Kyung Hee University · 工学
Professor Seung-Ho Yu's research lab specializes in advanced energy storage materials, with a primary focus on next-generation battery technologies. The lab investigates high-capacity anode materials for lithium-ion batteries, including nanostructured transition metal oxides and silicon-based composites, aiming to enhance energy density, cycling stability, and reaction kinetics. A key research direction involves operando characterization techniques—such as synchrotron X-ray diffraction, X-ray microscopy, and tomography—to visualize dynamic structural and morphological changes during battery operation, particularly in lithium metal and lithium-sulfur batteries. The lab also explores innovative nanoarchitectured materials, such as carbon-based cellular nanosheets, for superior electrochemical performance in sustainable energy applications.
Figures are computed from collected data and may differ slightly.
Developing high-energy-density electrodes for lithium ion batteries (LIBs) is of primary importance to meet the challenges in electronics and automobile industries in the near future. Conversion reaction-based transition metal oxides are attractive candidates for LIB anodes because of their high theoretical capacities. This review summarizes recent advances on the development of nanostructured transition metal oxides for use in lithium ion battery anodes based on conversion reactions. The oxide
The need/desire to lower the consumption of fossil fuels and its environmental consequences has reached unprecedented levels in recent years. A global effort has been undertaken to develop advanced renewable energy generation and especially energy storage technologies, as they would enable a dramatic increase in the effective and efficient use of renewable (and often intermittent) energy sources. The development of electrical energy storage (EES) technologies with high energy and power densities
As the need for the development of "beyond lithium" ion battery technologies continuous unabated, lithium sulfur batteries have attracted widespread attention due to their very high theoretical energy density of 2,600 Wh kg<sup>-1</sup>. However, despite much effort, the detailed reaction mechanism remains poorly understood. In this study, we have combined <i>operando</i> X-ray diffraction and X-ray microscopy along with X-ray tomography, to visualize the evolution of both the morphology and cry
Although Li metal has long been considered to be the ideal anode material for Li rechargeable batteries, our limited understanding of the complex mechanism of Li plating has hindered the widespread deployment of Li metal anodes. Therefore, operando studies are required to unambiguously reveal the complex mechanistic steps involved. In this study, we employed synchrotron-based X-ray imaging methods to visualize the evolution of Li plating/stripping under operando and, more importantly, practical
Kinetic studies with two different anaerobic mixed cultures (the PM and the EV cultures) were conducted to evaluate inhibition between chlorinated ethylenes. The more chlorinated ethylenes inhibited the reductive dechlorination of the less chlorinated ethylenes, while the less chlorinated ethylenes weakly inhibited the dechlorination of the more chlorinated ethylenes. Tetrachloroethylene (PCE) inhibited reductive trichloroethylene (TCE) dechlorination but not cis-dichloroethylene (c-DCE) dechlor
We report a simple synthetic method of carbon-based hybrid cellular nanosheets that exhibit outstanding electrochemical performance for many key aspects of lithium-ion battery electrodes. The nanosheets consist of close-packed cubic cavity cells partitioned by carbon walls, resembling plant leaf tissue. We loaded carbon cellular nanosheets with SnO2 nanoparticles by vapor deposition method and tested the performance of the resulting SnO2-carbon nanosheets as anode materials. The specific capacit
Two biokinetic models employing the Michaelis-Menten equation for anaerobic reductive dechlorination of tetrachloroethylene (PCE) and trichloroethylene (TCE) were developed. The models were compared with results from batch kinetic tests conducted over a wide range of PCE and TCE concentrations with two different dechlorinating cultures. One model applies Michaelis-Menten kinetics with competitive inhibition among chlorinated aliphatic hydrocarbons (CAHs), while the other model includes both comp
Abstract Non‐aqueous sol‐gel routes involving the reaction of metal oxide precursors in organic solvents (e.g., benzyl alcohol) at moderate temperature and pressure, offer advantages such as high purity, high reproducibility and the ability to control the crystal growth without the need of using additional ligands. In this paper, a study carried out on a series of iron oxide/reduced graphene oxide composites is presented to elucidate a structure‐properties relationship leading to an improved ele
Abstract The limited lifespan of aqueous zinc‐ion batteries (with vanadium‐oxide based cathodes) is constrained by practical applications due to corrosion accelerated by vanadium ions leaching from the cathode and uneven dendrite growth on the zinc metal anode. To address these issues, the difference in size between hydrated zinc ions (4.30 Å) in electrolyte and vanadium ions (8.34 Å) is considered. Uniformly coating the MOF‐801 nanoparticles (with a pore size of 6.0 Å) on the zinc foil formed a
Abstract Lithium, the lightest metal with the lowest standard reduction potential, has been long considered as the ultimate anode material for next‐generation high‐energy‐density batteries. However, an unexpected Li dendrite formation, which causes poor reversibility of electrochemical reactions and safety concerns, is a major problem that has to be solved for the commercialization of Li metal anodes. For the implementation of stable Li metal anodes, complete understanding on the dendritic Li fo
A one-pot template-free solvothermal synthesis of crystalline Li4Ti5O12 nanostructures based on the “benzyl alcohol route” is introduced. The 1–2 µm sized nanostructured spherical particles are constituted of nanocrystallites in the size range of a few nm. This is the first report showing that crystalline Li4Ti5O12 can be directly obtained by soft chemistry solution routes. The as-synthesized crystalline nanostructures show good lithium intercalation/deintercalation performances at high rates (u
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