Can Nanocavities Significantly Enhance Resonance Energy Transfer in a Single Donor-Acceptor Pair?

被引:28
作者
Wei, Yu-Chen [1 ,2 ]
Lee, Ming-Wei [1 ]
Chou, Pi-Tai [2 ]
Scholes, Gregory D. [3 ]
Schatz, George C. [4 ]
Hsu, Liang-Yan [1 ]
机构
[1] Acad Sinica, Inst Atom & Mol Sci, Taipei 10617, Taiwan
[2] Natl Taiwan Univ, Dept Chem, Taipei 10617, Taiwan
[3] Princeton Univ, Dept Chem, Frick Chem Lab, Princeton, NJ 08544 USA
[4] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
关键词
DIPOLE-DIPOLE INTERACTION; QUANTUM ELECTRODYNAMICS; ELECTROMAGNETIC-FIELD; AB-INITIO; QUANTIZATION; CONSTANT; WAVE;
D O I
10.1021/acs.jpcc.1c04623
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 resonance energy transfer (RET) and the control of energy transfer on the nanoscale have received considerable attention both experimentally and theoretically during the past few decades. We have investigated the RET between a donor/acceptor pair in the nanocavities based on our previous theory developed in the framework of macroscopic quantum electrodynamics (QED). On the basis of this theory, the enhancements in the RET with respect to the rate in vacuum were evaluated for a Fabry-Pe ' rot cavity. When the displacement vector between the two molecules is aligned with the cavity axis of the Fabry-Pe ' rot cavity, we find that cavity modes give enhancements of less than a factor of 10 due to the interference between contributions from resonant and non-resonant cavity modes. By comparison, when the displacement vector between the two molecules is aligned in a plane perpendicular to the cavity axis, we find that the cavity modes can induce enhancements of more than a factor of 10, and the surface plasmon-polariton modes can induce enhancements of up to a factor of 300. We develop a convenient representation for understanding the effect of the displacement vector between the molecules and of the molecular dipole directions in terms of the H-dimer and J-dimer properties. To further enhance the RET, we propose a square silver cavity that gives a rate enhancement of a factor of 280 under cavity resonance conditions, which provides important insight into developing devices capable of long-range RET.
引用
收藏
页码:18119 / 18128
页数:10
相关论文
共 81 条
  • [1] Resonance energy transfer: Influence of neighboring matter absorbing in the wavelength region of the acceptor
    Andrews, David L.
    Ford, Jack S.
    [J]. JOURNAL OF CHEMICAL PHYSICS, 2013, 139 (01)
  • [2] Virtual photons, dipole fields and energy transfer: a quantum electrodynamical approach
    Andrews, DL
    Bradshaw, DS
    [J]. EUROPEAN JOURNAL OF PHYSICS, 2004, 25 (06) : 845 - 858
  • [3] [Anonymous], FDTD Solutions
  • [4] ABINITIO CALCULATION OF THE MACROSCOPIC DIELECTRIC-CONSTANT IN SILICON
    BARONI, S
    RESTA, R
    [J]. PHYSICAL REVIEW B, 1986, 33 (10) : 7017 - 7021
  • [5] Integrated optical components utilizing long-range surface plasmon polaritons
    Boltasseva, A
    Nikolajsen, T
    Leosson, K
    Kjaer, K
    Larsen, MS
    Bozhevolnyi, SI
    [J]. JOURNAL OF LIGHTWAVE TECHNOLOGY, 2005, 23 (01) : 413 - 422
  • [6] Brédas JL, 2017, NAT MATER, V16, P35, DOI [10.1038/nmat4767, 10.1038/NMAT4767]
  • [7] Single-molecule strong coupling at room temperature in plasmonic nanocavities
    Chikkaraddy, Rohit
    de Nijs, Bart
    Benz, Felix
    Barrow, Steven J.
    Scherman, Oren A.
    Rosta, Edina
    Demetriadou, Angela
    Fox, Peter
    Hess, Ortwin
    Baumberg, Jeremy J.
    [J]. NATURE, 2016, 535 (7610) : 127 - 130
  • [8] Choi Y, 2009, NAT NANOTECHNOL, V4, P742, DOI [10.1038/nnano.2009.258, 10.1038/NNANO.2009.258]
  • [9] Ab initio study of ionic solutions by a polarizable continuum dielectric model
    Cossi, M
    Barone, V
    Mennucci, B
    Tomasi, J
    [J]. CHEMICAL PHYSICS LETTERS, 1998, 286 (3-4) : 253 - 260
  • [10] How solvent controls electronic energy transfer and light harvesting: Toward a quantum-mechanical description of reaction field and screening effects
    Curutchet, Carles
    Scholes, Gregory D.
    Mennucci, Benedetta
    Cammi, Roberto
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2007, 111 (46) : 13253 - 13265