Seung Sang Hwang
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
Research Subjects
Seung Sang Hwang has a total of 102 co-authors. Here are the top co-authors by number of shared publications:
- Albert Sung Soo Lee
Materials Architecturing Research Center, Korea Institute of Science and Technology, Seoul, Republic of Korea
22 shared publications He Seung Lee
Korea Institute of Science Technology
10 shared publications- Kyung-Youl Baek
Materials Architecturing Research Center, Korea Institute of Science and Technology, Seoul 02792, Republic of Korea
10 shared publications Seung-Sock Choi
Materials Architecturing Research Center Korea Institute of Science and Technology Seoul 136-791 Korea
10 shared publicationsJiyoon Jung
6 shared publications- Hyeonyeol Jeon
Research Center for Bio-based Chemistry, Korea Research Institute of Chemical Technology (KRICT), Ulsan, Republic of Korea
5 shared publications
Latest Publications
- 27 January 2025
- Published by Royal Society of Chemistry (RSC) in Biomaterials Science
- Vol. 13 (5) , 1243-1260
Fabrication of a micropatterned shape-memory polymer patch with l -DOPA for tendon regeneration
A scaffold design for tendon regeneration has been proposed, which mimics the microstructural features of tendons and provides appropriate mechanical properties. We synthesized a temperature-triggered shape-memory polymer (SMP) using the ring-opening polymerization of polycaprolactone (PCL) with polyethylene glycol (PEG) as a macroinitiator. We fabricated a micropatterned patch using SMP via capillary force lithography, which mimicked a native tendon, for providing physical cues and guiding effects. The SMP patches (the SMP-flat patch is referred to as SMP-F, and the SMP-patterned patch is referred to as SMP-P) were surface-modified with 3,4-dihydroxy-L-phenylalanine (L-DOPA, referred to as D) for improving cell adhesion. We hypothesized that SMP patches could be applied in minimally invasive surgery and the micropatterned structure would improve tendon regeneration by providing geometrical cues. The SMP patches exhibited excellent shape-memory properties, mechanical performance, and biocompatibility in vitro and in vivo. Especially, SMP-DP demonstrated enhanced cell behaviors in vitro, including cell orientation, elongation, migration, and tenogenic differentiation potential. The in vivo data showed notable biomechanical functionality and histological morphometric findings in various analyses of SMP-DP in the ruptured Achilles tendon model.
- 27 January 2025
- Published by Royal Society of Chemistry (RSC) in Biomaterials Science
- Vol. 13 (5) , 1243-1260
Fabrication of a micropatterned shape-memory polymer patch with l -DOPA for tendon regeneration
A scaffold design for tendon regeneration has been proposed, which mimics the microstructural features of tendons and provides appropriate mechanical properties. We synthesized a temperature-triggered shape-memory polymer (SMP) using the ring-opening polymerization of polycaprolactone (PCL) with polyethylene glycol (PEG) as a macroinitiator. We fabricated a micropatterned patch using SMP via capillary force lithography, which mimicked a native tendon, for providing physical cues and guiding effects. The SMP patches (the SMP-flat patch is referred to as SMP-F, and the SMP-patterned patch is referred to as SMP-P) were surface-modified with 3,4-dihydroxy-L-phenylalanine (L-DOPA, referred to as D) for improving cell adhesion. We hypothesized that SMP patches could be applied in minimally invasive surgery and the micropatterned structure would improve tendon regeneration by providing geometrical cues. The SMP patches exhibited excellent shape-memory properties, mechanical performance, and biocompatibility in vitro and in vivo. Especially, SMP-DP demonstrated enhanced cell behaviors in vitro, including cell orientation, elongation, migration, and tenogenic differentiation potential. The in vivo data showed notable biomechanical functionality and histological morphometric findings in various analyses of SMP-DP in the ruptured Achilles tendon model.
