National Repository of Grey Literature 31 records found  beginprevious13 - 22next  jump to record: Search took 0.00 seconds. 
Effect of pH on the Oxide Film Formation on a Pristine Zr Electrode
Hromadová, Magdaléna ; Kocábová, Jana ; Kolivoška, Viliam ; Pospíšil, Lubomír
Effect of pH on the oxidation of zirconium metal was studied by cyclic voltammetry in\naqueous borate buffer solutions as a function of the potential scan rate and pH from 4.80 to\n9.17. The results show that the oxide growth kinetics depends on pH of the electrolyte\nsolution and the total amount of irreversibly formed oxide under the potentiodynamic\nconditions decreases with decreasing buffer pH in accord with thermodynamic considerations.\nCathodic current corresponding to hydrogen evolution reaction diminishes in the presence of\nanodically modified electrode compared to bare zirconium.
Charge Transport through Molecular Towers Based on Tetraphenylmethane Tripods
Kolivoška, Viliam ; Šebera, Jakub ; Lindner, M. ; Valášek, M. ; Mayor, M. ; Mészáros, G. ; Gasior, Jindřich ; Hromadová, Magdaléna
Molecular platforms with multiple anchors were introduced recently to provide robust\ncoupling between molecular electronic components and metallic electrodes. In this work,\ncharge transport in tower-shaped single molecule conductors based on tetraphenylmethane\ntripod possessing three thiol anchors is investigated by scanning tunneling microscopy break\njunction technique. The effect of tripod substitution pattern and number of repeating units in\nmolecule is addressed. The substitution was found to influence conductance value in early\nstages of molecular junction evolution, where tower lays parallel to surface. In late stages, the\ncharge is transported through principal molecular axis and junction breaks thermally in tilted\nconfiguration.
Single Molecule Conductance and Junction Formation in Solution. Solvent Effect
Lachmanová, Štěpánka ; Šebera, Jakub ; Gasior, Jindřich ; Dupeyre, G. ; Lainé, P. P. ; Mészáros, G. ; Hromadová, Magdaléna
The single molecule conductance of expanded pyridinium derivative terminated by pyridyl\nnitrogen as an anchoring group at both ends of the molecule in two different environments\nwas measured by scanning tunneling microscopy break junction technique (STM-BJ). The\nvalues obtained in commonly used 1,3,5-trimethylbenzene (TMB) significantly differ from\nthe values acquired in a mixture of TMB and ethanol. Markedly lower junction length and\nhigher conductance indicate strong influence of adsorption of the molecule to the substrate\nsurface in pure TMB compared to the TMB and ethanol mixture.
Characterization of electrode modified by pyridineporphyrazinate film and its utilization in electrochemical sensor
Klusáčková, Monika ; Nesměrák, Karel (advisor) ; Hromadová, Magdaléna (referee)
In the diploma thesis the charge transfer reaction on thin layer N,N',N'',N'''-tetramethyl-tetra-3,4-pyridinoporphyrazinocobalt mediator is studied. The mediator is deposited on electrode surface formed by basal plane of highly ordered pyrolytic graphite. The modified electrode, which displays electrocatalytic activity to oxidation of propylene, has been characterized by cyclic voltammetry, backscattering spectroscopy and atomic force microscopy.
Dependence of Single-Molecule Conductance of Pyridinium Derivatives on Their Structure
Lachmanová, Štěpánka ; Hromadová, Magdaléna ; Kolivoška, Viliam ; Pospíšil, Lubomír ; Gasior, Jindřich ; Mészáros, G. ; Lainé, P. P.
The derivates of pyridinium belong to promising group of molecules applicable in molecular electronics. For this purpose, four expanded branched pyridinium compounds were synthetized and the influence of the molecular structure on their electrochemical properties and single-molecule conductances has been studied. The highest values of conductance provided compounds 9-(pyridin-4-yl)benzo[c]benzo[1,2]quinolizino[3,4,5,6-ija][1,6]naphthyridin-15-ium tetrafluoroborate and 3,5-dimethyl-2´,6´-diphenyl-[4,1´:4´,4´´-terpyridin]-1´-ium tetrafluoroborate. By the electrochemical reduction both of these compounds received two electrons in two separated one-electron steps. On the other hand, the compounds 2´,6´-diphenyl-[4,1´:4´,4´´-terpyridin]-1´-ium tetrafluoroborate and 2,6-diphenyl-4-(4-(pyridin-4-yl)phenyl)-[1,4´-bipyridin]-1-ium tetrafluoroborate are reduced by different mechanism and their conductance was lower.
