Study on photodynamics of furan via strong field multiphoton ionization by velocity map imaging technique

被引:7
作者
Yan Yihui [1 ,2 ]
Long Jinyou [3 ]
Liu Yuzhu [1 ,2 ]
机构
[1] Nanjing Univ Informat Sci & Technol, Jiangsu Key Lab Optoelect Detect Atmosphere & Oce, Nanjing 210044, Jiangsu, Peoples R China
[2] Jiangsu Collaborat Innovat Ctr Atmospher Environm, Nanjing 210044, Jiangsu, Peoples R China
[3] Chinese Acad Sci, Wuhan Inst Phys & Math, State Key Lab Magnet Resonance & Atom & Mol Phys, Wuhan 430071, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Furan; Velocity map imaging; Photodissociation; PHOTOELECTRON; CONVERSION; ION;
D O I
10.1016/j.chemphys.2019.110611
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
The photodissociation dynamics of furan at 800 nm was studied using velocity map imaging technology coupled with time-of-flight mass spectrometry. Dissociation channels are obtained by analysis of furan multiphoton ionization dissociation under strong field. According to time-of-flight mass spectrometry experiments, C4H4O+, C3H3+, C3H4+, C2H2O+, HCO+ are obtained by multiphoton ionization dissociation of furan. By calculating the speed distribution and kinetic energy distribution using velocity map imaging technology, it can be seen that there are two channels of high energy channel and low energy channel in the process of photodissociation. The anisotropy parameters of furan dissociation for both channels are close to 0 (Isotropy) by analysis of the angular distribution of dissociated fragment ions. The density functional theory was employed to calculate the configuration change of the furan molecule before and after ionization, the energy level intensity of the ionic states and corresponding oscillator strength.
引用
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页数:5
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共 18 条
[1]   Conversion of plant biomass to furan derivatives and sustainable access to the new generation of polymers, functional materials and fuels [J].
Chernyshev, Victor M. ;
Kravchenko, Oleg A. ;
Ananikov, Valentine P. .
RUSSIAN CHEMICAL REVIEWS, 2017, 86 (05) :357-387
[2]   Electronic states of thiophenyl and furanyl radicals and dissociation energy of thiophene via photoelectron imaging of negative ions [J].
Culberson, Lori Marie ;
Sanov, Andrei .
JOURNAL OF CHEMICAL PHYSICS, 2011, 134 (20)
[3]   PHOTOELECTRON-SPECTROSCOPICAL STUDY OF VIBRATIONS OF FURAN, THIOPHENE, PYRROLE AND CYCLOPENTADIENE [J].
DERRICK, PJ ;
ASBRINK, L ;
EDQVIST, O ;
LINDHOLM, E .
SPECTROCHIMICA ACTA PART A-MOLECULAR SPECTROSCOPY, 1971, A 27 (12) :2525-&
[4]   High-resolution photoelectron imaging of cryogenically cooled α- and β-furanyl anions [J].
DeVine, Jessalyn A. ;
Weichman, Marissa L. ;
Lyle, Steven J. ;
Neumark, Daniel M. .
JOURNAL OF MOLECULAR SPECTROSCOPY, 2017, 332 :16-21
[5]   The chemistry of graphene oxide [J].
Dreyer, Daniel R. ;
Park, Sungjin ;
Bielawski, Christopher W. ;
Ruoff, Rodney S. .
CHEMICAL SOCIETY REVIEWS, 2010, 39 (01) :228-240
[6]   Reconstruction of abel-transformable images: The Gaussian basis-set expansion abel transform method [J].
Dribinski, V ;
Ossadtchi, A ;
Mandelshtam, VA ;
Reisler, H .
REVIEW OF SCIENTIFIC INSTRUMENTS, 2002, 73 (07) :2634-2642
[7]   MASS SPECTROMETRY IN STRUCTURAL AND STEREOCHEMICAL PROBLEMS .63. HYDROGEN REARRANGEMENTS INDUCED BY ELECTRON IMPACT ON N-N-BUTYL- AND N-N-PENTYLPYRROLES [J].
DUFFIELD, AM ;
BEUGELMA.R ;
BUDZIKIE.H ;
LIGHTNER, DA ;
WILLIAMS, DH ;
DJERASSI, C .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1965, 87 (04) :805-&
[8]   Velocity map imaging of ions and electrons using electrostatic lenses: Application in photoelectron and photofragment ion imaging of molecular oxygen [J].
Eppink, ATJB ;
Parker, DH .
REVIEW OF SCIENTIFIC INSTRUMENTS, 1997, 68 (09) :3477-3484
[9]   ELECTRON-TRANSFER KINETICS OF REDOX REACTIONS AT THE SEMICONDUCTOR ELECTROLYTE CONTACT - A NEW APPROACH [J].
GERISCHER, H .
JOURNAL OF PHYSICAL CHEMISTRY, 1991, 95 (03) :1356-1359
[10]   Slow photoelectron velocity-map imaging spectroscopy of cold negative ions [J].
Hock, Christian ;
Kim, Jongjin B. ;
Weichman, Marissa L. ;
Yacovitch, Tara I. ;
Neumark, Daniel M. .
JOURNAL OF CHEMICAL PHYSICS, 2012, 137 (24)