To elucidate the effect of calcite-regulated activated carbon(AC)structure on low-temperature denitrification performance of SCR catalysts,this work prepared a series of Mn-Ce/De-AC-xCaCO_(3)(x is the calcite content ...To elucidate the effect of calcite-regulated activated carbon(AC)structure on low-temperature denitrification performance of SCR catalysts,this work prepared a series of Mn-Ce/De-AC-xCaCO_(3)(x is the calcite content in coal)catalysts were prepared by the incipient wetness impregnation method,followed by acid washing to remove calcium-containing minerals.Comprehensive characterization and low-temperature denitrification tests revealed that calcite-induced structural modulation of coal-derived AC significantly enhances catalytic activity.Specifically,NO conversion increased from 88.3%of Mn-Ce/De-AC to 91.7%of Mn-Ce/De-AC-1CaCO_(3)(210℃).The improved SCR denitrification activity results from the enhancement of physicochemical properties including higher Mn^(4+)content and Ce^(4+)/Ce^(3+)ratio,an abundance of chemisorbed oxygen and acidic sites,which could strengthen the SCR reaction pathways(richer NH_(3)activated species and bidentate nitrate active species).Therefore,NO removal is enhanced.展开更多
Conventional Tb^(3+)-doped phosphors typically suffer from concentration quenching once the doping level exceeds a critical threshold.Consequently,the development of Tb^(3+)phosphors with intrinsic resistance to conce...Conventional Tb^(3+)-doped phosphors typically suffer from concentration quenching once the doping level exceeds a critical threshold.Consequently,the development of Tb^(3+)phosphors with intrinsic resistance to concentration quenching has become a key research focus.In this work,we successfully synthesized KBi(MoO_(4))_(2):x Tb^(3+)(x=0-100 at%)(denoted as KBM:x Tb^(3+))phosphors via a high-temperature solid-state reaction.Remarkably,no concentration quenching was observed across the entire doping range.This anti-quenching behavior originates from the large Tb^(3+)-Tb^(3+)interionic distance(>5Å)inherent to the quasi-layered crystal structure,which effectively suppresses multipole-interaction-mediated energy migration.At full Tb^(3+)substitution(x=100 at%),the material undergoes a structural phase transition from the monoclinic KBM phase to the triclinicα-KTb(MoO_(4))_(2)(α-KTM)phase.Theα-KTM phosphor exhibits excellent thermal stability(activation energy=0.6129 eV)and a single-exponential decay profile,whereas KBM:x Tb^(3+)(x<100%)display double-exponential decay behaviors,attributed to dual energy transfer pathways.These findings provide new insights into the luminescence mechanisms of high-concentration rare-earth-doped systems and offer guidance for designing nextgeneration anti-quenching phosphors.展开更多
Because of the developed surface of the Triply PeriodicMinimumSurface(TPMS)structures,polylactide(PLA)products with a TPMS structure are thought to be promising bio soluble implants with the potential for targeted dru...Because of the developed surface of the Triply PeriodicMinimumSurface(TPMS)structures,polylactide(PLA)products with a TPMS structure are thought to be promising bio soluble implants with the potential for targeted drug delivery.For implants,mechanical properties are key performance characteristics,so understanding the deformation and failure mechanisms is essential for selecting the appropriate implant structure.The deformation and fracture processes in PLA samples with different interior architectures have been studied through computer simulation and experimental research.Two TPMS topologies,the Schwarz Diamond and Gyroid architectures,were used for the sample construction by 3D printing.ANSYS software was utilized to simulate compressive deformation.It was found that under the same load,the vonMises stresses in the Gyroid structure are higher than those in the Schwartz Diamond structure,which was associated with the different orientations of the cells in the studied structures in relation to the direction of the loading axis.The deformation process occurs in the local regions of the studied TPMS structures.Maximum von Mises stresses were observed in the vertical parts of the structures oriented along the load direction.It was found that,unlike the Gyroid,the Schwartz Diamond structure contains a frame that forms unique stiffening ribs,which ensures the redistribution of the load under the vertical loading direction.An analysis of the mechanical characteristics of PLA samples with the Schwartz Diamond and Gyroid structures produced by the Fused Deposition Modeling(FDM)method was correlated with computer simulation.The Schwarz Diamond-type structure was shown to have a higher absorption energy than the Gyroid one.A study of the fracture in PLA samples with various cell sizes revealed a particular feature related to the samples’periodic surface topology and the 3D printing process.Scanning electron microscopic(SEM)studies of the samples deformed by compression showed thatwith an increase in the density of the samples,the failure mechanism changes from ductile to quasi-brittle due to the complex participation of both cell deformation and fiber deformation.展开更多
4-Bromo-3-methylphenol(BMP)is an important chemical intermediate with wide applications in the fields of medicine and pesticides.The synthesis of BMP from m-cresol via bromination is easy to carry out on an industrial...4-Bromo-3-methylphenol(BMP)is an important chemical intermediate with wide applications in the fields of medicine and pesticides.The synthesis of BMP from m-cresol via bromination is easy to carry out on an industrial scale.However,due to the formation of regioisomeric impurities during bromination and the low melting point of BMP,the separation process is prone to the formation of oily substances,resulting in low yield and purity.In this work,a new cocrystallization engineering approach was proposed to separate and purify BMP.Through design of experiments,the cocrystallization process of BMP and triethylenediamine(DABCO)was optimized using a minimum-run resolution IV screening design combined with response surface methodology.In addition,the obtained 2BMP-DABCO powder was characterized by thermal analysis,powder X-ray diffraction,infrared spectroscopy,and scanning electron microscopy.Single crystals of 2BMP-DABCO were grown from acetone by slow evaporation,and detailed structural information was obtained through single-crystal X-ray diffraction.The self-assembly mechanism was further clarified by density functional theory calculations.This study provides a simple,robust,and scalable method for the production of BMP and offers a reference for the separation and purification of phenolic substances.展开更多
With superior structural integrity and design flexibility,3D woven fabrics exhibit unique potential in ballistic protection applications.However,the anisotropic yarn distribution renders traditional 3D woven fabrics s...With superior structural integrity and design flexibility,3D woven fabrics exhibit unique potential in ballistic protection applications.However,the anisotropic yarn distribution renders traditional 3D woven fabrics susceptible to fixed boundaries,which is not conducive to practical applications.Inspired by the motion characteristics of yarn structures,this study investigates a hybrid 3D woven fabric structure that incorporates interlayer warp yarns and normal yarns.Bending stiffness tests,yarn pull-out tests,and ballistic tests are conducted and compared with single-binding yarn structures.Utilizing a validated meso-finite element model,the dynamic deformation and energy absorption mechanisms of the hybrid configuration under impact are elucidated.The results demonstrate that synergistic interactions among various binding yarn structures maintain fabric stability in the absence of boundaries.Normal yarns inhibit horizontal slippage of warp yarns,while multi-layer warp yarns enhance resistance to weft yarn pull-out,thereby facilitating greater yarn participation in direct energy absorption.The hybrid structure exhibited the highest specific energy absorption(SEA)across different boundary conditions,with an average SEA increase of approximately 27%.These insights will facilitate the design of novel hybrid-structured 3D woven fabrics and inform the customization of lightweight protective materials.展开更多
