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dc.contributor.authorZhang, Weiqi
dc.contributor.authorJin, Yuan
dc.contributor.authorTan, Meihui
dc.contributor.authorLiu, Huiyuan
dc.contributor.authorMa, Qiang
dc.contributor.authorXu, Qian
dc.contributor.authorSu, Huaneng
dc.date.accessioned2024-12-24T19:04:27Z
dc.date.available2024-12-24T19:04:27Z
dc.date.copyright1/12/2024 12:00:00 AM
dc.date.issued2024
dc.identifier.issn2381-6872
dc.identifier.otherjeecs_21_4_041006.pdf
dc.identifier.urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4303239
dc.description.abstractTo facilitate the large-scale application of direct methanol fuel cells (DMFCs), the issue of low Pt/C durability due to Pt degradation and carbon corrosion in harsh DMFC operating conditions must be addressed. A promising strategy is to hybridize metal oxides with carbon materials, resulting in a durable and conductive support that exhibits a strong metal-support interaction (SMSI) effect on platinum nanoparticles (Pt NPs). In this study, we introduced a TiO2 coating on carbon black, creating a TiO2 nanolayer between Pt and carbon black. The nanolayer not only protects the carbon black but also activates the SMSI effect on Pt. The resulting Pt/C@TiO2 electrocatalyst exhibits superior durability than commercial Pt/C. After the accelerated durability test, the mass activity loss of the methanol oxidation reaction (MOR) of Pt/C@TiO2 (32%) is significantly lower than that of Pt/C (46.8%). Moreover, the MOR activity of Pt/C@TiO2 is higher than Pt/C as well. It suggests that Pt/C@TiO2 shows great potential as a highly durable and active electrocatalyst for DMFCs.
dc.publisherThe American Society of Mechanical Engineers (ASME)
dc.titleTiO2 Nanolayer–Coated Carbon as Pt Support for Enhanced Methanol Oxidation Reaction
dc.typeJournal Paper
dc.journal.volume21
dc.journal.issue4
dc.journal.titleJournal of Electrochemical Energy Conversion and Storage
dc.identifier.doi10.1115/1.4064290
dc.journal.fristpage41006-1
dc.journal.lastpage41006-7
dc.page7
dc.treeJournal of Electrochemical Energy Conversion and Storage:;2024:;volume( 021 ):;issue: 004
dc.contenttypeFulltext


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