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The properties of correlated electron materials are often intricately linked to Van Hove singularities (VHS) in the vicinity of the Fermi energy. The class of these VHS is of great importance, with higher-order ones—with power-law divergence in the density of states—leaving frequently distinct signatures in physical properties. We use a new theoretical method to detect and analyse higher-order VHS (HOVHS) in two-dimensional materials and apply it to the electronic structure of the surface layer of Sr2RuO4. We then constrain a low energy model of the VHS of the surface layer of Sr2RuO4 against angle-resolved photoemission spectroscopy and quasiparticle interference data to analyse the VHS near the Fermi level. We show how these VHS can be engineered into HOVHS. The density of states is an important quantity for a quantum material. Here, we demonstrate how singularities in the density of states can be characterized and engineered, combining the theoretical analysis of different experiments on the paradigmatic quantum material Sr2RuO4. [ABSTRACT FROM AUTHOR]

The amount of global plastic waste on land or in marine environments is a critical environmental issue. Plastic biodegradation by microorganisms, insect larvae, and enzymes has become one of the most popular solutions due to the ability of this strategy to generate environmentally benign byproducts, addressing ecological plastic waste concerns. This study revealed the biodegradation of ethylene vinyl acetate (EVA) by the bacterial strain identified as Klebsiella aerogenes EM011, isolated from effective microorganisms. The study found that K. aerogenes EM011 can survive in a carbon-free medium for 30 days using EVA films as the sole energy source, decomposing 0.65 ± 0.04% of 1 g of EVA film. The surface changes of the film were detected using scanning electron microscopy after treatment with K. aerogenes EM011. In addition, elemental modifications were detected in the imaged area of the plastic surfaces by energy-dispersive X-ray spectroscopy. Fourier-transform infrared spectroscopy and X-ray photoelectron spectroscopy analyses were conducted to detect changes in the functional groups and chemical components, elucidating alterations on the surface of the EVA films. Through these physicochemical analyses, the formation of carbonyl groups (C=O), ester groups (C–O), and hydroxyl groups (–OH) confirmed the oxidation of EVA. Furthermore, the oxidation led to the decomposition of the EVA film, resulting in changes in its thermal stability and molecular weight distribution. These findings show that the K. aerogenes EM011 strain plays a role in accelerating the biodegradation of EVA. [ABSTRACT FROM AUTHOR]

Obstructed atomic insulator is recently proposed as an unconventional material, in which electric charge centers localized at sites away from the atoms. A half-filling surface state would emerge at specific interfaces cutting through these charge centers and avoid intersecting any atoms. In this article, we utilized photoemission spectroscopy and density functional theory calculations to study one of the obstructed atomic insulator candidates, NiP2. A floating surface state with large effective mass that is close to the Fermi level and isolated from all bulk states is resolved on the (100) cleavage plane, implying better catalytic activity in this plane than the previously studied surfaces. Density functional theory calculation results elucidate that this floating surface state is originated from the obstructed Wannier charge centers, albeit underwent surface reconstruction. Our findings not only shed lights on the study of obstructed atomic insulators, but also provide possible route for development of new catalysts. [ABSTRACT FROM AUTHOR]

We report the synthesis of phosphorus (P)-doped reduced graphene oxide (P-rGO) using a hydrothermal method at 180°C for 7 h. Furthermore, the amorphous nature and phase purity of the hydrothermally synthesized P-rGO was studied by powder x-ray diffraction. The characteristic sheet-like surface structure of the P-rGO was confirmed by scanning electron microscopy. The presence of P in the P-rGO was authenticated by using energy-dispersive x-ray spectroscopy and photoelectron x-ray spectroscopy. The synthesized P-rGO was employed as a low-cost and Pt-free counter electrode material for the construction of dye-sensitized solar cells (DSSCs). The effect of annealing temperature on the construction of the DSSCs using P-rGO was also studied, and the highest power conversion efficiency of 6.3% and photocurrent density of 15.37 mA/cm2 were obtained at 200°C. The platinum counter electrode-based DSSCs exhibited the power conversion efficiency of 7.4%. The performance of the P-rGO counter electrode-based DSSCs was reasonable and can be further improved by developing novel device architectures. This work proposes the simple, eco-friendly, and Pt-free counter electrode for the construction of DSSCs with a decent performance. [ABSTRACT FROM AUTHOR]

Magnetic kagome materials provide a fascinating playground for exploring the interplay of magnetism, correlation and topology. Many magnetic kagome systems have been reported including the binary FemXn (X = Sn, Ge; m:n = 3:1, 3:2, 1:1) family and the rare earth RMn6Sn6 (R = rare earth) family, where their kagome flat bands are calculated to be near the Fermi level in the paramagnetic phase. While partially filling a kagome flat band is predicted to give rise to a Stoner-type ferromagnetism, experimental visualization of the magnetic splitting across the ordering temperature has not been reported for any of these systems due to the high ordering temperatures, hence leaving the nature of magnetism in kagome magnets an open question. Here, we probe the electronic structure with angle-resolved photoemission spectroscopy in a kagome magnet thin film FeSn synthesized using molecular beam epitaxy. We identify the exchange-split kagome flat bands, whose splitting persists above the magnetic ordering temperature, indicative of a local moment picture. Such local moments in the presence of the topological flat band are consistent with the compact molecular orbitals predicted in theory. We further observe a large spin-orbital selective band renormalization in the Fe d x y + d x 2 − y 2 spin majority channel reminiscent of the orbital selective correlation effects in the iron-based superconductors. Our discovery of the coexistence of local moments with topological flat bands in a kagome system echoes similar findings in magic-angle twisted bilayer graphene, and provides a basis for theoretical effort towards modeling correlation effects in magnetic flat band systems. Spectroscopic study on a kagome magnet thin film uncovers the local-moment nature of the magnetism in the presence of topological flat bands, as well as a strong spin- and orbital-selective electronic correlation effect. [ABSTRACT FROM AUTHOR]

Harnessing electronic excitations involving coherent coupling to bosonic modes is essential for the design and control of emergent phenomena in quantum materials. In situations where charge carriers induce a lattice distortion due to the electron-phonon interaction, the conducting states get "dressed", which leads to the formation of polaronic quasiparticles. The exploration of polaronic effects on low-energy excitations is in its infancy in two-dimensional materials. Here, we present the discovery of an interlayer plasmon polaron in heterostructures composed of graphene on top of single-layer WS2. By using micro-focused angle-resolved photoemission spectroscopy during in situ doping of the top graphene layer, we observe a strong quasiparticle peak accompanied by several carrier density-dependent shake-off replicas around the single-layer WS2 conduction band minimum. Our results are explained by an effective many-body model in terms of a coupling between single-layer WS2 conduction electrons and an interlayer plasmon mode. It is important to take into account the presence of such interlayer collective modes, as they have profound consequences for the electronic and optical properties of heterostructures that are routinely explored in many device architectures involving 2D transition metal dichalcogenides. Here, the authors report the observation of an interlayer plasmon polaron in heterostructures composed of graphene and monolayer WS2. This is manifested in the ARPES spectra as a strong quasiparticle peak accompanied by several carrier density-dependent shake-off replicas around the WS2 conduction band minimum. [ABSTRACT FROM AUTHOR]

