Ultrathin films composed of ruthenate nanosheets (RuO(2)ns) were fabricated via electrostatic self-assembly of unilamellar RuO(2)ns crystallites derived by total exfoliation of an ion-exchangeable layered ruthenate. Ultrathin films with submonolayer to monolayer RuO(2)ns coverage and multilayered RuO(2)ns thin films were prepared by controlled electrostatic self-assembly and layer-by-layer deposition using a cationic copolymer as the counterion. Electrical properties of a single RuO(2)ns crystallite were successfully measured by means of scanning probe microscopy. The sheet resistance of an isolated single RuO(2)ns crystallite was 12 kΩ sq(-1). Self-assembled submonolayer films behaved as a continuous conducting film for coverage above 70%, which was discussed based on a two-dimensional percolation model. Low sheet resistance was attained for multilayered films with values less than 1 kΩ sq(-1). Interestingly, the grain boundary resistance between nanosheets seems to contribute only slightly to the sheet resistance of self-assembled films.
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J Colloid Interface Sci
January 2025
College of New Materials and New Energies, Shenzhen Technology University, Shenzhen 518118, PR China. Electronic address:
The efficiency of graphitic carbon nitride (g-CN) in photocatalytic reduction of carbon dioxide (CO) is inhibited by the constrained CO chemisorption, insufficient light absorption and quick charge recombination. To address these problems, we successfully synthesized g-CN/AgInS (CN/AgInS) heterostructured photocatalytic materials via an electrostatic self-assembly method. An intimate phase contact between CN and AgInS is formed, paving the way for the charge transfer and redistribution near the interface of the CN/AgInS heterostructures.
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January 2025
Department of Chemistry, Universitat de les Illes Balears, Crta de Valldemossa km 7.5, 07122 Palma de Mallorca, Baleares, Spain.
This perpective delves into the emerging field of matere bonds, a novel type of noncovalent interaction involving group 7 elements such as manganese, technetium, and rhenium. Matere bonds, a new member of the σ-hole family where metal atoms act as electron acceptors, have been shown experimentally and theoretically to play significant roles in the self-assembly and stabilization of supramolecular structures both in solid-state and solution-phase environments. This perspective article explores the physical nature of these interactions, emphasizing their directionality and structural influence in various supramolecular architectures.
View Article and Find Full Text PDFSmall
January 2025
Guangxi Key Laboratory of Petrochemical Resource Processing and Process Intensification Technology, School of Chemistry and Chemical Engineering, Guangxi University, Nanning, 530004, P. R. China.
Although Silicon monoxide (SiO) is regarded as the most promising next-generation anode material, the large volume expansion, poor conductivity, and low initial Coulombic efficiency (ICE) severely hamper its commercialization application. Designing a multilayer conductive skeleton combined with advanced prelithiation technology is considered an effective approach to address these problems. Herein, a reliable strategy is proposed that utilizes MXene and carbon nanotube (CNT) as dual-conductive skeletons to encapsulate SiO through simple electrostatic interaction for high-performance anodes in LIBs, while also performing chemical prelithiation.
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January 2025
Leicester Institute for Pharmaceutical Innovation, Leicester School of Pharmacy, De Montfort University, The Gateway, Leicester, LE1 9BH, UK.
Guiding molecular assembly of peptides into rationally engineered nanostructures remains a major hurdle against the development of functional peptide-based nanomaterials. Various non-covalent interactions come into play to drive the formation and stabilization of these assemblies, of which electrostatic interactions are key. Here, the atomistic mechanisms by which electrostatic interactions contribute toward controlling self-assembly and lateral association of ultrashort β-sheet forming peptides are deciphered.
View Article and Find Full Text PDFACS Nano
January 2025
School of Chemistry and Chemical Engineering, National Special Superfine Powder Engineering Research Center, Nanjing University of Science and Technology, Nanjing 210094, China.
Constructing a strong bonded interface is highly desired to build fast charge-transfer channels and tune reactive sites for optimizing CO photoreduction. In this work, a covalent triazine framework (CTF) combined with a BiSBr heterojunction is designed using an electrostatic self-assembly process. Due to the oppositely charged states between two components and ultrasonic treatment, a strong coupled interface is realized with the formation of Bi-C/N/O bonds, leading to robust interfacial polarization.
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