Heterostructure engineering of iridium species on nickel/molybdenum nitride for highly-efficient anion exchange membrane water electrolyzer

A novel kind of hybrid electrode is successfully developed by introducing trace Ir species onto a hierarchical Ni/Mo5N6 heterostructure on Ni foam, presenting as a highly-active bifunctional electrocatalyst for AEM water electrolyzer. [Display omitted] Developing highly active electrocatalysts is a...

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Veröffentlicht in:Journal of colloid and interface science 2022-12, Vol.628, p.306-314
Hauptverfasser: Wang, Huijie, Tong, Yun, Li, Kaixun, Chen, Pengzuo
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Sprache:eng
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Zusammenfassung:A novel kind of hybrid electrode is successfully developed by introducing trace Ir species onto a hierarchical Ni/Mo5N6 heterostructure on Ni foam, presenting as a highly-active bifunctional electrocatalyst for AEM water electrolyzer. [Display omitted] Developing highly active electrocatalysts is a pivotal issue for anion-exchange membrane water electrolyzers (AEMWE). However, realizing the continuous hydrogen generation at a large current density remains challenging. Herein, a novel kind of hybrid electrode is successfully developed by introducing trace iridium (Ir) species onto a hierarchical Ni/Mo5N6 heterostructure on Ni foam (Ir-Ni/Mo5N6/NF). The synergistic advantages of high conductivity, abundant active sites, and strong electronic interaction endow superior reaction kinetics, presenting a highly-active bifunctional electrocatalyst. Remarkably, the Ir-Ni/Mo5N6/NF exhibit extremely low overpotentials of 52 mV and 250 mV at 100 mA cm−2 for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). By exploiting the Ir-Ni/Mo5N6 as both anode/cathode, the constructed AEMWE device delivers superior performance. The current density reaches 2.1 A cm−2 at a voltage of 2.0 V and 250 mA cm−2 at 1.8 V in alkaline/neutral media. This work put forward a facile and effective strategy to synthesize advanced bifunctional electrocatalysts for water electrolysis.
ISSN:0021-9797
1095-7103
DOI:10.1016/j.jcis.2022.08.056