TY - JOUR
T1 - Metal-organic-framework-derived bi-metallic sulfide on N, S-codoped porous carbon nanocomposites as multifunctional electrocatalysts
AU - Chen, Binling
AU - Ma, Guiping
AU - Zhu, Yanqiu
AU - Wang, Jinbo
AU - Xiong, Wei
AU - Xia, Yongde
N1 - Publisher Copyright:
© 2016 Elsevier B.V.
PY - 2016/12/1
Y1 - 2016/12/1
N2 - A novel type of composite, consisting of a bi-metallic sulfide/carbon nanocomposite system, was developed as a multifunctional electrocatalyst. The nanocomposite system was facilely generated via a one-step simultaneous carbonization and sulfurization of a selected metal-organic framework. Sample Ni1Co4S@C-1000 is one of the most efficient electrocatalysts and exhibited superior activity and stability in oxygen evolution reaction (OER) due to the Ni substitution, the high porosity, the homogeneous dispersion of active components and the effect of N, S-codoping. This novel material showed a low onset potential of 1.43 V (vs reversible hydrogen electrode) and a stable current density of 10 mA cm−2 at 1.51 V in a 0.1 M KOH alkaline solution over a long-term operation, which is better than IrO2/C and other composites synthesized under the same conditions. The Ni1Co4S@C-1000 sample can also efficiently catalyse oxygen reduction reaction (ORR), with a four-electron pathway for reversible oxygen evolution and reduction. Furthermore, Ni1Co4S@C-800 showed enhanced electrocatalytic activity for hydrogen evolution reaction (HER) in water splitting. These findings pave a way to develop effective and promising alternative electrocatalysts towards OER, ORR and HER in the next generation of energy storage and conversion technologies.
AB - A novel type of composite, consisting of a bi-metallic sulfide/carbon nanocomposite system, was developed as a multifunctional electrocatalyst. The nanocomposite system was facilely generated via a one-step simultaneous carbonization and sulfurization of a selected metal-organic framework. Sample Ni1Co4S@C-1000 is one of the most efficient electrocatalysts and exhibited superior activity and stability in oxygen evolution reaction (OER) due to the Ni substitution, the high porosity, the homogeneous dispersion of active components and the effect of N, S-codoping. This novel material showed a low onset potential of 1.43 V (vs reversible hydrogen electrode) and a stable current density of 10 mA cm−2 at 1.51 V in a 0.1 M KOH alkaline solution over a long-term operation, which is better than IrO2/C and other composites synthesized under the same conditions. The Ni1Co4S@C-1000 sample can also efficiently catalyse oxygen reduction reaction (ORR), with a four-electron pathway for reversible oxygen evolution and reduction. Furthermore, Ni1Co4S@C-800 showed enhanced electrocatalytic activity for hydrogen evolution reaction (HER) in water splitting. These findings pave a way to develop effective and promising alternative electrocatalysts towards OER, ORR and HER in the next generation of energy storage and conversion technologies.
KW - Bi-metallic sulfide
KW - Electrocatalyst
KW - Hydrogen evolution reaction
KW - MOFs
KW - Oxygen evolution reaction
KW - Oxygen reduction reaction
KW - Porous carbon
UR - http://www.scopus.com/inward/record.url?scp=84991380579&partnerID=8YFLogxK
U2 - 10.1016/j.jpowsour.2016.10.022
DO - 10.1016/j.jpowsour.2016.10.022
M3 - Article
AN - SCOPUS:84991380579
SN - 0378-7753
VL - 334
SP - 112
EP - 119
JO - Journal of Power Sources
JF - Journal of Power Sources
ER -