGO)nanocomposite with a representative 2 D-2 D architecture has been constructed by an easy self-assembly approach and firstly investigated as anode materials for secondary sodium-ion batteries.The SnNb_(2)O_(6)nanosheets are evenly anchored with the aminofunctionalized graphene through electrostatic attractive interplay between the negatively charged SnNb_(2)O_(6)and positively charged En-RGO after modification.As a result,a remarkable reversible capacity of 300 mAh·g^(-1)was obtained at 50 mA·g^(-1),and significantly,the En-RGO electrode could also deliver ultra-long calendar life up to1900 cycles with a high reversible capacity of200 mAh·g^(-1)at current of 500 mA·g^(-1).Such excellent electrochemical characteristics can be mainly ascribed to its fast pseudo-capacitive energy storage mechanism,and the capacitive contribution can even reach up to 90%at1.2 mV·s^(-1).展开更多
Anisotropic Pr-Fe-B films with soft-magnetic layer （Fe） and/or antiferromagnetic layer （Mn, FeMn or MnO） were prepared by direct-current （DC） magnetron sputtering on Si （100） substrates heated at 650℃. The in...Anisotropic Pr-Fe-B films with soft-magnetic layer （Fe） and/or antiferromagnetic layer （Mn, FeMn or MnO） were prepared by direct-current （DC） magnetron sputtering on Si （100） substrates heated at 650℃. The influence of four types＇ different structures on the magnetic properties of Pr-Fe-B films was investigated. The phase and magnetic properties were characterized by means of X-ray diffraction （XRD） and superconducting quantum interference device （SQUID）. Addition of anti-ferromagnetic layer enhances both the coercivity and the remanence ratios of Pr-Fe-B films with suitable structures. The interface number increases and the antiferromagnetic-ferromagnetic exchange interaction is likely to become stronger, which affect the improvement of magnetic properties. To further understand the influence of structures with soft-magnetic Fe layer and/or antifer- romagnetic FeMn layer on the magnetic properties of Pr-Fe-B hard-magnetic films, the thickness of Pr-Fe-B layer was designed to decrease from 600 to 50 nm. The improvement of magnetic properties becomes obvious in Mo（50 nm）/Pr-Fe-B（25 nm）Mo（2 nm）FeMn（20 nm）Mo （2 nm）Pr-Fe-B（25 nm）/Mo（50 rim） film.展开更多
Cellulose is a renewable biomass material and natural polymer which is abundantly available on Earth,and includes agricultural wastes,forestry residues,and woody materials.The excellent and smart characteristics of ce...Cellulose is a renewable biomass material and natural polymer which is abundantly available on Earth,and includes agricultural wastes,forestry residues,and woody materials.The excellent and smart characteristics of cellulose materials,such as lightweight,biocompatibility,biodegradability,high mechanical strength/stiffness and low thermal expansibility,have made cellulose a highpotential material for various industry applications.Cellulose has recently been discovered as a smart material in the electroactive polymers family which carries the name of cellulose-based electroactive paper(EAPap).The shear piezoelectricity in cellulose polymers is able to induce large displacement output,low actuation voltage,and low power consumption in the application of biomimetic sensors/actuators and electromechanical system.The present study provides an overview of biomass pretreatment from various lignocellulosic cellulose(LC)resources and nanocellulose production via TEMPO-mediated oxidation reaction,followed by the production of different types of EAPap versus its performance,and lastly the applications of EAPap in different areas and industries.Specifically,LC biomass consists mainly of cellulose having a small content of hemicelluloses and lignins which form a defensive inner structure against the degradation of plant cell wall.Thus,selective approaches are discussed to ensure proper extraction of cellulosic fibers from complex biomass for further minimization to nano-dimensions.In addition,a comprehensive review of the development of cellulose-based EAPap as well as fabrication,characterization,performance enhancement and applications of EAPap devices are discussed herein.展开更多
Fabrication and characterization of electro-optic modulators based on the novel organic electro-optic materials composed of self-assembled superlattices (SAS) were presented, both wet-dipping self-assembly and vapor p...Fabrication and characterization of electro-optic modulators based on the novel organic electro-optic materials composed of self-assembled superlattices (SAS) were presented, both wet-dipping self-assembly and vapor phase deposition approaches were discussed. Prototype waveguide electro-optic modulators were fabricated using SAS films integrated with low-loss polymeric materials functioning as partial guiding and cladding layers.Promising electro-optic thin film materials including DTPT and PEPCOOH grown from the vapor phase were used for fabrication and test of electro-optic prototype modulators. Finally,the EO coefficient of tens of pm/V was obtained,which can sufficiently support high-speed and small size EO modulators.展开更多
