The mechanical and thermodynamic properties of W-Ti alloys(including W_(15)Ti_(1),W_(14)Ti_(2),W_(12)Ti_(4) and W_(8)Ti_(8) alloys)were investigated by the first-principles approach based on density functional theory....The mechanical and thermodynamic properties of W-Ti alloys(including W_(15)Ti_(1),W_(14)Ti_(2),W_(12)Ti_(4) and W_(8)Ti_(8) alloys)were investigated by the first-principles approach based on density functional theory.The results indicate that W-Ti alloys except W_(8)Ti_(8) are thermodynamically stable.The modulus and hardness of W-Ti alloys are smaller than those of pure tungsten and gradually decrease with increasing Ti concentration.However,their B/G ratios and Poisson's ratios exceed those of pure tungsten,suggesting that the introduction of Ti decreases the mechanical strength while enhancing the ductility of W-Ti alloys.The thermal expansion coefficients for W-Ti alloys all surpass those of pure tungsten,indicating that the introduction of titanium exacerbates the thermal expansion behavior of W-Ti alloys.Nevertheless,elevated pressure has the capacity to suppress the thermal expansion tendencies in titanium-doped tungsten alloys.This study offers theoretical insights for the design of nuclear materials by exploring the mechanical and thermodynamic properties of W-Ti alloys.展开更多
The adsorption properties of a magnesium porphyrin(MgP)molecule on Au(111)surface covered with up to three lay-ers of sodium chloride(NaCl)were investigated by means of first-principles calculations.The most stable ad...The adsorption properties of a magnesium porphyrin(MgP)molecule on Au(111)surface covered with up to three lay-ers of sodium chloride(NaCl)were investigated by means of first-principles calculations.The most stable adsorption configuration of MgP on the NaCl/Au(111)heterosurfaces was found to be at the Cl-top site with a 20°angle between the[110]lattice direction of NaCl and the Mg–N bond of the molecule.Compared with MgP molecule adsorbed on bare Au(111),the inclusion of NaCl lay-ers can lead to a significant decrease in the adsorption energy of the MgP molecule.The exis-tence of NaCl layers also reduced the charge transfer between the molecule and the surface.For heterosurfaces with two or three monolayers of NaCl,the charge transfer was almost com-pletely suppressed.The obtained partial density of states(PDOS)showed that hybridization between the electronic structures of the adsorbed MgP molecule and the metal surface can be significantly suppressed when NaCl layers were added.For the heterosurface with three lay-ers of NaCl,the PDOS around the Fermi level was almost identical with that of the free molecule,suggesting the electronic structure of the MgP molecule was nicely preserved.Influ-ence of the NaCl layers on the electronic structure of the MgP molecule was mainly found for molecular orbitals(MOs)away from the Fermi level as a result of the large band gap of the NaCl layers.展开更多
Solute segregation at grain boundaries(GBs)can significantly influence GB cohesion.In this work,the segregation energies of solutes(Zn,Al,Ag,Ca,and Gd)were first investigated at six symmetrical tilt GBs rotating aroun...Solute segregation at grain boundaries(GBs)can significantly influence GB cohesion.In this work,the segregation energies of solutes(Zn,Al,Ag,Ca,and Gd)were first investigated at six symmetrical tilt GBs rotating around[0001]axis of Mg,to uncover the impact of GB characteristics on solute segregation behavior.The results reveal that solute segregation propensity is closely related to the local geometric environment of GB sites,but has little correlation with intrinsic GB properties(such as GB misorientation and GB energy).Furthermore,relationships between GB site characteristics and solute segregation tendencies were established.Ca-like solutes tend to occupy GB sites with larger Voronoi volumes(V),while Zn-like solutes prefer GB sites with smaller V as well as smaller shortest bond lengths(SBL).Based on this finding,we further evaluated the segregation capacities of 26 solutes at their most energetically stable segregation sites and their impact on GB cohesion.A descriptor that can effectively capture the strengthening/embrittling potency of segregated solutes on GBs was proposed by performing the crystal orbital Hamilton population(COHP)analyses.It was found that the discrepancies in bond strength between GBs and free surface dominate the solute-strengthening behavior.Finally,a first-principles“design map”regarding the segregation energies and strengthening energies was provided,which offers a database for designing Mg alloys with high fracture toughness.展开更多
Second period elements(B,C,N,and O)usually appear at the grain boundary(GB)and strongly affect the mechanical performance in austenitic stainless steels.Therefore,it is significant to investigate the effect of solute ...Second period elements(B,C,N,and O)usually appear at the grain boundary(GB)and strongly affect the mechanical performance in austenitic stainless steels.Therefore,it is significant to investigate the effect of solute elements(B,C,N,and O)on the GB.The first-principles calculation based on the density function theory was applied to explore the effect of B,C,N,and O onγ-FeΣ5(210)[001]GB.The GB energy,the segregation energy,the Voronoi volume,and the theoretical tensile test were calculated to investigate the segregation behavior and the strengthening effect.The structural change and electronic evolution were also investigated by bond change,charge density distribution,and density of states.The results show that B is favored to segregate at the capped trigonal prism(CTP)position with a large void and has a strengthening effect on the GB strength,while O and N are preferred to locate at the octahedral(OCT)site and have an embrittling effect on GB cohesion.C can segregate at both the CTP site and the OCT location with little energy difference.As C segregates at the OCT site,it is beneficial for GB strength.However,it is detrimental at the CTP position.It can be seen that the influence of solutes is closely related to the element type and segregated position.展开更多
