Photoelectron imaging spectroscopy of S1(1B2u π,π*) benzene via 6(1)1n (n = 0-3) levels

We report resonance-enhanced two-photon ionization photo-electron spectroscopy of jet-cooled benzene via the 6(1)1(n) (n = 0-3) vibronic levels in S(1)((1)B(2u) π,π*) using a nanosecond UV laser and photoelectron imaging. The best energy resolution (ΔE/E) was 0.7%. The photoelectron spectrum from the S(1) 6(1)1(3) level (E(vib) = 3284 cm(-1)) in the channel three region exhibited a clear signature of intramolecular vibrational redistribution (IVR). The spectral features were consistent with picosecond zero kinetic energy photoelectron (ZEKE) spectra reported by Smith et al. [ J. Phys. Chem. 1995, 99, 1768]. The photoelectron angular anisotropy parameter β(2) was found to be negative in ionization from the 6(1)1(n) (n = 0-3) levels with photoelectron kinetic energies up to 5000 cm(-1). No influence of a shape resonance was identified.     

A new action photoelectron spectroscopy for anions

We present a new experimental approach, in which anion photodetachment spectroscopy is recorded with electrons of fixed kinetic energy. This approach circumvents some shortcomings of the zero electron kinetic energy method. Our method is based on a modified magnetic bottle photoelectron spectrometer (MBPES). A tunable laser is used to detach electrons from mass selected anions, drifting collinearly with the 40 cm MBPES drift tube. To avoid Doppler broadening, a low voltage pulse removes the velocity component of anions from the detached electrons. Spectra are recorded by collecting the wavelength dependence of electron-signal at a predetermined TOF window, corresponding to a specific electron-kinetic energy. We call this approach PEACE, denoting photoelectron action spectroscopy at constant kinetic energy. Our best resolution is 0.65 meV for 1.5 meV electrons. We present a PEACE spectrum of HgCl(-) together with the corresponding simulated theoretical spectrum. The method is similar in resolution and data collection rates to the slow electron velocity map imaging technique recently introduced by Neumark and co-workers.     

He I (584 Å) photoelectron spectra and photoionization cross sections of atomic chlorine and bromine

Well-resolved He I photoelectron spectra of atomic chlorine and bromine have been obtained without serious background electrons, giving rise to relative photoelectron intensities associated with differential photoionization cross sections at an angle of 90° with respect to the incident 584 Å radiation.     

Chiral signatures in angle-resolved valence photoelectron spectroscopy of pure glycidol enantiomers

Photoionization of the chiral molecule glycidol has been investigated in the valence region. Photoelectron circular dichroism (PECD) curves have been obtained at various photon energies by using circularly polarized VUV synchrotron radiation and a velocity map imaging technique to record angle-resolved photoelectron spectra (PES). The measured chiral asymmetries vary dramatically with the photon energy as well as with the ionized orbital, improving the effective orbital resolution of the PECD spectrum with respect to the PES. Typical asymmetry factors of 5% are observed, but the peak values measured range up to 15%. The experimental results are interpreted by continuum multiple scattering (CMS-Xalpha) calculations for several thermally accessible glycidol conformers. We find that a nearly quantitative agreement between theory and experiments can be achieved for the ionization of several molecular orbitals. Owing to the sensitivity of PECD to molecular conformation this allows us to identify the dominant conformer. The influence of intramolecular hydrogen bond orbital polarization is found to play a small yet significant role in determining the chiral asymmetry in the electron angular distributions.     

The X-ray photoelectron spectrum of sulphur vapour

The X-ray photoelectron spectrum of S₈ vapour obtained with Al Kα radiation in a spectrometer designed for high temperature work is reported. The S2s and 2p levels were found to lie at 10.1(1) eV and 10.5(1) eV lower binding energy than the corresponding levels in SF₆ and 0.5 eV lower than the levels in H₂S. A S2p/S2s intensity ratio per electron of 0.40(3) was determined, in very good agreement with theory. The photoelectron spectrum in the molecular optical region was obtained and is in good agreement with a previously published spectrum of sulphur powder.     

He (I) and He (II) photoelectron spectra of ozone

The he I (21.2 eV) and He II (40.8 eV) photoelectron spectra of ozone have been recorded under high resolution. Ionization potentials are identified at 12.75 eV, 13.02 eV, 13.57 eV, and two broad bands are centered at 17.7 eV and 20.1 eV. The experimental results and the orbital assignment are not completely in accord with those given recently in the literature.     

