Publications by authors named "JaeKook Kim"

The rapid capacity loss attributed to irreversible phase reactions and structural instability has consistently affected the development of P2-layered cathode materials. Moreover, the introduction of costly elements such as single or multiple dopants has failed to resolve the sustainability challenges in designing an optimal Mn-based layered oxide cathode. This study proposes a Co-Ni-free, poly-elemental doping strategy (Li, Mg, and Cu) combined with high sodium content for an Mn-based P2-layered cathode designed for Na ion storage.

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The current work describes a facile synthesis of spinel-type ZnCoO along with an additional phase, CoO, by simply maintaining a non-stoichiometric ratio of Zn and Co precursors. Pure ZnCoO and CoO were also synthesized using the same method to compare results. The obtained morphologies of samples show that small-sized nanoparticles are interconnected and form a porous nanosheet-like structure.

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Cationic alteration related to a sodium super ion conductor (NASICON)-structured NaV(PO) (NVP) is an effective strategy for formulating high-energy and stable cathodes for sodium-ion batteries (SIBs). In this study, we altered the structure of NVP with dual cations, namely, Cr and Fe, to develop NaVCrFe(PO) cathodes for SIBs with high-rate capability (∼71 mAh g at 100 C) and an extreme cycle life output (∼75 mAh g with 95% capacity retention for 10,000 cycles). These excellent electrochemical properties can be ascribed to the synergistic effects of Cr and Fe in the NVP structure, as verified experimentally and theoretically.

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Composite solid electrolytes (CSEs) have emerged as promising candidates for safe and high-energy-density solid-state lithium metal batteries (SSLMBs). However, concurrently achieving exceptional ionic conductivity and interface compatibility between the electrolyte and electrode presents a significant challenge in the development of high-performance CSEs for SSLMBs. To overcome these challenges, we present a method involving the in-situ polymerization of a monomer within a self-supported porous LiLaZrTaO (LLZT) to produce the CSE.

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Alloying-type metallic tin is perceived as a potential anode material for K-ion batteries owing to its high theoretical capacity and reasonable working potential. However, pure Sn still face intractable issues of inferior K storage capability owing to the mechanical degradation of electrode against large volume changes and formation of intermediary insulating phases K Sn and KSn during alloying reaction. Herein, the TiC/C-carbon nanotubes (CNTs) is prepared as an effective buffer matrix and composited with Sn particles (Sn-TiC/C-CNTs) through the high-energy ball-milling method.

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Recently, aqueous zinc ion batteries (AZIBs) have attracted significant attention owing to their high safety, low cost, and abundant raw materials. However, finding an affordable and stable cathode, which can reversibly store a substantial amount of Zn ions without damaging the original crystal structure, is still a major challenge for the practical application of ZIBs. It has already been demonstrated that δ-MnO is a promising cathode for AZIBs owing to its layered structure and superior electrochemical performance; however, the reported results are still unsatisfactory (especially cyclability).

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Lithium-sulfur (Li-S) batteries using LiS and Li-free anodes have emerged as a potential high-energy and safe battery technology. Although the operation of Li-S full batteries based on LiS has been demonstrated at room temperature, their effective use at a subzero temperature has not been realized due to the low electrochemical utilization of LiS. Here, ammonium nitrate (NHNO) is introduced as a functional additive that allows Li-S full batteries to operate at -10 °C.

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Solid-state batteries (SSBs) are ideal candidates for next-generation high-energy-density batteries in the Battery of Things era. Unfortunately, SSB application is limited by their poor ionic conductivity and electrode-electrolyte interfacial compatibility. Herein, in situ composite solid electrolytes (CSEs) are fabricated by infusing vinyl ethylene carbonate monomer into a 3D ceramic framework to address these challenges.