MgO is one of the most abundant minerals in the Earth’s interior,and its structure and properties at high temperature and pressure are important for us to understand the composition and behavior in the deep Earth.In ...MgO is one of the most abundant minerals in the Earth’s interior,and its structure and properties at high temperature and pressure are important for us to understand the composition and behavior in the deep Earth.In the present work,firstprinciples molecular dynamics calculations were performed to investigate the pressure-induced structural evolution of the MgO melts at 4000 K and 5000 K.The results predicted the liquid-solid phase boundaries,and the calculated viscosities of the melts may help us to understand the transport behavior under the corresponding Earth conditions.展开更多
Extensive first-principles calculations have been performed to examine the electrochemical properties of Na-ion-intercalatable heterostructures formed by transitional metal dichalcogenides(MS_(2),where M=Ti,V,Nb and M...Extensive first-principles calculations have been performed to examine the electrochemical properties of Na-ion-intercalatable heterostructures formed by transitional metal dichalcogenides(MS_(2),where M=Ti,V,Nb and Mo)and blue phosphorus(BlueP),which have been reported as potential anode materials for rechargeable sodium-ion batteries.Upon formation of heterostructures,much improved structural stabilities have observed compared with the pristine MS_(2) and BlueP.Metallic T-TiS_(2),T-MoS_(2),H(T)-VS_(2) and H(T)-NbS_(2) would retain the conductive character after formation of heterostructures with BlueP,however,HTiS_(2)/BlueP and H-MoS_(2)/BlueP would undergo a semiconductor to metallic transition accompanied by Na intercalation.Moreover,the presence of relatively low diffusion barriers ranging from 0.04 eV to 0.08 eV,coupled with the suitable average open-circuit voltage spanning from 0.12 eV to 0.89 eV,guarantee exceptional charge-discharge rates and ensure the safety of battery performance.Among these heterostructures,H(T)-NbS_(2)/BlueP and T-TiS_(2)/BlueP exhibit best Na adsorption ability of up to 4 layers,corresponding to theoretical capacities of 570.2 and 746.7 mAh/g,respectively.These encouraging properties indicate that T-TiS_(2)/BlueP and H(T)-NbS_(2)/BlueP could serve as suitable anode materials for high-performance sodiumion batteries.展开更多
The lattice thermal conductivity(κ_(latt))of mantle minerals plays a crucial role in the heat flow and temperature distribution within the Earth.MgSiO_(3)akimotoite is stable at the bottom of the mantle transition zo...The lattice thermal conductivity(κ_(latt))of mantle minerals plays a crucial role in the heat flow and temperature distribution within the Earth.MgSiO_(3)akimotoite is stable at the bottom of the mantle transition zone;it transitions to MgSiO_(3)perovskite(MgPv).Inκ_(latt)this work,we carry out a study of the of MgSiO_(3)akimotoite for pressures up to 25 GPa and temperatures up to 2500 K,based onκ_(latt)first-principles calculations combined with lattice dynamics theory.At 300 K and 25 GPa,the of MgSiO_(3)akimotoite is 37.66 W m^(-1)K^(-1),κ_(latt)larger than that of MgPv(13.46 W m^(-1)K^(-1)),which implies that the phase transition explains the reduction in.At 300 K,the pressureκ_(latt)κ_(latt)dependence of is 0.68 W m^(-1)K^(-1)GPa-1,stronger than that of MgPv(0.48 W m^(-1)K^(-1)GPa-1).The azimuthal anisotropy in of MgSiO_(3)akimotoite decreases from 45.5%at 0 GPa to 28.94%at 25 GPa,while the variation trend is opposite to that of MgPv.In MgSiO_(3)κ_(latt)akimotoite,Fe incorporating in the mineral leads to a decrease in and an increase in azimuthal anisotropy.Along the geotherm,theκ_(latt)of MgSiO_(3)akimotoite is lower than that of ringwoodite,which would suggest that MgSiO_(3)akimotoite slows down heat conduction at the bottom of mantle transition zone.These findings are useful for determining the thermal structure of,and understanding heat transfer in,the interior of the Earth.展开更多
Previous studies have demonstrated that increasing Fe doping content can enhance the saturation magnetization and maximum energy product of 2:17-type Sm-Co rare-earth permanent magnets.Howeve r,syste matic theo retica...Previous studies have demonstrated that increasing Fe doping content can enhance the saturation magnetization and maximum energy product of 2:17-type Sm-Co rare-earth permanent magnets.Howeve r,syste matic theo retical calculations and the effects of other transition metal dopants have yet to be explored.This study employed first-principles computational methods to investigate the effects of doping with 3d and Zr transition metal elements on the structural stability,magnetic properties,and electronic structure of Sm_(2)Co_(17)permanent magnets.The results indicate that Sc and Zr tend to occupy the Sm-6c site,while Ni,Cu and Zn preferentially occupy the 18h site,and Ti,V,Cr,Mn and Fe primarily occupy the Co-6c site.Except for V and Cu,all other elements effectively improve the structural stability of the doped systems.Additionally,Mn and Fe doping can significantly enhance the total magnetic moment and magnetocrystalline anisotropy energies of the Sm_(2)Co_(17)system,while Cr only increases the total magnetic moment.More importantly,doping with Cr,Mn and Fe within the doping co ntent range of9.8 at%<x<35.29 at% can simultaneously improve the structural stability,total magnetic moment and magnetocrystalline anisotropy energy of the Sm_(2)Co_(17) system.Our study provides valuable theoretical guidance for experimental exploration and is expected to promote the development and application of novel rare-earth permanent magnetic materials.展开更多
The mechanical,thermodynamic properties and electrical conductivities of L1_(2)-Al_(3)X(X=Zr,Sc,Er,Yb,Hf)structural phases in aluminum conductors were investigated through a first-principles study.The results demonstr...The mechanical,thermodynamic properties and electrical conductivities of L1_(2)-Al_(3)X(X=Zr,Sc,Er,Yb,Hf)structural phases in aluminum conductors were investigated through a first-principles study.The results demonstrate that all structural phases have good alloy-forming ability and structural stability,where Al_(3)Zr is the most superior.Al_(3)Zr,Al_(3)Hf and Al_(3)Sc have enhanced shear and deformation resistance in comparison to other phases.Within the temperature range of 200−600 K,Al_(3)Er and Al_(3)Yb possess the greatest thermodynamic stability,followed by Al_(3)Hf,Al_(3)Zr and Al_(3)Sc.Al_(3)Er and Al_(3)Yb have higher thermodynamic stability than Al_(3)Hf,Al_(3)Zr and Al_(3)Sc.All structural phases exhibit substantial metallic properties,indicating their good electrical conductivity.The electrical conductivities of Al_(3)Hf and Al_(3)Zr are higher than those of Al_(3)Er,Al_(3)Yb and Al_(3)Sc.The covalent bond properties in Al_(3)Sc,Al_(3)Er and Al_(3)Yb enhance the hardness,brittleness and thermodynamic stability of the structural phase.The thermodynamic stability of Al_(3)Sc is significantly reduced by ionic bonds.展开更多
