Equilibrium-reduced density matrix formulation: Influence of noise, disorder, and temperature on localization in excitonic systems

被引:100
作者
Moix, Jeremy M. [1 ,2 ]
Zhao, Yang [1 ]
Cao, Jianshu [2 ]
机构
[1] Nanyang Technol Univ, Sch Mat Sci & Engn, Singapore 639798, Singapore
[2] MIT, Dept Chem, Cambridge, MA 02139 USA
来源
PHYSICAL REVIEW B | 2012年 / 85卷 / 11期
基金
新加坡国家研究基金会; 美国国家科学基金会;
关键词
LIGHT-HARVESTING SYSTEMS; PHOTOSYNTHETIC ANTENNA COMPLEXES; NONADIABATIC QUANTUM DYNAMICS; PUMP-PROBE SPECTROSCOPY; ENERGY-TRANSFER; SEMICLASSICAL DESCRIPTION; RHODOBACTER-SPHAEROIDES; OPTICAL-PROPERTIES; MAPPING APPROACH; COHERENCE;
D O I
10.1103/PhysRevB.85.115412
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
An exact method to compute the entire equilibrium-reduced density matrix for systems characterized by a system-bath Hamiltonian is presented. The approach is based upon a stochastic unraveling of the influence functional that appears in the imaginary time path integral formalism of quantum statistical mechanics. This method is then applied to study the effects of thermal noise, static disorder, and temperature on the coherence length in excitonic systems. As representative examples of biased and unbiased systems, attention is focused on the well-characterized complexes of the Fenna-Matthews-Olson (FMO) protein and the light harvesting complex of purple bacteria, LH2, respectively. Due to the bias, FMO is completely localized in the site basis at low temperatures, whereas LH2 is completely delocalized. In the latter, the presence of static disorder leads to a plateau in the coherence length at low temperature that becomes increasingly pronounced with increasing strength of the disorder. The introduction of noise, however, precludes this effect. In biased systems, it is shown that the environment may increase the coherence length, but only decrease that of unbiased systems. Finally it is emphasized that for typical values of the environmental parameters in light harvesting systems, the system and bath are entangled at equilibrium in the single excitation manifold. That is, the density matrix cannot be described as a product state as is often assumed, even at room temperature. The reduced density matrix of LH2 is shown to be in precise agreement with the steady state limit of previous exact quantum dynamics calculations.
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页数:14
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共 52 条
[1]   How proteins trigger excitation energy transfer in the FMO complex of green sulfur bacteria [J].
Adolphs, Julia ;
Renger, Thomas .
BIOPHYSICAL JOURNAL, 2006, 91 (08) :2778-2797
[2]   A novel method for simulating quantum dissipative systems [J].
Cao, JS ;
Ungar, LW ;
Voth, GA .
JOURNAL OF CHEMICAL PHYSICS, 1996, 104 (11) :4189-4197
[3]   A unified framework for quantum activated rate processes .1. General theory [J].
Cao, JS ;
Voth, GA .
JOURNAL OF CHEMICAL PHYSICS, 1996, 105 (16) :6856-6870
[4]  
CHANDLER D, 1991, LES HOUCH S, V51, P193
[5]   Coherence in the B800 ring of purple bacteria LH2 [J].
Cheng, YC ;
Silbey, RJ .
PHYSICAL REVIEW LETTERS, 2006, 96 (02)
[6]   Scaling of fluorescence Stokes shift and superradiance coherence size in disordered molecular aggregates [J].
Chernyak, V ;
Meier, T ;
Tsiper, E ;
Mukamel, S .
JOURNAL OF PHYSICAL CHEMISTRY A, 1999, 103 (49) :10294-10299
[7]   Exciton analysis in 2D electronic spectroscopy [J].
Cho, MH ;
Vaswani, HM ;
Brixner, T ;
Stenger, J ;
Fleming, GR .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (21) :10542-10556
[8]   Exciton delocalization in the B850 light-harvesting complex:: Comparison of different measures [J].
Dahlbom, M ;
Pullerits, T ;
Mukamel, S ;
Sandström, V .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (23) :5515-5524
[9]   Excitons in a photosynthetic light-harvesting system:: A combined molecular dynamics, quantum chemistry, and polaron model study -: art. no. 031919 [J].
Damjanovic, A ;
Kosztin, I ;
Kleinekathöfer, U ;
Schulten, K .
PHYSICAL REVIEW E, 2002, 65 (03) :1-031919
[10]   Localization and coherent dynamics of excitons in the two-dimensional optical spectrum of molecular J-aggregates [J].
Dijkstra, Arend G. ;
Jansen, Thomas La Cour ;
Knoester, Jasper .
JOURNAL OF CHEMICAL PHYSICS, 2008, 128 (16)