Research on the mechanical–electrical properties is crucial for designing and preparing high-temperature superconducting(HTS)cables.Various winding core structures can influence the mechanical–electrical behavior of...Research on the mechanical–electrical properties is crucial for designing and preparing high-temperature superconducting(HTS)cables.Various winding core structures can influence the mechanical–electrical behavior of cables,but the impact of alterations in the winding core structure on the mechanical–electrical behavior of superconducting cables remains unclear.This paper presents a 3D finite element model to predict the performance of three cables with different core structures when subjected to transverse compression and axial tension.The three cables analyzed are CORC(conductor-on-round-core),CORT(conductor-on-round-tube),and HFRC(conductor-on-spiral-tube).A parametric analysis is carried out by varying the core diameter and inner-to-outer diameter ratio.Results indicate that the CORT cable demonstrates better performance in transverse compression compared to the CORC cable,aligning with experimental data.Among the three cables,the HFRC cables exhibit the weakest resistance to transverse deformation.However,the HFRC cable demonstrates superior tensile deformation resistance compared to the CORT cable,provided that the transverse compression properties are maintained.Finite element results also show that the optimum inner-to-outer diameter ratios for achieving the best transverse compression performance are approximately 0.8 for CORT cables and 0.6 for HFRC cables.Meanwhile,the study explores the effect of structural changes in HTS cable winding cores on their electromagnetic properties.It recommends utilizing small tape gaps,lower frequencies,and spiral core construction to minimize eddy losses.The findings presented in this paper offer valuable insights for the commercialization and practical manufacturing of HTS cables.展开更多
Dislocations are thought to be the principal mechanism of high ductility of the novel B2 structure intermetallic compounds YAg and YCu.In this paper, the edge dislocation core structures of two primary slip systems 〈...Dislocations are thought to be the principal mechanism of high ductility of the novel B2 structure intermetallic compounds YAg and YCu.In this paper, the edge dislocation core structures of two primary slip systems 〈100〉{010} and 〈100〉{01^-1} for YAg and YCu are presented theoretically within the lattice theory of dislocation.The governing dislocation equation is a nonlinear integro-differential equation and the variational method is applied to solve the equation.Peierls stresses for 〈100〉{010} and 〈100〉{01^-1} slip systems are calculated taking into consideration the contribution of the elastic strain energy.The core width and Peierls stress of a typical transition-metal aluminide NiAl is also reported for the purpose of verification and comparison.The Peierls stress of NiAl obtained here is in agreement with numerical results,which verifies the correctness of the results obtained for YAg and YCu.Peierls stresses of the 〈100〉{01^-1} slip system are smaller than those of 〈100〉{010} for the same intermetallic compounds originating from the smaller unstable stacking fault energy.The obvious high unstable stacking fault energy of NiAl results in a larger Peierls stress than those of YAg and YCu although they have the same B2 structure.The results show that the core structure and Peierls stress depend monotonically on the unstable stacking fault energy.展开更多
The extended core structure of the dissociated edge dislocation in Al, Au, Ag, Cu and Ni is determined within lattice theory of dislocation. The 2D dislocation equation governing the displacements is coupled by the re...The extended core structure of the dissociated edge dislocation in Al, Au, Ag, Cu and Ni is determined within lattice theory of dislocation. The 2D dislocation equation governing the displacements is coupled by the restoring forces that are determined by the parameterization of the generalized stacking fault energies. The Ritz variational method is presented to solve the dislocation equation and the trial solution is constituted by two arctan-type functions with two undetermined parameters. The core widths of partial dislocations are wider than that obtained in generalized Peierls-Nabarro model due to the consideration of discreteness of crystal.展开更多
The study of dislocation properties in B2 structure intermetallics NiAl and FeAl is crucial to understand their mechanical behaviors. In this paper, the core structure and Peierls stress of collinear dissociated （111...The study of dislocation properties in B2 structure intermetallics NiAl and FeAl is crucial to understand their mechanical behaviors. In this paper, the core structure and Peierls stress of collinear dissociated （111）{110} edge superdislocations in NiAl and FeAl are investigated with the modified P-N dislocation equation. The generalized stacking fault energy curve along （111） direction in {110} slip plane contains two modification factors that can assure the antiphase energy and the unstable stacking fault energy to change independently. The results show that the core width of superpartials decreases with the increasing unstable stacking fault energy, and increases with the increasing antiphase boundary energy. The calculated Peierls stress of （111）{ 110） edge superdislocations in NiAl and FeAl are 475 MPa and 3042 MPa, respectively. The values of Peierls stress in NiAl is in accordance in magnitude with the experimental and the molecular statics simulations results.展开更多
We give a brief review of the asymptotic theory of slender vortex filaments with emphases on (i) the choices of scalings and small parameters characterizing the physical problem,(ii) the key steps in the formulation o...We give a brief review of the asymptotic theory of slender vortex filaments with emphases on (i) the choices of scalings and small parameters characterizing the physical problem,(ii) the key steps in the formulation of the theory and (iii) the assumptions and/or restrictions on the theory of Callegari and Ting (1978).We present highlights of an extension of the 1978 asymptotic theory:the analyses for core structures with axial variation.Making use of the physical insights gained from the analyses,we present a new derivation of the evolution equations for the core structure.The new one is simpler and straightforward and shows the physics clearly.展开更多
