In order to improve the electrochemical performance of the NiCo₂O₄ material, Ni ions were partially substituted with Cu²⁺ ions having excellent reducing ability. All of the electrodes were fabricated by growing the Ni_1−xCu_xCo₂O₄ electrode spinel-structural active materials onto the graphite felt (GF). Five types of electrodes, NiCo₂O₄/GF, Ni_0.875Cu_0.125Co₂O₄/GF, Ni_0.75Cu_0.25Co₂O₄/GF, Ni_0.625Cu_0.375Co₂O₄/GF, and Ni_0.5Cu_0.5Co₂O₄/GF, were prepared for application to the oxygen evolution reaction (OER). As Cu²⁺ ions were substituted, the electrochemical performances of the NiCo₂O₄-based structures were improved, and eventually the OER activities were also greatly increased. In particular, the Ni_0.75Cu_0.25Co₂O₄/GF electrode exhibited the best OER activity in a 1.0 M KOH alkaline electrolyte: the cell voltage required to reach a current density of 10 mA cm⁻² was only 1.74 V (η = 509 mV), and a low Tafel slope of 119 mV dec⁻¹ was obtained. X-ray photoelectron spectroscopy (XPS) analysis of Ni_1−xCu_xCo₂O₄/GF before and after OER revealed that oxygen vacancies are formed around active metals by the insertion of Cu ions, which act as OH-adsorption sites, resulting in high OER activity. Additionally, the stability of the Ni_0.75Cu_0.25Co₂O₄/GF electrode was demonstrated through 1000th repeated OER acceleration stability tests with a high faradaic efficiency of 94.3%.

The purpose of this study was to evaluate the surface properties of ZnO nanomaterials based on their ability to photodegrade methyl blue dye (MB) and to show their antibacterial properties against different types of Gram-positive bacteria (Bacillus manliponensis, Micrococcus luteus, Staphylococcus aureus) and Gram-negative bacteria (Escherichia coli). In this study, ZnO nanomaterials were synthesized rapidly and easily in the presence of 1–4 M NaOH at a low temperature of 40 °C within 4 h. It was found that the ZnO nanomaterials obtained from the 1.0 M (ZnO–1M) and 2.0 M (ZnO–2M) aqueous solutions of NaOH had spherical and needle-shaped forms, respectively. As the concentration of NaOH increased, needle thickness increased and the particles became rod-like. Although the ZnO nanomaterial shapes were different, the bandgap size remained almost unchanged. However, as the NaOH concentration increased, the energy position of the conduction band shifted upward. Photo current curves and photoluminescence intensities suggested that the recombination between photoexcited electrons and holes was low in the ZnO–4M materials prepared in 4.0 M NaOH solution; however, charge transfer was easy. ∙O₂⁻ radicals were generated more than ∙OH radicals in ZnO–4M particles, showing stronger antibacterial activity against both Gram-positive and Gram-negative bacteria and stronger decomposition ability on MB dye. The results of this study suggest that on the ZnO nanomaterial surface, ∙O₂⁻ radicals generated are more critical for antibacterial activity than particle shape.

The layered Ni-rich NiCoMn (NCM)-based cathode active material Li[Ni_xCo_(1−x)/2Mn_(1−x)/2]O₂ (x ≥ 0.6) has the advantages of high energy density and price competitiveness over an LiCoO₂-based material. Additionally, NCM is beneficial in terms of its increasing reversible discharge capacity with the increase in Ni content; however, stable electrochemical performance has not been readily achieved because of the cation mixing that occurs during its synthesis. In this study, various layer-structured Li_1.0[Ni_0.8Co_0.1Mn_0.1]O₂ materials were synthesized, and their electrochemical performances were investigated. A NiCoMnCO₃ precursor, prepared using carbonate co-precipitation with Li₂CO₃ as the lithium source and having a sintering temperature of 850 °C, sintering time of 25 h, and metal to Li molar ratio of 1.00–1.05 were found to be the optimal parameters/conditions for the preparation of Li_1.0[Ni_0.8Co_0.1Mn_0.1]O₂. The material exhibited a discharge capacity of 160 mAhg⁻¹ and capacity recovery rate of 95.56% (from a 5.0–0.1 C-rate).