Electrodeposited p-Cu2O Films – Role of Redox-Active Compounds Under Photoelectrochemical Operation Revisited
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F25%3A43933583" target="_blank" >RIV/60461373:22310/25:43933583 - isvavai.cz</a>
Výsledek na webu
<a href="https://chemistry-europe.onlinelibrary.wiley.com/doi/pdf/10.1002/elsa.70003?getft_integrator=clarivate&utm_source=clarivate" target="_blank" >https://chemistry-europe.onlinelibrary.wiley.com/doi/pdf/10.1002/elsa.70003?getft_integrator=clarivate&utm_source=clarivate</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/elsa.70003" target="_blank" >10.1002/elsa.70003</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Electrodeposited p-Cu2O Films – Role of Redox-Active Compounds Under Photoelectrochemical Operation Revisited
Popis výsledku v původním jazyce
The p-type semiconducting copper oxides CuO and Cu<inf>2</inf>O are of interest for the conversion of solar energy due to their medium-wide bandgap and the position of their conduction band, allowing for reductive processes in junctions with electrolytes under irradiation. In this work, on Cu<inf>2</inf>O, the efficiency of several such processes in competition with self-reduction is critically reviewed and experimentally studied. Up to 2000 nm thick films were obtained via potentiostatic electrodeposition on fluorine-doped tin oxide on glass from alkaline solutions of CuSO<inf>4</inf> using lactic acid as a complexant. The films consisted of a dense arrangement of crystallites as seen by scanning electron microscopy and were of phase pure Cu<inf>2</inf>O as shown by X-ray diffraction (XRD). The films were specular, with an absorption coefficient of 50,000 cm−1 at 480 nm and a direct bandgap of 2.5 eV. In junctions with aqueous electrolytes, the material was found to be p-type. Under electrical bias, cathodic and photocathodic currents passed and increased dramatically when reducible redox compounds were added. The influence of various redox couples (O<inf>2</inf>, H<inf>2</inf>O<inf>2</inf>, and methylviologen [MV, 1,1'-dimethyl-4,4'-bipyridinium]) and their concentration in the electrolyte on the stability of the electrodes was studied. Long-time experiments showed that to avoid degradation of the electrodes, the use of oxygen-saturated solutions was mandatory when no other redox couple was added. H<inf>2</inf>O<inf>2</inf>-containing electrolytes gave rise to constant photocurrents and no alteration of the electrodes was found by XRD. MV yielded cathodic photocurrents. Reoxidation of its reduced form by dissolved oxygen was necessary in order to hinder dimerization or further reduction to MV0 and association of the latter to MV0<inf>n</inf>, producing a whitish layer on top of the electrodes which led to their inactivation. © 2025 The Author(s). Electrochemical Science Advances published by Wiley-VCH GmbH.
Název v anglickém jazyce
Electrodeposited p-Cu2O Films – Role of Redox-Active Compounds Under Photoelectrochemical Operation Revisited
Popis výsledku anglicky
The p-type semiconducting copper oxides CuO and Cu<inf>2</inf>O are of interest for the conversion of solar energy due to their medium-wide bandgap and the position of their conduction band, allowing for reductive processes in junctions with electrolytes under irradiation. In this work, on Cu<inf>2</inf>O, the efficiency of several such processes in competition with self-reduction is critically reviewed and experimentally studied. Up to 2000 nm thick films were obtained via potentiostatic electrodeposition on fluorine-doped tin oxide on glass from alkaline solutions of CuSO<inf>4</inf> using lactic acid as a complexant. The films consisted of a dense arrangement of crystallites as seen by scanning electron microscopy and were of phase pure Cu<inf>2</inf>O as shown by X-ray diffraction (XRD). The films were specular, with an absorption coefficient of 50,000 cm−1 at 480 nm and a direct bandgap of 2.5 eV. In junctions with aqueous electrolytes, the material was found to be p-type. Under electrical bias, cathodic and photocathodic currents passed and increased dramatically when reducible redox compounds were added. The influence of various redox couples (O<inf>2</inf>, H<inf>2</inf>O<inf>2</inf>, and methylviologen [MV, 1,1'-dimethyl-4,4'-bipyridinium]) and their concentration in the electrolyte on the stability of the electrodes was studied. Long-time experiments showed that to avoid degradation of the electrodes, the use of oxygen-saturated solutions was mandatory when no other redox couple was added. H<inf>2</inf>O<inf>2</inf>-containing electrolytes gave rise to constant photocurrents and no alteration of the electrodes was found by XRD. MV yielded cathodic photocurrents. Reoxidation of its reduced form by dissolved oxygen was necessary in order to hinder dimerization or further reduction to MV0 and association of the latter to MV0<inf>n</inf>, producing a whitish layer on top of the electrodes which led to their inactivation. © 2025 The Author(s). Electrochemical Science Advances published by Wiley-VCH GmbH.
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/EH22_008%2F0004617" target="_blank" >EH22_008/0004617: Konverze a skladování energie</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2025
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Electrochemical Science Advances
ISSN
2698-5977
e-ISSN
2698-5977
Svazek periodika
5
Číslo periodika v rámci svazku
2
Stát vydavatele periodika
DE - Spolková republika Německo
Počet stran výsledku
8
Strana od-do
nestránkováno
Kód UT WoS článku
001442463700001
EID výsledku v databázi Scopus
2-s2.0-105002571648