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Some anaerobic bacteria use insoluble minerals as terminal electron acceptors and discovering the ways in which electrons move through the membrane barrier to the exterior acceptor forms an active field of research with implications for both bacterial physiology and bioenergy. A previous study suggested that MR-1 utilizes a small, polar, redox active molecule that serves as an electron shuttle between the bacteria and insoluble acceptors, but the shuttle itself has never been identified. Through isolation and synthesis, we identify it as ACNQ (2-amino-3-carboxy-1,4-naphthoquinone), a soluble analog of menaquinone. ACNQ is derived from DHNA (1,4-dihydroxy-2-naphthoic acid) in a non-enzymatic process that frustrated genetic approaches to identify the shuttle. Both ACNQ and DHNA restore reduction of AQDS under anaerobic growth in menaquinone-deficient mutants. Bioelectrochemistry analyses reveal that ACNQ (-0.32 V) contributes to the extracellular electron transfer (EET) as an electron shuttle, without altering menaquinone generation or EET related cytochrome c expression.
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http://dx.doi.org/10.7554/eLife.48054 | DOI Listing |
J Colloid Interface Sci
August 2025
Beijing Key Laboratory of Advanced Functional Polymer Composites, Beijing University of Chemical Technology, Beijing 100029, China. Electronic address:
Lithium‑sulfur batteries (LSBs) are promising alternatives to lithium-ion batteries due to their high energy density and low cost. However, issues like the lithium polysulfide (LiPSs) shuttle effect, lithium dendrite growth, and flammable electrolytes hinder commercialization. In this study, we have developed a metal-based catalyst, bismuth oxychloride (BiOCl) nanoflowers coated with conductive polypyrrole (Bi@Ppy), via hydrothermal synthesis.
View Article and Find Full Text PDFAdv Mater
September 2025
School of Materials Science and Chemical Engineering, Harbin University of Science and Technology, Harbin, 150080, China.
The polysulfide shuttling and sluggish sulfur redox kinetics hinder the commercialization of lithium-sulfur (Li-S) batteries. Herein, the fabrication of phosphorus (P)-doped iron telluride (FeTe) nanoparticles with engineered Te vacancies anchored on nitrogen (N)-doped carbon (C) (P-FeTe@NC) is presented as a multifunctional sulfur host. Theoretical and experimental analyses show that Te vacancies create electron-deficient Fe sites, which chemically anchor polysulfides through enhanced Fe─S covalent interactions.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Department of Mechanical and Aerospace Engineering, University of Florida, Gainesville, Florida 32611, United States.
Lithium-sulfur batteries (LSBs) are extensively researched for their high energy densities but are hindered by the lithium polysulfide (LiPS) shuttling effect, which results in poor cyclability. A popular mitigation strategy is separator modification, where a LiPS trapping material is slurry-coated onto a conventional microporous polypropylene (PP) separator. This additional mass and volume unfortunately compromise the overall energy density of the LSB.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
Guangzhou Key Laboratory of Clean Transportation Energy Chemistry, School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006, China. Electronic address:
The practical application of lithium‑sulfur (LiS) batteries is often restricted by the uncontrolled diffusion of lithium polysulfides (LiPSs) and their intrinsically sluggish redox kinetics. To address these limitations, we designed a multidimensional composite separator by anchoring Zn-Co-Ni-S nanocrystals onto alkalized two-dimensional transition metal carbide/nitride (MXene) nanosheets, followed by the incorporation of one-dimensional carbon nanotubes (CNTs), yielding a robust and highly conductive interfacial architecture. This multidimensional configuration combines physical confinement, strong chemisorption, and catalytic enhancement to regulate sulfur redox behavior effectively.
View Article and Find Full Text PDFChem Sci
August 2025
School of Materials Science and Engineering, Institutes of Physical Science and Information Technology, Leibniz International Joint Research Center of Materials Sciences of Anhui Province, Anhui University Hefei 230601 China
Aqueous zinc-iodine batteries (ZIBs), exploiting reversible conversion among various iodine species, have drawn significant research interest due to their fast redox kinetics and capability for multi-electron transfer. Although significant progress has been made in ZIBs based on the two-electron I/I redox pathway (2eZIBs), their inherently limited energy density impedes practical deployment. Achieving the additional reversible conversion of high-valence iodine species, particularly the I/I redox chemistry, offers substantial potential for improving energy density up to 630 Wh kg based on the mass of I.
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