Yu-Min Wang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Yu-Min Wang has a total of 28 co-authors. Here are the top co-authors by number of shared publications:
- Ognen Pop-Georgievski
Institute of Macromolecular Chemistry Czech Academy of Sciences Prague Czech Republic
4 shared publications - Andres de Los Santos Pereira
Institute of Macromolecular Chemistry CAS Prague Czech Republic
2 shared publications Anna Kálosi
Centre for advanced materials application, Slovak Academy of Sciences, Dúbravská cesta 9, 84511 Bratislava, Slovakia
2 shared publications- Daniel V. Krogstad
Department of Material Science and Engineering, Grainger College of Engineering, University of Illinois Urbana-Champaign, 1304 W. Green St., Urbana, IL 61801, USA
2 shared publications - Katarína Ridzoňová
FZU—Institute of Physics of the Czech Academy of Sciences, Na Slovance 1999/2, 182 00 Prague, Czech Republic
2 shared publications - Maksym Buryi
Institute of Plasma Physics of the Czech Academy of Sciences, U Slovanky 2525/1a, 182 00 Prague, Czech Republic
2 shared publications
Latest Publications
- Open Access
- 30 September 2026
- Published by Royal Society of Chemistry (RSC) in Soft Matter
- Vol. 22 (37) , 6227-6237
Curing mechanisms of imidazolium- and phosphonium-based ionic liquids in epoxy resins: linking initiation pathways to network glass transition temperature
The choice of ionic liquid used in epoxy crosslinking influences not only the cure temperatures, but also the curing mechanisms and the glass transition temperatures of the resultant epoxy network.
- 30 September 2026
- Published by Royal Society of Chemistry (RSC) in Soft Matter
- Vol. 22 (37) , 6227-6237
Open AccessCuring mechanisms of imidazolium- and phosphonium-based ionic liquids in epoxy resins: linking initiation pathways to network glass transition temperature
The choice of ionic liquid used in epoxy crosslinking influences not only the cure temperatures, but also the curing mechanisms and the glass transition temperatures of the resultant epoxy network.
- Open Access
- 26 April 2024
- Published by Royal Society of Chemistry (RSC) in Polymer Chemistry
- Vol. 15 (20) , 2070-2080
Solvent effects on surface-grafted and solution-born poly[N-(2-hydroxypropyl)methacrylamide] during surface-initiated RAFT polymerization
Solvent effects influence grafting density and cause discrepancy between molar mass of surface-grafted and solution-born poly[N-(2-hydroxypropyl) methacrylamide] during surface-initiated RAFT polymerization.
- 26 April 2024
- Published by Royal Society of Chemistry (RSC) in Polymer Chemistry
- Vol. 15 (20) , 2070-2080
Open AccessSolvent effects on surface-grafted and solution-born poly[N-(2-hydroxypropyl)methacrylamide] during surface-initiated RAFT polymerization
Solvent effects influence grafting density and cause discrepancy between molar mass of surface-grafted and solution-born poly[N-(2-hydroxypropyl) methacrylamide] during surface-initiated RAFT polymerization.
- 17 October 2023
- Published by Elsevier in Optical Materials
- Vol. 145
Hydrothermally grown molybdenum doped ZnO nanorod arrays. The concept of novel ultrafast nanoscintillator
- 17 October 2023
- Published by Elsevier in Optical Materials
- Vol. 145
Hydrothermally grown molybdenum doped ZnO nanorod arrays. The concept of novel ultrafast nanoscintillator
- Open Access
Changes to Material Phase and Morphology Due to High-Level Molybdenum Doping of ZnO Nanorods: Influence on Luminescence and Defects
The influence of Mo on the electronic states and crystalline structure, as well as morphology, phase composition, luminescence, and defects in ZnO rods grown as free-standing nanoparticles, was studied using a variety of experimental techniques. Mo has almost no influence on the luminescence of the grown ZnO particles, whereas shallow donors are strongly affected in ZnO rods. Annealing in air causes exciton and defect-related bands to drop upon Mo doping level. The increase of the Mo doping level from 20 to 30% leads to the creation of dominating molybdates. This leads to a concomitant drop in the number of formed ZnO nanorods.
