Pub Date : 2020-11-19DOI: 10.1103/PhysRevB.102.180103
Churen Gui, S. Dong
Nitride perovskites are supposed to exhibit excellent properties as oxide analogues and may even have better performance in specific fields for their more covalent characters. However, till now, very limited nitride perovskites have been reported. In this work, a nitride perovskite LaMoN$_3$ has been systematically studied by first-principles calculations. The most interesting physical property is its ferroelectric $R3c$ phase, which can be stabilized under a moderate hydrostatic pressure ($sim1.5$ GPa) and probably remain meta-stable under the ambient condition. Its ferroelectric polarization is considerable large, $80.3$ $mu$C/cm$^2$, driven by the nominal $4d^0$ rule of Mo$^{6+}$, and the covalent hybridization between Mo's $4d$ and N's $2p$ orbitals is very strong. Our calculation not only predicts a new ferroelectric material with prominent properties, but also encourages more studies on pressure engineering of functional nitrides.
{"title":"Pressure-induced ferroelectric phase of \u0000LaMoN3","authors":"Churen Gui, S. Dong","doi":"10.1103/PhysRevB.102.180103","DOIUrl":"https://doi.org/10.1103/PhysRevB.102.180103","url":null,"abstract":"Nitride perovskites are supposed to exhibit excellent properties as oxide analogues and may even have better performance in specific fields for their more covalent characters. However, till now, very limited nitride perovskites have been reported. In this work, a nitride perovskite LaMoN$_3$ has been systematically studied by first-principles calculations. The most interesting physical property is its ferroelectric $R3c$ phase, which can be stabilized under a moderate hydrostatic pressure ($sim1.5$ GPa) and probably remain meta-stable under the ambient condition. Its ferroelectric polarization is considerable large, $80.3$ $mu$C/cm$^2$, driven by the nominal $4d^0$ rule of Mo$^{6+}$, and the covalent hybridization between Mo's $4d$ and N's $2p$ orbitals is very strong. Our calculation not only predicts a new ferroelectric material with prominent properties, but also encourages more studies on pressure engineering of functional nitrides.","PeriodicalId":8467,"journal":{"name":"arXiv: Materials Science","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2020-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87103876","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-11-18DOI: 10.1103/PHYSREVB.103.054111
Ke Liao, Tong Shen, Xin-Zheng Li, A. Alavi, A. Grüneis
We study the structural and electronic properties of phase III of solid hydrogen using accurate many-electron theories and compare to state-of-the-art experimental findings. The atomic structures of phase III modelled by C2/c-24 crystals are fully optimized on the level of second-order perturbation theory, demonstrating that previously employed structures optimized on the level of approximate density functionals exhibit errors in the H$_2$ bond lengths that cause significant discrepancies in the computed quasi particle band gaps and vibrational frequencies compared to experiment. Using the newly optimized atomic structures, we study the band gap closure and change in vibrational frequencies as a function of pressure. Our findings are in good agreement with recent experimental observations and may prove useful in resolving long-standing discrepancies between experimental estimates of metallization pressures possibly caused by disagreeing pressure calibrations.