Lead chalcohalides(PbYX,X=Cl,Br,I;Y=S,Se)is an extension of the classic Pb chalcogenides(PbY).Constructing the heterogeneous integration with PbYX and PbY material systems makes it possible to achieve significantly im...Lead chalcohalides(PbYX,X=Cl,Br,I;Y=S,Se)is an extension of the classic Pb chalcogenides(PbY).Constructing the heterogeneous integration with PbYX and PbY material systems makes it possible to achieve significantly improved optoelectronic performance.In this work,we studied the effect of introducing halogen precursors on the structure of classical PbS nanocrystals(NCs)during the synthesis process and realized the preparation of PbS/Pb_(3)S_(2)X_(2) core/shell structure for the first time.The core/shell structure can effectively improve their optical properties.Furthermore,our approach enables the synthesis of Pb_(3)S_(2)Br_(2) that had not yet been reported.Our results not only provide valuable insights into the heterogeneous integration of PbYX and PbY materials to elevate material properties but also provide an effective method for further expanding the preparation of PbYX material systems.展开更多
The novel core−shell SiC@CoCrFeNiMn high-entropy alloy(HEA)matrix composites(SiC@HEA)were successfully prepared via mechanical ball milling and vacuum hot-pressing sintering(VHPS).After sintering,the microstructure wa...The novel core−shell SiC@CoCrFeNiMn high-entropy alloy(HEA)matrix composites(SiC@HEA)were successfully prepared via mechanical ball milling and vacuum hot-pressing sintering(VHPS).After sintering,the microstructure was composed of FCC solid solution,Cr_(23)C_(6) carbide phases,and Mn_(2)SiO_(4) oxy-silicon phase.The relative density,hardness,tensile strength,and elongation of SiC@HEA composites with 1.0 wt.%SiC were 98.5%,HV 358.0,712.3 MPa,and 36.2%,respectively.The core−shell structure had a significant deflecting effect on the cracks.This effect allowed the composites to effectively maintain the excellent plasticity of the matrix.As a result,the core−shell SiC@HEA composites obtained superior strength and plasticity with multiple mechanisms.展开更多
Magnetically separable bismuth ferrite(BiFeO3)nanoparticles were fabricated by a citrate self‐combustion method and coated with titanium dioxide(TiO2)by hydrolysis of titanium butoxide(Ti(OBu)4)to form BiFeO3@TiO2cor...Magnetically separable bismuth ferrite(BiFeO3)nanoparticles were fabricated by a citrate self‐combustion method and coated with titanium dioxide(TiO2)by hydrolysis of titanium butoxide(Ti(OBu)4)to form BiFeO3@TiO2core-shell nanocomposites with different mass ratios of TiO2to BiFeO3.The photocatalytic performance of the catalysts was comprehensively investigated via photocatalytic oxidation of methyl violet(MV)under both ultraviolet and visible‐light irradiation.The BiFeO3@TiO2samples exhibited better photocatalytic performance than either BiFeO3or TiO2alone,and a BiFeO3@TiO2sample with a mass ratio of1:1and TiO2shell thickness of50-100nm showed the highest photo‐oxidation activity of the catalysts.The enhanced photocatalytic activity was ascribed to the formation of a p‐n junction of BiFeO3and TiO2with high charge separation efficiency as well as strong light absorption ability.Photoelectrochemical Mott-Schottky(MS)measurements revealed that both the charge carrier transportation and donor density of BiFeO3were markedly enhanced after introduction of TiO2.The mechanism of MV degradation is mainly attributed to hydroxyl radicals and photogenerated electrons based on energy band theory and the formation of an internal electrostatic field.In addition,the unique core-shell structure of BiFeO3@TiO2also promotes charge transfer at the BiFeO3/TiO2interface by increasing the contact area between BiFeO3and TiO2.Finally,the photocatalytic activity of BiFeO3@TiO2was further confirmed by degradation of other industrial dyes under visible‐light irradiation.展开更多
Material composition and structural design are important factors influencing the electromagnetic wave(EMW)absorption performance of materials.To alleviate the impedance mismatch attributed to the high dielectric const...Material composition and structural design are important factors influencing the electromagnetic wave(EMW)absorption performance of materials.To alleviate the impedance mismatch attributed to the high dielectric constant of Ti_(3)C_(2)T_(x)MXene,we have successfully synthesized core‐shell structured SiO_(2)@MXene@MoS_(2)nanospheres.This architecture,comprising SiO_(2) as the core,MXene as the intermediate layer,and MoS_(2) as the outer shell,is achieved through an electrostatic self‐assembly method combined with a hydrothermal process.This complex core‐shell structure not only provides a variety of loss mechanisms that effectively dissipate electromagnetic energy but also prevents self‐aggregation of MXene and MoS_(2) nanosheets.Notably,the synergistic combination of SiO_(2) and MoS_(2) with highly conductive MXene enables the suitable dielectric constant of the composites,ensuring optimal impedance matching.Therefore,the core‐shell structured SiO_(2)@MXene@MoS_(2) nanospheres exhibit excellent EMW absorption performance,featuring a remarkable minimum reflection loss(RL_(min))of−52.11 dB(2.4 mm).It is noteworthy that these nanospheres achieve an ultra‐wide effective absorption bandwidth(EAB)of 6.72 GHz.This work provides a novel approach for designing and synthesizing high‐performance EMW absorbers characterized by“wide bandwidth and strong reflection loss.”展开更多
In this paper, Fe30Pt70/Fe3O4 core/shell nanoparticles were synthesized by chemical routine and the layered polyethylenimine （PEI）-Fe30Pt70/Fe3O4 structure was constructed by molecule-mediated self-assembly techniqu...In this paper, Fe30Pt70/Fe3O4 core/shell nanoparticles were synthesized by chemical routine and the layered polyethylenimine （PEI）-Fe30Pt70/Fe3O4 structure was constructed by molecule-mediated self-assembly technique. The dimension of core/shell structured nanoparticles was that of 4nm core and 2 nm shell. After annealing under a flow of forming gas （50%Ar2＋30%H2） for 1 h at or above 400℃, the iron oxide shell was reduced to Fe and diffused to Pt-rieh core, which leaded to the formation of L1. phase FePt at low temperature. The x-ray diffraction results and magnetic properties measurement showed that the chemical ordering temperature of Fe30Pt70/Fe3O4 core/shell nanoparticles assembly can be reduced to as low as 400℃. The sample annealed at 400℃ showed the eoereivity of 4KOe with the applied field of 1.5T. The core/shell structure was suggested to be an effective way to reduce the ordering temperature obviously.展开更多