In the mouth, biofilm formation occurs on all soft and hard surfaces. Microbial colonization on such surfaces is always preceded by the formation of a pellicle. The physicochemical surface properties of a pellicle are...In the mouth, biofilm formation occurs on all soft and hard surfaces. Microbial colonization on such surfaces is always preceded by the formation of a pellicle. The physicochemical surface properties of a pellicle are largely dependent on the physical and chemical nature of the underlying surface. Thus, the surface structure and composition of the underlying surface will influence on the initial bacterial adhesion. The aim of this review is to evaluate the influence of the surface roughness and the restorative material composition on the adhesion process of oral bacteria. Both in vitro and in vivo studies underline the importance of both variables in dental plaque formation. Rough surfaces will promote plaque formation and maturation. Candida species are found on acrylic dentures, but dentures coating and soaking of dentures in disinfectant solutions may be an effective method to prevent biofilm formation. Biofilms on gold and amalgam are thick, but with low viability. Glass-ionomer cement collects a thin biofilm with a low viability. Biofilms on composites cause surface deterioration, which enhances biofilm formation. Biofilms on ceramics are thin and highly viable.展开更多
Soft robots complement the existing efforts of miniaturizing conventional,rigid robots,and have the potential to revolutionize areas such as military equipment and biomedical devices.This type of system can accomplish...Soft robots complement the existing efforts of miniaturizing conventional,rigid robots,and have the potential to revolutionize areas such as military equipment and biomedical devices.This type of system can accomplish tasks in complex and time-varying environments through geometric reconfiguration induced by diverse external stimuli,such as heat,solvent,light,electric field,magnetic field,and mechanical field.Approaches to achieve reconfigurable mesostructures are essential to the design and fabrication of soft robots.Existing studies mainly focus on four key aspects:reconfiguration mechanisms,fabrication schemes,deformation control principles,and practical applications.This review presents a detailed survey of methodologies for morphable mesostructures triggered by a wide range of stimuli,with a number of impressive examples,demonstrating high degrees of deformation complexities and varied multi-functionalities.The latest progress based on the development of new materials and unique design concepts is highlighted.An outlook on the remaining challenges and open opportunities is provided.展开更多
基金support by National Key Research and Development Program of China(2022YFB3803502)National Natural Science Foundation of China(52103076)+5 种基金Science and Technology Commission of Shanghai Municipality(23ZR1400300)special fund of Beijing Key Laboratory of Indoor Air Quality Evaluat ion and Control(NO.BZ0344KF21-02)State Key Laboratory of Electrical Insulation and Power Equipment(EIPE22203)JLF is a member of LSRE-LCM–Laboratory of Separation and Reaction Engineering-Laboratory of Catalysis and Materials,supported by national funds through FCT/MCTES(PIDDAC):LSRE-LCM,UIDB/50020/2020(DOI:10.54499/UIDB/50020/2020)UIDP/50020/2020(DOI:10.54499/UIDP/50020/2020)ALiCE,LA/P/0045/2020(DOI:10.54499/LA/P/0045/2020).
文摘Direct seawater splitting has emerged as a popular and promising research direction for synthesising clean,green,non-polluting,and sustainable hydrogen energy without depending on high-purity water in the face of the world’s shortage of fossil energy.However,efficient seawater splitting is hindered by slow kinetics caused by the ultra-low conductivity and the presence of bacteria,microorganisms,and stray ions in seawater.Additionally,producing hydrogen on an industrial scale is challenging due to the high production cost.The present review addresses these challenges from the catalyst point of view,namely,that designing catalysts with high catalytic activity and stability can directly affect the rate and effect of seawater splitting.From the ion transfer perspective,designing membranes can block harmful ions,improving the stability of seawater splitting.From the energy point of view,mixed seawater systems and self-powered systems also provide new and low-energy research systems for seawater splitting.Finally,ideas and directions for further research on direct seawater splitting in the future are pointed out,with the aim of achieving low-cost and high-efficiency hydrogen production.