{"title":"Structural and electronic properties of solid molecular hydrogen from many-electron theories","authors":"Ke Liao, Tong Shen, Xin-Zheng Li, A. Alavi, A. Grüneis","doi":"10.1103/PHYSREVB.103.054111","DOIUrl":"https://doi.org/10.1103/PHYSREVB.103.054111","url":null,"abstract":"We study the structural and electronic properties of phase III of solid hydrogen using accurate many-electron theories and compare to state-of-the-art experimental findings. The atomic structures of phase III modelled by C2/c-24 crystals are fully optimized on the level of second-order perturbation theory, demonstrating that previously employed structures optimized on the level of approximate density functionals exhibit errors in the H$_2$ bond lengths that cause significant discrepancies in the computed quasi particle band gaps and vibrational frequencies compared to experiment. Using the newly optimized atomic structures, we study the band gap closure and change in vibrational frequencies as a function of pressure. Our findings are in good agreement with recent experimental observations and may prove useful in resolving long-standing discrepancies between experimental estimates of metallization pressures possibly caused by disagreeing pressure calibrations.","PeriodicalId":8467,"journal":{"name":"arXiv: Materials Science","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2020-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76542626","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-11-18DOI: 10.1103/PhysRevApplied.15.044051
A. Morozovska, E. Eliseev, H. Shevliakova, Y. Lopatina, G. Dovbeshko, M. Glinchuk, Yunseok Kim, Sergei V. Kalinin
Tunability of polar and semiconducting properties of low-dimensional transition metal dichalcogenides (TMDs) have propelled them to the forefront of fundamental and applied physical research. These materials can vary from non-polar to ferroelectric, and from direct-band semiconductor to metallic. However, in addition to classical controls such as composition, doping, and field effect in TMDs the additional degrees of freedom emerge due to the curvature-induced electron redistribution and associated changes in electronic properties. Here we numerically explore the elastic and electric fields, flexoelectric polarization and free charge density for a TMD nanoflake placed on a rough substrate with a sinusoidal profile of the corrugation using finite element modelling (FEM). Numerical results for different flake thickness and corrugation depth yield insight into the flexoelectric nature of the out-of-plane electric polarization and establish the unambiguous correlation between the polarization and static conductivity modulation caused by inhomogeneous elastic strains coupled with deformation potential and strain gradients, which evolve in TMD nanoflake due to the adhesion between the flake surface and corrugated substrate. We revealed a pronounced maximum at the thickness dependences of the electron and hole conductivity of MoS2 and MoTe2 nanoflakes placed on a metallic substrate, which opens the way for their geometry optimization towards significant improvement their polar and electronic properties, necessary for their advanced applications in nanoelectronics and memory devices.
{"title":"Correlation Between Corrugation-Induced Flexoelectric Polarization and Conductivity of Low-Dimensional Transition Metal Dichalcogenides","authors":"A. Morozovska, E. Eliseev, H. Shevliakova, Y. Lopatina, G. Dovbeshko, M. Glinchuk, Yunseok Kim, Sergei V. Kalinin","doi":"10.1103/PhysRevApplied.15.044051","DOIUrl":"https://doi.org/10.1103/PhysRevApplied.15.044051","url":null,"abstract":"Tunability of polar and semiconducting properties of low-dimensional transition metal dichalcogenides (TMDs) have propelled them to the forefront of fundamental and applied physical research. These materials can vary from non-polar to ferroelectric, and from direct-band semiconductor to metallic. However, in addition to classical controls such as composition, doping, and field effect in TMDs the additional degrees of freedom emerge due to the curvature-induced electron redistribution and associated changes in electronic properties. Here we numerically explore the elastic and electric fields, flexoelectric polarization and free charge density for a TMD nanoflake placed on a rough substrate with a sinusoidal profile of the corrugation using finite element modelling (FEM). Numerical results for different flake thickness and corrugation depth yield insight into the flexoelectric nature of the out-of-plane electric polarization and establish the unambiguous correlation between the polarization and static conductivity modulation caused by inhomogeneous elastic strains coupled with deformation potential and strain gradients, which evolve in TMD nanoflake due to the adhesion between the flake surface and corrugated substrate. We revealed a pronounced maximum at the thickness dependences of the electron and hole conductivity of MoS2 and MoTe2 nanoflakes placed on a metallic substrate, which opens the way for their geometry optimization towards significant improvement their polar and electronic properties, necessary for their advanced applications in nanoelectronics and memory devices.","PeriodicalId":8467,"journal":{"name":"arXiv: Materials Science","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2020-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90300176","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-11-18DOI: 10.1103/PhysRevMaterials.4.124002
Estelle Mazaleyrat, M. Pozzo, D. Alfé, A. Artaud, A. G. Gómez Herrero, S. Lisi, V. Guisset, P. David, C. Chapelier, J. Coraux
Transition metal surfaces catalyse a broad range of thermally-activated reactions involving carbon-containing-species -- from atomic carbon to small hydrocarbons or organic molecules, and polymers. These reactions yield well-separated phases, for instance graphene and the metal surface, or, on the contrary, alloyed phases, such as metal carbides. Here, we investigate carbon phases on a rhenium (0001) surface, where the former kind of phase can transform into the latter. We find that this transformation occurs with increasing annealing time, which is hence not suitable to increase the quality of graphene. Our scanning tunneling spectroscopy and reflection high-energy electron diffraction analysis reveal that repeated short annealing cycles are best suited to increase the lateral extension of the structurally coherent graphene domains. Using the same techniques and with the support of density functional theory calculations, we next unveil, in real space, the symmetry of the many variants (two six-fold families) of a rhenium surface carbide observed with diffraction since the 1970s, and finally propose models of the atomic details. One of these models, which nicely matches the microscopy observations, consists of parallel rows of eight aligned carbon trimers with a so-called $(7timessqrt{mathrm{19}})$ unit cell with respect to Re(0001).
