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Dive into the research topics where Mihalis Fakis is active.

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Featured researches published by Mihalis Fakis.


Journal of Organic Chemistry | 2011

Benzothiazoles with Tunable Electron-Withdrawing Strength and Reverse Polarity: A Route to Triphenylamine-Based Chromophores with Enhanced Two-Photon Absorption

Peter Hrobárik; Veronika Hrobáriková; Ivica Sigmundová; Pavol Zahradník; Mihalis Fakis; I. Polyzos; P. Persephonis

A series of dipolar and octupolar triphenylamine-derived dyes containing a benzothiazole positioned in the matched or mismatched fashion have been designed and synthesized via palladium-catalyzed Sonogashira cross-coupling reactions. Linear and nonlinear optical properties of the designed molecules were tuned by an additional electron-withdrawing group (EWG) and by changing the relative positions of the donor and acceptor substituents on the heterocyclic ring. This allowed us to examine the effect of positional isomerism and extend the structure-property relationships useful in the engineering of novel heteroaromatic-based systems with enhanced two-photon absorption (TPA). The TPA cross-sections (δ(TPA)) in the target compounds dramatically increased with the branching of the triphenylamine core and with the strength of the auxiliary acceptor. In addition, a change from the commonly used polarity in push-pull benzothiazoles to a reverse one has been revealed as a particularly useful strategy (regioisomeric control) for enhancing TPA cross-sections and shifting the absorption and emission maxima to longer wavelengths. The maximum TPA cross-sections of the star-shaped three-branched triphenylamines are ∼500-2300 GM in the near-infrared region (740-810 nm); thereby the molecular weight normalized δ(TPA)/MW values of the best performing dyes within the series (2.0-2.4 GM·g(-1)·mol) are comparable to those of the most efficient TPA chromophores reported to date. The large TPA cross-sections combined with high emission quantum yields and large Stokes shifts make these compounds excellent candidates for various TPA applications, including two-photon fluorescence microscopy.


Journal of Organic Chemistry | 2010

Benzothiazole-Based Fluorophores of Donor−π-Acceptor−π-Donor Type Displaying High Two-Photon Absorption

Veronika Hrobáriková; Peter Hrobárik; Peter Gajdoš; I. Fitilis; Mihalis Fakis; P. Persephonis; Pavol Zahradník

A series of novel heterocycle-based dyes with donor-pi-bridge-acceptor-pi-bridge-donor (D-pi-A-pi-D) structural motif, where benzothiazole serves as an electron-withdrawing core, have been designed and synthesized via palladium-catalyzed Sonogashira and Suzuki-type cross-coupling reactions. All the target chromophores show strong one-photon and two-photon excited emission. The maximum two-photon absorption (TPA) cross sections delta(TPA) of the prepared derivatives bearing diphenylamino functionalities occur at wavelengths ranging from 760 to 800 nm and are as large as approximately 900-1100 GM. One- and two-photon absorption characteristics of the title dyes have also been investigated by using density functional theory (DFT) and the structure-property relationships are discussed. The TPA cross sections calculated by means of quadratic response time-dependent DFT using the Coulomb-attenuated CAM-B3LYP functional support the experimentally observed trends within the series, as well as higher delta(TPA) values of the title compounds compared to those of analogous fluorene or carbazole-derived dyes. In contrast, the traditional B3LYP functional was not successful in predicting the observed trend of TPA cross sections for systems with different central cores. In general, structural modification of the pi-bridge composition by replacement of ethynylene (alkyne) with E-ethenylene (alkene) linkages and/or replacement of dialkylamino electron-donating edge substituents by diarylamino ones results in an increase of delta(TPA) values. The combination of large TPA cross sections and high emission quantum yields makes the title benzothiazole-based dyes attractive for applications involving two-photon excited fluorescence (TPEF).