基金supported by the National Natural Science Foundation of China(52172120)Shanghai Science and Technology Development Funds(No.24CL2900500).
文摘Radiative cooling is a passive thermal management strategy that leverages the natural ability of materials to dissipate heat through infrared radiation.It has significant implications for energy efficiency,climate adaptation,and sustainable technology development,with applications in personal thermal management,building temperature regulation,and aerospace engineering.However,radiative cooling performance is susceptible to environmental aging and special environmental conditions,limiting its applicability in extreme environments.Herein,a critical review of extreme environmental radiative cooling is presented,focusing on enhancing environmental durability and cooling efficiency.This review first introduces the design principles of heat exchange channels,which are tailored based on the thermal flow equilibrium to optimize radiative cooling capacity in various extreme environments.Subsequently,recent advancements in radiative cooling materials and micronano structures that align with these principles are systematically discussed,with a focus on their implementation in terrestrial dwelling environments,terrestrial extreme environments,aeronautical environments,and space environments.Moreover,this review evaluates the cooling effects and anti-environmental abilities of extreme radiative cooling devices.Lastly,key challenges hindering the development of radiative cooling devices for extreme environmental applications are outlined,and potential strategies to overcome these limitations are proposed,aiming to prompt their future commercialization.
基金support of Isfahan University of Medical Sciences(Project code No.#1401262).
文摘Mimicking the hierarchical structure of the skin is one of the most important strategies in skin tissue engineering.Monolayer wound dressings are usually not able to provide several functions at the same time and cannot meet all clinical needs.In order to maximize therapeutic efficiency,herein,we fabricated a Tri-layer wound dressing,where the middle layer was fabricated via 3D-printing and composed of alginate,tragacanth and zinc oxide nanoparticles(ZnO NPs).Both upper and bottom layers were constructed using electrospinning technique;the upper layer was made of hydrophobic polycaprolactone to mimic epidermis,while the bottom layer consisted of Soluplus■ and insulin-like growth factor-1(IGF-1)to promote cell behavior.Swelling,water vapor permeability and tensile properties of the dressings were evaluated and the Tri-layer dressing exhibited impressive antibacterial activity and cell stimulation following by the release of ZnO NPs and IGF-1.Additionally,the Tri-layer dressing led to faster healing of full-thicknesswound in ratmodel compared to monolayer and Bilayer dressings.Overall,the evidence confirmed that the Trilayer wound dressing is extremely effective for full-thickness wound healing.
基金supported by the Agency for Defense Development Grant Funded by the Korean Government(Grant No.912822501).
文摘Unmanned combat aerial vehicles require lightweight,stealth-capable exhaust systems.However,traditional metallic nozzles increase radar detectability and reduce range,while advanced composites offer high performance but are expensive.Therefore,to improve the operational range and survivability of unmanned combat aerial vehicles,a lightweight,high-temperature-resistant,oxidation-resistant,and low-observable composite exhaust nozzle is developed to replace conventional metallic straight-type nozzles.The nozzle features a double serpentine shape to reduce radar and infrared signatures and is manufactured as a monolithic structure using the filament winding process,accommodating the complex geometry and large size(length:1.8 m,width:0.8 m).The exhaust nozzle consists of a ceramic matrix composite made of silicon carbide fibers and a silicon oxycarbide matrix,which absorbs and scatters radio frequency signals while withstanding prolonged exposure to high-temperature(700℃)oxidizing environments typical of engine exhaust gases.The polysiloxane resin used to produce the silicon oxycarbide matrix poses significant challenges owing to its low tackiness and high viscosity variations depending on the presence of nanoparticles,making filament winding difficult.These challenges are addressed by optimizing resin viscosity and winding pattern design.As a result,the tensile strength of the composite specimens fabricated with the optimized viscosity increases by 228.03% before pyrolysis and 97.68%after pyrolysis,compared with that of the non-optimized specimens.In addition,the density and tensile strength of the composite processed via three cycles of polymer infiltration and pyrolysis increased by 13.08% and 80.37%,respectively,compared to those of the non-densified composite.High-temperature oxidation and flame tests demonstrate exceptional thermal and oxidative stability.Furthermore,when compared with carbon fiber-reinforced ceramic matrix composites,the developed composite exhibits a permittivity at least two levels lower and a reflection loss below7 dB within the frequency range of 9.3-10.9 GHz,underscoring its superior electromagnetic stealth performance.
