The study of the shear behavior of bonded rock-cement interface is important for understanding the strength and stability of grouted rock masses.This research aims to reveal the failure mechanism behind the shear prop...The study of the shear behavior of bonded rock-cement interface is important for understanding the strength and stability of grouted rock masses.This research aims to reveal the failure mechanism behind the shear property of bonded rock-cement interfaces.For the study,sandstone and granite joint blocks with specific morphology were fabricated by using a three-dimensional(3D)engraving technique.Bonded rock-cement joints with asperity inclination angles of 15°,30°,and 45°were prepared.Shear tests were performed on these bonded rock-cement joints to investigate the shear response and failure modes considering the effect of applied normal stress and interface morphology.Meanwhile,the two-dimensional particle flow code(PFC2D)was utilized to model the entire shear process of bonded rock-cement interfaces.The macroscopic shear behavior and mesoscopic failure mechanism were comprehensively investigated by the laboratory test and numerical simulation.The results showed that the shear stress-displacement curves of bonded rock-cement joints exhibit two distinct peaks,and the shear stress evolution can be categorized into four stages including elastic growth,rapid stress drop,secondary stress growth,and progressive softening.Significantly,the number of acoustic emission events also exhibits two distinct peaks related to the double peak of the shear stress curves.The failure of bonded rock-cement interfaces is mainly induced by shear fractures,while the failure of rock and cement blocks is primarily caused by tensile fractures.The number of shear cracks in the bonded rock-cement interfaces reaches the peak when the shear stress reaches the primary peak;whereas as the shear stress continuously approaches the residual stage,the fracture of the bonded rock-cement joints is primarily characterized by tensile cracks in the blocks.展开更多
In the Pidgeon process involving a vertical pot,bonded slag pellets occasionally emerge at the bottom of the reduction pot,impeding smooth slag discharge.To reveal the formation mechanism of the bonded slag pellets,th...In the Pidgeon process involving a vertical pot,bonded slag pellets occasionally emerge at the bottom of the reduction pot,impeding smooth slag discharge.To reveal the formation mechanism of the bonded slag pellets,thermodynamic calculations,X-ray diffraction(XRD),X-ray fluorescence spectrometry(XRF),electron probe microanalyzer(EPMA),X-ray photoelectron spectroscopy(XPS),and differential scanning calorimetry(DSC)were employed.The bonded slag pellets mainly comprise MgO,CaSi_(2),CaO,and Ca2SiO_(4).CaSi_(2) in the bonded slag pellets is attributed to the reduction reaction between Si and CaO,yielding liquid CaSi_(2).Simultaneously,the reaction between CaSi_(2) and MgO,which will typically produce Mg vapor,is inhibited,resulting in the accumulation of CaSi_(2).Owing to the solid-liquid transition of CaSi_(2),this process culminates in the bonding of slag pellets.This study can guide the Pidgeon process optimization,enabling mitigation of the“dead pot”issue,thereby enhancing efficiency and reducing costs.展开更多
Efficient conversion and synergistic solar energy utilization are critical for advancing low-carbon and sustainable development.In this study,two Pt(Ⅱ)-based metal/halogen-bonded organic frameworks(MXOFBen and MXOF-A...Efficient conversion and synergistic solar energy utilization are critical for advancing low-carbon and sustainable development.In this study,two Pt(Ⅱ)-based metal/halogen-bonded organic frameworks(MXOFBen and MXOF-Anth)were designed to enhance photoconversion efficiency and enable multifunctional integration.The ligand L-terpyr is formed by coupling tripyridine with diphenylamine dipyridine,in which the tripyridine effectively acts as a metal-ligand to lower the band gap and promote nonradiative leaps,thereby enhancing the photoconversion ability.Meanwhile,diphenylamine dipyridine serves as a[N…I^(+)…N]halogen-bonding acceptor,imparting superhydrophilicity to the materials and increasing carrier density,further improving photocatalytic performance.Experimental results demonstrate that these two MXOFs achieve impressive interfacial water evaporation efficiencies of up to87.8%and 94.0%,respectively.Additionally,the materials exhibit excellent performance in photothermal power generation and photocatalysis of H_(2)O_(2).Notably,the MXOFs also deliver strong overall performance in integrated systems combining interfacial water evaporation with photothermal power generation or photocatalysis,underscoring their exceptional photoconversion efficiency and multifunctional potential.This work introduces a novel strategy by incorporating metal-ligand and halogen bonds,offering a pathway to enhance photoconversion efficiency and develop versatile materials for advanced solar energy applications,thereby fostering the progress of high-efficiency solar energy conversion and multifunctional organic materials.展开更多
To improve the seismic performance of unrein-forced masonry(URM)buildings in the Himalayan re-gions,including Western China,India,Nepal,and Paki-stan,a low-cost bonded scrap tire rubber isolator(BSTRI)is proposed,and ...To improve the seismic performance of unrein-forced masonry(URM)buildings in the Himalayan re-gions,including Western China,India,Nepal,and Paki-stan,a low-cost bonded scrap tire rubber isolator(BSTRI)is proposed,and a series of vertical compression and horizontal shear tests are conducted.Incremental dynamic analyses are conducted for five types of BSTRI-supported URM buildings subjected to 22 far-field and 28 near-field earthquake ground motions.The resulting fragility curves and probability of damage curves are presented and utilized to evaluate the damage states of these buildings.The results show that in the base-isolated(BI)URM buildings under seismic ground motion at a peak ground acceleration(PGA)of 1.102g,the probability of exceeding the collapse prevention threshold is less than 25%under far-field earthquake ground motions and 31%under near-field earthquake ground motions.Furthermore,the maximum average vulnerability index for the BI-URM buildings,which are designed to withstand rare earthquakes with 9°(PGA=0.632g),is 40.87%for far-field earthquake ground motions and 41.83%for near-field earthquake ground motions.Therefore,the adoption of BSTRIs can significantly reduce the collapse probability of URM buildings.展开更多
In order to improve the densification of Si_(3)N_(4) bonded SiC refractories and reduce the nitriding temperature of Si powder,Si_(3)N_(4) bonded SiC refractories were produced by reaction sintering at 1350℃ for 5 h ...In order to improve the densification of Si_(3)N_(4) bonded SiC refractories and reduce the nitriding temperature of Si powder,Si_(3)N_(4) bonded SiC refractories were produced by reaction sintering at 1350℃ for 5 h under a carbon embedded atmosphere,using SiC particles and fine powder,and Si powder as the main raw materials,and introducing Ti-Si-Fe alloy extracted from high-titanium blast furnace slag to partially replace the Si powder.The effects of the Ti-Si-Fe alloy addition(0,1.8%,3.6%,5.4%,and 7.2%,by mass)on the nitriding behavior of Si powder,as well as on the mechanical properties and microstructure of the material were investigated,and the nitriding reaction sintering mechanism was also explored.The results show that:(1)with the increase of the Ti-Si-Fe alloy addition,the cold mechanical properties and the hot modulus of rupture of the refractories are obviously improved,and the refractoriness under load exceeds 1700℃;the property enhancement slows down with Ti-Si-Fe alloys addition above 3.6%;(2)Ti-Si-Fe alloy promotes the complete nitridation of Si powder and the reaction sintering of the material at a lower temperature;the volume growth during the nitridation process of the Ti-Si-Fe alloys and Si powder can effectively fill pores,nitriding products improve the bonding state between aggregates and matrix,and that inside matrix,thereby increasing the densification and improving the mechanical properties of the material;(3)after the introduction of Ti-Si-Fe alloys,the liquid phase rich in Ti,Si,N,and Fe components is formed in the reaction system;besides the traditional VS and VLS mechanisms,the dissolution-precipitation mechanism plays a leading role in the formation of short columnar β-Si_(3)N_(4) and granular TiN;and the cross-linked α-Si_(3)N_(4) whisker,short columnar β-Si_(3)N_(4) and granular TiN enhance the mechanical properties of the material.展开更多