Optimizing the oxygen reduction reaction(ORR)kinetics requires precise control of intermediate adsorption at active sites,which can be achieved through orbital engineering by regulating the electronic structure.This s...Optimizing the oxygen reduction reaction(ORR)kinetics requires precise control of intermediate adsorption at active sites,which can be achieved through orbital engineering by regulating the electronic structure.This study addresses the challenge by exploring how modulation of the 3d-orbital electronic structure of FeN_(4) active sites influences ORR electrocatalysis.To realize this,a catalyst composed of Fe_(3)C nanoparticles and FeN_(4) single atoms anchored on carbon black(Fe_(3)C-FeN_(4)/CB)was synthesized via a synergistic strategy of spatial confinement and atmosphere control.This unique heterostructure creates interfaces between Fe_(3)C and FeN_(4) that modulate the electronic configuration of the FeN_(4) center,transforming its geometry from square-planar to quasi-octahedral.Spectroscopic characterizations and theoretical calculations reveal that this orbital modulation results in a downward shift of the Fe dband center,altering the reaction pathway and lowering the energy barrier for ORR.Consequently,the Fe_(3)C-FeN_(4)/CB catalyst exhibits outstanding ORR activity,four-electron selectivity,excellent methanol tolerance,and remarkable electrochemical stability.When applied in a zinc-air battery,it achieves a peak power density of 178.4 mW cm^(-2)and superior cycling stability compared to commercial Pt/C catalysts.This work provides valuable insights into heterointerface-induced orbital modulation as a promising design principle for high-performance ORR electrocatalysts.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
MgO has been shown to facilitate the precipitation of MgO-rich crystalline phases within the MgO-CaO-Al_(2)O_(3)-SiO_(2)(MCAS)glassy inclusion system,which possesses a high liquidus temperature and a significant Young...MgO has been shown to facilitate the precipitation of MgO-rich crystalline phases within the MgO-CaO-Al_(2)O_(3)-SiO_(2)(MCAS)glassy inclusion system,which possesses a high liquidus temperature and a significant Young’s modulus.The underlying linkage between the structural evolution and the crystallization characteristics of the MCAS system was systematically investigated using molecular dynamics simulation and thermodynamic calculation.The results revealed that Mg^(2+) ions played a dual role,constructing networks through the formation of tricluster oxygens while consuming bridging oxygens(BOs)in a mechanism similar to Ca^(2+) ions.However,despite this dual role,the network connectivity was still decreased with the increase in MgO/(MgO+Al_(2)O_(3))(M/(M+A))and CaO/(CaO+SiO_(2))(C/(C+S))ratios,primarily due to the reduction in BOs.This microscopic structural evolution resulted in a reduction in viscosity and an enhancement of crystallization ability.Furthermore,the remarkable diffusion capability of Mg^(2+) ions,coupled with the increased proportion of 6-coordinated Mg^(2+)ions,unveiled the mechanism underlying the precipitation of MgSiO_(3) and Mg_(2)SiO_(4) crystals,which exhibited high Young’s moduli of 165.23 and 196.67 GPa,respectively.To prevent the precipitation of MgO-rich crystalline phases,it was crucial to maintain the M/(M+A)ratio below 0.42 and the C/(C+S)ratio below 0.16 within the MCAS system.展开更多
Hydrogel scaffolds have numerous potential applications in the tissue engineering field.However,tough hydrogel scaffolds implanted in vivo are seldom reported because it is difficult to balance biocompatibility and hi...Hydrogel scaffolds have numerous potential applications in the tissue engineering field.However,tough hydrogel scaffolds implanted in vivo are seldom reported because it is difficult to balance biocompatibility and high mechanical properties.Inspired by Chinese ramen,we propose a universal fabricating method(printing-P,training-T,cross-linking-C,PTC&PCT)for tough hydrogel scaffolds to fill this gap.First,3D printing fabricates a hydrogel scaffold with desired structures(P).Then,the scaffold could have extraordinarily high mechanical properties and functional surface structure by cycle mechanical training with salting-out assistance(T).Finally,the training results are fixed by photo-cross-linking processing(C).The tough gelatin hydrogel scaffolds exhibit excellent tensile strength of 6.66 MPa(622-fold untreated)and have excellent biocompatibility.Furthermore,this scaffold possesses functional surface structures from nanometer to micron to millimeter,which can efficiently induce directional cell growth.Interestingly,this strategy can produce bionic human tissue with mechanical properties of 10 kPa-10 MPa by changing the type of salt,and many hydrogels,such as gelatin and silk,could be improved with PTC or PCT strategies.Animal experiments show that this scaffold can effectively promote the new generation of muscle fibers,blood vessels,and nerves within 4 weeks,prompting the rapid regeneration of large-volume muscle loss injuries.展开更多
The study of BiFeO_(3)-0.3BaTiO_(3) ceramics has gained significant attention due to their high Curie temperature(TC≥450℃)and excellent piezoelectric properties(d33≥200 pC·N^(−1)).These are particularly pronou...The study of BiFeO_(3)-0.3BaTiO_(3) ceramics has gained significant attention due to their high Curie temperature(TC≥450℃)and excellent piezoelectric properties(d33≥200 pC·N^(−1)).These are particularly pronounced near the morphotropic phase boundary(MPB)region where coexisting rhombohedral and pseudocubic(R-PC)phases are observed.In addition,as the BaTiO_(3) content increases,BiFeO_(3)-BaTiO_(3) ceramics gradually become dominated by a single pseudocubic(PC-)phase.This shift results in a decrease in piezoelectric properties but an enhancement in strain performance.However,the underlying mechanism remains unclear.The high strain properties observed in non-MPB compositions provide a motivation for further investigation into these mechanisms.This paper presents a detailed analysis of the electric-field and temperature-induced domain structure evolution in BiFeO_(3)-0.4BaTiO_(3),which is predominately characterized by the PC phase.Piezoresponse force microscope(PFM)observations reveal the presence of nanodomains and stripy domains associated with polar nanoregions(PNRs),as well as relaxor ferroelectrics(RFEs)and/or ferroelectrics(FEs).The RFEs exhibit a significantly better strain response than the FEs,providing direct evidence for the enhanced strain properties of RFEs.Elevated-temperature Raman spectroscopy confirms a decrease in B-O bonding and BO6 deformation,along with an increase in structural symmetry,indicating the formation of RFEs and/or PNRs.The phase diagram shows the Burns temperature(TB),dielectric maxima temperature(Tm)and freezing temperature(Tf)evaluated from the dielectric spectra;the temperature-induced evolution of domain structures;and the sequential quasi-dielectric states:PNRs,RFEs and FEs.The evolution of the domain structure,including the morphology and ratio of FEs,RFEs and PNRs,induced by either electric-fields or temperature strongly affects the strain properties of RFEs.A superior piezoelectric coefficient of d33*=533 pm·V^(−1) at 40 kV·cm^(−1) and a large electric strain of Suni=0.285%are obtained.These results further validate that domain modulation can effectively enhance the strain properties of BiFeO_(3)-BaTiO_(3) ceramics,which makes them promising candidates for actuator applications.展开更多