基金the National Natural Science Foundation of China (Nos. 52071179, 52271033)the Key Program of National Natural Science Foundation of China (No. 51931003)+2 种基金the Natural Science Foundation of Jiangsu Province, China (No. BK20221493)the Jiangsu Province Leading Edge Technology Basic Research Major Project, China (No. BK20222014)the Foundation of “Qinglan Project” for Colleges and Universities in Jiangsu Province, China。
文摘The composition−property relationship of 18 quaternary high entropy diborides(HEBs)consisting of boron and IVB,VB and VIB transition metals(TM)was investigated using first-principles calculations.A valence electron concentration−relative electronegativity(VEC−REN)composite descriptor was developed to effectively predict the mechanical properties of HEBs.The results demonstrate that with a fixed VEC,the rise of the REN makes HEBs harder but more brittle when the electronegativity of doped TM atoms is lower than that of boron atoms.However,HEBs become softer and more ductile as REN increases if the doped TM atoms have higher electronegativity than boron atoms.The VEC−REN composite descriptor can accurately classify and predict the mechanical properties of HEBs with different components,which provides important theoretical guidance for the rapid design and development of novel high-entropy ceramic materials.
基金the funding support from the National Natural Science Foundation of China(22373080)Fujian Pro-vincial Natural Science Foundation of China(2024J08008)+6 种基金the funding support from the National Natural Science Foundation of China(22402163)Fujian Provincial Science and Technology Program for International Cooperation(2025I0002)Natural Science Foundation of Xiamen,China(3502Z202472001)the funding support from the National Natural Science Foundation of China(22078274)the funding support from the Funda-mental Research Funds for the Central Universities(20720240054)Nan-Qiang Youth Scholar Program of Xiamen UniversityXiaomi Young Talents Program/Xiaomi Foundation。
文摘Electrocatalytic co-reduction of CO_(2)and nitrate offers an attractive and sustainable pathway for urea synthesis,as it enables the simultaneous valorization of nitrogenous waste and CO_(2)into value-added chemicals.However,achieving ambient and high-performance urea electrosynthesis remains a persistent challenge,as it requires the simultaneous activation of CO_(2)and efficient H_(2)O dissociation to supply active^(*)H for^(*)NO x hydrogenation—ultimately forming key Cand N-containing intermediates necessary for effective C-N coupling.The stringent,sequential nature of the reaction requirements continues to present substantial challenges for the rational design of advanced multifunctional catalysts.Herein,we report a creative two-in-one catalyst,bifunctional Pd-single-atom-modified Cu(Pd_(1)Cu)nanorods,to synergistically promote the adsorption and stepwise activation of dual species,that is,CO_(2)and H_(2)O,thereby effectively steering the reaction pathway toward the highly selective synthesis of urea.By integrating experimental evidence,in situ spectroscopy,and computational analyses,we clearly disclose that the atomically dispersed Pd sites kinetically favor the co-generation of^(*)CO and^(*)NH_(2)(via H_(2)O dissociation-driven proton transfer),thereby forming an optimal intermediate balance that facilitates urea synthesis.More importantly,the rationally designed Pd_(1)Cu leverages dual metal active sites to enhance C-N coupling via combined electronic and geometric effects,substantially lowering the reaction energy barrier and improving selectivity toward urea.
