Femtosecond chemical reactions

被引:3
作者
Roberts, G [1 ]
机构
[1] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
来源
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES A-MATHEMATICAL PHYSICAL AND ENGINEERING SCIENCES | 2000年 / 358卷 / 1766期
关键词
femtosecond lasers; ultrafast spectroscopy; wave-packet dynamics;
D O I
10.1098/rsta.2000.0535
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Chemical reactions take place over an amazingly rapid time-scale, measured in millionths of a billionth of a second (a femtosecond). On time-scales of this duration, atoms and molecules come together, exchange energy and transfer atoms in the very act of transforming one substance into another. The emergence during the last ten years of laser devices that emit bursts of light just a few femtoseconds long can, however, enable scientists to record a series of 'snapshots' in real time of the entire temporal development of chemical reactions, and to understand their dynamical evolution during the critical moments when bonds are broken and made. This article reviews the application of femtosecond lasers to the study of the dynamics of chemical reactions. and attempts to show how a close synergy between calculations and experiment enables the forces that control the conversion of reactants into products to be understood in terms of fundamental quantum theory This is illustrated through consideration of a hierarchy of problems, starting with photochemistry in gases, catalytic processes at metal surfaces, and ending with processes in the condensed phase. A speculative conclusion forecasts developments in new laser techniques, highlighting how the exploitation of ever shorter laser pulses would permit the study and possible manipulation of the nuclear and electronic effects that lie at the conceptual heart of chemistry.
引用
收藏
页码:345 / 366
页数:22
相关论文
共 32 条
[1]  
AICKEN AM, 2000, UNPUB
[2]   Femtosecond near-infrared laser desorption of multilayer benzene on Pt{111}: spatial origin of hyperthermal desorption [J].
Arnolds, H ;
Rehbein, CEM ;
Roberts, G ;
Levis, RJ ;
King, DA .
CHEMICAL PHYSICS LETTERS, 1999, 314 (5-6) :389-395
[3]   Control of chemical reactions by feedback-optimized phase-shaped femtosecond laser pulses [J].
Assion, A ;
Baumert, T ;
Bergt, M ;
Brixner, T ;
Kiefer, B ;
Seyfried, V ;
Strehle, M ;
Gerber, G .
SCIENCE, 1998, 282 (5390) :919-922
[4]   All-solid-state cavity-dumped sub-5-fs laser [J].
Baltuska, A ;
Wei, Z ;
Pshenichnikov, MS ;
Wiersma, DA ;
Szipocs, R .
APPLIED PHYSICS B-LASERS AND OPTICS, 1997, 65 (02) :175-188
[5]   Dynamical stereochemistry on several electronic states: A computational study of Na*+H-2 [J].
BenNun, M ;
Martinez, TJ ;
Levine, RD .
JOURNAL OF PHYSICAL CHEMISTRY A, 1997, 101 (41) :7522-7529
[6]   TIME-DEPENDENT ABSORPTION OF FRAGMENTS DURING DISSOCIATION [J].
BERSOHN, R ;
ZEWAIL, AH .
BERICHTE DER BUNSEN-GESELLSCHAFT-PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1988, 92 (03) :373-378
[7]   DYNAMICS OF NONTHERMAL REACTIONS - FEMTOSECOND SURFACE-CHEMISTRY [J].
CAVANAGH, RR ;
KING, DS ;
STEPHENSON, JC ;
HEINZ, TF .
JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (04) :786-798
[8]  
CHANG Z, 1997, HYS REV LETT, V79, P2967
[9]   Generation and propagation of attosecond x-ray pulses in gaseous media [J].
Christov, IP ;
Murnane, MM ;
Kapteyn, HC .
PHYSICAL REVIEW A, 1998, 57 (04) :R2285-R2288
[10]   SUBFEMTOSECOND PULSES [J].
CORKUM, PB ;
BURNETT, NH ;
IVANOV, MY .
OPTICS LETTERS, 1994, 19 (22) :1870-1872