With the acceleration of industrialization,the pollution problem of sulfur dioxide(SO_(2))emitted from coal-fired power plants has become increasingly severe.Although wet flue gas desulfurization(FGD)technology can re...With the acceleration of industrialization,the pollution problem of sulfur dioxide(SO_(2))emitted from coal-fired power plants has become increasingly severe.Although wet flue gas desulfurization(FGD)technology can remove about 95%of SO_(2),its high energy consumption and the corrosion risk of downstream equipment caused by residual SO_(2)(500–3000 ppm)still need to be addressed[1].Previous porous materials(such as MOFs)achieve selective adsorption of SO_(2) through open metal sites,M–OH sites or functional organic groups,but the problem of CO_(2) co-adsorption limits their practical application[2].In recent years,hydrogen-bonded organic frameworks(HOFs)have emerged as a research hotspot due to their reversible hydrogen-bonding networks and flexible structures[3],but their stability under extreme conditions and efficient separation performance still need to be improved[4].展开更多
Acidic-stable oxygen evolution reaction(OER)catalysts based on earth-abundant materials are important but rare for the proton exchange membrane-based water electrolysis.In this study,a metal-containing hydrogen-bonded...Acidic-stable oxygen evolution reaction(OER)catalysts based on earth-abundant materials are important but rare for the proton exchange membrane-based water electrolysis.In this study,a metal-containing hydrogen-bonded organic framework(HOF)of manganese coordinated with 2,2'-bipyridine-6,6'-dicarboxylate ligands,Mn(bda),interconnected through hydrogen bonding and π-π stacking is used as a heterogeneous OER catalyst(Mn(bda)-HOF)for acidic water oxidation and exhibits a considerable OER performance.Electrochemical results show that Mn(bda)-HOF displays a turn of frequency of 1 s^(-1) at an overpotential of 870 mV.Meanwhile,this Mn(bda)-HOF shows an unusual pH dependence on performance,where the reaction rate increases with the decrease of pH.A comprehensive mechanistic study reveals that the charge transfer triggered coupling of two metal-oxo species Mn^(5+)(O)is the rate-determining step,which leads to this unusual pH dependence on the OER performance.展开更多
The transient liquid-phase(TLP)diffusion bonding of GH5188 with a BNi-5 interlayer was focused on.Parameters were chosen and optimized for GH5188 alloy according to the TLP joining mechanism.The microstructure evoluti...The transient liquid-phase(TLP)diffusion bonding of GH5188 with a BNi-5 interlayer was focused on.Parameters were chosen and optimized for GH5188 alloy according to the TLP joining mechanism.The microstructure evolution and mechanical properties of the joints were studied.Results show that the relatively complete isothermal solidification zone(ISZ)ensures a reliable connection of the base metal(BM).Within the temperature range of 1110–1190°C,higher bonding temperatures can widen ISZ and promote joint composition homogenization,thus improving mechanical properties.However,the increase in precipitated phase has an adverse effect on the mechanical properties of the joint.The maximum shear strength,reaching 482 MPa,is achieved at 1130°C,representing 84.6%of BM strength.Within the pressure range of 5–15 MPa,both precipitated phases in adiabatic solidification zone(ASZ)and voids generated by partial melting increase.On the contrary,their sizes decrease significantly under higher bonding pressure,resulting in an upward trend in alloy mechanical properties.The maximum shear strength of 490 MPa is attained at a bonding pressure of 15 MPa.The joint exhibits a typical mixed fracture pattern,with the small brittle M_(23)C_(6) phase and voids significantly impacting mechanical properties.Nano-indentation tests indicate that ASZ is a potential source of cracks.展开更多
Introduction: Bracket debonding is a frequent issue that clinicians encounter, leading to increased chair time, lost revenue, and material usage. In addition to patient compliance with their diet recommendations, the ...Introduction: Bracket debonding is a frequent issue that clinicians encounter, leading to increased chair time, lost revenue, and material usage. In addition to patient compliance with their diet recommendations, the preparation and conditioning of teeth for bonding significantly influence bond strength and consequently impact orthodontic treatment success and efficiency. Because of OBA-MCP’s (orthodontic bonding adhesive with modified calcium phosphate) decreased shear bond strength (SBS), the purpose of this study was to evaluate the effects of conditioning with 5.25% sodium hypochlorite (NaOCl) before etching in the bonding protocol. Materials and Methods: 90 extracted teeth were divided into 3 groups to be bonded with orthodontic brackets with different bonding protocols: 1) Transbond XT with regular bonding protocol (etch + prime + adhesive);2) OBA-MCP with regular bonding protocol;and 3) OBA-MCP with NaOCl prior to acid etching in the regular bonding protocol. SBS (in Newtons) were measured using an MTS universal testing machine with a custom jig to apply a vertical force onto the bracket and ARI (adhesive remnant index) scores were recorded for each sample after de-bond to rate the amount of adhesive remaining. Results: The addition of NaOCl to the bonding protocol statistically significantly increased the SBS of OBA-MCP to comparable levels to Transbond XT. The ARI scores showed that when NaOCl was added, more adhesive remained. Conclusion: The addition of NaOCl to the bonding protocol can increase the SBS of adhesives with historically weaker bond strengths. However, the increased amount of adhesive remaining and the increased time spent during bonding must be considered. Further testing can be done in vivo to demonstrate the practicality of this new procedure.展开更多
Diffusion-bonded Ti_(2)AlNb-based alloys commonly present a low strength compared with the deformed or aged ones. In this study, the post heat treatment including solution and aging treatments is proposed to optimize ...Diffusion-bonded Ti_(2)AlNb-based alloys commonly present a low strength compared with the deformed or aged ones. In this study, the post heat treatment including solution and aging treatments is proposed to optimize the microstructure, contributing to strength improvement and appropriate ductility sacrifice. An available method by the introduction of fine size (both 20-100 nm) and a high fraction (59.7% and 13.7%) of O and α_(2) phases using both solution at 1000℃ for 1 h and aging at 750℃ for 5 h can result in excellent tensile strength (992 MPa and 858 MPa) at room temperature and 650℃, respectively, which increases 5.3% and 44.5% than that of as-received sample. The aging treatment can contribute to lamellar O and α2 grains precipitated from the B_(2) parent, which results in limited dislocation slip systems and slip spaces to resist plastic deformation. Moreover, the crack propagation and fracture surfaces are also comparatively analyzed to reveal the fracture behaviors in the samples with high and low strength. This study can provide a new method for the mechanical property optimization of the welded Ti_(2)AlNb alloys.展开更多