基金supported by Young Elite Scientists Sponsorship Program by China Association for Science and Technology(No.2022QNRC001)the National Natural Science Foundation of China(No.52273053)the Chenguang Program of Shanghai Education Development Foundation and Shanghai Municipal Education Commission(No.21CGA41)。
文摘Extreme cold weather seriously harms human thermoregulatory system,necessitating high-performance insulating garments to maintain body temperature.However,as the core insulating layer,advanced fibrous materials always struggle to balance mechanical properties and thermal insulation,resulting in their inability to meet the demands for both washing resistance and personal protection.Herein,inspired by the natural spring-like structures of cucumber tendrils,a superelastic and washable micro/nanofibrous sponge(MNFS)based on biomimetic helical fibers is directly prepared utilizing multiple-jet electrospinning technology for high-performance thermal insulation.By regulating the conductivity of polyvinylidene fluoride solution,multiple-jet ejection and multiple-stage whipping of jets are achieved,and further control of phase separation rates enables the rapid solidification of jets to form spring-like helical fibers,which are directly entangled to assemble MNFS.The resulting MNFS exhibits superelasticity that can withstand large tensile strain(200%),1000 cyclic tensile or compression deformations,and retain good resilience even in liquid nitrogen(-196℃).Furthermore,the MNFS shows efficient thermal insulation with low thermal conductivity(24.85 mW m^(-1)K^(-1)),close to the value of dry air,and remains structural stability even after cyclic washing.This work offers new possibilities for advanced fibrous sponges in transportation,environmental,and energy applications.
文摘We are sorry for the mistakes of Affiliation,"a State Key Laboratory of Advanced Fiber Materials,Center for Advanced Low-Dimension Materials,Donghua University,Shanghai 201620,China"should be replaced by"a State Key Laboratory of Advanced Fiber Materials,Center for Advanced Low-Dimension Materials,College of Materials Science and Engineering,Donghua University,Shanghai 201620,China".We apologized for the inconvenience caused by this error.
文摘CO_(2)utilization powered by sustainable energy offers a promising route to mitigate carbon emissions while producing value-added chemicals[1].Among these pathways,CO_(2)hydrogenation is especially attractive because it integrates renewable H 2 with carbon resources,which have achieved notable success in producing methanol,CO,etc.[2,3].
基金support from the National Natural Science Foundation of China(Nos.82030107,82304443,82373944)the Hainan Provincial Natural Science Foundation of China(No.825QN288).
文摘PEGylation,the controlled covalent conjugation of polyethylene glycol to therapeutics,enhances therapeutic efficacy through optimized pharmacokinetics.However,to date no high-molecular-weight PEGylated small-molecule prodrugs have received regulatory approval.This technological gap can be partially attributed to the exponential proliferation of metabolic intermediates resulting from multi-payload conjugation strategies,which introduces unprecedented analytical complexities in metabolite profiling and pharmacokinetic characterization.To address this challenge,we developed a liquid chromatography-triple-quadrupole/time-of-flight mass spectrometry platform for PEG20k-(irinotecan)3,a Phase III clinical candidate.Our methodology employs payload stoichiometry-based chromatographic resolution for clustering isomeric PEG species.Complementarily,diagnostic product ions at m/z 699.83,569.27,and 587.28 enable systematic differentiation between double-loaded,single-loaded,and released irinotecan payload.This approach successfully identifies eight metabolic clusters spanning from PEG-conjugates,cleaved PEG segments,and released small-molecule species.Its demonstrated capacity to deconvolute complex metabolic profiles—through payload-stoichiometry based chromatographic resolution coupled with diagnostic ion analysis—positions this workflow as an attractive tool for accelerating the development of PEGylated small-molecule therapeutics.
基金support received from the National Research Foundation of Korea(NRF)through the Ministry of Science,ICT(Information and Communication Technology),under grant numbers RS-2023-00302646 and RS-2025-02316700.
文摘Tin-lead(Sn-Pb)halide perovskite single crystals combine narrow bandgaps,long carrier diffusion lengths,and low trap densities,positioning them as ideal candidates for near-infrared(NIR)optoelectronics.However,conventional growth strategies rely on bulk crystallization at elevated temperatures,leading to uncontrolled nucleation,Sn^(2+)oxidation,and poor compatibility with planar integration.Here,we develop a coordination-engineered crystallization strategy that enables direct,lowtemperature growth of micrometer-thick Sn-Pb single-crystal thin films on device-compatible substrates.By modulating metal-solvent coordination strength using a low-donor number cosolvent system,we delineate a narrow processing window that stabilizes precursor speciation,lowers the nucleation barrier,and guides directional crystal growth under mild thermal conditions(<40℃).The resulting crystal films exhibit smooth morphology,high crystallinity,compositional uniformity,and ultralow trap densities(~3.98×10^(12)cm^(-3)).When integrated into NIR photodetectors,these films deliver high responsivity(0.51 A W^(-1)at 900 nm),specific detectivity up to 3.6×10^(12)Jones,fast response(~188μs),and>25,000 cycles of ambient operational stability.This approach establishes a scalable platform for redox-stable,low-temperature growth of Sn-Pb perovskite crystal films and expands the processing-structure-function landscape for next-generation infrared optoelectronics.
