Seung Jun Lee
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Seung Jun Lee has a total of 20 co-authors. Here are the top co-authors by number of shared publications:
- Myong Yong Choi
Department of Chemistry (BK21 FOUR), Research Institute of Advanced Chemistry Gyeongsang National University Jinju Republic of Korea
4 shared publications - Jagannathan Madhavan
Solar Energy Lab, Department of Chemistry, Thiruvalluvar University, Vellore 632 115, Tamil Nadu, India
2 shared publications - Jayaraman Theerthagiri
Department of Chemistry (BK21 FOUR), Research Institute of Advanced Chemistry Gyeongsang National University Jinju Republic of Korea
2 shared publications - Bavani Thirugnanam
Department of Chemistry & Centre for Energy and Environment Karpagam Academy of Higher Education Coimbatore India
1 shared publication - Bruno Georges Pollet
Clean Hydrogen Lab (CleanH2Lab) Hydrogen Research Institute (HRI) Université du Québec à Trois‐Rivières (UQTR) Trois‐Rivières Québec Canada
1 shared publication - Dhandapani Balaji
Solar Energy Lab, Department of Chemistry, Thiruvalluvar University, Vellore 632 115, India
1 shared publication
Latest Publications
- Open Access
- 4 November 2020
- Published by MDPI AG in Nanomaterials
- Vol. 10 (11) , 2195
Cost-Effective Synthesis of Efficient CoWO4/Ni Nanocomposite Electrode Material for Supercapacitor Applications
In the present study, the synthesis of CoWO4 (CWO)–Ni nanocomposites was conducted using a wet chemical method. The crystalline phases and morphologies of the Ni nanoparticles, CWO, and CWO–Ni composites were analyzed using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy-dispersive X-ray spectroscopy (EDAX). The electrochemical properties of CWO and CWO–Ni composite electrode materials were assessed by cyclic voltammetry (CV), and galvanostatic charge–discharge (GCD) tests using KOH as a supporting electrolyte. Among the CWO–Ni composites containing different amounts of Ni1, Ni2, and Ni3, CWO–Ni3 exhibited the highest specific capacitance of 271 F g−1 at 1 A g−1, which was greater than that of bare CWO (128 F g−1). Moreover, the CWO–Ni3 composite electrode material displayed excellent reversible cyclic stability and maintained 86.4% of its initial capacitance after 1500 discharge cycles. The results obtained herein demonstrate that the prepared CWO–Ni3 nanocomposite is a promising electrode candidate for supercapacitor applications.
- 4 November 2020
- Published by MDPI AG in Nanomaterials
- Vol. 10 (11) , 2195
Open AccessCost-Effective Synthesis of Efficient CoWO4/Ni Nanocomposite Electrode Material for Supercapacitor Applications
In the present study, the synthesis of CoWO4 (CWO)–Ni nanocomposites was conducted using a wet chemical method. The crystalline phases and morphologies of the Ni nanoparticles, CWO, and CWO–Ni composites were analyzed using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy-dispersive X-ray spectroscopy (EDAX). The electrochemical properties of CWO and CWO–Ni composite electrode materials were assessed by cyclic voltammetry (CV), and galvanostatic charge–discharge (GCD) tests using KOH as a supporting electrolyte. Among the CWO–Ni composites containing different amounts of Ni1, Ni2, and Ni3, CWO–Ni3 exhibited the highest specific capacitance of 271 F g−1 at 1 A g−1, which was greater than that of bare CWO (128 F g−1). Moreover, the CWO–Ni3 composite electrode material displayed excellent reversible cyclic stability and maintained 86.4% of its initial capacitance after 1500 discharge cycles. The results obtained herein demonstrate that the prepared CWO–Ni3 nanocomposite is a promising electrode candidate for supercapacitor applications.
- Open Access
- 23 February 2020
- Published by MDPI AG in Nanomaterials
- Vol. 10 (2) , 392
Nanofiber NiMoO4/g-C3N4 Composite Electrode Materials for Redox Supercapacitor Applications
NiMoO4/g-C3N4 was fabricated by a hydrothermal method and used as an electrode material in a supercapacitor. The samples were characterized by XRD, FTIR, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) to study the physical and structural properties of the as-prepared NiMoO4/g-C3N4 material. The electrochemical responses of pristine NiMoO4 and the NiMoO4/g-C3N4 nanocomposite material were investigated by cyclic voltammetry (CV), galvanostatic charge-discharge (GCD) and electrochemical impedance spectroscopy (EIS). From the CD studies, the NiMoO4/g-C3N4 nanocomposite revealed a higher maximum specific capacitance (510 Fg−1) in comparison to pristine NiMoO4 (203 Fg−1). In addition, the NiMoO4/g-C3N4 composite electrode material exhibited high stability, which maintained up to 91.8% capacity even after 2000 charge-discharge cycles. Finally, NiMoO4/g-C3N4 was found to exhibit an energy density value of 11.3 Whkg−1. These findings clearly suggested that NiMoO4/g-C3N4 could be a suitable electrode material for electrochemical capacitors.
