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We explore the merits of linear-response range-separated time-dependent density-functional theory (TDDFT) for the calculation of photoionization spectra. We consider two variants of range-separated TDDFT, namely, the time-dependent range-separated hybrid (TDRSH) scheme, which uses a global range-separation parameter, and the time-dependent locally range-separated hybrid (TDLRSH), which uses a local range-separation parameter, and compare with standard time-dependent local-density approximation (TDLDA) and time-dependent Hartree-Fock (TDHF). We show how to calculate photoionization spectra with these methods using the Sternheimer approach formulated in a non-orthogonal B-spline basis set with appropriate frequency-dependent boundary conditions. We illustrate these methods on the photoionization spectrum of the Be atom, focusing, in particular, on the core resonances. Both the TDRSH and TDLRSH photoionization spectra are found to constitute a large improvement over the TDLDA photoionization spectrum and a more modest improvement over the TDHF photoionization spectrum.
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http://dx.doi.org/10.1063/5.0091073 | DOI Listing |
Angew Chem Int Ed Engl
August 2025
Lehrstuhl für Organische Chemie II, Ruhr-Universität Bochum, Universitätsstraße 150, 44801, Bochum, Germany.
We report the first direct observation of the pentafluorophenyl cation in the gas phase via vacuum ultraviolet (VUV) photoionization (PI) of the thermally generated pentafluorophenyl radical. The reactive intermediates and stable reaction products were characterized utilizing photoelectron photoion coincidence (PEPICO) spectroscopy with synchrotron radiation. Electron removal from the pentafluorophenyl radical yields the cation with an adiabatic ionization energy (AIE) of 9.
View Article and Find Full Text PDFJ Phys Chem A
August 2025
University of Potsdam, Institute of Chemistry, Karl-Liebknecht-Straße 24-25, Potsdam 14476, Germany.
Thionated nucleobases have drawn considerable attention due to their role in medical treatment and biology, which triggered studies of their photophysics and photochemistry using various experimental and theoretical techniques. In particular, vacuum ultraviolet (VUV)-induced dissociative photoionization of 2-thiouracil (2-TU) has been recently studied using synchrotron radiation [Robinson et al., , 28, 2354].
View Article and Find Full Text PDFJ Phys Chem A
August 2025
College of Chemistry, State Key Laboratory of Advanced Chemical Power Sources, Tianjin Key Laboratory of Biosensing and Molecular Recognition, Frontiers Science Centre for New Organic Matter, Nankai University, Tianjin 300071, China.
Microdroplet chemistry has been utilized in different fields due to a plethora of unique properties such as the existence of a high electric field up to 10 V/m at the surface of the microdroplets or between two oppositely charged microdroplets. Such a high field endows microdroplets with the ability of ionizing ambient air. In this study, we compare the ionization capability of microdroplets with several other ionization methods, including photoionization (vacuum ultraviolet photons, X-ray), nuclear decay (α-ray from Am), and discharge ionization (piezoelectric discharge, dielectric barrier discharge, and arc discharge) using mass spectrometry to detect ionic products.
View Article and Find Full Text PDFJ Phys Chem A
July 2025
Department of Chemistry, National Tsing Hua University, Hsinchu 300044 Taiwan, Republic of China.
Ultrafast photoionization-induced ionic relaxation dynamics in -propylbenzene and 2,2-dimethylpropylbenzene cations were investigated using time- and spectrally resolved ion photofragmentation spectroscopy with a femtosecond photoionization-photofragmentation (PI-PF) detection scheme. Photoionization was initiated via 1 + 1 REMPI using femtosecond UV pump pulses well below the strong-field ionization regime, and the evolving ionic systems were probed by delayed visible-wavelength probe pulses to induce photofragmentation. Despite substantial ionic fragmentation induced by UV photoionization, the observed parent ion depletion transient signals can be attributed exclusively to the relaxation dynamics of intact parent cations generated at the two-photon level.
View Article and Find Full Text PDFPhys Chem Chem Phys
July 2025
Université de Lille, CNRS, PC2A, F-59000 Lille, France.
A novel coupling of a stagnation plate burner and the SAPHIRS instrument located at synchrotron SOLEIL has been performed to enable the observation of labile species and radicals within stabilized cool flames. Gases were extracted from a dimethyl ether/O/O/N cool flame with a capillary probe and expanded through two consecutive skimmers to reach the synchrotron vacuum ultraviolet-photoelectron photoion coincidence spectrometer. threshold photoelectron spectra (TPES) and total ion yields (TIY) were recorded as a function of the photon energy, and led to the identification of species that have so far never been observed in cool flames, including the only expected keto- or aldo-hydroperoxide (hydroperoxymethylformate), hydrogen peroxide, methyl and hydroperoxyl radicals.
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