Polarization-sensitive IR-pump-x-ray-probe spectroscopy

被引:6
|
作者
Liu, Ji-Cai [1 ]
Savchenko, Viktoriia [2 ,3 ]
Kimberg, Victor [2 ,3 ]
Odelius, Michael [4 ]
Gel'mukhanov, Faris [2 ,3 ,5 ,6 ]
机构
[1] North China Elect Power Univ, Dept Math & Phys, Beijing 102206, Peoples R China
[2] KTH Royal Inst Technol, Dept Theoret Chem & Biol, S-10691 Stockholm, Sweden
[3] Siberian Fed Univ, Int Res Ctr Spect & Quantum Chem IRC SQC, Krasnoyarsk 660041, Russia
[4] Stockholm Univ, AlbaNova Univ Ctr, Dept Phys, SE-10691 Stockholm, Sweden
[5] Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Krasnoyarsk 660036, Russia
[6] Helmholtz Zentrum Berlin Mat & Energie, Inst Methods & Instrumentat Synchrotron Radiat Re, Albert Einstein Str 15, D-12489 Berlin, Germany
基金
中国国家自然科学基金; 瑞典研究理事会; 俄罗斯基础研究基金会; 欧盟地平线“2020”;
关键词
45;
D O I
10.1103/PhysRevA.103.022829
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
X-ray absorption and core-ionization spectra of molecules pumped by two coherent infrared pulses with different polarizations are studied theoretically. We have found a sensitivity of the vibrational profile of x-ray probe spectra to polarizations of the IR and x-ray pulses. This polarization dependence is qualitatively different for x-ray absorption and x-ray photoelectron spectra. Measurements of this polarization dependence allow to select the difference in Franck-Condon distributions from the lowest and pumped vibrational levels of the electronic ground state. The proposed technique is exemplified numerically using x-ray absorption spectra of the pumped CO molecule. We also show that this kind of pump-probe spectroscopy can enable studies of the dynamics of molecular rotation.
引用
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页数:10
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