X-ray Photoemission Spectroscopy Research Articles

Electronic structure of 2(5H)-thiophenone studied by UPS and soft X-ray spectroscopy

Abstract The electronic structure of 2(5H)-thiophenone in the gas phase was investigated by ultraviolet photoelectron spectroscopy (UPS) and x-ray photoemission spectroscopy (XPS) and near edge x-ray absorption fine structure (NEXAFS) spectroscopy at the C 1s, O 1s, and S 2p edges. All assignments of the experimental results are supported by both ab-initio electron propagator OVGF calculations for the valence photoemission bands and density functional theory (DFT) and relativistic time dependent DFT calculations for the core levels XPS and NEXAFS spectra. Overall good agreement between experiment and theory is observed; this is especially true for core electron excitations which has permitted an unambiguous assignment of the observed spectral features in terms of single-particle excitations to virtual molecular orbitals. The assignment of the valence band spectra based on OVGF calculations, although satisfactory, points to the importance of electron correlations effects that partially break the single particle picture of ionization.

Origin of Persisting Photoresponse of One-Year Aged Two-Dimensional Lead Halide Perovskites Stored in Air under Dark Conditions.

Two-dimensional halide perovskites are promising for advanced photonic, optoelectronic, and photovoltaic applications. However, their long-term stability is still a critical factor limiting their implementation into further commercial applications. Here, we present an environmental stability analysis of BA2(MA)n-1PbnI3n+1 (BA = C4H12N+, MA = CH6N+) two-dimensional perovskites with the lowest quantum well thicknesses of n = 1 and n = 2, after 1 year of aging under ambient humidity, oxygen content, and light conditions. We observed that both crystal phases (n = 1 and 2) degraded similarly, resulting in the removal of organic components and crystal decomposition into PbI2, Pb oxides, and Pb hydroxides. However, we have found a significant difference between their aging under ambient light and dark conditions, affecting their degraded morphology and photoactivity. Both crystal phases exposed to ambient light aged into a morphology characterized by the formation of several pinholes and voids, accompanied by photoluminescence degradation. Samples stored under dark conditions surprisingly preserved their photoluminescence activity, which morphologically aged into microrod structures. We conclude that the observed loss of photoactivity of 2D perovskites aged under ambient light is attributed to photoaccelerated degradation processes causing faster crystal surface photo-oxidation accompanied by a creation of multiple I vacancies and hydration of the inner crystal. The retainment of photoactivity in 2D perovskites aged under dark conditions is attributed to slower surface oxidation processes into Pb salts, as confirmed by X-ray photoemission spectroscopy. The formed surface layer even allows for a layer-by-layer degradation and acts as a protection barrier against further additional loss of I atoms and the consequent hydration of the inner part of samples. We demonstrate that light is the most critical external factor accelerating 2D perovskite degradation processes in ambient air and thus affecting their long-term stability. We conclude in this work that perovskite material structural engineering together with their surface passivation or encapsulation strategical techniques applied is an essential step for their further application into long-term stable commercial devices.

DFT + U Study of Plutonium Hydrides with Occupation Matrix Control.

The magnetic order of plutonium hydrides (PuHx) has long been a subject of controversy, both experimentally and theoretically. The magnetic, structural, electronic, and thermodynamic properties of PuHx are investigated using Hubbard-corrected density functional theory (DFT + U), with U derived from linear response calculations. To address the issue of electronic metastable states within DFT + U, we employ an occupation matrix control method as well as allowing 5f orbitals to break the structural symmetry. This advanced computational approach establishes that the ground-state magnetic order for PuH2 is antiferromagnetic and that for PuH3 is ferromagnetic, consistent with Faraday and nuclear magnetic resonance experiments. Using the conventional hydrogen-vacancy model for PuHx, the hydrogen-content-induced magnetic transition and anomalous variation of the magnetic moment are successfully reproduced. In particular, the calculated transition point of x matches the experimental findings. Furthermore, the electronic configuration of the Pu atom in PuHx is determined to be 5f5, which is consistent with observations from X-ray photoemission spectroscopy. Our calculated values for enthalpy of formation, heat capacity, and entropy are in good agreement with experimental data, thereby validating the robustness of our theoretical framework.

