Timing the recoherences of attosecond electronic charge migration by quantum control of femtosecond nuclear dynamics: A case study for HCCI+

被引:23
作者
Jia, Dongming [1 ]
Manz, Joern [1 ,2 ,3 ]
Yang, Yonggang [1 ,3 ]
机构
[1] Shanxi Univ, Inst Laser Spect, State Key Lab Quantum Opt & Quantum Opt Devices, 92 Wucheng Rd, Taiyuan 030006, Peoples R China
[2] Free Univ Berlin, Inst Chem & Biochem, Takustr 3, D-14195 Berlin, Germany
[3] Shanxi Univ, Collaborat Innovat Ctr Extreme Opt, 92 Wucheng Rd, Taiyuan 030006, Peoples R China
基金
中国国家自然科学基金;
关键词
RADICAL CATIONS; LASER-PULSES; LOCALIZATION; SELECTIVITY; MODEL; TIME; MOLECULES; DRIVEN; STATE; FIELD;
D O I
10.1063/1.5134665
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This work suggests an approach to a new target of laser control of charge migration in molecules or molecular ions. The target is motivated by the fact that nuclear motions can not only cause decoherence of charge migration, typically within few femtoseconds, but they may also enable the reappearance of charge migration after much longer times, typically several tens or even hundreds of femtoseconds. This phenomenon is called recoherence of charge migration, opposite to its decoherence. The details depend on the initiation of the original charge migration by an ultrashort strong intense pump laser pulse. It may reappear quasiperiodically, with reference period T-r. We show that a well-designed pump-dump laser pulse can enforce recoherences of charge migration at different target times T-c, for example, at T-c approximate to T-r/2. The approach is demonstrated by quantum dynamics simulations of the laser driven electronic and nuclear motions in the oriented linear cation HCCI+. First, the concept is explained in terms of a didactic one-dimensional (1D) model that accounts for the decisive CI stretch. The 1D results are then confirmed by a three-dimensional model for the complete set of the CH, CC, and CI stretches. Published under license by AIP Publishing.
引用
收藏
页数:14
相关论文
共 60 条
[11]   Ultrafast charge migration by electron correlation [J].
Cederbaum, LS ;
Zobeley, J .
CHEMICAL PHYSICS LETTERS, 1999, 307 (3-4) :205-210
[12]   SPIN-ORBIT INDUCED RADIATIONLESS TRANSITIONS IN ORGANOMETALLICS - QUANTUM SIMULATION OF THE (1)E-](3)A(1) INTERSYSTEM CROSSING PROCESS IN HCO(CO)(4) [J].
DANIEL, C ;
HEITZ, MC ;
MANZ, J ;
RIBBING, C .
JOURNAL OF CHEMICAL PHYSICS, 1995, 102 (02) :905-912
[13]   Quantum Control of Electron-Proton Symmetry Breaking in Dissociative Ionization of H2 by Intense Laser Pulses [J].
Daud, Mohammad Noh ;
Lu, Huizhong ;
Chelkowski, Szczepan ;
Bandrauk, Andre D. .
INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, 2015, 115 (06) :369-380
[14]   Attosecond Hole Migration in Benzene Molecules Surviving Nuclear Motion [J].
Despre, V. ;
Marciniak, A. ;
Loriot, V. ;
Galbraith, M. C. E. ;
Rouzee, A. ;
Vrakking, M. J. J. ;
Lepine, F. ;
Kuleff, A. I. .
JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 2015, 6 (03) :426-431
[15]   Charge Migration in Propiolic Acid: A Full Quantum Dynamical Study [J].
Despre, Victor ;
Golubev, Nikolay V. ;
Kuleff, Alexander I. .
PHYSICAL REVIEW LETTERS, 2018, 121 (20)
[16]   Charge Migration in Eyring, Walter and Kimball's 1944 Model of the Electronically Excited Hydrogen-Molecule Ion [J].
Diesder, Dennis J. ;
Hermann, Gunter ;
Manz, Joern .
JOURNAL OF PHYSICAL CHEMISTRY A, 2017, 121 (28) :5332-5340
[17]   Na2 Vibrating in the Double-Well Potential of State 21Σu+ (JM=00): A Pulsating "Quantum Bubble" with Antagonistic Electronic Flux [J].
Diestler, D. J. ;
Jia, D. ;
Manz, J. ;
Yang, Y. .
JOURNAL OF PHYSICAL CHEMISTRY A, 2018, 122 (08) :2150-2159
[18]   Reconstruction of the electronic flux during adiabatic attosecond charge migration in HCCI+ [J].
Ding, Hao ;
Jia, Dongming ;
Manz, Joern ;
Yang, Yonggang .
MOLECULAR PHYSICS, 2017, 115 (15-16) :1813-1825
[19]  
Eyring H., 1944, QUANTUM CHEM
[20]   Electron dynamics in molecules: a new combination of nuclear quantum dynamics and electronic structure theory [J].
Geppert, Dorothee ;
von den Hoff, Philipp ;
de Vivie-Riedle, Regina .
JOURNAL OF PHYSICS B-ATOMIC MOLECULAR AND OPTICAL PHYSICS, 2008, 41 (07)