Crystallization-Induced Charge-Transfer Change in TiOPc Thin Films Revealed by Resonant Photoemission Spectroscopy
Author
Summary, in English
Organic semiconductors usually demonstrate crystal structure dependent electronic properties, and through precise control of film structure, the performance of novel organic electronic devices can be greatly improved. Understanding the crystal structure dependent charge-transfer mechanism thus becomes critical. In this work, we have prepared amorphous titanyl phthalocyanine films by vacuum molecular beam evaporation and have further crystallized them through vacuum annealing. In the crystalline phase, an excited electron is rapidly transferred into neighboring molecules; while in the amorphous phase, it is mainly localized and recombines with the core hole as revealed by resonant photoemission spectroscopy (RPES). The fast electron transfer time is determined to be around 16 fs in the crystalline film, which is in good agreement with the charge-transfer hopping time estimated from the best device performance reported. The crystallized film shows more p-type characteristics than the amorphous with all the energy levels shifting toward the vacuum level. However, the greatly improved charge transfer is assigned to the molecular orbital coupling rather than this shift. From density functional theory and RPES, we specify the contribution of two differently coordinated nitrogen atoms (N2c and N3c) to the experimental results and illustrate that the N3c related orbital has experienced a dramatic change, which is keenly related to the improved charge transfer.
Department/s
Publishing year
2011
Language
English
Pages
14969-14977
Publication/Series
Journal of Physical Chemistry C
Volume
115
Issue
30
Document type
Journal article
Publisher
The American Chemical Society (ACS)
Topic
- Natural Sciences
- Physical Sciences
Status
Published
ISBN/ISSN/Other
- ISSN: 1932-7447