TY - JOUR
T1 - Nanotubular Iridium-Cobalt Mixed Oxide Crystalline Architectures Inherited from Cobalt Oxide for Highly Efficient Oxygen Evolution Reaction Catalysis
AU - Yu, Areum
AU - Lee, Chongmok
AU - Kim, Myung Hwa
AU - Lee, Youngmi
N1 - Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/10/11
Y1 - 2017/10/11
N2 - Here, we report the unique transformation of one-dimensional tubular mixed oxide nanocomposites of iridium (Ir) and cobalt (Co) denoted as IrxCo1-xOy, where x is the relative Ir atomic content to the overall metal content. The formation of a variety of IrxCo1-xOy (0 ≤ x ≤ 1) crystalline tubular nanocomposites was readily achieved by electrospinning and subsequent calcination process. Structural characterization clearly confirmed that IrxCo1-xOy polycrystalline nanocomposites had a tubular morphology consisting of Ir/IrO2 and Co3O4, where Ir, Co, and O were homogeneously distributed throughout the entire nanostructures. The facile formation of IrxCo1-xOy nanotubes was mainly ascribed to the inclination of Co3O4 to form the nanotubes during the calcination process, which could play a critical role in providing a template of tubular structure and facilitating the formation of IrO2 by being incorporated with Ir precursors. Furthermore, the electroactivity of obtained IrxCo1-xOy nanotubes was characterized for oxygen evolution reaction (OER) with rotating disk electrode voltammetry in 1 M NaOH aqueous solution. Among diverse IrxCo1-xOy, Ir0.46Co0.54Oy nanotubes showed the best OER activity (the least-positive onset potential, greatest current density, and low Tafel slope), which was even better than that of commercial Ir/C. The Ir0.46Co0.54Oy nanotubes also exhibited a high stability in alkaline electrolyte. Expensive Ir mixed with cheap Co at an optimum ratio showed a greater OER catalytic activity than pure Ir oxide, one of the most efficient OER catalysts.
AB - Here, we report the unique transformation of one-dimensional tubular mixed oxide nanocomposites of iridium (Ir) and cobalt (Co) denoted as IrxCo1-xOy, where x is the relative Ir atomic content to the overall metal content. The formation of a variety of IrxCo1-xOy (0 ≤ x ≤ 1) crystalline tubular nanocomposites was readily achieved by electrospinning and subsequent calcination process. Structural characterization clearly confirmed that IrxCo1-xOy polycrystalline nanocomposites had a tubular morphology consisting of Ir/IrO2 and Co3O4, where Ir, Co, and O were homogeneously distributed throughout the entire nanostructures. The facile formation of IrxCo1-xOy nanotubes was mainly ascribed to the inclination of Co3O4 to form the nanotubes during the calcination process, which could play a critical role in providing a template of tubular structure and facilitating the formation of IrO2 by being incorporated with Ir precursors. Furthermore, the electroactivity of obtained IrxCo1-xOy nanotubes was characterized for oxygen evolution reaction (OER) with rotating disk electrode voltammetry in 1 M NaOH aqueous solution. Among diverse IrxCo1-xOy, Ir0.46Co0.54Oy nanotubes showed the best OER activity (the least-positive onset potential, greatest current density, and low Tafel slope), which was even better than that of commercial Ir/C. The Ir0.46Co0.54Oy nanotubes also exhibited a high stability in alkaline electrolyte. Expensive Ir mixed with cheap Co at an optimum ratio showed a greater OER catalytic activity than pure Ir oxide, one of the most efficient OER catalysts.
KW - cobalt
KW - electrocatalyst
KW - electrospinning
KW - iridium
KW - mixed metal oxide nanotubes
KW - oxygen evolution reaction
UR - http://www.scopus.com/inward/record.url?scp=85031104048&partnerID=8YFLogxK
U2 - 10.1021/acsami.7b12247
DO - 10.1021/acsami.7b12247
M3 - Article
C2 - 28920424
AN - SCOPUS:85031104048
SN - 1944-8244
VL - 9
SP - 35057
EP - 35066
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 40
ER -