Photoemission spectroscopy

About: Photoemission spectroscopy is a research topic. Over the lifetime, 10821 publications have been published within this topic receiving 250888 citations. The topic is also known as: photoelectron spectroscopy & PES.

Dependence of indium–tin–oxide work function on surface cleaning method as studied by ultraviolet and x-ray photoemission spectroscopies

Abstract: The effect of the method used to clean indium–tin–oxide (ITO) on its work function was investigated by ultraviolet photoemission spectroscopy (UPS) and x-ray photoemission spectroscopy. With only ultrasonic cleaning in the organic solvent, considerable carbon contamination remained on the ITO surface and the work function was low (4.5 eV). In contrast, ultraviolet (UV)–ozone treatment removed significant carbon contamination, with an increase in the work function to 4.75 eV, which improves the hole-injection efficiency into the organic hole-transport layer in organic electroluminescent devices. Although carbon contamination on the ITO surface was also removed by Ar+ sputtering, it was accompanied by the removal of oxygen from ITO, and the work function was reduced (4.3 eV). Three factors, i.e.,: (i) C-containing contaminants, (ii) the O/In ratio, and (iii) the In/Sn ratio on the ITO surface affect the work function. The present results and those of other workers suggest that these three factors affect the...

Conjugated organic molecules on metal versus polymer electrodes: Demonstration of a key energy level alignment mechanism

Abstract: Ultraviolet photoemission spectroscopy is used to determine the energy level alignment at interfaces between three electroactive conjugated organic molecular materials, i.e., N,N′-bis-(1-naphthyl)-N,N′-diphenyl1-1,1-biphenyl1-4,4′-diamine; para-sexiphenyl; pentacene, and two high work function electrode materials, i.e., gold and poly(3,4-ethylenedioxythiophene)/poly(styrenesulfonate). Although both electrode surfaces have a similar work function (∼5 eV), the hole injection barrier and the interfacial dipole barrier are found to be significantly smaller for all the interfaces formed on the polymer as compared to the metal. This important and very general result is linked to one of the basic mechanisms that control molecular level alignment at interfaces with metals, i.e., the reduction of the electronic surface dipole contribution to the metal work function by adsorbed molecules.

Imaging Quasiparticle Interference in Bi2Sr2CaCu2O8+δ

Abstract: Scanning tunneling spectroscopy of the high-Tc superconductor Bi2Sr2CaCu2O8+delta reveals weak, incommensurate, spatial modulations in the tunneling conductance. Images of these energy-dependent modulations are Fourier analyzed to yield the dispersion of their wavevectors. Comparison of the dispersions with photoemission spectroscopy data indicates that quasiparticle interference, due to elastic scattering between characteristic regions of momentum-space, provides a consistent explanation for the conductance modulations, without appeal to another order parameter. These results refocus attention on quasiparticle scattering processes as potential explanations for other incommensurate phenomena in the cuprates. The momentum-resolved tunneling spectroscopy demonstrated here also provides a new technique with which to study quasiparticles in correlated materials.

Inelastic light scattering from correlated electrons

Abstract: Inelastic light scattering is an intensively used tool in the study of electronic properties of solids. Triggered by the discovery of high-temperature superconductivity in the cuprates and by new developments in instrumentation, light scattering in both the visible (Raman effect) and x-ray part of the electromagnetic spectrum has become a method complementary to optical (infrared) spectroscopy while providing additional and relevant information. The main purpose of the review is to position Raman scattering with regard to single-particle methods like angle-resolved photoemission spectroscopy, and other transport and thermodynamic measurements in correlated materials. Particular focus will be placed on photon polarizations and the role of symmetry to elucidate the dynamics of electrons in different regions of the Brillouin zone. This advantage over conventional transport (usually measuring averaged properties) provides new insights into anisotropic and complex many-body behavior of electrons in various systems. Recent developments in the theory of electronic Raman scattering in correlated systems and experimental results in paradigmatic materials such as the A15 superconductors, magnetic and paramagnetic insulators, compounds with competing orders, as well as the cuprates with high superconducting transition temperatures are reviewed. An overview of the manifestations of complexity in the Raman response due to the impact of correlations and developing competing orders is presented. In a variety of materials, observations which may be understood and a summary of important open questions that pave the way to a detailed understanding of correlated electron systems, are discussed.

Electron thermalization in gold.

Abstract: We report the direct observation of the thermalization of electrons in gold following 180 fs optical pulse excitation. The evolution of the electron energy distribution from the nascent (as photoexcited) to a hot Fermi-Dirac distribution was measured by time-resolved photoemission spectroscopy. Depending on the excitation density, thermalization times as long as \ensuremath{\approxeq}1 ps were observed. A model incorporating both electron-electron and electron-phonon scattering, and using Fermi-liquid theory to properly account for screening is found to reproduce the main features of the experiment.