Throughout the 20th century, several large megathrust earthquakes were observed in the Colombia–Ecuador subduction zone which widely ruptured plate interfaces, causing considerable damage and loss of life. The occurr...Throughout the 20th century, several large megathrust earthquakes were observed in the Colombia–Ecuador subduction zone which widely ruptured plate interfaces, causing considerable damage and loss of life. The occurrence of earthquakes in subduction zones is thought to be closely related to the thermal structure of the incoming plate. However, in the case of the subducting Nazca Plate beneath the Colombia–Ecuador zone, the thermal structure remains unclear, especially its hydraulic distribution. On the basis of 3D thermal models, we present new insights into the plate interface conditions of Colombia–Ecuador interplate and megathrust earthquakes. We show that the plate geometry strongly affects the along-strike thermal structure of the slab beneath Colombia and Ecuador, with the subduction of the Carnegie Ridge playing an important role. Our results further reveal that the unique geometry of the Nazca Plate is the primary reason for the relatively high temperatures of the slab beneath Colombia. We suggest that the positions of the100–200 ℃ and 350–450 ℃ isotherms on the plate interface determine the updip and downdip limits of the seismogenic zone. For Colombia–Ecuador interplate earthquakes, the released fluids control the distribution of shallow-depth earthquakes, whereas the age and geometry of the slab control the distribution of intermediate-depth earthquakes. The average temperature of the plate interface at the upper limit of large megathrust earthquakes is hotter than previously thought, which is more consistent with our understanding of the Colombia–Ecuador subduction zone. We predict that the potential location of future large seismic events could be in the rupture zone of past seismic events or offshore of northern Colombia.展开更多
Designing cathode possessing crystalline@amorphous core-shell structure with both active core and shell is a meaningful work for resolving the low specific capacity,unstable cycling performance and sluggish reaction ki...Designing cathode possessing crystalline@amorphous core-shell structure with both active core and shell is a meaningful work for resolving the low specific capacity,unstable cycling performance and sluggish reaction kinetics issues of rechargeable magnesium batteries(RMBs)by providing more active sites as well as releasing inner stress during cycling.Herein,WO_(3)@WO_(3-x)S_(x) owning crystalline@amorphous core-shell structure containing both active core and active shell is constructed successfully by introducing S into metastable WO3 structure under temperaturefield applying.In such structure,amorphous shell would provide continuous Mg^(2+)diffusion channels due to its isotropy property for most Mg^(2+)migrating rapidly to interface and then adsorb at ions reservoir formed by interfacial electricfield for increasing specific capacity.It also makes security for stable structure of WO_(3)@WO_(3-x)S_(x) by alleviating volume expansion of crystalline core WO_(3) during cycling to prolong cycling life.Additionally,“softer”ions S^(2-)would weaken interaction between hard acid Mg^(2+) and ionic lattice to enhance Mg^(2+)storage kinetics.Therefore,WO_(3)@WO_(3-x)S_(x) delivers the superior cycling performance(1000 cycles with 83.3%),rate capability(88.5 mAh g^(-1) at 1000 mA g^(-1))and specific capacity(about 150 mAh g^(-1) at 50 mA g^(-1)),which is near 2 times higher than that of WO3.It is believed that the crystalline@amorphous core-shell structure with both active core and shell designing via doping strategy is enlightening for the development of high-performance RMBs,and such design can be extended to other energy storage devices for better electrochemical performance.展开更多
Hierarchical porous structure,which include macropores,minor pores,and micropores in scaffolds,are essential in the multiple biological functions of bone repair and regeneration.In this study,patientcustomized calcium...Hierarchical porous structure,which include macropores,minor pores,and micropores in scaffolds,are essential in the multiple biological functions of bone repair and regeneration.In this study,patientcustomized calcium-deficient hydroxyapatite(CDHA)scaffolds with three-level hierarchical porous structure were fabricated by indirect 3D printing technology and particulate leaching method.The sacrificial template scaffolds were fabricated using a photo-curing 3D printer,which provided a prerequisite for the integral structure and interconnected macropores of CDHA scaffolds.Additionally,20 wt%pore former was incorporated into the slurry to enhance the content of smaller pores within the CDHA-2 scaffolds,and then the CDHA-2 scaffolds were sintered to remove the sacrificial template scaffolds and pore former.The obtained CDHA-2 scaffolds exhibited interconnected macropores(300-400μm),minor pores(∼10-100μm),and micropores(<10μm)distributed throughout the scaffolds,which could promote bone tissue ingrowth,increase surface roughness,and enhance protein adsorption of scaffolds.In vitro studies identified that CDHA-2 scaffolds had nanocrystal grains,high specific surface area,and outstanding protein adsorption capacity,which could provide a microenvironment for cell adhesion,spreading,and proliferation.In addition,the murine intramuscular implantation experiment suggested that CDHA-2 scaffolds exhibited excellent osteoinductivity and were superior to traditional BCP ceramics under conditions without the addition of live cells and exogenous growth factors.The rabbit calvarial defect repair results indicated that CDHA-2 scaffolds could enhance in situ bone regeneration.In conclusion,these findings demonstrated that the hierarchical porous structure of CDHA scaffolds was a pivotal factor in modulating osteoinductivity and bone regeneration,and CDHA-2 scaffolds were potential candidates for bone regeneration.展开更多
In-space 3D printing is transforming the manufacturing paradigm of space structures from ground-based production to in-situ space manufacturing,effectively addressing the challenges of high costs,long response times,a...In-space 3D printing is transforming the manufacturing paradigm of space structures from ground-based production to in-situ space manufacturing,effectively addressing the challenges of high costs,long response times,and structural size limitations associated with traditional rocket launches.This technology enables rapid on-orbit emergency repairs and significantly expands the geometric dimensions of space structures.High-performance polymers and their composites are widely used in in-space 3D printing,yet their implementation faces complex challenges posed by extreme space environmental conditions and limited energy or resources.This paper reviews the state-of-the-art in 3D printing of polymer and composites for on-orbit structure manufacturing.Based on existing research activities,the review focuses on three key aspects including the impact of extreme space environments on forming process and performance,innovative design and manufacturing methods for space structures,and on-orbit recycling and remanufacturing of raw materials.Some experiments that have already been conducted on-orbit and simulated experiments completed on the ground are systematically analyzed to provide a more comprehensive understanding of the constraints and objectives for on-orbit structure manufacturing.Furthermore,several perspectives requiring further research in future are proposed to facilitate the development of new in-space 3D printing technologies and space structures,thereby supporting increasingly advanced space exploration activities.展开更多
03-type layered oxide serves as dominant components in sodium ion batteries;however,the unstable electronic structure between transition metal and oxygen inevitably induces framework instability and severe kinetic hin...03-type layered oxide serves as dominant components in sodium ion batteries;however,the unstable electronic structure between transition metal and oxygen inevitably induces framework instability and severe kinetic hindrance.In this study,a two-in-one approach to synergistically modulate the local electro nic and interfacial structure of NaNi_(1/3)Fe_(1/3)Mn_(1/3)O_(2)by Ce modification is proposed.We present an indepth study to reveal the strong-covalent Ce-O bonds,which make local charge around oxygen more negative,enhance O 2p-Mn 3d hybridization,and preserve the octahedral structural integrity.This modification tailors local electronic structure between the octahedral metal center and oxygen,thus enhancing reversibility of 03-P3-03 phase transition and expanding Na+octahedral-tetrahedral-octahedral transport channel.Additionally,the nanoscale perovskite layer induced by Ce element is in favor of minimizing interfacial side reaction as well as enhancing Na^(+)diffusivity.As a result,the designed 03-NaNi_(0.305)Fe_(0.33)Mn_(0.33)Ce_(0.025)O_(2)material delivers an exceptionally low volume variation,an ultrahigh rate capacity of 76.9 mA h g^(-1)at 10 C,and remarkable cycling life over 250 cycles with capacity retention of 80% at 5 C.展开更多