Open AccessChanges to Material Phase and Morphology Due to High-Level Molybdenum Doping of ZnO Nanorods: Influence on Luminescence and Defects
The influence of Mo on the electronic states and crystalline structure, as well as morphology, phase composition, luminescence, and defects in ZnO rods grown as free-standing nanoparticles, was studied using a variety of experimental techniques. Mo has almost no influence on the luminescence of the grown ZnO particles, whereas shallow donors are strongly affected in ZnO rods. Annealing in air causes exciton and defect-related bands to drop upon Mo doping level. The increase of the Mo doping level from 20 to 30% leads to the creation of dominating molybdates. This leads to a concomitant drop in the number of formed ZnO nanorods.
- 7 June 2022
- Published by Royal Society of Chemistry (RSC) in Polymer Chemistry
- Vol. 13 (25) , 3815-3826
Grafting density and antifouling properties of poly[N-(2-hydroxypropyl) methacrylamide] brushes prepared by “grafting to” and “grafting from”
Antifouling polymer brushes are widely utilized in biomedical applications to prevent non-specific interactions with biological fluids. They consist of surface-tethered polymer chains and are commonly formed when the chains are “grafted to” (GT) a surface by chemisorption or “grafted from” (GF) a surface in a surface-initiated polymerization. Although the antifouling polymer brushes have been studied for years, an accurate comparison between the GT and GF methods in terms of the ability of the prepared brushes to resist fouling has not been established yet. In this study, we investigate physical and antifouling properties of poly[N-(2-hydroxypropyl) methacrylamide] (poly(HPMA)) brushes synthesized by GT and GF methods using reversible addition–fragmentation chain-transfer (RAFT) polymerization. Using size exclusion chromatography and single-molecule force spectroscopy, we are able to ensure that grafted polymer chains in the layers prepared by both methods have comparable composition and molar mass. Thus, we attribute the differences in fouling resistance and physical properties of the polymer layers to the physical conformation of the chains achieved by the selected grafting method. While both types of poly(HPMA) brushes are shown to substantially reduce fouling from blood plasma, the GF polymer brushes suppress fouling by an order of magnitude better than the GT polymer brushes. The observed difference in the antifouling performance is related to the much higher grafting density that can be achieved in the GF method. This study highlights the importance of the selection of the grafting method for achieving a high antifouling performance.
- 7 June 2022
- Published by Royal Society of Chemistry (RSC) in Polymer Chemistry
- Vol. 13 (25) , 3815-3826
Grafting density and antifouling properties of poly[N-(2-hydroxypropyl) methacrylamide] brushes prepared by “grafting to” and “grafting from”
Antifouling polymer brushes are widely utilized in biomedical applications to prevent non-specific interactions with biological fluids. They consist of surface-tethered polymer chains and are commonly formed when the chains are “grafted to” (GT) a surface by chemisorption or “grafted from” (GF) a surface in a surface-initiated polymerization. Although the antifouling polymer brushes have been studied for years, an accurate comparison between the GT and GF methods in terms of the ability of the prepared brushes to resist fouling has not been established yet. In this study, we investigate physical and antifouling properties of poly[N-(2-hydroxypropyl) methacrylamide] (poly(HPMA)) brushes synthesized by GT and GF methods using reversible addition–fragmentation chain-transfer (RAFT) polymerization. Using size exclusion chromatography and single-molecule force spectroscopy, we are able to ensure that grafted polymer chains in the layers prepared by both methods have comparable composition and molar mass. Thus, we attribute the differences in fouling resistance and physical properties of the polymer layers to the physical conformation of the chains achieved by the selected grafting method. While both types of poly(HPMA) brushes are shown to substantially reduce fouling from blood plasma, the GF polymer brushes suppress fouling by an order of magnitude better than the GT polymer brushes. The observed difference in the antifouling performance is related to the much higher grafting density that can be achieved in the GF method. This study highlights the importance of the selection of the grafting method for achieving a high antifouling performance.