LaF^3＋ Yb^3＋ , Er^3＋ nanoparticles were successfully synthesized using solvothermal treatment, and LaF^3＋ Yb^3＋ , Er^3＋/SiO2 core/shell nanoparticles were also prepared with reverse microemulsion technique. The ...LaF^3＋ Yb^3＋ , Er^3＋ nanoparticles were successfully synthesized using solvothermal treatment, and LaF^3＋ Yb^3＋ , Er^3＋/SiO2 core/shell nanoparticles were also prepared with reverse microemulsion technique. The crystal structure, morphology and photoluminescence properties of as-prepared core/shell nanoparticles were in- vestigated by X-ray diffraction, transmission electron microscopy and fluorescence spectrophotometer. The re- sults showed thatLaF^3＋ Yb^3＋ , Er^3＋ nanoparticles are of hexagonal structure and SiO2 shell is amorphous. The size ofLaF^3＋ Yb^3＋ , Er^3＋. nanoparticles is 13 nm and the LaF^3＋ Yb^3＋ , Er^3＋/SiO2 nanoparticles present clearly a core/shell structure with 12 nm shell thickness. The solubility of LaF^3＋ Yb^3＋ , Er^3＋ nanocrystals in water and the biocompatibility are both improved by the SiO2 shell. The upconversion luminescence spectra suggested that the SiO~ shell has small effect on the upconversion luminescence properties of the LaF^3＋ Yb^3＋ , Er^3＋ nanocrys- tals. The core/shell structure LaF^3＋ Yb^3＋ , Er^3＋ /SiO2. nanopartlcles are expected to be used in biological appli- cations.展开更多
In order to restrain the huge volume expansion of bismuth(Bi)anodes in sodium ion batteries(SIBs),the core-shell structure Bi@mesoporous carbon nanospheres(Bi@mC)composite was designed and prepared by sol-gel method c...In order to restrain the huge volume expansion of bismuth(Bi)anodes in sodium ion batteries(SIBs),the core-shell structure Bi@mesoporous carbon nanospheres(Bi@mC)composite was designed and prepared by sol-gel method coupled heat treatment.Structural characterization displays that the average diameter of the as-prepared Bi@mC composites is about 200 nm and thickness of the N-doped mesoporous carbon shells is 20-30 nm.Electrochemical test and kinetic analysis results show that the mesoporous carbon shell can not only effectively relieve the stress caused by volume expansion of Bi and protect active material from pulverization caused by the stress during charging/discharging process,but also facilitate quick diffusion of sodium ions,thus improving rate and cycling performance.Bi@mC delivers a high specific capacity of 279 mA·h/g and a capacity retention of 97.6%after 3500 cycles at a current density of 5 A/g.Even at a high current density of 20 A/g,Bi@mC can still maintain a high specific capacity of 266 mA·h/g.Additionally,the Bi@mC//NVP full button sodium-ion batteries(SIBs)assembled using Bi@mC anode and Na_(3)V_(2)(PO_(4))_(3)(NVP)cathode deliver an energy density of 182 W·h/kg.展开更多
Vanadium nitride(VN),a promising cathode material for aqueous zinc ion batteries(AZIBs),undergoes irreversible phase transitions accompanied by structural variation and sustained vanadium dissolution,which impair cycl...Vanadium nitride(VN),a promising cathode material for aqueous zinc ion batteries(AZIBs),undergoes irreversible phase transitions accompanied by structural variation and sustained vanadium dissolution,which impair cycling stability and reaction kinetics.To address these challenges,we designed a core–shell heterostructure(VONC-T,T represents temperature)composed of a VN core and a porous carbon shell.This structure was synthesized via in-situ construction,involving optimized ratio of coating a zinc-based zeolitic imidazolate framework(ZIF-8)onto a vanadium-based metal-organic framework(MIL-47(V)),followed by a thermal treatment.This process ensures a high degree of interfacial stability between the core and shell,effectively mitigating the structural variation of VN during irreversible phase transitions and enhancing the overall structural stability.During thermal driving,the volatilization of zinc within the shell layer created a porous channel effect,which facilitating Zn^(2+)diffusion.The enhancement of Zn²⁺diffusion strengthens the efficient conversion of VN to amorphous VOx,labeled as VONC-T-a,which provides more active sites and consequently results in a high specific capacity.The optimized heterostructure of VONC-900-a presented high reversible capacity of 387.2 mAh g^(−1)at 0.2 A g^(−1)and demonstrated excellent rate performance,achieving 274.5 mAh g^(−1)at 20 A g^(−1),while maintaining a capacity retention rate of 93.3%after 5000 cycles at 10 A g^(−1).Density functional theory calculations confirmed improved reaction kinetics in the core–shell structure.This study not only highlights the potential of amorphous vanadium oxide core–shell heterostructure for AZIBs but also provides new insights into the conversion mechanisms of VN.展开更多
This paper presents a high-resolution simulation of a remarkable polar low observed over the Sea of Japan on 21 January 1997 by using a 5-km mesh non-hydrostatic model MRI-NHM (Meteorological Research Institute Non-Hy...This paper presents a high-resolution simulation of a remarkable polar low observed over the Sea of Japan on 21 January 1997 by using a 5-km mesh non-hydrostatic model MRI-NHM (Meteorological Research Institute Non-Hydrostatic Model). A 24-hour simulation starting from 0000 UTC 21 January 1997 successfully reproduced the observed features of the polar low such as the wrapping of western part of an initial E-W orientation vortex, the spiral-shaped bands, the cloud-free 'eye', and the warm core structure at its mature stage. The 'eye' of the simulated polar low was relatively dry, and was associated with a strong downdraft. A thermodynamic budget analysis indicates that the 'warm core' in the 'eye' region was mainly caused by the adiabatic warming associated with the downdraft. The relationship among the condensational diabatic heating, the vertical velocity, the convergence of the moisture flux, and the circulation averaged within a 50 km×50 km square area around the polar low center shows that they form a positive feedback loop, and this loop is not inconsistent with the CISK (Conditional Instability of the Second Kind) mechanism during the developing stage of the polar low.展开更多
This paper presents an analysis of the coupled vibration of asymmetric core structures in tall buildings. The governing equation of free vibration and its corresponding eigenvalue problem, which is a set of equations ...This paper presents an analysis of the coupled vibration of asymmetric core structures in tall buildings. The governing equation of free vibration and its corresponding eigenvalue problem, which is a set of equations for laterally flexural vibrations in two different directions coupled by a warping-St. Venant torsional vibration, are derived. Based on the Calerkin method, a generalized approximate method is developed for the analysis of coupled vibration and thus proposed for determining the natural frequencies and mode shapes of the structure in triply-coupled vibration. The results of the proposed method for the example structure show good agreement with those of the FEM analysis. The proposed method has been shown to provide a simple and rapid, yet accurate, means for coupled vibration analysis of core structures.展开更多
