Electronic non-equilibrium conditions at C60-pentacene heterostructures

被引:13
作者
Duhm, Steffen [1 ]
Salzmann, Ingo [1 ]
Johnson, Robert L. [2 ]
Koch, Norbert [1 ]
机构
[1] Humboldt Univ, Inst Phys, D-12489 Berlin, Germany
[2] Univ Hamburg, Inst Expt Phys, D-22761 Hamburg, Germany
关键词
Organic heterostructures; Thermodynamic equilibrium; Energy level alignment; Photoelectron spectroscopy; Thin film morphology; ENERGY-LEVEL ALIGNMENT; LIGHT-EMITTING-DIODES; SOLAR-CELLS; CHARGE-TRANSFER; WORK FUNCTION; INTERFACES; FILMS; SURFACES; HETEROJUNCTIONS; PHOTOEMISSION;
D O I
10.1016/j.elspec.2009.04.008
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
The electronic structure of vacuum-sublimed layered organic heterostructures of pentacene (PEN) and fullerene (C-60) on conducting polymer substrates was investigated using ultraviolet photoelectron spectroscopy (UPS). The conditions at the PEN/C-60 interface changed from thermodynamic non-equilibrium (i.e. the onset of the PEN highest occupied molecular orbital above the substrate Fermi-energy) for thin PEN coverages on C-60 to thermodynamic equilibrium for thicker PEN coverages (i.e. Fermi-level pinning of PEN). This finding is attributed to a coverage-dependent pinhole connection of PEN through the C-60 layer with the substrate. The experiments demonstrate the importance of organic thin film morphology for UPS measurements to assess the energy level alignment at organic/organic heterointerfaces. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:40 / 44
页数:5
相关论文
共 48 条
[1]   Low voltage organic light emitting diodes featuring doped phthalocyanine as hole transport material [J].
Blochwitz, J ;
Pfeiffer, M ;
Fritz, T ;
Leo, K .
APPLIED PHYSICS LETTERS, 1998, 73 (06) :729-731
[2]   Electron energetics at surfaces and interfaces: Concepts and experiments [J].
Cahen, D ;
Kahn, A .
ADVANCED MATERIALS, 2003, 15 (04) :271-277
[3]  
Dimitrakopoulos CD, 2002, ADV MATER, V14, P99, DOI 10.1002/1521-4095(20020116)14:2<99::AID-ADMA99>3.0.CO
[4]  
2-9
[5]   PTCDA on Au(111), Ag(111) and Cu(111):: Correlation of interface charge transfer to bonding distance [J].
Duhm, S. ;
Gerlach, A. ;
Salzmann, I. ;
Broeker, B. ;
Johnson, R. L. ;
Schreiber, F. ;
Koch, N. .
ORGANIC ELECTRONICS, 2008, 9 (01) :111-118
[6]   Spontaneous charge transfer at organic-organic homointerfaces to establish thermodynamic equilibrium [J].
Duhm, S. ;
Glowatzki, H. ;
Rabe, J. P. ;
Koch, N. ;
Johnson, R. L. .
APPLIED PHYSICS LETTERS, 2007, 90 (12)
[7]   Orientation-dependent ionization energies and interface dipoles in ordered molecular assemblies [J].
Duhm, Steffen ;
Heimel, Georg ;
Salzmann, Ingo ;
Glowatzki, Hendrik ;
Johnson, Robert L. ;
Vollmer, Antje ;
Rabe, Juergen P. ;
Koch, Norbert .
NATURE MATERIALS, 2008, 7 (04) :326-332
[8]   Weak charge transfer between an acceptor molecule and metal surfaces enabling organic/metal energy level tuning [J].
Duhm, Steffen ;
Glowatzki, Hendrik ;
Cimpeanu, Valentin ;
Klankermayer, Jurgen ;
Rabe, Jurgen P. ;
Johnson, Robert L. ;
Koch, Norbert .
JOURNAL OF PHYSICAL CHEMISTRY B, 2006, 110 (42) :21069-21072
[9]   IMAGE STATES AND LOCAL WORK FUNCTION FOR AG/PD(111) [J].
FISCHER, R ;
SCHUPPLER, S ;
FISCHER, N ;
FAUSTER, T ;
STEINMANN, W .
PHYSICAL REVIEW LETTERS, 1993, 70 (05) :654-657
[10]   The role of the ionization potential in vacuum-level alignment at organic semiconductor interfaces [J].
Fukagawa, Hirohiko ;
Kera, Satoshi ;
Kataoka, Takashi ;
Hosoumi, Shunsuke ;
Watanabe, Yasuyuki ;
Kudo, Kazuhiko ;
Ueno, Nobuo .
ADVANCED MATERIALS, 2007, 19 (05) :665-+