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Park, Noejung
Computational Physics & Electronic Structure Lab.
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dc.citation.endPage 446 -
dc.citation.number 5 -
dc.citation.startPage 441 -
dc.citation.title NATURE NANOTECHNOLOGY -
dc.citation.volume 12 -
dc.contributor.author Mahmood, Javeed -
dc.contributor.author Li, Feng -
dc.contributor.author Jung, Sun-Min -
dc.contributor.author Okyay, Mahmut Sait -
dc.contributor.author Ahmad, Ishfaq -
dc.contributor.author Kim, Seok-Jin -
dc.contributor.author Park, Noejung -
dc.contributor.author Jeong, Hu Young -
dc.contributor.author Baek, Jong-Beom -
dc.date.accessioned 2023-12-21T22:17:11Z -
dc.date.available 2023-12-21T22:17:11Z -
dc.date.created 2017-02-07 -
dc.date.issued 2017-05 -
dc.description.abstract The hydrogen evolution reaction (HER) is a crucial step in electro-chemical water splitting and demands an efficient, durable and cheap catalyst if it is to succeed in real applications(1-3). For an energy-efficient HER, a catalyst must be able to trigger proton reduction with minimal overpotential(4) and have fast kinetics(5-9). The most efficient catalysts in acidic media are platinum-based, as the strength of the Pt-H bond(10) is associated with the fastest reaction rate for the HER11,12. The use of platinum, however, raises issues linked to cost and stability in non-acidic media. Recently, non-precious-metal-based catalysts have been reported, but these are susceptible to acid corrosion and are typically much inferior to Pt-based catalysts, exhibiting higher overpotentials and lower stability(13-15). As a cheaper alternative to platinum, ruthenium possesses a similar bond strength with hydrogen (similar to 65 kcal mol(-1))(16), but has never been studied as a viable alternative for a HER catalyst. Here, we report a Ru-based catalyst for the HER that can operate both in acidic and alkaline media. Our catalyst is made of Ru nanoparticles dispersed within a nitrogenated holey two-dimensional carbon structure (Ru@C2N). The Ru@C2N electrocatalyst exhibits high turnover frequencies at 25 mV (0.67 H-2 s(-1) in 0.5 M H2SO4 solution; 0.75 H-2 s(-1) in 1.0 M KOH solution) and small overpotentials at 10 mA cm(-2) (13.5 mV in 0.5 M H2SO4 solution; 17.0 mV in 1.0 M KOH solution) as well as superior stability in both acidic and alkaline media. These performances are comparable to, or even better than, the Pt/C catalyst for the HER. -
dc.identifier.bibliographicCitation NATURE NANOTECHNOLOGY, v.12, no.5, pp.441 - 446 -
dc.identifier.doi 10.1038/nnano.2016.304 -
dc.identifier.issn 1748-3387 -
dc.identifier.scopusid 2-s2.0-85012260274 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/21346 -
dc.identifier.url http://www.nature.com/nnano/journal/vaop/ncurrent/full/nnano.2016.304.html -
dc.identifier.wosid 000400650200012 -
dc.language 영어 -
dc.publisher NATURE PUBLISHING GROUP -
dc.title An efficient and pH-universal ruthenium-based catalyst for the hydrogen evolution reaction -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Nanoscience & Nanotechnology; Materials Science, Multidisciplinary -
dc.relation.journalResearchArea Science & Technology - Other Topics; Materials Science -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus ELECTROLYTIC HYDROGEN -
dc.subject.keywordPlus METAL -
dc.subject.keywordPlus COBALT -
dc.subject.keywordPlus ELECTROCATALYSTS -
dc.subject.keywordPlus NANOCATALYSTS -
dc.subject.keywordPlus ADSORPTION -
dc.subject.keywordPlus PHOSPHIDE -
dc.subject.keywordPlus KINETICS -
dc.subject.keywordPlus CARBON -
dc.subject.keywordPlus NI -

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