The purpose of this study is to explore the adsorption performance of meso-2,3-dimercaptosuccinic acid(DMSA)modified Fe3O4@SiO2 magnetic nanocomposite(Fe3O4@SiO2@DMSA)for Pb2+ions removal from aqueous solutions.The ef...The purpose of this study is to explore the adsorption performance of meso-2,3-dimercaptosuccinic acid(DMSA)modified Fe3O4@SiO2 magnetic nanocomposite(Fe3O4@SiO2@DMSA)for Pb2+ions removal from aqueous solutions.The effects of solution pH,initial concentration of Pb2+ions,contact time,and temperature on the amount of Pb2+adsorbed were investigated.Adsorption isotherms,adsorption kinetics,and thermodynamic analysis were also studied.The results showed that the maximum adsorption capacity of the Fe3O4@SiO2@DMSA composite is 50.5 mg/g at 298 K,which is higher than that of Fe3O4 and Fe3O4@SiO2 magnetic nanoparticles.The adsorption process agreed well with Langmuir adsorption isotherm models and pseudo second-order kinetics.The thermodynamic analysis revealed that the adsorption was spontaneous,endothermic and energetically driven in nature.展开更多
Rational construction of highly efficient and cheap bifunctional electrocatalysts to boost both oxygen evolution reaction(OER)and oxygen reduction reaction(ORR)is extremely essential for the wide application of rechar...Rational construction of highly efficient and cheap bifunctional electrocatalysts to boost both oxygen evolution reaction(OER)and oxygen reduction reaction(ORR)is extremely essential for the wide application of rechargeable metal-air battery.In this work,we design a core-shell structural catalyst of CoNi dual-metal embedded in nitrogen doped porous carbon(NPC,CoNi@NPC),which is developed via the pyrolysis of CoNiMOFs,assisting by mesoporous SiO_(2) to effectively inhibit the aggregation of metal sites.Consequently,the asprepared CoNi@NPC manifests good ORR activity with half-wave potential up to 0.77 V.Specifically,the CoNi@NPC gives a very low OER over-potential of merely 101 mV in 6 M KOH along with high stability,outperforming the commercial Pt/C-RuO_(2).Moreover,the home-made zinc air battery with CoNi@NPC air cathode demonstrates excellent stability over long-term charging–discharging test,and delivers the maximum power density of 224 mW cm^(-2).The enhanced high performance of CoNi@NPC bifunctional catalyst for both ORR and OER can be ascribed to its unique core-shell structure and strong synergistic effect between the dual-bimetal active sites and the heteroatom doped carbon.This work opens a new avenue for the rational design of nonprecious metal bifunctional catalysts for rechargeable metal-air battery.展开更多
The hydrogenation of CO_(2) into methanol has attracted much attention and In_(2)O_(3) is a promising catalyst.Introducing metal elements into In_(2)O_(3)(M/In_(2)O_(3))is one of the main strategies to improve its per...The hydrogenation of CO_(2) into methanol has attracted much attention and In_(2)O_(3) is a promising catalyst.Introducing metal elements into In_(2)O_(3)(M/In_(2)O_(3))is one of the main strategies to improve its performance.However,its mechanism and active sites remain unclear and need to be further elucidated.Here,the noble‐metal‐free In_(x)‐Co_(y) oxides catalysts were prepared.Much‐improved performance and obvious product selectivity shift were observed.The optimized catalyst(In_(1)‐Co_(4))(9.7 mmol g_(cat)^(–1) h^(–1))showed five times methanol yields than pure In_(2)O_(3)(2.2 mmol g_(cat)^(–1) h^(–1))(P=4.0 MPa,T=300°C,GHSV=24000 cm^(3)_(STP) g_(cat)^(–1) h^(–1),H_(2):CO_(2)=3).And the cobalt‐catalyzed CO_(2) methanation activity was suppressed,although cobalt was most of the metal element.To unravel this selectivity shift,detailed catalysts performance evaluation,together with several in‐situ and ex‐situ characterizations,were employed on cobalt and In‐Co for comparative study.The results indicated CO_(2) hydrogenation on cobalt and In‐Co catalyst both followed the formate pathway,and In‐Co reconstructed and generated a surface In_(2)O_(3)‐enriched core‐shell‐like structure under a reductive atmosphere.The enriched In_(2)O_(3) at the surface significantly enhanced CO_(2) adsorption capacity and well stabilized the intermediates of CO_(2) hydrogenation.CO_(2) and carbon‐containing intermediates adsorbed much stronger on In‐Co than cobalt led to a feasible surface C/H ratio,thus allowing the*CH_(3)O to desorb to produce CH_(3)OH instead of being over‐hydrogenated to CH_(4).展开更多
The reaction of molybdenum hexacarbonyl with C6H5CH2OC6H4ONa and Et4NBr in CH3CN at 60 ℃ afforded the di-nuclear Mo（0） compound [Et4N]3[Mo2（CO）6（μ-OC6H4OCH2C6H5）3] 1. 1 crystallizes in monoclinic, space group ...The reaction of molybdenum hexacarbonyl with C6H5CH2OC6H4ONa and Et4NBr in CH3CN at 60 ℃ afforded the di-nuclear Mo（0） compound [Et4N]3[Mo2（CO）6（μ-OC6H4OCH2C6H5）3] 1. 1 crystallizes in monoclinic, space group P21/c with a = 15.359（2）, b = 18.378（3）, c = 24.952（2） A, β = 102.268（4）°, V = 6882.3（1 6） A^3, Mr = 1348.34, Z = 4, Dc = 1.301 g/cm^3, F（000） = 2832 and μ= 0.424 mm^-1 The final R = 0.0606 and wR = 0.1552 for 9396 observed reflections （I 〉 2σ（I））. I contains a [Mo2O3]^3 core in triangular bi-pyralnidal configuration and each Mo atom adopts a distorted octahedral geometry with three carbon atoms from carbonyls and three ,μ-O atoms from C6H5CH2OC6H4O^- bridging ligands. The Mo…Mo distance is 3.30（8） A, indicating no metalmetal bonding. A formation pathway via forming a di-molybdenum（0） di-bridging OR compound [Mo2（μ-OR）2（CO）8]2 has been figured out and the reaction of Mo（CO）6 with alkoxide has also been discussed.展开更多
Many networks exhibit the core/periphery structure.Core/periphery structure is a type of meso-scale structure that consists of densely connected core nodes and sparsely connected peripheral nodes.Core nodes tend to be...Many networks exhibit the core/periphery structure.Core/periphery structure is a type of meso-scale structure that consists of densely connected core nodes and sparsely connected peripheral nodes.Core nodes tend to be well-connected,both among themselves and to peripheral nodes,which tend not to be well-connected to other nodes.In this brief report,we propose a new method to detect the core of a network by the centrality of each node.It is discovered that such nodes with non-negative centralities often consist in the core of the networks.The simulation is carried out on different real networks.The results are checked by the objective function.The checked results may show the effectiveness of the simulation results by the centralities of the nodes on the real networks.Furthermore,we discuss the characters of networks with the single core/periphery structure and point out the scope of the application of our method at the end of this paper.展开更多
基金supported by the National Natural Science Foundation of China(12072136).