基金supported by Basic Science Research Program(Priority Research Institute)through the NRF of Korea funded by the Ministry of Education(2021R1A6A1A10039823)by the Korea Basic Science Institute(National Research Facilities and Equipment Center)grant funded by the Ministry of Education(2020R1A6C101B194)。
文摘Lithium-oxygen(Li-O2)batteries are perceived as a promising breakthrough in sustainable electrochemical energy storage,utilizing ambient air as an energy source,eliminating the need for costly cathode materials,and offering the highest theoretical energy density(~3.5 k Wh kg^(-1))among discussed candidates.Contributing to the poor cycle life of currently reported Li-O_(2)cells is singlet oxygen(1O_(2))formation,inducing parasitic reactions,degrading key components,and severely deteriorating cell performance.Here,we harness the chirality-induced spin selectivity effect of chiral cobalt oxide nanosheets(Co_(3)O_(4)NSs)as cathode materials to suppress 1O_(2)in Li-O_(2)batteries for the first time.Operando photoluminescence spectroscopy reveals a 3.7-fold and 3.23-fold reduction in 1O_(2)during discharge and charge,respectively,compared to conventional carbon paperbased cells,consistent with differential electrochemical mass spectrometry results,which indicate a near-theoretical charge-to-O_(2)ratio(2.04 e-/O_(2)).Density functional theory calculations demonstrate that chirality induces a peak shift near the Fermi level,enhancing Co 3d-O 2p hybridization,stabilizing reaction intermediates,and lowering activation barriers for Li_(2)O_(2)formation and decomposition.These findings establish a new strategy for improving the stability and energy efficiency of sustainable Li-O_(2)batteries,abridging the current gap to commercialization.
基金supported by the National Research Foundation of Korea(NRF)grant funded by the Korea government(MSIT)(No.2022M3H4A6A0103720142)the National Research Council of Science&Technology(NST)grant by the Korea government(MSIT)(No.GTL24011-000)+1 种基金the Technology Innovation Program(RS-2024-00404165)through the Korea Planning&Evaluation Institute of Industrial Technology(KEIT)funded by the Ministry of Trade,Industry&Energy(MOTIE,Korea)supported by the Samsung SDI Co.Ltd.and the Korea Institute of Science and Technology(KIST)institutional program(2E33942,2E3394B)。
文摘Strategies for achieving high-energy-density lithium-ion batteries include using high-capacity materials such as high-nickel NCM,increasing the active material content in the electrode by utilizing high-conductivity carbon nanotubes(CNT)conductive materials,and electrode thickening.However,these methods are still limited due to the limitation in the capacity of high-nickel NCM,aggregation of CNT conductive materials,and nonuniform material distribution of thick-film electrodes,which ultimately damage the mechanical and electrical integrity of the electrode,leading to a decrease in electrochemical performance.Here,we present an integrated binder-CNT composite dispersion solution to realize a high-solids-content(>77 wt%)slurry for high-mass-loading electrodes and to mitigate the migration of binder and conductive additives.Indeed,the approach reduces solvent usage by approximately 30%and ensures uniform conductive additive-binder domain distribution during electrode manufacturing,resulting in improved coating quality and adhesive strength for high-mass-loading electrodes(>12 mAh cm^(−2)).In terms of various electrode properties,the presented electrode showed low resistance and excellent electrochemical properties despite the low CNT contents of 0.6 wt%compared to the pristine-applied electrode with 0.85 wt%CNT contents.Moreover,our strategy enables faster drying,which increases the coating speed,thereby offering potential energy savings and supporting carbon neutrality in wet-based electrode manufacturing processes.
基金This work was financially supported by the National Metal and Materials Technology Center,Thailand(Project No.P-18-50327).