Design and fabrication of an ultraviolet photoelectron spectrometer for the study of free molecules

An ultraviolet photoelectron spectrometer for the study of free atoms and molecules has been designed and fabricated with indigeneous components. The spectrometer consists of a 100 mA HeI discharge lamp, 180° hemispherical electron energy analyser (127 mm mean dia) and electron multiplier ratemeter electron detection systems. The resolution of the spectrometer is 90 meV/and the intensity of N₂ (5σ) band is 10⁵ c/sec. The sample inlet and the collision chamber can be heated to 500 K so that solids of low vapour pressure can be studied. Typical spectra of molecules recorded with the instrument are shown. Contribution No. 373 from the Solid State and Structural Chemistry Unit.     

UV photoelectron spectra of 5- and 6-azauracil

The He(I) photoelectron spectra of 5-azauracil (1,3,5-triazine-2,4(1H,3H)-dione) and 6-azauracil (1,2,4-triazine-3, 5(2H,4H)-dione) are presented. The spectra are assigned by using INDO/S calculations and comparison arguments with uracil. The first ionization energy in the title compounds is higher than in the usual nucleic acid bases.     

Two-color visible/vacuum ultraviolet photoelectron imaging dynamics of Br2

An experimental two-color photoionization dynamics study of laser-excited Br2 molecules is presented, combining pulsed visible laser excitation and tunable vacuum ultraviolet (VUV) synchrotron radiation with photoelectron imaging. The X 1Sigmag + -B 3Pi0+u transition in Br2 is excited at 527 nm corresponding predominantly to excitation of the v' = 28 vibrational level in the B 3Pi0+u state. Tunable VUV undulator radiation in the energy range of 8.40-10.15 eV is subsequently used to ionize the excited molecules to the X 2Pi32,12 state of the ion, and the ionic ground state is probed by photoelectron imaging. Similar experiments are performed using single-photon synchrotron ionization in the photon energy range of 10.75-12.50 eV without any laser excitation. Photoelectron kinetic energy distributions are extracted from the photoelectron images. In the case of two-color photoionization using resonant excitation of the intermediate B 3Pi0+u state, a broad distribution of photoelectron kinetic energies is observed, and in some cases even a bimodal distribution, which depends on the VUV photon energy. In contrast, for single-photon ionization, a single nearly Gaussian-shaped distribution is observed, which shifts to higher energy with photon energy. Simulated spectra based on Franck-Condon factors for the transitions Br2(X 1Sigmag+, v" = 0)-Br2 +(X 2Pi12,32, v+) and Br2(B 3Pi0+u, v' = 28)-Br2 +(X 2Pi12,32, v+) are generated. Comparison of these calculated spectra with the measured images suggests that the differences in the kinetic energy distributions for the two ionization processes reflect the different extensions of the vibrational wave functions in the v" = 0 electronic ground state (X 1Sigmag+) versus the electronically and vibrationally excited state (B 3Pi0+u, v' = 28).     

VUV photoelectron imaging of biological nanoparticles: ionization energy determination of nanophase glycine and phenylalanine-glycine-glycine

The ionization energies of biological nanoparticles are determined using the velocity map photoelectron imaging technique. A beam of nanoparticles produced by aerosol methods is photoionized with tunable vacuum ultraviolet (VUV) synchrotron radiation. The resulting photoelectrons are detected and their angular and energy distributions are measured, yielding an angle-resolved photoelectron spectrum. The ionization energies of the nanoparticles are derived from plots of the photoelectron spectrum versus incident photon energy. The ionization energies of nanophase glycine and phenylalanine-glycine-glycine are 7.6 +/- 0.2 eV, and 7.5 +/- 0.2 eV, respectively. X-Ray powder diffraction studies on the glycine nanoparticles indicate that they are crystalline in nature. The reduced ionization energy when compared to gas phase results suggests that the polarization energy in the solid is significant. The difference in the ionization energy between the nano and gas phase reflects this polarization energy and is derived to be 1.7 +/- 0.2 eV and 1.6 +/- 0.2 eV for glycine and phenylalanine-glycine-glycine, respectively. Using these results the molecular polarizability of glycine is estimated to be 4.7 +/- 0.3 A3 (31.9 +/- 1.9 au).     