文摘Research on the mechanical–electrical properties is crucial for designing and preparing high-temperature superconducting(HTS)cables.Various winding core structures can influence the mechanical–electrical behavior of cables,but the impact of alterations in the winding core structure on the mechanical–electrical behavior of superconducting cables remains unclear.This paper presents a 3D finite element model to predict the performance of three cables with different core structures when subjected to transverse compression and axial tension.The three cables analyzed are CORC(conductor-on-round-core),CORT(conductor-on-round-tube),and HFRC(conductor-on-spiral-tube).A parametric analysis is carried out by varying the core diameter and inner-to-outer diameter ratio.Results indicate that the CORT cable demonstrates better performance in transverse compression compared to the CORC cable,aligning with experimental data.Among the three cables,the HFRC cables exhibit the weakest resistance to transverse deformation.However,the HFRC cable demonstrates superior tensile deformation resistance compared to the CORT cable,provided that the transverse compression properties are maintained.Finite element results also show that the optimum inner-to-outer diameter ratios for achieving the best transverse compression performance are approximately 0.8 for CORT cables and 0.6 for HFRC cables.Meanwhile,the study explores the effect of structural changes in HTS cable winding cores on their electromagnetic properties.It recommends utilizing small tape gaps,lower frequencies,and spiral core construction to minimize eddy losses.The findings presented in this paper offer valuable insights for the commercialization and practical manufacturing of HTS cables.
基金Project supported by the National Natural Science Foundation of China (Grant No 10774196)Science Foundation Project of CQ Chongqing Science & Technology Commission (CSTC) (Grant No 2006BB4156)Chongqing University Postgraduates’Science and Innovation Fund (Grant No 200707A1A0030240)
文摘Dislocations are thought to be the principal mechanism of high ductility of the novel B2 structure intermetallic compounds YAg and YCu.In this paper, the edge dislocation core structures of two primary slip systems 〈100〉{010} and 〈100〉{01^-1} for YAg and YCu are presented theoretically within the lattice theory of dislocation.The governing dislocation equation is a nonlinear integro-differential equation and the variational method is applied to solve the equation.Peierls stresses for 〈100〉{010} and 〈100〉{01^-1} slip systems are calculated taking into consideration the contribution of the elastic strain energy.The core width and Peierls stress of a typical transition-metal aluminide NiAl is also reported for the purpose of verification and comparison.The Peierls stress of NiAl obtained here is in agreement with numerical results,which verifies the correctness of the results obtained for YAg and YCu.Peierls stresses of the 〈100〉{01^-1} slip system are smaller than those of 〈100〉{010} for the same intermetallic compounds originating from the smaller unstable stacking fault energy.The obvious high unstable stacking fault energy of NiAl results in a larger Peierls stress than those of YAg and YCu although they have the same B2 structure.The results show that the core structure and Peierls stress depend monotonically on the unstable stacking fault energy.
基金supported by the National Natural Science Foundation of China (No.10774196)the Science Founda-tion Project of CQ CSTC (No.2006BB4156)Chongqing University Postgraduates’Science and Innovation Fund(No.200707A1A0030240)
文摘The extended core structure of the dissociated edge dislocation in Al, Au, Ag, Cu and Ni is determined within lattice theory of dislocation. The 2D dislocation equation governing the displacements is coupled by the restoring forces that are determined by the parameterization of the generalized stacking fault energies. The Ritz variational method is presented to solve the dislocation equation and the trial solution is constituted by two arctan-type functions with two undetermined parameters. The core widths of partial dislocations are wider than that obtained in generalized Peierls-Nabarro model due to the consideration of discreteness of crystal.
基金supported by the Fundamental Research Funds for the Central Universities(No.CDJZR10100019).
文摘The study of dislocation properties in B2 structure intermetallics NiAl and FeAl is crucial to understand their mechanical behaviors. In this paper, the core structure and Peierls stress of collinear dissociated （111）{110} edge superdislocations in NiAl and FeAl are investigated with the modified P-N dislocation equation. The generalized stacking fault energy curve along （111） direction in {110} slip plane contains two modification factors that can assure the antiphase energy and the unstable stacking fault energy to change independently. The results show that the core width of superpartials decreases with the increasing unstable stacking fault energy, and increases with the increasing antiphase boundary energy. The calculated Peierls stress of （111）{ 110） edge superdislocations in NiAl and FeAl are 475 MPa and 3042 MPa, respectively. The values of Peierls stress in NiAl is in accordance in magnitude with the experimental and the molecular statics simulations results.
文摘We give a brief review of the asymptotic theory of slender vortex filaments with emphases on (i) the choices of scalings and small parameters characterizing the physical problem,(ii) the key steps in the formulation of the theory and (iii) the assumptions and/or restrictions on the theory of Callegari and Ting (1978).We present highlights of an extension of the 1978 asymptotic theory:the analyses for core structures with axial variation.Making use of the physical insights gained from the analyses,we present a new derivation of the evolution equations for the core structure.The new one is simpler and straightforward and shows the physics clearly.
基金supported by the National Key Research and Development Program of China(Grant No.2022YFE0110300)the National Natural Science Foundation of China(Grant Nos.52372215,92163114,and 52202274)+5 种基金the Natural Science Foundation of Jiangsu Province of China(Grant No.BK20230504)the Special Fund for the"Dual Carbon"Science and Technology Innovation of Jiangsu province(Industrial Prospect and Key Technology Research program)(Grant Nos.BE2022023 and BE2022021)the Natural Science Foundation of the Jiangsu Higher Education Institutions of China(Grant No.21KJA430004)Gusu Innovation and Entre preneurship Leading Talent Program(Grant No.ZXL2022451)the China Postdoctoral Science Foundation(Grant No.2023M732523)supported by Suzhou Key Laboratory of Functional Nano&Soft Materials,Collaborative Innovation Center of Suzhou Nano Science&Technology,the 111 Project.