Analogous to the condensation of Cooper pairs in superconductors, the Bose–Einstein condensation (BEC) of electron–hole pairs in semiconductors and semimetals leads to an emergence of an exotic ground state — the excitonic insulator state. In this paper, we study the electronic structure of 1T-TiSe2 utilizing angle-resolved photoemission spectroscopy and alkali-metal deposition. Alkali-metal adatoms are deposited in-situ on the sample surface, doping the system with electrons. The conduction bands of 1T-TiSe2 are thereby pushed down below the Fermi energy, which enables us to characterize its temperature dependence with precision. We found that the formation of the charge density wave (CDW) in 1T-TiSe2 at ~ 205 K is accompanied by a significant increase of the band gap, supporting the existence of excitonic pairing in the CDW state of 1T-TiSe2. More importantly, by analyzing the linewidth of the single-particle excitation spectrum, we unveiled an incoherence-to-coherence crossover at 165 K, which could be attributed to a possible exciton condensation that occurs beneath the CDW transition in 1T-TiSe2. Our results not only explain the exotic transport properties of 1T-TiSe2, but also highlight the possible existence of an excitonic condensate in this semiconducting material. Excitonic insulators remain a topic of great interest in condensed matter physics. Here, the authors provide spectroscopic evidence of increased electronic coherence in the charge-density-wave state of semiconducting 1T-TiSe2. [ABSTRACT FROM AUTHOR]

Charge transfer between molecules lies at the heart of many chemical processes. Here, we focus on the ultrafast electron dynamics associated with the formation of charge-transfer-to-solvent (CTTS) states following X-ray absorption in aqueous solutions of Na+, Mg2+, and Al3+ ions. To explore the formation of such states in the aqueous phase, liquid-jet photoemission spectroscopy is employed. Using the core-hole-clock method, based on Auger–Meitner (AM) decay upon 1s excitation or ionization of the respective ions, upper limits are estimated for the metal-atom electron delocalization times to the neighboring water molecules. These delocalization processes represent the first steps in the formation of hydrated electrons, which are determined to take place on a timescale ranging from several hundred attoseconds (as) below the 1s ionization threshold to only 20 as far above the 1s ionization threshold. The decrease in the delocalization times as a function of the photon energy is continuous. This indicates that the excited electrons remain in the vicinity of the studied ions even above the ionization threshold, i.e., metal-ion electronic resonances associated with the CTTS state manifolds are formed. The three studied isoelectronic ions exhibit quantitative differences in their electron energetics and delocalization times, which are linked to the character of the respective excited states. The authors investigate the X-ray-induced electron dynamics, on the sub-femtosecond timescale, of hydrated Na+, Mg2+, and Al3+ ions providing insights into the ultrafast charge-transfer processes in aqueous environments. [ABSTRACT FROM AUTHOR]

Understanding the mechanisms underlying a stable polarization at the surface of ferroelectric thin films is of particular importance both from a fundamental point of view and to achieve control of the surface polarization itself. In this study, we demonstrate that the X-ray standing wave technique allows the surface polarization profile of a ferroelectric thin film, as opposed to the average film polarity, to be probed directly. The X-ray standing wave technique provides the average Ti and Ba atomic positions, along the out-of-plane direction, near the surface of three differently strained thin films. This technique gives direct access to the local ferroelectric polarization at and below the surface. By employing X-ray photoelectron spectroscopy, a detailed overview of the oxygen-containing species adsorbed on the surface is obtained. The different amplitude and orientation of the local ferroelectric polarizations are associated with surface charges attributed to different type, amount and spatial distribution of the oxygen-containing adsorbates. [ABSTRACT FROM AUTHOR]

In present work, we investigated single-walled carbon nanotubes (SWCNTs) filled with nickelocene utilizing the gas phase method. We investigated the electronic properties of sorted metallic and semiconducting nickelocene-filled SWCNTs using angle-resolved photoemission spectroscopy. This allowed observing the variation of the Fermi level between different measurement angles, which is connected with the modification of the electronic properties of the nanotubes. The Fermi level varied significantly between nanotubes with different metallicity. This is explained by different effectivity of charge transfer in different samples due to different conductivity type, length of nickel clusters and homogeneity of filling of SWCNTs. [ABSTRACT FROM AUTHOR]

The experimental efficiency has been a central concern for time-consuming experiments. Spin- and angle-resolved photoemission spectroscopy (spin-resolved ARPES) is renowned for its inefficiency in spin-detection, despite its outstanding capability to directly determine the spin-polarized electronic properties of materials. Here, we investigate the potential enhancement of the efficiency of spin-resolved ARPES experiments through the integration of measurement informatics. We focus on a representative topological insulator Bi 2 Te 3 , which has well-understood spin-polarized electronic states. We employ Gaussian process regression (GPR) to assess the accumulation of spin polarization information using an indicator known as the GPR score. Our analyses based on the GPR model suggest that the GPR score can serve as a stopping criterion for spin-resolved ARPES experiments. This criterion enables us to conduct efficient spin-resolved ARPES experiments, significantly reducing the time costs by 5-10 times, compared to empirical stopping criteria. [ABSTRACT FROM AUTHOR]

Rich momentum-dependent electronic structure naturally arises in solids with long-range crystalline symmetry. Reliable and scalable quantum technologies rely on materials that are either not perfect crystals or non-crystalline, breaking translational symmetry. This poses the fundamental questions of whether coherent momentum-dependent electronic states can arise without long-range order, and how they can be characterized. Here we investigate Bi2Se3, which exists in crystalline, nanocrystalline, and amorphous forms, allowing direct comparisons between varying degrees of spatial ordering. Through angle-resolved photoemission spectroscopy, we show for the first time momentum-dependent band structure with Fermi surface repetitions in an amorphous solid. The experimental data is complemented by a model that accurately reproduces the vertical, dispersive features as well as the replication at higher momenta in the amorphous form. These results reveal that well-defined real-space length scales are sufficient to produce dispersive band structures, and that photoemission can expose the imprint of these length scales on the electronic structure. Recent studies showing dispersive surface states in an amorphous topological insulator has deepened the understanding of momentum-space electronic structure. Here the authors report dispersive electronic states and a distinct Fermi surface with Brillouin-zone-like repetitions in amorphous Bi2Se3. [ABSTRACT FROM AUTHOR]

The charge density wave (CDW), as a hallmark of vanadium-based kagome superconductor AV3Sb5 (A = K, Rb, Cs), has attracted intensive attention. However, the fundamental controversy regarding the underlying mechanism of CDW therein persists. Recently, the vanadium-based bi-layered kagome metal ScV6Sn6, reported to exhibit a long-range charge order below 94 K, has emerged as a promising candidate to further clarify this core issue. Here, employing micro-focusing angle-resolved photoemission spectroscopy (μ-ARPES) and first-principles calculations, we systematically studied the unique CDW order in vanadium-based bi-layered kagome metals by comparing ScV6Sn6 with its isostructural counterpart YV6Sn6, which lacks a CDW ground state. Combining ARPES data and the corresponding joint density of states (DOS), we suggest that the VHS nesting mechanism might be invalid in these materials. Besides, in ScV6Sn6, we identified multiple hybridization energy gaps resulting from CDW-induced band folding, along with an anomalous band dispersion, implying a potential electron-phonon coupling-driven mechanism underlying the formation of the CDW order. Our finding not only comprehensively maps the electronic structure of V-based bi-layer kagome metals but also provides constructive experimental evidence for the unique origin of CDW in this system. We investigated the origins of charge density wave (CDW) mechanisms in the bi-layered kagome metal ScV6Sn6 by comparing its electronic structure with that of its isostructural counterpart YV6Sn6, which does not exhibit a CDW state. Our ARPES measurements reveal that the Van Hove singularity (VHS) nesting mechanism may not be valid in the CDW state. In ScV6Sn6, the electronic structure shows a CDW-induced band gap accompanied by anomalous band dispersion near the M point of the Brillouin zone. These findings provide experimental evidence for the origin of CDW in vanadium-based kagome metals. [ABSTRACT FROM AUTHOR]

