Chemical and Structural Insights into Solid Electrolyte Interphase Evolution for Sodium Metal Electrodes
Source abstract
Abstract
The solid electrolyte interphase (SEI) critically governs the reversibility of sodium metal batteries, through dynamically mediating ion transport and interfacial reactions. However, its kinetic evolution under operating conditions, and how it influences interfacial stability, remains poorly understood. Here, we reveal that the SEI undergoes coupled chemical and mechanical changes during sodium plating and stripping, leading to spatial and temporal heterogeneity that drives interfacial degradation. Synchrotron operando grazing-incidence wide-angle X-ray scattering and soft X-ray absorption spectroscopy capture the sequential formation and dissolution of inorganic SEI phases (NaF, NaH, NaOH, Na 2 PO 3 F), accompanied by depth-dependent alterations in organic SEI components. Mesoscale modeling connects this evolving SEI heterogeneity to localized current density fluctuations and stress accumulation at the Na interface, identifying pathways to electrically isolated sodium formation. These findings show that SEI instability fundamentally limits reversibility in sodium metal batteries, and that controlling SEI chemistry–mechanics coupling is essential to achieving its durability.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Thermal Expansion and Ionic Conductivity · Advanced Battery Materials and Technologies · Advancements in Battery Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science and Chemical Engineering
Stony Brook University
School of Mechanical Engineering
Purdue University
National Synchrotron Light Source II
Brookhaven National Laboratory
Material Measurement Laboratory
National Institute of Standards and Technology
Funding
Basic Energy Sciences
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