Quasi-solid-state rechargeable zinc-air batteries (ZABs) are suitable for the generation of portable clean energy due to their high energy and power density, safety, and cost-effectiveness. Compared to the typical alkaline aqueous electrolyte in a ZAB, polymer or gel-based electrolytes can suppress the dissolution of zinc, preventing the precipitation of undesirable irreversible zinc compounds. Their low electronic conductivity minimizes zinc dendrite formation. However, gel electrolytes suffer from capacity fade due to the loss of the volatile solvent, failing to deliver high-energy and high-power ZABs. Consequently, developing polymers with high hydroxide ion conductivity and chemical durability is paramount. We report cationic C-C bonded robust polymers with stoichiometrically controlled mobile hydroxide ions as solid-state hydroxide ion transporters. To boot, we increased the viologen-hydroxide-ion concentration through "by-design" monomers. The polymers constructed with these designer monomers exhibit a commensurate increase in their ionic conductivity. The polymer prepared with 4 OH ion-containing monomer was superior to the one with 3 OH. The conductivity increases from 7.30 × 10 S cm (30 °C) to 2.96 × 10 S cm (30 °C) at 95% RH for IISERP-POF12_OH (2_OH) and IISERP-POF13_OH (3_OH), respectively. A rechargeable ZAB (RZAB) constructed using 3_OH@PVA (polyvinyl alcohol) as the electrolyte membrane and Pt/C + RuO catalyst delivers a power density of 158 mW cm. In comparison, RZABs with a PVA interlayer provided only 72 mW cm. Notably, the device suffered an initial charge-discharge voltage gap of merely 0.55 V at 10 mA cm, which increased by only 2 mV after 50 hours of running. The battery operated at 10 mA cm and worked steadily for 67 hours. We accomplished a flexible and rechargeable zinc-air battery (F-RZAB) exhibiting a maximum power density of 79 mW cm. This demonstration of a cationic viologen-bakelite polymer-based flexible secondary ZAB with versatile stochiometric hydroxide-ion tunability marks an important achievement in hydroxide-ion conducting solid-state electrolyte development.
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http://dx.doi.org/10.1039/d4sc00121d | DOI Listing |
J Colloid Interface Sci
January 2025
College of Biological, Chemical Sciences and Engineering, Jiaxing University, Jiaxing, Zhejiang 314001, China. Electronic address:
Electro-reforming of organics such as alcohols into commodity chemicals and H powered by renewables is intriguing and prevailing with the remarkable renaissance of electrochemical technology. Integrating Pt/Pd with an auxiliary metal, metal oxide, and metal hydroxide are feasible strategies to design the desirable catalysts toward alcohols electro-oxidation reactions. These catalysts however have high affinity toward carbonyl intermediates that occupy and poison the active sites.
View Article and Find Full Text PDFACS Nano
January 2025
Department of Chemical and Biomolecular Engineering, University of Pennsylvania, Philadelphia, Pennsylvania 19104, United States.
Ordered nanoporous polymer membranes offer opportunities for systematically probing the mechanisms of ion transport under confinement and for realizing useful materials for electrochemical devices. Here, we examine the impact of morphology and ion hydration on the transport of hydroxide and bromide anions in nanostructured polymer membranes with 1 nm scale pores. We use aqueous lyotropic self-assembly of an amphiphilic monomer, with a polymerizable surfactant to create direct hexagonal (H) and gyroid mesophases.
View Article and Find Full Text PDFJ Chem Phys
January 2025
Key Laboratory of Chemistry and Chemical Engineering on Heavy-Carbon Resources, School of Chemistry and Chemical Engineering, Yili Normal University, Yining 835000, People's Republic of China.
E2 elimination and SN2 substitution reactions are of central importance in preparative organic synthesis due to their stereospecificity. Herein, atomistic dynamics of a prototype reaction of ethyl chloride with hydroxide ion are uncovered that show strikingly distinct features from the case with fluoride anion. Chemical dynamics simulations reproduce the experimental reaction rate and reveal that the E2 proceeding through a direct elimination mechanism dominates over SN2 for the hydroxide ion reaction.
View Article and Find Full Text PDFACS Omega
December 2024
Center for Quantum Information and Quantum Biology, Osaka University, Toyonaka, Osaka 560-0043, Japan.
Photosynthetic water oxidation is a vital process responsible for producing dioxygen and supplying the energy necessary to sustain life on Earth. This fundamental reaction is catalyzed by the oxygen-evolving complex (OEC) of photosystem II, which houses the MnCaO cluster as its catalytic core. In this study, we specifically focus on the D1-Glu189 amino acid residue, which serves as a direct ligand to the MnCaO cluster.
View Article and Find Full Text PDFEur J Med Chem
February 2025
State Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, 611137, China. Electronic address:
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