Oxidation corrosion of steels usually occurs in contact with the oxygen-contained environment, which is accelerated by high oxygen concentration and irradiation. The oxidation mechanism of steels is investigated by th...Oxidation corrosion of steels usually occurs in contact with the oxygen-contained environment, which is accelerated by high oxygen concentration and irradiation. The oxidation mechanism of steels is investigated by the adsorption/solution of oxygen atoms on/under body-centered-cubic(bcc) iron surfaces, and diffusion of oxygen atoms on the surface and in the near-surface region. Energetic results indicate that oxygen atoms prefer to adsorb at hollow and long-bridge positions on the Fe(100) and(110) surfaces, respectively. As the coverage of oxygen atoms increases, oxygen atoms would repel each other and gradually dissolve in the near-surface and bulk region. As vacancies exist, oxygen atoms are attracted by vacancies, especially in the near-surface and bulk region. Dynamic results indicate that the diffusion of O atoms on surfaces is easier than that into near-surface, which is affected by oxygen coverage and vacancies. Moreover, the effects of oxygen concentration and irradiation on oxygen density in the near-surface and bulk region are estimated by the Mc Lean’s model with a simple hypothesis.展开更多
The paper reports on the atomic investigation aboutβphase in Mg_(96)Gd_(2)Y_(1)Ni_(1) alloy by using the first-principles study and the high-angle annular dark-field scanning transmission electron microscope(HAADF-ST...The paper reports on the atomic investigation aboutβphase in Mg_(96)Gd_(2)Y_(1)Ni_(1) alloy by using the first-principles study and the high-angle annular dark-field scanning transmission electron microscope(HAADF-STEM)corrected by atomic Cs.By using HAADF-STEM,the rectangularβphases were observed in the underage and peak aging stages in Mg_(96)Gd_(2)Y_(1)Ni_(1) alloy.Theβphase could be precipitated from the previously precipitatedβphase,and theβphase grew in steps when it was precipitated.A special transition structure of three atomic layer thicknesses was first observed at the edge of theβphase and the structure of this interface is probably as theβ/Mg_(1) interface for the analysis of thermodynamic characterization and electronic characterization.Theβ'phase and theβ_(H) structure were precipitated only at the edge of the length directions of theβphase.Theβ'phase continues to grow into aβphase directly without the formation ofβ_(1) phase,resulting in an increase in the length of theβphase,which is discovered for the first time.展开更多
First-principles calculations were carried out to investigate the structural stabilities and electronic properties of RhZr.The plane wave based pseudopotential method was used,in which both the local density approxima...First-principles calculations were carried out to investigate the structural stabilities and electronic properties of RhZr.The plane wave based pseudopotential method was used,in which both the local density approximation（LDA） and the generalized gradient approximation（GGA） implanted in the CASTEP code were employed.The internal positions of atoms in the unit cell were optimized and the ground state properties such as lattice parameter,density of state,cohesive energies and enthalpies of formation of ortho-RhZr and cubic-RhZr were calculated.The calculation results indicate that ortho-RhZr can form more easily than cubic-RhZr and the ortho-RhZr is more stable than cubic-RhZr.The density of states（DOS） reveals that the strong bonding in the Rh-Zr and Rh-Rh or Zr-Zr interaction chains accounts for the structural stability of ortho-RhZr and the hybridization between Rh-4d states and Zr-4d states is strong.展开更多
The first-principles method based on the projector augmented wave method within the generalized gradient approximation was employed to calculate the superlattice intrinsic stacking fault（SISF） and complex stacking f...The first-principles method based on the projector augmented wave method within the generalized gradient approximation was employed to calculate the superlattice intrinsic stacking fault（SISF） and complex stacking fault（CSF） energies of the binary Ni3Al alloys with different Al contents and the ternary Ni3Al intermetallic alloys with addition of alloying elements,such as Pd,Pt,Ti,Mo,Ta,W and Re.The results show that the energies of SISF and CSF increase significantly with increase of Al contents in Ni3Al.Addition of Pd and Pt occupying the Ni sublattices does not change the SISF and CSF energies of Ni3Al markedly in comparison with the Ni-23.75Al alloy.While addition of alloying elements,such as Ti,Mo,Ta,W and Re,occupying the Al sublattices dramatically increases the SISF and CSF energies of Ni3Al.The results suggest that the energies of SISF and CSF are dependent both on the Al contents and on the site occupancy of the ternary alloying element in Ni3Al intermetallic alloys.展开更多
The electronic structures and mechanical properties of Al4Sr, Mg2Sr and Mg23Sr6 phases were determined by the use of first-principles calculations. The calculated heat of formation and cohesive energy indicate that Al...The electronic structures and mechanical properties of Al4Sr, Mg2Sr and Mg23Sr6 phases were determined by the use of first-principles calculations. The calculated heat of formation and cohesive energy indicate that Al4Sr has the strongest alloying ability as well as the highest structural stability. The elastic parameters were calculated, and then the bulk modulus, shear modulus, elastic modulus and Poisson ratio were derived. The ductility and plasticity were discussed. The results show that Al4Sr and Mg2Sr phases both are ductile, on the contrary, Mg23Sr6 is brittle, and among the three phases, Mg2Sr is a phase with the best plasticity.展开更多
