Polariton-mediated energy transfer between organic dyes in a strongly coupled optical microcavity

被引:0
|
作者
Coles, David M. [1 ]
Somaschi, Niccolo [2 ,3 ]
Michetti, Paolo [4 ]
Clark, Caspar [5 ]
Lagoudakis, Pavlos G. [2 ]
Savvidis, Pavlos G. [3 ,6 ]
Lidzey, David G. [1 ]
机构
[1] Univ Sheffield, Dept Phys & Astron, Sheffield S3 7RH, S Yorkshire, England
[2] Univ Southampton, Sch Phys & Astron, Southampton SO17 1BJ, Hants, England
[3] IESL FORTH, Iraklion 71110, Crete, Greece
[4] Tech Univ Dresden, Inst Theoret Phys, D-01062 Dresden, Germany
[5] Helia Photon, Livingston EH54 7EJ, Scotland
[6] Univ Crete, Dept Mat Sci & Technol, Iraklion 71003, Crete, Greece
基金
英国工程与自然科学研究理事会;
关键词
EXCITON ANNIHILATION; PHOTOLUMINESCENCE; RELAXATION; PSEUDOISOCYANINE; HYBRIDIZATION; PICOSECOND; BOTTLENECK; EMISSION; DYNAMICS;
D O I
10.1038/NMAT3950
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
Strongly coupled optical microcavities containing different exciton states permit the creation of hybrid-polariton modes that can be described in terms of a linear admixture of cavity-photon and the constituent excitons. Such hybrid states have been predicted to have optical properties that are different from their constituent parts, making them a test bed for the exploration of light-matter coupling. Here, we use strong coupling in an optical microcavity to mix the electronic transitions of two J-aggregated molecular dyes and use both non-resonant photoluminescence emission and photoluminescence excitation spectroscopy to show that hybrid-polariton states act as an efficient and ultrafast energy-transfer pathway between the two exciton states. We argue that this type of structure may act as a model system to study energy-transfer processes in biological light-harvesting complexes.
引用
收藏
页码:712 / 719
页数:8
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