Hee Cheul Choi

In Vivo Near-Infrared Mediated Tumor Destruction by Photothermal Effect of Carbon Nanotubes

The photothermal therapy using nanomaterials has been recently attracted as an efficient strategy for the next generation of cancer treatments. Single walled carbon nanotube (SWNT) is an upcoming potent candidate for the photothermal therapeutic agent since it generates significant amounts of heat upon excitation with near-infrared light (NIR, lambda = 700-1100 nm) which is transparent to biological systems including skins. Such a photothermal effect can be employed to induce thermal cell death in a noninvasive manner. Here, we demonstrate in vivo obliteration of solid malignant tumors by the combined treatments of SWNTs and NIR irradiation. The photothermally treated mice displayed complete destruction of the tumors without harmful side effects or recurrence of tumors over 6 months, while the tumors treated in other control groups were continuously grown until the death of the mice. Most of the injected SWNTs were almost completely excreted from mice bodies in about 2 months through biliary or urinary pathway. These results suggest that SWNTs may potentially serve as an effective photothermal agent and pave the way to future cancer therapeutics.

Electroluminescence from Graphene Quantum Dots Prepared by Amidative Cutting of Tattered Graphite

Size-controlled graphene quantum dots (GQDs) are prepared via amidative cutting of tattered graphite. The power of this method is that the size of the GQDs could be varied from 2 to over 10 nm by simply regulating the amine concentration. The energy gaps in such GQDs are narrowed down with increasing their size, showing colorful photoluminescence from blue to brown. We also reveal the roles of defect sites in photoluminescence, developing long-wavelength emission and reducing exciton lifetime. To assess the viability of the present method, organic light-emitting diodes employing our GQDs as a dopant are first demonstrated with the thorough studies in their energy levels. This is to our best knowledge the first meaningful report on the electroluminescence of GQDs, successfully rendering white light with the external quantum efficiency of ca. 0.1%.

Synthesis and properties of molybdenum disulphide: from bulk to atomic layers

Molybdenum disulphide (MoS2) has been one of the most interesting materials for scientists and engineers for a long time. While its bulk form has been in use in conventional industries as an intercalation agent and a dry lubricant for many years, its two-dimensional forms have attracted growing attention in recent years for applications in nano-electronic applications. Specifically, the single layer form of MoS2 shows significant potential as a semiconductor analogue of graphene. These exciting applications are spread over many fields, from flexible and transparent transistor devices, to low-power, high efficiency biological and chemical sensing applications. This Review Article, for the first time, provides a comprehensive overview of the synthesis, structural polytypes, properties, and applications of bulk, few layer, and single layer MoS2.

Catalyst-free Direct Growth of a Single to a Few Layers of Graphene on a Germanium Nanowire for the Anode Material of a Lithium Battery†

Direct growth of a single to a few layers of graphene on a germanium nanowire (Gr/Ge NW; see picture) was achieved by a metal-catalyst-free chemical vapor deposition (CVD) process. The Gr/Ge NW was used as anode in a lithium ion battery. This material has a specific capacity of 1059 mA h g(-1) at 4.0 C, a long cycle life over 200 cycles, and a high capacity retention of 90%.

Copper-vapor-assisted chemical vapor deposition for high-quality and metal-free single-layer graphene on amorphous SiO2 substrate.

We report that high-quality single-layer graphene (SLG) has been successfully synthesized directly on various dielectric substrates including amorphous SiO2/Si by a Cu-vapor-assisted chemical vapor deposition (CVD) process. The Cu vapors produced by the sublimation of Cu foil that is suspended above target substrates without physical contact catalyze the pyrolysis of methane gas and assist nucleation of graphene on the substrates. Raman spectra and mapping images reveal that the graphene formed on a SiO2/Si substrate is almost defect-free and homogeneous single layer. The overall quality of graphene grown by Cu-vapor-assisted CVD is comparable to that of the graphene grown by regular metal-catalyzed CVD on a Cu foil. While Cu vapor induces the nucleation and growth of SLG on an amorphous substrate, the resulting SLG is confirmed to be Cu-free by synchrotron X-ray photoelectron spectroscopy. The SLG grown by Cu-vapor-assisted CVD is fabricated into field effect transistor devices without transfer steps that are generally required when SLG is grown by regular CVD process on metal catalyst substrates. This method has overcome two important hurdles previously present when the catalyst-free CVD process is used for the growth of SLG on fused quartz and hexagonal boron nitride substrates, that is, high degree of structural defects and limited size of resulting graphene, respectively.

