Interface Engineering of SRu-mC3N4 Heterostructures for Enhanced Electrochemical Hydrazine Oxidation Reactions
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989100%3A27640%2F22%3A10251055" target="_blank" >RIV/61989100:27640/22:10251055 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/61989592:15640/22:73617428
Výsledek na webu
<a href="https://www.mdpi.com/2073-4344/12/12/1560" target="_blank" >https://www.mdpi.com/2073-4344/12/12/1560</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3390/catal12121560" target="_blank" >10.3390/catal12121560</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Interface Engineering of SRu-mC3N4 Heterostructures for Enhanced Electrochemical Hydrazine Oxidation Reactions
Popis výsledku v původním jazyce
Hydrazine oxidation in single-atom catalysts (SACs) could exploit the efficiency of metal atom utilization, which is a substitution for noble metal-based electrolysers that results in reduced overall cost. A well-established ruthenium single atom over mesoporous carbon nitride (SRu-mC3N4) catalyst is explored for the electro-oxidation of hydrazine as one of the model reactions for direct fuel cell reactions. The electrochemical activity observed with linear sweep voltammetry (LSV) confirmed that SRu-mC3N4 shows an ultra-low onset potential of 0.88 V vs. RHE, and with a current density of 10 mA/cm2 the observed potential was 1.19 V vs. RHE, compared with mesoporous carbon nitride (mC3N4) (1.77 V vs. RHE). Electrochemical impedance spectroscopy (EIS) and chronoamperometry (i-t) studies on SRu-mC3N4 show a smaller charge-transfer resistance (RCt) of 2950 Ω and long-term potential, as well as current stability of 50 h and 20 mA/cm2, respectively. Herein, an efficient and enhanced activity toward HzOR was demonstrated on SRu-mC3N4 from its synergistic platform over highly porous C3N4, possessing large and independent active sites, and improving the subsequent large-scale reaction.
Název v anglickém jazyce
Interface Engineering of SRu-mC3N4 Heterostructures for Enhanced Electrochemical Hydrazine Oxidation Reactions
Popis výsledku anglicky
Hydrazine oxidation in single-atom catalysts (SACs) could exploit the efficiency of metal atom utilization, which is a substitution for noble metal-based electrolysers that results in reduced overall cost. A well-established ruthenium single atom over mesoporous carbon nitride (SRu-mC3N4) catalyst is explored for the electro-oxidation of hydrazine as one of the model reactions for direct fuel cell reactions. The electrochemical activity observed with linear sweep voltammetry (LSV) confirmed that SRu-mC3N4 shows an ultra-low onset potential of 0.88 V vs. RHE, and with a current density of 10 mA/cm2 the observed potential was 1.19 V vs. RHE, compared with mesoporous carbon nitride (mC3N4) (1.77 V vs. RHE). Electrochemical impedance spectroscopy (EIS) and chronoamperometry (i-t) studies on SRu-mC3N4 show a smaller charge-transfer resistance (RCt) of 2950 Ω and long-term potential, as well as current stability of 50 h and 20 mA/cm2, respectively. Herein, an efficient and enhanced activity toward HzOR was demonstrated on SRu-mC3N4 from its synergistic platform over highly porous C3N4, possessing large and independent active sites, and improving the subsequent large-scale reaction.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10511 - Environmental sciences (social aspects to be 5.7)
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)
Ostatní
Rok uplatnění
2022
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Catalysts
ISSN
2073-4344
e-ISSN
2073-4344
Svazek periodika
12
Číslo periodika v rámci svazku
12
Stát vydavatele periodika
CH - Švýcarská konfederace
Počet stran výsledku
12
Strana od-do
nestrankovano
Kód UT WoS článku
000902281200001
EID výsledku v databázi Scopus
2-s2.0-85144834332