Exciton dynamics at interfaces of organic semiconductors

被引:18
作者
Muntwiler, Matthias [1 ]
Yang, Qingxin [1 ]
Zhu, X. -Y. [1 ]
机构
[1] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
基金
美国国家科学基金会;
关键词
Organic semiconductor; Fullerene; Pentacene; Exciton dynamics; Photoelectron spectroscopy; SOLAR-CELLS; SOLID C-60; BAND-GAP; EXCITATION; ENERGY; METAL; PHOTOGENERATION; PHOTOEMISSION; SPECTROSCOPY; SEPARATION;
D O I
10.1016/j.elspec.2009.02.016
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
We review recent progress of using time-resolved two-photon photoelectron spectroscopy (2PPE) to study the energetics and dynamics of excitons at surfaces and interfaces of two prototypical organic semiconductors: C(60) and pentacene. For C(60) thin films epitaxially grown on Au(1 1 1) and Cu(1 1 1) surfaces, we observe both charge transfer and exciton states. For excitons in C(60), the proximity of a metal Surface leads to rapid, exciton band-mediated quenching. At the surface of pentacene thin films we observe a series of charge-transfer excitons where the electron and the photohole are bound across the interface. The ability of 2PPE to measure and directly relate exciton levels to single-electron levels is illustrated. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:116 / 124
页数:9
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