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Published on: August 17, 2019
Corrosion-driven Fe3+-assisted dynamic healing endows NiFe-(oxy)hydroxides with durable industrial-level water
Shanfu Sun1, Siyuan Wang1, Ningning Cao2
1School of Aerospace Science and Technology, Xidian University, Xi'an 710126, PR China.
Abstract:
The reasonable design of oxygen evolution reaction (OER) catalysts that simultaneously combine low energy consumption, high activity, and long-term durability under industrial-level conditions is crucial for the practical deployment of water electrolysis for hydrogen production. In the present work, a novel spontaneous electrochemical corrosion (SEC) strategy is employed to in-situ prepare the well-aligned NiFe-based (oxy)hydroxides nanosheet array film on Ni foam (NiFe-OH/NF). The resulting electrode can be fabricated at a cost of only $0.0058 per cm2 and is readily scalable. Operating as an OER catalyst in alkaline solution, NiFe-OH/NF requires an overpotential of merely 213 ± 2 mV to deliver 10 mA cm-2. More importantly, the SEC-derived NiFe-OH/NF exhibits a dynamic Fe-replenishment process during OER, in which dissolved Fe species are partially reincorporated into the catalyst surface, thereby mitigating deactivation and enabling superior durability. As a result, NiFe-OH/NF operates stably for more than 126 days (> 3024 h) at an industrial-level current density of 500 mA cm-2 in 1 M KOH containing 0.1 mM Fe3+. This work demonstrates a low-cost and scalable route to NiFe-based OER electrodes that simultaneously deliver competitive activity and remarkable durability, offering strong promise for practical alkaline water electrolysis.
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