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Single-ion-selective membranes are indispensable for efficient ion separations in environmental, energy, and biomedical technologies. Inspired by biological ion channels, this work harnessed the selective and reversible ion binding features of ionophores to fabricate an ultrathin, ionophore-based K-selective polyamide membrane through molecular layer-by-layer (m-LbL) polymerization with 18-crown-6-functionalized monomers. Compared with Cs, Li, and Mg, K exhibited the highest binding energy to 18-crown-6, facilitating its transport over the competing cations across the sub-10 nm polyamide film in a binary salt mixture. The need for competitive binding for selective K transport was further demonstrated through investigations of ion selectivity at varying concentration ratios between K and competing cations. Additionally, we extended the Nernst-Planck equation to describe individual ion flux in a binary system, identifying factors that govern ion transport. Our findings demonstrate the potential of selective single-ion transport enabled by preferential ion binding, showing promise for the development of biomimetic ion-selective polymeric membranes.
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http://dx.doi.org/10.1021/acsami.5c02331 | DOI Listing |
Chem Biodivers
September 2025
College of Environmental & Chemical Engineering, Yanshan University, Qinhuangdao, China.
β-Adrenergic agonists are employed in the livestock industry to promote the growth of poultry and livestock. However, due to the frequent lack of scientific guidance in medication administration among farmers, issues such as indiscriminate use, misuse, and noncompliance with withdrawal periods have arisen. These practices result in drug residues, triggering food safety concerns and posing a threat to consumer health.
View Article and Find Full Text PDFAdv Sci (Weinh)
August 2025
School of Chemistry and Energy, Sungshin Women's University, Seoul, 01133, Republic of Korea.
Molecular thermoelectric materials, which harness molecular-level design principles to optimize energy conversion, have emerged as a promising strategy for addressing the limitations of bulk inorganic thermoelectrics, such as brittleness and high production costs. In this study, a layer-by-layer (LbL) engineered HKUST-1 surface-mounted metal-organic framework (SURMOF) nanofilm is proposed as a promising thermoelectric nanostructure, systematically characterized across its thickness. By employing LbL growth of HKUST-1 on self-assembled monolayers (SCCOOH, n = 2, 10), nanofilms ranging from 5 to 30 nm in thickness are successfully fabricated.
View Article and Find Full Text PDFChem Asian J
August 2025
Research Center for Macromolecules and Biomaterials, National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, 305-0044, Japan.
The term "nanoarchitectonics" emerged as the 21st century approached, and it has been in use for around 20 years. We here look back accomplishments of nanoarchitectonics. However, this review will explore several typical topics and their trends instead of a comprehensive description in a chronicle-like manner.
View Article and Find Full Text PDFSmall
August 2025
Physics Department, Lancaster University, Lancaster, LA1 4YB, UK.
Despite the significant potential of molecular-scale devices for miniaturized electronics and energy conversion applications, conventional self-assembled monolayers (SAMs) exhibit limitations in simultaneously optimizing electrical conductivity and thermopower due to constrained electronic pathway modulation. This study demonstrates a molecular engineering strategy employing a discretely arranged conjugated molecular backbone to construct ordered cage-like supramolecular cavities, enabling controlled intercalation of fullerene within bipyridine-based SAMs grown on graphene-substrates. Quartz crystal microbalance and atomic force microscopy measurements confirmed the structural integrity of the fullerene-trapped SAMs.
View Article and Find Full Text PDFChem Sci
July 2025
Department of Chemistry, Indiana University Bloomington IN 47405 USA
Post-synthetic metalation and metathesis chemistry are central to rational synthesis of metal-organic frameworks (MOFs) that are unavailable by direct self-assembly. The inherent microcrystallinity and heterogeneous nature of many MOFs renders characterization of the rate, extent, and distribution of post-synthetic modifications challenging. Here we describe the deposition of optically transparent, permanently porous thin films comprised of peripherally carboxylated free-base porphyrins and cationic porous molecular cages.
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