Athanasios Katsouras

Dr. Athanasios Katsouras

Materials, University of Ioannina, Ioánnina, Ípeiros, Greece
orcid

Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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26 June 2015 in Advanced Functional Materials
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Journal Article
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NGNicola Gasparini
Nicola Gasparini
AKAthanasios Katsouras
Athanasios Katsouras
MAMAS PRODROMIDISMAMAS PRODROMIDIS
MAMAS PRODROMIDIS
AAApostolos Avgeropoulos
Apostolos Avgeropoulos
DBDerya Baran
Derya Baran
CBChristoph J. Brabec
Christoph J. Brabec

30 September 2015 in Advanced Energy Materials
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Journal Article
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NGNicola Gasparini
Nicola Gasparini
MSMichael Salvador
Michael Salvador
SFStefanie Fladischer
Stefanie Fladischer
AKAthanasios Katsouras
Athanasios Katsouras
AAApostolos Avgeropoulos
Apostolos Avgeropoulos
Tayebeh AmeriTayebeh Ameri
Tayebeh Ameri

21 September 2015 in Macromolecular Rapid Communications
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Journal Article
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AKAthanasios Katsouras
Athanasios Katsouras
NGNicola Gasparini
Nicola Gasparini
CKChrysanthos Koulogiannis
Chrysanthos Koulogiannis
MSMichael Spanos
Michael Spanos
TATayebeh Ameri
Tayebeh Ameri
AAApostolos Avgeropoulos
Apostolos Avgeropoulos

1 April 2019 in Progress in Polymer Science
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Journal Article
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Christos ChochosChristos Chochos
Christos Chochos
MSMichael Spanos
Michael Spanos
AKAthanasios Katsouras
Athanasios Katsouras
ETElisavet Tatsi
Elisavet Tatsi
SDSofia Drakopoulou
Sofia Drakopoulou
AAApostolos Avgeropoulos
Apostolos Avgeropoulos

14 November 2017 in Journal of Materials Chemistry A
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Christos ChochosChristos Chochos
Christos Chochos
NLNicolas Leclerc
Nicolas Leclerc
NGNicola Gasparini
Nicola Gasparini
NZNicolas Zimmerman
Nicolas Zimmerman
ETElisavet Tatsi
Elisavet Tatsi
AAApostolos Avgeropoulos
Apostolos Avgeropoulos
It is of upmost importance to gain an in-depth understanding of the role of the polymer chemical structure in the performance of the corresponding organic solar cell (OSC) and its degradation behavior, which is currently insufficiently explored. Achieving these correlations will set new design rules towards further optimization of polymer chemical structures for OSCs exhibiting high performances and long stability. In this study, our efforts have been focused on identifying how the nature of aryl substituents and the number of fluorine atoms anchored in the backbone of indacenodithieno[3,2-b]thiophene (IDTT) based polymers influence their optoelectronic properties, the OSC performances and their degradation mechanisms. The most important outcome of this study is the demonstration that standard initial burn-in loss is primary attributed to microstructure instabilities. Furthermore, the initial burn-in loss could be substantially reduced through the rational design of the polymeric semiconductor's chemical structure, leading to improved lifetimes and low (20%) initial power conversion efficiency loss. In particular, we identify the beneficial effect of the presence of the two fluorine atoms on the benzo[c][1,2,5]thiadiazole (BTD), as compared to the non-fluorinated and mono-fluorinated analogues, in decreasing the burn-in by reducing the microstructure instabilities regardless of the aryl substituent that is present in the polymer backbone.

6 March 2015 in Polymer Chemistry
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RSRanbir Singh
Ranbir Singh
GPGeorgia Pagona
Georgia Pagona
VGVasilis G. Gregoriou
Vasilis G. Gregoriou
Nikos TagmatarchisNikos Tagmatarchis
Nikos Tagmatarchis
DTDimosthenis Toliopoulos
Dimosthenis Toliopoulos
Christos ChochosChristos Chochos
Christos Chochos
The influence of the monomer's isomeric structure on the optical, electrochemical, charge transporting properties and photovoltaic performance of donor–acceptor (D–A) conjugated polymers has been demonstrated for the first time by studying two D–A copolymers consisting of bis(3-octyloxy)phenyl)quinoxaline as the electron deficient unit and the two isomeric structures of thienothiophene (thieno[3,2-b]thiophene and thieno[2,3-b]thiophene) as the electron rich units. The drastic effect of incorporating two different isomeric structures on the polymer backbone of these copolymers, manifests in changes observed in their optical, electrochemical and charge transporting properties. In contrast, the overall photovoltaic performance of the copolymers is similar, but distinct differences in the device photocurrents occur. These differences were attributed to morphology variations rather than the balanced mobility ratio. For further developments in the field, the isomeric structures of different functional monomers should be considered in the designing of new materials with even superior performance.