Porous and Amorphous Mn(x)Mo(3)S(13) Chalcogel Electrode for High-Capacity Conversion-Based Lithium-Ion Batteries.

TitlePorous and Amorphous Mn(x)Mo(3)S(13) Chalcogel Electrode for High-Capacity Conversion-Based Lithium-Ion Batteries.
Publication TypeJournal Article
Year of Publication2025
JournalJournal of the American Chemical Society
Volume147
Issue9
Pagination7400-7410
Date Published2025
ISSN0002-7863
Abstract

While Li-ion batteries (LIBs) are a leading energy storage technology, their energy densities are limited by the low capacity of conventional intercalation cathodes, driving interest in high energy-density Li-S batteries that make use of conversion chemistry. Achieving high capacity, reversibility, and cycle stability, and controlling volume changes in conversion batteries during the charge-discharge process, however, remains challenging. Here, we present a porous, amorphous, sulfide-based MnMoS chalcogel, which concurrently offers high capacity and cycle stability. The solution-processable room temperature synthesized MnMoS ( = 0.25) chalcogel exhibits a local structure that resembles the MoS cluster with Mn distributed across the MoS matrix, as determined by synchrotron X-ray pair distribution function (PDF) and extended X-ray absorption fine structure (EXAFS). Ab initio molecular dynamics (AIMD) simulations reveal that Mn incorporation shortens the polysulfide chain in the gel matrix compared to the MoS chalcogel, while forming a coordination environment with disulfide groups, analogous to the experimental findings. A Li/MnMoS half-cell delivers 897 mAh g capacity during the first discharge and retains 571 mAh g capacity after 100 cycles at a C/3 rate. Distribution of relaxation time (DRT) unveils a stable solid-electrolyte interphase (SEI) formation upon cycling that enables charge-discharge reversibility. Here, the enhanced capacity retention and cycle stability compared to those of the Li/MoS cell are attributed to the reduced dissolution of active mass into the electrolyte, facilitated by the formation of shorter polysulfide chains within the MnMoS structure and the strong affinity of Lewis-acidic Mn for polysulfide anions generated during the charge-discharge process of the Li/MnMoS cell. Thus, this work illustrates a design principle of material for high-capacity and cycle-stable Li-metal sulfide batteries.

URLhttps://doi.org/10.1021/jacs.4c15552
DOI10.1021/jacs.4c15552
Short TitleJ Am Chem Soc