Spinel-type NiCo2O4 with abundant oxygen vacancies as a high-performance catalyst for the oxygen reduction reaction

Spinel-type nickel cobaltite with numerous oxygen vacancies is successfully synthesized by hydrothermal and thermal reduction using hydrogen. The effects of oxygen vacancies on the electrochemical activity and stability for the oxygen reduction reaction are investigated. The prepared catalyst displa...

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Published in:International journal of hydrogen energy Vol. 44; no. 42; pp. 23775 - 23783
Main Authors: Lim, Dongwook, Kong, Hyungseok, Lim, Chaewon, Kim, Namil, Shim, Sang Eun, Baeck, Sung-Hyeon
Format: Journal Article
Language:English
Published: Elsevier Ltd 03-09-2019
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Abstract Spinel-type nickel cobaltite with numerous oxygen vacancies is successfully synthesized by hydrothermal and thermal reduction using hydrogen. The effects of oxygen vacancies on the electrochemical activity and stability for the oxygen reduction reaction are investigated. The prepared catalyst displays significantly enhanced oxygen reduction reaction (ORR) catalytic performance under alkaline conditions, which is comparable to that of commercial Pt/C. The oxygen-deficient NiCo2O4 exhibits a very high limiting current density of −5.44 mA cm−2 with onset and half-wave potentials of 0.93 and 0.78 V versus the reversible hydrogen electrode (RHE), respectively. Additionally, it shows excellent durability and resistance to methanol. The enhanced ORR activity and stability of the catalyst can be ascribed to the synergistic effects of the relatively large electrochemical surface area, more exposed active sites, and good electrical conductivity derived from abundant oxygen vacancies. [Display omitted] •NiCo2O4 nanoparticles with oxygen vacancies were synthesized by a hydrothermal method followed by mild H2 reduction.•The H2-treated NiCo2O4 exhibited a low overpotential and substantial long-term stability for oxygen reduction reaction.•This outstanding ORR performance and stability can be attributed to the improved physicochemical properties by H2 treatment.
AbstractList Spinel-type nickel cobaltite with numerous oxygen vacancies is successfully synthesized by hydrothermal and thermal reduction using hydrogen. The effects of oxygen vacancies on the electrochemical activity and stability for the oxygen reduction reaction are investigated. The prepared catalyst displays significantly enhanced oxygen reduction reaction (ORR) catalytic performance under alkaline conditions, which is comparable to that of commercial Pt/C. The oxygen-deficient NiCo2O4 exhibits a very high limiting current density of −5.44 mA cm−2 with onset and half-wave potentials of 0.93 and 0.78 V versus the reversible hydrogen electrode (RHE), respectively. Additionally, it shows excellent durability and resistance to methanol. The enhanced ORR activity and stability of the catalyst can be ascribed to the synergistic effects of the relatively large electrochemical surface area, more exposed active sites, and good electrical conductivity derived from abundant oxygen vacancies. [Display omitted] •NiCo2O4 nanoparticles with oxygen vacancies were synthesized by a hydrothermal method followed by mild H2 reduction.•The H2-treated NiCo2O4 exhibited a low overpotential and substantial long-term stability for oxygen reduction reaction.•This outstanding ORR performance and stability can be attributed to the improved physicochemical properties by H2 treatment.
Author Lim, Dongwook
Kong, Hyungseok
Baeck, Sung-Hyeon
Lim, Chaewon
Kim, Namil
Shim, Sang Eun
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  fullname: Baeck, Sung-Hyeon
  email: shbaeck@inha.ac.kr
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Keywords NiCo2O4
Spinel structure
Oxygen reduction reaction
Oxygen vacancy
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Snippet Spinel-type nickel cobaltite with numerous oxygen vacancies is successfully synthesized by hydrothermal and thermal reduction using hydrogen. The effects of...
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SubjectTerms NiCo2O4
Oxygen reduction reaction
Oxygen vacancy
Spinel structure
Title Spinel-type NiCo2O4 with abundant oxygen vacancies as a high-performance catalyst for the oxygen reduction reaction
URI https://dx.doi.org/10.1016/j.ijhydene.2019.07.091
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