Impacts of Mg doping on the structural properties and degradation mechanisms of a Li and Mn rich layered oxide cathode for lithium-ion batteries.

The Li- and Mn-rich layered oxide cathode material class is a promising cathode material type for high energy density lithium-ion batteries. However, this cathode material type suffers from layer to spinel structural transition during electrochemical cycling, resulting in energy density losses during repeated cycling. Thus, improving structural stability is an essential key for developing this cathode material family. Elemental doping is a useful strategy to improve the structural properties of cathode materials. This work examines the influences of Mg doping on the structural characteristics and degradation mechanisms of a Li1.2Mn0.4Co0.4O2 cathode material. The results reveal that the prepared cathode materials are a composite, exhibiting phase separation of the Li2MnO3 and LiCoO2 components. Li2MnO3 and LiCoO2 domain sizes decreased as Mg content increased, altering the electrochemical mechanisms of the cathode materials. Moreover, Mg doping can retard phase transition, resulting in reduced structural degradation. Li1.2Mn0.36Mg0.04Co0.4O2 with optimal Mg doping demonstrated improved electrochemical performance. The current work provides deeper understanding about the roles of Mg doping on the structural characteristics and degradation mechanisms of Li-and Mn-rich layered oxide cathode materials, which is an insightful guideline for the future development of high energy density cathode materials for lithium-ion batteries.

Disinfection efficiency test for contaminated surgical mask by using Ozone generator.

BACKGROUND: Ozone (O3) is an effective disinfectant agent that leaves no harmful residues. Due to the global health crisis caused by the COVID-19 pandemic, surgical masks are in high demand, with some needing to be reused in certain regions. This study aims to evaluate the effects of O3 for pathogen disinfection on reused surgical masks in various conditions. METHODS: O3 generators, a modified PZ 2-4 for Air (2000 mg O3/L) and a modified PZ 7 -2HO for Air (500 mg O3/L), were used together with 1.063 m3 (0.68 × 0.68 × 2.3 m) and 0.456 m3 (0.68 × 0.68 × 1.15 m) acrylic boxes as well as a room-sized 56 m3 (4 × 4 × 3.5 m) box to provide 3 conditions for the disinfection of masks contaminated with enveloped RNA virus (105 FFU/mL), bacteria (103 CFU/mL) and fungi (102 spores/mL). RESULTS: The virucidal effects were 82.99% and 81.70% after 15 min of treatment with 2000 mg/L O3 at 1.063 m3 and 500 mg/L O3 at 0.456 m3, respectively. The viral killing effect was increased over time and reached more than 95% after 2 h of incubation in both conditions. By using 2000 mg/L O3 in a 1.063 m3 box, the growth of bacteria and fungi was found to be completely inhibited on surgical masks after 30 min and 2 h of treatment, respectively. Using a lower-dose O3 generator at 500 mg O3/L in 0.456 m3 provided lower efficiency, although the difference was not significant. Using O3 at 2000 mg O3/L or 500 mg O3/L in a 56 m3 room is efficient for the disinfection of all pathogens on the surface of reused surgical masks. CONCLUSIONS: This study provided the conditions for using O3 (500-2000 mg/L) to reduce pathogens and disinfect contaminated surgical masks, which might be applied to reduce the inappropriate usage of reused surgical masks.

A multiscale investigation elucidating the structural complexities and electrochemical properties of layered-layered composite cathode materials synthesized at low temperatures.

Layered-layered composite (xLi2MnO3·(1 -x) LiMO2, M = Mn, Ni, Co, and Fe) cathode materials have attracted much attention as cathodes for high energy density lithium ion batteries. However, these materials are structurally unstable resulting from complicated phase transformation mechanisms during cycling. Additionally, the complex structural characteristics and structural stability of these materials largely depend on their preparation methods. Studying the correlation between multiscale structural properties and preparation methods is important in the development of layered-layered composite cathode materials. In this work, 0.5Li2MnO3·0.5LiCoO2 composite materials were prepared with different heating and cooling rates with a maximum temperature of 600 °C. The structural properties of the 0.5Li2MnO3·0.5LiMO2 composite materials were investigated using combined in situ X-ray absorption spectroscopy (XAS), in situ X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), and high resolution transmission electron microscopy (HRTEM) techniques. Heating and cooling rates have no significant effect on either the crystal or local atomic structures of the prepared samples. However, the microstructure was critically important for its impact on electrochemical properties.

Data on effect of electrospinning conditions on morphology and effect of heat-treatment temperature on the cycle and rate properties of core-shell LiFePO4/FeS/C composite fibers for use as cathodes in Li-ion batteries.

