Quantum Process Tomography Quantifies Coherence Transfer Dynamics in Vibrational Exciton

被引:9
|
作者
Chuntonov, Lev [1 ]
Ma, Jianqiang [1 ]
机构
[1] Univ Penn, Dept Chem, Ultrafast Opt Proc Lab, Philadelphia, PA 19104 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2013年 / 117卷 / 43期
关键词
2-DIMENSIONAL IR-SPECTROSCOPY; 2D IR; ENERGY-TRANSFER; WATER-MOLECULES; HYDROGEN-BOND; PHOTON-ECHO; RELAXATION; PEPTIDES; SPECTRA; SYSTEMS;
D O I
10.1021/jp4075493
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Quantum coherence has been a subject of great interest in many scientific disciplines. However, detailed characterization of the quantum coherence in molecular systems, especially its transfer and relaxation mechanisms, still remains a major challenge. The difficulties arise in part because the spectroscopic signatures of the coherence transfer are typically overwhelmed by other excitation-relaxation processes. We use quantum process tomography (QPT) via two-dimensional infrared spectroscopy to quantify the rate of the elusive coherence transfer between two vibrational exciton states. QPT retrieves the dynamics of the dissipative quantum system directly from the experimental observables. It thus serves as an experimental alternative to theoretical models of the system bath interaction and can be used to validate these theories. Our results for coupled carbonyl groups of a diketone molecule in chloroform, used as a benchmark system, reveal the nonsecular nature of the interaction between the exciton and the Markovian bath and open the door for the systematic studies of the dissipative quantum systems dynamics in detail.
引用
收藏
页码:13631 / 13638
页数:8
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