Angle-resolved Photoemission Spectra Research Articles

Computational method for angle-resolved photoemission spectra from repeated-slab band structure calculations

Computational method for angle-resolved photoemission spectra from repeated-slab band structure calculations

Order parameter and spectral function in d -wave holographic superconductors

We consider the d-wave holographic superconductor model with full backreaction on the metric, addressing a missing part in the literature. We have identified the gap function by comparing the fermionic spectral function with the momentum-dependent order parameter. By numerical investigations of the fermionic spectral function in the presence of a tensor condensate, we find the Fermi arc and the gapped behavior, which closely resembles angle resolved photoemission spectrum data. Moreover, we have examined the influence of the coupling constant, chemical potential, and temperature on the spectral function. We find that d-wave fermionic spectral function can be obtained through px and py condensates combined with two fermion flavors. Similarly, combining dx2−y2 and dxy orbitals symmetry with two fermion flavors leads to a g-wave spectral function. Published by the American Physical Society 2024

Observation of time-reversal symmetry breaking in the band structure of altermagnetic RuO2.

Altermagnets are an emerging elementary class of collinear magnets. Unlike ferromagnets, their distinct crystal symmetries inhibit magnetization while, unlike antiferromagnets, they promote strong spin polarization in the band structure. The corresponding unconventional mechanism of time-reversal symmetry breaking without magnetization in the electronic spectra has been regarded as a primary signature of altermagnetism but has not been experimentally visualized to date. We directly observe strong time-reversal symmetry breaking in the band structure of altermagnetic RuO2 by detecting magnetic circular dichroism in angle-resolved photoemission spectra. Our experimental results, supported by ab initio calculations, establish the microscopic electronic structure basis for a family of interesting phenomena and functionalities in fields ranging from topological matter to spintronics, which are based on the unconventional time-reversal symmetry breaking in altermagnets.

Two-dimensional heavy fermions in the van der Waals metal CeSiI.

Heavy-fermion metals are prototype systems for observing emergent quantum phases driven by electronic interactions1-6. A long-standing aspiration is the dimensional reduction of these materials to exert control over their quantum phases7-11, which remains a significant challenge because traditional intermetallic heavy-fermion compounds have three-dimensional atomic and electronic structures. Here we report comprehensive thermodynamic and spectroscopic evidence of an antiferromagnetically ordered heavy-fermion ground state in CeSiI, an intermetallic comprising two-dimensional (2D) metallic sheets held together by weak interlayer van der Waals (vdW) interactions. Owing to its vdW nature, CeSiI has a quasi-2D electronic structure, and we can control its physical dimension through exfoliation. The emergence of coherenthybridization of f and conduction electrons at low temperature is supported by the temperature evolution of angle-resolved photoemission and scanning tunnelling spectra near the Fermi level andby heat capacity measurements. Electrical transport measurements on few-layer flakes reveal heavy-fermion behaviour and magnetic order down to the ultra-thin regime. Our work establishes CeSiI and related materials as a unique platform for studying dimensionally confined heavy fermions in bulk crystals and employing 2D device fabrication techniques and vdW heterostructures12 to manipulate the interplay between Kondo screening, magnetic order and proximity effects.

Removing grid structure in angle-resolved photoemission spectra via deep learning method

Spectroscopic data may often contain unwanted extrinsic signals. For example, in the angle-resolved photoemission spectroscopy (ARPES) experiment, a wire mesh is typically placed in front of the charge-coupled device to block stray photoelectrons but could cause a gridlike structure in the spectra during quick measurement mode. In the past, this structure was often removed using the mathematical Fourier filtering method by erasing the periodic structure. However, this method may lead to information loss and vacancies in the spectra because the grid structure is not strictly linearly superimposed. Here, we propose a deep learning method to overcome this problem effectively. Our method takes advantage of the self-correlation information within the spectra themselves and can greatly optimize the quality of the spectra while removing the grid structure and noise simultaneously. It has the potential to be extended to all spectroscopic measurements to eliminate other extrinsic signals and enhance the spectral quality based on the self-correlation of the spectra solely.

