Electrochemical Properties of Cu(II/I)-Based Redox Mediators for Dye-Sensitized Solar Cells
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F17%3A00468650" target="_blank" >RIV/61388955:_____/17:00468650 - isvavai.cz</a>
Výsledek na webu
<a href="http://dx.doi.org/10.1016/j.electacta.2016.12.185" target="_blank" >http://dx.doi.org/10.1016/j.electacta.2016.12.185</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.electacta.2016.12.185" target="_blank" >10.1016/j.electacta.2016.12.185</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Electrochemical Properties of Cu(II/I)-Based Redox Mediators for Dye-Sensitized Solar Cells
Popis výsledku v původním jazyce
Three Cu(II/I)-phenanthroline and Cu(II/I)-bipyridine redox mediators are studied on various electrodes and in variety of electrolyte solutions using cyclic voltammetry and impedance spectroscopy on symmetrical dummy cells. Graphene-based catalysts provide comparably high activity to PEDOT, and both catalysts outperform the activity of platinum. The charge-transfer kinetics and the diffusion rate significantly slowdown in the presence 4-tert-butylpyridine. This effect is specific only for Cu-mediators (is missing for Co-mediators), and is ascribed to a sensitivity of the coordination sphere of the Cu(II)-species to structural and substitutional changes. The ‘Zombie Cells’ made from symmetrical PEDOT/PEDOT devices exhibit enhanced charge-transfer rate and enhanced diffusion resistance. Electrochemically clean Cu(II)-bipyridine species are prepared, for the first time, by electrochemical oxidation of the parent Cu(I) complexes. Our preparative electrolysis brings numerous advantages over the standard chemical syntheses of the Cu(II)-bipyridine complexes. The superior performance of electrochemically-grown clean Cu(II)-bipyridine complex is demonstrated on practical dye-sensitized solar cells.
Název v anglickém jazyce
Electrochemical Properties of Cu(II/I)-Based Redox Mediators for Dye-Sensitized Solar Cells
Popis výsledku anglicky
Three Cu(II/I)-phenanthroline and Cu(II/I)-bipyridine redox mediators are studied on various electrodes and in variety of electrolyte solutions using cyclic voltammetry and impedance spectroscopy on symmetrical dummy cells. Graphene-based catalysts provide comparably high activity to PEDOT, and both catalysts outperform the activity of platinum. The charge-transfer kinetics and the diffusion rate significantly slowdown in the presence 4-tert-butylpyridine. This effect is specific only for Cu-mediators (is missing for Co-mediators), and is ascribed to a sensitivity of the coordination sphere of the Cu(II)-species to structural and substitutional changes. The ‘Zombie Cells’ made from symmetrical PEDOT/PEDOT devices exhibit enhanced charge-transfer rate and enhanced diffusion resistance. Electrochemically clean Cu(II)-bipyridine species are prepared, for the first time, by electrochemical oxidation of the parent Cu(I) complexes. Our preparative electrolysis brings numerous advantages over the standard chemical syntheses of the Cu(II)-bipyridine complexes. The superior performance of electrochemically-grown clean Cu(II)-bipyridine complex is demonstrated on practical dye-sensitized solar cells.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10405 - Electrochemistry (dry cells, batteries, fuel cells, corrosion metals, electrolysis)
Návaznosti výsledku
Projekt
<a href="/cs/project/GA13-07724S" target="_blank" >GA13-07724S: Materiálové inženýrství pro inovativní Graetzelovy solární články</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2017
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Electrochimica acta
ISSN
0013-4686
e-ISSN
—
Svazek periodika
227
Číslo periodika v rámci svazku
FEB 2017
Stát vydavatele periodika
GB - Spojené království Velké Británie a Severního Irska
Počet stran výsledku
9
Strana od-do
194-202
Kód UT WoS článku
000394399600023
EID výsledku v databázi Scopus
2-s2.0-85008883743