LiMnxFe1-xPO_(4) is a promising cathode candidate due to its high security and the availability of a high 4.1 V operating voltage and high energy density.However,the poor electrochemical kinetics and structural instab...LiMnxFe1-xPO_(4) is a promising cathode candidate due to its high security and the availability of a high 4.1 V operating voltage and high energy density.However,the poor electrochemical kinetics and structural instability currently hinder its broader application.Herein,inspired by the hydrogen-bonded cross-linking and steric hindrance effect between short-chain polymer molecules(polyethylene glycol-400,PEG-400),the pomegranate-type LiMn_(0.5)Fe_(0.5)PO_(4)-0.5@C(P-LMFP@C)cathode materials with 3D ion/electron dual-conductive network structure were constructed through ball mill-assisted spray-drying method.The intermolecular effects of PEG-400 promote the spheroidization and uniform PEG coating of LMFP precursor,which prevents agglomeration during sintering.The 3D ion/electron dual-conductive network structure in P-LMFP@C accelerates the Li^(+)transport kinetics,improving the rate performance and cycling stability.As a result,the designed P-LMFP@C has remarkable electrochemical behavior,boasting excellent capacity retention(98%after 100 cycles at the 1C rate)and rate capability(91 mAh·g^(-1)at 20C).Such strategy introduces a novel window for designing high-performance olivine cathodes and offers compatibility with a range of energy storage materials for diverse applications.展开更多
Devising exceptional S-scheme heterojunction photocatalysts utilized in annihilating pharmaceuticals and chromium contamination is significant for addressing the problem of global water pollution.In this work,a chemic...Devising exceptional S-scheme heterojunction photocatalysts utilized in annihilating pharmaceuticals and chromium contamination is significant for addressing the problem of global water pollution.In this work,a chemically bonded Mn0.5Cd_(0.5)S/BiOBr S-scheme heterostructure with oxygen vacancies is ingeniously developed through a facile in-situ solvothermal synthesis.The designed Mn0.5Cd_(0.5)S/BiOBr heterojunction exhibits eminently reinforced photo-activity for destruction of tetracycline hydrochloride and Cr(VI)as compared with its individual components.This substantial photo-redox performance amelioration is benefitted from the creation of an intense internal electric field(IEF)via supplying powerful driving force and migration highway by interfacial chemical bond to foster the S-scheme electron/hole disintegration.More intriguingly,the IEF at the hetero-interface drives the fast consumption of the photo-induced holes in Mn0.5Cd_(0.5)S by the photoelectrons from BiOBr,profoundly boosting the enrichment of active photo-carriers and sparing the photo-corrosion of Mn0.5Cd_(0.5)S.Furthermore,Mn0.5Cd_(0.5)S/BiOBr with exceptional anti-interference property can work efficiently in real water matrices.Multiple uses of the recycled Mn0⋅5Cd0⋅5S/BiOBr evidence its prominent robustness and stability.This achievement indicates the vast potential of chemically bonded S-scheme photosystems with structural defects in the design of photo-responsive materials for effective wastewater treatment.展开更多
This paper presents the static and fatigue tests of hybrid(bonded/bolted)glass fiber reinforced polymer(GFRP)joints.Nine specimens of single-lap hybrid GFRP joints have been fabricated to study the static and fatigue ...This paper presents the static and fatigue tests of hybrid(bonded/bolted)glass fiber reinforced polymer(GFRP)joints.Nine specimens of single-lap hybrid GFRP joints have been fabricated to study the static and fatigue behaviors in the experimental campaign.The static tests of uniaxial tension loading are first conducted,from which the static ultimate bearing capacities of the joints are obtained.High-cycle fatigue tests are subsequently carried out so that the fatigue failure mode,fatigue life,and stiffness degradation of joints can be obtained.The measuring techniques including acoustic emission monitoring and three-dimensional digital image correlation have been employed in the tests to record the damage development process.The results revealed that the static strength and fatigue behavior of such thick hybrid GFRP joints were controlled by the bolted connections.The four stages of fatigue failure process are obtained from tests and acoustic emission signals analysis:cumulative damage of adhesive layer,damage of the adhesive layer,cumulative damage of GFRP plate,and damage of GFRP plate.The fatigue life and stiffness degradation can be improved by more bolts.The S-N(fatigue stress versus life)curves for the fatigue design of the single-lap hybrid GFRP joints under uniaxial tension loading are also proposed.展开更多
Transient liquid phase(TLP)bonding is a promising process for the joining and repairing of nickel-base superalloys.One of the most important parameters in TLP bonding is the bonding time required for suf-ficient isoth...Transient liquid phase(TLP)bonding is a promising process for the joining and repairing of nickel-base superalloys.One of the most important parameters in TLP bonding is the bonding time required for suf-ficient isothermal solidification which prevents the formation of undesirable precipitated phases.In the present work,the effect of bonding time on the microstructure,type,and evolution of precipitates in the non-isothermal solidified zone(NSZ)and their effect on micro-mechanical properties were systemat-ically investigated using multi-scale tests in TLP bonded Mar-M247 superalloy joints with Ni-15.2Cr-3.74B interlayer at 1230℃.For a bonding time of 5 min,dual-phase M_(23)(C,B)_(6)-γ/γ’(where M is a mix-ture of Hf,Ta,Cr,and Ni)with eutectic configuration was formed in NSZ.With the increase in bonding time,the evolution of NSZ microstructure can be summed up as eutectic M_(23)(C,B)_(6)-γ/γ’,semi-striping dual-phase M_(23)(C,B)_(6)-γ/γ’,discontinuously striping M_(23)(C,B)_(6)-γ/γ’,followed by the disintegration of NSZ.As the NSZ counterpart,the isothermal solidified zone(ISZ)is mainly composed ofγ/γ’.Ac-companied by the dissolution of M_(23)(C,B)_(6) in the centerline,the proportion of the ISZ increases greatly until the joints are completely occupied by ISZ.Finally,a bamboo-like structure with domain size of-100μm was formed in the joint centerline,along withγ’reorganized themselves all into cubic shapes and distributed homogeneously.Mechanical property tests demonstrated that in comparison to samples with longer bonding time,the NSZ of the shortest bonding time(5 min)has the highest strength and a subsequent decrease in strength was observed with prolonging the bonding time and post-bond heat treatment.Furthermore,possible solidification/transformation path,segregation behavior,and formation mechanism of NSZ/ISZ evolution were discussed.展开更多