Emergent phases often appear when the electronic kinetic energy is comparable to the Coulomb interactions. One approach to seek material systems as hosts of such emergent phases is to realize localization of electronic wavefunctions due to the geometric frustration inherent in the crystal structure, resulting in flat electronic bands. Recently, such efforts have found a wide range of exotic phases in the two-dimensional kagome lattice, including magnetic order, time-reversal symmetry breaking charge order, nematicity, and superconductivity. However, the interlayer coupling of the kagome layers disrupts the destructive interference needed to completely quench the kinetic energy. Here we demonstrate that an interwoven kagome network—a pyrochlore lattice—can host a three dimensional (3D) localization of electron wavefunctions. Meanwhile, the nonsymmorphic symmetry of the pyrochlore lattice guarantees all band crossings at the Brillouin zone X point to be 3D gapless Dirac points, which was predicted theoretically but never yet observed experimentally. Through a combination of angle-resolved photoemission spectroscopy, fundamental lattice model and density functional theory calculations, we investigate the novel electronic structure of a Laves phase superconductor with a pyrochlore sublattice, CeRu2. We observe evidence of flat bands originating from the Ce 4f orbitals as well as flat bands from the 3D destructive interference of the Ru 4d orbitals. We further observe the nonsymmorphic symmetry-protected 3D gapless Dirac cone at the X point. Our work establishes the pyrochlore structure as a promising lattice platform to realize and tune novel emergent phases intertwining topology and many-body interactions. [ABSTRACT FROM AUTHOR]

Owing to their exceptional mechanical, electronic, and phononic transport properties, compositionally complex alloys, including high-entropy alloys, represent an important class of materials. However, the interplay between chemical disorder and electronic correlations, and its influence on electronic structure-derived properties, remains largely unexplored. This is addressed for the archetypal CrMnFeCoNi alloy using resonant and valence band photoemission spectroscopy, electrical resistivity, and optical conductivity measurements, complemented by linear response calculations based on density functional theory. Utilizing dynamical mean-field theory, correlation signatures and damping in the spectra are identified, highlighting the significance of many-body effects, particularly in states distant from the Fermi edge. Electronic transport remains dominated by disorder and potentially short-range order, especially at low temperatures, while visible-spectrum optical conductivity and high-temperature transport are influenced by short quasiparticle lifetimes. These findings improve our understanding of element-specific electronic correlations in compositionally complex alloys and facilitate the development of advanced materials with tailored electronic properties. Compositionally complex alloys have attracted significant attention recently, but the role of electronic correlations in these materials is unknown. Redka et al. study the CrMnFeCoNi alloy using a combination of experimental and theoretical techniques, revealing strong correlation effects far from the Fermi edge. [ABSTRACT FROM AUTHOR]

Homogeneous mixed-valence (MV) behaviour is one of the most intriguing phenomena of f-electron systems. Despite extensive efforts, a fundamental aspect which remains unsettled is the experimental determination of the limiting cases for which MV emerges. Here we address this question for SmB6, a prototypical MV system characterized by two nearly-degenerate Sm2+ and Sm3+ configurations. By combining angle-resolved photoemission spectroscopy (ARPES) and x-ray absorption spectroscopy (XAS), we track the evolution of the mean Sm valence, vSm, in the SmxLa1−xB6 series. Upon substitution of Sm ions with trivalent La, we observe a linear decrease of valence fluctuations to an almost complete suppression at x = 0.2, with vSm ~ 2; surprisingly, by further reducing x, a re-entrant increase of vSm develops, approaching the value of vimp ~ 2.35 in the dilute-impurity limit. Such behaviour departs from a monotonic evolution of vSm across the whole series, as well as from the expectation of its convergence to an integer value for x → 0. Our ARPES and XAS results, complemented by a phenomenological model, demonstrate an unconventional evolution of the MV character in the SmxLa1−xB6 series, paving the way to further theoretical and experimental considerations on the concept of MV itself, and its influence on the macroscopic properties of rare-earth compounds in the dilute-to-intermediate impurity regime. This study reveals a non-monotonic evolution of the mixed-valence character in the SmxLa1−xB6 series, with near-complete suppression of valence fluctuations in the intermediate substitution regime, followed by a re-emergent mixed-valence behavior in the dilute-impurity limit. [ABSTRACT FROM AUTHOR]

TiN–Ag@Ag composite substrates were prepared via ammonia reduction nitridation followed by electrochemical deposition. Fabricated TiN–Ag@Ag substrates were characterized using X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscopy, and ultraviolet-visible spectrophotometry. The surface-enhanced Raman spectroscopy activity of these substrates was evaluated using ibuprofen as the probe molecule. The size of the Ag particles prepared via electrochemical deposition was approximately 1 μm, and Ag nanoparticles with an average particle size of 100 nm were uniformly distributed on the surface of TiN–Ag films. The Raman signal of ibuprofen was significantly enhanced, and the minimum detection concentration of ibuprofen was 10–5 M. The mechanism by which the TiN–Ag@Ag composite substrate enhanced the Raman signals was analyzed using ultraviolet photoelectron spectroscopy and density functional theory implemented in the Gaussian software. Overall, charge transfer and the local electromagnetic field effect enhanced the Raman signals of ibuprofen. [ABSTRACT FROM AUTHOR]

Solar-driven photo-thermal catalytic CO2 methanation reaction is a promising technology to alleviate the problems posed by greenhouse gases emissions. However, designing advanced photo-thermal catalysts remains a research challenge for CO2 methanation reaction. In this work, a series of ABO3 (A = lanthanide, B = transition metal) perovskite catalysts with Ce-substituted LaNiO3 (La1−xCexNiO3, x = 0, 0.2, 0.5, 0.8, 1) were synthesized for CO2 methanation. The La0.2Ce0.8NiO3 exhibited the highest CH4 formation rate of 258.9 mmol·g−1·hcat−1, CO2 conversion of 55.4% and 97.2% CH4 selectivity at 300 °C with the light intensity of 2.9 W·cm−2. Then the catalysts were thoroughly analyzed by physicochemical structure and optical properties characterizations. The partial substitution of the A-site provided more active sites for the adsorption and activation of CO2/H2. The sources of the active sites were considered to be the oxygen vacancies (Ov) created by lattice distortions due to different species of ions (La3+, Ce4+, Ce3+) and exsolved Ni0 by H2 reduction. The catalysts have excellent light absorption absorbance and low electron–hole (e−/h+) recombination rate, which greatly contribute to the excellent performance in photo-thermal synergistic catalysis (PTC) CO2 methanation. The results of in situ irradiated electron paramagnetic resonance spectrometer (ISI-EPR) and ISI-X-ray photoelectron spectroscopy (XPS) indicated that the aggregation of unpaired electrons near the defects and Ni metal (from La and Ce ions to Ov and Ni0) accelerated adsorption and activation of CO2/H2. At last, the catalyst properties and structure were correlated with the proposed reaction mechanism from the in situ diffuse reflection infrared Fourier transform spectrum (DRIFTS) measurements. The in situ precipitation of the B-site enhanced the dispersion of Ni, while its enriched photoelectrons upon illumination further promote hydrogen dissociation. More H* spillover accelerated the rate-determining step (RDS) of HCOO* hydrogenation. This work provides the theoretical basis for the development of catalysts and industrial application. [ABSTRACT FROM AUTHOR]

