사진

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Park, Young S. (박영석)

Department
Department of Chemistry(화학과)
Website
https://sites.google.com/site/youngsparkunist
Lab
Advanced Organic Materials Lab. (첨단 유기 재료 연구실)
Research Keywords
유기 합성, 합성 방법론, organic synthesis, synthetic methodology, polycyclic aromatic hydrocarbon, graphene nanoribbon, bottom-up synthesis, heteroatom-doping
Research Interests
Our laboratory is interested in developing general, facile yet selective synthetic strategies towards broad range of polycyclic aromatic hydrocarbon (PAH) systems. Through these general synthetic methodologies, we aim to build previously unknown low dimensional and multidimensional organic materials that hold great potential for applications in organic electronics.We design, synthesize, and characterize organic materials and seek for their applications in organic electronics. Particularly, we are interested in controlling the frontier molecular orbital energy levels by heteroatom-doping. By bottom-up approach using organic chemistry, we carefully introduce heteroatoms into the molecule and control their positions at atomic level.
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Issue DateTitleAuthor(s)TypeViewAltmetrics
2022-12Versatile Hole Selective Molecules Containing a Series of Heteroatoms as Self-Assembled Monolayers for Efficient p-i-n Perovskite and Organic Solar CellsUllah, Asmat; Park, Keun Hyeong; Lee, YoungWan, et alARTICLE552 Versatile Hole Selective Molecules Containing a Series of Heteroatoms as Self-Assembled Monolayers for Efficient p-i-n Perovskite and Organic Solar Cells
2022-01Novel Phenothiazine-Based Self-Assembled Monolayer as a Hole Selective Contact for Highly Efficient and Stable p-i-n Perovskite Solar CellsUllah, Asmat; Park, Keun Hyeong; Hieu Dinh Nguyen, et alARTICLE288 Novel Phenothiazine-Based Self-Assembled Monolayer as a Hole Selective Contact for Highly Efficient and Stable p-i-n Perovskite Solar Cells
2021-11PN-Doped tetraphenylnaphthalene: a straightforward synthetic strategy analogous to BN-annulationPark, Jupil; Kim, So Jung; Kwon, Hansol, et alARTICLE308 PN-Doped tetraphenylnaphthalene: a straightforward synthetic strategy analogous to BN-annulation
2021-04An aza-Diels–Alder approach to chlorinated quinolines, benzoquinolines, and polybenzoquinolinesKim, Juhwan; Umerani, Mehran J.; Kurakake, Reina, et alARTICLE339 An aza-Diels–Alder approach to chlorinated quinolines, benzoquinolines, and polybenzoquinolines
2021-02Impact of sphingosine and acetylsphingosines on the aggregation and toxicity of metal-free and metal-treated amyloid-betaYi, Yelim; Lin, Yuxi; Han, Jiyeon, et alARTICLE246 Impact of sphingosine and acetylsphingosines on the aggregation and toxicity of metal-free and metal-treated amyloid-beta
2020-08Unveiling 79-year-old ixene and its BN-doped derivativePati, Palas Baran; Jin, Eunji; Kim, Yohan, et alARTICLE674 Unveiling 79-year-old ixene and its BN-doped derivative
2018-07Contorted polycyclic aromatic hydrocarbon: promising Li insertion organic anodePark, Jaehyun; Lee, Cheol Woo; Joo, Se Hun, et alARTICLE1205 Contorted polycyclic aromatic hydrocarbon: promising Li insertion organic anode
2018-06ipso-Arylative polymerization as a route to π-conjugated polymers: synthesis of poly(3-hexylthiophene)Shih, Feng-Yang; Tian, Sisi; Gallagher, Nicholas, et alARTICLE671 ipso-Arylative polymerization as a route to π-conjugated polymers: synthesis of poly(3-hexylthiophene)
2016-03Synthesis of Nitrogen-Containing Rubicene and Tetrabenzopentacene DerivativesPark, Young S.; Dibble, David J.; Kim, Juhwan, et alARTICLE1057 Synthesis of Nitrogen-Containing Rubicene and Tetrabenzopentacene Derivatives
2016-01An Aza-Diels-Alder Approach to Crowded BenzoquinolinesMazaheripour, Amir; Dibble, David J.; Umerani, Mehran J., et alARTICLE1037 An Aza-Diels-Alder Approach to Crowded Benzoquinolines
2015-05Synthesis of Polybenzoquinolines as Precursors for Nitrogen-Doped Graphene NanoribbonsDibble, David J.; Park, Young S.; Mazaheripour, Amir, et alARTICLE856 Synthesis of Polybenzoquinolines as Precursors for Nitrogen-Doped Graphene Nanoribbons
2015-02An Aza-Diels-Alder Route to PolyquinolinesDibble, David J.; Umerani, Mehran J.; Mazaheripour, Amir, et alARTICLE937 An Aza-Diels-Alder Route to Polyquinolines
2014-09Polymerization of Tellurophene Derivatives by Microwave-Assisted Palladium-Catalyzed ipso-Arylative PolymerizationPark, Young S.; Wu, Qin; Nam, Chang-Yong, et alARTICLE962 Polymerization of Tellurophene Derivatives by Microwave-Assisted Palladium-Catalyzed ipso-Arylative Polymerization
2014-07Effects of heteroatom substitution in conjugated heterocyclic compounds on photovoltaic performance: from sulfur to telluriumPark, Y. S.; Kale, T. S.; Nam, C. -Y., et alARTICLE709 Effects of heteroatom substitution in conjugated heterocyclic compounds on photovoltaic performance: from sulfur to tellurium
2012-03Photo-Cross-Linkable Azide-Functionalized Polythiophene for Thermally Stable Bulk Heterojunction Solar CellsNam, Chang-Yong; Qin, Yang; Park, Young S., et alARTICLE906 Photo-Cross-Linkable Azide-Functionalized Polythiophene for Thermally Stable Bulk Heterojunction Solar Cells
2011-06Conductance of Single Cobalt Chalcogenide Cluster JunctionsBoardman, Brycelyn M.; Widawsky, Jonathan R.; Park, Young S., et alARTICLE749 Conductance of Single Cobalt Chalcogenide Cluster Junctions
2010-07Reliable Formation of Single Molecule Junctions with Air-Stable Diphenylphosphine LinkersParameswaran, R.; Widawsky, J. R.; Vazquez, H., et alARTICLE984 Reliable Formation of Single Molecule Junctions with Air-Stable Diphenylphosphine Linkers
2009-08Frustrated Rotations in Single-Molecule JunctionsPark, Young S.; Widawsky, Jonathan R.; Kamenetska, Maria, et alARTICLE854 Frustrated Rotations in Single-Molecule Junctions
2009-03Formation and Evolution of Single-Molecule JunctionsKamenetska, M.; koentopp, M.; Whalley, A. C., et alARTICLE826 Formation and Evolution of Single-Molecule Junctions
2007-12Contact chemistry and single-molecule conductance: A comparison of phosphines, methyl sulfides, and aminesPark, Young S.; Whalley, Adam C.; Kamenetska, Maria, et alARTICLE898 Contact chemistry and single-molecule conductance: A comparison of phosphines, methyl sulfides, and amines

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