AI Article Synopsis

  • Metal-sulfide electrodes have theoretical energy density advantages but face practical limitations, prompting the exploration of a sulfur-rich MoS chalcogel for lithium-sulfide batteries (LiSBs).
  • The structure of the MoS chalcogel was analyzed using advanced techniques like Raman spectroscopy and X-ray absorption, revealing a unique 3D network bonded by S-S connections.
  • Li/MoS half-cells exhibited impressive initial capacity and maintained stable performance over 140 cycles, suggesting the MoS chalcogel's promise as an effective electrode material for energy storage systems.

Article Abstract

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.

Download full-text PDF

Source
http://dx.doi.org/10.1002/cssc.202400084DOI Listing

Publication Analysis

Top Keywords

mos chalcogel
16
x-ray absorption
8
mos
6
chalcogel high-capacity
4
high-capacity electrode
4
electrode conversion-based
4
conversion-based li-ion
4
li-ion batteries
4
batteries despite
4
despite large
4

Similar Publications

Article Synopsis
  • Metal-sulfide electrodes have theoretical energy density advantages but face practical limitations, prompting the exploration of a sulfur-rich MoS chalcogel for lithium-sulfide batteries (LiSBs).
  • The structure of the MoS chalcogel was analyzed using advanced techniques like Raman spectroscopy and X-ray absorption, revealing a unique 3D network bonded by S-S connections.
  • Li/MoS half-cells exhibited impressive initial capacity and maintained stable performance over 140 cycles, suggesting the MoS chalcogel's promise as an effective electrode material for energy storage systems.
View Article and Find Full Text PDF

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 PDF

Chemically activating MoS via spontaneous atomic palladium interfacial doping towards efficient hydrogen evolution.

Nat 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 PDF

Anion-Redox Mechanism of MoO(S)(2,2'-bipyridine) for Electrocatalytic Hydrogen Production.

J 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 PDF

Chalcogenide Aerogels as Sorbents for Noble Gases (Xe, Kr).

ACS 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.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!