Namjo Jeong

High power density of reverse electrodialysis with pore-filling ion exchange membranes and a high-open-area spacer

In the present study, a novel reverse electrodialysis (RED) stack with ultrathin lab-made pore-filling membranes and a high-open-area spacer was proposed to enhance the gross power density. The proposed stack had much lower internal resistance than a typical RED stack at optimum flow rates of seawater and river water. Therefore, a gross power density of 2.4 W m−2 was achieved.

Direct printing and reduction of graphite oxide for flexible supercapacitors

We report direct printing and photo-thermal reduction of graphite oxide (GO) to obtain a highly porous pattern of interdigitated electrodes, leading to a supercapacitor on a flexible substrate. Key parameters optimized include the amount of GO delivered, the suitable photo-thermal energy level for effective flash reduction, and the substrate properties for appropriate adhesion after reduction. Tests with supercapacitors based on the printed-reduced GO showed performance comparable with commercial supercapacitors: the energy densities were 1.06 and 0.87 mWh/cm3 in ionic and organic electrolytes, respectively. The versatility in the architecture and choice of substrate makes this material promising for smart power applications.

Single-crystal apatite nanowires sheathed in graphitic shells: synthesis, characterization, and application.

Vertically aligned one-dimensional hybrid structures, which are composed of apatite and graphitic structures, can be beneficial for orthopedic applications. However, they are difficult to generate using the current method. Here, we report the first synthesis of a single-crystal apatite nanowire encapsulated in graphitic shells by a one-step chemical vapor deposition. Incipient nucleation of apatite and its subsequent transformation to an oriented crystal are directed by derived gaseous phosphorine. Longitudinal growth of the oriented apatite crystal is achieved by a vapor-solid growth mechanism, whereas lateral growth is suppressed by the graphitic layers formed through arrangement of the derived aromatic hydrocarbon molecules. We show that this unusual combination of the apatite crystal and the graphitic shells can lead to an excellent osteogenic differentiation and bony fusion through a programmed smart behavior. For instance, the graphitic shells are degraded after the initial cell growth promoted by the graphitic nanostructures, and the cells continue proliferation on the bare apatite nanowires. Furthermore, a bending experiment indicates that such core-shell nanowires exhibited a superior bending stiffness compared to single-crystal apatite nanowires without graphitic shells. The results suggest a new strategy and direction for bone grafting materials with a highly controllable morphology and material conditions that can best stimulate bone cell differentiation and growth.

Microscopic and spectroscopic analyses of Pt-decorated carbon nanowires formed on carbon fiber paper.

We report the synthesis of carbon nanowires (CNWs) via chemical vapor deposition using catalytic decomposition of ethanol on nanosized transition metals such as Co, Fe, and Ni. Dip-coating process was used for the formation of catalytic nanoparticles, inducing the growth of CNWs on the surface of the carbon fiber paper (CFP). The liquid ethanol used as carbon source was atomized by an ultrasonic atomizer and subsequently flowed into the reactor that was heated up to a synthesis temperature of 600-700°C. Microscopic images show that CNWs of <50 nm were densely synthesized on the surface of the CFP. Raman spectra reveal that a higher synthesis temperature leads to the growth of higher crystalline CNWs. In addition, we demonstrate the successful decoration of platinum nanoparticles on the surface of the prepared CNWs/CFP using the electrochemical deposition technique.

Effect of graphitic layers encapsulating single-crystal apatite nanowire on the osteogenesis of human mesenchymal stem cells.

An ideally designed scaffold for tissue engineering must be able to provide an environment that recapitulates the physiological conditions to control stem cell function. Here, we compared vertically aligned single-crystal apatite nanowires sheathed in graphitic layers (SANGs) with single-crystal apatite nanowires (SANs), which had the same geometric properties as--but differing nanotopographic surface chemistry than--SANGs, in order to evaluate the effect of the graphitic layer on the behavior of human mesenchymal stem cells (hMSCs). The difference in nanotopographic surface chemistry did not affect hMSC adhesion, growth, or morphology. However, hMSCs were more effectively differentiated into bone cells on SANGs through interaction with graphitic layers, which later degraded and thereby allowed the cells to continue differentiation on the bare apatite nanowires. Thus, SANGs provide an excellent microenvironment for the osteogenic differentiation of hMCS.

High-density growth of carbon nanotubes with catalytic sites activated on nickel substrate

We describe the growth of carbon nanotubes (CNTs) from catalytic nanoparticles formed on a nickel surface. For the growth of CNTs, a chemical vapor deposition (CVD) furnace was set up and ethanol was used as carbon source. Observation of SEM images shows that CNTs grew densely on the nickel surface and that nanoparticles play a key role in the growth of the CNTs. XRD and Raman analyses reveal that the obtained products have graphitic pattern of multi-walled carbon nanotubes (MWCNTs). Also HRTEM images confirm clearly that the product was a MWCNT and their diameter was in the range of 20–50 nm.

