Rechargeable aqueous Zn-ion batteries have been deemed a promising energy storage device. However, the dendrite growth and side reactions have hindered their practical application. Herein, inspired by the ultrafluidic and K ion-sieving flux through enzyme-gated potassium channels (KcsA) in biological plasma membranes, a metal-organic-framework (MOF-5) grafted with -ClO groups (MOF-ClO) as functional enzymes is fabricated to mimic the ultrafluidic lipid-bilayer structure for gating Zn 'on' and anions 'off' states. The MOF-ClO achieved perfect Zn/SO selectivity (∼10), enhanced Zn transfer number ([Formula: see text]) and the ultrafluidic Zn flux (1.9 × 10 vs. 1.67 mmol m s for KcsA). The symmetric cells based on MOF-ClO achieve a lifespan of over 5400 h at 10 mA cm/20 mAh cm. Specifically, the performance of the PMCl-Zn//VO pouch cell keeps 81% capacity after 2000 cycles at 1 A g. The regulated ion transport, by learning from a biological plasma membrane, opens a new avenue towards ultralong lifespan aqueous batteries.
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http://dx.doi.org/10.1093/nsr/nwae199 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
Shaanxi Key Laboratory of Energy Chemical Process Intensification, School of Chemical Engineering and Technology, Xi'an Jiaotong University, Xi'an 710049, Shaanxi, China.
Aqueous halogen batteries are gaining recognition for large-scale energy storage due to their high energy density, safety, environmental sustainability, and cost-effectiveness. However, the limited electrochemical stability window of aqueous electrolytes and the absence of desirable carbonaceous hosts that facilitate halogen redox reactions have hindered the advancement of halogen batteries. Here, a low-cost, high-concentration 26 m Li-B-C-O aqueous solution incorporating lithium bromide (LiBr), lithium chloride (LiCl), and lithium acetate (LiOAc) was developed for aqueous batteries, which demonstrated an expanded electrochemical stability window of .
View Article and Find Full Text PDFNatl Sci Rev
February 2025
PCFM Lab and GDHPRC Lab, School of Chemistry, Sun Yat-sen University, Guangzhou 510006, China.
Unstable anode/electrolyte interfaces have significantly hindered the development of lithium (Li) metal batteries under high rates and large capacities. In this study, a versatile reactive layer based on sulfur-selenium crosslinked polyacrylonitrile brushes has been developed by a combined strategy of polymer topology design and chemical crosslinking. The sulfur-selenium crosslinked polyacrylonitrile side-chains can react with Li to generate passivated LiS-LiSe-containing solid electrolyte interphase while 3D lithiophilic porous nanonetworks enable Li penetration, contributing to achieving rapid and uniform Li ion flux and a dendrite-free anode.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Laboratory of Advanced Materials, Aqueous Battery Center, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, School of Chemistry and Materials, Fudan University, Shanghai, 200433, P. R. China.
Tellurium (Te), with its rich valence states (-2 to +6), could endow aqueous batteries with potentially high specific capacity. However, achieving complete and stable hypervalent Te/Te electrochemistry in an aqueous environment poses significant challenges, owing to the sluggish reduction kinetics, easy dissolution of Te species, and a controversial energy storage mechanism. Herein, we demonstrate a crystallographic regulation strategy for robust aqueous Te redox electrochemistry.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Wuhan National Laboratory for Optoelectronics, School of Optical and Electronic Information, Huazhong University of Science and Technology, Wuhan 430074, China.
As a leading candidate for high-voltage, cobalt-free cathodes, spinel LiNiMnO (LNMO) oxide is highly attractive for next-generation lithium-ion batteries. However, the instability of cation-oxygen bonds (especially Mn-O) and the adverse two-phase transition of LNMO result in rapid crystal collapse during cycling, thus limiting its practical deployment. To address these issues, herein we exploit the differences in miscibility between dopants and the spinel matrix to embed high-entropy doped microregions (HEDRs, 5-15 nm in size) within the spinel.
View Article and Find Full Text PDFSmall
December 2024
State Key Laboratory of Organic-Inorganic Composites, Beijing Advanced Innovation Center for Soft Matter Science and Engineering, College of Chemical Engineering, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.
Aqueous Zinc-iodine batteries (ZIBs) are widely viewed as promising energy storage devices due to their high energy density and intrinsic safety. However, they encounter great challenges such as grievous polyiodides shuttle and sluggish iodine (I) redox reaction kinetics, thus undesirable cycling performance. Here a high-performance ZIB with an ultra-long lifespan is reported through the rational I cathode catalyst design.
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