The structure,stability and elastic properties of di-transition-metal carbides TixV1-xC were investigated by using the first-principles with a pseudopotential plane-waves method.The results show that the equilibrium l...The structure,stability and elastic properties of di-transition-metal carbides TixV1-xC were investigated by using the first-principles with a pseudopotential plane-waves method.The results show that the equilibrium lattice constants of TixV1-xC show a nearly linear reduction with increasing addition of V.The elastic properties of TixV1-xC are varied by doping with V.The bulk modulus of Ti0.5V0.5C is larger than that of pure TiC,as well as Ti0.5V0.5C has the largest C44 among TixV1-xC（0≤x≤1）,indicating that Ti0.5V0.5C has higher hardness than pure TiC.However,Ti0.5V0.5C presents brittleness based on the analysis of ductile/brittle behavior.The Ti0.5V0.5C carbide has the lowest formation energy,indicating that Ti0.5V0.5C is more stable than all other alloys.展开更多
A first-principles study was reported based on density functional theory of hydrogen vacancy,metal dopants,metal dopant-vacancy complex in LiBH4,a promising material for hydrogen storage.The formation of H vacancy and...A first-principles study was reported based on density functional theory of hydrogen vacancy,metal dopants,metal dopant-vacancy complex in LiBH4,a promising material for hydrogen storage.The formation of H vacancy and metal doping in LiBH4 is difficult,and their concentrations are low.The presence of one kind of defect is helpful to the formation of other kind of defect.Based on the analysis of electronic structure,the improvement of the dehydrogenating kinetics of LiBH4 by metal catalysts is due to the weaker bonding of B—H and the new metal-like system,which makes H atom diffuse easily;H vacancy accounts for a trace amount of BH3 release during the decomposing process of LiBH4;metal dopant weakens the strength of B—H bonds,which reduces the dehydriding temperature of LiBH4.The roles of metal and vacancy in the metal dopant-vacancy complex can be added in LiBH4 system.展开更多
The origins of magnetism in transition-metal doped Na0.5Bi0.5TiO3 system are investigated by ab initio calculations. The calculated results indicate that a transition-metal atom sub- stitution for a Ti atom produces m...The origins of magnetism in transition-metal doped Na0.5Bi0.5TiO3 system are investigated by ab initio calculations. The calculated results indicate that a transition-metal atom sub- stitution for a Ti atom produces magnetic moments, which are due to the spin-polarization of transition-metal 3d electrons. The characteristics of exchange coupling are also calculated, which shows that in Cr-/Mn-/Fe-/Co- doped Na0.5Bi0.5TiO3 system, the antiferromagnetic coupling is favorable. The results can successfully explain the experimental phenomenon that, in Mn-/Fe- doped Nao.sBio.sTiO3 system, the ferromagnetism disappears at low tem- perature and the paramagnetic component becomes stronger with the increase of doping concentration of Mn/Fe/Co ions. Unexpectedly, we find the Na0.5Bi0.5Ti0.67V0.33iO3 sys- tem with ferromagnetic coupling is favorable and produces a magnetic moment of 2.00 P-B, which indicates that low temperature ferromagnetism materials could be made by intro- ducing V atoms in Na0.5Bi0.5TiO3. This may be a new way to produce low temperature multiferroic materials.展开更多
The impacts of strain and polar discontinuities on the performance of superlattices have attracted widespread attention. Using first-principles calculation, we study the polarization and piezoelectricity of PbTiO3/KTa...The impacts of strain and polar discontinuities on the performance of superlattices have attracted widespread attention. Using first-principles calculation, we study the polarization and piezoelectricity of PbTiO3/KTa03 （PTO//KTO） superl^ttices with strain and polsr discontinuities. The strain caused by lattice mismatch between the superlattice and the substrate induces lattice distortion, the displacement of each atom and dynamical charge transfer between the Ti atom or Ta atom and the 0 atoms in the PTO//KTO superlattice. With more compressive or less tensile strain, the polarization value increases linearly, piezoelectric tensor e31 （e32） increases while e33 and e25 （e16） increase negatively. Polarity discontinuity caused by the interracial charge will produce large irreversible polarization. Proved by F-point phonons of PTO//KTO superlattices of different strain values, the polar discontinuity and the piezoelectric properties are just weakly dependent on temperature as found in PTO//KTO superlattices.展开更多
Doping is an effective approach for improving the photovoltaic performance of Cu2 ZnSnS4（CZTS）. The doping by substitution of Cu atoms in CZTS with Li and Ag atoms is investigated using density functional theory. Th...Doping is an effective approach for improving the photovoltaic performance of Cu2 ZnSnS4（CZTS）. The doping by substitution of Cu atoms in CZTS with Li and Ag atoms is investigated using density functional theory. The results show that the band gaps of Li（2 x）Cu2（1-x）ZnSnS4 and Ag（2 x）Cu2（1-x）ZnSnS4 can be tuned in the ranges of 1.30-3.43 and 1.30-1.63 eV, respectively. The calculation also reveals a phase transition from kesterite to wurtzite-kesterite for Li（2 x）Cu2（1-x）ZnSnS4 as x is larger than 0.9. The tunable band gaps of Li（2 x）Cu2（1-x）ZnSnS4 and Ag（2 x）Cu2（1-x） ZnSnS4 make them beneficial for achieving band-gap-graded solar cells.展开更多
基金Funded by National Key R&D Program of China(No.2021YFB3802300)the National Natural Science Foundation of China(No.52171045)the Joint Fund(No.8091B022108)。
文摘The mechanical and thermodynamic properties of W-Ti alloys(including W_(15)Ti_(1),W_(14)Ti_(2),W_(12)Ti_(4) and W_(8)Ti_(8) alloys)were investigated by the first-principles approach based on density functional theory.The results indicate that W-Ti alloys except W_(8)Ti_(8) are thermodynamically stable.The modulus and hardness of W-Ti alloys are smaller than those of pure tungsten and gradually decrease with increasing Ti concentration.However,their B/G ratios and Poisson's ratios exceed those of pure tungsten,suggesting that the introduction of Ti decreases the mechanical strength while enhancing the ductility of W-Ti alloys.The thermal expansion coefficients for W-Ti alloys all surpass those of pure tungsten,indicating that the introduction of titanium exacerbates the thermal expansion behavior of W-Ti alloys.Nevertheless,elevated pressure has the capacity to suppress the thermal expansion tendencies in titanium-doped tungsten alloys.This study offers theoretical insights for the design of nuclear materials by exploring the mechanical and thermodynamic properties of W-Ti alloys.
