Spatial Progression of Polysulfide Reactivity with Lithium Nitrate in Li–Sulfur Batteries
Source abstract
Abstract
LiNO 3 is a common electrolyte additive in Li–S batteries, but its stabilizing effect is not well-understood due to the complex electrolyte chemistry. This complexity often hampers the clear characterization and interpretation of data. Herein, we explore the LiNO 3 reactivity with polysulfide through in operando sulfur K-edge spectroscopy, using a sulfur-free electrolyte with LiNO 3 as the sole salt. We reveal a spatially progressing chemical reaction influenced by the polysulfide concentration gradient. Polysulfides are electrochemically generated near the sulfur cathode, leading to a high local concentration. As a result, they are incompletely oxidized by LiNO 3 to sulfites, which are gradually further oxidized into sulfonates and sulfates. Conversely, polysulfides near the anode side have a lower local concentration as they are diffused from the cathode side, thus leading to more highly oxidized species like sulfonates and sulfates. These reaction products are stable during electrochemical cycling, suggesting their capabilities to passivate the electrodes and contribute to the cycling stabilities of Li–S batteries.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Advanced Battery Technologies Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Chemistry Division, Brookhaven National Laboratory, Upton, New York 11973, United States
National Synchrotron Radiation Lightsource II, Brookhaven National Laboratory, Upton, New York 11973, United States
Funding
Vehicle Technologies Office
References (28)
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