文摘Lead chalcohalides(PbYX,X=Cl,Br,I;Y=S,Se)is an extension of the classic Pb chalcogenides(PbY).Constructing the heterogeneous integration with PbYX and PbY material systems makes it possible to achieve significantly improved optoelectronic performance.In this work,we studied the effect of introducing halogen precursors on the structure of classical PbS nanocrystals(NCs)during the synthesis process and realized the preparation of PbS/Pb_(3)S_(2)X_(2) core/shell structure for the first time.The core/shell structure can effectively improve their optical properties.Furthermore,our approach enables the synthesis of Pb_(3)S_(2)Br_(2) that had not yet been reported.Our results not only provide valuable insights into the heterogeneous integration of PbYX and PbY materials to elevate material properties but also provide an effective method for further expanding the preparation of PbYX material systems.
基金supported by Key Laboratory of Infrared Imaging Materials and Detectors,Shanghai Institute of Technical Physics,Chinese Academy of Sciences(No.IIMDKFJJ-21-10)China Postdoctoral Science Foundation(No.2018T110993)。
文摘The novel core−shell SiC@CoCrFeNiMn high-entropy alloy(HEA)matrix composites(SiC@HEA)were successfully prepared via mechanical ball milling and vacuum hot-pressing sintering(VHPS).After sintering,the microstructure was composed of FCC solid solution,Cr_(23)C_(6) carbide phases,and Mn_(2)SiO_(4) oxy-silicon phase.The relative density,hardness,tensile strength,and elongation of SiC@HEA composites with 1.0 wt.%SiC were 98.5%,HV 358.0,712.3 MPa,and 36.2%,respectively.The core−shell structure had a significant deflecting effect on the cracks.This effect allowed the composites to effectively maintain the excellent plasticity of the matrix.As a result,the core−shell SiC@HEA composites obtained superior strength and plasticity with multiple mechanisms.
基金supported by the Australian Research Council(ARC DP150103026)the National Natural Science Foundation of China(51278242)~~
文摘Magnetically separable bismuth ferrite(BiFeO3)nanoparticles were fabricated by a citrate self‐combustion method and coated with titanium dioxide(TiO2)by hydrolysis of titanium butoxide(Ti(OBu)4)to form BiFeO3@TiO2core-shell nanocomposites with different mass ratios of TiO2to BiFeO3.The photocatalytic performance of the catalysts was comprehensively investigated via photocatalytic oxidation of methyl violet(MV)under both ultraviolet and visible‐light irradiation.The BiFeO3@TiO2samples exhibited better photocatalytic performance than either BiFeO3or TiO2alone,and a BiFeO3@TiO2sample with a mass ratio of1:1and TiO2shell thickness of50-100nm showed the highest photo‐oxidation activity of the catalysts.The enhanced photocatalytic activity was ascribed to the formation of a p‐n junction of BiFeO3and TiO2with high charge separation efficiency as well as strong light absorption ability.Photoelectrochemical Mott-Schottky(MS)measurements revealed that both the charge carrier transportation and donor density of BiFeO3were markedly enhanced after introduction of TiO2.The mechanism of MV degradation is mainly attributed to hydroxyl radicals and photogenerated electrons based on energy band theory and the formation of an internal electrostatic field.In addition,the unique core-shell structure of BiFeO3@TiO2also promotes charge transfer at the BiFeO3/TiO2interface by increasing the contact area between BiFeO3and TiO2.Finally,the photocatalytic activity of BiFeO3@TiO2was further confirmed by degradation of other industrial dyes under visible‐light irradiation.
基金Joint Fund of Research and Development Program of Henan Province,Grant/Award Number:222301420002National Natural Science Foundation of China,Grant/Award Number:U21A2064Scientific and Technological Innovation Talents in Colleges and Universities in Henan Province,Grant/Award Number:22HASTIT001。
文摘Material composition and structural design are important factors influencing the electromagnetic wave(EMW)absorption performance of materials.To alleviate the impedance mismatch attributed to the high dielectric constant of Ti_(3)C_(2)T_(x)MXene,we have successfully synthesized core‐shell structured SiO_(2)@MXene@MoS_(2)nanospheres.This architecture,comprising SiO_(2) as the core,MXene as the intermediate layer,and MoS_(2) as the outer shell,is achieved through an electrostatic self‐assembly method combined with a hydrothermal process.This complex core‐shell structure not only provides a variety of loss mechanisms that effectively dissipate electromagnetic energy but also prevents self‐aggregation of MXene and MoS_(2) nanosheets.Notably,the synergistic combination of SiO_(2) and MoS_(2) with highly conductive MXene enables the suitable dielectric constant of the composites,ensuring optimal impedance matching.Therefore,the core‐shell structured SiO_(2)@MXene@MoS_(2) nanospheres exhibit excellent EMW absorption performance,featuring a remarkable minimum reflection loss(RL_(min))of−52.11 dB(2.4 mm).It is noteworthy that these nanospheres achieve an ultra‐wide effective absorption bandwidth(EAB)of 6.72 GHz.This work provides a novel approach for designing and synthesizing high‐performance EMW absorbers characterized by“wide bandwidth and strong reflection loss.”
基金Project supported by the National Natural Science Foundation of China （Grant No 50641006） and the Science Foundation of Education Commission of Beijing, China.
文摘In this paper, Fe30Pt70/Fe3O4 core/shell nanoparticles were synthesized by chemical routine and the layered polyethylenimine （PEI）-Fe30Pt70/Fe3O4 structure was constructed by molecule-mediated self-assembly technique. The dimension of core/shell structured nanoparticles was that of 4nm core and 2 nm shell. After annealing under a flow of forming gas （50%Ar2＋30%H2） for 1 h at or above 400℃, the iron oxide shell was reduced to Fe and diffused to Pt-rieh core, which leaded to the formation of L1. phase FePt at low temperature. The x-ray diffraction results and magnetic properties measurement showed that the chemical ordering temperature of Fe30Pt70/Fe3O4 core/shell nanoparticles assembly can be reduced to as low as 400℃. The sample annealed at 400℃ showed the eoereivity of 4KOe with the applied field of 1.5T. The core/shell structure was suggested to be an effective way to reduce the ordering temperature obviously.
