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Unveiling the potential of (CoFeNiMnCr)$_3$O$_4$ high-entropy oxide synthesized from CoFeNiMnCr high-entropy alloy for efficient oxygen-evolution reaction
ID Ljubec Božiček, Barbara (Author), ID Hreščak, Jitka (Author), ID Kušter, Monika (Author), ID Kovač, Janez (Author), ID Naglič, Iztok (Author), ID Markoli, Boštjan (Author), ID Šetina Batič, Barbara (Author), ID Šala, Martin (Author), ID Drev, Sandra (Author), ID Marinko, Živa (Author), ID Čeh, Miran (Author), ID Alcantara Marinho, Belisa (Author)

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Abstract
Electrochemical water-splitting is a promising green technology for the production of hydrogen. One of the bottlenecks, however, is the oxygen evolution half-reaction (OER), which could be overcome with the development of a suitable electrocatalyst. Recently, non-noble metal, high-entropy oxides (HEO) have been investigated as potential OER electrocatalysts, but complex synthesis approaches that usually produce the material in powder form limit their wider utilization. Here, an innovative synthesis strategy of formulating a nanostructured (CoFeNiMnCr)$_3$O$_4$ HEO thin film on a CoFeNiMnCr high entropy alloy (HEA) using facile electrochemical and thermal treatment methods is presented. The CoFeNiMnCr HEA serves as exceptional support to be electrochemically treated in an ethylene glycol electrolyte with ammonium fluoride to form a rough and microporous structure with nanopits. The electrochemically treated CoFeNiMnCr HEA surface is more prone to oxidation during a low-temperature thermal treatment, leading to the growth of a spinel (CoFeNiMnCr)$_3$O$_4$ HEO thin film. The (CoFeNiMnCr)$_3$O$_4$ HEO exhibits a superior overpotential of 341 mV at 10 mA cm$^{−2}$ and a Tafel slope of 50 mV dec$^{−1}$ along with remarkable long-term stability in alkaline media. The excellent catalytic activity and stability for the OER can serve as a promising platform for the practical utilization of (CoFeNiMnCr)$_3$O$_4$ HEO.

Language:English
Keywords:electrochemical water-spliting, electrocatalysts
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:NTF - Faculty of Natural Sciences and Engineering
Publication status:Published
Publication version:Version of Record
Year:2024
Number of pages:Str. 9189–9207
Numbering:Vol. 59, iss. 21
PID:20.500.12556/RUL-158419 This link opens in a new window
UDC:54
ISSN on article:1573-4803
DOI:10.1007/s10853-024-09710-5 This link opens in a new window
COBISS.SI-ID:195390211 This link opens in a new window
Publication date in RUL:07.06.2024
Views:135
Downloads:15
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Record is a part of a journal

Title:Journal of materials science
Shortened title:J. mater. sci.
Publisher:Springer Nature
ISSN:1573-4803
COBISS.SI-ID:513194009 This link opens in a new window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

Secondary language

Language:Slovenian
Keywords:nanostrukturni materiali, kataliza, elektrokemija

Projects

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P2-0084
Name:Nanostrukturni materiali

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:PR-11484

Funder:EC - European Commission
Funding programme:HE
Project number:101090289
Name:Development of new high-entropy oxide catalysts by the anodic oxidation of high-entropy alloys
Acronym:HEO4CAT

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