TY - JOUR
T1 - Three-dimensional core–shell structured NiCo2O4@CoS/Ni-Foam electrocatalyst for oxygen evolution reaction and electrocatalytic oxidation of urea
AU - Adhikari, Sangeeta
AU - Kwon, Yongchai
AU - Kim, Do Heyoung
N1 - Publisher Copyright:
© 2020 Elsevier B.V.
PY - 2020/12/15
Y1 - 2020/12/15
N2 - Rational construction of non-noble metal-based electrocatalysts for energy generation and environmental electrooxidation receives attention because of their simplicity, versatility, and high efficiency. In this study, a novel core–shell electroactive material architecture is developed by electrodepositing cobalt sulfide shell over core NiCo2O4 structure on Ni-Foam substrate, which is developed by hydrothermal process. The synergistic effect of the three-dimensional chrysanthemum-like NiCo2O4 with CoS shell exhibits superior activity towards oxygen evolution reaction with high durability and lower onset potential obtained at 1.52 V vs. RHE (overpotential 290 mV @ 10 mA/cm2) in alkaline solution. The electron pairs from NiCo2O4 and CoS along with increased active sites from their interfacial interaction considerably improve the charge transfer phenomena. The electrocatalytic activity in the presence of urea is also investigated, which aids in reducing the onset potential to 118.4 mV vs. RHE. A considerably higher current density of 78 mA/cm2 is achieved at the potential of 0.5 V, which is comparatively higher than that of other electrocatalysts. Thus, the activity from sulfide/oxide core–shell architectures proves to have a high potential in efficient electrochemical reactivity producing green energy.
AB - Rational construction of non-noble metal-based electrocatalysts for energy generation and environmental electrooxidation receives attention because of their simplicity, versatility, and high efficiency. In this study, a novel core–shell electroactive material architecture is developed by electrodepositing cobalt sulfide shell over core NiCo2O4 structure on Ni-Foam substrate, which is developed by hydrothermal process. The synergistic effect of the three-dimensional chrysanthemum-like NiCo2O4 with CoS shell exhibits superior activity towards oxygen evolution reaction with high durability and lower onset potential obtained at 1.52 V vs. RHE (overpotential 290 mV @ 10 mA/cm2) in alkaline solution. The electron pairs from NiCo2O4 and CoS along with increased active sites from their interfacial interaction considerably improve the charge transfer phenomena. The electrocatalytic activity in the presence of urea is also investigated, which aids in reducing the onset potential to 118.4 mV vs. RHE. A considerably higher current density of 78 mA/cm2 is achieved at the potential of 0.5 V, which is comparatively higher than that of other electrocatalysts. Thus, the activity from sulfide/oxide core–shell architectures proves to have a high potential in efficient electrochemical reactivity producing green energy.
KW - Core-shell
KW - NiCoO@CoS/NF
KW - Oxygen evolution
KW - Three-dimensional
KW - Urea electrooxidation
UR - http://www.scopus.com/inward/record.url?scp=85087752944&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2020.126192
DO - 10.1016/j.cej.2020.126192
M3 - Article
AN - SCOPUS:85087752944
SN - 1385-8947
VL - 402
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 126192
ER -