Despite 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 MoS chalcogel as a conversion-based electrode for lithium-sulfide batteries (LiSBs). The structure of the amorphous MoS 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 MoS units through S-S bonds. Li/MoS half-cells deliver initial capacity of 1013 mAh g during the first discharge. After the activation cycles, the capacity stabilizes and maintains 312 mAh g 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 MoS chalcogel. These findings showcase the potential of MoS chalcogels as metal-sulfide electrode materials for LiSBs.
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http://dx.doi.org/10.1002/cssc.202400084 | DOI Listing |
ChemSusChem
June 2024
Department of Chemistry, Physics, and Atmospheric Sciences, Jackson State University, 39217, Jackson, MS, USA.
Nanoscale
July 2022
School of Advanced Materials Science and Engineering, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Molybdenum disulfide (MoS)-based materials are extensively studied as promising hydrogen evolution reaction (HER) catalysts. In order to bring out the full potential of chalcogenide chemistry, precise control over the active sulfur sites and enhancement of electronic conductivity need to be achieved. This study develops a highly active HER catalyst with an optimized active site-controlled cobalt molybdenum sulfide (CoMoS) chalcogel/graphene oxide aerogel heterostructure.
View Article and Find Full Text PDFNat Commun
May 2018
State Key Laboratory of Electroanalytical Chemistry, Jilin Province Key Laboratory of Low Carbon Chemical Power, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 130022, Changchun, China.
Lacking strategies to simultaneously address the intrinsic activity, site density, electrical transport, and stability problems of chalcogels is restricting their application in catalytic hydrogen production. Herein, we resolve these challenges concurrently through chemically activating the molybdenum disulfide (MoS) surface basal plane by doping with a low content of atomic palladium using a spontaneous interfacial redox technique. Palladium substitution occurs at the molybdenum site, simultaneously introducing sulfur vacancy and converting the 2H into the stabilized 1T structure.
View Article and Find Full Text PDFJ Am Chem Soc
March 2017
Department of Chemistry and Biochemistry, The Ohio State University, 100 West 18th Avenue, Columbus, Ohio 43210, United States.
Redox processes of molybdenum-sulfide (Mo-S) compounds are important in the function of materials for various applications from electrocatalysts for the hydrogen evolution reaction (HER) to cathode materials for batteries. Our group has recently described a series of Mo-S molecular HER catalysts based on a MoO(S)L structural motif. Herein, reductive pathways of MoO(S)bpy (Mo-bpy) (bpy = 2,2'-bipyridine) are presented from both experimental and theoretical studies.
View Article and Find Full Text PDFACS Appl Mater Interfaces
October 2017
Department of Chemistry, Northwestern University, Evanston, Illinois 60208, United States.
High-surface-area molybdenum sulfide (MoS) and antimony sulfide (SbS) chalcogels were studied for Xe/Kr gas separation. The intrinsic soft Lewis basic character of the chalcogel framework is a unique property among the large family of porous materials and lends itself to a potential new approach toward the selective separation of Xe over Kr. Among these chalcogels, MoS shows the highest Xe and Kr uptake, reaching 0.
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