Growing concerns regarding the presence of pharmaceuticals in wastewater necessitate their removal. Membrane filtration offers a promising approach. This study explores the development of biochar incorporated mixed matrix membranes (MMMs) for ciprofloxacin removal from water. Biochar, derived from the pyrolysis of agricultural waste, was blended with polyether sulfone (PES) and polyvinylpyrrolidone in varying ratios. The resulting MMMs exhibited progressively improved properties with increasing biochar content. Notably, membrane M11, comprising equal parts PES and biochar, displayed the highest porosity, lowest surface roughness (12.0), and lowest contact angle (31.05°), indicating enhanced hydrophilicity (increased by 58.19% compared to the biochar-free membrane). M11 effectively removed ciprofloxacin along with three additional antibiotics from different classes. Fourier-transform infrared spectroscopy and X-ray photoelectron spectroscopy analyses corroborated the removal of ciprofloxacin. Furthermore, M11 demonstrated excellent regenerability, retaining over 57% removal efficiency after four cycles. These findings highlight the potential of M11 as a sustainable and cost-effective membrane for pharmaceutical removal from wastewater. [ABSTRACT FROM AUTHOR]

The interplay of topology, magnetism, and correlations gives rise to intriguing phases of matter. In this study, through state-of-the-art angle-resolved photoemission spectroscopy, density functional theory, and dynamical mean-field theory calculations, we visualize a fourfold degenerate Dirac nodal line at the boundary of the bulk Brillouin zone in the antiferromagnet YMn2Ge2. We further demonstrate that this gapless, antiferromagnetic Dirac nodal line is enforced by the combination of magnetism, space-time inversion symmetry, and nonsymmorphic lattice symmetry. The corresponding drumhead surface states traverse the whole surface Brillouin zone. YMn2Ge2 thus serves as a platform to exhibit the interplay of multiple degenerate nodal physics and antiferromagnetism. Interestingly, the magnetic nodal line displays a d-orbital dependent renormalization along its trajectory in momentum space, thereby manifesting Hund's coupling. Our findings offer insights into the effect of electronic correlations on magnetic Dirac nodal lines, leading to an antiferromagnetic Hund nodal line. The interplay of magnetism, various symmetries and correlations can lead to intriguing physics in the solid state. Here, the authors report signatures of a Hund nodal line in the antiferromagnet YMn2Ge2. [ABSTRACT FROM AUTHOR]

The utilization of biowastes for producing biochar to remove potentially toxic elements from water represents an important pathway for aquatic ecosystem decontamination. Here we explored the significance of thiol-functionalization on sugarcane bagasse biochar (Th/SCB–BC) and rice husk biochar (Th/RH–BC) to enhance arsenite (As(III)) removal capacity from water and compared their efficiency with both pristine biochars (SCB–BC and RH–BC). The maximum As(III) sorption was found on Th/SCB–BC and Th/RH–BC (2.88 and 2.51 mg g−1, respectively) compared to the SCB–BC and RH–BC (1.51 and 1.40 mg g−1). Relatively, a greater percentage of As(III) removal was obtained with Th/SCB–BC and Th/RH–BC (92% and 83%, respectively) at a pH 7 compared to pristine SCB–BC and RH–BC (65% and 55%) at 6 mg L−1 initial As(III) concentration, 2 h contact time and 1 g L−1 sorbent dose. Langmuir (R2 = 0.99) isotherm and pseudo-second-order kinetic (R2 = 0.99) models provided the best fits to As(III) sorption data. Desorption experiments indicated that the regeneration ability of biochars decreased and it was in the order of Th/SCB–BC (88%) > Th/RH–BC (82%) > SCB–BC (77%) > RH–BC (69%) up to three sorption–desorption cycles. Fourier-transform infrared spectroscopy and X-ray photoelectron spectroscopy results demonstrated that the thiol (-S–H) functional groups were successfully grafted on the surface of two biochars and as such contributed to enhance As(III) removal from water. Spectroscopic data indicated that the surface functional moieties, such as -S–H, − OH, − COOH, and C = O were involved to increase As(III) sorption on thiol-functionalized biochars. This study highlights that thiol-grafting on both biochars, notably on SCB–BC, enhanced their ability to remove As(III) from water, which can be used as an effective technique for the treatment of As from drinking water. [ABSTRACT FROM AUTHOR]

We present the evolution of the electronic structure of CrSBr from its antiferromagnetic ground state to the paramagnetic phase above TN = 132 K, in both experiment and theory. Low-temperature angle-resolved photoemission spectroscopy (ARPES) results are obtained using a novel method to overcome sample charging issues, revealing quasi-2D valence bands in the ground state. The results are very well reproduced by our QSG W ̂ calculations, which further identify certain bands at the X points to be exchange-split pairs of states with mainly Br and S character. By tracing band positions as a function of temperature, we show the splitting disappears above TN. The energy splitting is interpreted as an effective exchange splitting in individual layers in which the Cr moments all align, within the so-called A-type antiferromagnetic arrangement. Our results lay firm foundations for the interpretation of the many other intriguing physical and optical properties of CrSBr. [ABSTRACT FROM AUTHOR]

The oxidation of phenolic compounds is one of the most important reactions prevalent in various biological processes, often explicitly coupled with proton transfers (PTs). Quantitative descriptions and molecular-level understanding of these proton-coupled electron transfer (PCET) reactions have been challenging. This work reports a direct observation of PCET in photodetachment (PD) photoelectron spectroscopy (PES) of hydrogen-bonded phenolic (ArOH) nitrate (NO3−) complexes, in which a much slower rising edge provides a spectroscopic signature to evidence PCET. Electronic structure calculations unveil the PCET processes to be isomer-specific, occurred only in those with their HOMOs localized on ArOH, leading to charge-separated transient states ArOH•+·NO3− triggered by ionizing phenols while simultaneously promoting PT from ArOH•+ to NO3−. Importantly, this study showcases that gas-phase PD-PES is a generic means enabling to identify PCET reactions with explicit structural and binding information. The oxidation of phenolic compounds is one of the most important reactions prevalent in various biological processes, but quantitative descriptions and molecular-level understanding of these proton-coupled electron transfer (PCET) reactions have been challenging. Here, the authors use photodetachment photoelectron spectroscopy to directly observe PCET in hydrogen-bonded phenolic nitrate complexes, in which a much slower rising edge provides a spectroscopic signature to evidence PCET [ABSTRACT FROM AUTHOR]

Density fluctuation potential induced by a screening of the photohole scatters the photoelectron and generally causes its emission delay from the scattering matrix in the photoemission spectroscopy, where the photoemission delay usually quantifies the extrinsic loss of the photoelectron depending on the atomic orbital. Without the potential scattering, however, the photoemission from the coherent two-state mixture created by the laser driving is found to undergo the unexpected photoemission delay, which originates from the mixed photoemission matrix. Using the Haldane model, we analytically calculate such coherent mixing induced photoemission delay in an angle-resolved mode, which is found to reveal the local Berry curvature structure as long as the coherent mixing is sustained. This finding is confirmed through the streaking computation for the photoemission delay by solving the time-dependent Schrödinger equation and suggests that the photoemission delay be a new spectroscopic diagnosis of the material topology of two-dimensional semiconductors. [ABSTRACT FROM AUTHOR]

