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Highly ion-conductive solid electrolytes of nonlithium ions (sodium or potassium ions) are necessary for pursuing a more cost-effective and sustainable energy storage. Here, two classes of sulfonated -NH-linked covalent organic frameworks (COFs), specifically designed for sodium or potassium ion conduction (named i-COF-2 (Na or K) and i-COF-3 (Na or K)), were synthesized through a straightforward, one-step process using affordable starting materials. Remarkably, these COFs demonstrate high ionic conductivity at room temperature─3.17 × 10 and 1.02 × 10 S cm for i-COF-2 (Na) and i-COF-2 (K) and 2.75 × 10 and 1.42 × 10 S cm for i-COF-3 (Na) and i-COF-3 (K)─without the need for additional salt or solvent. This enhanced performance, including low activation energies of 0.21 eV for both i-COF-2 (Na) and i-COF-2 (K) and of 0.24 and 0.25 eV for i-COF-3 (Na) and i-COF-3 (K), is attributed to the strategic incorporation of sulfonate groups and the directional channels within the COF structure. The Na and K ion high conductivities, low cost, and intrinsic framework stability of i-COF-2 (Na or K) and i-COF-3 (Na or K) provide promising solid electrolyte candidates for the exploration of sustainable energy storage.
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http://dx.doi.org/10.1021/acsami.4c09568 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
Department of Materials Science and Engineering, University of Wisconsin─Madison, Madison, Wisconsin 53706, United States.
Highly ion-conductive solid electrolytes of nonlithium ions (sodium or potassium ions) are necessary for pursuing a more cost-effective and sustainable energy storage. Here, two classes of sulfonated -NH-linked covalent organic frameworks (COFs), specifically designed for sodium or potassium ion conduction (named i-COF-2 (Na or K) and i-COF-3 (Na or K)), were synthesized through a straightforward, one-step process using affordable starting materials. Remarkably, these COFs demonstrate high ionic conductivity at room temperature─3.
View Article and Find Full Text PDFBioorg Med Chem Lett
June 2004
Cancer Research, Global Pharmaceutical R & D, Abbott Laboratories, 100 Abbott Park Road, Abbott Park, IL 60064-6101, USA.
Several 8-substituted 2-naphthamidine-based inhibitors of the serine protease urokinase plasminogen activator (uPA) are described. Direct attachment of five-membered saturated or unsaturated rings improved inhibitor performance; substitution with sulfones further improved binding profiles. Combination of these substituents or of previously described NH-linked heteroaromatic rings with 6-phenyl amide substituents provided further enhancements to potency and selectivity.
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