基金supported by the National Natural Science Foundation of China(No.22373084,No.62201494)Hebei Natural Science Foundation(B2022203007)the Cultivation Project for Basic Research and Innovation of Yanshan University(2024LGZD002).
文摘The adsorption properties of a magnesium porphyrin(MgP)molecule on Au(111)surface covered with up to three lay-ers of sodium chloride(NaCl)were investigated by means of first-principles calculations.The most stable adsorption configuration of MgP on the NaCl/Au(111)heterosurfaces was found to be at the Cl-top site with a 20°angle between the[110]lattice direction of NaCl and the Mg–N bond of the molecule.Compared with MgP molecule adsorbed on bare Au(111),the inclusion of NaCl lay-ers can lead to a significant decrease in the adsorption energy of the MgP molecule.The exis-tence of NaCl layers also reduced the charge transfer between the molecule and the surface.For heterosurfaces with two or three monolayers of NaCl,the charge transfer was almost com-pletely suppressed.The obtained partial density of states(PDOS)showed that hybridization between the electronic structures of the adsorbed MgP molecule and the metal surface can be significantly suppressed when NaCl layers were added.For the heterosurface with three lay-ers of NaCl,the PDOS around the Fermi level was almost identical with that of the free molecule,suggesting the electronic structure of the MgP molecule was nicely preserved.Influ-ence of the NaCl layers on the electronic structure of the MgP molecule was mainly found for molecular orbitals(MOs)away from the Fermi level as a result of the large band gap of the NaCl layers.
基金supported by the National Natural Science Foundation of China(Nos.52222409 and U24A20104)the National Key Research and Development Program(No.2024YFB3408900)+1 种基金Partial financial support came from the Fundamental Research Funds for the Central Universities,JLUsupported by the High Performance Computing Center of Jilin University,China.
文摘Solute segregation at grain boundaries(GBs)can significantly influence GB cohesion.In this work,the segregation energies of solutes(Zn,Al,Ag,Ca,and Gd)were first investigated at six symmetrical tilt GBs rotating around[0001]axis of Mg,to uncover the impact of GB characteristics on solute segregation behavior.The results reveal that solute segregation propensity is closely related to the local geometric environment of GB sites,but has little correlation with intrinsic GB properties(such as GB misorientation and GB energy).Furthermore,relationships between GB site characteristics and solute segregation tendencies were established.Ca-like solutes tend to occupy GB sites with larger Voronoi volumes(V),while Zn-like solutes prefer GB sites with smaller V as well as smaller shortest bond lengths(SBL).Based on this finding,we further evaluated the segregation capacities of 26 solutes at their most energetically stable segregation sites and their impact on GB cohesion.A descriptor that can effectively capture the strengthening/embrittling potency of segregated solutes on GBs was proposed by performing the crystal orbital Hamilton population(COHP)analyses.It was found that the discrepancies in bond strength between GBs and free surface dominate the solute-strengthening behavior.Finally,a first-principles“design map”regarding the segregation energies and strengthening energies was provided,which offers a database for designing Mg alloys with high fracture toughness.
基金supported by National Key R&D Program of China(No.2022YFB3705202)National Natural Science Foundation of China(Nos.51831008,52171049 and 52104330).
文摘Second period elements(B,C,N,and O)usually appear at the grain boundary(GB)and strongly affect the mechanical performance in austenitic stainless steels.Therefore,it is significant to investigate the effect of solute elements(B,C,N,and O)on the GB.The first-principles calculation based on the density function theory was applied to explore the effect of B,C,N,and O onγ-FeΣ5(210)[001]GB.The GB energy,the segregation energy,the Voronoi volume,and the theoretical tensile test were calculated to investigate the segregation behavior and the strengthening effect.The structural change and electronic evolution were also investigated by bond change,charge density distribution,and density of states.The results show that B is favored to segregate at the capped trigonal prism(CTP)position with a large void and has a strengthening effect on the GB strength,while O and N are preferred to locate at the octahedral(OCT)site and have an embrittling effect on GB cohesion.C can segregate at both the CTP site and the OCT location with little energy difference.As C segregates at the OCT site,it is beneficial for GB strength.However,it is detrimental at the CTP position.It can be seen that the influence of solutes is closely related to the element type and segregated position.
基金supported by the National Natural Science Foundation of China(Grant No.51701180)the Foundation of the State Key Laboratory of Coal Conversion(Grant No.J22-23-103).