Lithium(Li)metal is considered the most promising anode material for the next generation of secondary batteries due to its high theoretical specific capacity and low potential.However,the application of Li anode in re...Lithium(Li)metal is considered the most promising anode material for the next generation of secondary batteries due to its high theoretical specific capacity and low potential.However,the application of Li anode in rechargeable Li metal batteries(LMBs)is hindered due to the short cycle life caused by uncontrolled dendrite growth.In this work,a dendrite-free anode(Li–Sn/Cu)is reinforced synergistically by lithophilic alloy,and a 3D grid structure is designed.Li^(+)diffusion and uniform nucleation are effectively induced by the lithophilic alloy Li_(22)Sn_(5).Moreover,homogeneous deposition of Li^(+)is caused by the reversible gridded Li plating/stripping effect of Cu mesh.Furthermore,the local space electric field is redistributed throughout the 3D conductive network,whereby the tip effect is suppressed,thus inhibiting the growth of Li dendrites.Also,the volume expansion of the anode during cycling is eased by the 3D grid structure.The results show that the Li–Sn/Cu symmetric battery can stably cycle for more than 10,000 h at 2 mA.cm^(-2)and 1 mAh.cm^(-2)with a low overpotential.The capacity retention of the LiFePO_(4)full battery remains above 90.7%after 1,000 cycles at 1C.This work provides a facile,low-cost,and effective strategy for obtaining Li metal batteries with ultra-long cycle life.展开更多
Transforming a scattering medium into a lens for imaging very simple binary objects is possible;however,it remains challenging to image complex grayscale objects,let alone measure 3D continuous distribution objects.He...Transforming a scattering medium into a lens for imaging very simple binary objects is possible;however,it remains challenging to image complex grayscale objects,let alone measure 3D continuous distribution objects.Here,we propose and demonstrate the use of a ground glass diffuser as a scattering lens for imaging complex grayscale fringes,and we employ it to achieve microscopic structured light 3D imaging(MSL3DI).The ubiquitous property of the speckle patterns permits the exploitation of the scattering medium as an ultra-thin scattering lens with a variable focal length and a flexible working distance for microscale object measurement.The method provides a light,flexible,and cost-effective imaging device as an alternative to microscope objectives or telecentric lenses in conventional MSL3DI systems.We experimentally demonstrate that employing a scattering lens allows us to achieve relatively good phase information and robust 3D imaging from depth measurements,yielding measurement accuracy only marginally lower than that of a telecentric lens,typically within approximately 10μm.Furthermore,the scattering lens demonstrates robust performance even when the imaging distance exceeds the typical working distance of a telecentric lens.The proposed method facilitates the application of scattering imaging techniques,providing a more flexible solution for MSL3DI.展开更多
The influence of the growth of rare earth on the viscosity during the uniform cooling of CaO-SiO_(2-)CaF_(2)-Ce_(2)O_(3)slag was investigated by the high temperature viscometer.The results show that Ce_(2)O_(3)affects...The influence of the growth of rare earth on the viscosity during the uniform cooling of CaO-SiO_(2-)CaF_(2)-Ce_(2)O_(3)slag was investigated by the high temperature viscometer.The results show that Ce_(2)O_(3)affects the viscosity variedly before and after the break temperature.At higher temperatures Ce_(2)O_(3)reduces the viscosity.When the temperature is below the break temperature,at a Ce_(2)O_(3)content of≥3 mol%,a rareearth crystalline phase is observed during the slag cooling process,and the break temperature progressively increases with the increase of Ce_(2)O_(3)concentration.There are no crystallized rare earths in the slag under the condition of Ce_(2)O_(3)concentration lower than 3 mol%.Too low or too high CaF_(2)content is found to be unfavorable for rare-earth crystallisation.The increase of Ce_(2)O_(3)content facilitates the depolymerization of silica-oxygen tetrahedral structure.Ca-F bond exists between structural units,weakening the flow resistance of structural units and lowering the viscosity of slag.展开更多
Constrained by severe bulk charge recombination,the actual photocurrent density of tantalum nitride(Ta_(3)N_(5))photoanode is much lower than the theoretical maximum value.Herein,we report the doping of phosphorus,a n...Constrained by severe bulk charge recombination,the actual photocurrent density of tantalum nitride(Ta_(3)N_(5))photoanode is much lower than the theoretical maximum value.Herein,we report the doping of phosphorus,a non-metallic element distinct from oxygen,into Ta_(3)N_(5),resulting in a photocurrent density 9 times higher than that of pristine Ta_(3)N_(5).Systematic characterization reveals that the phosphorus doping simultaneously enhances the bulk charge separation efficiency and surface charge injection efficiency of Ta_(3)N_(5),and induces favorable band energy restructuring.Specifically,a type-II homojunction formed between phosphorus-doped near-surface region and bulk Ta_(3)N_(5) effectively promotes the separation and transfer of photogenerated holes and electrons.Further modification with a Ni Fe-based cocatalyst enables the optimized photoanode to deliver a photocurrent density of 10 mA/cm^(2) at 1.23 V versus the reversible hydrogen electrode(RHE)and an applied bias photo-to-current efficiency of 1.78%at 0.95 V versus RHE.Our work provides a foundation for the development of a broader range of non-metal doped semiconductors.展开更多
Herein we report novel photocatalysts ZnIn_(2)S_(4)-Ag-LaFeO_(3) with the core-shell structured materials prepared by hydrothermal method.In order to improve the efficiency of photocatalytic degradation of pollutants,...Herein we report novel photocatalysts ZnIn_(2)S_(4)-Ag-LaFeO_(3) with the core-shell structured materials prepared by hydrothermal method.In order to improve the efficiency of photocatalytic degradation of pollutants,LaFeO_(3) was prepared by hydrothermal followed by calcination,and further Ag nanoparticle(NP)was loaded onto the spherical structure of LaFeO_(3) by photolysis of silver nitrate,and finally the spherical Znln_(2)S_(4)-Ag-LaFeO_(3) photocatalyst was prepared by hydrothermal method again.The structure and properties of the as-prepared materials were characterized by X-ray photoelectron spectroscopy,ultraviolet-visible absorption spectroscopy,X-ray diffraction,scanning electron microscopy and fluorescence spectra.The results show that the synthesized composite photocatalysts display a significant improvement in photocatalytic efficiency relative to the single LaFeO_(3) and ZnIn_(2)S_(4)and form a core-shell structure.Furthermore,the effect of the ratio of each component on the photocatalytic efficiency was investigated in detail,and it is discovered that at an Methylene Blue(MB)concentration of 0.219 mol/L,the degradation rate of MB is 95%at 120 min using 0.02 g of catalyst with an ideal ZnIn_(2)S_(4):Ag:LaFeO_(3)ratio of 10:0.5:1.The possible mechanisms to improve the photocatalytic efficiency were explored.展开更多
基金Supported by the Science and Technology Cooperation and Exchange special project of Cooperation of Shanxi Province(202404041101014)the Fundamental Research Program of Shanxi Province(202403021212333)+3 种基金the Joint Funds of the National Natural Science Foundation of China(U24A20555)the Lvliang Key R&D of University-Local Cooperation(2023XDHZ10)the Initiation Fund for Doctoral Research of Taiyuan University of Science and Technology(20242026)the Outstanding Doctor Funding Award of Shanxi Province(20242080).