Single crystal growth of topological semimetals and magnetic topological materials

Topological materials have attracted much attention due to their novel physical properties. These materials can not only serve as a platform for studying the fundamental physics, but also demonstrate a significant potential application in electronics, and they are studied usually in two ways. One is to constantly explore new experimental phenomena and physical problems in existing topological materials, and the other is to predict and discover new topological material systems and carry out synthesis for further studies. In a word, high-quality crystals are very important for studying quantum oscillations, angle resolved photoemission spectra or scanning tunneling microscopy. In this work, the classifications and developments of topological materials, including topological insulators, topological semimetals, and magnetic topological materials, are introduced. As usually employed growth methods in growing topological materials, flux and vapour transport methods are introduced in detail. Other growth methods, such as Bridgman, float-zone, vapour deposition and molecular beam epitaxy methods, are also briefly mentioned. Then the details about the crystal growth of some typical topological materials, including topological insulators/semimetals, high Chern number chiral topological semimetals and magnetic topological materials, are elaborated. Meanwhile, the identification of crystal quality is also briefly introduced, including the analysis of crystal composition and structure, which are greatly important.

Single crystal growth of topological semimetals and magnetic topological materials

Topological materials have attracted much attention due to their novel physical properties. These materials can not only serve as a platform for studying the fundamental physics, but also demonstrate a significant potential application in electronics, and they are studied usually in two ways. One is to constantly explore new experimental phenomena and physical problems in existing topological materials, and the other is to predict and discover new topological material systems and carry out synthesis. In a word, high-quality crystals are very important for studying quantum oscillations, angle resolved photoemission spectra or scanning tunneling microscopy. In this work, the classifications and developments of topological materials, including topological insulators, topological semimetals, and magnetic topological materials, are introduced. As usually employed growth methods in growing topological materials, flux and vapour transport methods are introduced in detail. Other growth methods, such as Bridgman, float-zone, vapour deposition and molecular beam epitaxy methods, are also briefly mentioned. Then the details about the crystal growth of some typical topological materials, including topological insulators/semimetals, high Chern number chiral topological semimetals and magnetic topological materials, are elaborated. Meanwhile, the identification of crystal quality is also briefly introduced, including the analysis of crystal composition and structure, which are greatly important.

Observation of electronic structure replicas in photoemission spectra of graphite upon adsorption of tin phthalocyanine

Cone-type bands near the center of the surface Brillouin zone were observed in low-energy angle-resolved photoemission spectra of tin phthalocyanine adsorbed on graphite. Simulations in comparison with the experimental data show that the spectral features represent replicas of the electronic structure of graphite near resulting from high-order momentum transfer processes up to the fourth order owing to the interaction of substrate electrons with the long-range structural order of the adsorbate overlayer. The analysis of time-resolved photoemission data from one of the replicas yields a quantitative and very good agreement with previous studies on the excited carrier dynamics in the Dirac cones of graphite and graphene.

Fabrication of honeycomb AuTe monolayer with Dirac nodal line fermions

Two-dimensional honeycomb lattices show great potential in the realization of Dirac nodal line fermions (DNLFs). Here, we successfully synthesized a gold telluride (AuTe) monolayer by direct tellurizing an Au(111) substrate. Low energy electron diffraction measurements reveal that it is (2×2) AuTe layer stacked onto (3×3) Au(111) substrate. Moreover, scanning tunneling microscopy images show that the AuTe layer has a honeycomb structure. Scanning transmission electron microscopy reveals that it is a single-atom layer. In addition, first-principles calculations demonstrate that the honeycomb AuTe monolayer exhibits Dirac nodal line features protected by mirror symmetry, which is validated by angle-resolved photoemission spectra. Our results establish that monolayer AuTe can be a good candidate to investigate 2D DNLFs and provides opportunities to realize high-speed low-dissipation devices.

Fourier-based methods for removing mesh anomalies from angle resolved photoemission spectra

Recent improvements to spatial resolution in angle-resolved photo-emission spectroscopy (ARPES) have made it common to perform measurements with a very brief dwell time, for the purpose of mapping the spectral function over large surface regions. However, rapid measurement modalities can suffer a grid-like intensity modulation due to a wire mesh that is typically placed in front of the ARPES detector to block stray electrons. Here, we explore Fourier-based methods that can effectively remove this artifact, and improve the quality of ARPES images obtained in rapid scanning modes. An open source software package is provided containing implementations of demonstrated algorithms.