文摘LaF^3＋ Yb^3＋ , Er^3＋ nanoparticles were successfully synthesized using solvothermal treatment, and LaF^3＋ Yb^3＋ , Er^3＋/SiO2 core/shell nanoparticles were also prepared with reverse microemulsion technique. The crystal structure, morphology and photoluminescence properties of as-prepared core/shell nanoparticles were in- vestigated by X-ray diffraction, transmission electron microscopy and fluorescence spectrophotometer. The re- sults showed thatLaF^3＋ Yb^3＋ , Er^3＋ nanoparticles are of hexagonal structure and SiO2 shell is amorphous. The size ofLaF^3＋ Yb^3＋ , Er^3＋. nanoparticles is 13 nm and the LaF^3＋ Yb^3＋ , Er^3＋/SiO2 nanoparticles present clearly a core/shell structure with 12 nm shell thickness. The solubility of LaF^3＋ Yb^3＋ , Er^3＋ nanocrystals in water and the biocompatibility are both improved by the SiO2 shell. The upconversion luminescence spectra suggested that the SiO~ shell has small effect on the upconversion luminescence properties of the LaF^3＋ Yb^3＋ , Er^3＋ nanocrys- tals. The core/shell structure LaF^3＋ Yb^3＋ , Er^3＋ /SiO2. nanopartlcles are expected to be used in biological appli- cations.
基金the support from National Natural Science Foundation of China (No.52004179)the Fundamental Research Program of Shanxi Province,China (Nos.202403021211028,202303021211036)+1 种基金Shanxi Water and Wood New Carbon Materials Technology Co.,Ltd.,ChinaGuangdong One Nano Technology Co.,Ltd.,China。
文摘In order to restrain the huge volume expansion of bismuth(Bi)anodes in sodium ion batteries(SIBs),the core-shell structure Bi@mesoporous carbon nanospheres(Bi@mC)composite was designed and prepared by sol-gel method coupled heat treatment.Structural characterization displays that the average diameter of the as-prepared Bi@mC composites is about 200 nm and thickness of the N-doped mesoporous carbon shells is 20-30 nm.Electrochemical test and kinetic analysis results show that the mesoporous carbon shell can not only effectively relieve the stress caused by volume expansion of Bi and protect active material from pulverization caused by the stress during charging/discharging process,but also facilitate quick diffusion of sodium ions,thus improving rate and cycling performance.Bi@mC delivers a high specific capacity of 279 mA·h/g and a capacity retention of 97.6%after 3500 cycles at a current density of 5 A/g.Even at a high current density of 20 A/g,Bi@mC can still maintain a high specific capacity of 266 mA·h/g.Additionally,the Bi@mC//NVP full button sodium-ion batteries(SIBs)assembled using Bi@mC anode and Na_(3)V_(2)(PO_(4))_(3)(NVP)cathode deliver an energy density of 182 W·h/kg.
基金financially supported by the National Key Research and Development Program of China(No.2022YFB4003801)the National Natural Science Foundation of China(No.52076091)We appreciate the analysis and characterization assistance of FESEM,XRD,and Raman from the Analytical and Testing Center at Huazhong University of Science&Technology.The author acknowledges the tubular furnace from Anhui Chem-n Instrument Co.,Ltd.
文摘Vanadium nitride(VN),a promising cathode material for aqueous zinc ion batteries(AZIBs),undergoes irreversible phase transitions accompanied by structural variation and sustained vanadium dissolution,which impair cycling stability and reaction kinetics.To address these challenges,we designed a core–shell heterostructure(VONC-T,T represents temperature)composed of a VN core and a porous carbon shell.This structure was synthesized via in-situ construction,involving optimized ratio of coating a zinc-based zeolitic imidazolate framework(ZIF-8)onto a vanadium-based metal-organic framework(MIL-47(V)),followed by a thermal treatment.This process ensures a high degree of interfacial stability between the core and shell,effectively mitigating the structural variation of VN during irreversible phase transitions and enhancing the overall structural stability.During thermal driving,the volatilization of zinc within the shell layer created a porous channel effect,which facilitating Zn^(2+)diffusion.The enhancement of Zn²⁺diffusion strengthens the efficient conversion of VN to amorphous VOx,labeled as VONC-T-a,which provides more active sites and consequently results in a high specific capacity.The optimized heterostructure of VONC-900-a presented high reversible capacity of 387.2 mAh g^(−1)at 0.2 A g^(−1)and demonstrated excellent rate performance,achieving 274.5 mAh g^(−1)at 20 A g^(−1),while maintaining a capacity retention rate of 93.3%after 5000 cycles at 10 A g^(−1).Density functional theory calculations confirmed improved reaction kinetics in the core–shell structure.This study not only highlights the potential of amorphous vanadium oxide core–shell heterostructure for AZIBs but also provides new insights into the conversion mechanisms of VN.
基金The first author was partly supported by the Chinese Ministry of Education,and the Japanese Ministry of Education,Science and Culture through their scholarship exchange programsthe National Natural Science Foundation of China under the Grant Nos.40275033 and 40240420564This work was also supported by the State Key Laboratory of Atmospheric Boundary Layer Physics and Atmospheric Chemistry(LAPC)of the Institute of Atmospheric Physics of the Chinese Academy of Sciences under Grant No.LAPC-KF-2003-10.
文摘This paper presents a high-resolution simulation of a remarkable polar low observed over the Sea of Japan on 21 January 1997 by using a 5-km mesh non-hydrostatic model MRI-NHM (Meteorological Research Institute Non-Hydrostatic Model). A 24-hour simulation starting from 0000 UTC 21 January 1997 successfully reproduced the observed features of the polar low such as the wrapping of western part of an initial E-W orientation vortex, the spiral-shaped bands, the cloud-free 'eye', and the warm core structure at its mature stage. The 'eye' of the simulated polar low was relatively dry, and was associated with a strong downdraft. A thermodynamic budget analysis indicates that the 'warm core' in the 'eye' region was mainly caused by the adiabatic warming associated with the downdraft. The relationship among the condensational diabatic heating, the vertical velocity, the convergence of the moisture flux, and the circulation averaged within a 50 km×50 km square area around the polar low center shows that they form a positive feedback loop, and this loop is not inconsistent with the CISK (Conditional Instability of the Second Kind) mechanism during the developing stage of the polar low.
文摘This paper presents an analysis of the coupled vibration of asymmetric core structures in tall buildings. The governing equation of free vibration and its corresponding eigenvalue problem, which is a set of equations for laterally flexural vibrations in two different directions coupled by a warping-St. Venant torsional vibration, are derived. Based on the Calerkin method, a generalized approximate method is developed for the analysis of coupled vibration and thus proposed for determining the natural frequencies and mode shapes of the structure in triply-coupled vibration. The results of the proposed method for the example structure show good agreement with those of the FEM analysis. The proposed method has been shown to provide a simple and rapid, yet accurate, means for coupled vibration analysis of core structures.
