Hyeran Kim

Carboxymethyl chitosan-modified magnetic-cored dendrimer as an amphoteric adsorbent.

Carboxymethyl chitosan-modified magnetic-cored dendrimers (CCMDs) were successfully synthesized in a three step method. The synthesized samples were characterized using X-ray diffraction, transmission electron microscopy, scanning electron microscopy, vibrating sample magnetometer, thermogravimetry analysis, zeta potential analyzer, X-ray photoelectron spectroscopy, surface area analysis, and Fourier transform infrared spectroscopy. The CCMD exhibited selective adsorption for anionic and cationic compounds at specific pH conditions. With the substitution of amino groups of MD with carboxymethyl chitosan moieties, the adsorption sites for cationic compounds were greatly increased. Since the adsorption onto CCMD was mainly electrostatic interaction, the adsorption of MB and MO was significantly affected by the pHs. The optimal adsorption pH values were 3 and 11 for MO and MB. The maximal adsorption of MO and MB on the CCMD at pH values of 3 and 11 were 20.85mgg(-1) and 96.31mgg(-1), respectively. Reuse of the CCMD as an adsorbent was experimentally tested through adsorption and desorption with simple pH control. More than 99% and 91% of the initial adsorption of MB and MO on the CCMD was maintained with five consecutive recycling.

Influence of visible-light irradiation on physicochemical and photocatalytic properties of nitrogen-doped three-dimensional (3D) titanium dioxide.

We report highly active visible-light driven nitrogen-doped three-dimensional polycrystalline anatase TiO2 photocatalysts (N-3D TiO2) for environmental and biomedical applications. N-3D TiO2 is synthesized at a low temperature (<90°C) without thermal treatment via a modified hydrothermal process (HP) and ultrasound irradiation (UI). The N-3D TiO2 is additionally irradiated with visible-light to improve the hydroxylation of its surface. Under visible-light irradiation, the photocatalytic activity of visible-light irradiated N-3D TiO2 (*N-3D TiO2; [k]=1.435 h(-1)) is 26.1 times higher than that of 3D TiO2 ([k]=0.055 h(-1)). The *N-3D TiO2 is highly recyclable and retained 91.8% of the initial decolorization rate after fifteen cycles. Interestingly, the *N-3D TiO2 shows very strong antibacterial properties against both Gram-negative Escherichia coli (E. coli) and Gram-positive Staphylococcus aureus (S. aureus) after exposure to visible-light for 3h. The antibacterial properties of *N-3D TiO2 are more effective than those of TiO2, 3D TiO2, and N-3D TiO2. More than 91.3% of the E. coli is sterilized after ten cycles. There are a large increase in the photocatalytic and antibacterial activity of *N-3D TiO2 relative to that of N-3D TiO2 owing to the hydroxylation of the N-3D TiO2 surface as a result of the visible-light irradiation. These results indicate that *N-3D TiO2 might have utility in several promising applications such as highly efficient water/air treatment, inactivation of pathogenic microorganisms, and solar-energy conversion.

Advanced nanoporous TiO2 photocatalysts by hydrogen plasma for efficient solar-light photocatalytic application

We report an effect involving hydrogen (H2)-plasma-treated nanoporous TiO2(H-TiO2) photocatalysts that improve photocatalytic performance under solar-light illumination. H-TiO2 photocatalysts were prepared by application of hydrogen plasma of assynthesized TiO2(a-TiO2) without annealing process. Compared with the a-TiO2, the H-TiO2 exhibited high anatase/brookite bicrystallinity and a porous structure. Our study demonstrated that H2 plasma is a simple strategy to fabricate H-TiO2 covering a large surface area that offers many active sites for the extension of the adsorption spectra from ultraviolet (UV) to visible range. Notably, the H-TiO2 showed strong ·OH free-radical generation on the TiO2 surface under both UV- and visible-light irradiation with a large responsive surface area, which enhanced photocatalytic efficiency. Under solar-light irradiation, the optimized H-TiO2 120(H2-plasma treatment time: 120 min) photocatalysts showed unprecedentedly excellent removal capability for phenol (Ph), reactive black 5(RB 5), rhodamine B (Rho B) and methylene blue (MB) — approximately four-times higher than those of the other photocatalysts (a-TiO2 and P25) — resulting in complete purification of the water. Such well-purified water (>90%) can utilize culturing of cervical cancer cells (HeLa), breast cancer cells (MCF-7), and keratinocyte cells (HaCaT) while showing minimal cytotoxicity. Significantly, H-TiO2 photocatalysts can be mass-produced and easily processed at room temperature. We believe this novel method can find important environmental and biomedical applications.