Multiplet XPS analysis of the Mn 2p for Mn3O4 thin films

In this work, we performed a detailed analysis of the x-ray photoemission spectroscopy (XPS) of the Mn 2ppeak for Mn3O4(001) thin films. This is a challenging task since Mn3O4is composed of two different cations, Mn2+at tetrahedral and Mn3+at octahedral sites, which both contribute to the XPS spectra. The oxide spectra consist of many multiplets arising from the angular momentum coupling of the open Mn 2pand 3dshells, thus increasing the spectrums' complexity. Moreover, the energy spacing and intensities of the different multiplets also reflect the covalent mixing between Mn 3dand O 2pshells. However, we show that a detailed analysis, which provides relevant information about the cations in the oxide structure, is possible. We prepared experimentally different Mn3O4films on Au(111), and their structure was monitored with the diffraction pattern obtained with low-energy electron diffraction. The Mn 2pspectra were fit, guided by cluster model theoretical predictions, and checked for films prepared at different oxygen partial pressures. Therefore, we could observe the Mn2+and Mn3+cations' relative concentration in the Mn 2pmains peaks.

Nonlinear Optical Properties of La3+-Doped Tellurite-Zinc Glasses: Impact of Chemical Bonding and Physical Properties via Raman and XPS

Understanding the connection between the local environments of lanthanum ions in tellurite glasses and their nonlinear optical (NLO) properties is essential for various technological applications. Rare earth ions can serve as probes for the local environments of the host material if the structure-property correlations are well understood. In this study, we investigated glasses with compositions 70TeO2 - (30-x)ZnO - (x)La2O3 (mol%) (x = 0, 5, 7, 9) fabricated by the melt-quenching technique. The capabilities of combined Raman and X-ray photoemission (XPS) spectroscopy were used to identify these glasses and define spectral deconvolution for distinguishing them in the formation of bridging oxygens (BO) and non-bridging oxygens (NBO). NLO properties were evaluated using open-aperture (OA) and closed-aperture (CA) Z-scan measurements with femtosecond (fs) laser pulses (∼220 fs, 750 Hz) at wavelengths ranging from 600 to 1500 nm. Raman spectra revealed a shift to higher frequencies from 731 to 746 cm-1, with increasing of La3+ ions, indicating the conversion of TeO4 polyhedra to TeO3 structural units, affecting the Te-O- Zn2+ or Te=O bonds and resulting in a variation of the polarizability. Besides the conventional analysis of oxidation state and chemical shifts of the core-level peaks, XPS spectroscopy included a careful analysis of the type oxygen bridges and metal-oxygen bond length to distinguish otherwise similar spectral contributions of different TZL glasses. Glasses with a high fraction of Zn2⁺ ions bonded with oxygen form NBO and modify the local structure of the glass network, while La³⁺ ions coordinate with oxygen atoms or interact with the lone pairs of tellurium atoms. By analyzing the correlation in different concentrations of La3+ ions, the Te-O bonds and NBO/(BO+NBO) ratio were clearly demonstrated. These findings suggest charge compensation between the Zn2⁺ and La³⁺ ions, for maintaining structural stability within the glass network. This study also reveals an enhancement of NLO properties as a function of La3+ ions concentration in TZL glasses under fs laser excitation due to resonant nonlinearity. The third-order optical nonlinearities showed an increase in the two-photon absorption coefficient (β) from 0.26×10-2 cm GW-1 (TZL5) to 0.62×10-2 cm GW-1 (TZL9), along with an increase in the nonlinear refractive index (n2) from 0.32×10-18 m2 W-1 to 0.65×10-18 m2 W-1. This enhancement is attributed to the increased number of NBOs and the high polarizability of La3+ ions. For all-optical switching (AOS) applications, two figures of merit were applied using the n2, α0, and β coefficients. The results suggest that the TZL glasses studied are potential candidates for AOS devices. Thus, this work not only elucidates the factors underlying the NLO properties but also highlights the promising potential of these glasses for use in AOS devices.

Unravelling the effect of crystal lattice compression on the supercapacitive performance of hydrothermally grown nanostructured hollandite α-MnO2 induced by incremental growth time