文摘High calcium-fly ash(HCFA)collected from the Mae Moh electricity generating plant in Thailand was utilized as a raw material for ceramic production.The main compositions of HCFA characterized by X-ray fluorescence mainly consisted of 28.55wt%SiO_(2),16.06wt%Al_(2)O_(3),23.40wt%CaO,and 17.03wt%Fe_(2)O_(3).Due to high proportion of calcareous and ferruginous contents,HCFA was used for replacing the potash feldspar in amounts of 10wt%-40wt%.The influence of substituting high-calcium fly ash(0-40wt%)and sintering temperatures(1000-1200℃)on physical,mechanical,and thermal properties of ceramic-based materials was investigated.The results showed that the in-corporation of HCFA in appropriate amounts could enhance the densification and the strength as well as reduce the thermal conductivity of ceramic samples.High proportion of calcareous and ferruginous constituents in fly ash promoted the vitrification behavior of ceramic samples.As a result,the densification was enhanced by liquid phase formation at optimum fly ash content and sintering temperature.In addition,these components also facilitated a more abundant mullite formation and consequently improved flexural strength of the ceramic samples.The op-timum ceramic properties were achieved with adding fly ash content between 10wt%-30wt%sintered at 1150-1200℃.At 1200℃,the max-imum flexural strength of ceramic-FA samples with adding fly ash 10wt%-30wt%(PSW-FA(10)-(30))was obtained in the range of 92.25-94.71 MPa when the water absorption reached almost zero(0.03%).In terms of thermal insulation materials,the increase in fly ash addi-tion had a positively effect on the thermal conductivity,due to the higher levels of porosity created by gas evolving from the inorganic decom-position reactions inside the ceramic-FA samples.The addition of 20wt%-40wt%high-calcium fly ash in ceramic samples sintered at 1150℃reduced the thermal conductivity to 14.78%-49.25%,while maintaining acceptable flexural strength values(~45.67-87.62 MPa).Based on these promising mechanical and thermal characteristics,it is feasible to utilize this high-calcium fly ash as an alternative raw material in clay compositions for manufacturing of ceramic tiles.
基金the National Natural Science Foundation of China(Nos.51871113 and21601071)the Natural Science Foundation of Jiangsu Province(No.BK20160211)the Key Research and Development Program of Xuzhou(No.KC17004)。
文摘A two-dimensional(2 D)SnNb_(2)O_(6)/amino-functionalized graphene(En-RGO)nanocomposite with a representative 2 D-2 D architecture has been constructed by an easy self-assembly approach and firstly investigated as anode materials for secondary sodium-ion batteries.The SnNb_(2)O_(6)nanosheets are evenly anchored with the aminofunctionalized graphene through electrostatic attractive interplay between the negatively charged SnNb_(2)O_(6)and positively charged En-RGO after modification.As a result,a remarkable reversible capacity of 300 mAh·g^(-1)was obtained at 50 mA·g^(-1),and significantly,the En-RGO electrode could also deliver ultra-long calendar life up to1900 cycles with a high reversible capacity of200 mAh·g^(-1)at current of 500 mA·g^(-1).Such excellent electrochemical characteristics can be mainly ascribed to its fast pseudo-capacitive energy storage mechanism,and the capacitive contribution can even reach up to 90%at1.2 mV·s^(-1).
基金financially supported by the National Key Basic Research Program of China (No. 2010CB934603)the National Nature Science Foundation of China (Nos. 50931006 and 50971123)
文摘Anisotropic Pr-Fe-B films with soft-magnetic layer （Fe） and/or antiferromagnetic layer （Mn, FeMn or MnO） were prepared by direct-current （DC） magnetron sputtering on Si （100） substrates heated at 650℃. The influence of four types＇ different structures on the magnetic properties of Pr-Fe-B films was investigated. The phase and magnetic properties were characterized by means of X-ray diffraction （XRD） and superconducting quantum interference device （SQUID）. Addition of anti-ferromagnetic layer enhances both the coercivity and the remanence ratios of Pr-Fe-B films with suitable structures. The interface number increases and the antiferromagnetic-ferromagnetic exchange interaction is likely to become stronger, which affect the improvement of magnetic properties. To further understand the influence of structures with soft-magnetic Fe layer and/or antifer- romagnetic FeMn layer on the magnetic properties of Pr-Fe-B hard-magnetic films, the thickness of Pr-Fe-B layer was designed to decrease from 600 to 50 nm. The improvement of magnetic properties becomes obvious in Mo（50 nm）/Pr-Fe-B（25 nm）Mo（2 nm）FeMn（20 nm）Mo （2 nm）Pr-Fe-B（25 nm）/Mo（50 rim） film.
