База данных: Каталог библиотеки СФУ
Библиографическое описание: Time-resolved study of recoil-induced rotation by X-ray pump - X-ray probe spectroscopy : научное издание / J. Liu [et al.]. - Текст : непосредственный // Phys. Chem. Chem. Phys. = Physical Chemistry Chemical Physics. - 2022. - Vol. 24, Is. 11. - P. 6627-6638. - The reported study was funded by the Russian Science Foundation, Project No. 21-12-00193. J.-C. L. acknowledges support by the National Natural Science Foundation of China under Grant No. 11974108 and No. 11574082, and the Fundamental Research Funds for the Central Universities (No. 2021MS046). A. F. acknowledges from the European Research Council through ERC-ADG-2014 (Advanced Investigator Grant No. 669531 EDAX) at the University of Potsdam within the Horizon 2020 EU Framework Programme for Research and Innovation. A. F. and F. G. acknowledge support by Helmholtz-Zentrum Berlin für Materialien und Energie GmbH. N.I. acknowledges funding from the Foundation for the Advancement of Theoretical Physics and Mathematics “BASIS” (Grant No. 19-1-4-66-1). Support from the Swedish Research Council, Project No. 2019-03470, is acknowledged. - MAR 16. - ISSN 1463-9076. - ISSN 1463-9084, DOI 10.1039/d1cp05000a. Скопировать
Аннотация: Modern stationary X-ray spectroscopy is unable to resolve rotational structure. In the present paper, we propose to use time-resolved two color X-ray pump-probe spectroscopy with picosecond resolution for real-time monitoring of the rotational dynamics induced by the recoil effect. The proposed technique consists of two steps. The first short pump X-ray pulse ionizes the valence electron, which transfers angular momentum to the molecule. The second time-delayed short probe X-ray pulse resonantly excites a 1s electron to the created valence hole. Due to the recoil-induced angular momentum the molecule rotates and changes the orientation of transition dipole moment of core-excitation with respect to the transition dipole moment of the valence ionization, which results in a temporal modulation of the probe X-ray absorption as a function of the delay time between the pulses. We developed an accurate theory of the X-ray pump-probe spectroscopy of the recoil-induced rotation and study how the energy of the photoelectron and thermal dephasing affect the structure of the time-dependent X-ray absorption using the CO molecule as a case-study. We also discuss the feasibility of experimental observation of our theoretical findings, opening new perspectives in studies of molecular rotational dynamics.
Modern stationary X-ray spectroscopy is unable to resolve rotational structure. In the present paper, we propose to use time-resolved two color X-ray pump-probe spectroscopy with picosecond resolution for real-time monitoring of the rotational dynamics induced by the recoil effect. The proposed technique consists of two steps. The first short pump X-ray pulse ionizes the valence electron, which transfers angular momentum to the molecule. The second time-delayed short probe X-ray pulse resonantly excites a 1s electron to the created valence hole. Due to the recoil-induced angular momentum the molecule rotates and changes the orientation of transition dipole moment of core-excitation with respect to the transition dipole moment of the valence ionization, which results in a temporal modulation of the probe X-ray absorption as a function of the delay time between the pulses. We developed an accurate theory of the X-ray pump-probe spectroscopy of the recoil-induced rotation and study how the energy of the photoelectron and thermal dephasing affect the structure of the time-dependent X-ray absorption using the CO molecule as a case-study. We also discuss the feasibility of experimental observation of our theoretical findings, opening new perspectives in studies of molecular rotational dynamics. © 2022 the Owner Societies.
Год издания: 2022
Издательство: ROYAL SOC CHEMISTRY, CAMBRIDGE
Источник: PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Выпуск: Vol. 24, Is. 11
Номера страниц: 6627-6638
Держатель оригинала документа: North China Elect Power Univ, Dept Math & Phys, Beijing 102206, Peoples R China; , Siberian Fed Univ, Int Res Ctr Spect & Quantum Chem IRC SQC, Krasnoyarsk 660041, Russia; , KTH Royal Inst Technol, Dept Theoret Chem & Biol, S-10691 Stockholm, Sweden; , Helmholtz Zentrum Berlin Mat & Energie, Inst Methods & Instrumentat Synchrotron Radiat Re, FG ISRR, Albert Einstein Str 15, D-12489 Berlin, Germany; , Univ Potsdam, Inst Phys & Astron, Karl Liebknecht Str 24-25, D-14476 Potsdam, Germany; , Sorbonne Univ, Lab Chim Phys Matiere & Rayonnement, LCPMR, CNRS, F-75005 Paris, France
Количество экземпляров: Твёрдая копия издания отсутствует в фонде библиотеки
Рубрики: Chemistry, Physical, Physics, Atomic, Molecular & Chemical, Angular momentum, Dipole moment, Molecules, Optical pumping, Probes, X ray spectroscopy, Probe spectroscopy, Rotational dynamics, Rotational structures, Time resolved studies, Time-resolved, Transition dipole moments, X ray pulse, X ray pump-probe spectroscopy, X-ray absorptions, X-ray spectroscopy, X ray absorption, article, crystal structure, dipole, excitation, feasibility study, ionization, pump probe spectroscopy, rotation, theoretical study, X ray
ISSN: 1463-9076