Charge Transport in Single Molecule Junctions of Spirobifluorene Scaffold
Hromadová, Magdaléna ; Kolivoška, Viliam ; Sokolová, Romana ; Šebera, Jakub ; Mészáros, G. ; Valášek, M. ; Mayor, C.
Single molecule conductance of two spirobifluorene molecules of different length have been studied by scanning tunneling break junction (STM–BJ) methodology. First molecule contains a tripodal spirobifluorene platform, whereas a second one contains the same platform with chemically attached p-phenyleneethynylene molecular wire. The conductance values change only slightly between these two molecules, which demonstrated that such a platform provides both highly conducting pathway and stable anchor for the future molecular electronic devices.
Comparison of Techniques for Single-Molecule Conductance Measurements of Expanded Pyridinium Molecules
Lachmanová, Štěpánka ; Hromadová, Magdaléna ; Sokolová, Romana ; Kocábová, Jana ; Gasior, Jindřich ; Mészáros, G. ; Lainé, P. P.
This work is focused on the comparison of two techniques of single-molecule conductance measurements: Scanning Tunneling Microscopy Break Junction technique and Mechanically Controlled Break Junction technique. The structure of studied compound 9-(pyridin-4-yl)benzo[c]benzo[1,2]quinolizino[3,4,5,6-ija][1,6]naphthyridin-15-ium allows the formation of the molecular bridge between two gold electrodes, which are connected to a source of the constant voltage in both of the used methods. The differences, advantages and disadvantages of both of the techniques will be discussed. Both techniques provided two values of conductance of studied compound depending on the experimantal conditions.
Spectroelectrochemical Study of Electron Transfer in the Extended 1,1 '-Bipyridinium Cation
Hromadová, Magdaléna ; Kolivoška, Viliam ; Pospíšil, Lubomír ; Valášek, M. ; Tarábek, Ján
Electron transfer (ET) in the extended 1, 1 ' -bipyridinium has been investigated by UV Nis/NIR and EPR in-situ spectroelectrochemical techniques. During the in-situ cyclic voltammetric scan no EPR signal was observed at the potential corresponding to the first electron transfer at room temperature, whereas the EPR signal for the subsequent ET steadily increased and was observed even at the potentials corresponding to the fourth electron transfer. The EPR signal was detected for the first electron transfer step only at elevated temperature. The evidence for the presence of comproportionation processes and for the formation of n-dimer is discussed.
Electrochemical Properties of Branched Pyridinium Cations
Lachmanová, Štěpánka ; Hromadová, Magdaléna ; Pospíšil, Lubomír ; Lainé, P. P.
The electrochemical properties of branched extended pyridinium cations depend strongly on the structure of the molecule. This work is focused on the redox processes of the electron transfer of four derivatives of pyridinium. The electron transfer mechanism was studied by various electrochemical methods. Although the structures of the studied molecules seem to be quite similar, 1-N-methyl-2,4,6-triphenylpyridinium and 1',3',5'-trimethyl-2,4,6-triphenyl-1,4'-bipyridine-1,1'-diium are reduced in two separate one-electron transfer steps. On the other hand, 1'-methyl-2,4,6-triphenyl-1,4'-bipyridine-1,1'-diium and 1',3,5-trimethyl-2,4,6-triphenyl-1,4'-bipyridine-1,1'-diium accept two electrons, but in a single two-electron transfer. The heterogeneous rate constants of the electron-transfer processes were determined.
Properties of some radiosensitizers studied by means of the electrochemical methods
Gál, Miroslav ; Kolivoška, Viliam ; Ambrová, M. ; Híveš, J. ; Sokolová, Romana ; Hromadová, Magdaléna
To determine the correlation between reduction potential and some physicochemical properties of selected radiosensitizers cyclic voltammetry and theoretical calculations based on the DFT method with B3LYP functional of the level of 6-311++G** basis set in vacuum were utilized. Very good correlation was found between electron affinities of radiosensitizers and their reduction potential and so called E1(7) potential.

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2 Hromadová, Marcela
1 Hromadová, Michaela
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