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High‐entropy sulfides as highly effective catalysts for the oxygen evolution reaction

Lin, Ling ; Ding, Ziming ; Karkera, Guruprakash ; Diemant, Thomas ; Kante, Mohana V. ; Agrawal, Daisy ; Hahn, Horst ; Aghassi‐Hagmann, Jasmin ; Fichtner, Maximilian ; Breitung, Ben ; Schweidler, Simon (2023)
High‐entropy sulfides as highly effective catalysts for the oxygen evolution reaction.
In: Small Structures, 4 (9)
doi: 10.1002/sstr.202300012
Artikel, Bibliographie

Dies ist die neueste Version dieses Eintrags.

Kurzbeschreibung (Abstract)

With respect to efficient use of diminishing or harder to reach energy resources, the catalysis of processes that will otherwise require high overpotentials is a very important application in today's world. As a newly developed class of materials, high‐entropy sulfides (HESs) are promising electrocatalysts for a variety of different reactions. In this report, HESs containing five or six transition metals are synthesized in a one‐step mechanochemical process. Seven HESs of Pnma (M:S≈1:1) and three Pa‐3 (M:S = 1:2) structures are investigated as electrocatalysts for the oxygen evolution reaction (OER). The performances and properties of the HESs with different compositions and structures are compared with each other and with commercial IrO₂ as reference material, in terms of OER overpotential, Tafel slope, electrochemically active surface area, ionic conductivity, and durability. The structural and chemical properties of these HESs are determined by X‐ray diffraction, transmission electron microscopy, scanning electron microscopy, X‐ray photoelectron spectroscopy, and energy‐dispersive X‐ray spectroscopy. Most of the HESs show excellent and promising performance as OER electrocatalysts under alkaline conditions, and outperform the reference OER catalyst IrO₂.

Typ des Eintrags: Artikel
Erschienen: 2023
Autor(en): Lin, Ling ; Ding, Ziming ; Karkera, Guruprakash ; Diemant, Thomas ; Kante, Mohana V. ; Agrawal, Daisy ; Hahn, Horst ; Aghassi‐Hagmann, Jasmin ; Fichtner, Maximilian ; Breitung, Ben ; Schweidler, Simon
Art des Eintrags: Bibliographie
Titel: High‐entropy sulfides as highly effective catalysts for the oxygen evolution reaction
Sprache: Englisch
Publikationsjahr: 2023
Ort: Weinheim
Verlag: Wiley-VCH
Titel der Zeitschrift, Zeitung oder Schriftenreihe: Small Structures
Jahrgang/Volume einer Zeitschrift: 4
(Heft-)Nummer: 9
Kollation: 9 Seiten
DOI: 10.1002/sstr.202300012
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Kurzbeschreibung (Abstract):

With respect to efficient use of diminishing or harder to reach energy resources, the catalysis of processes that will otherwise require high overpotentials is a very important application in today's world. As a newly developed class of materials, high‐entropy sulfides (HESs) are promising electrocatalysts for a variety of different reactions. In this report, HESs containing five or six transition metals are synthesized in a one‐step mechanochemical process. Seven HESs of Pnma (M:S≈1:1) and three Pa‐3 (M:S = 1:2) structures are investigated as electrocatalysts for the oxygen evolution reaction (OER). The performances and properties of the HESs with different compositions and structures are compared with each other and with commercial IrO₂ as reference material, in terms of OER overpotential, Tafel slope, electrochemically active surface area, ionic conductivity, and durability. The structural and chemical properties of these HESs are determined by X‐ray diffraction, transmission electron microscopy, scanning electron microscopy, X‐ray photoelectron spectroscopy, and energy‐dispersive X‐ray spectroscopy. Most of the HESs show excellent and promising performance as OER electrocatalysts under alkaline conditions, and outperform the reference OER catalyst IrO₂.

Freie Schlagworte: catalysts, high-entropy materials, high-entropy sulfides, oxygen evolution reaction
ID-Nummer: Artikel-ID: 2300012
Sachgruppe der Dewey Dezimalklassifikatin (DDC): 600 Technik, Medizin, angewandte Wissenschaften > 660 Technische Chemie
Fachbereich(e)/-gebiet(e): 11 Fachbereich Material- und Geowissenschaften
11 Fachbereich Material- und Geowissenschaften > Materialwissenschaft
11 Fachbereich Material- und Geowissenschaften > Materialwissenschaft > In-Situ Elektronenmikroskopie
11 Fachbereich Material- und Geowissenschaften > Materialwissenschaft > Gemeinschaftslabor Nanomaterialien
11 Fachbereich Material- und Geowissenschaften > Materialwissenschaft > Fachgebiet Strukturforschung
Hinterlegungsdatum: 12 Feb 2024 07:22
Letzte Änderung: 12 Feb 2024 09:30
PPN: 515503223
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