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Transition fields in organic materials: From percolation to inverted Marcus regime. A consistent Monte Carlo simulation in disordered PPV
Linköpings universitet, Institutionen för fysik, kemi och biologi, Teoretisk kemi. Linköpings universitet, Tekniska högskolan.
Linköpings universitet, Institutionen för fysik, kemi och biologi, Teoretisk kemi. Linköpings universitet, Tekniska högskolan.
Linköpings universitet, Institutionen för fysik, kemi och biologi, Teoretisk kemi. Linköpings universitet, Tekniska högskolan.
2015 (Engelska)Ingår i: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 142, nr 9, s. 094503-Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

In this article, we analyze the electric field dependence of the hole mobility in disordered poly (p-phenylene vinylene). The charge carrier mobility is obtained from Monte Carlo simulations. Depending on the field strength three regions can be identified: the percolation region, the correlation region, and the inverted region. Each region is characterized by a different conduction mechanism and thus a different functional dependence of the mobility on the electric field. Earlier studies have highlighted that Poole-Frenkel law, which appears in the correlation region, is based on the type of correlation caused by randomly distributed electric dipoles. This behavior is thus observed in a limited range of field strengths, and by studying a broader range of electric fields, a more fundamental understanding of the transport mechanism is obtained. We identify the electric fields determining the transitions between the different conduction mechanisms in the material and we explain their physical origin. In principle, this allows us to characterize the mobility field dependence for any organic material. Additionally, we study the charge carrier trapping mechanisms due to diagonal and off-diagonal disorder, respectively. (C) 2015 AIP Publishing LLC.

Ort, förlag, år, upplaga, sidor
American Institute of Physics (AIP), 2015. Vol. 142, nr 9, s. 094503-
Nationell ämneskategori
Kemi
Identifikatorer
URN: urn:nbn:se:liu:diva-117234DOI: 10.1063/1.4913733ISI: 000350973900041PubMedID: 25747090OAI: oai:DiVA.org:liu-117234DiVA, id: diva2:807099
Anmärkning

Funding Agencies|Swedish Research Council (VR); MATTER Network; SERC (Swedish e-Science Research Center)

Tillgänglig från: 2015-04-22 Skapad: 2015-04-21 Senast uppdaterad: 2017-12-04
Ingår i avhandling
1. Charge Transport Simulations for Organic Electronics: A Kinetic Monte Carlo Approach
Öppna denna publikation i ny flik eller fönster >>Charge Transport Simulations for Organic Electronics: A Kinetic Monte Carlo Approach
2015 (Engelska)Licentiatavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

In this thesis we focus on the modelling and simulation of organic electronic devices, investigating their structural and electronic properties. Organic devices have attracted great interest for their innovative properties, but their functioning still represent a theoretical and technological challenge. They are composed by one or more organic materials depending on the particular application. The morphology of organic devices in the single phase or at the interface is known to strongly determine mobility and efficiency of the devices. The structural disorder is studied through molecular dynamics (MD) simulations. Marcus formula is used to calculate the hopping rate of the charge carriers and the model developed is tested by simulations in a Kinetic Monte Carlo scheme. The dependence of the transfer integrals on the relative molecular orientation is achieved through a weighted Mulliken formula or through a dimer projection approach using the semi-empirical Hartree Fock method ZINDO. Electrostatic effects, have been included through atomic charges and atomic polarizabilities, calculated at the B3LYP level of theory. The inclusion of electrostatic effects has been shown (through simulations in 4PV and C60) to be crucial to obtain a good qualitative agreement with experiments, for both mobility field and temperature dependence in the single phase. In particular the external reorganization energy, calculated through the polarization of the environment, has been shown to have a great impact on the conduction, shifting the inverse Marcus region and helping CT state separation at the interface (between C60 and anthracene).

Ort, förlag, år, upplaga, sidor
Linköping: Linköping University Electronic Press, 2015. s. 64
Serie
Linköping Studies in Science and Technology. Thesis, ISSN 0280-7971 ; 1738
Nationell ämneskategori
Kemi
Identifikatorer
urn:nbn:se:liu:diva-122991 (URN)10.3384/lic.diva-122991 (DOI)978-91-7685-878-3 (ISBN)
Presentation
2016-01-15, Planck, Fisikhuset, Campus Valla, Linköpings universitet, Linköping, 13:00 (Engelska)
Opponent
Handledare
Tillgänglig från: 2015-12-01 Skapad: 2015-12-01 Senast uppdaterad: 2019-11-18Bibliografiskt granskad
2. Modelling Charge Transport for Organic Solar Cells within Marcus Theory
Öppna denna publikation i ny flik eller fönster >>Modelling Charge Transport for Organic Solar Cells within Marcus Theory
2017 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

With the technological advancement of modern society, electronic devices are getting progressively more integrated in our everyday lives. Their continuouslygrowing presence is generating numerous concerns about costs, efficiency and the environmental impact of the electronic waste. In this context, organic electronics is finding its way through the market, allowing for potentially low-cost, light, flexible, transparent and environmentally friendly electronics. Despite the numerous successes of organic electronics, the functioning of several categories of organic devices still represents a technological challenge, due to problems like low efficiencies and stabilities (degradation over time).

Organic devices are composed by one or more organic materials depending on the particular application. The conformation and electronic structure of the organic molecules as well as their supramolecular arrangement in the single phase or at the interface are known to strongly a affect the mobility and/or the efficiency of the device. While there is consensus on the fundamental physics of organic devices, we still lack a detailed comprehensive theory able to fully explain experimental data. In this thesis we focus on trying to expand our knowledge of charge transport in organic materials through theoretical modelling and simulation of organic electronic devices. While the methodology developed is generally valid for any organic device, we will particularly focus on the case represented by organic photovoltaics.

The morphology of the system is obtained by molecular dynamics simulations. Marcus theory is used to calculate the hopping rate of the charge carriers and subsequently study the possibility of free charge carriers production in an organic solar cell. The theory is then compared both with Kinetic Monte Carlo simulations and with experiments to identify the main pitfalls of the actual theory and ways to improve it. The Marcus rate between two molecules depends on the molecular orbital energies, the transfer integral between the two molecules and the reorganization energy. The orbital energies and the transfer integrals between two neighbouring molecules are obtained through quantum mechanical calculations in vacuum. Electrostatic effects of the environment are included through atomic charges and atomic polarizabilities, producing a correction both to the orbital energy and to the reorganization energy. We have studied several systems in the single phase (polyphenylene vinylene, C60, PC61BM) and at the interface between two organic materials (anthracene/C60, TQ1/PC71BM).

We show how a combination of different methodologies can be used to obtain a realistic ab-initio model of organic devices taking into account environmental effects. This allows us to obtain qualitative agreement with experimental data of mobility in the single phase and to determine whether or not two materials are suitable to be used together in an organic solar cell.

Ort, förlag, år, upplaga, sidor
Linköping: Linköping University Electronic Press, 2017. s. 54
Serie
Linköping Studies in Science and Technology. Dissertations, ISSN 0345-7524 ; 1815
Nationell ämneskategori
Teoretisk kemi Den kondenserade materiens fysik Fysikalisk kemi
Identifikatorer
urn:nbn:se:liu:diva-133329 (URN)10.3384/diss.diva-133329 (DOI)9789176856192 (ISBN)
Disputation
2017-02-10, Planck (J206), Fysikhuset, Campus Valla, Linköping, 10:15 (Engelska)
Opponent
Handledare
Tillgänglig från: 2016-12-20 Skapad: 2016-12-20 Senast uppdaterad: 2019-10-12Bibliografiskt granskad

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