- 23 February 2020
- Published by MDPI AG in Nanomaterials
- Vol. 10 (2) , 392
Open AccessNanofiber NiMoO4/g-C3N4 Composite Electrode Materials for Redox Supercapacitor Applications
NiMoO4/g-C3N4 was fabricated by a hydrothermal method and used as an electrode material in a supercapacitor. The samples were characterized by XRD, FTIR, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) to study the physical and structural properties of the as-prepared NiMoO4/g-C3N4 material. The electrochemical responses of pristine NiMoO4 and the NiMoO4/g-C3N4 nanocomposite material were investigated by cyclic voltammetry (CV), galvanostatic charge-discharge (GCD) and electrochemical impedance spectroscopy (EIS). From the CD studies, the NiMoO4/g-C3N4 nanocomposite revealed a higher maximum specific capacitance (510 Fg−1) in comparison to pristine NiMoO4 (203 Fg−1). In addition, the NiMoO4/g-C3N4 composite electrode material exhibited high stability, which maintained up to 91.8% capacity even after 2000 charge-discharge cycles. Finally, NiMoO4/g-C3N4 was found to exhibit an energy density value of 11.3 Whkg−1. These findings clearly suggested that NiMoO4/g-C3N4 could be a suitable electrode material for electrochemical capacitors.
- Open Access
Enhanced Catalytic Dechlorination of 1,2-Dichlorobenzene Using Ni/Pd Bimetallic Nanoparticles Prepared by a Pulsed Laser Ablation in Liquid
Bimetallic nanoparticles (NPs) exhibit advantageous electrical, optical, and catalytic properties. Among the various NP synthesis methods, pulsed laser ablation in liquid (PLAL) is currently attracting much attention because of its simplicity and versatility. In this study, a pulsed laser was used to produce nickel/palladium (Ni/Pd) bimetallic NPs in methanol and deionized water. The morphological and optical properties of the resulting Ni/Pd bimetallic NPs were characterized. The synthesized Ni/Pd bimetallic NPs were used for the dechlorination of 1,2-dichlorobenzene (1,2-DCB) under various conditions. The dechlorination rates of 1,2-DCB while using single (Ni and Pd) and bimetallic (Ni powder/Pd and Ni/Pd) NPs were investigated. The results showed that the Ni/Pd bimetallic NPs with 19.16 wt.% Pd exhibited much enhanced degradation efficiency for 1,2-DCB (100% degradation after 30 min). Accordingly, the results of enhanced the degradation of 1,2-DCB provide plausible mechanism insights into the catalytic reaction.
Open AccessEnhanced Catalytic Dechlorination of 1,2-Dichlorobenzene Using Ni/Pd Bimetallic Nanoparticles Prepared by a Pulsed Laser Ablation in Liquid
Bimetallic nanoparticles (NPs) exhibit advantageous electrical, optical, and catalytic properties. Among the various NP synthesis methods, pulsed laser ablation in liquid (PLAL) is currently attracting much attention because of its simplicity and versatility. In this study, a pulsed laser was used to produce nickel/palladium (Ni/Pd) bimetallic NPs in methanol and deionized water. The morphological and optical properties of the resulting Ni/Pd bimetallic NPs were characterized. The synthesized Ni/Pd bimetallic NPs were used for the dechlorination of 1,2-dichlorobenzene (1,2-DCB) under various conditions. The dechlorination rates of 1,2-DCB while using single (Ni and Pd) and bimetallic (Ni powder/Pd and Ni/Pd) NPs were investigated. The results showed that the Ni/Pd bimetallic NPs with 19.16 wt.% Pd exhibited much enhanced degradation efficiency for 1,2-DCB (100% degradation after 30 min). Accordingly, the results of enhanced the degradation of 1,2-DCB provide plausible mechanism insights into the catalytic reaction.