Observation and theory of strong circular dichroism in angle-revolved photoemission from graphite

Experimental angle-resolved photoemission spectra (ARPES) and its circular dichroism (CD) from a graphite surface are reported together with calculations in the one-step model of photoemission. For photoelectrons emitted with surface parallel momentum k∥ perpendicular to the incoming light, a strong and complex CD signal is observed and analyzed along the Γ-K and Γ-M lines of the Brillouin zone. Calculations using real-space multiple scattering theory agree well with the data both for the total ARPES and the CD intensity maps. In the independent atomic approximation, i.e. when photoelectron scattering is neglected, the total ARPES intensity map is still well described, but not the CD. We find that photoelectron scattering makes a large contribution to the CD signal and may change its sign. Moreover, the CD of the bands depends strongly on photon energy, while this is much less the case for the total ARPES intensity. The present findings show that an accurate description of the photoemission final state, including photoelectron scattering effects, is crucial for understanding the CD in ARPES from surfaces and two-dimensional materials.

Hydrogen Spillover and Storage on Graphene with Single-Site Ti Catalysts

Hydrogen spillover and storage for single-site metal catalysts, including single-atom catalysts (SACs) and single nanocluster catalysts, have been elucidated for various supports but remain poorly understood for inert carbon supports. Here, we use synchrotron radiation-based methods to investigate the role of single-site Ti catalysts on graphene for hydrogen spillover and storage. Our in-situ angle-resolved photoemission spectra results demonstrate a bandgap opening and the X-ray absorption spectra reveal the formation of C-H bonds, both indicating the partial graphene hydrogenation. With increasing Ti deposition and H2 exposure, the Ti atoms tend to aggregate to form nanocluster catalysts and yield 13.5% sp3-hybridized carbon atoms corresponding to a hydrogen-storage capacity of 1.11 wt% (excluding the weight of the Ti nanoclusters [1]). Our results demonstrate how a simple spillover process at Ti SACs can lead to covalent hydrogen bonding on graphene, thereby providing a strategy for a rational design of carbon-supported single-site catalysts.

Thickness dependent band structure of α-bismuthene grown on epitaxial graphene

Along with the great interest in two-dimensional elemental materials that has emerged in recent years, atomically thin layers of bismuth have attracted attention due to physical properties on account of a strong spin–orbit coupling. Thickness dependent electronic band structure must be explored over the whole Brillouin zone in order to further explore their topological electronic properties. The anisotropic band structures along zig-zag and armchair directions of α-bismuthene (α-Bi) were resolved using the two-dimensional mapping of angle-resolved photoemission spectra. An increase in the number of layers from 1- to 2-bilayers (BLs) shifts the top of a hole band on line to high wavenumber regions. Subsequently, an electron pocket on line and a hole pocket centred at point appears in the 3 BL α-Bi. Gapless Dirac-cone features with a large anisotropy were clearly resolved on point in the 1-BL and 2-BL α-Bi, which can be attributed to the strong spin–orbit coupling and protection by the nonsymmorphic symmetry of the α-Bi lattice.

Two-orbital model for possible superconductivity pairing mechanism in nickelates

The newly synthesized strontium doped $R{\mathrm{NiO}}_{2}$ ($R$=Nd, Pr, and La) superconductors have stimulated extensive interests in understanding their pairing mechanism and pairing nature. Here we study the pairing mechanism in this family from a two-orbital model comprising the Ni- $3{d}_{{x}^{2}\ensuremath{-}{y}^{2}}$ and $3{d}_{xy}$ orbitals, equipped with extended Hubbard interactions and induced low-energy effective superexchange interactions. We then study the pairing symmetry in this system by using large scale variational Monte Carlo approach. Our results yield the intraorbital ${d}_{{x}^{2}\ensuremath{-}{y}^{2}}$-wave singlet pairing as the leading pairing symmetry in the nickelates, which is analogous to the cuprates. However, there exist two important differences between the physical properties of the two families due to the fact that at the low Sr-doping regime, while the Ni-$3{d}_{{x}^{2}\ensuremath{-}{y}^{2}}$ orbitals remain half-filled and singlyins occupied to form a Mott-insulating background, the Ni-$3{d}_{xy}$ orbitals accommodate nearly all the extra doped holes, which move freely on this background. The first difference lies in the single-particle aspect: while the $3{d}_{{x}^{2}\ensuremath{-}{y}^{2}}$ degree of freedom remains Mott insulating with spectra weight pinned down at zero at low dopings, the $3{d}_{xy}$ one behaves as Fermi liquid with spectra weight near 1. The second difference lies in the pairing aspect: while the huge intra-$3{d}_{{x}^{2}\ensuremath{-}{y}^{2}}$-orbital pairing gap is actually a pseudogap which has nothing to do with the SC, the small intra-$3{d}_{xy}$-orbital pairing gap serves as the true superconducting pairing gap, which is related to the ${T}_{c}$ via the BCS relation. Both differences can be verified by the angle-resolved photoemission spectrum.