Spatially Resolved Spontaneous Reactivity of Diazonium Salt on Edge and Basal Plane of Graphene without Surfactant and Its Doping Effect

The site-dependent and spontaneous functionalization of 4-bromobenzene diazonium tetrafluoroborate (4-BBDT) and its doping effect on a mechanically exfoliated graphene (MEG) were investigated. The spatially resolved Raman spectra obtained from both edge and basal region of MEG revealed that 4-BBDT molecules were noncovalently functionalized on the basal region of MEG, while they were covalently bonded to the edge of MEG. The chemical doping effect induced by noncovalently functionalized 4-BBDT molecules on a basal plane region of MEG was successfully explicated by Raman spectroscopy. The position of Fermi level of MEG and the type of doping charge carrier induced by the noncovalently adsorbed 4-BBDT molecules were determined from systematic G band and 2D band changes. The successful spectroscopic elucidation of the different bonding characters of 4-BBDT depending on the site of graphene is beneficial for the fundamental studies about the charge transfer phenomena of graphene as well as for the potential applications, such as electronic devices, hybridized composite structures, etc.

A 3.5 V lithium-iodine hybrid redox battery with vertically aligned carbon nanotube current collector.

A lithium-iodine (Li-I2) cell using the triiodide/iodide (I3(-)/I(-)) redox couple in an aqueous cathode has superior gravimetric and volumetric energy densities (∼ 330 W h kg(-1) and ∼ 650 W h L(-1), respectively, from saturated I2 in an aqueous cathode) to the reported aqueous Li-ion batteries and aqueous cathode-type batteries, which provides an opportunity to construct cost-effective and high-performance energy storage. To apply this I3(-)/I(-) aqueous cathode for a portable and compact 3.5 V battery, unlike for grid-scale storage as general target of redox flow batteries, we use a three-dimensional and millimeter thick carbon nanotube current collector for the I3(-)/I(-) redox reaction, which can shorten the diffusion length of the redox couple and provide rapid electron transport. These endeavors allow the Li-I2 battery to enlarge its specific capacity, cycling retention, and maintain a stable potential, thereby demonstrating a promising candidate for an environmentally benign and reusable portable battery.

Direct growth of graphene pad on exfoliated hexagonal boron nitride surface

A direct and metal layer-free growth of flat graphene pads on exfoliated hexagonal boron nitride substrate (h-BN) are demonstrated by atmospheric chemical vapour deposition (CVD) process. Round shape with high flatness graphene pads are grown in high yield (∼95%) with a pad thickness of ∼0.5 nm and homogenous diameter.

The critical effect of solvent geometry on the determination of fullerene (C60) self-assembly into dot, wire and disk structures

Geometrically defined C60 self-assembled disks, wires and dots have been systematically obtained via a solution drop-drying process at room temperature; during this process, we discovered that there is a critical correlation between the geometry of the solvent and the final geometry of the self-assembled C60 structure.

Synthesis of Single‐Crystal Tetra(4‐pyridyl)porphyrin Rectangular Nanotubes in the Vapor Phase

Stacking up: One-dimensional single-crystalline rectangular nanotubes (RNTs) of 5,10,15,20-tetra(4-pyridyl)porphyrin (H(2)TPyP, see picture) are synthesized by a vaporization-condensation-recrystallization process. The single-crystal X-ray diffraction and selected-area electron diffraction data reveal that the H(2)TPyP RNTs form by self-stacking of H(2)TPyP units through hydrogen-bonding, H-pi, and pi-pi intermolecular interactions.