{"title":"Structure of graphene and a surface carbide grown on the (0001) surface of rhenium","authors":"Estelle Mazaleyrat, M. Pozzo, D. Alfé, A. Artaud, A. G. Gómez Herrero, S. Lisi, V. Guisset, P. David, C. Chapelier, J. Coraux","doi":"10.1103/PhysRevMaterials.4.124002","DOIUrl":"https://doi.org/10.1103/PhysRevMaterials.4.124002","url":null,"abstract":"Transition metal surfaces catalyse a broad range of thermally-activated reactions involving carbon-containing-species -- from atomic carbon to small hydrocarbons or organic molecules, and polymers. These reactions yield well-separated phases, for instance graphene and the metal surface, or, on the contrary, alloyed phases, such as metal carbides. Here, we investigate carbon phases on a rhenium (0001) surface, where the former kind of phase can transform into the latter. We find that this transformation occurs with increasing annealing time, which is hence not suitable to increase the quality of graphene. Our scanning tunneling spectroscopy and reflection high-energy electron diffraction analysis reveal that repeated short annealing cycles are best suited to increase the lateral extension of the structurally coherent graphene domains. Using the same techniques and with the support of density functional theory calculations, we next unveil, in real space, the symmetry of the many variants (two six-fold families) of a rhenium surface carbide observed with diffraction since the 1970s, and finally propose models of the atomic details. One of these models, which nicely matches the microscopy observations, consists of parallel rows of eight aligned carbon trimers with a so-called $(7timessqrt{mathrm{19}})$ unit cell with respect to Re(0001).","PeriodicalId":8467,"journal":{"name":"arXiv: Materials Science","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2020-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72575313","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-11-17DOI: 10.1103/PHYSREVB.103.094407
D. M. Juraschek, Derek S. Wang, P. Narang
Coherent excitation of magnons is conventionally achieved through Raman scattering processes, in which the difference-frequency components of the driving field are resonant with the magnon energy. Here, we describe mechanisms by which the sum-frequency components of the driving field can be used to coherently excite magnons through two-particle absorption processes. We use the Landau-Lifshitz-Gilbert formalism to compare the spin-precession amplitudes that different types of impulsive stimulated and ionic Raman scattering processes and their sum-frequency counterparts induce in an antiferromagnetic model system. We show that sum-frequency mechanisms enabled by linearly polarized driving fields yield excitation efficiencies comparable or larger than established Raman techniques, while elliptical polarizations produce only weak and circularly polarizations no sum-frequency components at all. The mechanisms presented here complete the map for dynamical spin control by the means of Raman-type processes.