Triangular Black Phosphorus Atomic Layers by Liquid Exfoliation

Few-layer black phosphorus (BP) is the most promising material among the two-dimensional materials due to its layered structure and the excellent semiconductor properties. Currently, thin BP atomic layers are obtained mostly by mechanical exfoliation of bulk BP, which limits applications in thin-film based electronics due to a scaling process. Here we report highly crystalline few-layer black phosphorus thin films produced by liquid exfoliation. We demonstrate that the liquid-exfoliated BP forms a triangular crystalline structure on SiO2/Si (001) and amorphous carbon. The highly crystalline BP layers are faceted with a preferred orientation of the (010) plane on the sharp edge, which is an energetically most favorable facet according to the density functional theory calculations. Our results can be useful in understanding the triangular BP structure for large-area applications in electronic devices using two-dimensional materials. The sensitivity and selectivity of liquid-exfoliated BP to gas vapor demonstrate great potential for practical applications as sensors.

Hierarchically three-dimensional (3D) nanotubular sea urchin-shaped iron oxide and its application in heavy metal removal and solar-induced photocatalytic degradation

In this study, hierarchically three-dimensional (3D) nanotubular sea urchin-shaped iron oxide nanostructures (3D-Fe2O3) were synthesized by a facile and rapid ultrasound irradiation method. Additives, templates, inert gas atmosphere, pH regulation, and other complicated procedures were not required. Dense 3D-Fe2O3 with a relatively large Brunauer-Emmett-Teller (BET) surface area of 129.4 m2/g was synthesized within 23 min, and the BET surface area was further improved to 282.7 m2/g by a post heat-treatment process. In addition, this post processing led to phase changes from maghemite (γ phase) to hematite (α phase) Fe2O3. Subsequent characterization suggested that the growth mechanism of the 3D-Fe2O3 follows self-assembly and oriented attachment. The prepared 3D-Fe2O3 was applied to wastewater purification. Ultrasound-irradiated 3D-Fe2O3 can eliminate a As(V) and Cr(VI) from water with 25 times faster removal rate by using a one third smaller amount than commercial α-Fe2O3. This was attributed to the inter-particle pores and relatively positively charged surface of the nanostructure. In addition, post heat treatment on ultrasound-irradiated 3D-Fe2O3 significantly influenced the photocatalytic degradation of methylene blue and phenol, with a 25 times higher removal efficiency than that of commercial α-Fe2O3, because of both high BET surface area and good crystallization of the prepared samples.

Studies on mass production and highly solar light photocatalytic properties of gray hydrogenated-TiO2 sphere photocatalysts

In this paper, it is first reported that gray hydrogenated TiO2 sphere photocatalysts (H-TiO2) with high reactivity to solar light are mass produced within a few minutes using an underwater discharge plasma modified sol-gel method at room temperature and atmospheric pressure. This plasma modified system is an easy one-step in-situ synthetic process and the crystallinity, hydrogenation, and spherical structure of H-TiO2 are achieved by the synergy effect between the continuous reaction of highly energetic atomic and molecular species generated from the underwater plasma and surface tension of water. The resultant H-TiO2 demonstrated high anatase/rutile bicrystallinity and extended optical absorption spectrum from the ultraviolet (UV) to visible range. Furthermore, various defects including oxygen vacancies and hydroxyl species on the TiO2 surface permitted the enhancement of the photocatalytic performance. It was demonstrated that H-TiO2 photocatalysts showed significant degradation efficiencies for reactive black 5 (RB 5), rhodamine B (Rho B), and phenol (Ph) under solar light irradiation, up to approximately 5 times higher than that of commercial anatase TiO2 (C-TiO2), which resulted in good water purification. Notably, it was also possible to cultivate HepG2 cells using such well-purified water (to degrees up to 76%), with minimal cytotoxicity. Considering all these results, we believe that this novel plasma technology is promising for important environmental applications.

Computational calculation identified optimal binding sites in nano-sized magnetic-cored dendrimer

Magnetic-cored dendrimers (MDs) with amino groups were prepared with the formation of poly(amidoamine) dendrimer on the surface of magnetite nanoparticles (MNPs). The experiment involved the binding of four different heavy metal ions including Pb (II), Cu (II), Zn (II), and Cr (VI). Density functional theory (DFT) calculation was applied to the experimental results to determine the optimal configurations between the heavy metal species and generation 1 amino (NH2) functionalized MD (G1-NH2-MD). Different binding configurations among the possible binding positions of inner and outer G1-NH2-MD were determined with the ionic radius and coordination number of each heavy metal ion. Although Pb2+ and Zn2+ were stable in the terminal positions, Cu2+ was the most stable in the internal position. The oxygen and hydrogen atoms of HCrO4- formed a hydrogen bond with the NH2 groups, and thus dipole-nonpolar molecular interaction occurred with the CH2 groups of G1-NH2-MD. Specific binding positions and energies of different heavy metal species were identified through the DFT calculation in the study. The DFT calculation results also contributed to an understanding of the binding priority of each metal ions in the mixed solution. Furthermore, Pb2+ was preferably adsorbed in the mixed solution of Pb2+, Cu2+, and Zn2+.