Dae-Chul Kim

Bio: Dae-Chul Kim is an academic researcher from KAIST. The author has contributed to research in topics: Catalysis & Sputtering. The author has an hindex of 9, co-authored 16 publications receiving 358 citations.

Application of Spinel-Type Cobalt Chromite as a Novel Catalyst for Combustion of Chlorinated Organic Pollutants

Abstract: Various chromium-containing catalysts were tested for the total oxidation of trichloroethylene (TCE) as a model reaction for the catalytic combustion of chlorinated organic pollutants. A spinel-type cobalt chromite (CoCr2O4) among others was proven to be a very promising catalyst showing higher activity and higher CO2 selectivity than traditional alumina supported chromia. Even if both Cr3+ and Cr6+ species were observed on the surface of CoCr2O4, the Cr6+ species was stable under reducing environment. The presence of Cr3+-Cr6+ pair sites and the effect of redox treatments on the activity were investigated to explain the nature of possible active sites for TCE decomposition. Higher selectivity to CO2 of CoCr2O4 was ascribed to the abundance of its Cr3+ species, together with its activity for water gas shift reaction.

Scalable functionalized graphene nano-platelets as tunable cathodes for high-performance lithium rechargeable batteries.

Abstract: High-performance and cost-effective rechargeable batteries are key to the success of electric vehicles and large-scale energy storage systems. Extensive research has focused on the development of (i) new high-energy electrodes that can store more lithium or (ii) high-power nano-structured electrodes hybridized with carbonaceous materials. However, the current status of lithium batteries based on redox reactions of heavy transition metals still remains far below the demands required for the proposed applications. Herein, we present a novel approach using tunable functional groups on graphene nano-platelets as redox centers. The electrode can deliver high capacity of ~250 mAh g−1, power of ~20 kW kg−1 in an acceptable cathode voltage range, and provide excellent cyclability up to thousands of repeated charge/discharge cycles. The simple, mass-scalable synthetic route for the functionalized graphene nano-platelets proposed in this work suggests that the graphene cathode can be a promising new class of electrode.

Rapid, High-Resolution 3D Interference Printing of Multilevel Ultralong Nanochannel Arrays for High-Throughput Nanofluidic Transport.

Abstract: 3D interference printing enables the single-step production of multilayered ultralong nanochannel arrays with nanoscale regularity. The superior depth-of-focus of this technique realizes a state-of-the-art nanostructure which has intensively stacked 32 layers of inch-long, horizonontal nanochannels with sub-100 nm holes in a monolithic matrix (≈15 μm). This exceptional structure can be integrated into microfluidic devices, facilitating high-flux rheological platforms using nanocapillarity.

Connected open structures from close-packed colloidal crystals by hyperthermal neutral beam etching.

Abstract: We report the fabrication of connected open structures from close-packed colloidal crystals by hyperthermal neutral beam etching. Colloidal crystal films of polystyrene microspheres were prepared by a vertical deposition method. Exposure of the colloidal crystal films to hyperthermal neutral beam made isolated microspheres in the face-centered cubic lattice, each of which was connected with its twelve nearest neighbors through very thin cylinders. Due to the charge neutrality of impinging gas molecules of the hyperthermal neutral beam, the spherical shape of polymer microspheres was almost maintained during the etching process. The Bragg reflection peaks were modulated by the etched volume of colloidal crystals. Finally, the inverse structures of such open structures were replicated by a simple room-temperature chemical vapor deposition and subsequently burning out polymer template spheres.

Aqueous Rechargeable Li and Na Ion Batteries

Abstract: Haegyeom Kim,†,∥ Jihyun Hong,†,∥ Kyu-Young Park,†,∥ Hyungsub Kim,†,∥ Sung-Wook Kim, and Kisuk Kang*,†,‡ †Department of Materials Science and Engineering, Research Institute of Advanced Materials (RIAM), Seoul National University, Gwanak-ro 1, Gwanak-gu, Seoul 151-742, Republic of Korea ‡Center for Nanoparticle Research, Institute for Basic Science (IBS), Seoul National University, Gwanak-ro 1, Gwanak-gu, Seoul 151-742, Republic of Korea Nuclear Fuel Cycle Development Group, Korea Atomic Energy Research Institute, 989-111 Daedeok-daero, Yuseong-gu, Daejeon 305-353, Republic of Korea

Recent Advances in the Catalytic Oxidation of Volatile Organic Compounds: A Review Based on Pollutant Sorts and Sources.