文摘To elucidate the effect of calcite-regulated activated carbon(AC)structure on low-temperature denitrification performance of SCR catalysts,this work prepared a series of Mn-Ce/De-AC-xCaCO_(3)(x is the calcite content in coal)catalysts were prepared by the incipient wetness impregnation method,followed by acid washing to remove calcium-containing minerals.Comprehensive characterization and low-temperature denitrification tests revealed that calcite-induced structural modulation of coal-derived AC significantly enhances catalytic activity.Specifically,NO conversion increased from 88.3%of Mn-Ce/De-AC to 91.7%of Mn-Ce/De-AC-1CaCO_(3)(210℃).The improved SCR denitrification activity results from the enhancement of physicochemical properties including higher Mn^(4+)content and Ce^(4+)/Ce^(3+)ratio,an abundance of chemisorbed oxygen and acidic sites,which could strengthen the SCR reaction pathways(richer NH_(3)activated species and bidentate nitrate active species).Therefore,NO removal is enhanced.
基金supported by the Natural Science Research Project of Anhui Province Education Department for Excellent Young Scholars(Grant No.2024AH030007)the National Natural Science Foundation of China(Grant No.52202001)。
文摘Conventional Tb^(3+)-doped phosphors typically suffer from concentration quenching once the doping level exceeds a critical threshold.Consequently,the development of Tb^(3+)phosphors with intrinsic resistance to concentration quenching has become a key research focus.In this work,we successfully synthesized KBi(MoO_(4))_(2):x Tb^(3+)(x=0-100 at%)(denoted as KBM:x Tb^(3+))phosphors via a high-temperature solid-state reaction.Remarkably,no concentration quenching was observed across the entire doping range.This anti-quenching behavior originates from the large Tb^(3+)-Tb^(3+)interionic distance(>5Å)inherent to the quasi-layered crystal structure,which effectively suppresses multipole-interaction-mediated energy migration.At full Tb^(3+)substitution(x=100 at%),the material undergoes a structural phase transition from the monoclinic KBM phase to the triclinicα-KTb(MoO_(4))_(2)(α-KTM)phase.Theα-KTM phosphor exhibits excellent thermal stability(activation energy=0.6129 eV)and a single-exponential decay profile,whereas KBM:x Tb^(3+)(x<100%)display double-exponential decay behaviors,attributed to dual energy transfer pathways.These findings provide new insights into the luminescence mechanisms of high-concentration rare-earth-doped systems and offer guidance for designing nextgeneration anti-quenching phosphors.
文摘Because of the developed surface of the Triply PeriodicMinimumSurface(TPMS)structures,polylactide(PLA)products with a TPMS structure are thought to be promising bio soluble implants with the potential for targeted drug delivery.For implants,mechanical properties are key performance characteristics,so understanding the deformation and failure mechanisms is essential for selecting the appropriate implant structure.The deformation and fracture processes in PLA samples with different interior architectures have been studied through computer simulation and experimental research.Two TPMS topologies,the Schwarz Diamond and Gyroid architectures,were used for the sample construction by 3D printing.ANSYS software was utilized to simulate compressive deformation.It was found that under the same load,the vonMises stresses in the Gyroid structure are higher than those in the Schwartz Diamond structure,which was associated with the different orientations of the cells in the studied structures in relation to the direction of the loading axis.The deformation process occurs in the local regions of the studied TPMS structures.Maximum von Mises stresses were observed in the vertical parts of the structures oriented along the load direction.It was found that,unlike the Gyroid,the Schwartz Diamond structure contains a frame that forms unique stiffening ribs,which ensures the redistribution of the load under the vertical loading direction.An analysis of the mechanical characteristics of PLA samples with the Schwartz Diamond and Gyroid structures produced by the Fused Deposition Modeling(FDM)method was correlated with computer simulation.The Schwarz Diamond-type structure was shown to have a higher absorption energy than the Gyroid one.A study of the fracture in PLA samples with various cell sizes revealed a particular feature related to the samples’periodic surface topology and the 3D printing process.Scanning electron microscopic(SEM)studies of the samples deformed by compression showed thatwith an increase in the density of the samples,the failure mechanism changes from ductile to quasi-brittle due to the complex participation of both cell deformation and fiber deformation.
基金supported by the National Natural Science Foundation of China(22177011(R.Z.Qiao),21977012(R.Z.Qiao),and 21572018(C.Li))the National High-Level Hospital Clinical Research Funding(2023-NHLHCRF-YXHZ-ZRMS-02)the Joint Project of BRCBC(Biomedical Translational Engineering Research Center of BUCT-CJFH)(XK2020-06).
文摘4-Bromo-3-methylphenol(BMP)is an important chemical intermediate with wide applications in the fields of medicine and pesticides.The synthesis of BMP from m-cresol via bromination is easy to carry out on an industrial scale.However,due to the formation of regioisomeric impurities during bromination and the low melting point of BMP,the separation process is prone to the formation of oily substances,resulting in low yield and purity.In this work,a new cocrystallization engineering approach was proposed to separate and purify BMP.Through design of experiments,the cocrystallization process of BMP and triethylenediamine(DABCO)was optimized using a minimum-run resolution IV screening design combined with response surface methodology.In addition,the obtained 2BMP-DABCO powder was characterized by thermal analysis,powder X-ray diffraction,infrared spectroscopy,and scanning electron microscopy.Single crystals of 2BMP-DABCO were grown from acetone by slow evaporation,and detailed structural information was obtained through single-crystal X-ray diffraction.The self-assembly mechanism was further clarified by density functional theory calculations.This study provides a simple,robust,and scalable method for the production of BMP and offers a reference for the separation and purification of phenolic substances.
基金supports from National Key R&D Program for Young Scientists of China(No.2022YFC3080900)the opening project of State Key Laboratory of Explosion Science and Safety Protection,Beijing Institute of Technology(No.KFJJ25-25M).
文摘With superior structural integrity and design flexibility,3D woven fabrics exhibit unique potential in ballistic protection applications.However,the anisotropic yarn distribution renders traditional 3D woven fabrics susceptible to fixed boundaries,which is not conducive to practical applications.Inspired by the motion characteristics of yarn structures,this study investigates a hybrid 3D woven fabric structure that incorporates interlayer warp yarns and normal yarns.Bending stiffness tests,yarn pull-out tests,and ballistic tests are conducted and compared with single-binding yarn structures.Utilizing a validated meso-finite element model,the dynamic deformation and energy absorption mechanisms of the hybrid configuration under impact are elucidated.The results demonstrate that synergistic interactions among various binding yarn structures maintain fabric stability in the absence of boundaries.Normal yarns inhibit horizontal slippage of warp yarns,while multi-layer warp yarns enhance resistance to weft yarn pull-out,thereby facilitating greater yarn participation in direct energy absorption.The hybrid structure exhibited the highest specific energy absorption(SEA)across different boundary conditions,with an average SEA increase of approximately 27%.These insights will facilitate the design of novel hybrid-structured 3D woven fabrics and inform the customization of lightweight protective materials.