Chemical Physics Letters | 2003

Two-photon absorption properties of novel organic materials for three-dimensional optical memories

I. Polyzos; G. Tsigaridas; Mihalis Fakis; V. Giannetas; P. Persephonis; John A. Mikroyannidis

Abstract The two-photon absorption (TPA) properties of a novel group of pyrylium-based compounds were studied. The molecules of this group were synthesized by systematically changing the chemical structure of a specific substituent in an initial chromophore. TPA cross-sections as large as 1.8×10 −47 cm 4 s photon −1 and high quantum yields were obtained. The results combined with the low cost and ease of synthesis of these compounds make them candidates for TPA applications. Particularly, three-dimensional data storage in polymer matrices of the synthesized compounds was realized through the photobleaching process. The high efficiency of recording and the submicron resolution reveal the great potential of this group of molecules as memory materials.


Chemical Physics Letters | 2001

Intensity dependent nonlinear absorption of pyrylium chromophores

Mihalis Fakis; G. Tsigaridas; I. Polyzos; V. Giannetas; P. Persephonis; Ioakim K. Spiliopoulos; John A. Mikroyannidis

Abstract The intensity dependence of nonlinear absorption (NLA) of a series of pyrylium chromophores was studied with femtosecond pulses in their two-photon absorption spectral region to assess their potential as optical limiters. The open z-scan technique using different excitation intensities was employed. Fifth-order effects appear above a critical value of the irradiance and consequently of the first excited singlet-state population. Reverse saturable absorption (RSA) based on two-photon (TPA) and excited-state absorption (ESA) was dominant in most cases. The third- and fifth-order NLA coefficients and high ESA cross-sections of the order of 10 −15 cm 2 are presented at 760, 790 and 840 nm.


Journal of Materials Chemistry | 2014

Porphyrin oriented self-assembled nanostructures for efficient exciton dissociation in high-performing organic photovoltaics

Maria Vasilopoulou; Dimitra G. Georgiadou; Antonios M. Douvas; Anastasia Soultati; Vassilios Constantoudis; Dimitris Davazoglou; Spyros Gardelis; Leonidas C. Palilis; Mihalis Fakis; S. Kennou; Theodore Lazarides; Athanassios G. Coutsolelos; Panagiotis Argitis

Herein we report on enhanced organic solar cell performance through the incorporation of cathode interfacial layers consisting of self-organized porphyrin nanostructures with a face-on configuration. In particular, a water/methanol-soluble porphyrin molecule, the free base meso-tetrakis(1-methylpyridinium-4-yl)porphyrin chloride, is employed as a novel cathode interlayer in bulk heterojunction organic photovoltaics. It is demonstrated that the self-organization of this porphyrin compound into aggregates in which molecules adopt a face-to-face orientation parallel to the organic semiconducting substrate induces a large local interfacial electric field that results in a significant enhancement of exciton dissociation. Consequently, enhanced photocurrent and open circuit voltage were obtained resulting in overall device efficiency improvement in organic photovoltaics based on bulk heterojunction mixtures of different polymeric donors and fullerene acceptors, regardless of the specific combination of donor–acceptor employed. To highlight the impact of molecular orientation a second porphyrin compound, the Zn-metallated meso-tetrakis(1-methylpyridinium-4-yl)porphyrin chloride, was also studied and it was found that it forms aggregates with an edge-to-edge molecular configuration inducing a smaller increase in the device performance.


Chemical Physics Letters | 2000

Novel class of pyrylium dyes with high efficiency in lasing and two-photon absorption fluorescence

Mihalis Fakis; J Polyzos; G. Tsigaridas; John Parthenios; A Fragos; V. Giannetas; P. Persephonis; John A. Mikroyannidis

Abstract We report the synthesis of a promising class of pyrylium dyes concerning laser and two-photon absorption action. Three representatives of this class, 4-(2,4-dichlorophenyl)-2,6-bisphenylpyrylium tetrafluoroborate, 4-phenyl-2,6-bis(4-methoxyphenyl)pyrylium tetrafluoroborate, and 4-(2,4-dichlorophenyl)-2,6-bis(4-biphenyl)pyrylium tetrafluoroborate, were investigated. Each dye was synthesized by a convenient and inexpensive method. Efficient laser action was shown at ∼500, ∼560, ∼615 nm. Changing the conjugation length i.e. the length of the oligophenyl moiety, or introducing various substituents on the aromatic rings, the emission maximum can be controlled. Two-photon absorption induced fluorescence was also observed. These pyrylium dyes constitute excellent candidates for laser technology and two-photon absorption applications.