Manganese oxide (α-MnO2) nanoparticles are highly recognised for their use in supercapacitor applications. This study demonstrates the successful synthesis of flower-like and nanorods hollandite α-MnO2 by a simple one-pot hydrothermal technique at various reaction times. The synthesised nanoparticles were characterised by various physicochemical and electrochemical characterisation techniques. The influence of the various reaction times on the structural and morphological properties was evaluated by X-ray diffraction (XRD) and scanning electron microscope. XRD patterns revealed that the synthesized MnO2 nanoparticles are tetragonal structures with crystallite sizes ranging from 13.69 to 20.37 nm estimated from the Williamson–Hall method. Moreover, the functional groups and surface area were examined by Fourier transform infrared spectroscopy and Bruner–Emmert–Teller, respectively. Furthermore, the compositional elements were studied by X-ray photoemission spectroscopy and energy-dispersive X-ray spectroscopy. Finally, the electrochemical performances were studied using cyclic voltammetry, galvanostatic charge–discharge and electrochemical impedance spectroscopy (EIS). The GCD characteristics revealed that the optimised α-MnO2 has a good capacitive behaviour, which predicts the potential application in energy storage. Electrochemical studies revealed that the 3 h-MnO2 sample exhibited a superior electrochemical behaviour and demonstrated a high specific capacitance of 132 F/g at a current density of 1A/g.

Double exchange interaction in Mn-based topological kagome ferrimagnet

Recently discovered Mn-based kagome materials, such as RMn6Sn6 (R = rare-earth element), exhibit the coexistence of topological electronic states and long-range magnetic order, offering a platform for studying quantum phenomena. However, understanding the electronic and magnetic properties of these materials remains incomplete. Here, we investigate the electronic structure and magnetic properties of GdMn6Sn6 using x-ray magnetic circular dichroism, photoemission spectroscopy, and theoretical calculations. We observe localized electronic states from spin frustration in the Mn-based kagome lattice and induced magnetic moments in the nonmagnetic element Sn experimentally, which originate from the Sn-p\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$p$$\\end{document} and Mn-d\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$d$$\\end{document} orbital hybridization. Our calculations also reveal ferromagnetic coupling within the kagome Mn-Mn layer, driven by double exchange interaction. This work provides insights into the mechanisms of magnetic interaction and magnetic tuning in the exploration of topological quantum materials.

Hydrogenation of graphene on Ni(111) by H2 under near ambient pressure conditions

Graphene hydrogenation on Ni(111) in the mbar region has been investigated by combining Near Ambient Pressure X-ray Photoemission Spectroscopy and Density Functional Theory calculations. A complete and nearly perfect graphene single layer and an incomplete defective monolayer were exposed to a methanation mixture (H2 + CO and H2 + CO2, respectively) with a large excess of H2. The observed behavior is quite different for the two systems. In the former case, the C 1s spectrum of the initially strongly interacting graphene shows the appearance of new components corresponding to hydrogenated C atoms and their first nearest neighbors. The defective carbon layer, grown in the presence of sulfur contamination and consisting of a mixture of strongly and weakly interacting graphene with a significant amount of dissolved C, initially shows the same C species and then evolves with the formation of sp3 carbon and patches of Ni oxide/hydroxide. NiO forms by CO2 dissociation, while sp3 carbon is indicative of a rumpling of the graphene adlayer induced by hydrogenation. Both species disappear when annealing in H2. Dissociation of H2 and graphene hydrogenation is possible thanks to the presence of the Ni substrate which makes the reaction weakly exothermic and significantly reduces the barrier for H2 dissociation.

Investigation on electronic and magnetic properties of Cr doped V2O5 thin films prepared by chemical solution deposition method

The present study examines the role of Cr doping on the electronic and magnetic behaviour of V2O5i.e. V2-xCrxO5 (x = 0, 0.05, and 0.10) thin films, prepared by chemical-solution deposition technique on Si (111) substrate. X-Ray diffraction technique shows the purity of the films and confirms no secondary phase formation. The atomic force microscopy was used to confirm the roughness of the films. A morphological investigation is done using High-resolution scanning electron microscopy associated with Energy dispersive X-Ray mapping of each element of the film. Fourier transform Infrared spectroscopy is utilised to identify functional groups that are present in obtained samples. The band-gap of these obtained samples is in the range of 0.8–0.6 eV, as examined by UV–Vis i.e., its value is decreasing with Cr doping. Using vibrating sample magnetometer, it is clear that samples shows ferromagnetic (FM) behaviour with saturation magnetization 0.3–0.6 μB/cc consistent with Langevin function fitting. It concludes the presence of FM behaviour of films and magnetization increases with carrier density, consistent with the carrier-induced origin of the ferromagnetism. X-ray photoemission spectroscopy (XPS) is utilised to understand its electronic properties. Core level spectra measurements suggest that V is in mixed state of 5+ and 4+. However Cr is in 3+ states. XPS and UV–Vis measurements imply that oxygen vacancies significantly contribute to the declination of the band gap and the promotion of FM-like behaviour. This discovery offers a promising pathway for engineering novel devices.

