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Jonathan Maeyer

Bio: Jonathan Maeyer is an academic researcher. The author has contributed to research in topics: Dimethoxyethane & Gas evolution reaction. The author has an hindex of 1, co-authored 1 publications receiving 22 citations.

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Journal ArticleDOI
TL;DR: In this paper, the typical applications of computational chemistry in Li-S battery studies, correlating to characterization techniques, such as X-ray diffraction, infra-red & Raman spectra, X -ray absorption spectroscopy, binding energy, and nuclear magnetic resonance, are reviewed.

367 citations

Journal ArticleDOI
TL;DR: Lithium-sulfur batteries are considered a possible next-generation energy storage solution, but their commercial viability is still in question because of several technical challenges, including th... as mentioned in this paper.
Abstract: Lithium–sulfur batteries are considered a possible next-generation energy-storage solution, but their commercial viability is still in question because of several technical challenges, including th...

107 citations

Journal ArticleDOI
TL;DR: In this paper, the authors investigate the reaction processes and their correlation to cell cycling behavior and failure mechanisms, and find that catastrophic failure of high-energy Li-sulfur (Li-S) pouch cells results from uneven sulfur/polysulfide reactions and electrolyte depletion for the first tens of cycles.
Abstract: The lithium–sulfur (Li–S) battery is a promising next-generation energy storage technology because of its high theoretical energy and low cost. Extensive research efforts have been made on new materials and advanced characterization techniques for mechanistic studies. However, it is uncertain how discoveries made on the material level apply to realistic batteries due to limited analysis and characterization of real high-energy cells, such as pouch cells. Evaluation of pouch cells (>1 A h) (instead of coin cells) that are scalable to practical cells provides a critical understanding of current limitations which enables the proposal of strategies and solutions for further performance improvement. Herein, we design and fabricate pouch cells over 300 W h kg−1, compare the cell parameters required for high-energy pouch cells, and investigate the reaction processes and their correlation to cell cycling behavior and failure mechanisms. Spatially resolved characterization techniques and fluid-flow simulation reveal the impacts of the liquid electrolyte diffusion within the pouch cells. We found that catastrophic failure of high-energy Li–S pouch cells results from uneven sulfur/polysulfide reactions and electrolyte depletion for the first tens of cycles, rather than sulfur dissolution as commonly reported in the literature. The uneven reaction stems from limited electrolyte diffusion through the porous channels into the central part of thick cathodes during cycling, which is amplified both across the sulfur electrodes and within the same electrode plane. A combination of strategies is suggested to increase sulfur utilization, improve nanoarchitectures for electrolyte diffusion and reduce consumption of the electrolytes and additives.

100 citations

Journal ArticleDOI
TL;DR: In this paper, the main advances in this field since the first attempts in the mid 1970s are reviewed, including specific applications in all-solid-state (inorganic and polymeric), Li-Sulfur (Li-S) and Lithium-O2 (air) batteries.

85 citations