文摘MgO is one of the most abundant minerals in the Earth’s interior,and its structure and properties at high temperature and pressure are important for us to understand the composition and behavior in the deep Earth.In the present work,firstprinciples molecular dynamics calculations were performed to investigate the pressure-induced structural evolution of the MgO melts at 4000 K and 5000 K.The results predicted the liquid-solid phase boundaries,and the calculated viscosities of the melts may help us to understand the transport behavior under the corresponding Earth conditions.
基金supported by the Fund of Education Department of Shaanxi Provincial Government(No.23JP172)the National Natural Science Foundation of China(No.22309189)financial support from Xiaomi Young Talents Program.
文摘Extensive first-principles calculations have been performed to examine the electrochemical properties of Na-ion-intercalatable heterostructures formed by transitional metal dichalcogenides(MS_(2),where M=Ti,V,Nb and Mo)and blue phosphorus(BlueP),which have been reported as potential anode materials for rechargeable sodium-ion batteries.Upon formation of heterostructures,much improved structural stabilities have observed compared with the pristine MS_(2) and BlueP.Metallic T-TiS_(2),T-MoS_(2),H(T)-VS_(2) and H(T)-NbS_(2) would retain the conductive character after formation of heterostructures with BlueP,however,HTiS_(2)/BlueP and H-MoS_(2)/BlueP would undergo a semiconductor to metallic transition accompanied by Na intercalation.Moreover,the presence of relatively low diffusion barriers ranging from 0.04 eV to 0.08 eV,coupled with the suitable average open-circuit voltage spanning from 0.12 eV to 0.89 eV,guarantee exceptional charge-discharge rates and ensure the safety of battery performance.Among these heterostructures,H(T)-NbS_(2)/BlueP and T-TiS_(2)/BlueP exhibit best Na adsorption ability of up to 4 layers,corresponding to theoretical capacities of 570.2 and 746.7 mAh/g,respectively.These encouraging properties indicate that T-TiS_(2)/BlueP and H(T)-NbS_(2)/BlueP could serve as suitable anode materials for high-performance sodiumion batteries.
基金supported by the National Natural Science Foundation of China(Nos.41474067,12174352).
文摘The lattice thermal conductivity(κ_(latt))of mantle minerals plays a crucial role in the heat flow and temperature distribution within the Earth.MgSiO_(3)akimotoite is stable at the bottom of the mantle transition zone;it transitions to MgSiO_(3)perovskite(MgPv).Inκ_(latt)this work,we carry out a study of the of MgSiO_(3)akimotoite for pressures up to 25 GPa and temperatures up to 2500 K,based onκ_(latt)first-principles calculations combined with lattice dynamics theory.At 300 K and 25 GPa,the of MgSiO_(3)akimotoite is 37.66 W m^(-1)K^(-1),κ_(latt)larger than that of MgPv(13.46 W m^(-1)K^(-1)),which implies that the phase transition explains the reduction in.At 300 K,the pressureκ_(latt)κ_(latt)dependence of is 0.68 W m^(-1)K^(-1)GPa-1,stronger than that of MgPv(0.48 W m^(-1)K^(-1)GPa-1).The azimuthal anisotropy in of MgSiO_(3)akimotoite decreases from 45.5%at 0 GPa to 28.94%at 25 GPa,while the variation trend is opposite to that of MgPv.In MgSiO_(3)κ_(latt)akimotoite,Fe incorporating in the mineral leads to a decrease in and an increase in azimuthal anisotropy.Along the geotherm,theκ_(latt)of MgSiO_(3)akimotoite is lower than that of ringwoodite,which would suggest that MgSiO_(3)akimotoite slows down heat conduction at the bottom of mantle transition zone.These findings are useful for determining the thermal structure of,and understanding heat transfer in,the interior of the Earth.
基金Project supported by the National Key R&D Program of China(2022YFB3505301)the National Key R&D Program of Shanxi Province(202302050201014)+2 种基金the National Natural Science Foundation of China(12304148)the Natural Science Basic Research Program of Shanxi Province(202203021222219)the China Postdoctoral Science Foundation(2023M731452)。
文摘Previous studies have demonstrated that increasing Fe doping content can enhance the saturation magnetization and maximum energy product of 2:17-type Sm-Co rare-earth permanent magnets.Howeve r,syste matic theo retical calculations and the effects of other transition metal dopants have yet to be explored.This study employed first-principles computational methods to investigate the effects of doping with 3d and Zr transition metal elements on the structural stability,magnetic properties,and electronic structure of Sm_(2)Co_(17)permanent magnets.The results indicate that Sc and Zr tend to occupy the Sm-6c site,while Ni,Cu and Zn preferentially occupy the 18h site,and Ti,V,Cr,Mn and Fe primarily occupy the Co-6c site.Except for V and Cu,all other elements effectively improve the structural stability of the doped systems.Additionally,Mn and Fe doping can significantly enhance the total magnetic moment and magnetocrystalline anisotropy energies of the Sm_(2)Co_(17)system,while Cr only increases the total magnetic moment.More importantly,doping with Cr,Mn and Fe within the doping co ntent range of9.8 at%<x<35.29 at% can simultaneously improve the structural stability,total magnetic moment and magnetocrystalline anisotropy energy of the Sm_(2)Co_(17) system.Our study provides valuable theoretical guidance for experimental exploration and is expected to promote the development and application of novel rare-earth permanent magnetic materials.
