Plasma‐Engineering of Oxygen Vacancies on NiCo2O4 Nanowires with Enhanced Bifunctional Electrocatalytic Performance for Rechargeable Zinc‐air Battery

Author:

Li He1ORCID,Wang Jihao2,Tjardts Tim3,Barg Igor3,Qiu Haoyi4,Müller Martin5,Krahmer Jan2,Askari Sadegh6,Veziroglu Salih37,Aktas Cenk3,Kienle Lorenz57,Benedikt Jan17ORCID

Affiliation:

1. Institute of Experimental and Applied Physics Kiel University Leibnizstraße 19 D‐24098 Kiel Germany

2. Institute of Inorganic Chemistry Kiel University Max‐Eyth‐Straße 2/Otto‐Hahn‐Platz 6 D‐24118. Kiel Germany

3. Chair for Multicomponent Materials Department of Materials Science Faculty of Engineering Kiel University Kaiserstraße 2 D‐24143 Kiel Germany

4. Chair for Functional Nanomaterials Department of Materials Science Faculty of Engineering Kiel University Kaiserstraße 2 D‐24143 Kiel Germany

5. Chair for Synthesis and Real Structure Department of Materials Science Faculty of Engineering Kiel University Kaiserstraße 2 D‐24143 Kiel Germany

6. Department of Fiber and Polymer Technology KTH Royal Institute of Technology Stockholm SE‐10044 Sweden

7. Kiel Nano Surface, and Interface Science KiNSIS Kiel University Christian‐Albrechts‐Platz 4 D‐24118 Kiel Germany

Abstract

AbstractDesigning an efficient, durable, and inexpensive bifunctional electrocatalyst toward oxygen evolution reactions (OER) and oxygen reduction reactions (ORR) remains a significant challenge for the development of rechargeable zinc‐air batteries (ZABs). The generation of oxygen vacancies plays a vital role in modifying the surface properties of transition‐metal‐oxides (TMOs) and thus optimizing their electrocatalytic performances. Herein, a H2/Ar plasma is employed to generate abundant oxygen vacancies at the surfaces of NiCo2O4 nanowires. Compared with the Ar plasma, the H2/Ar plasma generated more oxygen vacancies at the catalyst surface owing to the synergic effect of the Ar‐related ions and H‐radicals in the plasma. As a result, the NiCo2O4 catalyst treated for 7.5 min in H2/Ar plasma exhibited the best bifunctional electrocatalytic activities and its gap potential between Ej = 10 for OER and E1/2 for ORR is even smaller than that of the noble‐metal‐based catalyst. In situ electrochemical experiments are also conducted to reveal the proposed mechanisms for the enhanced electrocatalytic performance. The rechargeable ZABs, when equipped with cathodes utilizing the aforementioned catalyst, achieved an outstanding charge–discharge gap, as well as superior cycling stability, outperforming batteries employing noble‐metal catalyst counterparts.

Funder

China Scholarship Council

Publisher

Wiley

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