Assessing the behavior of the feed-water constituents of a pilot-scale 1000-cell-pair reverse electrodialysis with seawater and municipal wastewater effluent

Reverse electrodialysis (RED) has vast potential as a clean, nonpolluting, and sustainable renewable energy source; however, pilot-scale RED studies employing real waters remain rare. This study reports the largest RED (1000 cell pairs, 250 m2) with municipal wastewater effluent (1.3-5.7 mS/cm) and seawater (52.9-53.8 mS/cm) as feed solutions. The RED stack was operated at a velocity of 1.5 cm/s and the pilot plant produced 95.8 W of power (0.38 W/m2total membrane or 0.76 W/m2cell pair). During operation of the RED, the inlet design of the stack, comprising thin spacers, and the water dissociation reaction at the cathode were revealed as vulnerabilities of the stack. Specifically, pressure drops at the fluid inlet parts had the most detrimental effects on power output due to clogged spacers around the inlet parts. In addition, precipitates resulting in inorganic fouling were inevitable during the water dissociation reaction due to significant potential generated by the stack in the cathode chamber. Na+ and Cl- accounted for the majority of ions transferred from seawater to wastewater effluent through ion exchange membranes (IEMs). Moreover, some divalent cations in seawater, Mg2+ and Ca2+, were also transferred to the wastewater effluent. Some organics with relatively low molecular weights in the wastewater effluent passed through the IEMs, and their hydrophobic properties elevated the specific UV absorbance (SUVA) level in the seawater.

Fabrication of an Anion-Exchange Membrane by Pore-Filling Using Catechol–1,4-Diazabicyclo-[2,2,2]octane Coating and Its Application to Reverse Electrodialysis

We have successfully exploited the Michael-type addition reaction between catechol and DABCO (1,4-diazabicyclo-[2,2,2]octane) molecules under alkaline conditions for the formation of new quaternary ammonium (QA) groups in an anion-exchange membrane. The anion-exchange membranes (AEMs) were prepared using the pore-filling method by addition of electrolytes (vinyl benzyl trimethylammonium chloride (VBTMA), dopamine methacrylamide (DMA) bearing a catechol group, and ethylene glycol diacrylate as a cross-linker) to a porous substrate. The formation of new QA groups by the reaction of DABCO with catechol components was confirmed by characterization of new peaks in the Fourier transform infrared spectra of the AEMs. The DABCO-bound AEM demonstrated a significant decrease in area resistance (0.4 Ω·cm2) and increase in permselectivity (94%). Furthermore, the electrochemical properties of the AEMs could be controlled by altering the concentrations of VBTMA and DMA and the formation of new bonds between DMA and DABCO. The calculated theoretical (4.31 W/m2) and practical (1.52 W/m2) power densities during a reverse electrodialysis (RED) process employing the membrane with the best properties (E2C1-DMA0.5-DABCO) were by 33 and 18% higher than those of a system utilizing a commercial membrane, Neosepta AMX (3.25 and 1.29 W/m2). Therefore, the AEM synthesized in this study is a good candidate for use in RED applications.

Direct Growth of Graphitic Carbon-Encapsulating Carbonate Apatite Nanowires from Calcium Carbonate

We report the direct chemical vapor deposition of graphitic carbon-encapsulating carbonate apatite nanowires (GCECANs)/hexagonal portlandite-phased Ca(OH)2 hybrid structures from CaCO3 powder at 900 °C. The formation mechanism of the GCECANs is investigated in detail through a structural and morphological characterization of the final products. Spectroscopic analyses elucidate the effect of H2 concentration in the reactor on the transformation of the calcite-phased CaCO3 into vaterite-phased CaCO3 and subsequently portlandite-phased Ca(OH)2. The results show that GCECANs are formed on the surface of the derived Ca(OH)2. It is especially remarkable that a higher H2 concentration results in the precipitated growth of such hybrid structures. Microscopic images show that GCECANs 20 nm in diameter grew up to 3 μm in length along the direction corresponding to the [001] plane of the hexagonal apatite crystal. In addition, the electrical properties of the GCECANs are measured by using an electrode with 150 nm gap.

Facile and controllable synthesis of carbon-encapsulating carbonate apatite nanowires from biomass containing calcium compounds such as CaC2O4 and CaCO3

We report the synthesis of carbon-encapsulating carbonate apatite nanowires through vapor–solid growth by heat-treatment of biomass comprising calcium compounds such as CaC2O4 or CaCO3 at 900 °C using both PH3 and C2H2 as the reactants. The thermal decomposition of CaC2O4 or CaCO3 to CaO with increasing temperature (CaC2O4 → CaCO3 + CO → CaO + CO2) is the key to achieving the growth of such core–shell nanowires. First, vapor-phase reactions between the gaseous calcium species generated from the derived CaO and gaseous molecules derived from thermal reactions of the reactants (PH3 and C2H2) lead to the oriented growth of core–shell nanowires along the [001] plane. Second, the CO2 generated during the decomposition of CaCO3 may be primarily responsible for the incorporation of carbonate ions into the apatite structure. Nanowire growth with knots along the growth direction reveals that our approach is very controllable. Additional demonstrations using kenaf fibers further verify that other types of biomass too are usable.