基金supported by the National Natural Science Foundation of China(Grant Nos.22272105 and 22572118)Natural Science Foundation of Shanghai(Grant No.23ZR1423900)。
文摘Optimizing the oxygen reduction reaction(ORR)kinetics requires precise control of intermediate adsorption at active sites,which can be achieved through orbital engineering by regulating the electronic structure.This study addresses the challenge by exploring how modulation of the 3d-orbital electronic structure of FeN_(4) active sites influences ORR electrocatalysis.To realize this,a catalyst composed of Fe_(3)C nanoparticles and FeN_(4) single atoms anchored on carbon black(Fe_(3)C-FeN_(4)/CB)was synthesized via a synergistic strategy of spatial confinement and atmosphere control.This unique heterostructure creates interfaces between Fe_(3)C and FeN_(4) that modulate the electronic configuration of the FeN_(4) center,transforming its geometry from square-planar to quasi-octahedral.Spectroscopic characterizations and theoretical calculations reveal that this orbital modulation results in a downward shift of the Fe dband center,altering the reaction pathway and lowering the energy barrier for ORR.Consequently,the Fe_(3)C-FeN_(4)/CB catalyst exhibits outstanding ORR activity,four-electron selectivity,excellent methanol tolerance,and remarkable electrochemical stability.When applied in a zinc-air battery,it achieves a peak power density of 178.4 mW cm^(-2)and superior cycling stability compared to commercial Pt/C catalysts.This work provides valuable insights into heterointerface-induced orbital modulation as a promising design principle for high-performance ORR electrocatalysts.
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support from the National Key R&D Program of China(Grant Nos.2023YFB3709900 and 2023YFB3709903)the National Natural Science Foundation of China(Grant Nos.52174293 and U22A20171)+1 种基金the High Steel Center(HSC)at North China University of TechnologyUniversity of Science and Technology Beijing(USTB).
文摘MgO has been shown to facilitate the precipitation of MgO-rich crystalline phases within the MgO-CaO-Al_(2)O_(3)-SiO_(2)(MCAS)glassy inclusion system,which possesses a high liquidus temperature and a significant Young’s modulus.The underlying linkage between the structural evolution and the crystallization characteristics of the MCAS system was systematically investigated using molecular dynamics simulation and thermodynamic calculation.The results revealed that Mg^(2+) ions played a dual role,constructing networks through the formation of tricluster oxygens while consuming bridging oxygens(BOs)in a mechanism similar to Ca^(2+) ions.However,despite this dual role,the network connectivity was still decreased with the increase in MgO/(MgO+Al_(2)O_(3))(M/(M+A))and CaO/(CaO+SiO_(2))(C/(C+S))ratios,primarily due to the reduction in BOs.This microscopic structural evolution resulted in a reduction in viscosity and an enhancement of crystallization ability.Furthermore,the remarkable diffusion capability of Mg^(2+) ions,coupled with the increased proportion of 6-coordinated Mg^(2+)ions,unveiled the mechanism underlying the precipitation of MgSiO_(3) and Mg_(2)SiO_(4) crystals,which exhibited high Young’s moduli of 165.23 and 196.67 GPa,respectively.To prevent the precipitation of MgO-rich crystalline phases,it was crucial to maintain the M/(M+A)ratio below 0.42 and the C/(C+S)ratio below 0.16 within the MCAS system.
基金supported by the Innovative Research Group Project of the National Natural Science Foundation of China(T2121004)Key Programme(52235007)National Outstanding Youth Foundation of China(52325504).
文摘Hydrogel scaffolds have numerous potential applications in the tissue engineering field.However,tough hydrogel scaffolds implanted in vivo are seldom reported because it is difficult to balance biocompatibility and high mechanical properties.Inspired by Chinese ramen,we propose a universal fabricating method(printing-P,training-T,cross-linking-C,PTC&PCT)for tough hydrogel scaffolds to fill this gap.First,3D printing fabricates a hydrogel scaffold with desired structures(P).Then,the scaffold could have extraordinarily high mechanical properties and functional surface structure by cycle mechanical training with salting-out assistance(T).Finally,the training results are fixed by photo-cross-linking processing(C).The tough gelatin hydrogel scaffolds exhibit excellent tensile strength of 6.66 MPa(622-fold untreated)and have excellent biocompatibility.Furthermore,this scaffold possesses functional surface structures from nanometer to micron to millimeter,which can efficiently induce directional cell growth.Interestingly,this strategy can produce bionic human tissue with mechanical properties of 10 kPa-10 MPa by changing the type of salt,and many hydrogels,such as gelatin and silk,could be improved with PTC or PCT strategies.Animal experiments show that this scaffold can effectively promote the new generation of muscle fibers,blood vessels,and nerves within 4 weeks,prompting the rapid regeneration of large-volume muscle loss injuries.
基金supported by the National Key Research and Development Program(No.2022YFB3807400)the National Natural Science Foundation of China(Nos.52072028 and 52032007).
文摘The study of BiFeO_(3)-0.3BaTiO_(3) ceramics has gained significant attention due to their high Curie temperature(TC≥450℃)and excellent piezoelectric properties(d33≥200 pC·N^(−1)).These are particularly pronounced near the morphotropic phase boundary(MPB)region where coexisting rhombohedral and pseudocubic(R-PC)phases are observed.In addition,as the BaTiO_(3) content increases,BiFeO_(3)-BaTiO_(3) ceramics gradually become dominated by a single pseudocubic(PC-)phase.This shift results in a decrease in piezoelectric properties but an enhancement in strain performance.However,the underlying mechanism remains unclear.The high strain properties observed in non-MPB compositions provide a motivation for further investigation into these mechanisms.This paper presents a detailed analysis of the electric-field and temperature-induced domain structure evolution in BiFeO_(3)-0.4BaTiO_(3),which is predominately characterized by the PC phase.Piezoresponse force microscope(PFM)observations reveal the presence of nanodomains and stripy domains associated with polar nanoregions(PNRs),as well as relaxor ferroelectrics(RFEs)and/or ferroelectrics(FEs).The RFEs exhibit a significantly better strain response than the FEs,providing direct evidence for the enhanced strain properties of RFEs.Elevated-temperature Raman spectroscopy confirms a decrease in B-O bonding and BO6 deformation,along with an increase in structural symmetry,indicating the formation of RFEs and/or PNRs.The phase diagram shows the Burns temperature(TB),dielectric maxima temperature(Tm)and freezing temperature(Tf)evaluated from the dielectric spectra;the temperature-induced evolution of domain structures;and the sequential quasi-dielectric states:PNRs,RFEs and FEs.The evolution of the domain structure,including the morphology and ratio of FEs,RFEs and PNRs,induced by either electric-fields or temperature strongly affects the strain properties of RFEs.A superior piezoelectric coefficient of d33*=533 pm·V^(−1) at 40 kV·cm^(−1) and a large electric strain of Suni=0.285%are obtained.These results further validate that domain modulation can effectively enhance the strain properties of BiFeO_(3)-BaTiO_(3) ceramics,which makes them promising candidates for actuator applications.
基金benefited from the financial support of the CAS Pioneer Hundred Talents Program and the Second Tibetan Plateau Scientific Expedition and Research Program (2019QZKK0708)。
文摘Throughout the 20th century, several large megathrust earthquakes were observed in the Colombia–Ecuador subduction zone which widely ruptured plate interfaces, causing considerable damage and loss of life. The occurrence of earthquakes in subduction zones is thought to be closely related to the thermal structure of the incoming plate. However, in the case of the subducting Nazca Plate beneath the Colombia–Ecuador zone, the thermal structure remains unclear, especially its hydraulic distribution. On the basis of 3D thermal models, we present new insights into the plate interface conditions of Colombia–Ecuador interplate and megathrust earthquakes. We show that the plate geometry strongly affects the along-strike thermal structure of the slab beneath Colombia and Ecuador, with the subduction of the Carnegie Ridge playing an important role. Our results further reveal that the unique geometry of the Nazca Plate is the primary reason for the relatively high temperatures of the slab beneath Colombia. We suggest that the positions of the100–200 ℃ and 350–450 ℃ isotherms on the plate interface determine the updip and downdip limits of the seismogenic zone. For Colombia–Ecuador interplate earthquakes, the released fluids control the distribution of shallow-depth earthquakes, whereas the age and geometry of the slab control the distribution of intermediate-depth earthquakes. The average temperature of the plate interface at the upper limit of large megathrust earthquakes is hotter than previously thought, which is more consistent with our understanding of the Colombia–Ecuador subduction zone. We predict that the potential location of future large seismic events could be in the rupture zone of past seismic events or offshore of northern Colombia.