Basing on vacuum diffusion bonding technique,Mg1 and Al1060 were welded under different welding temperatures.Inspection equipment such as scanning electron microscopy,energy dispersive spectroscopy,X-ray diffractomete...Basing on vacuum diffusion bonding technique,Mg1 and Al1060 were welded under different welding temperatures.Inspection equipment such as scanning electron microscopy,energy dispersive spectroscopy,X-ray diffractometer,and tensile machine were applied to observe and investigate the microstructure,phase composition and mechanical property of Mg/Al diffusion welding joints.The results indic-ate that Mg1/Al1060 diffusion layers generate in the joints,and the thickness progressively increases with ascending welding temperature.From Al to Mg side,diffusion layers are comprised of Mg2Al3,Mg17Al12,and Mg17Al12+Mg based solid solutions sequentially.The shear resistance of the joints increases and then decreases with the increasing welding temperature.At 440℃,the maximal shear strength of 13 MPa can be obtained,and fracture results from Mg2Al3 phase near Al side.展开更多
Surface charge localization and inferior charge transfer efficiency seriously restrict the supply of reactive hydrogen and the reaction dynamics of CO_(2) photoreduction performance of photocatalysts.Herein,chemically...Surface charge localization and inferior charge transfer efficiency seriously restrict the supply of reactive hydrogen and the reaction dynamics of CO_(2) photoreduction performance of photocatalysts.Herein,chemically bonded BiVO_(4)/Bi_(19)Cl_(3)S_(27)(BVO/BCS)S-scheme heterojunction with a strong internal electric field is designed.Experimental and density function theory calculation results confirm that the elaborated heterojunction accelerates the vectorial migration of photogenerated charges from BiVO_(4) to Bi_(19)Cl_(3)S_(27) via the interfacial chemical bonding interactions(i.e.,Bi-O and Bi-S bonds)between Bi atoms of BVO and S atoms of BCS or Bi atoms of BCS and O atoms of BVO under light irradiation,breaking the interfacial barrier and surface charge localization of Bi_(19)Cl_(3)S_(27),and further decreasing the energy of reactive hydrogen generation,CO_(2) absorption and activation.The separation efficiency of photogenerated carriers is much more efficient than that counterpart individual in BVO/BCS S-scheme heterojunction system.As a result,BVO/BCS heterojunction exhibits a significantly improved continuous photocatalytic performance for CO_(2) reduction and the 24 h CO yield reaches 678.27μmol⋅g^(-1).This work provides an atomic-level insight into charge transfer kinetics and CO_(2) reduction mechanism in S-scheme heterojunction.展开更多
Despite advancements in silicon-based anodes for high-capacity lithium-ion batteries,their widespread commercial adoption is still hindered by significant volume expansion during cycling,especially at high active mass...Despite advancements in silicon-based anodes for high-capacity lithium-ion batteries,their widespread commercial adoption is still hindered by significant volume expansion during cycling,especially at high active mass loadings crucial for practical use.The root of these challenges lies in the mechanical instability of the material,which subsequently leads to the structural failure of the electrode.Here,we present a novel synthesis of a composite combining expanded graphite and silicon nanoparticles.This composite features a unique interlayer-bonded graphite structure,achieved through the application of a modified spark plasma sintering method.Notably,this innovative structure not only facilitates efficient ion and electron transport but also provides exceptional mechanical strength(Vickers hardness:up to658 MPa,Young's modulus:11.6 GPa).This strength effectively accommodates silicon expansion,resulting in an impressive areal capacity of 2.9 mA h cm^(-2)(736 mA h g^(-1)) and a steady cycle life(93% after 100cycles).Such outsta nding performance is paired with features appropriate for large-scale industrial production of silicon batteries,such as active mass loading of at least 3.9 mg cm^(-2),a high-tap density electrode material of 1.68 g cm^(-3)(secondary clusters:1.12 g cm^(-3)),and a production yield of up to 1 kg per day.展开更多
We study the friction properties of interlayer bonded bilayer graphene by simulating the movement of a slider on the surface of bilayer graphene using molecular dynamics.The results show that the presence of the inter...We study the friction properties of interlayer bonded bilayer graphene by simulating the movement of a slider on the surface of bilayer graphene using molecular dynamics.The results show that the presence of the interlayer covalent bonds due to the local sp^(3) hybridization of carbon atoms in the bilayer graphene seriously reduces the frictional coefficient of the bilayer graphene surface to 30%,depending on the coverage of interlayer sp^(3) bonds and normal loads.For a certain coverage of interlayer sp3bonds,when the normal load of the slider reaches a certain value,the surface of this interlayer bonded bilayer graphene will lose the friction reduction effect on the slider.Our findings provide guidance for the regulation and manipulation of the frictional properties of bilayer graphene surfaces through interlayer covalent bonds,which may be useful for applications of friction related graphene based nanodevices.展开更多
Covalently bonded bridging between different semiconductors is a remarkable approach to improve the transfer of charge carriers at interfaces.In this study,we designed a ternary heterojunction(MBG)combining of molybde...Covalently bonded bridging between different semiconductors is a remarkable approach to improve the transfer of charge carriers at interfaces.In this study,we designed a ternary heterojunction(MBG)combining of molybdenum diselenide(Mo Se_(2)),black phosphorus nanosheets(Bpn)and graphitic carbon nitride(GCN).Among this MBG of Mo Se_(2)/Bpn/GCN,(i)the covalently bonded bridging effect between Bpn/GCN facilitates directional charge carrier transfer,meanwhile(ii)a Z-scheme heterojunction is formed between Mo Se_(2)/GCN to enhance the separation of photogenerated carriers.Furthermore,(iii)this composite exhibits an increased absorption for visible light.Using this MBG,photocatalytic degradation of over 98%of moxifloxacin is achieved within 20 min,with O_(2)·-confirmed as the primary photocatalytic active species.These findings provide novel insights into the construction of efficient heterojunction by covalently bonded bridging.展开更多
Cement-free castables have attracted significant attention due to their superior thermal-mechanical properties and rapid dry-out in comparison to cement-bonded refractory castables.However,drying industrial-scale spec...Cement-free castables have attracted significant attention due to their superior thermal-mechanical properties and rapid dry-out in comparison to cement-bonded refractory castables.However,drying industrial-scale specimens can pose more challenges than lab-scale samples.In this study,the dry-out behavior and explosion resistance of microsilica-gel bonded nocement castables(NCCs)were investigated on both lab-and industrial-scale specimens,employing various drying agents.First,the fast dry-out mechanism was assessed using thermogravimetric analysis(TGA),differential scanning calorimetry(DSC),and scanning electron microscopy(SEM)on lab-scale small samples.Then,the drying behavior of industrial-scale large samples(300 mm×300 mm×300 mm cubes,approximately 80 kg)was studied using a unique macro-thermo-balance(macro-TGA).The results showed that EMSIL-DRY^(®)reduced the temperature level for maximum dewatering rate and effectively prevented explosions during heat-up,compared to other polymer fibres.The use of a specialty drying agent(EMSIL-DRY^(®))significantly improved the explosion resistance,as demonstrated by the production of a perfect 400 kg block fired to 850℃at a rate of 50℃·h^(-1).This research contributes to the understanding and application of cement-free castables in industrial settings.展开更多
基金supported by the National Natural Science Foundation of China(Grant Nos.52369019,52004127)the Young Elite Scientists Sponsorship Program by JXAST(Grant No.2023QT06).
