Ultrafast two dimensional-infrared spectroscopy of a molecular monolayer

被引:83
作者
Bredenbeck, Jens [1 ]
Ghosh, Avishek [1 ]
Smits, Marc [1 ]
Bonn, Mischa [1 ]
机构
[1] FOM, Inst Atom & Mol Phys, NL-1098 SJ Amsterdam, Netherlands
关键词
D O I
10.1021/ja710099c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The study of vibrational coupling and energy flow in bulk (bio)molecular systems using two-dimensional infrared spectroscopy, has dramatically broadened our ability to elucidate structures and their dynamic evoluton on uttrafast timescales. For molecules at surfaces, however, these insights have been lacking. In our study, vibrational coupling in a molecular monolayer is revealed by ultrafast two-dimensional vibrational spectroscopy, with interface specificity and (sub)monolayer sensitivity. This technique provides information on vibrational coupling and energy transfer at surfaces and interfaces with subpicosecond time resolution rendering it a unique tool for the investigation of both structural and dynamical surface processes in a wide variety of disciplines.
引用
收藏
页码:2152 / +
页数:3
相关论文
共 23 条
[1]   Protein ligand migration mapped by nonequilibrium 2D-IR exchange spectroscopy [J].
Bredenbeck, Jens ;
Helbing, Jan ;
Nienhaus, Karin ;
Nienhaus, G. Ulrich ;
Hamm, Peter .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (36) :14243-14248
[2]   Double-resonance versus pulsed Fourier transform two-dimensional infrared spectroscopy: An experimental and theoretical comparison [J].
Cervetto, V ;
Helbing, J ;
Bredenbeck, J ;
Hamm, P .
JOURNAL OF CHEMICAL PHYSICS, 2004, 121 (12) :5935-5942
[3]   Theoretical description of two-dimensional vibrational spectroscopy by infrared-infrared-visible sum frequency generation [J].
Cho, M .
PHYSICAL REVIEW A, 2000, 61 (02) :12
[4]   Two-dimensional vibrational spectroscopy. V. Novel 2-dimensional surface vibrational spectroscopies of adsorbed molecules on surfaces or at interfaces [J].
Cho, MH .
JOURNAL OF CHEMICAL PHYSICS, 2000, 112 (22) :9978-9985
[5]   Ultrafast memory loss and energy redistribution in the hydrogen bond network of liquid H2O [J].
Cowan, ML ;
Bruner, BD ;
Huse, N ;
Dwyer, JR ;
Chugh, B ;
Nibbering, ETJ ;
Elsaesser, T ;
Miller, RJD .
NATURE, 2005, 434 (7030) :199-202
[6]   Hydrogen bonds in liquid water are broken only fleetingly [J].
Eaves, JD ;
Loparo, JJ ;
Fecko, CJ ;
Roberts, ST ;
Tokmakoff, A ;
Geissler, PL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (37) :13019-13022
[7]   SURFACE VIBRATIONAL-ENERGY RELAXATION BY SUM FREQUENCY GENERATION - 5-WAVE MIXING AND COHERENT TRANSIENTS [J].
HARRIS, AL ;
ROTHBERG, L .
JOURNAL OF CHEMICAL PHYSICS, 1991, 94 (04) :2449-2457
[8]   Two-dimensional spectroscopy at infrared and optical frequencies [J].
Hochstrasser, Robin M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (36) :14190-14196
[9]   Watching hydrogen-bond dynamics in a β-turn by transient two-dimensional infrared spectroscopy [J].
Kolano, Christoph ;
Helbing, Jan ;
Kozinski, Mariusz ;
Sander, Wolfram ;
Hamm, Peter .
NATURE, 2006, 444 (7118) :469-472
[10]   Lateral hopping of molecules induced by excitation of internal vibration mode [J].
Komeda, T ;
Kim, Y ;
Kawai, M ;
Persson, BNJ ;
Ueba, H .
SCIENCE, 2002, 295 (5562) :2055-2058