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

김봉수

Kim, BongSoo
Polymer & Organic Semiconductor Lab.
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 192 -
dc.citation.startPage 185 -
dc.citation.title SOLAR ENERGY MATERIALS AND SOLAR CELLS -
dc.citation.volume 104 -
dc.contributor.author Son, Seon Kyoung -
dc.contributor.author Kim, Bong Soo -
dc.contributor.author Lee, Chun-Young -
dc.contributor.author Lee, Joong Suk -
dc.contributor.author Cho, Jeong Ho -
dc.contributor.author Ko, Min Jae -
dc.contributor.author Lee, Doh-Kwon -
dc.contributor.author Kim, Honggon -
dc.contributor.author Choi, Dong Hoon -
dc.contributor.author Kim, Kyungkon -
dc.date.accessioned 2023-12-22T04:41:57Z -
dc.date.available 2023-12-22T04:41:57Z -
dc.date.created 2018-09-10 -
dc.date.issued 2012-09 -
dc.description.abstract Two low band gap copolymers (PQTDPP and PQTVTDPP) having quaterthiophene (QT) or bithiophene-vinylene-bithiophene (QTVT) as donor unit and diketopyrrolopyrrole (DPP) as acceptor unit have been synthesized via Stille cross-coupling polymerization. The polymers showed high thermal stability and broad light absorption with optical band gaps around 1.3 eV. Cyclic voltammetry measurements revealed that the HOMO and LUMO energy levels of QT and DPP copolymer (PQTDPP) were found to be -5.19 and -3.64 eV, respectively and those of PQTVTDPP -5.05 and -3.66 eV, respectively. X-ray diffraction patterns showed highly crystalline phase in the PQTDPP film and nearly amorphous in the PQTVTDPP film. This dramatic difference in crystallinity was attributed to the structural isomerization around vinyl groups in the PQTVTDPP polymer. Field-effect transistor measurement revealed that the PQTDPP showed high hole mobility of 0.06 cm(2)/Vs and on/off ratio of 106 while the PQTVTDPP showed hole mobility of 3.57 x 10(-4) cm(2)/Vs and on/off ratio of 10(5), which is consistent with X-ray diffraction results. Photovoltaic devices were also fabricated using polymer:PCBM blends in the structure of ITO/PEDOT:PSS/blend/Al. The PQTDPP devices exhibited an open circuit voltage (V-oc) of 0.58 V, a short circuit current (J(sc)) of 7.16 mA/cm(2), a fill factor (FF) of 0.55 and a power conversion efficiency (PCE) of 2.28%, and the PQTVTDPP devices exhibited an V-oc of 0.50 V, a J(sc) of 7.60 mA/cm(2), a FF of 0.51 and a PCE of 1.97% under AM 1.5 illumination. -
dc.identifier.bibliographicCitation SOLAR ENERGY MATERIALS AND SOLAR CELLS, v.104, pp.185 - 192 -
dc.identifier.doi 10.1016/j.solmat.2012.04.043 -
dc.identifier.issn 0927-0248 -
dc.identifier.scopusid 2-s2.0-84862190161 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/24843 -
dc.identifier.url https://www.sciencedirect.com/science/article/pii/S092702481200219X?via%3Dihub -
dc.identifier.wosid 000306775400030 -
dc.language 영어 -
dc.publisher ELSEVIER SCIENCE BV -
dc.title Synthesis and photovoltaic properties of low band gap quarterthiophenes-alt-diketopyrrolopyrroles polymers having high hole mobility -
dc.type Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor Low band gap polymer -
dc.subject.keywordAuthor Polymer solar cell -
dc.subject.keywordAuthor Organic solar cell -
dc.subject.keywordPlus HETEROJUNCTION SOLAR-CELLS -
dc.subject.keywordPlus OPEN-CIRCUIT VOLTAGE -
dc.subject.keywordPlus FIELD-EFFECT TRANSISTORS -
dc.subject.keywordPlus THIN-FILM TRANSISTORS -
dc.subject.keywordPlus PHOTOCURRENT GENERATION -
dc.subject.keywordPlus CONVERSION EFFICIENCY -
dc.subject.keywordPlus ORGANIC PHOTOVOLTAICS -
dc.subject.keywordPlus CHARGE-TRANSPORT -
dc.subject.keywordPlus CARRIER MOBILITY -
dc.subject.keywordPlus METHANOFULLERENE -

qrcode

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