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The synthesis of Ni-Co-Fe-Se@NiCo-LDH nanoarrays on Ni foam as efficient overall water splitting electrocatalyst.

Authors :
Dai, Zhixin
Du, Xiaoqiang
Zhang, Xiaoshuang
Source :
Journal of Alloys & Compounds. Jun2023, Vol. 946, pN.PAG-N.PAG. 1p.
Publication Year :
2023

Abstract

The development of efficient, stable and low-cost electrocatalysts for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) is the key to promote the industrialization of electrocatalytic water splitting. In this paper, the CoFe-LDH@NiCo-LDH precursor was first synthesized and then the target catalyst named Ni-Co-Fe-Se@NiCo-LDH was finally synthesized by a selenization reaction based on this precursor. In a three-electrode system with 1.0 M KOH alkaline atmosphere, Ni-Co-Fe-Se@NiCo-LDH requires an overpotential of 286 mV to deliver a current density of 100 mA/cm2 for OER and 113 mV at a current density of 10 mA/cm2 for HER. In addition, the material shows excellent overall water splitting performance and a low cell voltage of 1.55 V at 10 mA/cm2 is expected. By comparing the test results of CoFe-LDH@NiCo-LDH and NiCo-LDH, we found that increasing the number of metal species only slightly reduces the electron transfer impedance and does not help to increase the electrochemical surface area of the material. Density functional theory calculation shows that the presence of the Co-NiSe 2 material accelerates the kinetics of hydrogen production and the Fe 7 Se 8 material enhances the conductivity of the material. Their synergistic effect makes the Ni-Co-Fe-Se@NiCo-LDH catalyst exhibit enhanced hydrogen production activity. • Ni-Co-Fe-Se@NiCo-LDH nanoarrays was synthesized through typical hydrothermal processes. • This Ni-Co-Fe-Se@NiCo-LDH exhibits enhanced water splitting activity (1.55 V @10 mA cm-2). • The Ni-Co-Fe-Se@NiCo-LDH nanoarrays maintains good stability. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09258388
Volume :
946
Database :
Academic Search Index
Journal :
Journal of Alloys & Compounds
Publication Type :
Academic Journal
Accession number :
162386309
Full Text :
https://doi.org/10.1016/j.jallcom.2023.169451