Ridwan P. Putra, I. B. Rachman, H. Horino, I. Rzeznicka
{"title":"Bifunctional Catalytic Activity of γ-NiOOH toward Oxygen Reduction and Oxygen Evolution Reactions in Alkaline Solutions","authors":"Ridwan P. Putra, I. B. Rachman, H. Horino, I. Rzeznicka","doi":"10.3390/oxygen2040031","DOIUrl":null,"url":null,"abstract":"Nickel oxyhydroxides (NiOOHs) are well-known for their superior activity toward oxygen evolution reaction (OER) in alkaline solutions. However, their activity toward oxygen reduction reaction (ORR) has been largely unexplored. There exist three NiOOH polymorphs: α-, β-, and γ-NiOOH, characterized by different interlayer spacing. Although still debated, γ-NiOOH with a large layer spacing has been indicated as the active phase for OER. Here, a highly crystalline γ-NiOOH was prepared in a carbon matrix by the in situ electrochemical transformation of nickel dithiooxamide Ni(dto) in 1 M KOH solution. The catalyst prepared in this way showed low overpotential not only for OER, but also for ORR in alkaline solutions. The onset potential for ORR is ~0.81 V vs. RHE, and the reaction proceeds via the 2e− transfer pathway. The high OER catalytic activity and relatively low ORR overpotential make this nanocomposite catalyst a good candidate for bifunctional OER/ORR catalyst, stable in alkaline solutions.","PeriodicalId":74387,"journal":{"name":"Oxygen (Basel, Switzerland)","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Oxygen (Basel, Switzerland)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/oxygen2040031","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 4
Abstract
Nickel oxyhydroxides (NiOOHs) are well-known for their superior activity toward oxygen evolution reaction (OER) in alkaline solutions. However, their activity toward oxygen reduction reaction (ORR) has been largely unexplored. There exist three NiOOH polymorphs: α-, β-, and γ-NiOOH, characterized by different interlayer spacing. Although still debated, γ-NiOOH with a large layer spacing has been indicated as the active phase for OER. Here, a highly crystalline γ-NiOOH was prepared in a carbon matrix by the in situ electrochemical transformation of nickel dithiooxamide Ni(dto) in 1 M KOH solution. The catalyst prepared in this way showed low overpotential not only for OER, but also for ORR in alkaline solutions. The onset potential for ORR is ~0.81 V vs. RHE, and the reaction proceeds via the 2e− transfer pathway. The high OER catalytic activity and relatively low ORR overpotential make this nanocomposite catalyst a good candidate for bifunctional OER/ORR catalyst, stable in alkaline solutions.