Modulations of electronic tunneling rates through flexible molecular bridges by a dissipative superexchange mechanism

被引:10
作者
Abu-Hilu, M [1 ]
Peskin, U [1 ]
机构
[1] Technion Israel Inst Technol, Lise Meitner Ctr Computat Quantum Chem, Dept Chem, IL-32000 Haifa, Israel
基金
以色列科学基金会;
关键词
D O I
10.1016/j.chemphys.2003.09.026
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
Long-range coherent electron transfer between a donor and an acceptor is often assisted by intermediate molecular bridge, via the superexchange tunneling mechanism. The effect of electronic-nuclear coupling intensity on the tunneling rate and mechanism is analyzed using a generalized spin-boson model, in which the two level system, representing the donor and the acceptor is coupled to a dissipative nuclear bath only indirectly, via additional N bridge sites. A Langevin-Schroedinger equation, based on a mean field approximation, is applied in order to study the corresponding many-body dynamics, and the results are supported by numerically exact calculations for a single nuclear bridge mode. At zero temperature and when the electron tunneling is slower than the nuclear motion, the main effect of electronic-nuclear coupling is the dissipation of electronic energy at the bridge into nuclear vibrations. At small coupling intensities, the electronic tunneling rate increases due to this dissipative mechanism, but as the coupling intensity increases the tunneling into the acceptor is suppressed and efficient dissipation leads to electronic trapping (solvation) at the bridge. This analysis agrees with numerous experimental and theoretical studies, emphasizing the importance of the nuclear bridge conformation and the bridge flexibility in controlling the electron transfer rate in donor-bridge-acceptor systems. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:231 / 241
页数:11
相关论文
共 61 条
[1]   Current-triggered vibrational excitation in single-molecule transistors [J].
Alavi, S ;
Larade, B ;
Taylor, J ;
Guo, H ;
Seideman, T .
CHEMICAL PHYSICS, 2002, 281 (2-3) :293-303
[2]   Anomalous distance dependence of electron transfer across peptide bridges [J].
Antonello, S ;
Formaggio, F ;
Moretto, A ;
Toniolo, C ;
Maran, F .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (10) :2874-2875
[3]   FAR-INFRARED PERTURBATION OF ELECTRON-TUNNELING IN REACTION CENTERS [J].
AUSTIN, RH ;
HONG, MK ;
MOSER, C ;
PLOMBON, J .
CHEMICAL PHYSICS, 1991, 158 (2-3) :473-486
[4]   ELECTRON-TUNNELING PATHWAYS IN PROTEINS [J].
BERATAN, DN ;
ONUCHIC, JN ;
WINKLER, JR ;
GRAY, HB .
SCIENCE, 1992, 258 (5089) :1740-1741
[5]   ELECTRON-TUNNELING PATHWAYS IN RUTHENATED PROTEINS [J].
BERATAN, DN ;
ONUCHIC, JN ;
BETTS, JN ;
BOWLER, BE ;
GRAY, HB .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (22) :7915-7921
[6]   Electron transfer via bridges [J].
Bixon, M ;
Jortner, J .
JOURNAL OF CHEMICAL PHYSICS, 1997, 107 (13) :5154-5170
[7]   Conformational dynamics of semiflexibly bridged electron donor-acceptor systems comprising long aliphatic tails [J].
Bleisteiner, B ;
Marian, T ;
Schneider, S ;
Brouwer, AM ;
Verhoeven, JW .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2001, 3 (11) :2070-2079
[8]   Large on-off ratios and negative differential resistance in a molecular electronic device [J].
Chen, J ;
Reed, MA ;
Rawlett, AM ;
Tour, JM .
SCIENCE, 1999, 286 (5444) :1550-1552
[9]   Room temperature single electron transistor by local chemical modification of carbon nanotubes [J].
Cui, JB ;
Burghard, M ;
Kern, K .
NANO LETTERS, 2002, 2 (02) :117-120
[10]   Competition between conformational relaxation and intramolecular electron transfer within phenothiazine-pyrene dyads [J].
Daub, J ;
Engl, R ;
Kurzawa, J ;
Miller, SE ;
Schneider, S ;
Stockmann, A ;
Wasielewski, MR .
JOURNAL OF PHYSICAL CHEMISTRY A, 2001, 105 (23) :5655-5665