Nonresonant Multiphoton Ionization of Stark Decelerated Molecules by Femtosecond Laser Pulses

被引:0
|
作者
孟从森 [1 ]
治辉 [1 ]
王小伟 [1 ]
张栋文 [1 ]
赵增秀 [1 ]
袁建民 [1 ,2 ]
机构
[1] Department of Physics, National University of Defense Technology
[2] Department of Physics, Graduate School of China Academy of Engineering Physics
基金
中国国家自然科学基金;
关键词
D O I
暂无
中图分类号
O56 [分子物理学、原子物理学]; TN24 [激光技术、微波激射技术];
学科分类号
070203 ; 1406 ;
摘要
Nonresonant multiphoton ionization by femtosecond laser pulses can be applied to any molecule virtually,thereby greatly enhancing the scope of Stark decelerated molecules.For comparison,we detect decelerated and trapped ammonia molecules using two different schemes:(ⅰ) nonresonant multiphoton ionization using intense femtosecond(fs) pulses in the near infrared,and(ⅱ) resonance-enhanced multiphoton ionization using nanosecond(ns) pulses from a tunable UV laser.The observed number of ions per shot for both schemes is similar.The fs laser detection scheme suffers from an increased background,which can be effectively eliminated by subsequent mass and velocity selection.To determine the detection volume of the ns laser detection scheme,we present measurements in which the decelerated ammonia molecules are bunched to a packet with a longitudinal spread well below~100 μm.It is concluded that the detection volume for the ns laser detection scheme is 1.5-2 times larger than that of the fs laser detection scheme.
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页码:27 / 30
页数:4
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