This work reviews the impact of cobalt phthalocyanine (CoPc) interlayers on the electrical and current transport properties of Au/undoped-InP Schottky diodes (SDs). The crystalline quality of CoPc films was confirmed using dominant vibrational bands observed in Raman measurements. Using X-ray photoemission spectroscopy (XPS), the chemical properties were assessed and the results confirmed that the CoPc interfacial layer was deposited on undoped-InP (un-InP). The Au/CoPc/un-InP metal/polymer/semiconductor (MPS) diode showed a better rectification ratio than did the SD. The estimated barrier height (ΦB) of the MPS diode (0.77 eV (I-V)) was greater than the SD (0.66 eV (I-V)), signifying that ΦB was modified by a CoPc layer. Using Cheung's, and Norde methods and Ψs-V plots, the ΦB, ideality factor and series resistance were assessed. The ΦB values estimated by these techniques were well matched with one another demonstrating their constancy and validity. A lower density of states (NSS) is attained for the MPS diode than for the SD, demonstrating that the CoPc layer reduced the NSS. The forward log I-log V plot of both the SD and MPS suggests ohmic-type behavior and space charge limited current (SCLC) in the lower-bias and upper-bias regions. The Poole–Frenkel emission (PFE) is ruled at the lower-bias, while, the Schottky emission (SE) is governed in the upper-bias regions under reverse bias in both the SD and MPS diodes. The findings confirmed that the CoPc layer is a probable material for the construction of organic–inorganic devices. [ABSTRACT FROM AUTHOR]

The paper presents an investigation into the reduction and adsorption performance of hierarchically structured carbon films (HSCFs). The HSCFs are synthesized from glucose using a molten magnesium catalyst under a layer of molten salts during their reaction with an aqueous sodium permanganate solution at pH values from 1 to 14 and temperatures from 20 to 80 °C. By increasing the temperature from 20 to 80 °C, the reduction and adsorption of Mn (VII) on the HSCFs is accelerated by a factor of 150; moreover, the reaction products are not temperature-dependent. According to Raman and photoelectron spectroscopy data, synthesis in the neutral and basic sodium permanganate solutions produces an "HSCF-sodium-manganese spinel" nanocomposite, the greater part (≈ 80%) of whose manganese is in a tetravalent state, while the remainder is in a trivalent state. The predominant precipitation of manganese spinel nanocrystals on the developed side of the carbon film may be related to the full disappearance of the sp hybridized carbon peak on the XPS spectra. It is shown for the first time that the reactivity of carbon varies with its valence state. Of the three hybridized states of carbon, sp hybridized carbon is demonstrated to have the highest reactivity. It is confirmed that 100% reduction and adsorption from 0.01 to 0.1 M sodium permanganate solutions occur in neutral and basic media. The adsorption capacity of the hierarchically structured carbon film interacting with 0.1 M sodium permanganate solution is more than 450 mg/g, representing a high adsorption performance as compared to other carbon nanomaterials investigated earlier. [ABSTRACT FROM AUTHOR]

As a most promising environmental technology, the substantial enhancement of photocatalytic efficiency is still a big challenge for practical applications. In this work, the surface of Bi2O2CO3 (BOC) nanotubes are modified by Cl and I. The as-obtained samples at different hydrothermal temperatures (T) are designated as T-X-BOC (X = Cl, I). X-ray diffraction (XRD), energy dispersive X-ray (EDX) spectroscopy and X-ray photoelectron spectroscopy (XPS) prove that Cl and I merely chemically adsorb on the BOC surface, rather than dope into the crystal lattice. The surface modification of Cl and I slightly increases light absorption range, while significantly promotes the photoelectron migration from bulk to the surface that greatly enhances the carrier separation efficiency. Density functional theory (DFT) calculations further prove that surface Cl and I have adjusted band structure and surface charge distribution. Besides, the surface Cl and I favor the O2 adsorption and trap the surface photoelectrons, thus promoting the formation of •O2–; while the surface Cl and I impede the surface adsorption of H2O, thus refraining the generation of •OH. In the degradation of rhodamine B (RhB), holes and •O2− radicals play the crucial role. Under ultraviolet light irradiation (λ < 420 nm) for 45 min, the RhB degradation ratios over 150-Cl-BOC (94%) and 150-I-BOC (85%) are 4.2 and 3.7 times higher than that of original BOC (18%), respectively. This work demonstrates that the simple surface halogenation modification greatly improves the photocatalytic activity. [ABSTRACT FROM AUTHOR]

The kink structure in band dispersion usually refers to a certain electron-boson interaction, which is crucial in understanding the pairing in unconventional superconductors. Here we report the evidence of the observation of a kink structure in Fe-based superconductor CsCa2Fe4As4F2 using angle-resolved photoemission spectroscopy. The kink shows an orbital selective and momentum dependent behavior, which is located at 15 meV below Fermi level along the Γ − M direction at the band with dxz orbital character and vanishes when approaching the Γ − X direction, correlated with a slight decrease of the superconducting gap. Most importantly, this kink structure disappears when the superconducting gap closes, indicating that the corresponding bosonic mode (~ 9 ± 1 meV) is closely related to superconductivity. However, the origin of this mode remains unidentified, since it cannot be related to phonons or the spin resonance mode (~15 meV) observed by inelastic neutron scattering. The behavior of this mode is rather unique and challenges our present understanding of the superconducting paring mechanism of the bilayer FeAs-based superconductors. The kink structure in the band dispersion can be linked to electron-boson interaction and has been reported in unconventional superconductors. Here the authors observe an orbital selective and momentum dependent kink feature in an Fe-based superconductor, which is highly correlated with superconductivity. [ABSTRACT FROM AUTHOR]

Surface templating by electrostatic surface potentials is the least invasive way to design large-scale artificial nanostructures. However, generating sufficiently large potential gradients remains challenging. Here, we lay the groundwork for significantly enhancing local electrostatic fields by chemical modification of the surface. We consider the hexagonal boron nitride (h-BN) nanomesh on Rh(111), which already exhibits small surface potential gradients between its pore and wire regions. Using photoemission spectroscopy, we show that adding Au atoms to the Rh(111) surface layer leads to a local migration of Au atoms below the wire regions of the nanomesh. This significantly increases the local work function difference between the pore and wire regions that can be quantified experimentally by the changes in the h-BN valence band structure. Using density functional theory, we identify an electron transfer from Rh to Au as the microscopic origin for the local enhancement of potential gradients within the h-BN nanomesh. [ABSTRACT FROM AUTHOR]

ZnO and Zn₀․₉₈Mn₀․₀₂CoₓO (0.00 ≤ x ≤ 0.025) nanoparticles were synthesized via the sol-gel method and subjected to a comprehensive analysis of their structural, electronic, morphological, dielectric, and magnetic properties. X-ray diffraction (XRD) confirmed the presence of a single-phase hexagonal ZnO structure, while transmission electron microscopy (TEM) revealed spherical particles with minor facets, consistent with high-resolution TEM (HR-TEM) data. X-ray photoemission spectroscopy (XPS) analysis demonstrated successful Co and Mn incorporation into the ZnO lattice without secondary phases. Dielectric properties were investigated via impedance spectroscopy, with results interpreted using the Maxwell-Wagner model to elucidate interfacial polarization mechanisms. Magnetic measurements revealed complex interactions in Mn-doped ZnO nanoparticles, including ferromagnetic, paramagnetic, and antiferromagnetic behaviors. However, the introduction of Co as a co-dopant stabilized the ferromagnetic moment in the (Zn, Mn)O system, attributed to the presence of sufficient oxygen vacancies. Notably, our findings provide strong evidence for defect-mediated ferromagnetism in (Mn, Co) co-doped ZnO nanoparticles, contributing to our understanding of magnetic phenomena in nanomaterials. [ABSTRACT FROM AUTHOR]

