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Dive into the research topics where Sung-Jin Chang is active.

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Featured researches published by Sung-Jin Chang.


Advanced Materials | 2013

Microporous Carbon Nanoplates from Regenerated Silk Proteins for Supercapacitors

Young Soo Yun; Se Youn Cho; Jinyong Shim; Byung Hoon Kim; Sung-Jin Chang; Seung Jae Baek; Yun Suk Huh; Yongsug Tak; Yung Woo Park; Sungjin Park; Hyoung-Joon Jin

Novel carbon-based microporous nanoplates containing numerous heteroatoms (H-CMNs) are fabricated from regenerated silk fibroin by the carbonization and activation of KOH. The H-CMNs exhibit superior electrochemical performance, displaying a specific capacitance of 264 F/g in aqueous electrolytes, a specific energy of 133 Wh/kg, a specific power of 217 kW/kg, and a stable cycle life over 10000 cycles.


Advanced Materials | 2013

Hierarchical Hollow Spheres of Fe2O3@Polyaniline for Lithium Ion Battery Anodes

Jae-Min Jeong; Bong Gill Choi; Soon Chang Lee; Kyoung G. Lee; Sung-Jin Chang; Young-Kyu Han; Young Boo Lee; Hyun Uk Lee; Soonjo Kwon; Gaehang Lee; Chang-Soo Lee; Yun Suk Huh

Hierarchical hollow spheres of Fe2 O3 @polyaniline are fabricated by template-free synthesis of iron oxides followed by a post in- and exterior construction. A combination of large surface area with porous structure, fast ion/electron transport, and mechanical integrity renders this material attractive as a lithium-ion anode, showing superior rate capability and cycling performance.


Nanoscale | 2012

High performance of a solid-state flexible asymmetric supercapacitor based on graphene films

Bong Gill Choi; Sung-Jin Chang; Hyun-Wook Kang; Chan Pil Park; Hae Jin Kim; Won Hi Hong; SangGap Lee; Yun Suk Huh

Solid-state flexible energy storage devices hold the key to realizing portable and flexible electronic devices. Achieving fully flexible energy storage devices requires that all of the essential components (i.e., electrodes, separator, and electrolyte) with specific electrochemical and interfacial properties are integrated into a single solid-state and mechanically flexible unit. In this study, we describe the fabrication of solid-state flexible asymmetric supercapacitors based on an ionic liquid functionalized-chemically modified graphene (IL-CMG) film (as the negative electrode) and a hydrous RuO(2)-IL-CMG composite film (as the positive electrode), separated with polyvinyl alcohol-H(2)SO(4) electrolyte. The highly ordered macroscopic layer structures of these films arising through direct flow self-assembly make them simultaneously excellent electrical conductors and mechanical supports, allowing them to serve as flexible electrodes and current collectors in supercapacitor devices. Our asymmetric supercapacitors have been optimized with a maximum cell voltage up to 1.8 V and deliver a high energy density (19.7 W h kg(-1)) and power density (6.8 kW g(-1)), higher than those of symmetric supercapacitors based on IL-CMG films. They can operate even under an extremely high rate of 10 A g(-1) with 79.4% retention of specific capacitance. Their superior flexibility and cycling stability are evident in their good performance stability over 2000 cycles under harsh mechanical conditions including twisted and bent states. These solid-state flexible asymmetric supercapacitors with their simple cell configuration could offer new design and fabrication opportunities for flexible energy storage devices that can combine high energy and power densities, high rate capability, and long-term cycling stability.


Nano Letters | 2013

Hydrogen-induced morphotropic phase transformation of single-crystalline vanadium dioxide nanobeams.

