Mo3S13 Chalcogel: A High‐Capacity Electrode for Conversion‐Based Li‐Ion Batteries

Author:

Islam Taohedul1,Chandra Roy Subrata1,Bayat Sahar2,Adigo Weret Misganaw1,Hoffman Justin M.3,Rao Keerthan R.2,Sawicki Conrad4,Nie Jing1,Alam Robiul1,Oketola Oluwaseun1,Donley Carrie L.5,Kumbhar Amar5,Feng Renfei6,Wiaderek Kamila M.3,Risko Chad2,Amin Ruhul4ORCID,Islam Saiful M.1ORCID

Affiliation:

1. Department of Chemistry Physics, and Atmospheric Sciences Jackson State University 39217 Jackson MS USA

2. Department of Chemistry & Center for Applied Energy Research University of Kentucky 40506-0055 Lexington KY USA

3. X-ray Science Division Advanced Photon Source Argonne National Laboratory 60439 Argonne Illinois USA

4. Electrification and Energy Infrastructures Division Oak Ridge National Laboratory Hardin Valley Campus 37830 Knoxville TN USA

5. Department of Chemistry University of North Carolina at Chapel Hill 27599-3290 Chapel Hill NC USA

6. Canadian Light Source S7 N 2 V3 Saskatoon Saskatchewan Canada

Abstract

AbstractDespite large theoretical energy densities, metal‐sulfide electrodes for energy storage systems face several limitations that impact the practical realization. Here, we present the solution‐processable, room temperature (RT) synthesis, local structures, and application of a sulfur‐rich Mo3S13 chalcogel as a conversion‐based electrode for lithium‐sulfide batteries (LiSBs). The structure of the amorphous Mo3S13 chalcogel is derived through operando Raman spectroscopy, synchrotron X‐ray pair distribution function (PDF), X‐ray absorption near edge structure (XANES), and extended X‐ray absorption fine structure (EXAFS) analysis, along with ab initio molecular dynamics (AIMD) simulations. A key feature of the three‐dimensional (3D) network is the connection of Mo3S13 units through S−S bonds. Li/Mo3S13 half‐cells deliver initial capacity of 1013 mAh g−1 during the first discharge. After the activation cycles, the capacity stabilizes and maintains 312 mAh g−1 at a C/3 rate after 140 cycles, demonstrating sustained performance over subsequent cycling. Such high‐capacity and stability are attributed to the high density of (poly)sulfide bonds and the stable Mo−S coordination in Mo3S13 chalcogel. These findings showcase the potential of Mo3S13 chalcogels as metal‐sulfide electrode materials for LiSBs.

Funder

Savannah River National Laboratory

Publisher

Wiley

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