High-density nonvolatile memories can be realized by fabricating resistive random-access memories (RRAMs) as 4F2 (F: minimum feature size) cells in a crossbar array (CBA) configuration. However, the CBA configuration induces leakage currents in the nearby cells, which significantly reduces the read-out margin and limits the CBA size extension. One solution to this problem is to integrate an RRAM with a bidirectional selector. Research on the various type of selector devices has been extensively explored so far, however, a device that satisfies all requirements has not been developed. In this paper, we propose a novel bidirectional diode selector with a Pt/HfNx/Pt stack. We implement a one-selector–one-resistor configuration in a 10 × 10 CBA by integrating Pt/HfNx/Pt with a Ti/HfO2/Pt RRAM stack. We confirm the stable resistive switching operation and good thermal stability of the selector and its integrated device. Chemical analyses aided by Auger electron spectroscopy and X-ray photoelectron spectroscopy reveal the gradient-oxidation of the HfNx film, which explains the nonlinear and asymmetric current–voltage characteristics. This novel nonlinear selector with simple structure and high thermal stability can be applied to build CBAs for high-density nonvolatile memories or neuromorphic computing elements, in the future. [ABSTRACT FROM AUTHOR]

Two-dimensional electrides can acquire topologically non-trivial phases due to intriguing interplay between the cationic atomic layers and anionic electron layers. However, experimental evidence of topological surface states has yet to be verified. Here, via angle-resolved photoemission spectroscopy (ARPES) and scanning tunnelling microscopy (STM), we probe the magnetic Weyl states of the ferromagnetic electride [Gd2C]2+·2e−. In particular, the presence of Weyl cones and Fermi-arc states is demonstrated through photon energy-dependent ARPES measurements, agreeing with theoretical band structure calculations. Notably, the STM measurements reveal that the Fermi-arc states exist underneath a floating quantum electron liquid on the top Gd layer, forming double-stacked surface states in a heterostructure. Our work thus not only unveils the non-trivial topology of the [Gd2C]2+·2e− electride but also realizes a surface heterostructure that can host phenomena distinct from the bulk. Electrides are an emerging family of materials with potential for hosting topological states. Here, the authors demonstrate the presence of Fermi-arc surface states in close proximity to the floating electron layer on the surface of an electride. [ABSTRACT FROM AUTHOR]

Modification is widely used to enhance the adsorption performance of pristine hydrochar (HBC) and pyrochar (BC). However, comparisons between modified HBC and BC toward pollutant removal have rarely been reported. In this study, pristine HBC and BC derived from rice straw were first produced, and then citric acid (CA) was used as a modifier to synthesize CA-modified HBC (CAHBC) and CA-modified BC (CABC). Furthermore, the adsorption performance of biochars toward methylene blue (MB) was investigated. The results showed that BC exhibits relatively rough surfaces and contains more minerals (ash), whereas HBC has plentiful O-containing functional groups and fewer minerals. CA modification partially removed minerals from the surface of BC, which weakened the ion exchange, surface complexation, and n–π interaction, resulting in a lower adsorption ability toward MB. By contrast, CA produced more O-containing functional groups on the surface of HBC, which strengthened the hydrogen bonding and electrostatic interaction, thus increasing the adsorption capacity toward MB. The two-compartment model showed a good fit to the adsorption process of MB on CAHBC, and the isotherm data for MB adsorption by HBC and CAHBC are suitable for the Freundlich model. The highest adsorption amount of MB using CAHBC was 80.13 mg·g–1, which was 27.66% higher than that for CABC. Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy analysis indicated that the carboxyl groups in the surface functional groups of CAHBC played a crucial role in the MB adsorption process. In addition, CAHBC showed a good performance for a wide range of pH values (4.0–10.0) and under the interference of coexisting ions, and also presented a recycling ability. Furthermore, the adsorption of MB on CAHBC biochar was a spontaneous, exothermic, degree-of-randomness-increasing process. Consequently, CA modification of HBC is a promising strategy and could be used for MB removal from aquatic environments. [ABSTRACT FROM AUTHOR]

Kagome vanadates AV3Sb5 display unusual low-temperature electronic properties including charge density waves (CDW), whose microscopic origin remains unsettled. Recently, CDW order has been discovered in a new material ScV6Sn6, providing an opportunity to explore whether the onset of CDW leads to unusual electronic properties. Here, we study this question using angle-resolved photoemission spectroscopy (ARPES) and scanning tunneling microscopy (STM). The ARPES measurements show minimal changes to the electronic structure after the onset of CDW. However, STM quasiparticle interference (QPI) measurements show strong dispersing features related to the CDW ordering vectors. A plausible explanation is the presence of a strong momentum-dependent scattering potential peaked at the CDW wavevector, associated with the existence of competing CDW instabilities. Our STM results further indicate that the bands most affected by the CDW are near vHS, analogous to the case of AV3Sb5 despite very different CDW wavevectors. The authors use angle-resolved photoemission spectroscopy (ARPES) and scanning tunneling microscopy (STM) to study the charge density wave (CDW) in the kagome material ScV6Sn6. The ARPES data shows minimal changes to the electronic structure in the CDW state, while STM quasiparticle interference measurements imply a strong reconstruction of the electronic structure in the CDW state. [ABSTRACT FROM AUTHOR]

Polycyclic aromatic hydrocarbons (PAHs) are widely established as ubiquitous in the interstellar medium (ISM), but considering their prevalence in harsh vacuum environments, the role of ionisation in the formation of PAH clusters is poorly understood, particularly if a chirality-dependent aggregation route is considered. Here we report on photoelectron spectroscopy experiments on [4]helicene clusters performed with a vacuum ultraviolet synchrotron beamline. Aggregates (up to the heptamer) of [4]helicene, the smallest PAH with helical chirality, were produced and investigated with a combined experimental and theoretical approach using several state-of-the-art quantum-chemical methodologies. The ionisation onsets are extracted for each cluster size from the mass-selected photoelectron spectra and compared with calculations of vertical ionisation energies. We explore the complex aggregation topologies emerging from the multitude of isomers formed through clustering of P and M, the two enantiomers of [4]helicene. The very satisfactory benchmarking between experimental ionisation onsets vs. predicted ionisation energies allows the identification of theoretically predicted potential aggregation motifs and corresponding energetic ordering of chiral clusters. Our structural models suggest that a homochiral aggregation route is energetically favoured over heterochiral arrangements with increasing cluster size, hinting at potential symmetry breaking in PAH cluster formation at the scale of small grains. Polycyclic aromatic hydrocarbons such as [4]helicenes are important interstellar molecules. Here, the authors show their evolution of chiral clusters upon aggregation through coincidence spectroscopy and quantum chemical calculations. [ABSTRACT FROM AUTHOR]

The superconducting gap symmetry is crucial in understanding the underlying superconductivity mechanism. Angle-resolved photoemission spectroscopy (ARPES) has played a key role in determining the gap symmetry in unconventional superconductors. However, it has been considered so far that ARPES can only measure the magnitude of the superconducting gap but not its phase; the phase has to be detected by other phase-sensitive techniques. Here we propose a method to directly detect the superconducting gap sign by ARPES. This method is successfully validated in a cuprate superconductor Bi2Sr2CaCu2O8+δ with a well-known d-wave gap symmetry. When two bands have a strong interband interaction, the resulted electronic structures in the superconducting state are sensitive to the relative gap sign between the two bands. Our present work provides an approach to detect the gap sign and can be applied to various superconductors, particularly those with multiple orbitals like the iron-based superconductors. According to conventional wisdom, angle-resolved photoemission spectroscopy (ARPES) can only measure the magnitude of the superconducting gap but not its phase. Here, the authors propose a new method to directly detect the superconducting gap phase using ARPES and validate this technique on a cuprate superconductor. [ABSTRACT FROM AUTHOR]