Woong-Ki Hong; Jong Bae Park; Jongwon Yoon; Bong-Joong Kim; Jung Inn Sohn; Young Boo Lee; Tae-Sung Bae; Sung-Jin Chang; Yun Suk Huh; Byoungchul Son; Eric A. Stach; Takhee Lee; Mark E. Welland

We report a morphotropic phase transformation in vanadium dioxide (VO2) nanobeams annealed in a high-pressure hydrogen gas, which leads to the stabilization of metallic phases. Structural analyses show that the annealed VO2 nanobeams are hexagonal-close-packed structures with roughened surfaces at room temperature, unlike as-grown VO2 nanobeams with the monoclinic structure and with clean surfaces. Quantitative chemical examination reveals that the hydrogen significantly reduces oxygen in the nanobeams with characteristic nonlinear reduction kinetics which depend on the annealing time. Surprisingly, the work function and the electrical resistance of the reduced nanobeams follow a similar trend to the compositional variation due mainly to the oxygen-deficiency-related defects formed at the roughened surfaces. The electronic transport characteristics indicate that the reduced nanobeams are metallic over a large range of temperatures (room temperature to 383 K). Our results demonstrate the interplay between oxygen deficiency and structural/electronic phase transitions, with implications for engineering electronic properties in vanadium oxide systems.


Nanoscale | 2014

In situ probing of doping- and stress-mediated phase transitions in a single-crystalline VO2 nanobeam by spatially resolved Raman spectroscopy

Sung-Jin Chang; Jong Bae Park; Gaehang Lee; Hae Jin Kim; Jin-Bae Lee; Tae-Sung Bae; Young-Kyu Han; Tae Jung Park; Yun Suk Huh; Woong-Ki Hong

We demonstrate an experimental in situ observation of the temperature-dependent evolution of doping- and stress-mediated structural phase transitions in an individual single-crystalline VO₂ nanobeam on a Au-coated substrate under exposure to hydrogen gas using spatially resolved Raman spectroscopy. The nucleation temperature of the rutile R structural phase in the VO₂ nanobeam upon heating under hydrogen gas was lower than that under air. The spatial structural phase evolution behavior along the length of the VO₂ nanobeam under hydrogen gas upon heating was much more inhomogeneous than that along the length of the same nanobeam under air. The triclinic T phase of the VO₂ nanobeam upon heating under hydrogen gas transformed to the R phase and this R phase was stabilized even at room temperature in air after sample cooling. In particular, after the VO₂ nanobeam with the R phase was annealed at approximately 250 °C in air, it exhibited the monoclinic M1 phase (not the T phase) at room temperature during heating and cooling cycles. These results were attributed to the interplay between hydrogen doping and stress associated with nanobeam-substrate interactions. Our study has important implications for engineering metal-insulator transition properties and developing functional devices based on VO₂ nanostructures through doping and stress.


ACS Applied Materials & Interfaces | 2015

Dopamine-Assisted Synthesis of Carbon-Coated Silica for PCR Enhancement

Ji Young Park; Seung Hun Back; Sung-Jin Chang; Seok Jae Lee; Kyoung G. Lee; Tae Jung Park

Polymerase chain reaction (PCR) has become one of the most popular methods to identify genomic information on cells and tissues as well as to solve crimes and check genetic diseases. Recently, the nanomaterials including nanocomposite and nanoparticles have been considered as a next generation of solution to improve both quality and productivity of PCR. Herein, taking into these demands, carbon-coated silica was synthesized using silica particles via polymerization of biocompatible dopamine (PD) to form polydopamine (PDA) film and carbonization of PDA into graphitic structures. For further investigation of the effects of as-prepared silica, PDA-coated silica (PDA silica), and carbonized PDA silica (C-PDA silica), two different types of genes were adopted to investigate the influences of them in the PCR. Furthermore, the strong interaction between the nanocomposites and PCR reagents including polymerase and primers enables regulation of the PCR performance. The effectiveness of the nanocomposites was also confirmed through adopting the conventional PCR and real-time PCR with two different types of DNA as realistic models and different kinds of analytical methods. These findings could provide helpful insight for the potential application in biosensors and biomedical diagnosis.