{"title":"Sum-frequency excitation of coherent magnons","authors":"D. M. Juraschek, Derek S. Wang, P. Narang","doi":"10.1103/PHYSREVB.103.094407","DOIUrl":"https://doi.org/10.1103/PHYSREVB.103.094407","url":null,"abstract":"Coherent excitation of magnons is conventionally achieved through Raman scattering processes, in which the difference-frequency components of the driving field are resonant with the magnon energy. Here, we describe mechanisms by which the sum-frequency components of the driving field can be used to coherently excite magnons through two-particle absorption processes. We use the Landau-Lifshitz-Gilbert formalism to compare the spin-precession amplitudes that different types of impulsive stimulated and ionic Raman scattering processes and their sum-frequency counterparts induce in an antiferromagnetic model system. We show that sum-frequency mechanisms enabled by linearly polarized driving fields yield excitation efficiencies comparable or larger than established Raman techniques, while elliptical polarizations produce only weak and circularly polarizations no sum-frequency components at all. The mechanisms presented here complete the map for dynamical spin control by the means of Raman-type processes.","PeriodicalId":8467,"journal":{"name":"arXiv: Materials Science","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2020-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90940551","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-11-17DOI: 10.1103/PHYSREVB.103.085138
Xinlei Zhao, P. Guo, Fengjie Ma, Zhong-yi Lu
Magnetic topological quantum materials have attracted great attention due to their exotic topological quantum physics induced by the interplay among crystalology, magnetism, and topology, which is of profound importance to fundamental research and technology applications. However, limited materials are experimentally available, most of whom are realized by magnetic impurity doping or heterostructural constructions. In this work, based on the first-principles calculations, we predict that double perovskite Ba2CdReO6 is an intrinsic ferromagnetic topological semi-half-metal, while the ferrimagnetic double perovskite with space group symmetry Fm-3m, such as Ba2FeMoO6, belongs to topological half-metal. One pair of Weyl points and fully spin-polarized nodal-ring states are found in the vicinity of the Fermi level in Ba2CdReO6. Its two-dimensional nearly flat drumhead surface states are fully spin-polarized. In Ba2FeMoO6, however, there exist four pairs of Weyl points and two fully spin-polarized nodal-rings near the Fermi level. These topological properties are stable in the presence of spin-orbit coupling. This makes these materials be an appropriate platform for studying the emerging intriguing properties, especially for the applications in spintronics, information technology, and topological superconductivity.
{"title":"Coexistence of topological Weyl and nodal-ring states in ferromagnetic and ferrimagnetic double perovskites","authors":"Xinlei Zhao, P. Guo, Fengjie Ma, Zhong-yi Lu","doi":"10.1103/PHYSREVB.103.085138","DOIUrl":"https://doi.org/10.1103/PHYSREVB.103.085138","url":null,"abstract":"Magnetic topological quantum materials have attracted great attention due to their exotic topological quantum physics induced by the interplay among crystalology, magnetism, and topology, which is of profound importance to fundamental research and technology applications. However, limited materials are experimentally available, most of whom are realized by magnetic impurity doping or heterostructural constructions. In this work, based on the first-principles calculations, we predict that double perovskite Ba2CdReO6 is an intrinsic ferromagnetic topological semi-half-metal, while the ferrimagnetic double perovskite with space group symmetry Fm-3m, such as Ba2FeMoO6, belongs to topological half-metal. One pair of Weyl points and fully spin-polarized nodal-ring states are found in the vicinity of the Fermi level in Ba2CdReO6. Its two-dimensional nearly flat drumhead surface states are fully spin-polarized. In Ba2FeMoO6, however, there exist four pairs of Weyl points and two fully spin-polarized nodal-rings near the Fermi level. These topological properties are stable in the presence of spin-orbit coupling. This makes these materials be an appropriate platform for studying the emerging intriguing properties, especially for the applications in spintronics, information technology, and topological superconductivity.","PeriodicalId":8467,"journal":{"name":"arXiv: Materials Science","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2020-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77828771","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
T. Scheike, Q. Xiang, Z. Wen, H. Sukegawa, T. Ohkubo, K. Hono, S. Mitani
Giant tunnel magnetoresistance (TMR) ratios of 417% at room temperature (RT) and 914% at 3 K were demonstrated in epitaxial Fe/MgO/Fe(001) exchanged-biased spin-valve magnetic tunnel junctions (MTJs) by tuning growth conditions for each layer, combining sputter deposition for the Fe layers, electron-beam evaporation of the MgO barrier, and barrier interface tuning. Clear TMR oscillation as a function of the MgO thickness with a large peak-to-valley difference of ~80% was observed when the layers were grown on a highly (001)-oriented Cr buffer layer. Specific features of the observed MTJs are symmetric differential conductance (dI/dV) spectra for the bias polarity and plateau-like deep local minima in dI/dV (parallel configuration) at |V| = 0.2~0.5 V. At 3K, fine structures with two dips emerge in the plateau-like dI/dV, reflecting highly coherent tunneling through the Fe/MgO/Fe. We also observed a 496% TMR ratio at RT by a 2.24-nm-thick-CoFe insertion at the bottom-Fe/MgO interface.