文摘The study of the shear behavior of bonded rock-cement interface is important for understanding the strength and stability of grouted rock masses.This research aims to reveal the failure mechanism behind the shear property of bonded rock-cement interfaces.For the study,sandstone and granite joint blocks with specific morphology were fabricated by using a three-dimensional(3D)engraving technique.Bonded rock-cement joints with asperity inclination angles of 15°,30°,and 45°were prepared.Shear tests were performed on these bonded rock-cement joints to investigate the shear response and failure modes considering the effect of applied normal stress and interface morphology.Meanwhile,the two-dimensional particle flow code(PFC2D)was utilized to model the entire shear process of bonded rock-cement interfaces.The macroscopic shear behavior and mesoscopic failure mechanism were comprehensively investigated by the laboratory test and numerical simulation.The results showed that the shear stress-displacement curves of bonded rock-cement joints exhibit two distinct peaks,and the shear stress evolution can be categorized into four stages including elastic growth,rapid stress drop,secondary stress growth,and progressive softening.Significantly,the number of acoustic emission events also exhibits two distinct peaks related to the double peak of the shear stress curves.The failure of bonded rock-cement interfaces is mainly induced by shear fractures,while the failure of rock and cement blocks is primarily caused by tensile fractures.The number of shear cracks in the bonded rock-cement interfaces reaches the peak when the shear stress reaches the primary peak;whereas as the shear stress continuously approaches the residual stage,the fracture of the bonded rock-cement joints is primarily characterized by tensile cracks in the blocks.
基金China Postdoctoral Science Foundation (No. 2020M682337)。
文摘In the Pidgeon process involving a vertical pot,bonded slag pellets occasionally emerge at the bottom of the reduction pot,impeding smooth slag discharge.To reveal the formation mechanism of the bonded slag pellets,thermodynamic calculations,X-ray diffraction(XRD),X-ray fluorescence spectrometry(XRF),electron probe microanalyzer(EPMA),X-ray photoelectron spectroscopy(XPS),and differential scanning calorimetry(DSC)were employed.The bonded slag pellets mainly comprise MgO,CaSi_(2),CaO,and Ca2SiO_(4).CaSi_(2) in the bonded slag pellets is attributed to the reduction reaction between Si and CaO,yielding liquid CaSi_(2).Simultaneously,the reaction between CaSi_(2) and MgO,which will typically produce Mg vapor,is inhibited,resulting in the accumulation of CaSi_(2).Owing to the solid-liquid transition of CaSi_(2),this process culminates in the bonding of slag pellets.This study can guide the Pidgeon process optimization,enabling mitigation of the“dead pot”issue,thereby enhancing efficiency and reducing costs.
基金supported by the National Natural Science Foundation of China(Nos.22371218,21702153,52270070,and 21801194)the Wuhan Science and Technology Bureau(No.whkxjsj009)+1 种基金support of the Core Facility of Wuhan Universitythe Large-scale Instrument and Equipment Sharing Foundation of Wuhan University。
文摘Efficient conversion and synergistic solar energy utilization are critical for advancing low-carbon and sustainable development.In this study,two Pt(Ⅱ)-based metal/halogen-bonded organic frameworks(MXOFBen and MXOF-Anth)were designed to enhance photoconversion efficiency and enable multifunctional integration.The ligand L-terpyr is formed by coupling tripyridine with diphenylamine dipyridine,in which the tripyridine effectively acts as a metal-ligand to lower the band gap and promote nonradiative leaps,thereby enhancing the photoconversion ability.Meanwhile,diphenylamine dipyridine serves as a[N…I^(+)…N]halogen-bonding acceptor,imparting superhydrophilicity to the materials and increasing carrier density,further improving photocatalytic performance.Experimental results demonstrate that these two MXOFs achieve impressive interfacial water evaporation efficiencies of up to87.8%and 94.0%,respectively.Additionally,the materials exhibit excellent performance in photothermal power generation and photocatalysis of H_(2)O_(2).Notably,the MXOFs also deliver strong overall performance in integrated systems combining interfacial water evaporation with photothermal power generation or photocatalysis,underscoring their exceptional photoconversion efficiency and multifunctional potential.This work introduces a novel strategy by incorporating metal-ligand and halogen bonds,offering a pathway to enhance photoconversion efficiency and develop versatile materials for advanced solar energy applications,thereby fostering the progress of high-efficiency solar energy conversion and multifunctional organic materials.
基金The National Natural Science Foundation of China(No.52208195)the Independent Subject of State Key Laboratory of Disaster Reduction in Civil Engineering of Tongji University(No.SLDRCE19-A-10).
文摘To improve the seismic performance of unrein-forced masonry(URM)buildings in the Himalayan re-gions,including Western China,India,Nepal,and Paki-stan,a low-cost bonded scrap tire rubber isolator(BSTRI)is proposed,and a series of vertical compression and horizontal shear tests are conducted.Incremental dynamic analyses are conducted for five types of BSTRI-supported URM buildings subjected to 22 far-field and 28 near-field earthquake ground motions.The resulting fragility curves and probability of damage curves are presented and utilized to evaluate the damage states of these buildings.The results show that in the base-isolated(BI)URM buildings under seismic ground motion at a peak ground acceleration(PGA)of 1.102g,the probability of exceeding the collapse prevention threshold is less than 25%under far-field earthquake ground motions and 31%under near-field earthquake ground motions.Furthermore,the maximum average vulnerability index for the BI-URM buildings,which are designed to withstand rare earthquakes with 9°(PGA=0.632g),is 40.87%for far-field earthquake ground motions and 41.83%for near-field earthquake ground motions.Therefore,the adoption of BSTRIs can significantly reduce the collapse probability of URM buildings.
文摘In order to improve the densification of Si_(3)N_(4) bonded SiC refractories and reduce the nitriding temperature of Si powder,Si_(3)N_(4) bonded SiC refractories were produced by reaction sintering at 1350℃ for 5 h under a carbon embedded atmosphere,using SiC particles and fine powder,and Si powder as the main raw materials,and introducing Ti-Si-Fe alloy extracted from high-titanium blast furnace slag to partially replace the Si powder.The effects of the Ti-Si-Fe alloy addition(0,1.8%,3.6%,5.4%,and 7.2%,by mass)on the nitriding behavior of Si powder,as well as on the mechanical properties and microstructure of the material were investigated,and the nitriding reaction sintering mechanism was also explored.The results show that:(1)with the increase of the Ti-Si-Fe alloy addition,the cold mechanical properties and the hot modulus of rupture of the refractories are obviously improved,and the refractoriness under load exceeds 1700℃;the property enhancement slows down with Ti-Si-Fe alloys addition above 3.6%;(2)Ti-Si-Fe alloy promotes the complete nitridation of Si powder and the reaction sintering of the material at a lower temperature;the volume growth during the nitridation process of the Ti-Si-Fe alloys and Si powder can effectively fill pores,nitriding products improve the bonding state between aggregates and matrix,and that inside matrix,thereby increasing the densification and improving the mechanical properties of the material;(3)after the introduction of Ti-Si-Fe alloys,the liquid phase rich in Ti,Si,N,and Fe components is formed in the reaction system;besides the traditional VS and VLS mechanisms,the dissolution-precipitation mechanism plays a leading role in the formation of short columnar β-Si_(3)N_(4) and granular TiN;and the cross-linked α-Si_(3)N_(4) whisker,short columnar β-Si_(3)N_(4) and granular TiN enhance the mechanical properties of the material.