Nanotechnology | 2013

Probing the photothermally induced phase transitions in single-crystalline vanadium dioxide nanobeams

Sung-Jin Chang; Woong-Ki Hong; Hae Jin Kim; Jin Bae Lee; Jongwon Yoon; Heung Cho Ko; Yun Suk Huh

Using Raman spectroscopy, we demonstrated photothermally induced crystallographic phase transitions of vanadium dioxide (VO2) nanobeams clamped to and free-standing on a substrate. Compared to the temperature-dependent Raman measurements, the laser-power-dependent Raman characteristics provide substantial evidence for the photothermal origin of the phase transitions of the VO2 nanobeams. The laser power necessary to cause phase transitions in the free-standing nanobeam was approximately eight times smaller than the laser power used in the substrate-clamped nanobeam. Our study will enhance the understanding of the complex phase transitions of strongly correlated oxides and thereby provide a foundation for engineering desirable properties in novel devices.


Scientific Reports | 2015

Substrate-mediated strain effect on the role of thermal heating and electric field on metal-insulator transition in vanadium dioxide nanobeams

Min-Woo Kim; Wan-Gil Jung; Hyun-Cho; Tae-Sung Bae; Sung-Jin Chang; Ja-Soon Jang; Woong-Ki Hong; Bong-Joong Kim

Single-crystalline vanadium dioxide (VO2) nanostructures have recently attracted great attention because of their single domain metal-insulator transition (MIT) nature that differs from a bulk sample. The VO2 nanostructures can also provide new opportunities to explore, understand, and ultimately engineer MIT properties for applications of novel functional devices. Importantly, the MIT properties of the VO2 nanostructures are significantly affected by stoichiometry, doping, size effect, defects, and in particular, strain. Here, we report the effect of substrate-mediated strain on the correlative role of thermal heating and electric field on the MIT in the VO2 nanobeams by altering the strength of the substrate attachment. Our study may provide helpful information on controlling the properties of VO2 nanobeam for the device applications by changing temperature and voltage with a properly engineered strain.


Scientific Reports | 2016

Graphene growth from reduced graphene oxide by chemical vapour deposition: seeded growth accompanied by restoration.

Sung-Jin Chang; Moon Seop Hyun; Sung Myung; Min-A Kang; Jung Ho Yoo; Kyoung G. Lee; Bong Gill Choi; Youngji Cho; Gaehang Lee; Tae Jung Park

Understanding the underlying mechanisms involved in graphene growth via chemical vapour deposition (CVD) is critical for precise control of the characteristics of graphene. Despite much effort, the actual processes behind graphene synthesis still remain to be elucidated in a large number of aspects. Herein, we report the evolution of graphene properties during in-plane growth of graphene from reduced graphene oxide (RGO) on copper (Cu) via methane CVD. While graphene is laterally grown from RGO flakes on Cu foils up to a few hundred nanometres during CVD process, it shows appreciable improvement in structural quality. The monotonous enhancement of the structural quality of the graphene with increasing length of the graphene growth from RGO suggests that seeded CVD growth of graphene from RGO on Cu surface is accompanied by the restoration of graphitic structure. The finding provides insight into graphene growth and defect reconstruction useful for the production of tailored carbon nanostructures with required properties.


RSC Advances | 2015

A hybrid composite of gold and graphene oxide as a PCR enhancer

Ha Young Jeong; Seung Hun Baek; Sung-Jin Chang; MinHo Yang; Seok Jae Lee; Kyoung G. Lee; Tae Jung Park

A hybrid composite of gold-decorated graphene oxide (GO) was synthesized and applied as a PCR enhancer. The analysis of the results of PCR demonstrates that the gold and graphene oxide (Au/GO) hybrid composite improves PCR performance. The chemical interaction of the hybrid composite and the PCR components and the potential mechanism behind the hybrid composite-assisted PCR were also investigated and discussed.

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Bong Gill Choi

Kangwon National University

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Hae Jin Kim

Chungnam National University

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Woong-Ki Hong

Gwangju Institute of Science and Technology

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Gaehang Lee

University of Science and Technology

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Byung Hoon Kim

Incheon National University

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