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Compared with layered materials such as graphite and transitional metal dichalcogenides with highly anisotropic in-plane covalent bonds, freestanding metallic two-dimensional (2D) films with atomic thickness are intrinsically more difficult to achieve. The omnidirectional nature of typical metallic bonds prevents the formation of highly anisotropic atomically thin metallic layers. Herein, we report a ligand regulation strategy to stabilize monoatomic platinum layers by forming a unique lamellar superlattice structure with self-assembled organic ligand layers. We show that the interlayer spacings and coordination environments could be systematically tuned by varying programmable molecular ligands with the designed length and structural motifs, which further modulate the electronic states and catalytic performances. The strategy can be extended for preparing lamellar superlattices with monoatomic metallic layers from silver and gold. Such general and delicate synthetic control provides an exciting model system for systematic investigation of the intriguing structure-property correlation of monoatomic layers and promises a molecular design pathway for heterogeneous catalysts.
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http://dx.doi.org/10.1021/jacs.2c11928 | DOI Listing |
ACS Cent Sci
June 2025
Department of Applied Plasma & Quantum Beam Engineering, Jeonbuk National University, Jeonju 54896, Republic of Korea.
For a wide range of practical applications of boron nitride nanotubes (BNNTs), it is essential to achieve their highly ordered self-assembled structures. This study reports on a two-dimensional (2D) binary superlattice of individually exfoliated BNNTs with a negative surface charge (p-BNNT25) and cationic surfactant vesicles (CTAT/SDBS vesicles, prepared by mixing cetyltrimethylammonium tosylate (CTAT) and sodium dodecylbenzenesulfonate (SDBS)) complexes through electrostatic interactions. Depending on the surface charge density of the CTAT/SDBS vesicles and the mass ratio between the CTAT/SDBS vesicle and p-BNNT25, the CTAT/SDBS-BNNT complexes formed highly ordered superstructures.
View Article and Find Full Text PDFNano Lett
June 2025
State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun 130012, China.
Electrolyte materials with responsive conductive properties are highly desired in electronic and sensing technologies, which rely on the construction of ion transport channels that combine orderliness with dynamic adjustability. However, achieving such structures remains a significant challenge. In this study, we fabricate a lamellar liquid crystal electrolyte enabling deformation-responsive proton conduction.
View Article and Find Full Text PDFChemistry
August 2023
Jiangsu Engineering Laboratory of Novel Functional Polymeric Materials State and Local Joint Engineering Laboratory for Novel Functional Polymeric Materials College of Chemistry Chemical Engineering and Materials Science, Soochow University, Suzhou, 215123, P. R. China.
Here the supramolecular liquid crystalline (LC) phase behavior of a series of fullerene block molecules was investigated regarding spacer length, alkyl tail length and temperature. These compounds exhibit several lamellar LC phases with different packings of self-organized fullerene two-dimensional (2D) crystals. With a short hexamethylene spacer, they form sandwich-like structures with triple or quadruple fullerene layers.
View Article and Find Full Text PDFJ Am Chem Soc
January 2023
School of Chemistry, Key Laboratory of Bio-Inspired Smart Interfacial Science and Technology, Beijing Advanced Innovation Center for Biomedical Engineering, Beihang University, Beijing 100191, China.
Compared with layered materials such as graphite and transitional metal dichalcogenides with highly anisotropic in-plane covalent bonds, freestanding metallic two-dimensional (2D) films with atomic thickness are intrinsically more difficult to achieve. The omnidirectional nature of typical metallic bonds prevents the formation of highly anisotropic atomically thin metallic layers. Herein, we report a ligand regulation strategy to stabilize monoatomic platinum layers by forming a unique lamellar superlattice structure with self-assembled organic ligand layers.
View Article and Find Full Text PDFACS Nano
December 2022
Department of Applied Chemistry, School of Chemistry, Xi'an Jiaotong University, Engineering Research Center of Energy Storage Materials and Devices, Ministry of Education, Xi'an Key Laboratory of Sustainable Energy Material Chemistry, Xi'an710049, P. R. China.
The use of polyoxometalate clusters (POMs) with multitudinous structures and surface properties as building blocks has sparked the development of cluster-assembled materials with many prospective applications. In comparison to classic molecules and assembly processes, control over the steric interactions and linkage of large POMs to achieve superlattices with multiple levels of organization remains a great challenge. This work presents a universal approach to modulate the spatial coordination behavior and configurations, and achieves a class of cluster superlattice architectures formed by linear alignment and two-dimensional arrangement of POM units.
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