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Batteries using potassium metal (K-metal) anode are considered a new type of low-cost and high-energy storage device. However, the thermodynamic instability of the K-metal anode in organic electrolyte solutions causes uncontrolled dendritic growth and parasitic reactions, leading to rapid capacity loss and low Coulombic efficiency of K-metal batteries. Herein, an advanced electrolyte comprising 1 M potassium bis(fluorosulfonyl)imide (KFSI) + 0.

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Recently, a novel electrochemical regulation associated with a deposition/dissolution reaction on an electrode surface has been proven to show superiority in large-scale energy storage systems (ESSs). Hence, in the search for high-performance electrodes showcasing these novel regulations, we utilized a low-cost ZnO microsphere electrode to construct aqueous rechargeable batteries (ARBs) that supplied a harvestable and storable charge through electrochemical deposition/dissolution via a reversible manganese oxidation reaction (MOR)/manganese reduction reaction (MRR), respectively, induced by the inherent formation/dissolution of zinc basic sulfate in a mild aqueous electrolyte solution containing 2 M ZnSO and 0.2 M MnSO.

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Herein, we report the effect of using nanoparticles of LiFePO on the electrochemical properties of all-solid-state batteries (ASSBs) with a solid electrolyte. LiFePO (LFP) cathode materials are promising cathode materials in polymer-based composite solid electrolytes because of their limited electrochemical window range. However, LFP cathodes exhibit poor electric conductivity and sluggish lithium ion diffusion.

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In this study, V doped sodium titanate nanorods were successfully synthesized by a sol-gel method with different optimized vanadium concentrations. Before testing as a promising anode material for sodium ion battery (SIB) application, the samples were systematically characterized. It was clearly observed that V doping significantly affects the phase formation of sodium titanate samples and leads to the alteration of the major phase of NaTiO to a single NaTiO phase with increasing doping concentrations.

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In this article, we report the effect of a Li6LaZrAlO (LLZAO) composite Li(NiCoMn)O (NCM811) cathode material on the performance of all-solid-state batteries (ASSBs) with oxide-based organic/inorganic hybrid solid electrolytes. The layered structure of Ni-rich cathode material Li(Ni CoMn)O ( > 0.6) (NCM) exhibiting a high specific capacity is among the suitable cathode materials for next-generation energy storage systems, particularly electric vehicles and portable devices for all-solid-state batteries.

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In this study, we evaluated the properties exhibited by a composite solid electrolyte (CSE) prepared tailoring the particle size of an active filler, LiLaZrTaO (LLZTO). The average particle size was reduced to 2.53 μm ball milling and exhibited a specific surface area of 3.

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In this study, magnesium-ion-substituted, sodium-deficient, P3- and P2-layered manganese oxide cathodes (NaMgMnO) were synthesized through a facile polyol-assisted combustion technique for applications in sodium-ion batteries. The electrochemical reaction pathways, structural integrity, and long cycling ability at low current rates of the P3- and P2-phases of the NaMgMnO cathodes were investigated using time-consuming techniques, such as galvanostatic titration and series cyclic voltammetry. The results obtained from these techniques were supported by those obtained from operando X-ray diffraction (XRD) analysis.

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Aqueous rechargeable zinc ion batteries (ARZIBs) have gained wide interest in recent years as prospective high power and high energy devices to meet the ever-rising commercial needs for large-scale eco-friendly energy storage applications. The advancement in the development of electrodes, especially cathodes for ARZIB, is faced with hurdles related to the shortage of host materials that support divalent zinc storage. Even the existing materials, mostly based on transition metal compounds, have limitations of poor electrochemical stability, low specific capacity, and hence apparently low specific energies.

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Metal-sulfur batteries (MSBs) provide high specific capacity due to the reversible redox mechanism based on conversion reaction that makes this battery a more promising candidate for next-generation energy storage systems. Recently, along with elemental sulfur (S ), sulfurized polyacrylonitrile (SPAN), in which active sulfur moieties are covalently bounded to carbon backbone, has received significant attention as an electrode material. Importantly, SPAN can serve as a universal cathode with minimized metal-polysulfide dissolution because sulfur is immobilized through covalent bonding at the carbon backbone.

