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신태주

Shin, Tae Joo
Synchrotron Radiation Research Lab.
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dc.citation.endPage 515 -
dc.citation.number 7749 -
dc.citation.startPage 511 -
dc.citation.title NATURE -
dc.citation.volume 567 -
dc.contributor.author Jung, Eui Hyuk -
dc.contributor.author Jeon, Nam Joong -
dc.contributor.author Park, Eun Young -
dc.contributor.author Moon, Chan Su -
dc.contributor.author Shin, Tae Joo -
dc.contributor.author Yang, Tae-Youl -
dc.contributor.author Noh, Jun Hong -
dc.contributor.author Seo, Jangwon -
dc.date.accessioned 2023-12-21T19:19:34Z -
dc.date.available 2023-12-21T19:19:34Z -
dc.date.created 2019-04-11 -
dc.date.issued 2019-03 -
dc.description.abstract Perovskite solar cells typically comprise electron-and hole-transport materials deposited on each side of a perovskite active layer. So far, only two organic hole-transport materials have led to state-of-the-art performance in these solar cells(1): poly(triarylamine) (PTAA)(2-5) and 2,2',7,7'-tetrakis(N,N-di-p-methoxyphenylamine)-9,9'-spirobifluorene (spiro-OMeTAD)(6,7). However, these materials have several drawbacks in terms of commercialization, including high cost(8), the need for hygroscopic dopants that trigger degradation of the perovskite layer(9) and limitations in their deposition processes(10). Poly(3-hexylthiophene) (P3HT) is an alternative hole-transport material with excellent optoelectronic properties(11-13), low cost(8,14) and ease of fabrication(15-18), but so far the efficiencies of perovskite solar cells using P3HT have reached only around 16 per cent(19). Here we propose a device architecture for highly efficient perovskite solar cells that use P3HT as a hole-transport material without any dopants. A thin layer of wide-bandgap halide perovskite is formed on top of the narrow-bandgap light-absorbing layer by an in situ reaction of n-hexyl trimethyl ammonium bromide on the perovskite surface. Our device has a certified power conversion efficiency of 22.7 per cent with hysteresis of +/- 0.51 per cent; exhibits good stability at 85 per cent relative humidity without encapsulation; and upon encapsulation demonstrates long-term operational stability for 1,370 hours under 1-Sun illumination at room temperature, maintaining 95 per cent of the initial efficiency. We extend our platform to large-area modules (24.97 square centimetres)-which are fabricated using a scalable bar-coating method for the deposition of P3HT-and achieve a power conversion efficiency of 16.0 per cent. Realizing the potential of P3HT as a hole-transport material by using a wide-bandgap halide could be a valuable direction for perovskite solar-cell research. -
dc.identifier.bibliographicCitation NATURE, v.567, no.7749, pp.511 - 515 -
dc.identifier.doi 10.1038/s41586-019-1036-3 -
dc.identifier.issn 0028-0836 -
dc.identifier.scopusid 2-s2.0-85063609624 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/26611 -
dc.identifier.url https://www.nature.com/articles/s41586-019-1036-3 -
dc.identifier.wosid 000462655800047 -
dc.language 영어 -
dc.publisher NATURE PUBLISHING GROUP -
dc.title Efficient, stable and scalable perovskite solar cells using poly(3-hexylthiophene) -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Multidisciplinary Sciences -
dc.relation.journalResearchArea Science & Technology - Other Topics -
dc.type.docType Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus HOLE TRANSPORT MATERIALS -
dc.subject.keywordPlus MOBILITY -
dc.subject.keywordPlus LAYERS -
dc.subject.keywordPlus ROUTE -
dc.subject.keywordPlus FILMS -

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