- Open Access
- 19 January 2024
- Published by Elsevier in Journal of Cleaner Production
- Vol. 438
Ion-exchangeable and sorptive reinforced membranes for efficient electrochemical removal of heavy metal ions in wastewater
- 19 January 2024
- Published by Elsevier in Journal of Cleaner Production
- Vol. 438
Open AccessIon-exchangeable and sorptive reinforced membranes for efficient electrochemical removal of heavy metal ions in wastewater
- Open Access
- 13 January 2024
- Published by Elsevier in Applied Catalysis B: Environment and Energy
- Vol. 346
Unveiling the role of catalytically active MXene supports in enhancing the performance and durability of cobalt oxygen evolution reaction catalysts for anion exchange membrane water electrolyzers
- 13 January 2024
- Published by Elsevier in Applied Catalysis B: Environment and Energy
- Vol. 346
Open AccessUnveiling the role of catalytically active MXene supports in enhancing the performance and durability of cobalt oxygen evolution reaction catalysts for anion exchange membrane water electrolyzers
- 20 October 2023
- Published by Elsevier in International Journal of Adhesion and Adhesives
- Vol. 128
Reversible Fe3+-induced urushi organogels in gamma butyrolactone
- 20 October 2023
- Published by Elsevier in International Journal of Adhesion and Adhesives
- Vol. 128
Reversible Fe3+-induced urushi organogels in gamma butyrolactone
- 7 August 2023
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry A
- Vol. 11 (34) , 18426-18433
Mitigating p hosphoric acid migration in high temperature polymer electrolyte membrane fuel cells with hydrophobic polysilsesquioxane-based binders
Cross-linkable organosilsesquioxanes were synthesized for application as catalyst binders in high temperature polymer electrolyte membrane fuel cells (HT-PEMFCs). Four different organic functional groups were examined including methyl, phenyl, fluoroalkyl, and fluorophenyl and their chemical, physical, surface, and electrochemical properties were characterized. The effect of surface hydrophobicity on a HT-PEMFC membrane electrode assembly was elucidated, showing that organosilsesquioxanes with lower surface tension or higher hydrophobicity towards water and phosphoric acid could be considered as a key parameter for HT-PEMFC performance. Fuel cell tests showed that the pentafluorophenyl-functionalized organosilsesquioxane showed improved H2/air performance (a peak power density of 527 mW cm−2 at 0.4 V) compared to the MEA with PTFE (a peak power density of 425 mW cm−2 at 0.4 V). Short term durability tests for 500 h showed that membrane electrode assemblies with alternative binders were stable and the developed organosilsesquioxane binders are a viable alternative to PTFE-based binders, all the while having additional advantages in vastly simplified ink slurry preparation through increased dispersibility in alcohol–water mixtures.
- 7 August 2023
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry A
- Vol. 11 (34) , 18426-18433
Mitigating p hosphoric acid migration in high temperature polymer electrolyte membrane fuel cells with hydrophobic polysilsesquioxane-based binders
Cross-linkable organosilsesquioxanes were synthesized for application as catalyst binders in high temperature polymer electrolyte membrane fuel cells (HT-PEMFCs). Four different organic functional groups were examined including methyl, phenyl, fluoroalkyl, and fluorophenyl and their chemical, physical, surface, and electrochemical properties were characterized. The effect of surface hydrophobicity on a HT-PEMFC membrane electrode assembly was elucidated, showing that organosilsesquioxanes with lower surface tension or higher hydrophobicity towards water and phosphoric acid could be considered as a key parameter for HT-PEMFC performance. Fuel cell tests showed that the pentafluorophenyl-functionalized organosilsesquioxane showed improved H2/air performance (a peak power density of 527 mW cm−2 at 0.4 V) compared to the MEA with PTFE (a peak power density of 425 mW cm−2 at 0.4 V). Short term durability tests for 500 h showed that membrane electrode assemblies with alternative binders were stable and the developed organosilsesquioxane binders are a viable alternative to PTFE-based binders, all the while having additional advantages in vastly simplified ink slurry preparation through increased dispersibility in alcohol–water mixtures.