{"title":"Exceeding 400% tunnel magnetoresistance at room temperature in epitaxial Fe/MgO/Fe(001) spin-valve-type magnetic tunnel junctions","authors":"T. Scheike, Q. Xiang, Z. Wen, H. Sukegawa, T. Ohkubo, K. Hono, S. Mitani","doi":"10.1063/5.0037972","DOIUrl":"https://doi.org/10.1063/5.0037972","url":null,"abstract":"Giant tunnel magnetoresistance (TMR) ratios of 417% at room temperature (RT) and 914% at 3 K were demonstrated in epitaxial Fe/MgO/Fe(001) exchanged-biased spin-valve magnetic tunnel junctions (MTJs) by tuning growth conditions for each layer, combining sputter deposition for the Fe layers, electron-beam evaporation of the MgO barrier, and barrier interface tuning. Clear TMR oscillation as a function of the MgO thickness with a large peak-to-valley difference of ~80% was observed when the layers were grown on a highly (001)-oriented Cr buffer layer. Specific features of the observed MTJs are symmetric differential conductance (dI/dV) spectra for the bias polarity and plateau-like deep local minima in dI/dV (parallel configuration) at |V| = 0.2~0.5 V. At 3K, fine structures with two dips emerge in the plateau-like dI/dV, reflecting highly coherent tunneling through the Fe/MgO/Fe. We also observed a 496% TMR ratio at RT by a 2.24-nm-thick-CoFe insertion at the bottom-Fe/MgO interface.","PeriodicalId":8467,"journal":{"name":"arXiv: Materials Science","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2020-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91417472","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-11-17DOI: 10.1103/PhysRevB.103.184102
D. Rehn, C. Greeff, L. Burakovsky, D. Sheppard, S. Crockett
We perform density functional theory (DFT) calculations of five solid phases and the liquid phase of tin. The calculations include cold curves of the five solid phases, phonon calculations in the quasi-harmonic approximation over a range of volumes for each solid phase, and DFT-based molecular dynamics (DFT-MD) calculations of the liquid phase. Using the DFT results, we construct a tabular multiphase SESAME equation of state for tin, referred to as SESAME 2162. Comparisons to experimental data are made and show a high level of agreement in isobaric data, isothermal data, shock data, and phase boundary measurements, including measurements of the melt curve. The 2162 EOS will be useful for hydrodynamics simulations and has been designed with an eye toward hydrodynamics simulations that incorporate materials strength models and allow for modeling of the kinetics of phase transitions.
{"title":"Multiphase tin equation of state using density functional theory","authors":"D. Rehn, C. Greeff, L. Burakovsky, D. Sheppard, S. Crockett","doi":"10.1103/PhysRevB.103.184102","DOIUrl":"https://doi.org/10.1103/PhysRevB.103.184102","url":null,"abstract":"We perform density functional theory (DFT) calculations of five solid phases and the liquid phase of tin. The calculations include cold curves of the five solid phases, phonon calculations in the quasi-harmonic approximation over a range of volumes for each solid phase, and DFT-based molecular dynamics (DFT-MD) calculations of the liquid phase. Using the DFT results, we construct a tabular multiphase SESAME equation of state for tin, referred to as SESAME 2162. Comparisons to experimental data are made and show a high level of agreement in isobaric data, isothermal data, shock data, and phase boundary measurements, including measurements of the melt curve. The 2162 EOS will be useful for hydrodynamics simulations and has been designed with an eye toward hydrodynamics simulations that incorporate materials strength models and allow for modeling of the kinetics of phase transitions.","PeriodicalId":8467,"journal":{"name":"arXiv: Materials Science","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2020-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73909549","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-11-16DOI: 10.1103/physrevb.102.205136
H. Fukuyama, M. Ogata
Lee, Rice and Anderson, in their monumental paper, have proved the existence of a collective mode describing the coupled motion of electron density and phonons in one-dimensional incommensurate charge density wave (CDW) in the Peierls state. This mode, which represents the coherent sliding motion of electrons and lattice distortions and affects low energy transport properties, is described by the phase of the complex order parameter of the Peierls condensate, leading to Frohlich superconductivity in pure systems. Once spatial disorder is present, however, phason is pinned and system is transformed into an insulating ground state: a dramatic change. Since phason can be considered as an ultimate of phonon drag effect, it is of interest to see its effects on thermoelectricity, which has been studied in the present paper based linear response theory of Kubo and Luttinger. The result indicates that a large absolute value of Seebeck coefficient proportional to the square root of resistivity is expected at low temperatures k_B T/Delta <<1 (Delta: Peierls gap) with opposite sign to the electronic contributions in the absence of Peierls gap.
