Impact of Carbon Corrosion and Denitrogenation on the Deactivation of Fe-N-C Catalysts in Alkaline Media

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F24%3A10492026" target="_blank" >RIV/00216208:11320/24:10492026 - isvavai.cz</a>

Výsledek na webu

<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=.F6N24P42t" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=.F6N24P42t</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1021/acscatal.4c01219" target="_blank" >10.1021/acscatal.4c01219</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Impact of Carbon Corrosion and Denitrogenation on the Deactivation of Fe-N-C Catalysts in Alkaline Media

Popis výsledku v původním jazyce

Fe-N-C catalysts are considered an earth-abundant alternative to Pt in cathodes of anion exchange membrane fuel cells, although their stability still requires improvement for further commercialization. The degradation of Fe-N-C during both load cycles and start-stop events must be understood and mitigated to minimize system costs. Several approaches have recently been proposed to improve the durability of Fe active species during the oxygen reduction reaction in acidic media. On the other hand, knowledge of the degradation of Fe-N-C catalysts during start-stop events of anion exchange membrane fuel cells remains scarce. In this work, we use a gas diffusion electrode half-cell coupled with inductively coupled plasma mass spectrometry (GDE-ICP-MS) to quantify the Fe dissolution rates in the potential range between 0.93 and 1.5 V-RHE. It is shown that Fe dissolution accelerates with increased anodic potential and temperature, while it is independent of the presence/absence of O-2. The onset potential of Fe dissolution at room temperature agrees with the reported onset potentials of carbon corrosion and denitrogenation, C and N being oxidized to gaseous COx and NOx species, respectively. This correlation supports that the electrochemical oxidation of the N-C matrix triggers the observed catalyst demetalation in these conditions. Using a set of ex situ physicochemical characterization techniques, including spectroscopy and microscopy, the various degrees of degradation under three sets of experimental conditions of interest (O-2-RT, O-2-HT, and Ar-HT, where RT = 22 degrees C and HT = 62 degrees C) are rationalized. Combining the GDE-ICP-MS technique and post-mortem analyses, this work provides detailed insights into the degradation pathways of various Fe, N, and C species during start-stop events, which may inspire the next generation of durable Fe-N-C catalysts for anion exchange membrane fuel cells.

Název v anglickém jazyce

Impact of Carbon Corrosion and Denitrogenation on the Deactivation of Fe-N-C Catalysts in Alkaline Media

Popis výsledku anglicky

Fe-N-C catalysts are considered an earth-abundant alternative to Pt in cathodes of anion exchange membrane fuel cells, although their stability still requires improvement for further commercialization. The degradation of Fe-N-C during both load cycles and start-stop events must be understood and mitigated to minimize system costs. Several approaches have recently been proposed to improve the durability of Fe active species during the oxygen reduction reaction in acidic media. On the other hand, knowledge of the degradation of Fe-N-C catalysts during start-stop events of anion exchange membrane fuel cells remains scarce. In this work, we use a gas diffusion electrode half-cell coupled with inductively coupled plasma mass spectrometry (GDE-ICP-MS) to quantify the Fe dissolution rates in the potential range between 0.93 and 1.5 V-RHE. It is shown that Fe dissolution accelerates with increased anodic potential and temperature, while it is independent of the presence/absence of O-2. The onset potential of Fe dissolution at room temperature agrees with the reported onset potentials of carbon corrosion and denitrogenation, C and N being oxidized to gaseous COx and NOx species, respectively. This correlation supports that the electrochemical oxidation of the N-C matrix triggers the observed catalyst demetalation in these conditions. Using a set of ex situ physicochemical characterization techniques, including spectroscopy and microscopy, the various degrees of degradation under three sets of experimental conditions of interest (O-2-RT, O-2-HT, and Ar-HT, where RT = 22 degrees C and HT = 62 degrees C) are rationalized. Combining the GDE-ICP-MS technique and post-mortem analyses, this work provides detailed insights into the degradation pathways of various Fe, N, and C species during start-stop events, which may inspire the next generation of durable Fe-N-C catalysts for anion exchange membrane fuel cells.

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/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)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2024

Kód důvěrnosti údajů

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

Název periodika

ACS Catalysis

ISSN

2155-5435

e-ISSN

—

Svazek periodika

14

Číslo periodika v rámci svazku

11

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

16

Strana od-do

8576-8591

Kód UT WoS článku

001227290300001

EID výsledku v databázi Scopus

2-s2.0-85193750841