Thickness-dependent topological phase transition and Rashba-like preformed topological surface states of α-Sn(001) thin films on InSb(001)

Topological materials, possessing spin-momentum locked topological surface states (TSS), have attracted much interest due to their potential applications in spintronics. \ensuremath{\alpha}-phase Sn (\ensuremath{\alpha}-Sn), being one of them, displays enriched topological phases via band-gap engineering through a strain or confinement effect. In this work, we investigated the band evolution of in-plane compressively strained \ensuremath{\alpha}-Sn(001) thin films on InSb(001) in a wide range of thickness from 3 bilayers (BL) to 370 BL by combining angle-resolved photoemission spectra and first-principles calculations. Gapped surface states evolved to a linearly dispersive TSS at a critical thickness of 6 BL, indicating that the system undergoes a phase transition from topologically trivial to nontrivial. For films thicker than 30 BL, additional Rashba-like surface states (RSS) were identified. These RSS served as preformed TSS in another strain-induced topological phase transition. In thick films, 370-BL \ensuremath{\alpha}-Sn(001), so as to preclude the confinement effect in thin films, our results were consistent with a Dirac semimetal phase with Dirac nodes located along $\mathrm{\ensuremath{\Gamma}}--Z$. This thickness-dependent band-structure study deepens our understanding of topological phase transitions and the evolution of Dirac states. Furthermore, the coexistence of TSS and RSS in a Dirac semimetal \ensuremath{\alpha}-Sn might significantly enhance the potential for spintronic applications.

Temperature-independent localization of Ce 4f electrons in cerium monoarsenide

In order to reveal the valence state of Ce ions and the occupancy number of Ce 4f electrons versus temperature in cerium monoarsenide (CeAs), we perform an ab initio calculation by using a many-body scheme combing density functional theory (DFT) with dynamical mean field theory (DMFT), taking into account the spin-orbit coupling (SOC) interaction and on-site Coulomb repulsion between Ce 4f electrons. Results demonstrate that Ce 4f j=5/2 and j=7/2 manifolds exhibit the metallic and insulating characters, respectively, irrespective of temperature. Ce 4f-4f correlation, Ce 4f-conduction electrons hybridization, SOC interaction and final state effects yield a complicated spectrum function for CeAs. Coupling of 4f atomic configuration transition, hybridization and temperature does not change the localized Ce 4f regime in CeAs. Finally, momentum-resolved electronic spectrum function is also discussed for comparison with experimental angle-resolved photoemission spectrum (ARPES).

Mixed 5f atomic configurations in two polymorphic forms of uranium pentafluoride

A first principles calculation in this work is performed on two polymorphic forms of uranium pentafluoride (UF5) by using density functional theory (DFT) merging with dynamical mean-field theory (DMFT) scheme with spin–orbit coupling (SOC) and on-site Coulomb repulsion for correlation effect due to the incompletely filled U 5f orbitals. Calculation results suggest that U j = 5/2 and j = 7/2 manifolds both are in weakly correlated states in α and β phases UF5 and, Russel-Saunders (LS) coupling scheme is appropriate for U 5f electrons. Occupation probability analysis demonstrates that U ions are mostly composed of mixed atomic configurations 5f1, 5f2 and 5f3 with average occupation numbers of nf ∼ 2.002 and 1.862 for U 5f electrons in α and β phases UF5, respectively, mainly due to the complicated quantum mechanics processes including the dual nature of localized and itinerant U 5f electrons, as well as the flexible outer electronic configuration of U ions. Finally, we estimate the momentum-resolved electronic spectrum function (the so-called quasiparticle band structure) to compare with angle-resolved photoemission spectrum (ARPES).