- 19 April 2023
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry A
- Vol. 11 (20) , 10891-10900
Polydiallylammonium interpenetrating cationic network ion-solvating membranes for anion exchange membrane water electrolyzers
A facile methodology of fabricating alkaline exchange membranes was developed by blending an alkaline stable, ammonium network forming precursor with an ion-solvating polymer, poly(ethylene-co-vinyl alcohol) matrix, followed by thermal curing under mild conditions. The alkaline stable, ammonium network forming precursor was synthesized through the Menshutkin reaction of a multifunctional alkyl halide and methyldiallylamine, yielding an ammonium polymer precursor that under radical initiated thermal cyclo-polymerization forms pyrrolidinium cationic networks. The fabricated membranes exhibited tunable IEC, conductivity, and physical properties through the control of the poly(ethylene-co-vinyl alcohol) ion-solvating polymer content. The alkaline stability of the membranes was examined under 70 °C and 1 M KOH conditions for over 300 h, which showed impeccable retention of ion exchange capacity (IEC) and conductivity. The membrane electrode assembly (MEA) of anion exchange membrane electrolyzers with the fabricated membranes showed excellent performance (1.57 A cm−2 at 2.0 V) and a short-term durability test showed improved durability over a commercial anion exchange membrane.
- 19 April 2023
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry A
- Vol. 11 (20) , 10891-10900
Polydiallylammonium interpenetrating cationic network ion-solvating membranes for anion exchange membrane water electrolyzers
A facile methodology of fabricating alkaline exchange membranes was developed by blending an alkaline stable, ammonium network forming precursor with an ion-solvating polymer, poly(ethylene-co-vinyl alcohol) matrix, followed by thermal curing under mild conditions. The alkaline stable, ammonium network forming precursor was synthesized through the Menshutkin reaction of a multifunctional alkyl halide and methyldiallylamine, yielding an ammonium polymer precursor that under radical initiated thermal cyclo-polymerization forms pyrrolidinium cationic networks. The fabricated membranes exhibited tunable IEC, conductivity, and physical properties through the control of the poly(ethylene-co-vinyl alcohol) ion-solvating polymer content. The alkaline stability of the membranes was examined under 70 °C and 1 M KOH conditions for over 300 h, which showed impeccable retention of ion exchange capacity (IEC) and conductivity. The membrane electrode assembly (MEA) of anion exchange membrane electrolyzers with the fabricated membranes showed excellent performance (1.57 A cm−2 at 2.0 V) and a short-term durability test showed improved durability over a commercial anion exchange membrane.
- Open Access
Lanthanide and Ladder-Structured Polysilsesquioxane Composites for Transparent Color Conversion Layers
Ladder-type polysilsesquioxanes (LPSQs) containing phenyl as a high refractive index unit and cyclic epoxy as a curable unit were found to be excellent candidates for a transparent color conversion layer for displays due to being miscible with organic solvents and amenable to transparent film formation. Therefore, the LPSQs were combined with luminescent lanthanide metals, europium Eu(III), and terbium Tb(III), to fabricate transparent films with various emission colors, including red, orange, yellow, and green. The high luminescence and transmittance properties of the LPSQs–lanthanide composite films after thermal curing were attributed to chelating properties of hydroxyl and polyether side chains of LPSQs to lanthanide ions, as well as a light sensitizing effect of phenyl side chains of the LPSQs. Furthermore, Fourier-transform infrared (FT-IR) and X-ray photoelectron spectroscopy and nanoindentation tests indicated that the addition of the nanoparticles to the LPSQs moderately enhanced the epoxy conversion rate and substantially improved the wear resistance, including hardness, adhesion, and insusceptibility to atmospheric corrosion in a saline environment. Thus, the achieved LPGSG–lanthanide hybrid organic–inorganic material could effectively serve as a color conversion layer for displays.
