Platinum interlayers reduce charge transport barriers between amorphous Ir-oxide OER electrocatalysts and the porous transport layer
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F25%3A10510428" target="_blank" >RIV/00216208:11320/25:10510428 - isvavai.cz</a>
Výsledek na webu
<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=a3xJti-dCs" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=a3xJti-dCs</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.cej.2025.162887" target="_blank" >10.1016/j.cej.2025.162887</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Platinum interlayers reduce charge transport barriers between amorphous Ir-oxide OER electrocatalysts and the porous transport layer
Popis výsledku v původním jazyce
Significant research efforts are dedicated to reducing the iridium loading in proton-exchange membrane water electrolyzers. Recently, the focus shifted toward better understanding the interplay between the titanium porous transport layers (PTLs) and the Ir-oxide-based catalyst layers, where significant performance losses were observed for low-loaded anodes based on intrinsically highly active but poorly conductive amorphous IrOx. In the presented study, a gas-diffusion electrode half-cell setup is used to promote an understanding of the underlying phenomena leading to this low performance. The influence of the PTL platinization on the performance of realistic porous transport electrodes (PTEs) for the oxygen evolution reaction (OER) is investigated by gradually increasing the platinum layer thickness for PTEs based on amorphous and rutile Ir-oxide. Electrochemical measurements show a beneficial influence of platinization on the activity for amorphous, but not for rutile Iroxide. Impedance analysis corroborates the formation of a Schottky-type interface between the PTL and the amorphous IrOx catalyst layers, depending on the PTL's platinum layer thickness. We presume that this heterogeneous Schottky-type interface induces an additional voltage drop and influences the utilization of the catalyst layer, leading to increased overpotentials. The measurements were complemented by inductively coupled plasma mass spectrometry showing constant integral amounts of Ir dissolving from the catalyst layers during the OER, independent of the platinization. Transferring the obtained knowledge to single cells, the whole composite anode, including e.g. the interplay between PTL and catalyst layer, must be optimized in conjunction to achieve optimum OER performance and long-term stability.
Název v anglickém jazyce
Platinum interlayers reduce charge transport barriers between amorphous Ir-oxide OER electrocatalysts and the porous transport layer
Popis výsledku anglicky
Significant research efforts are dedicated to reducing the iridium loading in proton-exchange membrane water electrolyzers. Recently, the focus shifted toward better understanding the interplay between the titanium porous transport layers (PTLs) and the Ir-oxide-based catalyst layers, where significant performance losses were observed for low-loaded anodes based on intrinsically highly active but poorly conductive amorphous IrOx. In the presented study, a gas-diffusion electrode half-cell setup is used to promote an understanding of the underlying phenomena leading to this low performance. The influence of the PTL platinization on the performance of realistic porous transport electrodes (PTEs) for the oxygen evolution reaction (OER) is investigated by gradually increasing the platinum layer thickness for PTEs based on amorphous and rutile Ir-oxide. Electrochemical measurements show a beneficial influence of platinization on the activity for amorphous, but not for rutile Iroxide. Impedance analysis corroborates the formation of a Schottky-type interface between the PTL and the amorphous IrOx catalyst layers, depending on the PTL's platinum layer thickness. We presume that this heterogeneous Schottky-type interface induces an additional voltage drop and influences the utilization of the catalyst layer, leading to increased overpotentials. The measurements were complemented by inductively coupled plasma mass spectrometry showing constant integral amounts of Ir dissolving from the catalyst layers during the OER, independent of the platinization. Transferring the obtained knowledge to single cells, the whole composite anode, including e.g. the interplay between PTL and catalyst layer, must be optimized in conjunction to achieve optimum OER performance and long-term stability.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10305 - Fluids and plasma physics (including surface physics)
Návaznosti výsledku
Projekt
Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
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
Chemical Engineering Journal
ISSN
1385-8947
e-ISSN
1873-3212
Svazek periodika
514
Číslo periodika v rámci svazku
Jun
Stát vydavatele periodika
CH - Švýcarská konfederace
Počet stran výsledku
15
Strana od-do
162887
Kód UT WoS článku
001494495400001
EID výsledku v databázi Scopus
2-s2.0-105003975203