The data in this study are related to the research article "Core-shell electrospun and doped LiFePO4/FeS/C composite fibers for Li-ion batteries" [1]. Core-shell LiFePO4/FeS/C composites fiber were prepared via an electrospinning method for use as cathodes in Li-ion batteries. The data presented in this paper showed the effect of electrospinning parameters, including applied voltage, solution flow rate, the concentration of polyvinylpyrrolidone (PVP) (wt%) and a mixed PVP/PEO (polyethylene oxide) (w/w%) polymers on the morphological properties of composites fibers. These data were developed using scanning electron microscopy (SEM). Then, the effect of heat-treatment temperature on fiber morphology was investigated using transmission electron microscopy (TEM). The voltage profile and cycle rate properties of the core-shell LiFePO4/FeS/C composites obtained after various heat treatments were studied.

Rate dependent structural transition and cycling stability of a lithium-rich layered oxide material.

Lithium-rich layered oxide materials, xLi2MnO3·(1 - x)LiMO2 (M = Mn, Fe, Co, Ni, etc.), are a promising candidate for use as cathode materials in the batteries of electric vehicles (EVs). This is due to their high energy density (∼900 W h kg-1), which is larger than those of the currently used commercial cathode materials. Moreover, EV technologies require lithium ion batteries with a high rate performance to achieve short charging times. The high rate property largely depends on the electrochemical properties of the electrodes in these batteries. However, the correlation between the cycling rate, structural stability and electrochemical properties of cathode materials is not clearly understood. In this work, the influence of cycling rate on structural transition behaviors and cycling stability of a 0.5Li2MnO3·0.5LiCoO2 composite-based material was investigated. The experimental results reveal that cycling rates significantly affect the activation of the Li2MnO3 component. A high cycling rate retards Li2MnO3 activation, leading to a smaller spinel phase transition and a higher cycling stability.

Structural and Electrochemical Kinetic Properties of 0.5Li2MnO3∙0.5LiCoO2 Cathode Materials with Different Li2MnO3 Domain Sizes.

Lithium rich layered oxide xLi2MnO3∙(1-x)LiMO2 (M = Mn, Co, Ni, etc.) materials are promising cathode materials for next generation lithium ion batteries. However, the understanding of their electrochemical kinetic behaviors is limited. In this work, the phase separation behaviors and electrochemical kinetics of 0.5Li2MnO3∙0.5LiCoO2 materials with various Li2MnO3 domain sizes were studied. Despite having similar morphological, crystal and local atomic structures, materials with various Li2MnO3 domain sizes exhibited different phase separation behavior resulting in disparate lithium ion transport kinetics. For the first few cycles, the 0.5Li2MnO3∙0.5LiCoO2 material with a small Li2MnO3 domain size had higher lithium ion diffusion coefficients due to shorter diffusion path lengths. However, after extended cycles, the 0.5Li2MnO3∙0.5LiCoO2 material with larger Li2MnO3 domain size showed higher lithium ion diffusion coefficients, since the larger Li2MnO3 domain size could retard structural transitions. This leads to fewer structural rearrangements, reduced structural disorders and defects, which allows better lithium ion mobility in the material.

Li2MnO3 domain size and current rate dependence on the electrochemical properties of 0.5Li2MnO3·0.5LiCoO2 cathode material.

Layered-layered composite oxides of the form xLi2MnO3·(1-x) LiMO2 (M = Mn, Co, Ni) have received much attention as candidate cathode materials for lithium ion batteries due to their high specific capacity (>250mAh/g) and wide operating voltage range of 2.0-4.8 V. However, the cathode materials of this class generally exhibit large capacity fade upon cycling and poor rate performance caused by structural transformations. Since electrochemical properties of the cathode materials are strongly dependent on their structural characteristics, the roles of these components in 0.5Li2MnO3·0.5LiCoO2 cathode material was the focus of this work. In this work, the influences of Li2MnO3 domain size and current rate on electrochemical properties of 0.5Li2MnO3·0.5LiCoO2 cathodes were studied. Experimental results obtained showed that a large domain size provided higher cycling stability. Furthermore, fast cycling rate was also found to help reduce possible structural changes from layered structure to spinel structure that takes place in continuous cycling.

Virus-enabled synthesis and assembly of nanowires for lithium ion battery electrodes.

The selection and assembly of materials are central issues in the development of smaller, more flexible batteries. Cobalt oxide has shown excellent electrochemical cycling properties and is thus under consideration as an electrode for advanced lithium batteries. We used viruses to synthesize and assemble nanowires of cobalt oxide at room temperature. By incorporating gold-binding peptides into the filament coat, we formed hybrid gold-cobalt oxide wires that improved battery capacity. Combining virus-templated synthesis at the peptide level and methods for controlling two-dimensional assembly of viruses on polyelectrolyte multilayers provides a systematic platform for integrating these nanomaterials to form thin, flexible lithium ion batteries.