Capabilities of a novel electrochemical cell for operando XAS and SAXS investigations for PEM fuel cells and water electrolysers
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F24%3A10492077" target="_blank" >RIV/00216208:11320/24:10492077 - isvavai.cz</a>
Výsledek na webu
<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=EtS4OKPzVK" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=EtS4OKPzVK</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.jpowsour.2024.235070" target="_blank" >10.1016/j.jpowsour.2024.235070</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Capabilities of a novel electrochemical cell for operando XAS and SAXS investigations for PEM fuel cells and water electrolysers
Popis výsledku v původním jazyce
Catalyst stability is a key issue in current electrochemical devices, such as fuel cells (FCs) and water electrolysers (WEs). While for FCs, the main degradation process limiting catalyst stability have been highlighted, a clear picture is still missing concerning WEs. In this framework, in operando analyses are essential to characterize catalyst degradation over time. As X-Rays constitute the perfect probe for studying catalytic materials, we here present a reversible electrochemical cell designed for operando X-Ray Absorption Spectroscopy and Small and Wide Angle X-Ray Scattering analyses, which was used: (i) to study Pt/C catalyst degradation coupling the evolution of specific electrochemically active surface area (ECSA) with catalyst morphology, supported by the analysis of Pt oxidation state. As a result, an increase of particle (and particle cluster) size is connected to the diminishing of ECSA and to the changes in the fraction of metallic-to-oxidised Pt, underlying that changes mainly develop in the first 2000 cycles of applied stress tests. Finally, (ii) we introduce some preliminary results underlying the change in Ir oxidation state for a standard Ir/IrOX catalyst material for WEs, showing as such a change is not sufficient to induce any remarkable morphological variations within 500 cycles of stress tests.
Název v anglickém jazyce
Capabilities of a novel electrochemical cell for operando XAS and SAXS investigations for PEM fuel cells and water electrolysers
Popis výsledku anglicky
Catalyst stability is a key issue in current electrochemical devices, such as fuel cells (FCs) and water electrolysers (WEs). While for FCs, the main degradation process limiting catalyst stability have been highlighted, a clear picture is still missing concerning WEs. In this framework, in operando analyses are essential to characterize catalyst degradation over time. As X-Rays constitute the perfect probe for studying catalytic materials, we here present a reversible electrochemical cell designed for operando X-Ray Absorption Spectroscopy and Small and Wide Angle X-Ray Scattering analyses, which was used: (i) to study Pt/C catalyst degradation coupling the evolution of specific electrochemically active surface area (ECSA) with catalyst morphology, supported by the analysis of Pt oxidation state. As a result, an increase of particle (and particle cluster) size is connected to the diminishing of ECSA and to the changes in the fraction of metallic-to-oxidised Pt, underlying that changes mainly develop in the first 2000 cycles of applied stress tests. Finally, (ii) we introduce some preliminary results underlying the change in Ir oxidation state for a standard Ir/IrOX catalyst material for WEs, showing as such a change is not sufficient to induce any remarkable morphological variations within 500 cycles of stress tests.
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
2024
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Journal of Power Sources
ISSN
0378-7753
e-ISSN
1873-2755
Svazek periodika
615
Číslo periodika v rámci svazku
Sep 30
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
8
Strana od-do
235070
Kód UT WoS článku
001281956200001
EID výsledku v databázi Scopus
2-s2.0-85199100571