{"title":"Theory of phason drag effect on thermoelectricity","authors":"H. Fukuyama, M. Ogata","doi":"10.1103/physrevb.102.205136","DOIUrl":"https://doi.org/10.1103/physrevb.102.205136","url":null,"abstract":"Lee, Rice and Anderson, in their monumental paper, have proved the existence of a collective mode describing the coupled motion of electron density and phonons in one-dimensional incommensurate charge density wave (CDW) in the Peierls state. This mode, which represents the coherent sliding motion of electrons and lattice distortions and affects low energy transport properties, is described by the phase of the complex order parameter of the Peierls condensate, leading to Frohlich superconductivity in pure systems. Once spatial disorder is present, however, phason is pinned and system is transformed into an insulating ground state: a dramatic change. Since phason can be considered as an ultimate of phonon drag effect, it is of interest to see its effects on thermoelectricity, which has been studied in the present paper based linear response theory of Kubo and Luttinger. The result indicates that a large absolute value of Seebeck coefficient proportional to the square root of resistivity is expected at low temperatures k_B T/Delta <<1 (Delta: Peierls gap) with opposite sign to the electronic contributions in the absence of Peierls gap.","PeriodicalId":8467,"journal":{"name":"arXiv: Materials Science","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2020-11-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88112065","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Bi$_2$Se$_3$, a layered three dimensional (3D) material, exhibits topological insulating properties due to presence of surface states and a band gap of 0.3 eV in the bulk. We study the effect hydrostatic pressure $P$ and doping with rare earth elements on the topological aspect of this material in bulk from a first principles perspective. Our study shows that under a moderate pressure of P$>$7.9 GPa, the bulk electronic properties show a transition from an insulating to a Weyl semi-metal state due to band inversion. This transition may be correlated to a structural transition from a layered material to a 3D system observed at $P$=7.9 GPa. At large $P$ density of states have significant value at the Fermi-energy. Intercalating Gd with a small doping fraction between Bi$_2$Se$_3$ layers drives the system to a metallic anti-ferromagnetic state, with Weyl nodes below the Fermi-energy. At the Weyl nodes time reversal symmetry is broken due to finite local field induced by large magnetic moments on Gd atoms. However, substituting Bi with Gd induces anti-ferromagnetic order with an increased direct band gap. Our studies provides novel approaches to tune topological transitions, particularly in capturing the elusive Weyl semimetal states, in 3D topological materials.
{"title":"Topological transitions to Weyl states in bulk Bi2Se3: Effect of hydrostatic pressure and doping","authors":"S. Saha, H. Banerjee, Manoranjan Kumar","doi":"10.1063/5.0038952","DOIUrl":"https://doi.org/10.1063/5.0038952","url":null,"abstract":"Bi$_2$Se$_3$, a layered three dimensional (3D) material, exhibits topological insulating properties due to presence of surface states and a band gap of 0.3 eV in the bulk. We study the effect hydrostatic pressure $P$ and doping with rare earth elements on the topological aspect of this material in bulk from a first principles perspective. Our study shows that under a moderate pressure of P$>$7.9 GPa, the bulk electronic properties show a transition from an insulating to a Weyl semi-metal state due to band inversion. This transition may be correlated to a structural transition from a layered material to a 3D system observed at $P$=7.9 GPa. At large $P$ density of states have significant value at the Fermi-energy. Intercalating Gd with a small doping fraction between Bi$_2$Se$_3$ layers drives the system to a metallic anti-ferromagnetic state, with Weyl nodes below the Fermi-energy. At the Weyl nodes time reversal symmetry is broken due to finite local field induced by large magnetic moments on Gd atoms. However, substituting Bi with Gd induces anti-ferromagnetic order with an increased direct band gap. Our studies provides novel approaches to tune topological transitions, particularly in capturing the elusive Weyl semimetal states, in 3D topological materials.","PeriodicalId":8467,"journal":{"name":"arXiv: Materials Science","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2020-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85860575","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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