Abstract: It is well known that urbanization and industrialization have resulted in the rapidly increasing emissions of volatile organic compounds (VOCs), which are a major contributor to the formation of secondary pollutants (e.g., tropospheric ozone, PAN (peroxyacetyl nitrate), and secondary organic aerosols) and photochemical smog. The emission of these pollutants has led to a large decline in air quality in numerous regions around the world, which has ultimately led to concerns regarding their impact on human health and general well-being. Catalytic oxidation is regarded as one of the most promising strategies for VOC removal from industrial waste streams. This Review systematically documents the progresses and developments made in the understanding and design of heterogeneous catalysts for VOC oxidation over the past two decades. It addresses in detail how catalytic performance is often drastically affected by the pollutant sources and reaction conditions. It also highlights the primary routes for catalyst deactivation and discusses protocols for their subsequent reactivation. Kinetic models and proposed oxidation mechanisms for representative VOCs are also provided. Typical catalytic reactors and oxidizers for industrial VOC destruction are further discussed. We believe that this Review will provide a great foundation and reference point for future design and development in this field.

High-Power Lithium Batteries from Functionalized Carbon Nanotube Electrodes

Abstract: Energy storage devices that can deliver high powers have many applications, including hybrid vehicles and renewable energy. Much research has focused on increasing the power output of lithium batteries by reducing lithium-ion diffusion distances, but outputs remain far below those of electrochemical capacitors and below the levels required for many applications. Here, we report an alternative approach based on the redox reactions of functional groups on the surfaces of carbon nanotubes. Layer-by-layer techniques are used to assemble an electrode that consists of additive-free, densely packed and functionalized multiwalled carbon nanotubes. The electrode, which is several micrometres thick, can store lithium up to a reversible gravimetric capacity of approximately 200 mA h g(-1)(electrode) while also delivering 100 kW kg(electrode)(-1) of power and providing lifetimes in excess of thousands of cycles, both of which are comparable to electrochemical capacitor electrodes. A device using the nanotube electrode as the positive electrode and lithium titanium oxide as a negative electrode had a gravimetric energy approximately 5 times higher than conventional electrochemical capacitors and power delivery approximately 10 times higher than conventional lithium-ion batteries.

Peanut shell hybrid sodium ion capacitor with extreme energy–power rivals lithium ion capacitors

Abstract: This is the first report of a hybrid sodium ion capacitor (NIC) with the active materials in both the anode and the cathode being derived entirely from a single precursor: peanut shells, which are a green and highly economical waste globally generated at over 6 million tons per year. The electrodes push the envelope of performance, delivering among the most promising sodiation capacity–rate capability–cycling retention combinations reported in the literature for each materials class. Hence the resultant NIC also offers a state-of-the-art cyclically stable combination of energy and power, not only in respect to previously but also as compared to Li ion capacitors (LICs). The ion adsorption cathode based on Peanut Shell Nanosheet Carbon (PSNC) displays a hierarchically porous architecture, a sheet-like morphology down to 15 nm in thickness, a surface area on par with graphene materials (up to 2396 m2 g−1) and high levels of oxygen doping (up to 13.51 wt%). Scanned from 1.5–4.2 V vs. Na/Na+ PSNC delivers a specific capacity of 161 mA h g−1 at 0.1 A g−1 and 73 mA h g−1 at 25.6 A g−1. A low surface area Peanut Shell Ordered Carbon (PSOC) is employed as an ion intercalation anode. PSOC delivers a total capacity of 315 mA h g−1 with a flat plateau of 181 mA h g−1 occurring below 0.1 V (tested at 0.1 A g−1), and is stable at 10 000 cycles (tested at 3.2 A g−1). The assembled NIC operates within a wide temperature range (0–65 °C), yielding at room temperature (by active mass) 201, 76 and 50 W h kg−1 at 285, 8500 and 16 500 W kg−1, respectively. At 1.5–3.5 V, the hybrid device achieved 72% capacity retention after 10 000 cycles tested at 6.4 A g−1, and 88% after 100 000 cycles at 51.2 A g−1.