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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&lt;inf&gt;2&lt;/inf&gt;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&lt;inf&gt;2&lt;/inf&gt;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&lt;inf&gt;4&lt;/inf&gt; 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&lt;inf&gt;2&lt;/inf&gt;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&lt;inf&gt;2&lt;/inf&gt;, H&lt;inf&gt;2&lt;/inf&gt;O&lt;inf&gt;2&lt;/inf&gt;, and methylviologen [MV, 1,1&apos;-dimethyl-4,4&apos;-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&lt;inf&gt;2&lt;/inf&gt;O&lt;inf&gt;2&lt;/inf&gt;-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&lt;inf&gt;n&lt;/inf&gt;, 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&lt;inf&gt;2&lt;/inf&gt;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&lt;inf&gt;2&lt;/inf&gt;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&lt;inf&gt;4&lt;/inf&gt; 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&lt;inf&gt;2&lt;/inf&gt;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&lt;inf&gt;2&lt;/inf&gt;, H&lt;inf&gt;2&lt;/inf&gt;O&lt;inf&gt;2&lt;/inf&gt;, and methylviologen [MV, 1,1&apos;-dimethyl-4,4&apos;-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&lt;inf&gt;2&lt;/inf&gt;O&lt;inf&gt;2&lt;/inf&gt;-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&lt;inf&gt;n&lt;/inf&gt;, 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