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The growing demand for green energy has fueled the exploration of sustainable and eco-friendly energy storage systems. To date, the primary focus has been solely on the enhancement of lithium-ion battery (LIB) technologies. Recently, the increasing demand and uneven distribution of lithium resources have prompted extensive attention toward the development of other advanced battery systems.

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Manganese (Mn)-based cathode materials have garnered huge research interest for rechargeable aqueous zinc-ion batteries (AZIBs) due to the abundance and low cost of manganese and the plentiful advantages of manganese oxides including their different structures, wide range of phases, and various stoichiometries. A novel in situ generated Mn-deficient ZnMnO@C (Mn-d-ZMO@C) nanoarchitecture cathode material from self-assembly of ZnO-MnO@C for rechargeable AZIBs is reported. Analytical techniques confirm the porous and crystalline structure of ZnO-MnO@C and the in situ growth of Mn deficient ZnMnO@C.

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Lithium-ion batteries (LIBs) are widely used in various electronic devices and have garnered a huge amount of attention. In addition, evaluation of the intrinsic properties of LIB cathode materials is of considerable interest for practical applications. Therefore, through first-principles calculations based on the density functional theory, we investigated the structural, electronic, electrochemical, and kinetic properties of mixed transition metals, that is, Ni-substituted LiMnPO (LMP) and LiMnPOF (LMPF) cathode materials, that is, LiMnNiPO (LMNP) and LiMnNiPOF (LMNPF), respectively, which have not been extensively studied.

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Herein, we synthesize a nanostructured bismuth sulfide/carbon nanotube composite and demonstrate its potential use as a high-capacity anode for K-ion batteries, for the first time. The composite anode shows reversible K-ion storage capabilities that are supported by density functional theory calculations.

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A composite of Si nanoparticles (SiNPs) and a two-dimensional (2D) porous conductive Ni3(2,3,6,7,10,11-hexaiminotriphenylene)2 (Ni3(HITP)2) metal-organic framework (MOF), namely Si/Ni3(HITP)2, is suggested as a potential anode material for Li-ion batteries (LIBs). The Ni3(HITP)2 MOF with a carbon backbone and evenly dispersed Ni and N heteroatoms showed high potential for mitigating the volume expansion of Si and enhancing the electronic conductivity as well as Li storage ability of the Si/Ni3(HITP)2 anode. The Si/Ni3(HITP)2 electrode delivered a reversible capacity of 2657 mA h g-1 after 100 cycles of discharge-charge at a rate of 0.

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A simple one-pot polyol-assisted pyro-technique has been adopted to synthesize highly crystalline, carbon-coated LiMnO (LMO/C) nanoparticles for use as a cathode material in rechargeable Li-ion battery (LIB) applications. The phase purity, structure and stoichiometry of the prepared cathode was confirmed using X-ray techniques that included high-resolution powder X-ray diffraction and X-ray absorption fine structure spectroscopy. Electron microscopy studies established that the synthetic technique facilitated the production of nano-sized LMO particles with uniform carbon coating.

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Reduced graphene oxide (rGO) sheets were synthesized by a modified Hummer's method without additional reducing procedures, such as chemical and thermal treatment, by appropriate drying of graphite oxide under ambient atmosphere. The use of a moderate drying temperature (250°C) led to mesoporous characteristics with enhanced electrochemical activity, as confirmed by electron microscopy and N adsorption studies. The dimensions of the sheets ranged from nanometres to micrometres and these sheets were entangled with each other.

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We explore NaV6O15 (NVO) nanorod cathodes prepared by a sol-gel method for aqueous rechargeable zinc-ion battery applications for the first time. The NVO cathode delivers a high capacity of 427 mA h g-1 at 50 mA g-1 current density. Furthermore, based on the mass of the active materials, it exhibits a high energy density of 337 W h kg-1.

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