The kinetic properties of the chemical oxidation of aqueous polysulfide solutions have been studied in phosphate-buffered systems at pH 7-12, at temperatures between 20 and 40 degrees C, and ionic strength between 0.05 and 0.50 M. Polysulfide solutions were mixed with a buffer solution of known dissolved oxygen concentration, after which the decrease in the oxygen concentration of the solution was measured in time. The rate of oxygen consumption can be described by the empirical relation d[O2]/dt= -k[Sx(2-)][O2](0.59) . The reaction rate constant k is moderately dependent on pH and goes through a maximum at pH 10. The rate of oxygen consumption for polysulfide solutions is approximately four times higher than for sulfide solutions. At pH values below 9, reaction products were formed according to Sx(2-)+3/2O2-->S2O3(2-)+(x-2)S(0) . At pH values higher than 9, more thiosulfate and additional sulfide were formed, which is attributed to the low chemical stability of the sulfur of oxidation state zero, formed upon polysulfide oxidation. Our results strongly suggest that hydrolysis of this 'nascent' elemental sulfur to HS- and S2O3(2-) is faster than hydrolysis of crystalline inorganic sulfur or colloidal particles of biologically produced sulfur, and has a significant contribution already at 30 degrees C and pH 10.
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http://dx.doi.org/10.1016/j.watres.2005.08.006 | DOI Listing |
J Colloid Interface Sci
January 2025
School of Materials and Energy, and LONGi Institute of Future Technology, Lanzhou University, Lanzhou 730000 China. Electronic address:
Room-temperature sodium-sulfur (RT Na-S) batteries, known for their high-energy density, low cost and environmental friendliness, have attracted much attention. However, the development of RT Na-S batteries has encountered a number of challenges, including low conductivity and large volume changes of sulfur during the charge-discharge cycles. In this study, TiO nanoparticles modified porous carbon hosts for sulfur in RT Na-S batteries were prepared by a simple and efficient spray drying method combined with solution immersion.
View Article and Find Full Text PDFChemSusChem
January 2025
School of Mechanical and Materials Engineering, Washington State University, Pullman, WA-99164, USA.
Advancement of sulfur (S) cathode of lithium-sulfur (Li-S) batteries is hindered by issues such as insulating nature of sulfur, sluggish redox kinetics, polysulfide dissolution and shuttling. To address these issues, we initiate a study on applying an important amino acid of protein, arginine (Arg), as a functional additive into S cathode. Based on our simulation study, the positively charged Arg facilitates strong interactions with polysulfides.
View Article and Find Full Text PDFACS Energy Lett
December 2024
Catalan Institute of Nanoscience and Nanotechnology (ICN2), CSIC and BIST, Barcelona 08193, Spain.
Batteries based on sulfur cathodes offer a promising energy storage solution due to their potential for high performance, cost-effectiveness, and sustainability. However, commercial viability is challenged by issues such as polysulfide migration, volume changes, uneven phase nucleation, limited ion transport, and sluggish sulfur redox kinetics. Addressing these challenges requires insights into the structural, morphological, and chemical evolution of phases, the associated volume changes and internal stresses, and ion and polysulfide diffusion within the battery.
View Article and Find Full Text PDFAdv Sci (Weinh)
December 2024
Institute for Nanoscale Science and Technology, College of Science and Engineering, Flinders University, Bedford Park, South Australia, 5042, Australia.
Big data and artificial intelligence are driving increasing demand for high-density data storage. Probe-based data storage, such as mechanical storage using an atomic force microscope tip, is a potential solution with storage densities exceeding hard disks. However, the storage medium must be modifiable on the nanoscale.
View Article and Find Full Text PDFJ Colloid Interface Sci
March 2025
Hubei Engineering Technology Research Centre of Energy Polymer Materials, School of Chemistry and Materials Science, South-Central Minzu University, Wuhan 430074, China; Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Nankai University, Tianjin 300071, China. Electronic address:
In the quest for next-generation energy storage solutions, lithium-sulfur (Li-S) batteries present exceptional potential due to their high energy density and cost-effectiveness. Nevertheless, significant challenges, such as the shuttle effect of lithium polysulfides (LiPSs) and inadequate sulfur utilization, have impeded their practical application. In this study, we report the design and synthesis of a novel covalent organic polymer that integrates a triazine-linked framework with carbonyl-enriched polyimide moieties, serving as a highly effective sulfur host for Li-S batteries.
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