TY - JOUR
T1 - Partial-sacrificial-template Synthesis of Fe/Ni Phosphides on Ni Foam
T2 - A Strongly Stabilized and Efficient Catalyst for Electrochemical Water Splitting
AU - Xiao, Chunhui
AU - Zhang, Bo
AU - Li, Dan
N1 - Publisher Copyright:
© 2017 Elsevier Ltd
PY - 2017/7/10
Y1 - 2017/7/10
N2 - Electrochemical water splitting is considered to be one of the most promising strategies for clean and efficient hydrogen production. In this paper, an in-situ growth of iron-nickel phosphide on nickel foam (FeNiPx/NF) is demonstrated as a self-supported ternary catalyst for electrochemical water splitting. The FeNiPx/NF were prepared by a thermo-reaction between NaH2PO2 and NiFe hydroxide precursors that are in situ grown on Ni foam via a simple chemical precipitation reaction. In this newly proposed method, the nickel foam not only acts as an electrode substrate, but also serves as a slow-release Ni source in the reaction due to its oxidation by Fe3+ in solution. Benefiting from collaborative advantages of bimetallic composite, metallic phosphide, and unique electrode fabrication, the FeNiPx/NF exhibits extraordinarily high activities for both OER and HER with low overpotentials of of 192 and 106 mV at 10 mA cm−2, 236 and 161 mV at 100 mA cm−2, respectively. The voltage during the galvanostatic electrolysis is well maintained for almost 400 h without any visible elevation, representing the few most stable noble-metal-free catalysts for water splitting.
AB - Electrochemical water splitting is considered to be one of the most promising strategies for clean and efficient hydrogen production. In this paper, an in-situ growth of iron-nickel phosphide on nickel foam (FeNiPx/NF) is demonstrated as a self-supported ternary catalyst for electrochemical water splitting. The FeNiPx/NF were prepared by a thermo-reaction between NaH2PO2 and NiFe hydroxide precursors that are in situ grown on Ni foam via a simple chemical precipitation reaction. In this newly proposed method, the nickel foam not only acts as an electrode substrate, but also serves as a slow-release Ni source in the reaction due to its oxidation by Fe3+ in solution. Benefiting from collaborative advantages of bimetallic composite, metallic phosphide, and unique electrode fabrication, the FeNiPx/NF exhibits extraordinarily high activities for both OER and HER with low overpotentials of of 192 and 106 mV at 10 mA cm−2, 236 and 161 mV at 100 mA cm−2, respectively. The voltage during the galvanostatic electrolysis is well maintained for almost 400 h without any visible elevation, representing the few most stable noble-metal-free catalysts for water splitting.
KW - electrocatalysis
KW - electrochemical water splitting
KW - in situ growth
KW - iron nickel phosphide
KW - self-supported catalyst
UR - https://www.scopus.com/pages/publications/85018930539
U2 - 10.1016/j.electacta.2017.05.015
DO - 10.1016/j.electacta.2017.05.015
M3 - 文章
AN - SCOPUS:85018930539
SN - 0013-4686
VL - 242
SP - 260
EP - 267
JO - Electrochimica Acta
JF - Electrochimica Acta
ER -