Ultrafast electron dynamics in phenylalanine initiated by attosecond pulses

被引:643
|
作者
Calegari, F. [1 ]
Ayuso, D. [2 ]
Trabattoni, A. [3 ]
Belshaw, L. [4 ]
De Camillis, S. [4 ]
Anumula, S. [3 ]
Frassetto, F. [5 ]
Poletto, L. [5 ]
Palacios, A. [2 ]
Decleva, P. [6 ,7 ]
Greenwood, J. B. [4 ]
Martin, F. [2 ,8 ]
Nisoli, M. [1 ,3 ]
机构
[1] CNR, Inst Photon & Nanotechnol IFN, I-20133 Milan, Italy
[2] Univ Autonoma Madrid, Dept Quim, E-28049 Madrid, Spain
[3] Politecn Milan, Dept Phys, I-20133 Milan, Italy
[4] Queens Univ Belfast, Sch Maths & Phys, Ctr Plasma Phys, Belfast BT7 1NN, Antrim, North Ireland
[5] CNR, IFN, I-35131 Padua, Italy
[6] Univ Trieste, Dipartimento Sci Chim & Farmaceut, I-34127 Trieste, Italy
[7] CNR, Ist Officina Mat, I-34127 Trieste, Italy
[8] Inst Madrileno Estudios Avanzados Nanociencia, Madrid 28049, Spain
基金
英国工程与自然科学研究理事会; 欧洲研究理事会; 英国科学技术设施理事会;
关键词
REAL-TIME OBSERVATION; CHARGE MIGRATION; PEPTIDE CATIONS;
D O I
10.1126/science.1254061
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
In the past decade, attosecond technology has opened up the investigation of ultrafast electronic processes in atoms, simple molecules, and solids. Here, we report the application of isolated attosecond pulses to prompt ionization of the amino acid phenylalanine and the subsequent detection of ultrafast dynamics on a sub-4.5-femtosecond temporal scale, which is shorter than the vibrational response of the molecule. The ability to initiate and observe such electronic dynamics in polyatomic molecules represents a crucial step forward in attosecond science, which is progressively moving toward the investigation of more and more complex systems.
引用
收藏
页码:336 / 339
页数:4
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