We present a combined experimental and theoretical study on the unoccupied surface electronic structure of the Tl/Si(111) surface. Spin- and angle-resolved inverse-photoemission measurements with sensitivity to both the in-plane and the out-of-plane polarization direction detect a spin-orbit-split surface state, which is well described by theoretical calculations. We demonstrate that the spin polarization vector rotates from the classical in-plane Rashba polarization direction around Γ[over ¯] to the direction perpendicular to the surface at the K[over ¯](K[over ¯]') points-a direct consequence of the symmetry of the 2D hexagonal system. A giant splitting in energy of about 0.6 eV is observed and attributed to the strong localization of the unoccupied surface state close to the heavy Tl atoms. This leads to completely out-of-plane spin-polarized valleys in the vicinity of the Fermi level. As the valley polarization is oppositely oriented at the K[over ¯] and K[over ¯]' points, backscattering should be strongly suppressed in this system.
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http://dx.doi.org/10.1103/PhysRevLett.111.176402 | DOI Listing |
Phys Chem Chem Phys
January 2025
The Institute for Solid State Physics, The University of Tokyo, 5-1-5 Kashiwanoha, Kashiwa, Chiba 277-8581, Japan.
Formic acid (HCOOH) is one of the essential molecules for CO utilization including methanol synthesis and hydrogen carriers. In this study, we have investigated the chemical processes of hydrogen and HCOOH on a dilute-alloy Pd-Cu(111) surface using high-resolution X-ray photoelectron spectroscopy (HR-XPS) and density functional theory (DFT) calculations. The present Pd-Cu(111) surface was prepared at 500 K, and the observed core-level shifts of Pd 3d indicate that Pd atoms were located at the surface and subsurface sites: 335.
View Article and Find Full Text PDFAdv Sci (Weinh)
December 2024
Institute of Materials Science, Technische Universität Darmstadt, Peter-Grünberg-Str. 2, D-64287, Darmstadt, Germany.
The design of cathode/electrolyte interfaces in high-energy density Li-ion batteries is critical to protect the surface against undesirable oxygen release from the cathodes when batteries are charged to high voltage. However, the involvement of the engineered interface in the cationic and anionic redox reactions associated with (de-)lithiation is often ignored, mostly due to the difficulty to separate these processes from chemical/catalytic reactions at the cathode/electrolyte interface. Here, a new electron energy band diagrams concept is developed that includes the examination of the electrochemical- and ionization- potentials evolution upon batteries cycling.
View Article and Find Full Text PDFAnal Chem
December 2024
Phenikaa University Nano Institute (PHENA), Phenikaa University, Hanoi 12116, Vietnam.
Surface-enhanced Raman spectroscopy (SERS) is a powerful analytical technique, yet it faces challenges with certain probe molecules exhibiting weak or inactive signals, limiting their applicability. In a recent study, we investigated this phenomenon using a set of four probe molecules─chloramphenicol (CAP), 4-nitrophenol (4-NP), amoxicillin (AMX), and furazolidone (FZD)─deposited on Ag-based nanostructured SERS substrates. Despite being measured under identical conditions, CAP and 4-NP exhibited SERS activity, while AMX and FZD did not.
View Article and Find Full Text PDFJ Am Chem Soc
December 2024
Department of Chemical Engineering, Virginia Tech, Blacksburg, Virginia 24061, United States.
The decomposition of ozone on supported manganese oxide catalysts, studied here, exemplifies reactions involving electron transfer. In situ extended X-ray absorption fine-structure spectra (Mn K-edge) on in situ treated samples show that the supported phase in MnO/SiO resembles MnO while that in MnO/AlO samples resembles MnO. In situ Raman spectroscopy shows the involvement of a common peroxide surface species.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
Department of Creative Convergence Engineering, Hanbat National University, Daejeon 34158, Republic of Korea.
Heterobimetallic systems (HBS), known for their ability to facilitate the versatile design of surface workfunctions, offer significant potential as an electron-injection electrode layer for organic semiconductors. In this paper, we propose a universal and effective strategy to overcome the limitations of the erase operation in charge-trap memory with a small-bandgap organic semiconductor or diketopyrrolopyrrole-quaterthiophene-conjugated polymer (PDPP4T) by utilizing HBS-based source/drain (SD) electrodes. Conventional gold SD electrodes restrict electron injection into the PDPP4T layer during the electrical erase operation and impose a lower limit on the erasing voltage required for full threshold-voltage recovery.
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