TY - JOUR
T1 - One-step synthesis of heterostructured cobalt-iron selenide as bifunctional catalyst for overall water splitting
AU - Boakye, Felix Ofori
AU - Li, Yong
AU - Owusu, Kwadwo Asare
AU - Amiinu, Ibrahim Saana
AU - Cheng, Yapeng
AU - Zhang, Haining
N1 - Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2022/1/1
Y1 - 2022/1/1
N2 - Transition metal selenide catalysts have been identified as suitable materials for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) as a result of their high electrical conductivity, large surface area, and tunable electronic structure to generate clean hydrogen through electrocatalytic water splitting. In this work, we report the fabrication of cobalt-iron selenide nanoparticles to form a heterostructured Co-Fe Selenide catalyst through a one-step hydrothermal process. The fabricated Co-Fe Selenide shows an improved performance toward HER in both acidic and alkaline electrolyte as compared to individual CoSe2 and FeSe2 catalysts. The HER activity of Co-Fe Selenide, at a current density of 10 mA cm−2, generates an overpotential of 129 and 142 mV, a Tafel slope of 47 and 46 mV dec−1 in both acidic and alkaline electrolytes, respectively. Furthermore, the catalyst exhibits an OER activity with an overpotential of 270 mV at a current density of 10 mA cm−2 with a small Tafel slope (78 mV dec−1) in alkaline electrolyte. Moreover, a symmetric water electrolysis cell assembled using Co-Fe Selenide on carbon cloth as both anode and cathode in alkaline electrolyte achieves a cell voltage of 1.68 V at a current density of 10 mA cm−2 with strong stability for 9 h. This outcome renders Co-Fe Selenide as a low-cost material for efficient HER and OER activity and as a potential replacement to noble metal catalysts for overall water splitting devices.
AB - Transition metal selenide catalysts have been identified as suitable materials for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) as a result of their high electrical conductivity, large surface area, and tunable electronic structure to generate clean hydrogen through electrocatalytic water splitting. In this work, we report the fabrication of cobalt-iron selenide nanoparticles to form a heterostructured Co-Fe Selenide catalyst through a one-step hydrothermal process. The fabricated Co-Fe Selenide shows an improved performance toward HER in both acidic and alkaline electrolyte as compared to individual CoSe2 and FeSe2 catalysts. The HER activity of Co-Fe Selenide, at a current density of 10 mA cm−2, generates an overpotential of 129 and 142 mV, a Tafel slope of 47 and 46 mV dec−1 in both acidic and alkaline electrolytes, respectively. Furthermore, the catalyst exhibits an OER activity with an overpotential of 270 mV at a current density of 10 mA cm−2 with a small Tafel slope (78 mV dec−1) in alkaline electrolyte. Moreover, a symmetric water electrolysis cell assembled using Co-Fe Selenide on carbon cloth as both anode and cathode in alkaline electrolyte achieves a cell voltage of 1.68 V at a current density of 10 mA cm−2 with strong stability for 9 h. This outcome renders Co-Fe Selenide as a low-cost material for efficient HER and OER activity and as a potential replacement to noble metal catalysts for overall water splitting devices.
KW - Bifunctional catalyst
KW - Hydrogen evolution
KW - Oxygen evolution
KW - Transition metal selenide
KW - Water splitting
UR - https://www.scopus.com/pages/publications/85114189457
U2 - 10.1016/j.matchemphys.2021.125201
DO - 10.1016/j.matchemphys.2021.125201
M3 - Article
AN - SCOPUS:85114189457
SN - 0254-0584
VL - 275
JO - Materials Chemistry and Physics
JF - Materials Chemistry and Physics
M1 - 125201
ER -