基金National Natural Science Foundation of China (No. 52274403)。
文摘The mechanical,thermodynamic properties and electrical conductivities of L1_(2)-Al_(3)X(X=Zr,Sc,Er,Yb,Hf)structural phases in aluminum conductors were investigated through a first-principles study.The results demonstrate that all structural phases have good alloy-forming ability and structural stability,where Al_(3)Zr is the most superior.Al_(3)Zr,Al_(3)Hf and Al_(3)Sc have enhanced shear and deformation resistance in comparison to other phases.Within the temperature range of 200−600 K,Al_(3)Er and Al_(3)Yb possess the greatest thermodynamic stability,followed by Al_(3)Hf,Al_(3)Zr and Al_(3)Sc.Al_(3)Er and Al_(3)Yb have higher thermodynamic stability than Al_(3)Hf,Al_(3)Zr and Al_(3)Sc.All structural phases exhibit substantial metallic properties,indicating their good electrical conductivity.The electrical conductivities of Al_(3)Hf and Al_(3)Zr are higher than those of Al_(3)Er,Al_(3)Yb and Al_(3)Sc.The covalent bond properties in Al_(3)Sc,Al_(3)Er and Al_(3)Yb enhance the hardness,brittleness and thermodynamic stability of the structural phase.The thermodynamic stability of Al_(3)Sc is significantly reduced by ionic bonds.
基金Project supported by the National Key Research and Development Program of China(Grant Nos.2017YFE0302400 and 2017YFA0402803)the National Nature Science Foundation of China(Grant Nos.11735015,52071314,51871207,U1832206,12075274,U1967211,52171084)Hefei Advanced Computing Center。
文摘Oxidation corrosion of steels usually occurs in contact with the oxygen-contained environment, which is accelerated by high oxygen concentration and irradiation. The oxidation mechanism of steels is investigated by the adsorption/solution of oxygen atoms on/under body-centered-cubic(bcc) iron surfaces, and diffusion of oxygen atoms on the surface and in the near-surface region. Energetic results indicate that oxygen atoms prefer to adsorb at hollow and long-bridge positions on the Fe(100) and(110) surfaces, respectively. As the coverage of oxygen atoms increases, oxygen atoms would repel each other and gradually dissolve in the near-surface and bulk region. As vacancies exist, oxygen atoms are attracted by vacancies, especially in the near-surface and bulk region. Dynamic results indicate that the diffusion of O atoms on surfaces is easier than that into near-surface, which is affected by oxygen coverage and vacancies. Moreover, the effects of oxygen concentration and irradiation on oxygen density in the near-surface and bulk region are estimated by the Mc Lean’s model with a simple hypothesis.
基金financially supported by the National Natural Science Foundation of China(Grant No.51825101)the National Key Research and Development Program of China(Grant No.2016YFB0701201)。
文摘The paper reports on the atomic investigation aboutβphase in Mg_(96)Gd_(2)Y_(1)Ni_(1) alloy by using the first-principles study and the high-angle annular dark-field scanning transmission electron microscope(HAADF-STEM)corrected by atomic Cs.By using HAADF-STEM,the rectangularβphases were observed in the underage and peak aging stages in Mg_(96)Gd_(2)Y_(1)Ni_(1) alloy.Theβphase could be precipitated from the previously precipitatedβphase,and theβphase grew in steps when it was precipitated.A special transition structure of three atomic layer thicknesses was first observed at the edge of theβphase and the structure of this interface is probably as theβ/Mg_(1) interface for the analysis of thermodynamic characterization and electronic characterization.Theβ'phase and theβ_(H) structure were precipitated only at the edge of the length directions of theβphase.Theβ'phase continues to grow into aβphase directly without the formation ofβ_(1) phase,resulting in an increase in the length of theβphase,which is discovered for the first time.
基金Project(u0837601)supported by the National Natural Science Foundation of China
文摘First-principles calculations were carried out to investigate the structural stabilities and electronic properties of RhZr.The plane wave based pseudopotential method was used,in which both the local density approximation（LDA） and the generalized gradient approximation（GGA） implanted in the CASTEP code were employed.The internal positions of atoms in the unit cell were optimized and the ground state properties such as lattice parameter,density of state,cohesive energies and enthalpies of formation of ortho-RhZr and cubic-RhZr were calculated.The calculation results indicate that ortho-RhZr can form more easily than cubic-RhZr and the ortho-RhZr is more stable than cubic-RhZr.The density of states（DOS） reveals that the strong bonding in the Rh-Zr and Rh-Rh or Zr-Zr interaction chains accounts for the structural stability of ortho-RhZr and the hybridization between Rh-4d states and Zr-4d states is strong.
基金Project(50871065) supported by the National Natural Science Foundation of ChinaProjects(08DJ1400402,09JC1407200,10DZ2290904) supported by the Science and Technology Committee of Shanghai Municipality,China
文摘The first-principles method based on the projector augmented wave method within the generalized gradient approximation was employed to calculate the superlattice intrinsic stacking fault（SISF） and complex stacking fault（CSF） energies of the binary Ni3Al alloys with different Al contents and the ternary Ni3Al intermetallic alloys with addition of alloying elements,such as Pd,Pt,Ti,Mo,Ta,W and Re.The results show that the energies of SISF and CSF increase significantly with increase of Al contents in Ni3Al.Addition of Pd and Pt occupying the Ni sublattices does not change the SISF and CSF energies of Ni3Al markedly in comparison with the Ni-23.75Al alloy.While addition of alloying elements,such as Ti,Mo,Ta,W and Re,occupying the Al sublattices dramatically increases the SISF and CSF energies of Ni3Al.The results suggest that the energies of SISF and CSF are dependent both on the Al contents and on the site occupancy of the ternary alloying element in Ni3Al intermetallic alloys.
