The topology and transport behavior of the lamellar morphology self-assembled by block copolymers in thin films are shown to depend on the length scale over which they are characterized and can be described by percolation in a network under confinement. Gold nanowires replicating the lamellar morphology were fabricated via self-assembled poly(styrene-block-methyl methacrylate) thin films and a lift-off pattern transfer process. The lamellar morphology exhibits long-range connectivity (macroscopic scale); however, characterization of electrical conduction over confined areas (5-500 μm) demonstrates a discrete probability of disconnection that arises due to the underlying network structure and a lack of self-similarity at these microscale dimensions. In particular, it is proved that the lamellar network morphology under confinement has a conductance that is nonlinear with channel length or width. The experimental results are discussed in terms of percolation theory, and a simple, two-dimensional Monte Carlo model is shown to predict the key trends in the network topology and conductance in lamellar block copolymers, including the dependencies on composition, extent of spatial confinement, and confinement geometry. These results highlight the need to exquisitely control or engineer the self-assembled nanostructured pathways formed by block copolymers to ensure consistent device performance for any application that depends upon percolating material, ionic, or electrical transport, especially when confined in any dimension. It is also concluded that the two most promising approaches for enhancing conductivity in block copolymer materials may be achieved either at the limits of (1) perfectly oriented, single-crystalline or (2) high defect density, polycrystalline microphase separated morphologies and that nanostructured systems with intermediate defect densities would be detrimental to transport in confined systems.
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http://dx.doi.org/10.1021/acsnano.5b01321 | DOI Listing |
Chemistry
January 2025
Beijing Institute of Technology, Polymer Materials, 5 Zhongguancun Nandajie, 100081, Beijing, CHINA.
The self-assembly of block copolymers (BCPs) to form nanostructures of various morphologies and controllable dimensions has been a very promising research area in nanotechnology in recent decades. This review mainly summarizes the recent advances in precise and controllable self-assembly of BCPs through a tailored nucleation-growth strategy to modulate the self-assembly behavior of the BCPs. These efforts have led to a better understanding of the self-assembly mechanisms and opened new possibilities for creating novel materials with designable properties.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China.
While synthesizing circular polymers with telechelic polyolefin building blocks recently emerged as a promising strategy for addressing conventional polyethylenes' sustainability challenges, the lack of telechelic PP (PP) with sufficient difunctional purity for polycondensation has been limiting the development of circular polypropylenes with PP-like structures and properties. Here we described a combined approach of coordinative chain transfer polymerization and transition-metal-catalyzed quenching reaction with various acyl chlorides, affording PPs with a high difunctional ratio (up to ∼99%) and broad end functional group scope. The steric effect of polymeryl-Zn species and the role of Pd catalyst were revealed by DFT.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Fudan University, Department of Macromolecular Science, 2205 Songhu Rd, 200438, Shanghai, CHINA.
Nitrogen heterocyclic carbenes (NHCs) are emerging as effective substitutes for conventional thiol ligands in surface functionalization of nanoparticles (NPs), offering exceptional stability to NPs under harsh conditions. However, the highly reactive feature of NHCs limits their use in introducing chemically active groups onto the NP surface. Herein, we develop a general yet robust strategy for the efficient surface functionalization of NPs with copolymer ligands bearing various functional groups.
View Article and Find Full Text PDFJ Colloid Interface Sci
April 2025
Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Collaborative Innovation Center of Chemistry for Energy Materials, Department of Chemistry, Fudan University, Shanghai, China. Electronic address:
Triblock Pluronics of polyoxyethylene (PEO) and polyoxypropylene (PPO) are identified as competent suppressors for copper (Cu) electroplating in advanced electronics manufacturing. However, the specific interfacial roles of PEO and PPO blocks in Pluronic suppressors, are not yet fully understood, which is crucial for the rational design of effective suppressors. Herein, the influences of composition and block arrangement of such Pluronics on the inhibition against Cu plating are systematically investigated.
View Article and Find Full Text PDFChemistry
January 2025
Huazhong University of Science and Technology, 1037 Luoyu Road, 430074, Wuhan, CHINA.
Block copolymer (BCP) microparticles, which exhibit rapid change of morphology and physicochemical property in response to external stimuli, represent a promising avenue for the development of programmable smart materials. Among the methods available for generating BCP microparticles with adjustable morphologies, the confined assembly of BCPs within emulsions has emerged as a particularly facile and versatile approach. This review provides a comprehensive overview of the role of responsive surfactants in modulating interfacial interactions at the oil-water interface, which facilitates controlled BCP microparticle morphology.
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