Per- and polysulfides are sulfane sulfur species produced inside living cells, in organisms as diverse as bacteria, plants and humans, but their biological roles remain to be fully understood. Unfortunately, due to their reactivity, per- and polysulfides are easily altered, interconverted or lost during the processing and analysis of biological material. Thus, all current analytical methods make use of alkylating agents, to quench reactivity of hydropersulfides and hydropolysulfides and also to prevent free thiols from attacking sulfur chains in hydropolysulfides and dialkyl polysulfides. However, recent findings reveal that alkylating agents can also destroy per- and polysulfides, to varying degrees, depending on the choice of alkylating agent. Here, we discuss the challenges associated with the alkylation of per- and polysulfides, the single most important step for their preservation and detection in biological samples.
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http://dx.doi.org/10.1016/j.cbpa.2023.102368 | DOI Listing |
Mater Horiz
January 2025
National local joint engineering research center for Lithium-ion Batteries and Materials Preparation Technology, Key Laboratory of Advanced Batteries Materials of Yunnan Province, Faculty of Metallurgical and Energy Engineering, Kunming University of Science and Technology, Kunming, 650093, China.
The stable operation of high-capacity lithium-sulfur batteries (LSBs) has been hampered by slow conversion kinetics of lithium polysulfides (LiPSs) and instability of the lithium metal anodes. Herein, 6-(dibutylamino)-1,3,5-triazine-2,4-thiol (DTD) is introduced as a functional additive for accelerating the kinetics of cathodic conversion and modulating the anode interface. We proposed that a coordination interaction mechanism drives the polysulfide conversion and modulates the Li solvated structure during the binding of the N-active site of DTD to LiPSs and lithium salts.
View Article and Find Full Text PDFSmall
January 2025
State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.
The electrocatalytic conversion of 16-electron multistep polysulfides is crucial for lithium-sulfur batteries, while it is hard to achieve compatibility between intricate sulfur reduction processes and appropriate catalysts. Herein, a tandem conversion strategy is reported to boost multi-step intermediate reactions of polysulfides transformation by designing an electrocatalyst featuring cobalt and zinc sites (Co/Zn), where the Zn serve as sites for the conversion of long-chain lithium polysulfides (LiPSs), promoting the transformation of S to LiS; the Co sites accelerate the kinetics of the subsequent reduction of LiS. This tandem catalysis method not only enhances the conversion of the initial reactants but also provides additional support for the intermediates, thereby facilitating subsequent reactions to maximize capacity.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Wenzhou University, College of Chemistry and Materials Engineering, Chashan University Town, 325035, Wenzhou, CHINA.
Small
December 2024
College of Material Science and Engineering, Zhejiang University of Technology, Hangzhou, 310014, P. R. China.
Lithium-sulfur batteries (LSBs) face challenges from the shuttle effect of lithium polysulfides (LiPSs) and slow redox kinetics. In this study, a NiCo-Doped 3D Ordered Mesoporous Carbon (NiCo-3DOMC) composite material is synthesized using a gel-crystalline template and sol-gel method to modify polypropylene separators in LSBs. Density Functional Theory calculations and experiment results demonstrate that under a magnetic field, the NiCo-3DOMC enhances adsorption and catalyzes the conversion of LiPSs, effectively mitigating the shuttle effect and boosting redox kinetics.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
College of Materials Science and Engineering, Changchun University of Science and Technology, Changchun 130022, China; Key Laboratory of Applied Chemistry and Nanotechnology at Universities of Jilin Province, Changchun University of Science and Technology, Changchun 130022, China. Electronic address:
High-energy-density lithium-sulfur (Li-S) cells are identified as one of the most prospective next-generation energy storage appliances owing to their numerous advantages. Nonetheless, their widespread applications are restricted by the unwanted shuttling effect and tardy conversion reaction kinetics of lithium polysulfides (LiPSs). To address these puzzles, we present an innovative strategy for the one-pot synthesis of LaF@SiO yolk-shell heterostructure nanofibers (YSHNFs) through a straightforward uniaxial electrospinning process coupled with fluorination, avoiding the complexities of traditional methods.
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