Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Hanok Park"'
Publikováno v:
ACS Omega, Vol 3, Iss 12, Pp 18398-18410 (2018)
Externí odkaz:
https://doaj.org/article/97509743cb9540dc87e9b8c515a7c962
Publikováno v:
Dyes and Pigments. 163:30-39
We present design and synthesis of three new symmetrical and linear A-D-A type π-conjugated donor small molecules (2D-NDT(TPD)2, 2D-NDT(Ester)2 and 2D-NDT(Amide)2) containing two dimensional (2D) naphthodithiophene (NDT) unit as the central donor co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd27823d5d4b6b2200ba697481ffc7a6
https://doi.org/10.1016/j.dyepig.2018.11.037
https://doi.org/10.1016/j.dyepig.2018.11.037
Autor:
Soo-Hyoung Lee, Jang-Gun Han, Swapnil B. Ambade, Sushil S. Bagde, Rohan B. Ambade, Hanok Park, Yinji Li, ByeongCheol Kim
Publikováno v:
Dyes and Pigments. 137:117-125
Two new small molecules, composed of naphthodithiophene (NDT) donor core and thienopyrroledione (TPD) group acceptor group end-capped with and without an alkyl-bithiophene, defined as NDT(TPD)2 and NDT(TPDTT)2 were designed and synthesized by stille
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8aa7380e9b28e5ceab02e77bdc98387
https://doi.org/10.1016/j.dyepig.2016.10.007
https://doi.org/10.1016/j.dyepig.2016.10.007
Autor:
Nam Jeong Hong, Myoung-Jin Baek, Kyukwan Zong, Jun Hui Park, Soo-Hyoung Lee, Jo Jeong, Hanok Park
Publikováno v:
Organic Electronics. 35:101-111
Four BDT-TPD polymers (PA–PD) were synthesized by modifying the alkylthienyl chains on BDT, placing spacer group between BDT and TPD, and installing extended conjugated side chains on the BDT of the polymer to investigate the correlation between st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd0b777fda6bb42fc1cfdb5993aa296e
https://doi.org/10.1016/j.orgel.2016.05.007
https://doi.org/10.1016/j.orgel.2016.05.007
Publikováno v:
New Journal of Chemistry. 40:2063-2070
Two π-conjugated small molecules, BDT(TTBT)2 and BDT(PTBT)2, based on benzodithiophene (BDT) and benzothiadiazole (BT) substituted with different terminal groups such as hexyl-bithiophene and hexylphenyl-thiophene are investigated for use in solutio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d50734627a7d4d4f270a307f5d2bda3
https://doi.org/10.1039/c5nj02529j
https://doi.org/10.1039/c5nj02529j
Publikováno v:
ACS Omega
We report for the first time that alkali carbonates (Li2CO3, K2CO3, and Rb2CO3) based on a low-temperature solution process can be used as interfacial modifiers for SnO2 as robust electron-transport layers (ETL) for inverted organic solar cells (iOSC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::32ccdcaa40d8bee2af63823b912bf3b9
https://pubmed.ncbi.nlm.nih.gov/31458412
https://pubmed.ncbi.nlm.nih.gov/31458412
Publikováno v:
Chemical Physics Letters. 630:37-43
This study involves the development of two new small molecules comprising a diketopyrrolopyrrole (DPP) core flanked with donor units of triphenylamine (TPA-DPP-TPA) and fluorine (FL-DPP-FL) for application in bulk heterojunction (BHJ) organic solar c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3768b408d0dc84fff27dbb0838c8032
https://doi.org/10.1016/j.cplett.2015.04.032
https://doi.org/10.1016/j.cplett.2015.04.032
Publikováno v:
Bulletin of the Korean Chemical Society. 2014, Vol. 35 Issue 6, p1875-1878. 4p.
Publikováno v:
Journal of Nanoscience and Nanotechnology. 14:8561-8566
Polymer solar cells (PSCs) have attracted increasing attention in recent years. The rapid progress and mounting interest suggest the feasibility of PSC commercialization. However, critical issues such as stability and the weak nature of their interfa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbad594fdefee027480986818a231541
https://doi.org/10.1166/jnn.2014.9996
https://doi.org/10.1166/jnn.2014.9996
Publikováno v:
Chemical Physics Letters. :388-393
An isoindigo-dithienocarbazole-isoindigo oligomer (II-DTC-II) was synthesized by a Stille coupling reaction between N -hexadecyl-2,8-bis(trimethylstannyl)dithieno[3,2-b:6,7-b]carbazole and 6-bromo- N , N ′-dioctylisoindigo. The oligomer exhibited a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::126f4fdb6d72966d4c2d26afa43677e0
https://doi.org/10.1016/j.cplett.2014.07.071
https://doi.org/10.1016/j.cplett.2014.07.071