Dimensional modifications play a crucial role in various applications, especially in the context of device miniaturization, giving rise to novel quantum phenomena. The many-body dynamics induced by dimensional modifications, including electron-electron, electron-phonon, electron-magnon and electron-plasmon coupling, are known to significantly affect the atomic and electronic properties of the materials. By reducing the dimensionality of orthorhombic CoSe2 and forming heterostructure with bilayer graphene using molecular beam epitaxy, we unveil the emergence of two types of phase transitions through angle-resolved photoemission spectroscopy and scanning tunneling microscopy measurements. We disclose that the 2 × 1 superstructure is associated with charge density wave induced by Fermi surface nesting, characterized by a transition temperature of 340 K. Additionally, another phase transition at temperature of 160 K based on temperature dependent gap evolution are observed with renormalized electronic structure induced by electron-boson coupling. These discoveries of the electronic and atomic modifications, influenced by electron-electron and electron-boson interactions, underscore that many-body physics play significant roles in understanding low-dimensional properties of non-van der Waals Co-chalcogenides and related heterostructures. [ABSTRACT FROM AUTHOR]

The latest discovery of high temperature superconductivity near 80 K in La3Ni2O7 under high pressure has attracted much attention. Many proposals are put forth to understand the origin of superconductivity. The determination of electronic structures is a prerequisite to establish theories to understand superconductivity in nickelates but is still lacking. Here we report our direct measurement of the electronic structures of La3Ni2O7 by high-resolution angle-resolved photoemission spectroscopy. The Fermi surface and band structures of La3Ni2O7 are observed and compared with the band structure calculations. Strong electron correlations are revealed which are orbital- and momentum-dependent. A flat band is formed from the Ni-3d z 2 orbitals around the zone corner which is ~ 50 meV below the Fermi level and exhibits the strongest electron correlation. In many theoretical proposals, this band is expected to play the dominant role in generating superconductivity in La3Ni2O7. Our observations provide key experimental information to understand the electronic structure and origin of high temperature superconductivity in La3Ni2O7. Recently, superconductivity near 80 K was observed in La3Ni2O7 under high pressure, but the mechanism is debated. Here the authors report angle-resolved photoemission spectroscopy measurements under ambient pressure, revealing flat bands with strong electronic correlations that could be linked to superconductivity. [ABSTRACT FROM AUTHOR]

The Berry curvature dipole (BCD) serves as a one of the fundamental contributors to emergence of the nonlinear Hall effect (NLHE). Despite intense interest due to its potential for new technologies reaching beyond the quantum efficiency limit, the interplay between BCD and NLHE has been barely understood yet in the absence of a systematic study on the electronic band structure. Here, we report NLHE realized in NbIrTe4 that persists above room temperature coupled with a sign change in the Hall conductivity at 150 K. First-principles calculations combined with angle-resolved photoemission spectroscopy (ARPES) measurements show that BCD tuned by the partial occupancy of spin-orbit split bands via temperature is responsible for the temperature-dependent NLHE. Our findings highlight the correlation between BCD and the electronic band structure, providing a viable route to create and engineer the non-trivial Hall effect by tuning the geometric properties of quasiparticles in transition-metal chalcogen compounds. Previous work proposed the Berry curvature dipole as the mechanism of the nonlinear Hall effect. Lee et al. establish the sign-changing Berry curvature hot spots from spin-orbit split bands as the origin of the Berry curvature dipole and link it to the nonlinear Hall effect in the topological semimetal NbIrTe4. [ABSTRACT FROM AUTHOR]

Context: Mixed-metal clusters have long been studied because of their peculiar properties and how they change with cluster size, composition, and charge state and their potential roles in catalysis. The characterization of these clusters is therefore a very important issue. One of the main experimental tools for characterizing their electronic structure is photoelectron spectroscopy. Theoretical computation completes the task by fully determining the structural properties and matching the theoretical predictions to the measured spectra. We present density functional theory computations of the structural, magnetic, and electronic properties of negatively charged mixed AlnNi- clusters with up to 13 Al atoms. The lowest energy structures of the anionic clusters with up to 7 atoms are also found to be low-energy isomers of the neutral counterparts found in the literature. The 13-atom cluster is found to be a quartet and a perfect icosahedron. The predicted photoelectron spectra are also presented and can be used to interpret future experimental data. We also presented indicators that can be used to determine the potential of these systems for single-atom catalysis. These indicators point to smaller clusters to be more reactive as the gap between the Fermi energy and the center of the d-band increases with cluster size and that Ni occupies an internal site for n = 11–13. We speculate that reactivity can be enhanced if one adds an additional Ni atom. Methods: The DFT calculations were performed using the Becke exchange and Perdew-Wang/91 correlation functionals (BPW91), a DFT-optimized all-electron basis set for the aluminum atom, and the Stuttgart small core pseudopotential for the Ni atom. All of the computations used the Gaussian 03 software. [ABSTRACT FROM AUTHOR]

Spin-orbit coupling in noncentrosymmetric crystals leads to spin-momentum locking – a directional relationship between an electron's spin angular momentum and its linear momentum. Isotropic orthogonal Rashba spin-momentum locking has been studied for decades, while its counterpart, isotropic parallel Weyl spin-momentum locking has remained elusive in experiments. Theory predicts that Weyl spin-momentum locking can only be realized in structurally chiral cubic crystals in the vicinity of Kramers-Weyl or multifold fermions. Here, we use spin- and angle-resolved photoemission spectroscopy to evidence Weyl spin-momentum locking of multifold fermions in the chiral topological semimetal PtGa. We find that the electron spin of the Fermi arc surface states is orthogonal to their Fermi surface contour for momenta close to the projection of the bulk multifold fermion at the Γ point, which is consistent with Weyl spin-momentum locking of the latter. The direct measurement of the bulk spin texture of the multifold fermion at the R point also displays Weyl spin-momentum locking. The discovery of Weyl spin-momentum locking may lead to energy-efficient memory devices and Josephson diodes based on chiral topological semimetals. Spin-momentum locking is a fundamental property of condensed matter systems. Here, the authors evidence parallel Weyl spin-momentum locking of multifold fermions in the chiral topological semimetal PtGa. [ABSTRACT FROM AUTHOR]

The features of magnetic microstructure of La0.73Dy0.27Mn2Si2 at 293 K have been visualized by atomic force and magnetic force microscopy. Magnetic force images reveal the presence of low-contrast magnetic domains. The change of Raman spectral characteristics of light scattering in the process of cooling La0.73Dy0.27Mn2Si2 to a temperature of 263 K is experimentally detected. The electronic structure of La0.73Dy0.27Mn2Si2 is investigated by resonance photoemission spectroscopy with the use of the synchrotron radiation. Resonances at the 3d and 4d levels of electronic structure show different properties of valence electrons. Using the Dy 3d–4f (M4.5 absorption edge) resonance, the distribution of 4f states of dysprosium in the valence band is determined. Photoemission upon the giant Dy 4d–4f (N4.5 absorption edge) resonance is determined by the contribution of all states in the valence band due to the sudden involvement of the Coulomb interaction. The energies of the 5p and 4f levels of La, the 4f level of Dy, and the 3d level of Mn in the valence band are determined. [ABSTRACT FROM AUTHOR]

The glass compound eye bead is the exquisite embodiment of the glassmaking technology of ancient craftsmen, and is an example of the cultural exchange between China and the West during the Warring States Period. This study takes two dots and mesh beads with seriously weathered surfaces excavated from Hejia village, Zhouling as the research object. Micromorphology, X-ray fluorescence spectroscopy (XRF), microscopic laser Raman spectroscopy and X-ray photoelectron spectroscopy (XPS) were respectively used to determine the chemical elements, valence states and compositions of the glass matrix and its weathering products. In this study, the valence state analysis of group-d elements is used to reveal the electron transition mode and explain the colour formation reason of blue-black glass matrix. In terms of weathering products, in addition to the identification of common cerusite [PbCO3] and barite [BaSO4], the study also found the blue weathering product alforsite [Ba5(PO4)3Cl] for the first time. The study also makes reasonable assumptions about the reasons for their appearance. The X-ray photoelectron spectroscopy (XPS) used in this study has positive significance for the study of the formation mechanism of glass colour. The scientific and technological analysis data of these two glass beads provide basic data for the related research of the lead-barium glass system produced in China, and also provide a certain scientific basis for the related protection research. [ABSTRACT FROM AUTHOR]

