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Here, MgI is introduced as a bifunctional self-defense redox mediator into dimethyl sulfoxide-based Li-O batteries. During charging, I is first oxidized to I, which facilitates the decomposition of LiO, and thus reduces overpotential. In addition, Mg spontaneously reacts with the Li anode to form a very stable SEI layer containing MgO, which can resist the synchronous attack by the soluble I and improve the interface stability between the Li anode and the electrolyte. Therefore, a Li-O battery containing MgI exhibits an extended cycling life span (400 cycles) and a quite low overpotential (0.6 V).
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http://dx.doi.org/10.1039/d3cc02847j | DOI Listing |
Angew Chem Int Ed Engl
September 2025
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, Changchun, 130012, P.R. China.
Neutral aqueous Zn-air batteries (ZABs), while promising for extended lifespans and recyclability compared to alkaline systems, are hindered by sluggish kinetics that limit energy efficiency and power output. Here, we report an effective approach to construct a photo-assisted near-neutral ZAB based on a photo-responsive titanium silicalite-1 zeolite (TS-1). The incorporation of Ru active centers into the 3D porous architecture of TS@C (Ru@TS@C), which exhibits remarkably enhanced electronic conduction, creates interconnected conductive pathways.
View Article and Find Full Text PDFACS Nano
September 2025
Key Laboratory of Eco-chemical Engineering, International Science and Technology Cooperation Base of Eco-chemical Engineering and Green Manufacturing, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, P. R. China.
Development of aprotic lithium-oxygen (Li-O) batteries suffers from slow cathode reaction kinetics, numerous side reactions, and large polarization, which are intimately related to the discharge product of LiO. Here, we designed and prepared a modified CoO nanoparticle with atomic Ru substitution at octahedral Co sites supported by carbon nanocages (RuCoO@HCNs) as a cathode catalyst. The asymmetrical octahedral Ru-O-Co units trigger a strong electron coupling effect, leading to charge redistribution and optimization of the d-orbital energy levels, thus facilitating oxygen activation and conversion into superoxide anions during discharging.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
Department of Materials Science and Engineering, Chonnam National University, 77 Yongbong-ro, Buk-gu, Gwangju 61186, South Korea. Electronic address:
A composite quasi-solid-state electrolyte (QSE) integrating sulfonated poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) and silicon dioxide (SiO) nanofillers is developed for lithium‑oxygen (Li-O) batteries. The inclusion of SiO nanofillers into the host polymer matrix helps in retaining the liquid electrolyte, enhancing ionic conductivity, mechanical stability, and structural integrity. Sulfonation of PVDF-HFP improves lithium-ion transport, reduces the shuttle effect of the lithium iodide (LiI) redox mediator, and suppresses lithium dendrite growth through uniform lithium deposition.
View Article and Find Full Text PDFMaterials (Basel)
August 2025
Department of Chemistry, The George Washington University, Washington, DC 20052, USA.
Multiwalled carbon nanotube (MWCNT) Li-O cathodes can achieve high gravimetric capacity. However, the macropores of these cathodes require a relatively large mass of electrolyte to fill, resulting in lower true gravimetric and volumetric capacities. Here we report a simple method to incorporate a mesoporous material, carbon nanochains (CNCs), into the macropores of MWCNTs, resulting in composite cathodes that fully utilize their pore structure to store LiO product.
View Article and Find Full Text PDFNanomaterials (Basel)
August 2025
School of Materials Science and Engineering, Changsha University of Science and Technology, Changsha 410114, China.
Lithium-ion batteries (LIBs) have attracted extensive attention as a distinguished electrochemical energy storage system due to their high energy density and long cycle life. However, the initial irreversible lithium loss during the first cycle caused by the formation of the solid electrolyte interphase (SEI) leads to the prominent reduction in the energy density of LIBs. Notably, lithium formate (HCOOLi, LFM) is regarded as a promising cathode prelithiation reagent for effective lithium supplementation due to its high theoretical capacity of 515 mAh·g.
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