Open AccessLanthanide and Ladder-Structured Polysilsesquioxane Composites for Transparent Color Conversion Layers
Ladder-type polysilsesquioxanes (LPSQs) containing phenyl as a high refractive index unit and cyclic epoxy as a curable unit were found to be excellent candidates for a transparent color conversion layer for displays due to being miscible with organic solvents and amenable to transparent film formation. Therefore, the LPSQs were combined with luminescent lanthanide metals, europium Eu(III), and terbium Tb(III), to fabricate transparent films with various emission colors, including red, orange, yellow, and green. The high luminescence and transmittance properties of the LPSQs–lanthanide composite films after thermal curing were attributed to chelating properties of hydroxyl and polyether side chains of LPSQs to lanthanide ions, as well as a light sensitizing effect of phenyl side chains of the LPSQs. Furthermore, Fourier-transform infrared (FT-IR) and X-ray photoelectron spectroscopy and nanoindentation tests indicated that the addition of the nanoparticles to the LPSQs moderately enhanced the epoxy conversion rate and substantially improved the wear resistance, including hardness, adhesion, and insusceptibility to atmospheric corrosion in a saline environment. Thus, the achieved LPGSG–lanthanide hybrid organic–inorganic material could effectively serve as a color conversion layer for displays.
- 26 March 2022
- Published by Wiley in Advanced Optical Materials
- Vol. 10 (10)
Coupled Solid and Inverse Antenna Stacks Above Metal Ground as Metamaterial Perfect Electromagnetic Wave Absorbers with Extreme Subwavelength Thicknesses
The ability to completely absorb an electromagnetic (EM) wave with a material much thinner than the wavelength is a prerequisite for achieving ultracompact, flexible, and lightweight EM devices. Herein, a metamaterial microwave perfect absorber is demonstrated as thin as 1/1250 of the target wavelength by coupling an array of metal patches to inverse cross metal antennas through a dielectric separator and with a reflector placed underneath. Compared to a conventional three‐layer absorber, the modified design reduces the resonance frequency by up to tenfolds without altering the patch and dielectric layers, but by reconfiguring the induced current pathways that reorient the dipolar magnetic fields and dramatically boost the magnetic flux. With the reflector, the stack is framed for perfect absorption at the critical coupling condition, which is identified by monitoring the reflection phase shift across the resonance frequency. The study provides guidelines for shrinking the thickness further and can be extended to other frequencies.
- 26 March 2022
- Published by Wiley in Advanced Optical Materials
- Vol. 10 (10)
Coupled Solid and Inverse Antenna Stacks Above Metal Ground as Metamaterial Perfect Electromagnetic Wave Absorbers with Extreme Subwavelength Thicknesses
The ability to completely absorb an electromagnetic (EM) wave with a material much thinner than the wavelength is a prerequisite for achieving ultracompact, flexible, and lightweight EM devices. Herein, a metamaterial microwave perfect absorber is demonstrated as thin as 1/1250 of the target wavelength by coupling an array of metal patches to inverse cross metal antennas through a dielectric separator and with a reflector placed underneath. Compared to a conventional three‐layer absorber, the modified design reduces the resonance frequency by up to tenfolds without altering the patch and dielectric layers, but by reconfiguring the induced current pathways that reorient the dipolar magnetic fields and dramatically boost the magnetic flux. With the reflector, the stack is framed for perfect absorption at the critical coupling condition, which is identified by monitoring the reflection phase shift across the resonance frequency. The study provides guidelines for shrinking the thickness further and can be extended to other frequencies.
- 18 August 2021
- Published by American Chemical Society (ACS) in ACS Applied Polymer Materials
- Vol. 3 (9) , 4708-4716
Structure–Property Relationships of 3D-Printable Chain-Extended Block Copolymers with Tunable Elasticity and Biodegradability
- 18 August 2021
- Published by American Chemical Society (ACS) in ACS Applied Polymer Materials
- Vol. 3 (9) , 4708-4716
Structure–Property Relationships of 3D-Printable Chain-Extended Block Copolymers with Tunable Elasticity and Biodegradability
- 1 February 2021
- Published by Elsevier in Journal of Membrane Science
- Vol. 620
Tailoring selective pores of carbon molecular sieve membranes towards enhanced N2/CH4 separation efficiency
- 1 February 2021
- Published by Elsevier in Journal of Membrane Science
- Vol. 620
Tailoring selective pores of carbon molecular sieve membranes towards enhanced N2/CH4 separation efficiency