Rechargeable magnesium batteries (RMBs) have attracted a lot of attention in recent decades due to the theoretical properties of these systems in terms of energy density, safety, and price. Nevertheless, to date, fully rechargeable magnesium battery prototypes with sufficient longevity and reversibility were realized only with low voltage and low capacity intercalation cathode materials based on Cheverel phases. The community is therefore actively looking for high-capacity cathodes that can work with metallic magnesium anodes in viable RMB systems. One of the most promising cathode materials, in terms of very high theoretical specific capacity, is, naturally, sulfur. A number of recent works studied the electrochemical performances of rechargeable sulfur cathodes in RMB, with success to some extent on the cathode side. Nevertheless, as known from the lithium-sulfur rechargeable battery systems, the formation of soluble polysulfides during discharge affects strongly the behavior of the anode side. In this article and the work it describes, we focus on soluble polysulfides impact on Mg-S electrochemichal systems. We carefully designed herein conditions that mimic the Mg-S battery prototypes containing balanced Mg and elemental sulfur electrodes. Under these conditions, we extensively studied the Mg anode behavior. The study shows that when elemental sulfur cathodes are discharged in the Mg-S cells containing electrolyte solutions in which Mg anodes behave reversibly, the polysulfide species thus formed migrate to the anode and eventually fully passivate it by the formation of very stable surface layers. The work involved electrochemical, spectroscopic, and microscopic studies. The present study clearly shows that to realize practical rechargeable Mg-S batteries, the transport of any sulfide moieties from the sulfur cathode to the magnesium anode has to be completely avoided. Such a condition is mandatory for the operation of secondary Mg-S batteries.
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http://dx.doi.org/10.1021/acsami.8b11123 | DOI Listing |
Angew Chem Int Ed Engl
December 2024
Key Lab for Special Functional Materials of Ministry of Education, National & Local Joint Engineering Research Center for High-efficiency Display and Lighting Technology, School of Materials Science and Engineering, Collaborative Innovation Center of Nano Functional Materials and Applications, Henan University, Kaifeng, 475004, PR China.
Sluggish reaction kinetics of sulfur species fundamentally trigger the incomplete conversion of S↔LiS and restricted lifespan of lithium-sulfur batteries, especially under high sulfur loading and/or low electrolyte/sulfur (E/S) ratios. Developing redox mediators (RMs) is an effective strategy to boost the battery reaction kinetics, yet their multifunctionality and shuttle inhibition are still not available. Here, a unique ethyl viologen (EtV) RM with two highly reversible redox couples (EtV/EtV, EtV/EtV) is demonstrated to well match the redox chemistry of sulfur species, in terms of accelerating the electron transfer in S reduction, LiS nucleation and the LiS oxidation.
View Article and Find Full Text PDFACS Nano
December 2024
Shenzhen Geim Graphene Center, Tsinghua Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, China.
Carbon nanotubes (CNTs) with exceptional conductivity have been widely adopted in lithium-sulfur (Li-S) batteries. While trace metal impurities in CNTs have demonstrated electrocatalytic activity in various catalytic processes, their influence on sulfur electrocatalysis in Li-S batteries has been largely overlooked. Herein, we reveal that the trace metal impurities content in CNTs significantly improves the specific capacity and cycling performance of Li-S batteries by analyzing both our own results and previous literature with CNTs as the sulfur hosts.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
School of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, P. R. China.
The utilization of catalysts in lithium--sulfur batteries has proven to be an efficacious avenue for enhancing the kinetics of polysulfide conversion. Specially, the size and electronic structure of catalysts play a pivotal role in harnessing the active sites and intrinsic catalysis activity. Outstanding MoSe and NbSe are were selected from 16 universal transition metal selenides based on the proposed binary descriptor.
View Article and Find Full Text PDFLangmuir
December 2024
Physics Department, Faculty of Science, Benha University, 13518 Benha, Egypt.
Magnesium-sulfur (Mg-S) batteries offer a promising energy storage system due to their high theoretical capacity. However, the sluggish conversion reaction kinetics and the shuttle effect of magnesium polysulfides hinder their practical application. The high charge density of the divalent Mg cations leads to slow kinetics caused by significant electrostatic interactions between Mg and its surrounding solvent and anion species.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Key Laboratory for Soft Chemistry and Functional Material of Ministry of Education, Nanjing University of Science and Technology, Nanjing 210094, China.
Regulating the transformation of sulfur species is the key to improving the electrochemical performance of lithium-sulfur (Li-S) batteries, in particular, to accelerate the reversible conversion between solid phase LiS and LiS. Herein, we introduced Spidroin, which is a main protein in spider silk, as a dual functional separator coating in Li-S batteries to effectively adsorb polysulfides via the sequence of amino acids in its primary structure and regulate Li flux through the β-sheet of its secondary structure, thus accelerating the reversible transformation between LiS and LiS. Spidroin-based Li-S cells exhibited an exceptional electrochemical performance with a high specific capacity of 744.
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