Decoherence reduces thermal energy loss in graphene quantum dots

被引:14
|
作者
Jaeger, H. M. [1 ]
Green, J. R. [1 ]
Prezhdo, O. V. [1 ]
机构
[1] Univ Rochester, Dept Chem, Rochester, NY 14627 USA
基金
美国国家科学基金会;
关键词
MOLECULAR-DYNAMICS SIMULATIONS; AUGMENTED-WAVE METHOD; SEMICONDUCTOR NANOCRYSTALS; RAMAN-SPECTROSCOPY; CARBON NANOTUBES; SOLAR-CELLS; ELECTRON RELAXATION; BASIS-SET; NANORIBBONS; EFFICIENCY;
D O I
10.1063/1.4817269
中图分类号
O59 [应用物理学];
学科分类号
摘要
Intraband splitting energies in graphene quantum dots are on the order of the fundamental phonon energies, creating a single-phonon relaxation pathway. Yet, charge carrier thermalization is slow. Our time-domain, ab initio computations demonstrate that the slow rate of electronic relaxation is due to quantum decoherence. The relaxation through the discrete states occurs on a 30 ps timescale. Electron-hole recombination takes place within 660 ps, two orders of magnitude slower than a coherent mechanism. Disorder introduced by structural variations around the edge expedites coherence loss, increasing the lifetimes of excited charge carriers in graphene quantum dots. (C) 2013 AIP Publishing LLC.
引用
收藏
页数:4
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