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Singlet Exciton Diffusion in Vacuum‐Evaporated Films of Amine‐Based Materials as Studied by Photocurrent and Photoluminescence Quenching Methods
Author(s) -
Pelczarski Daniel,
Grygiel Piotr,
Stampor Waldemar
Publication year - 2018
Publication title -
physica status solidi (b)
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.51
H-Index - 109
eISSN - 1521-3951
pISSN - 0370-1972
DOI - 10.1002/pssb.201800043
Subject(s) - triphenylamine , electroluminescence , photocurrent , exciton , materials science , photoconductivity , quenching (fluorescence) , photochemistry , photoluminescence , luminescence , diffusion , singlet state , analytical chemistry (journal) , optoelectronics , chemistry , atomic physics , nanotechnology , optics , fluorescence , organic chemistry , condensed matter physics , physics , excited state , layer (electronics) , thermodynamics
The singlet exciton diffusion lengths are determined by the photoconductivity as well as the luminescence surface quenching technique, in vacuum‐evaporated layers of (4,4′,4″‐tris(N‐(3‐methylphenyl)‐N‐phenylylamino) triphenylamine) (m‐MTDATA), 4,4′,4″‐tris[2‐naphthyl(phenyl)amino] triphenylamine (2TNATA), and N,N′‐diphenyl‐N,N′‐bis(3‐methylphenyl)‐[1,1′‐biphenyl]‐4,4′‐diamine (TPD) which are frequently used for fabrication of electroluminescent and photovoltaic devices. The values are found to be as high as (30 ± 10) nm in 2TNATA and m‐MTDATA, as well as (46 ± 9) nm in TPD films. The corresponding singlet diffusion coefficients of the range between 1 × 10 −3 and 1 × 10 −2  cm 2  s −1 , according to a comprehensive study undertaken, are assigned to a sizable electronic coupling induced by strong interactions of intra‐ and inter‐molecular origin in the investigated materials.

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