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Identification and Catalysis of the Potential-Limiting Step in Lithium-Sulfur Batteries
The Li-S chemistry is thermodynamically promising for high-density energy storage but kinetically challenging. Over the past few years, many catalyst materials have been developed to improve the performance of Li-S batteries and their catalytic role has been increasingly accepted. However, the classic catalytic behavior, i.e., reduction of reaction barrier, has not been clearly observed. Crucial mechanistic questions, including what specific step is limiting the reaction rate, whether/how it can be catalyzed, and how the catalysis is sustained after the catalyst surface is covered by solid products, remain unanswered. Herein, we report the first identification of the potential-limiting step of Li-S batteries operating under lean electrolyte conditions and its catalysis that conforms to classic catalysis principles, where the catalyst lowers the kinetic barrier of the potential-limiting step and accelerates the reaction without affecting the product composition. After carefully examining the electrochemistry under lean electrolyte conditions, we update the pathway of the Li-S battery reaction: S 8 solid is first reduced to Li 2 S 8 and Li 2 S 4 molecular species sequentially; the following reduction of Li 2 S 4 to a Li 2 S 2 -Li 2 S solid with an almost constant ratio of 1:4 is the potential-limiting step; the previously believed Li 2 S 2 -to-Li 2 S solid-solid conversion does not occur; the recharging reaction is relatively fast. We further demonstrate that supported cobalt phthalocyanine molecules can effectively catalyze the potential-limiting step. After Li 2 S 2 /Li 2 S buries the active sites, it can self-catalyze the reaction and continue driving the discharging process.
Low-tortuous and dense single-particle-layer electrode for high-energy lithium-sulfur batteries
Single-particle-layer sulfur electrodes are designed to build low-tortuosity through-pores across both vertical and planar directions of an electrode, enabling operation of low-porosity cathodes under practical conditions.
Triphilic organochalcogen compounds for high-capacity and stable solid-state lithium–sulfur batteries
Triphilic organochalcogen compounds are added to solid-state sulfur cathodes to establish intimate and durable interfacial contact among cathode components, enhancing ion and electron transport, active material utilization, and cycling stability.
Mediated Lithium-Sulfur Flow Battery for Grid-Scale Energy Storage.
Abstract not provided.
Predictive Engineering of Interfaces and Cathodes for High-Performance All Solid-State Lithium-Sulfur Batteries
The primary goal of this project is to leverage data-driven methods and machine learning strategies to develop accurate multi-physics models for all-solid-state Li-S battery (ASLSB) materials that can capture electrochemical and transport phenomena over atomic to mesoscopic length/timescales. These models will be rigorously validated by synthesis and advanced characterization experiments. The team will leverage the predictive power of these models, alongside synthesis/characterization experiments and battery fabrication to address longstanding issues at the electrode/electrolyte interfaces in ASLSBs. The project’s proposed technology involves the following: (1) halide-doped solid sulfide electrolytes that can concurrently provide high Li + ion conductivity and suppress dendrite growth; (2) novel mesoporous cathode composed of super-P and carbon nanotubes co-infiltrated with sulfur and sulfide electrolyte, which hold potential to allow high sulfur loading and optimal ion/electron pathways; and (3) functionalization of sulfide electrolyte with ionic liquids to improve physical contact and minimize impedance at the cathode/electrolyte interface. Successful development of proposed predictive models (at multiple scales) will bridge this knowledge gap and will advance fundamental understanding of reaction chemistry, kinetics, charge transfer, and dendrite growth at electrified SSIs. This will enable predictive design of effective strategies to mitigate interfacial problems in ASSLSBs, including poor interfacial contact, interfacial impedance to Li + ion transport, and poor electron/ion conduction within cathodes. Ultimately, the fundamental knowledge gained will lead to development of high-performance ASSLSBs.
Higher Surface Area Lithium Anode for Mediated Lithium-Sulfur Flow Batteries.
Abstract not provided.
Higher Energy Density Mediated Lithium-Sulfur Flow Batteries.
Abstract not provided.
Higher Energy Density Mediated Lithium-Sulfur Flow Batteries.
Abstract not provided.
Higher Energy Density Mediated Lithium-Sulfur Flow Batteries
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Mediated Lithium-Sulfur Flow Batteries
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Rational Design and Control of Mixed Ionic-electronic Conducting Metal Organic Frameworks for Lithium-sulfur Batteries
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High temperature storage characteristics of lithium sulfur dioxide cells
Hermetically sealed SO2 cells were developed to eliminate SO2 diffusion and its adverse effects on shelf life. A two part barrier coating material was applied to the internal surface of the glass seal and cured under a predetermined thermal profile in order to prevent the self discharge associated with glass seal corrosion.
Advances in Lithium-Sulfur Rechargeable Batteries Powering the Electronic Future
This viewgraph presentation discusses the Moltech Corporation's history and structure, power systems development, product attributes, Li-S adapted products, cell construction, specific energy comparisons, and product requirements necessary for use in spacecraft applications.
High Energy Density Lithium-Sulfur Batteries for Aerospace Applications
No abstract available
Performance Assessment of Prototype Lithium- Sulfur Cells from Oxis Energy
UNKNOWN