Controlling degradable activities of water oxidation anode via facile surface reconstruction

[Display omitted] •It covered the post-treatment of hydrothermal-treated stainless-steel based anode.•Enhanced stability of post-treated sample was resulted from our novel preparation.•The presence of active chemical species leads to enhanced performance during OER. Robustness and efficiency are cru...

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Bibliographic Details
Published inApplied surface science Vol. 614; p. 155741
Main Authors Yu, Byounguk, Chan Choi, Byeong, Myung, Yoon, Rae Kim, Jung, Chan Kim, Hyoung, Choi, Yong-Wook
Format Journal Article
LanguageEnglish
Published Elsevier B.V 30.03.2023
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Summary:[Display omitted] •It covered the post-treatment of hydrothermal-treated stainless-steel based anode.•Enhanced stability of post-treated sample was resulted from our novel preparation.•The presence of active chemical species leads to enhanced performance during OER. Robustness and efficiency are crucial factors for being a highly active electrocatalyst in water electrolysis system (WES). In the case of metal oxide catalysts, the thermodynamic instability under oxygen evolution reaction (OER) condition has been a bottleneck that degrades electrode activity. In this study, we provide a post-treatment that enables further improvement of electrode activity by restructuring metal oxides. The SS-based metal oxide electrode was synthesized through hydrothermal synthesis (HY) and subsequent post-acidic immersion process (HYAi) using earth-abundant stainless steel (SS) 304 plate as a substrate material. The HYAi electrode showed improved electrochemical activities with a lower charge transfer resistance (Rct) and higher surface roughness factor (RF) compared to HY when the prolonged OER potential was applied under alkaline media. Moreover, even after 10,000 cycles of rapid cycling, HYAi showed reduced overpotential of 276.7 mV at 10 mA cm−2, while HY degraded to 304 mV. The enhanced electrochemical activities were confirmed by observing catalytic surface that conversion of oxide to stable (oxy)hydroxide was observed. Our novel approach to rearranging catalytic surface will provide deeper insights for designing improved OER catalyst.
ISSN:0169-4332
1873-5584
DOI:10.1016/j.apsusc.2022.155741