Quantum control of photodissociation using intense, femtosecond pulses shaped with third order dispersion

被引:15
作者
Lev, U. [1 ]
Graham, L. [1 ,2 ]
Madsen, C. B. [3 ]
Ben-Itzhak, I. [1 ,3 ]
Bruner, B. D. [4 ]
Esry, B. D. [3 ]
Frostig, H. [4 ]
Heber, O. [1 ]
Natan, A. [4 ,5 ]
Prabhudesai, V. S. [4 ,6 ]
Schwalm, D. [1 ,7 ]
Silberberg, Y. [4 ]
Strasser, D. [8 ]
Williams, I. D. [2 ]
Zajfman, D. [1 ]
机构
[1] Weizmann Inst Sci, Dept Particle Phys & Astrophys, IL-76100 Rehovot, Israel
[2] Queens Univ Belfast, Sch Math & Phys, Ctr Plasma Phys, Belfast BT7 1NN, Antrim, North Ireland
[3] Kansas State Univ, Dept Phys, JR Macdonald Lab, Manhattan, KS 66506 USA
[4] Weizmann Inst Sci, Dept Phys Complex Syst, IL-76100 Rehovot, Israel
[5] SLAC Natl Lab, Stanford PULSE Inst, Menlo Pk, CA 94025 USA
[6] Tata Inst Fundamental Res, Dept Nucl & Atom Phys, Mumbai 400005, Maharashtra, India
[7] Max Planck Inst Kernphys, D-69117 Heidelberg, Germany
[8] Hebrew Univ Jerusalem, Inst Chem, IL-91904 Jerusalem, Israel
关键词
quantum control; photodissociation; intense field; FIELD LASER-PULSES; DYNAMICS; FEMTOCHEMISTRY; MOLECULES; PHASE;
D O I
10.1088/0953-4075/48/20/201001
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We demonstrate the ability to control the molecular dissociation rate using femtosecond pulses shaped with third-order dispersion (TOD). Explicitly, a significant 50% enhancement in the dissociation yield for the low lying vibrational levels (v similar to 6) of an H-2(+) ion-beam target was measured as a function of TOD. The underlying mechanism responsible for this enhanced dissociation was theoretically identified as non-adiabatic alignment induced by the pre-pulses situated on the leading edge of pulses shaped with negative TOD. This control scheme is expected to work in other molecules as it does not rely on specific characteristics of our test-case H-2(+) molecule.
引用
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页数:6
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