Electronic structure of the intermediate-valence compound EuNi2P2 studied by soft x-ray photoemission spectroscopy

We carried out angle-resolved photoemission (ARPES) experiments using soft x rays to investigate the electronic structure of the intermediate-valence compound ${\mathrm{EuNi}}_{2}{\mathrm{P}}_{2}$. Both the ${\mathrm{Eu}}^{2+}$ and ${\mathrm{Eu}}^{3+}$ components arising from the $4{f}^{6}$ and $4{f}^{5}$ final states were observed in the valence spectra, directly confirming an intermediate-valence character of Eu ions. The three-dimensional band structure was studied by ARPES measurements, and the ARPES results were compared with calculations based on the density-functional theory for the non-4$f$ reference compounds ${\mathrm{SrNi}}_{2}{\mathrm{P}}_{2}$ and ${\mathrm{YNi}}_{2}{\mathrm{P}}_{2}$. We found that the ARPES spectra up to just below the Fermi level are better reproduced by the calculation of ${\mathrm{SrNi}}_{2}{\mathrm{P}}_{2}$ rather than that of ${\mathrm{YNi}}_{2}{\mathrm{P}}_{2}$. The heavy-fermion bands in ${\mathrm{EuNi}}_{2}{\mathrm{P}}_{2}$ are thus considered to be formed through the hybridization between the dispersive valence bands, which resemble those for ${\mathrm{SrNi}}_{2}{\mathrm{P}}_{2}$, and the ${\mathrm{Eu}}^{2+}$ components located at the very vicinity of the Fermi level.

Topological Proximity-Induced Dirac Fermion in Two-Dimensional Antimonene.

Antimonene is a promising two-dimensional (2D) material that is calculated to have a significant fundamental bandgap usable for advanced applications such as field-effect transistors, photoelectric devices, and the quantum-spin Hall (QSH) state. Herein, we demonstrate a phenomenon termed topological proximity effect, which occurs between a 2D material and a three-dimensional (3D) topological insulator (TI). We provide strong evidence derived from hydrogen etching on Sb2Te3 that large-area and well-ordered antimonene presents a 2D topological state. Delicate analysis with a scanning tunneling microscope of the evolutionary intermediates reveals that hydrogen etching on Sb2Te3 resulted in the formation of a large area of antimonene with a buckled structure. A topological state formed in the antimonene/Sb2Te3 heterostructure was confirmed with angle-resolved photoemission spectra and density-functional theory calculations; in particular, the Dirac point was located almost at the Fermi level. The results reveal that Dirac fermions are indeed realized at the interface of a 2D normal insulator (NI) and a 3D TI as a result of strong hybridization between antimonene and Sb2Te3. Our work demonstrates that the position of the Dirac point and the shape of the Dirac surface state can be tuned by varying the energy position of the NI valence band, which modifies the direction of the spin texture of Sb-BL/Sb2Te3 via varying the Fermi level. This topological phase in 2D-material engineering has generated a paradigm in that the topological proximity effect at the NI/TI interface has been realized, which demonstrates a way to create QSH systems in 2D-material TI heterostructures.

Correlation effect on electronic and lattice properties of cerium oxides: Insights from density functional theory to dynamical mean-field theory

In order to reveal static and dynamic correlation effect in Ce 2 O 3 and CeO 2 with an unified theoretical framework, we perform a first principles calculation on electronic and lattice properties of these two typical correlated systems using density functional theory (DFT) schemes as well as a many-body method merging DFT with dynamical mean field theory (DMFT), taking into account the spin–orbit coupling (SOC) interaction and on-site Coulomb repulsion between Ce 4 f states. Results show that ground state of Ce 2 O 3 is in the localized 4 f 1 atomic configuration, while CeO 2 is a mixed-valence n f = 0.82 correlated system, which are in agreement with recent theoretical calculations and experimental observations. Lattice parameters, bulk modulus and band gap are also consistent with other theoretical calculations and experimental values. In order to compare with experimental angle-resolved photoemission spectrum (ARPES), momentum-resolved electronic spectrum function is also discussed.