TY - JOUR
T1 - Template-free synthesis of one-dimensional cobalt sulfide nanorod array as an attractive architecture for overall water splitting
AU - Patil, Supriya A.
AU - Rabani, Iqra
AU - Vikraman, Dhanasekaran
AU - Bathula, Chinna
AU - Shrestha, Nabeen K.
AU - Kim, Hyungsang
AU - Hussain, Sajjad
AU - Im, Hyunsik
N1 - Publisher Copyright:
© 2020 John Wiley & Sons Ltd
PY - 2021/2
Y1 - 2021/2
N2 - One-dimensional (1D) nanoarrays are beneficial for electrochemical reactions, including water splitting, due to their directional electron transport through the array, large effective surface area, and porosity. Fabrication of such array without a template is, however, extremely challenging. Herein, an ion-exchange approach is employed to fabricate a 1D cobalt sulfide nanorod array (1D-CoS) from Co3O4 on stainless steel. The 1D-CoS electrode works as a bifunctional electrocatalyst, attaining the current density of 10 mA cm−2 for hydrogen evolution reaction and oxygen evolution reaction at a low overpotential of 159 and 280 mV, respectively in a 1 M KOH solution. A full electrolyzer with the same two 1D-CoS electrodes assembly demonstrates a low cell voltage of 1.75 V at 10 mA cm−2 and this performance value is well maintained for 20 hours. The efficient catalytic performance can be due to the controlled CoS phase with a unique 1D nanoarchitecture, which allows facile electrolyte diffusion and charge transfer between electrode/electrolyte interface.
AB - One-dimensional (1D) nanoarrays are beneficial for electrochemical reactions, including water splitting, due to their directional electron transport through the array, large effective surface area, and porosity. Fabrication of such array without a template is, however, extremely challenging. Herein, an ion-exchange approach is employed to fabricate a 1D cobalt sulfide nanorod array (1D-CoS) from Co3O4 on stainless steel. The 1D-CoS electrode works as a bifunctional electrocatalyst, attaining the current density of 10 mA cm−2 for hydrogen evolution reaction and oxygen evolution reaction at a low overpotential of 159 and 280 mV, respectively in a 1 M KOH solution. A full electrolyzer with the same two 1D-CoS electrodes assembly demonstrates a low cell voltage of 1.75 V at 10 mA cm−2 and this performance value is well maintained for 20 hours. The efficient catalytic performance can be due to the controlled CoS phase with a unique 1D nanoarchitecture, which allows facile electrolyte diffusion and charge transfer between electrode/electrolyte interface.
KW - CoS
KW - chemical bath deposition
KW - ion-exchange approach
KW - overall water splitting
UR - http://www.scopus.com/inward/record.url?scp=85090477837&partnerID=8YFLogxK
U2 - 10.1002/er.5973
DO - 10.1002/er.5973
M3 - Article
AN - SCOPUS:85090477837
SN - 0363-907X
VL - 45
SP - 2785
EP - 2796
JO - International Journal of Energy Research
JF - International Journal of Energy Research
IS - 2
ER -