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Ternary nickel iron phosphide supported on nickel foam as a high-efficiency electrocatalyst for overall water splitting
Electrochemical water splitting is a promising technology for mass hydrogen production. Efficient, stable, and cheap electrocatalysts are keys to realizing this strategy. However, high price and preciousness of commonly used noble metal based catalysts severely hinder this realization. Herein, we re...
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Published in: | International journal of hydrogen energy 2018-04, Vol.43 (15), p.7299-7306 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Electrochemical water splitting is a promising technology for mass hydrogen production. Efficient, stable, and cheap electrocatalysts are keys to realizing this strategy. However, high price and preciousness of commonly used noble metal based catalysts severely hinder this realization. Herein, we report nickel iron phosphide (Ni-FexP) bifunctional electrocatalyst via the in-situ growth of NiFe(OH)x on nickel foam (NiFe(OH)x/NF) followed by low-temperature phosphidation. As a hydrogen evolution reaction (HER) catalyst, the Ni-FexP/NF only needs an overpotential of 119 mV to drive a current density of −10 mA/cm2 in a base media. It also shows excellent activity toward oxygen evolution reaction (OER) with low overpotentials of 254 mV, 267 mV, and 282 mV at 50, 100 and 200 mA/cm2, respectively. Moreover, when this bifunctional catalyst is used for overall water splitting, a low cell voltage of 1.62 V is needed to deliver a current density of 10 mA/cm2, which is superior to commercial electrolyzer and it also shows remarkable stability.
•The ternary nickel iron phosphide (Ni-FexP) has been successfully synthesized.•The high catalytic activity for HER and OER of Ni-FexP has been demonstrated.•The built full cell based on this bifunctional catalyst exhibits a low overpotential and good stability. |
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ISSN: | 0360-3199 1879-3487 |
DOI: | 10.1016/j.ijhydene.2018.02.157 |