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Modification of Charge Transfer and Energy Level Alignment at Organic/TiO2 Interfaces
KTH, Skolan för informations- och kommunikationsteknik (ICT), Materialfysik, Materialfysik, MF.ORCID-id: 0000-0002-9663-7705
KTH, Skolan för informations- och kommunikationsteknik (ICT), Materialfysik, Materialfysik, MF.
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2009 (Engelska)Ingår i: The Journal of Physical Chemistry C, ISSN 1932-7447, E-ISSN 1932-7455, Vol. 113, nr 31, s. 13765-13771Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Adsorption of titanyl phthalocyanine (TiOPc) on rutile TiO2(110) modified by a set of pyridine derivatives (2,2'-bipyridine, 4,4'-bipyridine, and 4-tert-butyl pyridine) has been investigated using synchrotron radiation based X-ray photoelectron spectroscopy (XPS). For the unmodified TiOPc/TiO2 system, a strong charge transfer is observed from the first layer TiOPc into the substrate, which leads to a molecular layer at the interface with a depleted highest occupied molecular orbital (HOMO). However, precovering the TiO2 surface with a saturated pyridine monolayer effectively reduce this process and leave the TiOPc in a less perturbed molecular state. Furthermore, the TiOPc HOMO and core levels are observed at different binding energies ranging by 0.3 eV on the three pyridine monolayers, which is ascribed to differences in surface potentials set up by the different pyridine/TiO2 systems.

Ort, förlag, år, upplaga, sidor
2009. Vol. 113, nr 31, s. 13765-13771
Nyckelord [en]
electronic-structure, titanyl phthalocyanine, tio2(110)-(1x1) surface, stm observation, solar-cells, thin-film, metal, pyridine, molecules, layer
Identifikatorer
URN: urn:nbn:se:kth:diva-18640DOI: 10.1021/jp902814dISI: 000268478700047Scopus ID: 2-s2.0-68749107094OAI: oai:DiVA.org:kth-18640DiVA, id: diva2:336687
Anmärkning
QC 20100525Tillgänglig från: 2010-08-05 Skapad: 2010-08-05 Senast uppdaterad: 2017-12-12Bibliografiskt granskad
Ingår i avhandling
1. Molecular Interaction of Thin Film Photosensitive Organic Dyes on TiO2 Surfaces
Öppna denna publikation i ny flik eller fönster >>Molecular Interaction of Thin Film Photosensitive Organic Dyes on TiO2 Surfaces
2011 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

The photosensitive molecule adsorption on titanium dioxide (TiO2) forms the so-called “dye sensitized TiO2” system, a typical organic/oxide heterojunction, which is of great interest in catalysis and energy applications, e.g. dye-sensitized solar cell (DSSC). Traditionally, the transition metal complex dyes are the focus of the study. However, as the fast development of the organic semiconductors and invention of new pure organic dyes, it is necessary to expand the research horizon to cover these molecules and concrete the fundamental understanding of their basic properties, especially during sensitization.In this work, we focus on two different photosensitive molecules: phthalocyanines and triphenylamine-based dyes. Phthalocyanines are organic semiconductors with symmetric macro aromatic molecular structures. They possess good photoelectrical properties and good thermal and chemical stability, which make them widely used in the organic electronic industries. Triphenylamine-based dyes are new types of pure organic dyes which deliver high efficiency and reduce the cost of DSSC. They can be nominated as one of the strong candidates to substitute the ruthenium complex dyes in DSSC. The researches were carried out using classic surface science techniques on single crystal substrates and under ultrahigh vacuum condition. The photosensitive molecules were deposited by organic molecular beam deposition. The substrate reconstruction and ordering were checked by low energy electron diffraction. The molecular electronic, geometric structures and charge transfer properties were characterized by photoelectron spectroscopy, near edge X-ray absorption fine structure spectroscopy and resonant photoelectron spectroscopy (RPES). Scanning tunneling microscopy is used to directly image the molecular adsorption.For phthalocyanines, we select MgPc, ZnPc, FePc and TiOPc, which showed a general charge transfer from molecule to the substrate when adsorbed on rutile TiO2(110) surface with 1×1 and 1×2 reconstructions. This charge transfer can be prevented by modifying the TiO2 surface with pyridine derivatives (4-tert-butyl pyridine (4TBP), 2,2’-bipyridine and 4,4’-bipyridine), and furthermore the energy level alignment at the interface is modified by the surface dipole established by the pyridine molecules. Annealing also plays an important role to control the molecular structure and change the electronic structure together with the charge transfer properties, shown by TiOPc film. Special discussions were done for 4TBP for its ability to shift the substrate band bending by healing the oxygen vacancies, which makes it an important additive in the DSSC electrolyte. For the triphenylamine-based dye (TPAC), the systematic deposition enables the characterization of the coverage dependent changes of molecular electronic and geometric structures. The light polarization dependent charge transfer was revealed by RPES. Furthermore, the iodine doped TPAC on TiO2 were investigated to mimic the electrolyte/dye/TiO2 interface in the real DSSC.The whole work of this thesis aims to provide fundamental understanding of the interaction between photosensitive molecules on TiO2 surfaces at molecular level in the monolayer region, e.g. the formation of interfacial states and the coverage dependent atomic and electronic structures, etc. We explored the potential of the application of new dyes and modified of the existing system by identifying their advantage and disadvantage. The results may benefit the fields of dye syntheses, catalysis researches and designs of organic photovoltaic devices.

Ort, förlag, år, upplaga, sidor
Stockholm: KTH Royal Institute of Technology, 2011. s. xiii, 62
Serie
TRITA-ICT/MAP AVH, ISSN 1653-7610 ; 2011:14
Nyckelord
photoelectron spectroscopy, X-ray absorption spectroscopy, organic semiconductor, oxides, adsorption, dye sensitization, electronic structure, charge transfer
Nationell ämneskategori
Annan fysik
Identifikatorer
urn:nbn:se:kth:diva-47354 (URN)978-91-7501-144-8 (ISBN)
Disputation
2011-12-02, C2, KTH-Electrum, Isafjordsgatan 26, Kista,, Stockholm, 10:00 (Engelska)
Opponent
Handledare
Anmärkning

QC 20111114

Tillgänglig från: 2011-11-14 Skapad: 2011-11-08 Senast uppdaterad: 2020-01-02Bibliografiskt granskad

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Yu, Shun

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Yu, ShunAhmadi, SarehGöthelid, Mats
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Materialfysik, MF
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The Journal of Physical Chemistry C

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