B-N-, Si-N, and S-N-co-doped carbon quantum dots (CQD) were prepared by hydrothermal synthesis frominexpensive and non-toxic precursors. They were analysed by Raman, FTIR, and XPS spectroscopies and used asoxygen reduction reaction (ORR) electrocatalysts. The electrodes were prepared by drop-casting a slurry containingpoly(sulfone trimethylammonium) hydroxide (PSU-TMA) to enhance the hydroxide-ion transport nearthe catalytically active centers. Furthermore, polyaniline (PANI), reported to be catalytically active for the ORR,was added to some electrodes. A similar trend was observed for the electrode capacitance measured by cyclovoltammetryin the non-Faradaic region and impedance spectroscopy. The ORR kinetics studied by linear sweepvoltammetry showed the lowest onset and half-wave potentials and the lowest Tafel slopes for the B-N-co-dopedsamples, although the B concentration is low (0.5%). Data with and without PANI are quite similar. The S-N- andSi-N co-doped samples are slightly less efficient. The stability test demonstrated a decrease by about 10% of thediffusion-limited current after 500 cycles, indicating a microstructural change impacting the mass transportconditions, but the onset potential is not modified. Altogether, the good electrocatalytic activity of B-N-co-dopedCQD with a low boron concentration in presence of PSU-TMA indicated the high potential of these electrodes.The inexpensive synthesis of co-doped CQD from non-toxic precursors is an important advantage of these materialsvs other carbon-doped electrocatalysts.

Catalytic electrodes for the oxygen reduction reaction based on co-doped (B-N, Si-N, S-N) carbon quantum dots and anion exchange ionomer

S Kaciulis;
2022

Abstract

B-N-, Si-N, and S-N-co-doped carbon quantum dots (CQD) were prepared by hydrothermal synthesis frominexpensive and non-toxic precursors. They were analysed by Raman, FTIR, and XPS spectroscopies and used asoxygen reduction reaction (ORR) electrocatalysts. The electrodes were prepared by drop-casting a slurry containingpoly(sulfone trimethylammonium) hydroxide (PSU-TMA) to enhance the hydroxide-ion transport nearthe catalytically active centers. Furthermore, polyaniline (PANI), reported to be catalytically active for the ORR,was added to some electrodes. A similar trend was observed for the electrode capacitance measured by cyclovoltammetryin the non-Faradaic region and impedance spectroscopy. The ORR kinetics studied by linear sweepvoltammetry showed the lowest onset and half-wave potentials and the lowest Tafel slopes for the B-N-co-dopedsamples, although the B concentration is low (0.5%). Data with and without PANI are quite similar. The S-N- andSi-N co-doped samples are slightly less efficient. The stability test demonstrated a decrease by about 10% of thediffusion-limited current after 500 cycles, indicating a microstructural change impacting the mass transportconditions, but the onset potential is not modified. Altogether, the good electrocatalytic activity of B-N-co-dopedCQD with a low boron concentration in presence of PSU-TMA indicated the high potential of these electrodes.The inexpensive synthesis of co-doped CQD from non-toxic precursors is an important advantage of these materialsvs other carbon-doped electrocatalysts.
2022
Istituto per lo Studio dei Materiali Nanostrutturati - ISMN
oxygen reduction
carbon materials
electrocatalyst
fuel cells
stability
File in questo prodotto:
File Dimensione Formato  
prod_469441-doc_190120.pdf

solo utenti autorizzati

Descrizione: Catalytic electrodes for the oxygen reduction reaction based on co-doped (B-N, Si-N, S-N) carbon quantum dots and anion exchange ionomer
Tipologia: Versione Editoriale (PDF)
Licenza: NON PUBBLICO - Accesso privato/ristretto
Dimensione 2.33 MB
Formato Adobe PDF
2.33 MB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/417114
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 16
  • ???jsp.display-item.citation.isi??? 14
social impact