Pushing the Thickness Limit of the Giant Rashba Effect in Ferroelectric Semiconductor GeTe.

Ferroelectric Rashba semiconductors (FERSCs) such as α-GeTe are promising candidates for energy-efficient information technologies exploiting spin-orbit coupling (SOC) and are termed spin-orbitronics. In this work, the thickness limit of the Rashba-SOC effect in α-GeTe films is investigated. We demonstrate, using angle-resolved photoemission spectroscopy (ARPES) and first-principles calculations performed on pristine GeTe, that down to 1 nm, GeTe(111) films on a Sb-covered Si(111) substrate continuously exhibit a giant Rashba effect characterized, at 1 nm, by a constant of 5.2 ± 0.5 eV·Å. X-ray photoemission spectroscopy (XPS) allows the understanding of the persistence of the Rashba effect by evidencing a compensation of Ge vacancy defects resulting from the insertion of Sb interfacial atoms in the early stage growth of the GeTe(111) films.

Structure and physical properties of modified Ti2MnAl compound – Ti2Fe0.5Cr0.5Al and Ti2MnAl0.5In0.5 case

Ti2MnAl was believed to be Spin Gapless Semiconducting (SGS) material, but this state can be achieved only in an inverted variant of Heusler structure. This specific structure is not realized under normal conditions, however, earlier reports suggest that substituting Al by In or Sn should make it possible. This was the motivation for studying the structural and physical properties of Ti2MnAl0.5In0.5 alloy in this paper. We also studied isoelectronic Ti2Fe0.5Cr0.5Al material, as it is well known that properties of Heusler compounds strongly depend on the valence electron count. We report a combined experimental and theoretical study, where we synthesized substituted variants and measured their diffraction patterns. Additionally we performed ab initio calculations using several methods to study the stability of the resulting compounds. We also examined the impact of disorder within Coherent Potential Approximation. Experimental XPS (X-ray Photoemission Spectroscopy) spectra, magnetic susceptibility and electrical resistivity are also discussed.

Epitaxial growth and band offsets of β -(ScxGa1− x)2O3 thin films grown on (100) β -Ga2O3 substrate

β-(ScxGa1−x)2O3 (x = 0–0.36) thin films were epitaxially grown on (100) β-Ga2O3 substrates by oxygen-radical-assisted pulsed-laser deposition. β-(ScxGa1−x)2O3 epilayers were coherently strained up to x = 0.30, although the presence of a structural disorder was implied when x > 0.2. The bandgap energies measured by reflection electron energy loss spectroscopy increased from 4.56 to 5.25 eV with increasing Sc content. In β-(ScxGa1−x)2O3 epilayers, a slightly negative bandgap bowing behavior with a bowing parameter of −0.4 eV was observed, resulting in a larger bandgap increase than in β-(AlxGa1−x)2O3 epilayers with identical x. X-ray photoemission spectroscopy measurement revealed that the valence-band and conduction-band offsets of β-(Sc0.17Ga0.83)2O3 epilayer with respect to β-Ga2O3 were 0.0 and 0.3 eV, respectively.

Peeling-induced interfacial roughness and charging for enhanced triboelectric power generation

To date, there have been a lot of efforts to enhance the conversion efficiency of triboelectric nanogenerators (TENGs) via physical and chemical modifications of the polymer surface. Herein, we report that a facile peeling of polymer from a substrate can enhance the triboelectric power output. The peeling of spin-coated polydimethylsiloxane (PDMS) from glass and polytetrafluoroethylene (PTFE) substrates has revealed a considerable increase in interfacial roughness and lateral friction. Surface-sensitive X-ray photoemission spectroscopy and non-contact current measurements have also revealed the transfer of counter-material and interfacial charging. The surface roughness of peeled PDMS is significant for the PTFE substrate, while the surface charge is significant for the glass substrate. The triboelectric output power density for peeled PDMS from the substrate is similar, 10.3 µW/cm2, but significantly larger than that for as-grown PDMS (2.2 µW/cm2). The peeling strength of PDMS significantly increases for glass compared to PTFE after the oxygen plasma treatment of substrates. The triboelectric charge of peeled PDMS from a plasma-treated glass substrate is almost 1.3 times larger than that from a PTFE substrate. This work implies that peeling polymer from a rough substrate with a large adhesion force would be a facile and effective way to increase the triboelectric power output, without any delicate surface treatments.

