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Synthesis of PtCu/C Nanostructured Electrocatalysts for the Oxygen Reduction Reaction via One-Step Electrochemical Erosion

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216305%3A26620%2F26%3A0200769" target="_blank" >RIV/00216305:26620/26:0200769 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://pubs.acs.org/doi/10.1021/acsami.5c22270?src=getftr&utm_source=clarivate&getft_integrator=clarivate" target="_blank" >https://pubs.acs.org/doi/10.1021/acsami.5c22270?src=getftr&utm_source=clarivate&getft_integrator=clarivate</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/acsami.5c22270" target="_blank" >10.1021/acsami.5c22270</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Synthesis of PtCu/C Nanostructured Electrocatalysts for the Oxygen Reduction Reaction via One-Step Electrochemical Erosion

  • Popis výsledku v původním jazyce

    Reducing the precious metal loading while increasing the oxygen reduction reaction (ORR) mass activity of novel electrocatalysts constitutes one of the remaining key challenges in the widespread application of proton exchange membrane fuel cells, which is inevitable for the transition to the climate-neutral hydrogen economy. However, this requires a simple, scalable, and affordable production of active nanostructured electrocatalysts. Alloyed nanoparticles of Platinum (Pt) with transition metals like cobalt, nickel, or copper have shown promising activity toward ORR, but their preparation usually involves complex multistep processes and environmentally harmful surfactants or structure-capping agents. In this work, we present the successful synthesis of nonspherical copper-alloyed Pt nanoparticles (PtCu) by employing a simple one-step top-down approach without surfactants or capping agents. The electrocatalysts were characterized by high-resolution transmission electron microscopy, energy-dispersive X-ray spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and inductively coupled plasma mass spectrometry. The ORR kinetics were evaluated using the rotating (ring) disk electrode technique. The synthesized PtCu/C catalysts revealed outstanding mass activities of similar to 1.2 A mgPt -1 at 0.9 V vs the reversible hydrogen electrode, which clearly surpasses state-of-the-art Pt-based catalysts in the literature and demonstrates the highest ORR mass activities reported for PtCu nanoparticles.

  • Název v anglickém jazyce

    Synthesis of PtCu/C Nanostructured Electrocatalysts for the Oxygen Reduction Reaction via One-Step Electrochemical Erosion

  • Popis výsledku anglicky

    Reducing the precious metal loading while increasing the oxygen reduction reaction (ORR) mass activity of novel electrocatalysts constitutes one of the remaining key challenges in the widespread application of proton exchange membrane fuel cells, which is inevitable for the transition to the climate-neutral hydrogen economy. However, this requires a simple, scalable, and affordable production of active nanostructured electrocatalysts. Alloyed nanoparticles of Platinum (Pt) with transition metals like cobalt, nickel, or copper have shown promising activity toward ORR, but their preparation usually involves complex multistep processes and environmentally harmful surfactants or structure-capping agents. In this work, we present the successful synthesis of nonspherical copper-alloyed Pt nanoparticles (PtCu) by employing a simple one-step top-down approach without surfactants or capping agents. The electrocatalysts were characterized by high-resolution transmission electron microscopy, energy-dispersive X-ray spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and inductively coupled plasma mass spectrometry. The ORR kinetics were evaluated using the rotating (ring) disk electrode technique. The synthesized PtCu/C catalysts revealed outstanding mass activities of similar to 1.2 A mgPt -1 at 0.9 V vs the reversible hydrogen electrode, which clearly surpasses state-of-the-art Pt-based catalysts in the literature and demonstrates the highest ORR mass activities reported for PtCu nanoparticles.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    21001 - Nano-materials (production and properties)

Návaznosti výsledku

  • Projekt

    <a href="/cs/project/LM2023051" target="_blank" >LM2023051: Výzkumná infrastruktura CzechNanoLab</a><br>

  • Návaznosti

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Ostatní

  • Rok uplatnění

    2026

  • Kód důvěrnosti údajů

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

Údaje specifické pro druh výsledku

  • Název periodika

    ACS Applied Materials & Interfaces

  • ISSN

    1944-8244

  • e-ISSN

    1944-8252

  • Svazek periodika

    18

  • Číslo periodika v rámci svazku

    2

  • Stát vydavatele periodika

    US - Spojené státy americké

  • Počet stran výsledku

    15

  • Strana od-do

    4210-4224

  • Kód UT WoS článku

    001656094800001

  • EID výsledku v databázi Scopus

    2-s2.0-105028019774