Vacuum Ultraviolet and Soft X‐ray Photoelectron Spectroscopy of Liquid Beams Using a Hemispherical Photoelectron Spectrometer with a Multistage Differential Pumping System

We present photoelectron spectroscopy of liquid beams using a high‐resolution hemispherical photoelectron spectrometer with a multistage differential pumping system developed in our laboratory. Intense soft X‐ray synchrotron radiation (500‐1200 eV) at SPring‐8 and a relatively large detection solid angle (1.5 × 10^?2 π sr) of the spectrometer enable highly efficient measurements of X‐ray photoelectron spectra of liquids. Vacuum ultraviolet photoelectron spectroscopy using the same spectrometer provides sufficiently high spectral resolution to resolve rotational isomers of gas‐phase molecules.     

Threshold photoelectron spectroscopy of iodine monobromide

A high-resolution (1–7 meV) threshold photoelectron spectroscopic study of IBr was performed using synchrotron radiation and a penetrating-field electron spectrometer over the valence ionization region of the molecule. Extensive vibrational structure was found in all three electronic-state band systems (X²Π_i, A²Π_i and B²Σ⁺) of IBr⁺. In the (X²Π_i) band system both spin–orbit components exhibited extended vibrational structure in the Franck–Condon gap regions that is attributed to resonance autoionization of neutral Rydberg states lying in these energy regions. Analysis of this vibrational structure yielded accurate spectroscopic constants.     

Threshold photoelectron spectroscopy of ozone

Threshold photoelectron spectrum of ozone is presented for the first time at a resolution of 21-38 meV using synchrotron radiation in the energy region of 12-21 eV. The ionization energies of the first ionized states were determined and an interpretation of the O3 spectrum with respect to its first three ionic states, 1 2A1, 1 2B2, and 1 2A2, is presented. Above 16 eV the enhancement of the intensities of the 2 2B1, 3 2A1, and 4 2B2 band systems due to the contribution of indirect processes was observed, not accessible by conventional photoelectron spectroscopy. It was also resolved and assigned the extensive vibrational structures of ozone. Between 15.5 and 18.5 eV the main band contours are similar to those found in conventional photoelectron spectroscopy, except that our threshold photoelectron spectrum reveals extensive additional vibrational structures. The band 2 2B1 was found to present an irregular vibrational spacing DeltaE, with a minimum value of 80 meV at approximately 16.47 eV.     

Electronic state spectroscopy of c-C5F8 explored by photoabsorption, electron impact, photoelectron spectroscopies and ab initio calculations

The electronic transitions and resonance-enhanced vibrational excitations of octafluorocyclopentene (c-C5F8) have been investigated using high-resolution photoabsorption spectroscopy in the energy range 6-11 eV. In addition, the high-resolution electron energy loss spectrum (HREELS) was recorded under the electric dipolar excitation conditions (100 eV incident energy, approximately 0 degrees scattering angle) over the 5-14 eV energy loss range. A He(I) photoelectron spectrum (PES) has also been recorded between 11 and 20 eV, allowing us to derive a more precise value of (11.288 +/- 0.002) eV for the ground neutral state adiabatic ionization energy. All spectra presented in this paper represent the first and highest resolution data yet reported for octafluorocyclopentene. Ab initio calculations have been performed for helping in the assignment of the spectral bands for both neutral excited states and ionic states.     

Valence electron bands in the gas-phase x-ray photoelectron spectra of acetonitrile and nitromethane

The valence electron bands of the gas-phase X-ray photoelectron spectra were measured on acetonitrile and nitromethane. It is shown that the observed spectra can be interpreted successfully by comparison with the He I photoelectron spectra and the results of CNDO/2 calculations.     

