Heterostructured organic interfaces probed by resonant photoemission

被引:35
作者
Vilmercati, Paolo [1 ,4 ]
Cvetko, Dean [2 ]
Cossaro, Albano [3 ]
Morgante, Alberto [1 ,3 ]
机构
[1] Univ Trieste, Dipartmento Fis, I-34127 Trieste, Italy
[2] Fak Matemat Fiz, Ljubljana 1000, Slovenia
[3] CNR, INFM, Lab TASC, I-34012 Trieste, Italy
[4] Sincrotrone Trieste SCpA, I-34012 Trieste, Italy
关键词
Resonant photoemission; Organic molecules; Interfaces; Charge transfer; PHOTOINDUCED ELECTRON-TRANSFER; ULTRAFAST CHARGE-TRANSFER; GROWTH; DYNAMICS; PTCDA; AU(111); CONDUCTANCE; ADSORBATE; SURFACES; CU(111);
D O I
10.1016/j.susc.2008.11.050
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
The application of the resonant photoemission spectroscopy (RPES) to various organic molecule based systems is reviewed. The chemical specificity and the possibility to conduct experiments in the energy domain that provides a time scale for charge dynamics, make the RPES a powerful tool to study organic heterojunctions and in particular to probe the charge transfer processes at organic interfaces. We briefly discuss the models used in RPES data analysis to extract the time scale of the excited charge delocalisation and the spatial correlation of core, valence occupied and unoccupied molecular states. As an example we report on 3,4,9,10-perylene tetracarboxylic acid dianhydride (PTCDA) on (1 x 2) Au(110) surface where organic layer metallicity is directly evidenced in RPES experiments. A particular attention is dedicated to bio-mimetic model molecules whose electronic structure at interfaces is the fundamental key for the design of real devices. In the last section we consider recent experiments that could open the way to new fields of applications regarding biological molecules and single molecule systems where RPES could elucidate the link between the quantum and the meso-scopic properties of such systems. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:1542 / 1556
页数:15
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