4.6 Article

The FeOOH Decorated Fe-Doped Nickel Selenide Hierarchical Array for High-Performance Water Oxidation

Journal

INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
Volume 61, Issue 18, Pages 6146-6155

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.iecr.1c02592

Keywords

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Funding

  1. National Key R&D Program of China [2020YFB1505602, 2018YFE0202001]
  2. Nation Natural Science Foundation of China [21776154]

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In this study, an autologous growth approach was used to synthesize FeOOH-decorated Fe-doped NiSe on NiFe foam as an efficient electrocatalyst for the oxygen evolution reaction (OER). The designed electrocatalyst showed excellent electrocatalytic performance, remarkable stability, and superior aerophobicity. Experimental studies confirmed that Fe/NiOOH could serve as the intrinsic active sites for the OER, providing a new methodology for designing durable and efficient electrocatalysts.
For production hydrogen with water electrolysis to promote the development of a hydrogen-energy economy, it is crucial to develop efficient, durable, and non-noble metal electrocatalysts for the oxygen evolution reaction (OER). Transition metal selenides have been considered as promising alternatives for OER due to their excellent conductivity. Herein, FeOOH-decorated Fe-doped NiSe on NiFe foam (FeOOH@Fe-NiSe@NiFe) was synthesized with an autologous growth approach, where the NiFe foam was used as an Fe and Ni resource. The FeOOH@Fe-NiSe@NiFe electrode exhibits excellent electrocatalytic performance with an overpotential of 224 mV at 10 mA cm-2, a small Tafel slope of 52.67 mV dec-1, and remarkable stability. Results confirm that the morphology and electronic structure of designed electrocatalysts can be significantly tailored due to the introduction of Fe. The designed FeOOH@Fe-NiSe@NiFe electrode also possesses superior aerophobicity, which ensures fast mass transfer during water splitting processes. As a result, the electrocatalytic activity is improved remarkably. In addition, the actual active sites of designed electrocatalysts were also systematically investigated. Experimental studies demonstrate that the Fe/NiOOH on the surface of Fe-NiSe, which in situ converses from Fe-NiSe, can serve as the intrinsic active sites toward the OER. Thus, this work can provide a new methodology to designing durable and efficient electrocatalysts.

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