Redox reaction at buried ZnO/Ti thin film interface as seen by hard x-ray photoemission and thermal desorption spectroscopy

In the context of low-emissivity glazing, the redox reaction at a buried ZnO/Ti interface is studied in model nanometer-thick film stacks synthesized by magnetron sputtering deposition. For a given amount of Ti, the roles of annealing temperature up to 550 °C, of ZnO layer thickness, and of its crystalline quality are explored. The main originality of the approach is the use of hard x-ray photoemission spectroscopy to probe in situ chemical reactions at a buried interface in a non-destructive way. The detailed analysis of relevant core levels reveals the formation of a ZnxTiyOz ternary compound and the nearly complete oxidation of Ti into TiO2. Thanks to complementary measurements of thermal desorption spectroscopy and electron probe microanalysis, unexpected diffusion of the Zn redox reaction by-product through the upper part of the stack and its desorption in vacuum are clearly evidenced. The reaction and mass transport pathways are rationalized through thermodynamic simulations.

Balancing the redox activity against structure stability in high-voltage manganese/iron-based layered oxide cathodes through copper doping for potassium-ion batteries

Earth-abundant manganese/iron-based layered oxide cathodes display high energy densities in cost-effective potassium-ion batteries, but still encounter severe structure distortions and irreversible phase transformations upon cycling. To ameliorate its structural stability, the highly electronegative but electrochemically inactive Cu2+ is rationally introduced into Mn sites of P3-type K0.5Mn0.8Fe0.2O2 cathode materials to regulate crystal structures and elemental valences toward a balance between redox activity and structure stability. Ranging from 4.2 to 1.5 V, the optimal K0.5Mn0.7Fe0.2Cu0.1O2 cathode material with a lower formation energy and a narrower band gap could present a large initial discharging capacity of 91 mAh g−1 at 50 mA g−1 with an excellent capacity retention of 71.6 % over 50 cycles and a competitive capacity retention of 62.3 % at 100 mA g−1 after 100 cycles. Regardless of its compromised K+ diffusion capabilities from a slightly contracted interlayer, a superior rate performance of 71 mAh g−1 can be achieved at 500 mA g−1, implying a dominant function of structural stability in electrochemical depotassiation/potassiation. Additionally, the dynamic redox activities and high electrochemical reversibility of Mn4+/3+ and Fe4+/3+ couples are verified by ex-situ X-ray photoemission spectroscopies. This solid work would enlighten the novel structural manipulations of layered oxide cathodes for high-voltage potassium-ion batteries.

In situ photoemission spectroscopies to reveal surface transfer doping on hydrogenated milled nanodiamonds

Nanodiamonds (ND) exhibit exceptional chemical, electronic, thermal, and optical properties, making them valuable for applications in nanomedicine, energy, quantum technologies, advanced lubricants, and polymer composites. Surface analysis techniques such as X-ray photoemission spectroscopy (XPS), ultraviolet photoemission spectroscopy (UPS) and reflection electron energy loss spectroscopy (REELS) are critical for understanding the surface properties of nanomaterials, including nanodiamonds. This study investigates hydrogenated milled nanodiamonds (H-MND) by integrating UPS and XPS measurements with REELS. Through in situ annealing within an ultra-high vacuum (UHV) chamber, we examine the impact of surface termination on surface conductivity, focusing on the role of adsorbates. Our findings reveal that a surface transfer doping mechanism, akin to that observed in bulk diamond, governs a pseudo p-type conductivity in H-MND. The conductivity dependence on ambient exposure, water, and subsequent annealing demonstrates its reversibility. The study also discusses the nature of electron acceptors and the influence of ND facets on conductivity.

Antiferromagnetic Frustration Behavior with Face-Sharing CuAs4 Tetrahedrons in Conducting ACu6As3 (A = Li and Na).

New mixed-valence copper pnictides ACu6As3 (A = Li and Na) adopt a quasi-2D structure type, featuring alkalis and [Cu6As3]- slabs along the c-axis alternatively. The face-sharing connection between CuAs4 polyhedra leads to a higher valence state for the inside Cu ions than that of Cu ions with the other connectivity way. This is confirmed by X-ray photoemission spectroscopy results. The Cu2+ with near spin 1/2 located on bilayer triangular lattice is found to exhibit a peculiar hump in magnetic susceptibility along the c-axis and, most strikingly, nearly a constant at low temperatures from 1.8 K down to 0.4 K. Besides, high hole mobilities, 68.58 and 645.16 cm2 V-1 S-1, are observed in LiCu6As3 and NaCu6As3, respectively. These compounds provide a novel material system for researching the relationship among structure, valence state, and spin correlation in frustrated lattice.