Tunability of interfacial effects between two-dimensional (2D) crystals is crucial not only for understanding the intrinsic properties of each system, but also for designing electronic devices based on ultra-thin heterostructures. A prerequisite of such heterostructure engineering is the availability of 2D crystals with different degrees of interfacial interactions. In this work, we report a controlled epitaxial growth of monolayer TaSe2 with different structural phases, 1H and 1 T, on a bilayer graphene (BLG) substrate using molecular beam epitaxy, and its impact on the electronic properties of the heterostructures using angle-resolved photoemission spectroscopy. 1H-TaSe2 exhibits significant charge transfer and band hybridization at the interface, whereas 1 T-TaSe2 shows weak interactions with the substrate. The distinct interfacial interactions are attributed to the dual effects from the differences of the work functions as well as the relative interlayer distance between TaSe2 films and BLG substrate. The method demonstrated here provides a viable route towards interface engineering in a variety of transition-metal dichalcogenides that can be applied to future nano-devices with designed electronic properties. [ABSTRACT FROM AUTHOR]

4Hb-TaS2 is a superconductor that exhibits unique characteristics such as time-reversal symmetry breaking, hidden magnetic memory, and topological edge modes. It is a naturally occurring heterostructure comprising of alternating layers of 1H-TaS2 and 1T-TaS2. The former is a well-known superconductor, while the latter is a correlated insulator with a possible non- trivial magnetic ground state. In this study, we use angle resolved photoemission spectroscopy to investigate the normal state electronic structure of this unconventional superconductor. Our findings reveal that the band structure of 4Hb-TaS2 fundamentally differs from that of its constituent materials. Specifically, we observe a significant charge transfer from the 1T layers to the 1H layers that drives the 1T layers away from half-filling. In addition, we find a substantial reduction in inter-layer coupling in 4Hb-TaS2 compared to the coupling in 2H-TaS2 that results in a pronounced spin-valley locking within 4Hb-TaS2. [ABSTRACT FROM AUTHOR]

Van Hove singularities (VHss) in the vicinity of the Fermi energy often play a dramatic role in the physics of strongly correlated electron materials. The divergence of the density of states generated by VHss can trigger the emergence of phases such as superconductivity, ferromagnetism, metamagnetism, and density wave orders. A detailed understanding of the electronic structure of these VHss is therefore essential for an accurate description of such instabilities. Here, we study the low-energy electronic structure of the trilayer strontium ruthenate Sr4Ru3O10, identifying a rich hierarchy of VHss using angle-resolved photoemission spectroscopy and millikelvin scanning tunneling microscopy. Comparison of k-resolved electron spectroscopy and quasiparticle interference allows us to determine the structure of the VHss and demonstrate the crucial role of spin-orbit coupling in shaping them. We use this to develop a minimal model from which we identify a mechanism for driving a field-induced Lifshitz transition in ferromagnetic metals. [ABSTRACT FROM AUTHOR]

Transparent conducting aluminum-doped tin oxide (ATO) thin films were prepared on unheated glass substrates by a high-target utilization system (HiTUS). The effect of oxygen flow rates on the structural, optical, and electrical properties of ATO thin films were comprehensively examined. X-ray diffraction analysis (XRD) and transmission electron microscopy (TEM) were utilized to analyze the films' structural properties, x-ray photoemission spectroscopy (XPS) was employed to investigate their surface chemistry, UV–visible transmittance curves were recorded to study their optical properties, and Hall-effect measurements determined their electrical properties. At room temperature, the ATO thin films with 3 wt.% aluminum dopant concentration demonstrated resistivity, carrier concentration, and mobility values of 2.16 Ω m × 10−1 Ω m, 2.32 m−3 × 1014 m−3, and 1.24 m2 V−1 s−1 × 10−3 m2 V−1 s−1, respectively. The sheet resistance of the films was approximately 43 Ω/□, and the average optical transmittance between 400 nm and 800 nm exceeded 80%. These findings strongly suggest that ATO thin films exhibit great potential for use in multiple optoelectronic device applications, making them an attractive option. [ABSTRACT FROM AUTHOR]

X-ray free-electron lasers are sources of coherent, high-intensity X-rays with numerous applications in ultra-fast measurements and dynamic structural imaging. Due to the stochastic nature of the self-amplified spontaneous emission process and the difficulty in controlling injection of electrons, output pulses exhibit significant noise and limited temporal coherence. Standard measurement techniques used for characterizing two-coloured X-ray pulses are challenging, as they are either invasive or diagnostically expensive. In this work, we employ machine learning methods such as neural networks and decision trees to predict the central photon energies of pairs of attosecond fundamental and second harmonic pulses using parameters that are easily recorded at the high-repetition rate of a single shot. Using real experimental data, we apply a detailed feature analysis on the input parameters while optimizing the training time of the machine learning methods. Our predictive models are able to make predictions of central photon energy for one of the pulses without measuring the other pulse, thereby leveraging the use of the spectrometer without having to extend its detection window. We anticipate applications in X-ray spectroscopy using XFELs, such as in time-resolved X-ray absorption and photoemission spectroscopy, where improved measurement of input spectra will lead to better experimental outcomes. [ABSTRACT FROM AUTHOR]

The dynamical response of a quantum spin liquid upon injecting a hole is a pertinent open question. In experiments, the hole spectral function, measured momentum-resolved in angle-resolved photoemission spectroscopy (ARPES) or locally in scanning tunneling microscopy (STM), can be used to identify spin liquid materials. In this study, we employ tensor network methods to simulate the time evolution of a single hole doped into the Kitaev spin-liquid ground state. Focusing on the gapped spin liquid phase, we reveal two fundamentally different scenarios. For ferromagnetic spin couplings, the spin liquid is highly susceptible to hole doping: a Nagaoka ferromagnet forms dynamically around the doped hole, even at weak coupling. By contrast, in the case of antiferromagnetic spin couplings, the hole spectrum demonstrates an intricate interplay between charge, spin, and flux degrees of freedom, best described by a parton mean-field ansatz of fractionalized holons and spinons. Moreover, we find a good agreement of our numerical results to the analytically solvable case of slow holes. Our results demonstrate that dynamical hole spectral functions provide rich information on the structure of fractionalized quantum spin liquids. [ABSTRACT FROM AUTHOR]

Vanadium nitride (VN) is a transition-metal nitride with remarkable properties that have prompted extensive experimental and theoretical investigations in recent years. However, there is a current paucity of experimental research investigating the temperature-dependent electronic structure of single-crystalline VN. In this study, high-quality VN(111) films were successfully synthesized on α -Al 2 O 3 (0001) substrates using magnetron sputtering. The crystal and electronic structures of the VN films were characterized by a combination of high-resolution X-ray diffraction, low-energy electron diffraction, resonant soft X-ray absorption spectroscopy, and ultraviolet photoelectron spectroscopy. The electrical transport measurements indicate that the superconducting critical temperature of the VN films is around 8.1 K. Intriguingly, the temperature-dependent photoelectron spectroscopy measurements demonstrate a weak temperature dependence in the electronic structure of the VN films, which is significant for understanding the ground state of VN compounds. [ABSTRACT FROM AUTHOR]