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| 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 | - |
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