文摘Cellulose is a renewable biomass material and natural polymer which is abundantly available on Earth,and includes agricultural wastes,forestry residues,and woody materials.The excellent and smart characteristics of cellulose materials,such as lightweight,biocompatibility,biodegradability,high mechanical strength/stiffness and low thermal expansibility,have made cellulose a highpotential material for various industry applications.Cellulose has recently been discovered as a smart material in the electroactive polymers family which carries the name of cellulose-based electroactive paper(EAPap).The shear piezoelectricity in cellulose polymers is able to induce large displacement output,low actuation voltage,and low power consumption in the application of biomimetic sensors/actuators and electromechanical system.The present study provides an overview of biomass pretreatment from various lignocellulosic cellulose(LC)resources and nanocellulose production via TEMPO-mediated oxidation reaction,followed by the production of different types of EAPap versus its performance,and lastly the applications of EAPap in different areas and industries.Specifically,LC biomass consists mainly of cellulose having a small content of hemicelluloses and lignins which form a defensive inner structure against the degradation of plant cell wall.Thus,selective approaches are discussed to ensure proper extraction of cellulosic fibers from complex biomass for further minimization to nano-dimensions.In addition,a comprehensive review of the development of cellulose-based EAPap as well as fabrication,characterization,performance enhancement and applications of EAPap devices are discussed herein.
文摘Fabrication and characterization of electro-optic modulators based on the novel organic electro-optic materials composed of self-assembled superlattices (SAS) were presented, both wet-dipping self-assembly and vapor phase deposition approaches were discussed. Prototype waveguide electro-optic modulators were fabricated using SAS films integrated with low-loss polymeric materials functioning as partial guiding and cladding layers.Promising electro-optic thin film materials including DTPT and PEPCOOH grown from the vapor phase were used for fabrication and test of electro-optic prototype modulators. Finally,the EO coefficient of tens of pm/V was obtained,which can sufficiently support high-speed and small size EO modulators.
文摘In the mouth, biofilm formation occurs on all soft and hard surfaces. Microbial colonization on such surfaces is always preceded by the formation of a pellicle. The physicochemical surface properties of a pellicle are largely dependent on the physical and chemical nature of the underlying surface. Thus, the surface structure and composition of the underlying surface will influence on the initial bacterial adhesion. The aim of this review is to evaluate the influence of the surface roughness and the restorative material composition on the adhesion process of oral bacteria. Both in vitro and in vivo studies underline the importance of both variables in dental plaque formation. Rough surfaces will promote plaque formation and maturation. Candida species are found on acrylic dentures, but dentures coating and soaking of dentures in disinfectant solutions may be an effective method to prevent biofilm formation. Biofilms on gold and amalgam are thick, but with low viability. Glass-ionomer cement collects a thin biofilm with a low viability. Biofilms on composites cause surface deterioration, which enhances biofilm formation. Biofilms on ceramics are thin and highly viable.
文摘Soft robots complement the existing efforts of miniaturizing conventional,rigid robots,and have the potential to revolutionize areas such as military equipment and biomedical devices.This type of system can accomplish tasks in complex and time-varying environments through geometric reconfiguration induced by diverse external stimuli,such as heat,solvent,light,electric field,magnetic field,and mechanical field.Approaches to achieve reconfigurable mesostructures are essential to the design and fabrication of soft robots.Existing studies mainly focus on four key aspects:reconfiguration mechanisms,fabrication schemes,deformation control principles,and practical applications.This review presents a detailed survey of methodologies for morphable mesostructures triggered by a wide range of stimuli,with a number of impressive examples,demonstrating high degrees of deformation complexities and varied multi-functionalities.The latest progress based on the development of new materials and unique design concepts is highlighted.An outlook on the remaining challenges and open opportunities is provided.
