File Download

There are no files associated with this item.

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)
Related Researcher

이승걸

Lee, Seung Geol
Read More

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Full metadata record

DC Field Value Language
dc.citation.endPage 12415 -
dc.citation.number 12 -
dc.citation.startPage 12399 -
dc.citation.title ACS NANO -
dc.citation.volume 19 -
dc.contributor.author Park, Minjeong -
dc.contributor.author Jeon, Sohee -
dc.contributor.author Lee, Hoseok -
dc.contributor.author Jeong, Jaehoon -
dc.contributor.author Jun, Jong Han -
dc.contributor.author Jo, Jeong-Hyang -
dc.contributor.author Yang, Juchan -
dc.contributor.author Choi, Sung Mook -
dc.contributor.author Lee, Seung Geol -
dc.contributor.author Lee, Ji-Hoon -
dc.date.accessioned 2025-04-25T15:07:28Z -
dc.date.available 2025-04-25T15:07:28Z -
dc.date.created 2025-04-09 -
dc.date.issued 2025-03 -
dc.description.abstract Hydrogen production via water electrolysis is essential for achieving carbon-free energy. However, enhancing the performance of these systems, particularly at the electrode level, remains challenging. Photonic sintering (PS) is proposed as a highly effective post-treatment method for electrodes, highlighting the importance of electrode design and optimization. PS significantly enhances the catalytic activity and durability of spinel-type copper-cobalt oxide-based anodes for the oxygen evolution reaction and Pt@C-based cathodes for the hydrogen evolution reaction, which are attributed to structural and chemical modifications, including active site control, optimized surface chemical bonding, improved catalyst-substrate adhesion, and generation of a reduced surface. PS-treated electrodes maintain well-preserved electrochemical active sites and pore structures, which are crucial for activation polarization and mass transport kinetics. Consequently, an anion exchange membrane water electrolysis cell with PS-treated electrodes achieved 89.57% cell efficiency, 3.91 W cm-2 area-specific power at 1.8 V, and a low degradation rate of 0.049 mV h-1 (at 0.5 A cm-2) and 0.136 mV h-1 (at 1.0 A cm-2) over 500 h. This research overcomes the traditional trade-off between activity and durability, indicating that PS can be widely applied across various energy fields, including electrochemical storage and conversion. -
dc.identifier.bibliographicCitation ACS NANO, v.19, no.12, pp.12399 - 12415 -
dc.identifier.doi 10.1021/acsnano.5c03082 -
dc.identifier.issn 1936-0851 -
dc.identifier.scopusid 2-s2.0-105000492868 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/86679 -
dc.identifier.wosid 001450136600001 -
dc.language 영어 -
dc.publisher AMER CHEMICAL SOC -
dc.title Photonic Sintering as an Electrode Structuring Process to Improve Electrocatalytic Activity and Durability in Anion Exchange Membrane Water Electrolysis -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Chemistry, Multidisciplinary; Chemistry, Physical; Nanoscience & Nanotechnology; Materials Science, Multidisciplinary -
dc.relation.journalResearchArea Chemistry; Science & Technology - Other Topics; Materials Science -
dc.type.docType Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor photonic sintering -
dc.subject.keywordAuthor post-treatment -
dc.subject.keywordAuthor electrocatalysts -
dc.subject.keywordAuthor catalyticelectrodes -
dc.subject.keywordAuthor anion exchange membrane water electrolysis -
dc.subject.keywordPlus OXYGEN EVOLUTION -
dc.subject.keywordPlus HIGHLY-EFFICIENT -
dc.subject.keywordPlus OXIDE -
dc.subject.keywordPlus TEMPERATURE -
dc.subject.keywordPlus NANOPARTICLES -
dc.subject.keywordPlus SINTERABILITY -
dc.subject.keywordPlus FABRICATION -
dc.subject.keywordPlus RESISTANCE -
dc.subject.keywordPlus REDUCTION -

qrcode

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.