TY - JOUR
T1 - Iron-nickel nitride nanostructures in situ grown on surface-redox-etching nickel foam
T2 - Efficient and ultrasustainable electrocatalysts for overall water splitting
AU - Zhang, Bo
AU - Xiao, Chunhui
AU - Xie, Sanmu
AU - Liang, Jin
AU - Chen, Xu
AU - Tang, Yuhai
N1 - Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/10/11
Y1 - 2016/10/11
N2 - Water splitting is widely considered to be a promising strategy for clean and efficient energy production. In this paper, for the first time we report an in situ growth of iron-nickel nitride nanostructures on surface-redox-etching Ni foam (FeNi3N/NF) as a bifunctional electrocatalyst for overall water splitting. This method does not require a specially added nickel precursor nor an oxidizing agent, but achieves well-dispersed iron-nickel nitride nanostructures that are grown directly on the nickel foam surface. The commercial Ni foam in this work not only acts as a substrate but also serves as a slow-releasing nickel precursor that is induced by redox-etching of Fe3+. FeCl2 is a more preferable iron precursor than FeCl3 for no matter quality of FeNi3N growth or its electrocatalytic behaviors. The obtained FeNi3N/NF exhibits extraordinarily high activities for both oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) with low overpotentials of 202 and 75 mV at 10 mA cm-2, Tafel slopes of 40 and 98 mV dec-1, respectively. In addition, the presented FeNi3N/NF catalyst has an extremely good durability, reflecting in more than 400 h of consistent galvanostatic electrolysis without any visible voltage elevation.
AB - Water splitting is widely considered to be a promising strategy for clean and efficient energy production. In this paper, for the first time we report an in situ growth of iron-nickel nitride nanostructures on surface-redox-etching Ni foam (FeNi3N/NF) as a bifunctional electrocatalyst for overall water splitting. This method does not require a specially added nickel precursor nor an oxidizing agent, but achieves well-dispersed iron-nickel nitride nanostructures that are grown directly on the nickel foam surface. The commercial Ni foam in this work not only acts as a substrate but also serves as a slow-releasing nickel precursor that is induced by redox-etching of Fe3+. FeCl2 is a more preferable iron precursor than FeCl3 for no matter quality of FeNi3N growth or its electrocatalytic behaviors. The obtained FeNi3N/NF exhibits extraordinarily high activities for both oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) with low overpotentials of 202 and 75 mV at 10 mA cm-2, Tafel slopes of 40 and 98 mV dec-1, respectively. In addition, the presented FeNi3N/NF catalyst has an extremely good durability, reflecting in more than 400 h of consistent galvanostatic electrolysis without any visible voltage elevation.
UR - https://www.scopus.com/pages/publications/84991384257
U2 - 10.1021/acs.chemmater.6b02610
DO - 10.1021/acs.chemmater.6b02610
M3 - 文章
AN - SCOPUS:84991384257
SN - 0897-4756
VL - 28
SP - 6934
EP - 6941
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 19
ER -