基金supported by the National Natural Science Foundation of China under Grant No.52072196,52002200,52102106,52202262,22379081,22379080,Major Basic Research Program of Natural Science Foundation of Shandong Province under Grant No.ZR2020ZD09the Natural Science Foundation of Shandong Province under Grant No.ZR2020QE063,ZR202108180009,ZR2023QE059the Postdoctoral Program in Qingdao under No.QDBSH20220202019.
文摘Designing cathode possessing crystalline@amorphous core-shell structure with both active core and shell is a meaningful work for resolving the low specific capacity,unstable cycling performance and sluggish reaction kinetics issues of rechargeable magnesium batteries(RMBs)by providing more active sites as well as releasing inner stress during cycling.Herein,WO_(3)@WO_(3-x)S_(x) owning crystalline@amorphous core-shell structure containing both active core and active shell is constructed successfully by introducing S into metastable WO3 structure under temperaturefield applying.In such structure,amorphous shell would provide continuous Mg^(2+)diffusion channels due to its isotropy property for most Mg^(2+)migrating rapidly to interface and then adsorb at ions reservoir formed by interfacial electricfield for increasing specific capacity.It also makes security for stable structure of WO_(3)@WO_(3-x)S_(x) by alleviating volume expansion of crystalline core WO_(3) during cycling to prolong cycling life.Additionally,“softer”ions S^(2-)would weaken interaction between hard acid Mg^(2+) and ionic lattice to enhance Mg^(2+)storage kinetics.Therefore,WO_(3)@WO_(3-x)S_(x) delivers the superior cycling performance(1000 cycles with 83.3%),rate capability(88.5 mAh g^(-1) at 1000 mA g^(-1))and specific capacity(about 150 mAh g^(-1) at 50 mA g^(-1)),which is near 2 times higher than that of WO3.It is believed that the crystalline@amorphous core-shell structure with both active core and shell designing via doping strategy is enlightening for the development of high-performance RMBs,and such design can be extended to other energy storage devices for better electrochemical performance.
基金supported by the National Key Research and Development Program of China(No.2019YFA0110600)the Science and Technology Support Program of Sichuan Province(No.2019YJ0161).
文摘Hierarchical porous structure,which include macropores,minor pores,and micropores in scaffolds,are essential in the multiple biological functions of bone repair and regeneration.In this study,patientcustomized calcium-deficient hydroxyapatite(CDHA)scaffolds with three-level hierarchical porous structure were fabricated by indirect 3D printing technology and particulate leaching method.The sacrificial template scaffolds were fabricated using a photo-curing 3D printer,which provided a prerequisite for the integral structure and interconnected macropores of CDHA scaffolds.Additionally,20 wt%pore former was incorporated into the slurry to enhance the content of smaller pores within the CDHA-2 scaffolds,and then the CDHA-2 scaffolds were sintered to remove the sacrificial template scaffolds and pore former.The obtained CDHA-2 scaffolds exhibited interconnected macropores(300-400μm),minor pores(∼10-100μm),and micropores(<10μm)distributed throughout the scaffolds,which could promote bone tissue ingrowth,increase surface roughness,and enhance protein adsorption of scaffolds.In vitro studies identified that CDHA-2 scaffolds had nanocrystal grains,high specific surface area,and outstanding protein adsorption capacity,which could provide a microenvironment for cell adhesion,spreading,and proliferation.In addition,the murine intramuscular implantation experiment suggested that CDHA-2 scaffolds exhibited excellent osteoinductivity and were superior to traditional BCP ceramics under conditions without the addition of live cells and exogenous growth factors.The rabbit calvarial defect repair results indicated that CDHA-2 scaffolds could enhance in situ bone regeneration.In conclusion,these findings demonstrated that the hierarchical porous structure of CDHA scaffolds was a pivotal factor in modulating osteoinductivity and bone regeneration,and CDHA-2 scaffolds were potential candidates for bone regeneration.
基金supported by National Natural Science Foundation of China(Grant No.52205413)National Key Research and Development Program(Grant No.2022YFB3806101)+1 种基金K C Wong Education FoundationThe Youth Innovation Team of Shaanxi Universities。
文摘In-space 3D printing is transforming the manufacturing paradigm of space structures from ground-based production to in-situ space manufacturing,effectively addressing the challenges of high costs,long response times,and structural size limitations associated with traditional rocket launches.This technology enables rapid on-orbit emergency repairs and significantly expands the geometric dimensions of space structures.High-performance polymers and their composites are widely used in in-space 3D printing,yet their implementation faces complex challenges posed by extreme space environmental conditions and limited energy or resources.This paper reviews the state-of-the-art in 3D printing of polymer and composites for on-orbit structure manufacturing.Based on existing research activities,the review focuses on three key aspects including the impact of extreme space environments on forming process and performance,innovative design and manufacturing methods for space structures,and on-orbit recycling and remanufacturing of raw materials.Some experiments that have already been conducted on-orbit and simulated experiments completed on the ground are systematically analyzed to provide a more comprehensive understanding of the constraints and objectives for on-orbit structure manufacturing.Furthermore,several perspectives requiring further research in future are proposed to facilitate the development of new in-space 3D printing technologies and space structures,thereby supporting increasingly advanced space exploration activities.
基金supported by the Science and technology plan project of Yulin(2023-CXY-193)the Project funded by Shaanxi Postdoctoral Science Foundation(2023BSHEDZZ274)+2 种基金the Shaanxi Province(2023-ZDLGY-24,2023-JC-QN-0588,Z20210201)the Science and technology plan project of Beilin(GX2319)the Science and technology plan project of Ankang(AK2023-GY-08)。
文摘03-type layered oxide serves as dominant components in sodium ion batteries;however,the unstable electronic structure between transition metal and oxygen inevitably induces framework instability and severe kinetic hindrance.In this study,a two-in-one approach to synergistically modulate the local electro nic and interfacial structure of NaNi_(1/3)Fe_(1/3)Mn_(1/3)O_(2)by Ce modification is proposed.We present an indepth study to reveal the strong-covalent Ce-O bonds,which make local charge around oxygen more negative,enhance O 2p-Mn 3d hybridization,and preserve the octahedral structural integrity.This modification tailors local electronic structure between the octahedral metal center and oxygen,thus enhancing reversibility of 03-P3-03 phase transition and expanding Na+octahedral-tetrahedral-octahedral transport channel.Additionally,the nanoscale perovskite layer induced by Ce element is in favor of minimizing interfacial side reaction as well as enhancing Na^(+)diffusivity.As a result,the designed 03-NaNi_(0.305)Fe_(0.33)Mn_(0.33)Ce_(0.025)O_(2)material delivers an exceptionally low volume variation,an ultrahigh rate capacity of 76.9 mA h g^(-1)at 10 C,and remarkable cycling life over 250 cycles with capacity retention of 80% at 5 C.
