A survey of Earth-abundant metal oxides as oxygen evolution electrocatalysts in acidic media (pH < 1)

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F23%3A10477106" target="_blank" >RIV/00216208:11320/23:10477106 - isvavai.cz</a>

Výsledek na webu

<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=5M5oMxvHNN" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=5M5oMxvHNN</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1039/D3EY00101F" target="_blank" >10.1039/D3EY00101F</a>

Jazyk výsledku

angličtina

Název v původním jazyce

A survey of Earth-abundant metal oxides as oxygen evolution electrocatalysts in acidic media (pH < 1)

Popis výsledku v původním jazyce

Electrolytic hydrogen appears as one of the most promising options to store renewable energy. In this water splitting process, the sluggish kinetics of the 4-electron oxygen evolution reaction (OER) with its high overpotentials have been widely regarded as the bottleneck to facilitate a fast, energy-efficient process. In alkaline media, numerous earth-abundant metal oxides are efficient OER catalysts, stabilized by the high concentration of hydroxide anions in the electrolyte. However, under acidic conditions, where the hydrogen evolution reaction (HER) is technologically preferred, only noble metal-based oxides (RuO2 and IrO2) are suitable OER catalysts, putting into question the scalability to wide-spread applications due to their scarcity and high cost. Most earth abundant metal oxides dissolve at high proton concentrations. A promising strategy to avoid this drawback consists of incorporating these catalysts into partially hydrophobic composite electrodes. Following this strategy, we have been able to conduct an extensive survey of the activity and stability of mono-, bi- and trimetallic earth-abundant transition metal oxides during the electrocatalytic OER under strongly acidic conditions. Our results confirm the general validity of the strategy by using a hydrophobic electrode to confer high stability to common metal oxides under these harsh conditions. Among all OER catalysts investigated, we found that simple manganese oxides appeared as the most active also exhibiting high, long-term stability. In particular, the stability of Mn2O3 oxide in the OER in acidic media was well confirmed by post-electrolysis characterization data.

Název v anglickém jazyce

A survey of Earth-abundant metal oxides as oxygen evolution electrocatalysts in acidic media (pH < 1)

Popis výsledku anglicky

Electrolytic hydrogen appears as one of the most promising options to store renewable energy. In this water splitting process, the sluggish kinetics of the 4-electron oxygen evolution reaction (OER) with its high overpotentials have been widely regarded as the bottleneck to facilitate a fast, energy-efficient process. In alkaline media, numerous earth-abundant metal oxides are efficient OER catalysts, stabilized by the high concentration of hydroxide anions in the electrolyte. However, under acidic conditions, where the hydrogen evolution reaction (HER) is technologically preferred, only noble metal-based oxides (RuO2 and IrO2) are suitable OER catalysts, putting into question the scalability to wide-spread applications due to their scarcity and high cost. Most earth abundant metal oxides dissolve at high proton concentrations. A promising strategy to avoid this drawback consists of incorporating these catalysts into partially hydrophobic composite electrodes. Following this strategy, we have been able to conduct an extensive survey of the activity and stability of mono-, bi- and trimetallic earth-abundant transition metal oxides during the electrocatalytic OER under strongly acidic conditions. Our results confirm the general validity of the strategy by using a hydrophobic electrode to confer high stability to common metal oxides under these harsh conditions. Among all OER catalysts investigated, we found that simple manganese oxides appeared as the most active also exhibiting high, long-term stability. In particular, the stability of Mn2O3 oxide in the OER in acidic media was well confirmed by post-electrolysis characterization data.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10305 - Fluids and plasma physics (including surface physics)

Projekt

<a href="/cs/project/GN22-18079O" target="_blank" >GN22-18079O: POLAR-PEC: Objevení (foto/elektro) katalytických vlastností povrchů polárních oxidů kovů</a><br>

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2023

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

EES Catalysis

ISSN

2753-801X

e-ISSN

2753-801X

Svazek periodika

1

Číslo periodika v rámci svazku

5

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

9

Strana od-do

765-773

Kód UT WoS článku

001363337100001

EID výsledku v databázi Scopus

2-s2.0-85189979654