基金Project (200805321032) supported by Doctoral Fund of Ministry of Education of ChinaProject (51071065) supported by the National Natural Science Foundation of ChinaProject (71075003) supported by the Science Fund of State Key Laboratory of Advanced Design and Manufacturing for Vehicle Body, China
文摘The electronic structures and mechanical properties of Al4Sr, Mg2Sr and Mg23Sr6 phases were determined by the use of first-principles calculations. The calculated heat of formation and cohesive energy indicate that Al4Sr has the strongest alloying ability as well as the highest structural stability. The elastic parameters were calculated, and then the bulk modulus, shear modulus, elastic modulus and Poisson ratio were derived. The ductility and plasticity were discussed. The results show that Al4Sr and Mg2Sr phases both are ductile, on the contrary, Mg23Sr6 is brittle, and among the three phases, Mg2Sr is a phase with the best plasticity.
基金Project(Z2006F07)supported by Natural Science Foundation of Shandong Province,China
文摘The structure,stability and elastic properties of di-transition-metal carbides TixV1-xC were investigated by using the first-principles with a pseudopotential plane-waves method.The results show that the equilibrium lattice constants of TixV1-xC show a nearly linear reduction with increasing addition of V.The elastic properties of TixV1-xC are varied by doping with V.The bulk modulus of Ti0.5V0.5C is larger than that of pure TiC,as well as Ti0.5V0.5C has the largest C44 among TixV1-xC（0≤x≤1）,indicating that Ti0.5V0.5C has higher hardness than pure TiC.However,Ti0.5V0.5C presents brittleness based on the analysis of ductile/brittle behavior.The Ti0.5V0.5C carbide has the lowest formation energy,indicating that Ti0.5V0.5C is more stable than all other alloys.
基金Project (2009AA05Z105) supported by the High-tech Research and Development Program of ChinaProject (20102173) supported by the Natural Science Foundation of Liaoning Province,China
文摘A first-principles study was reported based on density functional theory of hydrogen vacancy,metal dopants,metal dopant-vacancy complex in LiBH4,a promising material for hydrogen storage.The formation of H vacancy and metal doping in LiBH4 is difficult,and their concentrations are low.The presence of one kind of defect is helpful to the formation of other kind of defect.Based on the analysis of electronic structure,the improvement of the dehydrogenating kinetics of LiBH4 by metal catalysts is due to the weaker bonding of B—H and the new metal-like system,which makes H atom diffuse easily;H vacancy accounts for a trace amount of BH3 release during the decomposing process of LiBH4;metal dopant weakens the strength of B—H bonds,which reduces the dehydriding temperature of LiBH4.The roles of metal and vacancy in the metal dopant-vacancy complex can be added in LiBH4 system.
文摘The origins of magnetism in transition-metal doped Na0.5Bi0.5TiO3 system are investigated by ab initio calculations. The calculated results indicate that a transition-metal atom sub- stitution for a Ti atom produces magnetic moments, which are due to the spin-polarization of transition-metal 3d electrons. The characteristics of exchange coupling are also calculated, which shows that in Cr-/Mn-/Fe-/Co- doped Na0.5Bi0.5TiO3 system, the antiferromagnetic coupling is favorable. The results can successfully explain the experimental phenomenon that, in Mn-/Fe- doped Nao.sBio.sTiO3 system, the ferromagnetism disappears at low tem- perature and the paramagnetic component becomes stronger with the increase of doping concentration of Mn/Fe/Co ions. Unexpectedly, we find the Na0.5Bi0.5Ti0.67V0.33iO3 sys- tem with ferromagnetic coupling is favorable and produces a magnetic moment of 2.00 P-B, which indicates that low temperature ferromagnetism materials could be made by intro- ducing V atoms in Na0.5Bi0.5TiO3. This may be a new way to produce low temperature multiferroic materials.
基金Supported by the National Natural Science Foundation of China under Grant Nos 11372085 and 10902029the Shenzhen Science and Technology Project under Grant No JCYJ20150625142543461
文摘The impacts of strain and polar discontinuities on the performance of superlattices have attracted widespread attention. Using first-principles calculation, we study the polarization and piezoelectricity of PbTiO3/KTa03 （PTO//KTO） superl^ttices with strain and polsr discontinuities. The strain caused by lattice mismatch between the superlattice and the substrate induces lattice distortion, the displacement of each atom and dynamical charge transfer between the Ti atom or Ta atom and the 0 atoms in the PTO//KTO superlattice. With more compressive or less tensile strain, the polarization value increases linearly, piezoelectric tensor e31 （e32） increases while e33 and e25 （e16） increase negatively. Polarity discontinuity caused by the interracial charge will produce large irreversible polarization. Proved by F-point phonons of PTO//KTO superlattices of different strain values, the polar discontinuity and the piezoelectric properties are just weakly dependent on temperature as found in PTO//KTO superlattices.
基金Supported by the National Natural Science Foundation of China under Grant No 61674073the Science and Technology Planning Project of Guangdong Province under Grant No 2017A050506056+1 种基金the Key Basic and Applied Research Project of Guangdong Province under Grant No 2016KZDXM021the Project of International as well as Hongkong,Macao and Taiwan Science and Technology Cooperation Innovation Platform in Universities in Guangdong Province under Grant No 2015KGJHZ028
文摘Doping is an effective approach for improving the photovoltaic performance of Cu2 ZnSnS4（CZTS）. The doping by substitution of Cu atoms in CZTS with Li and Ag atoms is investigated using density functional theory. The results show that the band gaps of Li（2 x）Cu2（1-x）ZnSnS4 and Ag（2 x）Cu2（1-x）ZnSnS4 can be tuned in the ranges of 1.30-3.43 and 1.30-1.63 eV, respectively. The calculation also reveals a phase transition from kesterite to wurtzite-kesterite for Li（2 x）Cu2（1-x）ZnSnS4 as x is larger than 0.9. The tunable band gaps of Li（2 x）Cu2（1-x）ZnSnS4 and Ag（2 x）Cu2（1-x） ZnSnS4 make them beneficial for achieving band-gap-graded solar cells.
