Remarkable influence of the local symmetry of substituted 3d metal ion on bifunctional electrocatalyst performance of α-MnO2 nanowire

Jang Mee Lee, Seong Ju Hwang

Research output: Contribution to journalArticle

Abstract

Efficient bifunctional electrocatalysts of V- and Co-substituted α-MnO2 materials can be synthesized by one-pot hydrothermal reaction of ion-adducts V3+/Co2+–MnO4 , leading to the successful substitution of both V and Co ions in the α-MnO2 lattice. According to extended X-ray absorption fine structure analysis, the substituted V ion is stabilized in highly distorted local symmetry whereas the substituted Co ion has regular octahedral local environment. Both the V- and Co-substituted α-MnO2 materials exhibit excellent bifunctional electrocatalytic functionalities with lowered overpotentials and enhanced current densities for oxygen evolution (OER) and oxygen reduction reactions (ORR), underscoring the beneficial role of cation substitution in enhancing the bifunctional electrocatalytic activity of α-MnO2. The Co-substituted α-MnO2 shows higher bifunctional oxygen electrocatalyst functionality than does the V-substituted homologue, which is attributable to the greater improvement of charge transfer kinetics upon the Co substitution than the V one. The poorer charge transfer property of V-substituted α-MnO2 can be ascribed to highly distorted local symmetry of V ion, which is unfavorable for increasing band width and depressing bandgap energy. Taking into account many advantages of the oxides of V, Mn, and Co elements such as low price, rich abundance, and environmentally benignity, the present study underscores that the partial substitution of neighboring 3d metal ion having regular octahedral symmetry can provide an effective and environmental friendly way of optimizing the oxygen electrocatalytic activity of manganese oxide.

Original languageEnglish
Pages (from-to)354-360
Number of pages7
JournalJournal of Solid State Chemistry
Volume269
DOIs
Publication statusPublished - 2019 Jan

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electrocatalysts
Electrocatalysts
Nanowires
Metal ions
metal ions
nanowires
Ions
Substitution reactions
substitutes
Oxygen
symmetry
oxygen
ions
Charge transfer
charge transfer
Manganese oxide
manganese oxides
X ray absorption
Oxides
adducts

All Science Journal Classification (ASJC) codes

  • Electronic, Optical and Magnetic Materials
  • Ceramics and Composites
  • Condensed Matter Physics
  • Physical and Theoretical Chemistry
  • Inorganic Chemistry
  • Materials Chemistry

Cite this

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title = "Remarkable influence of the local symmetry of substituted 3d metal ion on bifunctional electrocatalyst performance of α-MnO2 nanowire",
abstract = "Efficient bifunctional electrocatalysts of V- and Co-substituted α-MnO2 materials can be synthesized by one-pot hydrothermal reaction of ion-adducts V3+/Co2+–MnO4 −, leading to the successful substitution of both V and Co ions in the α-MnO2 lattice. According to extended X-ray absorption fine structure analysis, the substituted V ion is stabilized in highly distorted local symmetry whereas the substituted Co ion has regular octahedral local environment. Both the V- and Co-substituted α-MnO2 materials exhibit excellent bifunctional electrocatalytic functionalities with lowered overpotentials and enhanced current densities for oxygen evolution (OER) and oxygen reduction reactions (ORR), underscoring the beneficial role of cation substitution in enhancing the bifunctional electrocatalytic activity of α-MnO2. The Co-substituted α-MnO2 shows higher bifunctional oxygen electrocatalyst functionality than does the V-substituted homologue, which is attributable to the greater improvement of charge transfer kinetics upon the Co substitution than the V one. The poorer charge transfer property of V-substituted α-MnO2 can be ascribed to highly distorted local symmetry of V ion, which is unfavorable for increasing band width and depressing bandgap energy. Taking into account many advantages of the oxides of V, Mn, and Co elements such as low price, rich abundance, and environmentally benignity, the present study underscores that the partial substitution of neighboring 3d metal ion having regular octahedral symmetry can provide an effective and environmental friendly way of optimizing the oxygen electrocatalytic activity of manganese oxide.",
author = "Lee, {Jang Mee} and Hwang, {Seong Ju}",
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AU - Hwang, Seong Ju

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N2 - Efficient bifunctional electrocatalysts of V- and Co-substituted α-MnO2 materials can be synthesized by one-pot hydrothermal reaction of ion-adducts V3+/Co2+–MnO4 −, leading to the successful substitution of both V and Co ions in the α-MnO2 lattice. According to extended X-ray absorption fine structure analysis, the substituted V ion is stabilized in highly distorted local symmetry whereas the substituted Co ion has regular octahedral local environment. Both the V- and Co-substituted α-MnO2 materials exhibit excellent bifunctional electrocatalytic functionalities with lowered overpotentials and enhanced current densities for oxygen evolution (OER) and oxygen reduction reactions (ORR), underscoring the beneficial role of cation substitution in enhancing the bifunctional electrocatalytic activity of α-MnO2. The Co-substituted α-MnO2 shows higher bifunctional oxygen electrocatalyst functionality than does the V-substituted homologue, which is attributable to the greater improvement of charge transfer kinetics upon the Co substitution than the V one. The poorer charge transfer property of V-substituted α-MnO2 can be ascribed to highly distorted local symmetry of V ion, which is unfavorable for increasing band width and depressing bandgap energy. Taking into account many advantages of the oxides of V, Mn, and Co elements such as low price, rich abundance, and environmentally benignity, the present study underscores that the partial substitution of neighboring 3d metal ion having regular octahedral symmetry can provide an effective and environmental friendly way of optimizing the oxygen electrocatalytic activity of manganese oxide.

AB - Efficient bifunctional electrocatalysts of V- and Co-substituted α-MnO2 materials can be synthesized by one-pot hydrothermal reaction of ion-adducts V3+/Co2+–MnO4 −, leading to the successful substitution of both V and Co ions in the α-MnO2 lattice. According to extended X-ray absorption fine structure analysis, the substituted V ion is stabilized in highly distorted local symmetry whereas the substituted Co ion has regular octahedral local environment. Both the V- and Co-substituted α-MnO2 materials exhibit excellent bifunctional electrocatalytic functionalities with lowered overpotentials and enhanced current densities for oxygen evolution (OER) and oxygen reduction reactions (ORR), underscoring the beneficial role of cation substitution in enhancing the bifunctional electrocatalytic activity of α-MnO2. The Co-substituted α-MnO2 shows higher bifunctional oxygen electrocatalyst functionality than does the V-substituted homologue, which is attributable to the greater improvement of charge transfer kinetics upon the Co substitution than the V one. The poorer charge transfer property of V-substituted α-MnO2 can be ascribed to highly distorted local symmetry of V ion, which is unfavorable for increasing band width and depressing bandgap energy. Taking into account many advantages of the oxides of V, Mn, and Co elements such as low price, rich abundance, and environmentally benignity, the present study underscores that the partial substitution of neighboring 3d metal ion having regular octahedral symmetry can provide an effective and environmental friendly way of optimizing the oxygen electrocatalytic activity of manganese oxide.

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