基金Project(2013DFA51290)supported by International S&T Cooperation Program of China
文摘The purpose of this study is to explore the adsorption performance of meso-2,3-dimercaptosuccinic acid(DMSA)modified Fe3O4@SiO2 magnetic nanocomposite(Fe3O4@SiO2@DMSA)for Pb2+ions removal from aqueous solutions.The effects of solution pH,initial concentration of Pb2+ions,contact time,and temperature on the amount of Pb2+adsorbed were investigated.Adsorption isotherms,adsorption kinetics,and thermodynamic analysis were also studied.The results showed that the maximum adsorption capacity of the Fe3O4@SiO2@DMSA composite is 50.5 mg/g at 298 K,which is higher than that of Fe3O4 and Fe3O4@SiO2 magnetic nanoparticles.The adsorption process agreed well with Langmuir adsorption isotherm models and pseudo second-order kinetics.The thermodynamic analysis revealed that the adsorption was spontaneous,endothermic and energetically driven in nature.
基金supported by National Natural Science Foundation of China(21972017)the“Scientific and Technical Innovation Action Plan”Hong Kong,MacaoTaiwan Science&Technology Cooperation Project of Shanghai Science and Technology Committee(19160760600).
文摘Rational construction of highly efficient and cheap bifunctional electrocatalysts to boost both oxygen evolution reaction(OER)and oxygen reduction reaction(ORR)is extremely essential for the wide application of rechargeable metal-air battery.In this work,we design a core-shell structural catalyst of CoNi dual-metal embedded in nitrogen doped porous carbon(NPC,CoNi@NPC),which is developed via the pyrolysis of CoNiMOFs,assisting by mesoporous SiO_(2) to effectively inhibit the aggregation of metal sites.Consequently,the asprepared CoNi@NPC manifests good ORR activity with half-wave potential up to 0.77 V.Specifically,the CoNi@NPC gives a very low OER over-potential of merely 101 mV in 6 M KOH along with high stability,outperforming the commercial Pt/C-RuO_(2).Moreover,the home-made zinc air battery with CoNi@NPC air cathode demonstrates excellent stability over long-term charging–discharging test,and delivers the maximum power density of 224 mW cm^(-2).The enhanced high performance of CoNi@NPC bifunctional catalyst for both ORR and OER can be ascribed to its unique core-shell structure and strong synergistic effect between the dual-bimetal active sites and the heteroatom doped carbon.This work opens a new avenue for the rational design of nonprecious metal bifunctional catalysts for rechargeable metal-air battery.
文摘The hydrogenation of CO_(2) into methanol has attracted much attention and In_(2)O_(3) is a promising catalyst.Introducing metal elements into In_(2)O_(3)(M/In_(2)O_(3))is one of the main strategies to improve its performance.However,its mechanism and active sites remain unclear and need to be further elucidated.Here,the noble‐metal‐free In_(x)‐Co_(y) oxides catalysts were prepared.Much‐improved performance and obvious product selectivity shift were observed.The optimized catalyst(In_(1)‐Co_(4))(9.7 mmol g_(cat)^(–1) h^(–1))showed five times methanol yields than pure In_(2)O_(3)(2.2 mmol g_(cat)^(–1) h^(–1))(P=4.0 MPa,T=300°C,GHSV=24000 cm^(3)_(STP) g_(cat)^(–1) h^(–1),H_(2):CO_(2)=3).And the cobalt‐catalyzed CO_(2) methanation activity was suppressed,although cobalt was most of the metal element.To unravel this selectivity shift,detailed catalysts performance evaluation,together with several in‐situ and ex‐situ characterizations,were employed on cobalt and In‐Co for comparative study.The results indicated CO_(2) hydrogenation on cobalt and In‐Co catalyst both followed the formate pathway,and In‐Co reconstructed and generated a surface In_(2)O_(3)‐enriched core‐shell‐like structure under a reductive atmosphere.The enriched In_(2)O_(3) at the surface significantly enhanced CO_(2) adsorption capacity and well stabilized the intermediates of CO_(2) hydrogenation.CO_(2) and carbon‐containing intermediates adsorbed much stronger on In‐Co than cobalt led to a feasible surface C/H ratio,thus allowing the*CH_(3)O to desorb to produce CH_(3)OH instead of being over‐hydrogenated to CH_(4).
基金This research was supported by NNSFC (No. 90203017 29733090), NBRP (2004CB7201005) and SKLSC
文摘The reaction of molybdenum hexacarbonyl with C6H5CH2OC6H4ONa and Et4NBr in CH3CN at 60 ℃ afforded the di-nuclear Mo（0） compound [Et4N]3[Mo2（CO）6（μ-OC6H4OCH2C6H5）3] 1. 1 crystallizes in monoclinic, space group P21/c with a = 15.359（2）, b = 18.378（3）, c = 24.952（2） A, β = 102.268（4）°, V = 6882.3（1 6） A^3, Mr = 1348.34, Z = 4, Dc = 1.301 g/cm^3, F（000） = 2832 and μ= 0.424 mm^-1 The final R = 0.0606 and wR = 0.1552 for 9396 observed reflections （I 〉 2σ（I））. I contains a [Mo2O3]^3 core in triangular bi-pyralnidal configuration and each Mo atom adopts a distorted octahedral geometry with three carbon atoms from carbonyls and three ,μ-O atoms from C6H5CH2OC6H4O^- bridging ligands. The Mo…Mo distance is 3.30（8） A, indicating no metalmetal bonding. A formation pathway via forming a di-molybdenum（0） di-bridging OR compound [Mo2（μ-OR）2（CO）8]2 has been figured out and the reaction of Mo（CO）6 with alkoxide has also been discussed.
基金Project supported by the National Natural Science Foundation of China (Gant No.11872323)。
文摘Many networks exhibit the core/periphery structure.Core/periphery structure is a type of meso-scale structure that consists of densely connected core nodes and sparsely connected peripheral nodes.Core nodes tend to be well-connected,both among themselves and to peripheral nodes,which tend not to be well-connected to other nodes.In this brief report,we propose a new method to detect the core of a network by the centrality of each node.It is discovered that such nodes with non-negative centralities often consist in the core of the networks.The simulation is carried out on different real networks.The results are checked by the objective function.The checked results may show the effectiveness of the simulation results by the centralities of the nodes on the real networks.Furthermore,we discuss the characters of networks with the single core/periphery structure and point out the scope of the application of our method at the end of this paper.