基金supported by the National Natural Science Foundation of China(No.52401221)Shandong Provincial Natural Science Foundation,China(No.ZR2022QE014)+1 种基金the Basic Scientific Research Fund for Central Universities(No.202112018)the Key Laboratory of Advanced Energy Materials Chemistry(Ministry of Education)。
文摘Lithium(Li)metal is considered the most promising anode material for the next generation of secondary batteries due to its high theoretical specific capacity and low potential.However,the application of Li anode in rechargeable Li metal batteries(LMBs)is hindered due to the short cycle life caused by uncontrolled dendrite growth.In this work,a dendrite-free anode(Li–Sn/Cu)is reinforced synergistically by lithophilic alloy,and a 3D grid structure is designed.Li^(+)diffusion and uniform nucleation are effectively induced by the lithophilic alloy Li_(22)Sn_(5).Moreover,homogeneous deposition of Li^(+)is caused by the reversible gridded Li plating/stripping effect of Cu mesh.Furthermore,the local space electric field is redistributed throughout the 3D conductive network,whereby the tip effect is suppressed,thus inhibiting the growth of Li dendrites.Also,the volume expansion of the anode during cycling is eased by the 3D grid structure.The results show that the Li–Sn/Cu symmetric battery can stably cycle for more than 10,000 h at 2 mA.cm^(-2)and 1 mAh.cm^(-2)with a low overpotential.The capacity retention of the LiFePO_(4)full battery remains above 90.7%after 1,000 cycles at 1C.This work provides a facile,low-cost,and effective strategy for obtaining Li metal batteries with ultra-long cycle life.
基金supported by the National Natural Science Foundation of China(Grant Nos.62275188 and 62505216)the Central Guidance on Local Science and Technology Development Fund(Grant No.YDZJSX2024D019)+1 种基金the International Scientific and Technological Cooperative Project in Shanxi Province(Grant No.202104041101009)the Natural Science Foundation of Shanxi Province of China through Research Project(Grant No.20210302123195).
文摘Transforming a scattering medium into a lens for imaging very simple binary objects is possible;however,it remains challenging to image complex grayscale objects,let alone measure 3D continuous distribution objects.Here,we propose and demonstrate the use of a ground glass diffuser as a scattering lens for imaging complex grayscale fringes,and we employ it to achieve microscopic structured light 3D imaging(MSL3DI).The ubiquitous property of the speckle patterns permits the exploitation of the scattering medium as an ultra-thin scattering lens with a variable focal length and a flexible working distance for microscale object measurement.The method provides a light,flexible,and cost-effective imaging device as an alternative to microscope objectives or telecentric lenses in conventional MSL3DI systems.We experimentally demonstrate that employing a scattering lens allows us to achieve relatively good phase information and robust 3D imaging from depth measurements,yielding measurement accuracy only marginally lower than that of a telecentric lens,typically within approximately 10μm.Furthermore,the scattering lens demonstrates robust performance even when the imaging distance exceeds the typical working distance of a telecentric lens.The proposed method facilitates the application of scattering imaging techniques,providing a more flexible solution for MSL3DI.
基金Project supported by the Inner Mongolia University of Science and Technology Basic Research Business Fee Project(2022QNJS068,2024QNJS132)Inner Mongolia Autonomous Region Scientific and Technological Achievements Transformation Project(CGZH2018153)+1 种基金Inner Mongolia Autonomous Region Science and Technology Innovation Guidance Incentive Fund(0406041703)Project of Natural Science Foundation of Inner Mongolia(2024SHZR2341)。
文摘The influence of the growth of rare earth on the viscosity during the uniform cooling of CaO-SiO_(2-)CaF_(2)-Ce_(2)O_(3)slag was investigated by the high temperature viscometer.The results show that Ce_(2)O_(3)affects the viscosity variedly before and after the break temperature.At higher temperatures Ce_(2)O_(3)reduces the viscosity.When the temperature is below the break temperature,at a Ce_(2)O_(3)content of≥3 mol%,a rareearth crystalline phase is observed during the slag cooling process,and the break temperature progressively increases with the increase of Ce_(2)O_(3)concentration.There are no crystallized rare earths in the slag under the condition of Ce_(2)O_(3)concentration lower than 3 mol%.Too low or too high CaF_(2)content is found to be unfavorable for rare-earth crystallisation.The increase of Ce_(2)O_(3)content facilitates the depolymerization of silica-oxygen tetrahedral structure.Ca-F bond exists between structural units,weakening the flow resistance of structural units and lowering the viscosity of slag.
基金supported by the National Natural Science Foundation of China(Nos.22472071,21832005,22072168,22002175)the Natural Science Foundation of Gansu Province(No.21JR7RA440)Strategic Priority Research Program of the Chinese Academy of Sciences(No.XDA21061011)。
文摘Constrained by severe bulk charge recombination,the actual photocurrent density of tantalum nitride(Ta_(3)N_(5))photoanode is much lower than the theoretical maximum value.Herein,we report the doping of phosphorus,a non-metallic element distinct from oxygen,into Ta_(3)N_(5),resulting in a photocurrent density 9 times higher than that of pristine Ta_(3)N_(5).Systematic characterization reveals that the phosphorus doping simultaneously enhances the bulk charge separation efficiency and surface charge injection efficiency of Ta_(3)N_(5),and induces favorable band energy restructuring.Specifically,a type-II homojunction formed between phosphorus-doped near-surface region and bulk Ta_(3)N_(5) effectively promotes the separation and transfer of photogenerated holes and electrons.Further modification with a Ni Fe-based cocatalyst enables the optimized photoanode to deliver a photocurrent density of 10 mA/cm^(2) at 1.23 V versus the reversible hydrogen electrode(RHE)and an applied bias photo-to-current efficiency of 1.78%at 0.95 V versus RHE.Our work provides a foundation for the development of a broader range of non-metal doped semiconductors.
基金Project supported by the National Natural Science Foundation of China(21101107,51173107)State Key Laboratory of Pollution Control and Resource Reuse Foundation(PCRRF19017)。
文摘Herein we report novel photocatalysts ZnIn_(2)S_(4)-Ag-LaFeO_(3) with the core-shell structured materials prepared by hydrothermal method.In order to improve the efficiency of photocatalytic degradation of pollutants,LaFeO_(3) was prepared by hydrothermal followed by calcination,and further Ag nanoparticle(NP)was loaded onto the spherical structure of LaFeO_(3) by photolysis of silver nitrate,and finally the spherical Znln_(2)S_(4)-Ag-LaFeO_(3) photocatalyst was prepared by hydrothermal method again.The structure and properties of the as-prepared materials were characterized by X-ray photoelectron spectroscopy,ultraviolet-visible absorption spectroscopy,X-ray diffraction,scanning electron microscopy and fluorescence spectra.The results show that the synthesized composite photocatalysts display a significant improvement in photocatalytic efficiency relative to the single LaFeO_(3) and ZnIn_(2)S_(4)and form a core-shell structure.Furthermore,the effect of the ratio of each component on the photocatalytic efficiency was investigated in detail,and it is discovered that at an Methylene Blue(MB)concentration of 0.219 mol/L,the degradation rate of MB is 95%at 120 min using 0.02 g of catalyst with an ideal ZnIn_(2)S_(4):Ag:LaFeO_(3)ratio of 10:0.5:1.The possible mechanisms to improve the photocatalytic efficiency were explored.