基金the support of the National Natural Science Foundation of China(Nos.22205207 and 22378369).
文摘With the acceleration of industrialization,the pollution problem of sulfur dioxide(SO_(2))emitted from coal-fired power plants has become increasingly severe.Although wet flue gas desulfurization(FGD)technology can remove about 95%of SO_(2),its high energy consumption and the corrosion risk of downstream equipment caused by residual SO_(2)(500–3000 ppm)still need to be addressed[1].Previous porous materials(such as MOFs)achieve selective adsorption of SO_(2) through open metal sites,M–OH sites or functional organic groups,but the problem of CO_(2) co-adsorption limits their practical application[2].In recent years,hydrogen-bonded organic frameworks(HOFs)have emerged as a research hotspot due to their reversible hydrogen-bonding networks and flexible structures[3],but their stability under extreme conditions and efficient separation performance still need to be improved[4].
基金supported by the National Natural Science Foundation of China(Nos.22172011,22088102,and 22301248)the National Key R&D Program of China(2022YFA0911900)the Fundamental Research Funds for the Central Universities(DUT23LAB611).
文摘Acidic-stable oxygen evolution reaction(OER)catalysts based on earth-abundant materials are important but rare for the proton exchange membrane-based water electrolysis.In this study,a metal-containing hydrogen-bonded organic framework(HOF)of manganese coordinated with 2,2'-bipyridine-6,6'-dicarboxylate ligands,Mn(bda),interconnected through hydrogen bonding and π-π stacking is used as a heterogeneous OER catalyst(Mn(bda)-HOF)for acidic water oxidation and exhibits a considerable OER performance.Electrochemical results show that Mn(bda)-HOF displays a turn of frequency of 1 s^(-1) at an overpotential of 870 mV.Meanwhile,this Mn(bda)-HOF shows an unusual pH dependence on performance,where the reaction rate increases with the decrease of pH.A comprehensive mechanistic study reveals that the charge transfer triggered coupling of two metal-oxo species Mn^(5+)(O)is the rate-determining step,which leads to this unusual pH dependence on the OER performance.
基金National Natural Science Foundation of China(52075449,5197052086)。
文摘The transient liquid-phase(TLP)diffusion bonding of GH5188 with a BNi-5 interlayer was focused on.Parameters were chosen and optimized for GH5188 alloy according to the TLP joining mechanism.The microstructure evolution and mechanical properties of the joints were studied.Results show that the relatively complete isothermal solidification zone(ISZ)ensures a reliable connection of the base metal(BM).Within the temperature range of 1110–1190°C,higher bonding temperatures can widen ISZ and promote joint composition homogenization,thus improving mechanical properties.However,the increase in precipitated phase has an adverse effect on the mechanical properties of the joint.The maximum shear strength,reaching 482 MPa,is achieved at 1130°C,representing 84.6%of BM strength.Within the pressure range of 5–15 MPa,both precipitated phases in adiabatic solidification zone(ASZ)and voids generated by partial melting increase.On the contrary,their sizes decrease significantly under higher bonding pressure,resulting in an upward trend in alloy mechanical properties.The maximum shear strength of 490 MPa is attained at a bonding pressure of 15 MPa.The joint exhibits a typical mixed fracture pattern,with the small brittle M_(23)C_(6) phase and voids significantly impacting mechanical properties.Nano-indentation tests indicate that ASZ is a potential source of cracks.
文摘Introduction: Bracket debonding is a frequent issue that clinicians encounter, leading to increased chair time, lost revenue, and material usage. In addition to patient compliance with their diet recommendations, the preparation and conditioning of teeth for bonding significantly influence bond strength and consequently impact orthodontic treatment success and efficiency. Because of OBA-MCP’s (orthodontic bonding adhesive with modified calcium phosphate) decreased shear bond strength (SBS), the purpose of this study was to evaluate the effects of conditioning with 5.25% sodium hypochlorite (NaOCl) before etching in the bonding protocol. Materials and Methods: 90 extracted teeth were divided into 3 groups to be bonded with orthodontic brackets with different bonding protocols: 1) Transbond XT with regular bonding protocol (etch + prime + adhesive);2) OBA-MCP with regular bonding protocol;and 3) OBA-MCP with NaOCl prior to acid etching in the regular bonding protocol. SBS (in Newtons) were measured using an MTS universal testing machine with a custom jig to apply a vertical force onto the bracket and ARI (adhesive remnant index) scores were recorded for each sample after de-bond to rate the amount of adhesive remaining. Results: The addition of NaOCl to the bonding protocol statistically significantly increased the SBS of OBA-MCP to comparable levels to Transbond XT. The ARI scores showed that when NaOCl was added, more adhesive remained. Conclusion: The addition of NaOCl to the bonding protocol can increase the SBS of adhesives with historically weaker bond strengths. However, the increased amount of adhesive remaining and the increased time spent during bonding must be considered. Further testing can be done in vivo to demonstrate the practicality of this new procedure.
基金support by the National Key R&D Program of China(No.2022YFB3402200)the Program of Shanghai Academic Research Leader(No.22XD1421600).
文摘Diffusion-bonded Ti_(2)AlNb-based alloys commonly present a low strength compared with the deformed or aged ones. In this study, the post heat treatment including solution and aging treatments is proposed to optimize the microstructure, contributing to strength improvement and appropriate ductility sacrifice. An available method by the introduction of fine size (both 20-100 nm) and a high fraction (59.7% and 13.7%) of O and α_(2) phases using both solution at 1000℃ for 1 h and aging at 750℃ for 5 h can result in excellent tensile strength (992 MPa and 858 MPa) at room temperature and 650℃, respectively, which increases 5.3% and 44.5% than that of as-received sample. The aging treatment can contribute to lamellar O and α2 grains precipitated from the B_(2) parent, which results in limited dislocation slip systems and slip spaces to resist plastic deformation. Moreover, the crack propagation and fracture surfaces are also comparatively analyzed to reveal the fracture behaviors in the samples with high and low strength. This study can provide a new method for the mechanical property optimization of the welded Ti_(2)AlNb alloys.
