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Oxygen-deficient TiO2−x interlayer enabling Li-rich Mn-based layered oxide cathodes with enhanced reversible capacity and cyclability† † Electronic supplementary information (ESI) available. See DOI: https://doi.org/10.1039/d3ra02125d

ABSTRACT: The unique anion redox mechanism of Li-rich Mn-based layered oxide (LMLO) cathodes endows them with a higher specific capacity compared with conventional cathodes. However, the irreversible anion redox reactions can cause structural degradation and sluggish electrochemical kinetics in the cathode, resulting in a poor electrochemical performance in the batteries. Thus, to address these issues, a single-sided conductive oxygen-deficient TiO2−x interlayer was applied on a commercial Celgard separator as a coating layer towards the LMLO cathode. After coating TiO2−x, the initial coulombic efficiency (ICE) of the cathode increased from 92.1% to 95.8%, the capacity retention improved from 84.2% to 91.7% after 100 cycles, and the rate performance of the cathode was significantly enhanced from 91.3 mA h g−1 to 203.9 mA h g−1 at 5C. Operando differential electrochemical mass spectroscopy (DEMS) showed that the coating layer could restrain the release of oxygen in the battery, especially from the initial formation process. The X-ray photoelectron spectroscopy (XPS) results demonstrated that the favorable oxygen absorption by the TiO2−x interlayer benefitted the suppression of side reactions and cathode structural evolution and favored the formation of a uniform cathode-electrolyte interphase on the LMLO cathode. This work provides an alternative path to address the issue of oxygen release in LMLO cathodes. The oxygen vacancies in the TiO2−x interlayer inhibit the release of oxygen, while Li+ migrates to the anode, thus enhancing the reversibility of the cathode structural evolution and favoring the formation of a cathode electrolyte interface.

SUBMITTER: Lei Y

PROVIDER: S-EPMC10240256 | biostudies-literature | 2023 Jun

REPOSITORIES: biostudies-literature

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Project description:Nanoparticles produced by bacteria, fungi, or plants generally have physicochemical properties such as size, shape, crystalline structure, magnetic properties, and stability which are difficult to obtain by chemical synthesis. For instance, Mn(II)-oxidizing organisms promote the biomineralization of manganese oxides with specific textures under ambient conditions. Controlling their crystallinity and texture may offer environmentally relevant routes of Mn oxide synthesis with potential technological applications, e.g., for energy storage. However, whereas the electrochemical activity of synthetic (abiotic) Mn oxides has been extensively studied, the electroactivity of Mn biominerals has been seldom investigated yet. Here we evaluated the electroactivity of biologically induced biominerals produced by the Mn(II)-oxidizer bacteria Pseudomonas putida strain MnB1. For this purpose, we explored the mechanisms of Mn biomineralization, including the kinetics of Mn(II) oxidation, under different conditions. Manganese speciation, biomineral structure, and texture as well as organic matter content were determined by a combination of X-ray diffraction, electron and X-ray microscopies, and thermogravimetric analyses coupled to mass spectrometry. Our results evidence the formation of an organic-inorganic composite material and a competition between the enzymatic (biotic) oxidation of Mn(II) to Mn(IV) yielding MnO2 birnessite and the abiotic formation of Mn(III), of which the ratio depends on oxygenation levels and activity of the bacteria. We reveal that a subtle control over the conditions of the microbial environment orients the birnessite to Mn(III)-phases ratio and the porosity of the assembly, which both strongly impact the bulk electroactivity of the composite biomineral. The electrochemical properties were tested in lithium battery configuration and exhibit very appealing performances (voltage, capacity, reversibility, and power capability), thanks to the specific texture resulting from the microbially driven synthesis route. Given that such electroactive Mn biominerals are widespread in the environment, our study opens an alternative route for the synthesis of performing electrode materials under environment-friendly conditions.

Dataset Information

Oxygen-deficient TiO2−x interlayer enabling Li-rich Mn-based layered oxide cathodes with enhanced reversible capacity and cyclability† † Electronic supplementary information (ESI) available. See DOI: https://doi.org/10.1039/d3ra02125d

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