Soomin Park

Removal characteristics of engineered nanoparticles by activated sludge.

Environmental release of engineered nanoparticles (NPs) has been on the rise due to the increased use of NPs in commercial products. In addition, the fate of NPs in sewage treatment processes may play an important role in determining the environmental release pathway of NPs. In this study, we investigated the removal of engineered NPs (AgNPs, TiO2NPs, and SiO2NPs) using activated sludge by evaluating the effects of several important factors of the NPs, including physicochemical properties, contact time between NPs and activated sludge, aquatic chemistry of sewage, and the presence of extracellular polymeric substances (EPS) in the activated sludge. For all three types of NPs tested, a considerable amount of NPs were removed after exposure to activated sludge in a time-dependent manner; nevertheless, the removal efficiencies depended on the type of NPs and seemed to be affected by the NP stability relative to the hydrodynamic diameter (HDD) and zeta potential. In addition, the presences of both ionic compounds and EPS significantly enhanced the NP removal efficiency, indicating that the instability of the NPs resulting from the ionic strength in sewage and entrapment of NP by EPS played an important role in NP removal by activated sludge. These results suggest that the removal efficiencies can be affected by the operating conditions of the activated sludge process and the conditions of the activated sludge; therefore, these factors should be considered when developing approaches to sufficiently remove NPs from sewage treatment plants.

Preparation of energy storage material derived from a used cigarette filter for a supercapacitor electrode.

We report on a one-step method for preparing nitrogen doped (N-doped) meso-/microporous hybrid carbon material (NCF) via the heat treatment of used cigarette filters under a nitrogen-containing atmosphere. The used cigarette filter, which is mostly composed of cellulose acetate fibers, can be transformed into a porous carbon material that contains both the mesopores and micropores spontaneously. The unique self-developed pore structure allowed a favorable pathway for electrolyte permeation and contact probability, resulting in the extended rate capability for the supercapacitor. The NCF exhibited a better rate capability and higher specific capacitance (153.8 F g(-1)) compared to that of conventional activated carbon (125.0 F g(-1)) at 1 A g(-1). These findings indicate that the synergistic combination of well-developed meso-/micropores, an enlarged surface area and pseudocapacitive behavior leads to the desired supercapacitive performance. The prepared carbon material is capable of reproducing its electrochemical performance during the 6000 cycles required for charge and discharge measurements.

Transparent and ultra-bendable all-solid-state supercapacitors without percolation problems

A technological foundation for transparent and ultra-bendable supercapacitors without percolation effects and depth limitations is introduced, with demonstrated examples in in- and out-of-plain ultra-deformation states. This prototype system, built on large-scale interdigitated pattern type electrodes, constitutes significant advances over existing energy systems for optoelectronic systems in terms of electrochemical performance (capacitance ∼405 F g−1) and flexibility (bending radius ∼1.5 mm).

Hybrid MnO2 Film with Agarose Gel for Enhancing the Structural Integrity of Thin Film Supercapacitor Electrodes

We report on the fabrication of a robust hybrid film containing MnO2 for achieving large areal capacitances. An agarose gel, as an ion-permeable and elastic layer coated on a current collector, plays a key role in stabilizing the deposited pseudocapacitive MnO2. Cyclic voltammetry and electrochemical impedance spectroscopy data indicate that the hybrid electrode is capable of exhibiting a high areal capacitance up to 52.55 mF cm(-2), with its superior structural integrity and adhesiveness to the current collector being maintained, even at a high MnO2 loading.

Preferential growth of Co3O4 anode material with improved cyclic stability for lithium-ion batteries

A strategy for the synthesis of Co3O4 embedded in a carbonaceous matrix using an agarose gel template is described. The close-packed and porous structures were formed by a preferential growth mechanism within a short time. The resulting structured Co3O4 electrode had a long cycling stability and high conductivity.

Fabrication and design equation of film-type large-scale interdigitated supercapacitor chips.

We report large-scale interdigitated supercapacitor chips based on pseudo-capacitive metal oxide electrodes. A novel method is presented, which provides a powerful fabrication technology of interdigitated supercapacitors operated by a pseudo-capacitive reaction. Also, we empirically develop an equation that describes the relationship between capacitance, mass, and sweep rate in an actual supercapacitor system.