基金supported by the Key Technologies R&D Program of Xiamen(No.3502Z20231057)Industry Leading Key Projects of Fujian Province(No.2022H0057)+2 种基金the National Natural Science Foundation of China(No.21975212)High-Level Talent Start-Up Foundation of Xiamen Institute of Technology for financial support(No.YKJ23017R)Graduate Science and Technology Innovation Program of Xiamen University of Technology(No.YKJCX2023194).
文摘LiMnxFe1-xPO_(4) is a promising cathode candidate due to its high security and the availability of a high 4.1 V operating voltage and high energy density.However,the poor electrochemical kinetics and structural instability currently hinder its broader application.Herein,inspired by the hydrogen-bonded cross-linking and steric hindrance effect between short-chain polymer molecules(polyethylene glycol-400,PEG-400),the pomegranate-type LiMn_(0.5)Fe_(0.5)PO_(4)-0.5@C(P-LMFP@C)cathode materials with 3D ion/electron dual-conductive network structure were constructed through ball mill-assisted spray-drying method.The intermolecular effects of PEG-400 promote the spheroidization and uniform PEG coating of LMFP precursor,which prevents agglomeration during sintering.The 3D ion/electron dual-conductive network structure in P-LMFP@C accelerates the Li^(+)transport kinetics,improving the rate performance and cycling stability.As a result,the designed P-LMFP@C has remarkable electrochemical behavior,boasting excellent capacity retention(98%after 100 cycles at the 1C rate)and rate capability(91 mAh·g^(-1)at 20C).Such strategy introduces a novel window for designing high-performance olivine cathodes and offers compatibility with a range of energy storage materials for diverse applications.
基金supported by the National Natural Science Foundation of China(U1809214)the Natural Science Foundation of Zhejiang Province(LY20E080014 and LTGN23E080001)the Science and Technology Project of Zhoushan(2022C41011).
文摘Devising exceptional S-scheme heterojunction photocatalysts utilized in annihilating pharmaceuticals and chromium contamination is significant for addressing the problem of global water pollution.In this work,a chemically bonded Mn0.5Cd_(0.5)S/BiOBr S-scheme heterostructure with oxygen vacancies is ingeniously developed through a facile in-situ solvothermal synthesis.The designed Mn0.5Cd_(0.5)S/BiOBr heterojunction exhibits eminently reinforced photo-activity for destruction of tetracycline hydrochloride and Cr(VI)as compared with its individual components.This substantial photo-redox performance amelioration is benefitted from the creation of an intense internal electric field(IEF)via supplying powerful driving force and migration highway by interfacial chemical bond to foster the S-scheme electron/hole disintegration.More intriguingly,the IEF at the hetero-interface drives the fast consumption of the photo-induced holes in Mn0.5Cd_(0.5)S by the photoelectrons from BiOBr,profoundly boosting the enrichment of active photo-carriers and sparing the photo-corrosion of Mn0.5Cd_(0.5)S.Furthermore,Mn0.5Cd_(0.5)S/BiOBr with exceptional anti-interference property can work efficiently in real water matrices.Multiple uses of the recycled Mn0⋅5Cd0⋅5S/BiOBr evidence its prominent robustness and stability.This achievement indicates the vast potential of chemically bonded S-scheme photosystems with structural defects in the design of photo-responsive materials for effective wastewater treatment.
基金the National Natural Science Foundation of China(No.51978400)。
文摘This paper presents the static and fatigue tests of hybrid(bonded/bolted)glass fiber reinforced polymer(GFRP)joints.Nine specimens of single-lap hybrid GFRP joints have been fabricated to study the static and fatigue behaviors in the experimental campaign.The static tests of uniaxial tension loading are first conducted,from which the static ultimate bearing capacities of the joints are obtained.High-cycle fatigue tests are subsequently carried out so that the fatigue failure mode,fatigue life,and stiffness degradation of joints can be obtained.The measuring techniques including acoustic emission monitoring and three-dimensional digital image correlation have been employed in the tests to record the damage development process.The results revealed that the static strength and fatigue behavior of such thick hybrid GFRP joints were controlled by the bolted connections.The four stages of fatigue failure process are obtained from tests and acoustic emission signals analysis:cumulative damage of adhesive layer,damage of the adhesive layer,cumulative damage of GFRP plate,and damage of GFRP plate.The fatigue life and stiffness degradation can be improved by more bolts.The S-N(fatigue stress versus life)curves for the fatigue design of the single-lap hybrid GFRP joints under uniaxial tension loading are also proposed.
基金supported by the National Natural Science Foundation of China(No.52125101)the Basic and Applied Basic Research Major Program of Guangdong Province,China(Grant No.2021B0301030003)the Jihua Laboratory(Project No.X210141TL210).
文摘Transient liquid phase(TLP)bonding is a promising process for the joining and repairing of nickel-base superalloys.One of the most important parameters in TLP bonding is the bonding time required for suf-ficient isothermal solidification which prevents the formation of undesirable precipitated phases.In the present work,the effect of bonding time on the microstructure,type,and evolution of precipitates in the non-isothermal solidified zone(NSZ)and their effect on micro-mechanical properties were systemat-ically investigated using multi-scale tests in TLP bonded Mar-M247 superalloy joints with Ni-15.2Cr-3.74B interlayer at 1230℃.For a bonding time of 5 min,dual-phase M_(23)(C,B)_(6)-γ/γ’(where M is a mix-ture of Hf,Ta,Cr,and Ni)with eutectic configuration was formed in NSZ.With the increase in bonding time,the evolution of NSZ microstructure can be summed up as eutectic M_(23)(C,B)_(6)-γ/γ’,semi-striping dual-phase M_(23)(C,B)_(6)-γ/γ’,discontinuously striping M_(23)(C,B)_(6)-γ/γ’,followed by the disintegration of NSZ.As the NSZ counterpart,the isothermal solidified zone(ISZ)is mainly composed ofγ/γ’.Ac-companied by the dissolution of M_(23)(C,B)_(6) in the centerline,the proportion of the ISZ increases greatly until the joints are completely occupied by ISZ.Finally,a bamboo-like structure with domain size of-100μm was formed in the joint centerline,along withγ’reorganized themselves all into cubic shapes and distributed homogeneously.Mechanical property tests demonstrated that in comparison to samples with longer bonding time,the NSZ of the shortest bonding time(5 min)has the highest strength and a subsequent decrease in strength was observed with prolonging the bonding time and post-bond heat treatment.Furthermore,possible solidification/transformation path,segregation behavior,and formation mechanism of NSZ/ISZ evolution were discussed.
基金supported by Scientific Research Funding Project of the Education Department of Liaoning Province(LJ212410146074)Liaoning Provincial Department of Science and Technology Doctoral Initiation Fund(2021-BS-241).
