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Aqueous zinc ion batteries (AZIBs) have attracted intense attention due to their high safety and low cost. Unfortunately, the serious dendrite growth and side reactions of the Zn metal anode in an aqueous electrolyte result in rapid battery failure, hindering the practical application of AZIBs. Herein, sodium gluconate as a dual-functional electrolyte additive has been employed to enhance the electrochemical performance of AZIBs. Gluconate anions preferentially adsorb on the surface of the Zn anode, which effectively prevents H evolution and induces uniform Zn deposition to suppress dendrite growth. Moreover, the gluconate anions can highly coordinate with Zn, promoting the dissolution of [Zn(HO)] to inhibit side reactions and the water-induced corrosion reaction. As a result, the Zn||Zn symmetric battery exhibits a long-term cycling stability of over 3000 h at 1 mA cm/1 mA h cm and 600 h at 10 mA cm/10 mA h cm. Furthermore, the NHVO||Zn full battery also displays excellent cycling stability and a high reversible capacity of 193 mA h g at 2 A g after 1000 cycles. Given the low-cost advantage of SG, the proposed interface chemistry modulation strategy holds considerable potential for promoting the commercialization of AZIBs.
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http://dx.doi.org/10.1021/acsami.3c16717 | DOI Listing |
Lasers Med Sci
September 2025
Laser Research Center of Dentistry, Dentistry Research Institute, Tehran University of Medical Sciences, Tehran, Iran.
Microbial contamination of absorbable collagen membranes used in guided bone regeneration (GBR) may compromise healing outcomes. This study aimed to investigate whether the minimum inhibitory concentration (MIC) of hydrogen peroxide (HO) can improve the antibacterial effect of indocyanine green (ICG)-mediated antimicrobial photodynamic therapy (PDT) on absorbable collagen membranes while reducing the need for high HO concentrations. A laboratory-based model was developed using Streptococcus sanguinis and Staphylococcus aureus.
View Article and Find Full Text PDFSmall
September 2025
School of Energy and Chemical Engineering, UNIST, Ulsan, 44919, South Korea.
All-solid-state batteries (ASSBs), equipped with highly ion-conductive sulfide solid electrolytes and utilizing lithium plating/stripping as anode electrochemistry, suffer from 1) chemical vulnerability of the electrolytes with lithium and 2) physical growth of lithium to penetrate the electrolytes. By employing an ordered mesoporous graphitic carbon (OMGC) framework between a sulfide electrolyte layer and a copper current collector in ASSB, the concerns by are addressed 1) minimizing the chemically vulnerable interface (CVI) between electric conductor and solid electrolyte, and 2) allowing lithium ingrowth toward the porous structure via Coble creep, a diffusional deformation mechanism of lithium metal along the lithium-carbon interface. The void volume of the framework is fully filled with lithium metal, despite ionic pathways not being provided separately, even without additional lithiophiles, when an enough amount of lithium is allowed to be plated.
View Article and Find Full Text PDFChem Commun (Camb)
September 2025
Guangdong Provincial Key Laboratory of New Energy Materials Service Safety, College of Materials Science and Engineering, Shenzhen University, Shenzhen 518055, China.
Thermocells (TECs) represent a promising technology for sustainable low-grade waste heat (<100 °C) harvesting, offering distinct advantages such as scalability, structural versatility, and high thermopower. However, their practical applications are still hindered by low energy conversion efficiency and stability issues. In recent studies, electrolyte engineering has been highlighted as a critical strategy to enhance their thermopower by regulating the solvation structure and redox ion concentration gradient, thereby improving conversion efficiency.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
State Key Laboratory of Chemical Resource Engineering, Beijing Key Laboratory of Electrochemical Process and Technology of Materials, Beijing University of Chemical Technology, Beijing, 10029, P.R. China.
Lithium metal batteries (LMBs) have emerged as the most promising candidate for next-generation high-energy-density energy storage systems. However, their practical implementation is hindered by the inability of conventional carbonate electrolytes to simultaneously stabilize the lithium metal anode and LiNiCoMnO (NCM811) cathode interfaces, particularly under extreme operating conditions. Herein, we present a transformative molecular design using 3,5-difluorophenylboronic acid neopentyl glycol ester (DNE), which uniquely integrates dual interfacial stabilization mechanisms in a single molecule.
View Article and Find Full Text PDFCommun Chem
September 2025
Department of Chemistry-Ångström Laboratory, Uppsala University, Uppsala, Sweden.