Optics Letters | 2005

Three-photon induced photobleaching in a three-dimensional memory material

I. Polyzos; G. Tsigaridas; Mihalis Fakis; V. Giannetas; P. Persephonis

The photobleaching properties of a 3D memory material based on pyrylium salts are studied. It is shown that under ultrashort pulsed irradiation photobleaching occurs through two diverse mechanisms. One is major and causes fast bleaching, whereas the other is minor and causes slow bleaching. Furthermore, it is proved that both mechanisms are three- or more-photon processes. This fact gives the capability of significantly increasing data storage density.


RSC Advances | 2016

Solvent and branching effect on the two-photon absorption properties of push–pull triphenylamine derivatives

Daniel Cvejn; E. Michail; Kostas Seintis; Milan Klikar; Oldřich Pytela; Tomáš Mikysek; Numan Almonasy; Miroslav Ludwig; V. Giannetas; Mihalis Fakis; Filip Bureš

The photophysical and two-photon absorption (2PA) properties of two tri-podal molecules and of their quadrupolar and dipolar counterparts are reported for a series of solvents with varying polarity. The molecules possess a tri-phenylamine electron donating group and mono-cyano acceptors while olefinic and acetylenic π-linkers have been used. Branching led to an increase of the molar extinction coefficient and to a slight bathochromic shift of the absorption spectra while the fluorescence quantum yields decrease but they are maintained to relatively high values. Solvatochromic measurements in the tri-podal molecules revealed an emitting state with a polar nature. The 2PA cross sections in general increase upon branching but the observed behaviour strongly depends on the type of solvent. The highest 2PA cross sections are obtained in solvents of medium polarity and values as high as 1420 GM are reported.


Journal of The Optical Society of America B-optical Physics | 2003

Z-scan analysis for near-Gaussian beams through Hermite-Gaussian decomposition

G. Tsigaridas; Mihalis Fakis; I. Polyzos; M. Tsibouri; P. Persephonis; V. Giannetas

Gaussian decomposition is used as a theoretical infrastructure with which Z-scan experiments are analyzed. This procedure is extended here to the interesting, from a practical point of view, case in which the laser beam used is not perfectly Gaussian. We follow a perturbative approach to obtain the far-field pattern of the beam after the beam passes through a nonlinear sample. The procedure is based on the decomposition of the electric field at the exit plane of the sample to a linear combination of Hermite–Gaussian functions. To a first-order approximation, each mode of the incident beam is decomposed to a linear combination of different-order modes that do not exceed the order of the original mode. Finally, the effects of the simultaneous presence of first and higher-order refractive nonlinearities or first-order refractive nonlinearity and nonlinear absorption are studied.


Journal of Materials Chemistry C | 2015

Modulation of (non)linear optical properties in tripodal molecules by variation of the peripheral cyano acceptor moieties and the π-spacer

Daniel Cvejn; Eugene Michail; I. Polyzos; Numan Almonasy; Oldřich Pytela; Milan Klikar; Tomáš Mikysek; V. Giannetas; Mihalis Fakis; Filip Bureš

A series of twelve tripodal push-pull molecules with a central triphenylamine donor and peripheral cyano substituted acceptors has been prepared. These molecules possess systematically altered π-linkers as well as cyano acceptors. Based on the experimental properties measured by differential scanning calorimetry, electrochemistry, one and two photon absorption/emission spectroscopy, supported by the DFT calculations, thorough structure–property relationships were elucidated.

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Anastasia Soultati

National Technical University of Athens

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Spyros Gardelis

National and Kapodistrian University of Athens

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