文摘Basing on vacuum diffusion bonding technique,Mg1 and Al1060 were welded under different welding temperatures.Inspection equipment such as scanning electron microscopy,energy dispersive spectroscopy,X-ray diffractometer,and tensile machine were applied to observe and investigate the microstructure,phase composition and mechanical property of Mg/Al diffusion welding joints.The results indic-ate that Mg1/Al1060 diffusion layers generate in the joints,and the thickness progressively increases with ascending welding temperature.From Al to Mg side,diffusion layers are comprised of Mg2Al3,Mg17Al12,and Mg17Al12+Mg based solid solutions sequentially.The shear resistance of the joints increases and then decreases with the increasing welding temperature.At 440℃,the maximal shear strength of 13 MPa can be obtained,and fracture results from Mg2Al3 phase near Al side.
基金financially supported by Outstanding Talent Research Fund of Zhengzhou University,China Postdoc toral Science Foundation(2020TQ0277,2020M682328)Central Plains Science and Technology Innovation Leader Project(214200510006)+1 种基金China Scholarship Council(No.202108410356)Postdoctoral Science Foundation of Henan province(202002010).
文摘Surface charge localization and inferior charge transfer efficiency seriously restrict the supply of reactive hydrogen and the reaction dynamics of CO_(2) photoreduction performance of photocatalysts.Herein,chemically bonded BiVO_(4)/Bi_(19)Cl_(3)S_(27)(BVO/BCS)S-scheme heterojunction with a strong internal electric field is designed.Experimental and density function theory calculation results confirm that the elaborated heterojunction accelerates the vectorial migration of photogenerated charges from BiVO_(4) to Bi_(19)Cl_(3)S_(27) via the interfacial chemical bonding interactions(i.e.,Bi-O and Bi-S bonds)between Bi atoms of BVO and S atoms of BCS or Bi atoms of BCS and O atoms of BVO under light irradiation,breaking the interfacial barrier and surface charge localization of Bi_(19)Cl_(3)S_(27),and further decreasing the energy of reactive hydrogen generation,CO_(2) absorption and activation.The separation efficiency of photogenerated carriers is much more efficient than that counterpart individual in BVO/BCS S-scheme heterojunction system.As a result,BVO/BCS heterojunction exhibits a significantly improved continuous photocatalytic performance for CO_(2) reduction and the 24 h CO yield reaches 678.27μmol⋅g^(-1).This work provides an atomic-level insight into charge transfer kinetics and CO_(2) reduction mechanism in S-scheme heterojunction.
基金supported by the National Research Foundation, Prime Minister’s Office, Singapore, under its Competitive Research Programme (CRP award number NRF-CRP22-2019-008)Medium-Sized Centre Programme (CA2DM)+1 种基金the Ministry of Education of Singapore, under its Research Centre of Excellence award to the Institute for Functional Intelligent Materials (I-FIM, Project No. EDUNC-33-18-279-V12)by the EDB Singapore, under its Space Technology Development Programme (S2219013-STDP)。
文摘Despite advancements in silicon-based anodes for high-capacity lithium-ion batteries,their widespread commercial adoption is still hindered by significant volume expansion during cycling,especially at high active mass loadings crucial for practical use.The root of these challenges lies in the mechanical instability of the material,which subsequently leads to the structural failure of the electrode.Here,we present a novel synthesis of a composite combining expanded graphite and silicon nanoparticles.This composite features a unique interlayer-bonded graphite structure,achieved through the application of a modified spark plasma sintering method.Notably,this innovative structure not only facilitates efficient ion and electron transport but also provides exceptional mechanical strength(Vickers hardness:up to658 MPa,Young's modulus:11.6 GPa).This strength effectively accommodates silicon expansion,resulting in an impressive areal capacity of 2.9 mA h cm^(-2)(736 mA h g^(-1)) and a steady cycle life(93% after 100cycles).Such outsta nding performance is paired with features appropriate for large-scale industrial production of silicon batteries,such as active mass loading of at least 3.9 mg cm^(-2),a high-tap density electrode material of 1.68 g cm^(-3)(secondary clusters:1.12 g cm^(-3)),and a production yield of up to 1 kg per day.
基金supported by the Doctor Fund and the Program of independent Research for Young Teachers of Yanshan University (Grant Nos.B919 and 020000534)。
文摘We study the friction properties of interlayer bonded bilayer graphene by simulating the movement of a slider on the surface of bilayer graphene using molecular dynamics.The results show that the presence of the interlayer covalent bonds due to the local sp^(3) hybridization of carbon atoms in the bilayer graphene seriously reduces the frictional coefficient of the bilayer graphene surface to 30%,depending on the coverage of interlayer sp^(3) bonds and normal loads.For a certain coverage of interlayer sp3bonds,when the normal load of the slider reaches a certain value,the surface of this interlayer bonded bilayer graphene will lose the friction reduction effect on the slider.Our findings provide guidance for the regulation and manipulation of the frictional properties of bilayer graphene surfaces through interlayer covalent bonds,which may be useful for applications of friction related graphene based nanodevices.
基金financially supported by the National Natural Science Foundation of China(No.52100076)the Fundamental Research Funds for the Central Universities(No.2023MS064)。
文摘Covalently bonded bridging between different semiconductors is a remarkable approach to improve the transfer of charge carriers at interfaces.In this study,we designed a ternary heterojunction(MBG)combining of molybdenum diselenide(Mo Se_(2)),black phosphorus nanosheets(Bpn)and graphitic carbon nitride(GCN).Among this MBG of Mo Se_(2)/Bpn/GCN,(i)the covalently bonded bridging effect between Bpn/GCN facilitates directional charge carrier transfer,meanwhile(ii)a Z-scheme heterojunction is formed between Mo Se_(2)/GCN to enhance the separation of photogenerated carriers.Furthermore,(iii)this composite exhibits an increased absorption for visible light.Using this MBG,photocatalytic degradation of over 98%of moxifloxacin is achieved within 20 min,with O_(2)·-confirmed as the primary photocatalytic active species.These findings provide novel insights into the construction of efficient heterojunction by covalently bonded bridging.
文摘Cement-free castables have attracted significant attention due to their superior thermal-mechanical properties and rapid dry-out in comparison to cement-bonded refractory castables.However,drying industrial-scale specimens can pose more challenges than lab-scale samples.In this study,the dry-out behavior and explosion resistance of microsilica-gel bonded nocement castables(NCCs)were investigated on both lab-and industrial-scale specimens,employing various drying agents.First,the fast dry-out mechanism was assessed using thermogravimetric analysis(TGA),differential scanning calorimetry(DSC),and scanning electron microscopy(SEM)on lab-scale small samples.Then,the drying behavior of industrial-scale large samples(300 mm×300 mm×300 mm cubes,approximately 80 kg)was studied using a unique macro-thermo-balance(macro-TGA).The results showed that EMSIL-DRY^(®)reduced the temperature level for maximum dewatering rate and effectively prevented explosions during heat-up,compared to other polymer fibres.The use of a specialty drying agent(EMSIL-DRY^(®))significantly improved the explosion resistance,as demonstrated by the production of a perfect 400 kg block fired to 850℃at a rate of 50℃·h^(-1).This research contributes to the understanding and application of cement-free castables in industrial settings.