Antibacterial nanocarriers of resveratrol with gold and silver nanoparticles

This study focused on the preparation of resveratrol nanocarrier systems and the evaluation of their in vitro antibacterial activities. Gold nanoparticles (AuNPs) and silver nanoparticles (AgNPs) for resveratrol nanocarrier systems were synthesized using green synthetic routes. During the synthesis steps, resveratrol was utilized as a reducing agent to chemically reduce gold and silver ions to AuNPs and AgNPs. This system provides green and eco-friendly synthesis routes that do not involve additional chemical reducing agents. Resveratrol nanocarriers with AuNPs (Res-AuNPs) and AgNPs (Res-AgNPs) were observed to be spherical and to exhibit characteristic surface plasmon resonance at 547 nm and at 412-417 nm, respectively. The mean size of the nanoparticles ranged from 8.32 to 21.84 nm, as determined by high-resolution transmission electron microscopy. The face-centered cubic structure of the Res-AuNPs was confirmed by high-resolution X-ray diffraction. Fourier-transform infrared spectra indicated that the hydroxyl groups and C=C in the aromatic ring of resveratrol were involved in the reduction reaction. Res-AuNPs retained excellent colloidal stability during ultracentrifugation and re-dispersion, suggesting that resveratrol also played a role as a capping agent. Zeta potentials of Res-AuNPs and Res-AgNPs were in the range of -20.58 to -48.54 mV. Generally, against Gram-positive and Gram-negative bacteria, the Res-AuNPs and Res-AgNPs exhibited greater antibacterial activity compared to that of resveratrol alone. Among the tested strains, the highest antibacterial activity of the Res-AuNPs was observed against Streptococcus pneumoniae. The addition of sodium dodecyl sulfate during the synthesis of Res-AgNPs slightly increased their antibacterial activity. These results suggest that the newly developed resveratrol nanocarrier systems with metallic nanoparticles show potential for application as nano-antibacterial agents with enhanced activities.

All-solid-state, origami-type foldable supercapacitor chips with integrated series circuit analogues

Patterning-assembly technology for energy storage systems can be a breakthrough for physicochemically limited energy storage systems. In this study, a concept of design with experimental proof is provided for an all-solid-state origami-type foldable supercapacitor by a novel patterning approach. The proposed system is composed of periodically assembled isolated electrodes (IEs) and sectionalized ion transferring paper (SITP), which are key factors for the densely packed series circuit analogues in the single system. The system shows a linear relationship between the potential window and the number of IEs, which does not have any limited asymptotic line. This system could increase energy and power simultaneously, which was conventionally not possible. Also, its folding characteristics accommodate highly stable stretching. These characteristics are proven by simulations based on ab-initio calculations and the finite-element method.

Interfacial Adsorption and Redox Coupling of Li4Ti5O12 with Nanographene for High-Rate Lithium Storage

Despite the many efforts to solve the problem associated with lithium storage at high rates, it is rarely achieved up until now. The design with experimental proof is reported here for the high rate of lithium storage via a core-shell structure composite comprised of a Li4Ti5O12 (LTO) core and a nanographene (NG) shell. The LTO-NG core-shell was synthesized via a first-principles understanding of the adsorption properties between LTO and NG. Interfacial reactions are considered between the two materials by a redox coupling effect. The large interfacial area between the LTO core and the NG shell resulted in a high electron-conducting path. It allowed rapid kinetics to be achieved for lithium storage and also resulted in a stable contact between LTO and NG, affording cyclic performance stability.

Preparation via an electrochemical method of graphene films coated on both sides with NiO nanoparticles for use as high-performance lithium ion anodes

We report on a simple strategy for the direct synthesis of a thin film comprising interconnected NiO nanoparticles deposited on both sides of a graphene sheet via cathodic deposition. For the co-electrodeposition, graphene oxide (GO) is treated with water-soluble cationic poly(ethyleneimine) (PEI) which acts as a stabilizer and trapping agent to form complexes of GO and Ni2+. The positively charged complexes migrate toward the stainless steel substrate, resulting in the electrochemical deposition of PEI-modified GO/Ni(OH)2 at the electrode surface under an applied electric field. The as-synthesized film is then converted to graphene/NiO after annealing at 350 ° C. The interconnected NiO nanoparticles are uniformly deposited on both sides of the graphene surface, as evidenced by field emission scanning electron microscopy, transmission electron microscopy and energy dispersive spectrometry. This graphene/NiO structure shows enhanced electrochemical performance with a large reversible capacity, good cyclic performance and improved electronic conductivity as an anode material for lithium ion batteries. A reversible capacity is retained above 586 mA h g−1 after 50 cycles. The findings reported herein suggest that this strategy can be effectively used to overcome a bottleneck problem associated with the electrochemical production of graphene/metal oxide films for lithium ion battery anodes.