3s Rydberg and cationic States of pyrazine studied by photoelectron spectroscopy

We have studied 3s(n-1 and pi-1) Rydberg states and D0(n-1) and D1(pi-1) cationic states of pyrazine [1,4-diazabenzene] by picosecond (2 + 1) resonance-enhanced multiphoton ionization (REMPI), (2 + 1) REMPI photoelectron imaging, He(I) ultraviolet photoelectron spectroscopy (UPS), and vacuum ultraviolet pulsed field ionization photoelectron spectroscopy (VUV-PFI-PE). The new He(I) photoelectron spectrum of pyrazine in a supersonic jet revealed a considerably finer vibrational structure than a previous photoelectron spectrum of pyrazine vapor. We performed Franck-Condon analysis on the observed photoelectron and REMPI spectra in combination with ab initio density functional theory and molecular orbital calculations to determine the equilibrium geometries in the D0 and 3s(n-1) states. The equilibrium geometries were found to differ slightly between the D0 and 3s states, indicating the influence of a Rydberg electron on the molecular structure. The locations of the D1-D0 and 3s(pi-1)-3s(n-1) conical intersections were estimated. From the line width in the D1 <-- S0 spectrum, we estimated the lifetime of D1 to be 12 fs for pyrazine and 15 fs for fully deuterated pyrazine. A similar lifetime was estimated for the 3s(pi-1) state of pyrazine by REMPI spectroscopy. The vibrational feature of D1 observed in the VUV-PFI-PE measurement differed dramatically from that in the UPS spectrum, which suggests that the high-n Rydberg (ZEKE) states converging to the D1 vibronic state are short-lived due to electronic autoionization to the D0 continuum.     

Information depth determination for hard X‐ray photoelectron spectroscopy up to 15 keV photoelectron kinetic energy

In the present work, we have determined the information depth in a solid for hard X‐ray photoelectron spectroscopy (HAXPES) up to a photoelectron kinetic energy of 15 keV. For that, we have followed the evolution of the photoemission signal from different core levels of a gold overlayer grown in situ on a polycrystalline copper substrate as a function of the photoelectron kinetic energy. We demonstrate that in the case of gold, an information depth of 57 nm can be achieved by detecting photoelectrons with 15‐keV kinetic energy. The photoemission signal produced at this depth corresponds to 0.2% of the signal coming from a semi‐infinite solid bulk. Such a high sensitivity can only be reached with the combination of a third‐generation synchrotron radiation beam with a high‐transmission electron analyzer. Copyright © 2008 John Wiley & Sons, Ltd.     

Limonene: electronic state spectroscopy by high-resolution vacuum ultraviolet photoabsorption, electron scattering, He(I) photoelectron spectroscopy and ab initio calculations

Electronic state spectroscopy of limonene has been investigated using vacuum ultraviolet photoabsorption spectroscopy in the energy range 5.0-10.8 eV. The availability of a high resolution photon beam (~0.075 nm) enabled detailed analysis of the vibrational progressions and allowed us to propose, for the first time, new assignments for several Rydberg series. Excited states located in the 7.5-8.4 eV region have been studied for the first time. A He(I) photoelectron spectrum has also been recorded from 8.2 to 9.5 eV and compared to previous low resolution works. A new value of 8.521 ± 0.002 eV for the ground ionic state adiabatic ionisation energy is proposed. Absolute photoabsorption cross sections were derived in the 10-26 eV range from electron scattering data. All spectra presented in this paper represent the highest resolution data yet reported for limonene. These experiments are complemented by new ab initio calculations performed for the three most abundant conformational isomers of limonene, which we then used in the assignment of the spectral bands.     

The photoelectron spectrum of phosphorus pentafluoride

The He(I) photoelectron spectrum of PF₅ has been determined. Assignments for the six observed bands are suggested and comparisons with several semi-empirical molecular orbital calculations are made. Particular interest is associated with the fifth band since it exhibits vibrational fine structure.     

Electronic Structures of Copper(I) and Silver(I) beta-Diketonate Complexes

The valence electronic structures of [Cu(hfac)L] (hfac = CF(3)C(O)CHC(O)CF(3); L = PMe(3), CNMe), [Ag(hfac)(PMe(3))], and [Ag(fod)(PEt(3))] (fod = t-BuC(O)CHC(O)C(3)F(7)) have been studied by recording their photoelectron spectra and by performing Xalpha-SW calculations on the model compounds [M(dfm)(PH(3))] (dfm = HC(O)CHC(O)H; M = Cu, Ag) and [Cu(dfm)(CNH)]. For the copper complexes, the spectra were recorded between 21 and 160 eV using He I, He II and synchrotron radiation; while, for the silver complexes, He I and He II, spectra were recorded. Assignments were made by comparison of experimental and calculated values of band energies, and, for the copper complexes, by similar comparison of experimental and theoretical branching ratios as a function of photon energy. For the silver complexes, a more limited comparison of band intensities in the He I and He II spectra was made. In analogous compounds, it is shown that the binding energies follow the sequence Ag 4d > Cu 3d, with an energy difference of almost 2 eV.