Details

Autor(en) / Beteiligte

• Yu, Areum
• Lee, Chongmok
• Lee, Nam-Suk
• Kim, Myung Hwa
• Lee, Youngmi

Titel

Highly Efficient Silver–Cobalt Composite Nanotube Electrocatalysts for Favorable Oxygen Reduction Reaction

Ist Teil von

• ACS applied materials & interfaces, 2016-12, Vol.8 (48), p.32833-32841

Ort / Verlag

United States: American Chemical Society

Erscheinungsjahr

2016

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• This paper reports the synthesis and characterization of silver–cobalt (AgCo) bimetallic composite nanotubes. Cobalt oxide (Co3O4) nanotubes were fabricated by electrospinning and subsequent calcination in air and then reduced to cobalt (Co) metal nanotubes via further calcination under a H2/Ar atmosphere. As-prepared Co nanotubes were then employed as templates for the following galvanic replacement reaction (GRR) with silver (Ag) precursor (AgNO3), which produced AgCo composite nanotubes. Various AgCo nanotubes were readily synthesized with applying different reaction times for the reduction of Co3O4 nanotubes and GRR. One hour reduction was sufficiently long to convert Co3O4 to Co metal, and 3 h GRR was enough to deposit Ag layer on Co nanotubes. The tube morphology and copresence of Ag and Co in AgCo composite nanotubes were confirmed with SEM, HRTEM, XPS, and XRD analyses. Electroactivity of as-prepared AgCo composite nanotubes was characterized for ORR with rotating disk electrode (RDE) voltammetry. Among differently synthesized AgCo composite nanotubes, the one synthesized via 1 h reduction and 3 h GRR showed the best ORR activity (the most positive onset potential, greatest limiting current density, and highest number of electrons transferred). Furthermore, the ORR performance of the optimized AgCo composite nanotubes was superior compared to pure Co nanotubes, pure Ag nanowires, and bare platinum (Pt). High ethanol tolerance of AgCo composite nanotubes was also compared with the commercial Pt/C and then verified its excellent resistance to ethanol contamination.