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Despite their promising theoretical performance, lithium-sulfur (Li-S) batteries are often limited by low efficiency, primarily due to the solubility of lithium polysulfides and the low conductivity of sulfur electrodes. Enhancing the incorporation of sulfur into porous carbon with improved polarity could significantly boost the Li-S battery performance. In this study, we doped carbon xerogels with nitrogen atoms and decorated them with iron-based nanostructures using a straightforward and scalable method. The decomposition of nitrogen-containing additives at varying temperatures─specifically 750 °C (FeNC-750) and 950 °C (FeNC-950)─resulted in alterations to the porosity of the xerogel compared to the pristine structure. After impregnating these structures with sulfur to develop the sulfur electrode, we assessed the electrochemical performance of FeNC-750@S and FeNC-950@S, varying the sulfur content and the electrolyte-to-sulfur (E/S) ratio. Our results indicated that the electrochemical performance of the sulfur electrode with high sulfur content was significantly influenced by both the E/S ratio and the porosity of the host materials. Notably, the sulfur electrode with over 80% sulfur content, designated FeNC-950@S, achieved a discharge capacity of 600 mA h g with an E/S ratio of 7.5 mL g and an electrode loading of 3.5 g cm, demonstrating an excellent capacity retention of 96% over 100 cycles at a rate of 0.1 C.
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http://dx.doi.org/10.1021/acsami.5c05993 | DOI Listing |
Dalton Trans
September 2025
Department of Chemistry, University of Zululand, Private Bag X1001, KwaDlangezwa 3880, South Africa.
To overcome the potential issue of active site blockage by surfactants in colloidal synthesis, alternative synthetic approaches must be explored. In this study, we investigated both solvent-free and colloidal thermolysis routes to synthesize nickel sulfides (NiS and NiS) using sulfur-based Ni complexes, [Ni(SCO(CH))] (Ni-Xan) and [Ni(SCN(CH))] (Ni-DTC) as precursors. The solvent-free decomposition of these complexes produced ligand-free NiS and NiS in the absence or presence of triphenylphosphine (TPP), respectively.
View Article and Find Full Text PDFNatl Sci Rev
September 2025
College of Chemistry, Huazhong Agricultural University, Wuhan 430070, China.
The stress distribution in Li metal strongly affects the interfacial Li-ion diffusion, thereby influencing the morphology of plated Li and the performance of the battery. Here, we report a mechano-electrochemical coupling strategy that utilizes an arched structured carbon aerogel to achieve stable Li-plating/stripping electrochemistry. The arch-structured carbon aerogel can actively regulate stress distributions in response to the compressive stresses induced by Li deposition, generating the transition of stress from compressive on the convex surface to tensile on the concave surface, which can effectively promote the Li-migration kinetics and thus suppress the non-uniform deposition of Li.
View Article and Find Full Text PDFACS Sustain Chem Eng
September 2025
Electrochemical Innovation Lab, Department of Chemical Engineering, University College London, Torrington Place, London WC1E 7JE, U.K.
Traditionally, binders such as poly-(vinylidene fluoride) (PVDF) have been used within lithium-sulfur (Li-S) batteries, but these present environmental and recyclability challenges and have little to no impact on the processes that drive degradation in the cell's chemistry. Ideally, a Li-S battery binder would contribute to the mitigation of the polysulfide shuttle effect and negate the impacts of positive electrode volume expansion while being compatible with aqueous ink preparation and low-energy, low-toxicity recycling processes. In this work, we demonstrate that fibroin, an economical and sustainable biological polymer with an abundance of functional groups, can effectively trap polysulfides while still offering the durability, cyclability, and ease of use offered by the current state-of-the-art binder (PVDF).
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Shandong Key Laboratory of Advanced Chemical Energy Storage and Intelligent Safety, Advanced Technology Research Institute, Beijing Institute of Technology, Jinan, 250300, China.
Lithium-sulfur batteries have been regarded as a promising candidate for next-generation energy storage systems owing to their high energy density and low cost. Sulfurized polyacrylonitrile (SPAN) as a cathode material has received wide interest due to the solid-solid conversion mechanism, while the Li-SPAN cell performance has been limited by the notorious issue of lithium metal anode. Developing solid-state electrolytes for lithium-sulfur batteries with favorable electrode-electrolyte compatibility is urgently desired.
View Article and Find Full Text PDFChem Commun (Camb)
September 2025
Department of Chemistry, Indian Institute of Technology Ropar, Punjab 140001, India.
Aqueous metal batteries are emerging as promising candidates for next-generation energy storage, offering safer, more sustainable, and cost-effective alternatives to lithium-ion batteries (LIBs). Leveraging earth-abundant metals such as zinc, aluminium, magnesium, and silicon, these systems benefit from non-flammable, water-based electrolytes and simplified manufacturing, making them attractive for grid-scale and off-grid applications. This review highlights recent progress in aqueous battery chemistries, including metal-ion, metal-sulfur, and metal-air systems, emphasizing advancements in electrode design, electrolyte engineering, and interface optimization to improve energy density and cycling stability.
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