Femtosecond electron diffraction: 'making the molecular movie'

被引:159
作者
Dwyer, JR
Hebeisen, CT
Ernstorfer, R
Harb, M
Deyirmenjian, VB
Jordan, RE
Miller, RJD [1 ]
机构
[1] Univ Toronto, Inst Opt Sci, Toronto, ON M5S 3H6, Canada
[2] Univ Toronto, Dept Chem, Toronto, ON M5S 3H6, Canada
[3] Univ Toronto, Dept Phys, Toronto, ON M5S 3H6, Canada
来源
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY A-MATHEMATICAL PHYSICAL AND ENGINEERING SCIENCES | 2006年 / 364卷 / 1840期
关键词
femtosecond electron diffraction; transition states; atomic level view of dynamics; electron-electron correlations; space charge effects; laser ponderomotive effects;
D O I
10.1098/rsta.2005.1735
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
Femtosecond electron diffraction (FED) has the potential to directly observe transition state processes. The relevant motions for this barrier-crossing event occur on the hundred femtosecond time-scale. Recent advances in the development of high-flux electron pulse sources with the required time resolution and sensitivity to capture barrier-crossing processes are described in the context of attaining atomic level details of such structural dynamics-seeing chemical events as they occur. Initial work focused on the ordered-to-disordered phase transition of Al under strong driving conditions for which melting takes on mn or molecular scale dimensions. This work has been extended to Au, which clearly shows a separation in time-scales for lattice heating and melting. It also demonstrates that superheated face-centred cubic (FCC) metals melt through thermal mechanisms involving homogeneous nucleation to propagate the disordering process. A new concept exploiting electron-electron correlation is introduced for pulse characterization and determination of t=0 to within 100 fs as well as for spatial manipulation of the electron beam. Laser-based methods are shown to provide further improvements in time resolution with respect to pulse characterization, absolute t=0 determination, and the potential for electron acceleration to energies optimal for time-resolved diffraction.
引用
收藏
页码:741 / 778
页数:38
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