Probing Surface Dynamics of SiOx Thin-Film Electrodes during Cycling through X-Ray Photoemission Spectroscopy and Operando X-Ray Reflectivity.

SiOx electrodes are promising for high-energy-density lithium-ion batteries (LIBs) due to their ability to mitigate volume expansion-induced degradation. Here, we investigate the surface dynamics of SiOx thin-film electrodes cycled in different carbonate-based electrolytes using a combination of ex situ X-ray photoelectron spectroscopy (XPS) and operando synchrotron X-ray reflectivity analyses. The thin-film geometry allows us to probe the depth-dependent chemical composition and electron density from surface to current collector through the solid electrolyte interphase (SEI), the active material, and the thickness evolution during cycling. Results reveal that SiOx lithiation initiates below 0.4 V vs Li+/Li and indicate a close relationship between SEI formation and SiOx electrode lithiation, likely due to the high resistivity of SiOx. We find similar chemical compositions for the SEI in FEC-containing and FEC-free electrolytes but observe a reduced thickness in the former case. In both cases, the SEI thickness decreases during delithiation due to the removal or dissolution of some carbonate species. These findings give insights into the (de)lithiation of SiOx, in particular, during the formation stage, and the effect of the presence of FEC in the electrolyte on the evolution of the SEI during cycling.

Eupatorium adenophorum Spreng root extract as an efficient inhibitor for the corrosion of steel in sulfamic acid solution

Eupatorium adenophorum Spreng root extract (EASRE) was prepared using a reflux extraction method with 40 % ethanol (C2H5OH) as the extractant solvent. The corrosion inhibitory impact of EASRE on cold rolled steel (CRS) in 0.10 M sulfamic acid (NH2SO3H) solution was explored through gravimetric tests, potentiodynamic polarization curves, and electrochemical impedance spectroscopy (EIS) methods. Metallographic microscopy (MM), scanning electron microscopy (SEM), atomic force microscopy (AFM), and confocal laser scanning microscopy (CLSM) were employed to examine the micrographs of CRS specimens. The adsorbed chemical substances on the inhibited CRS surface were examined via X-ray photoemission spectroscopy (XPS). And the main chemical constituents of EASRE were analysed by high performance liquid chromatography-mass spectrometry (HPLC-MS). The results of the study showed that EASRE at a concentration of 500 mg L−1 in 0.10 M NH2SO3H at 30 °C for 12 h had a significant inhibitory effect on CRS, with a maximum inhibitory efficiency of 89.7 %. At all set temperatures, the adsorption of EASRE onto CRS surface adheres to Langmuir isotherm. EASRE functions as a mixed-type inhibitor through a “geometric covering effect”. EIS show that the addition of EASRE significantly improves the charge transfer resistance at the steel/sulfamic acid interface, and the charge transfer resistance increases with increasing inhibitor concentration. XPS analysis confirm the presence of a “protective film” generated by EASRE on the CRS surface, and it consists of O-H, N-H, C-O, C-H, CC, CN, CO. Microscopic graphs of MM, SEM, AFM and CLSM reveal that EASRE efficiently alleviates the corrosion on the CRS surface. The HPLC-MS suggest that the main components of EASRE are flavonoids and phenylpropanoid compounds.

Room Temperature Synthesis of Tellurium by Solution Atomic Layer Deposition.

This study demonstrates the deposition of tellurium (Te) on silicon/silicon nitride substrates using solution atomic layer deposition (sALD) at ambient temperature. The process employs tellurium tetrachloride (TeCl4) and bis(triethylsilyl)-telluride ((TES)2Te) as precursors, with toluene as the solvent. Growth parameters were optimized through systematic variation of the pulse and purge times. Morphological characterization via scanning and transmission electron microscopy revealed needle-like crystallites, while X-ray diffractometry confirmed the crystalline nature of the deposited Te. Increasing the number of deposition cycles resulted in larger Te crystallites and enhanced substrate surface coverage. A thin amorphous carbon shell surrounding the crystallites and carbon inclusions was observed, likely originating from the organic solvent. X-ray photoemission spectroscopy analysis indicated high-purity Te films with minimal surface oxidation. The small chlorine signal suggested a near-complete precursor reaction and the efficient purging of byproducts. This novel sALD approach presents a promising method for depositing Te on various surfaces under mild conditions.