Depositing carbon nanotubes (CNTs) into carbon fiber reinforced polymer composites (CFRPs) is challenging because of the need for complicated lab-scale processes and toxic chemical dispersants that makes conventional means of processing less compatible with existing industrial procedures for large-scale applications. In this work, a scalable supercritical CO2-assisted atomization technique is used to effectively deposit hybrid CNTs in CFRPs allowing them to boost their functionality and tailor the microstructure. Cellulose nanocrystals (CNCs) are utilized to create hybrid nanostructures with CNTs (CNC bonded CNT) that enables stabilization of CNTs in nontoxic media, i.e., water, and this promotes the scalability of the process. According to Zeta potential values, CNCs successfully stabilize CNTs in water suspension. Scanning electron microscopy (SEM) micrographs show hybrid CNC bonded CNTs are homogeneously dispersed on the carbon fiber surface. According to the in-situ bending test under the optical microscope, crack propagation is hindered by engineered hybrid CNT nanostructures in the modified CFRP whereas neat CFRP exhibits low crack growth resistance due to the uninterrupted crack propagation in the continuous epoxy matrix. Our results imply that this strategy probes the importance of new controlled manufacturing of hybrid nanostructures through evaporation‑induced self‑assembly of nanocolloidal droplets, and allows for tailoring of the desired properties of nanostructured composites.
Achieving desired performance from self‐assembly of nanoparticles (NPs) is challenging due to the stochastic nature of interactions among the constituent building blocks. Self‐assembly of nano‐colloids through evaporation of particle‐laden droplets can be exploited to fabricate tailored nanostructures that add functionality and engineer the properties of manufactured components. The particle–particle and particle–solvent interactions, and delicate force balance among them are the main factors that define the pattern of the final 3D nanostructure. Here, a nanoparticle‐agnostic approach that allows the fabrication of nanostructures with precisely engineered patterns is introduced. Evaporative droplets of aqueous suspensions of pristine Carbon Nanotubes, Graphene Nanoplatelets, and Boron Nitride Nanotubes representing NPs of different elemental compositions, sizes, and shapes are investigated. Cellulose nanocrystals (CNCs) are used as a platform to make hybrid systems of CNC‐NP and utilize the repulsive‐attractive‐directional interactions in these multimaterial systems to enforce the desired final pattern between ring and disk. It is shown that irrespective of the type of NPs, the amphiphilicity of the hybrid system dictates the formation of deposited patterns. Finally, the effect of self‐assembled patterns on the functionality of multi‐material systems is demonstrated. The proposed method creates new capabilities in the precisely controlled nanostructures and facilitates smart self‐assembly systems.
more » « less- Award ID(s):
- 2134465
- NSF-PAR ID:
- 10393036
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Advanced Materials Technologies
- Volume:
- 8
- Issue:
- 7
- ISSN:
- 2365-709X
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
Abstract Light‐induced self‐assembly offers a new route to build mesoscale optical matter arrays from nanoparticles (NPs), yet the low stability of optical matter systems limits the assembly of large‐scale NP arrays. Here it is shown that the interferometric optical fields created by illuminating a single Ag nanowire deposited on a coverslip can enhance the electrodynamic interactions among NPs. The Ag nanowire serves as a plasmonic antenna to shape the incident laser beam and guide the optical assembly of colloidal metal (Ag and Au) and dielectric (polystyrene) NPs in solution. By controlling the laser polarization direction, both the mesoscale interactions among multiple NPs and the near‐field coupling between the NPs and nanowire can be tuned, leading to large‐scale and stable optical matter arrays consisting of up to 60 NPs. These results demonstrate that single Ag nanowires can serve as multifunctional antennas to guide the optical trapping and binding of multiple NPs and provide a new strategy to control electrodynamic interactions using hybrid nanostructures.
-
null (Ed.)Hybrid organic–inorganic composites possessing both electronic and magnetic properties are promising materials for a wide range of applications. Controlled and ordered arrangement of the organic and inorganic components is key for synergistic cooperation toward desired functions. In this work, we report the self-assemblies of core–shell composite nanofibers from conjugated block copolymers and magnetic nanoparticles through the cooperation of orthogonal non-covalent interactions. We show that well-defined core–shell conjugated polymer nanofibers can be obtained through solvent induced self-assembly and polymer crystallization, while hydroxy and pyridine functional groups located at the shell of nanofibers can immobilize magnetic nanoparticles via hydrogen bonding and coordination interactions. These precisely arranged nanostructures possess electronic properties intrinsic to the polymers and are simultaneously responsive to external magnetic fields. We applied these composite nanofibers in organic solar cells and found that these non-covalent interactions led to controlled thin film morphologies containing uniformly dispersed nanoparticles, although high loadings of these inorganic components negatively impact device performance. Our methodology is general and can be utilized to control the spatial distribution of functionalized organic/inorganic building blocks, and the magnetic responsiveness and optoelectronic activities of these nanostructures may lead to new opportunities in energy and electronic applications.more » « less
-
Abstract Self-organized complex structures in nature, e.g., viral capsids, hierarchical biopolymers, and bacterial flagella, offer efficiency, adaptability, robustness, and multi-functionality. Can we program the self-assembly of three-dimensional (3D) complex structures using simple building blocks, and reach similar or higher level of sophistication in engineered materials? Here we present an analytic theory for the self-assembly of polyhedral nanoparticles (NPs) based on their crystal structures in non-Euclidean space. We show that the unavoidable geometrical frustration of these particle shapes, combined with competing attractive and repulsive interparticle interactions, lead to controllable self-assembly of structures of complex order. Applying this theory to tetrahedral NPs, we find high-yield and enantiopure self-assembly of helicoidal ribbons, exhibiting qualitative agreement with experimental observations. We expect that this theory will offer a general framework for the self-assembly of simple polyhedral building blocks into rich complex morphologies with new material capabilities such as tunable optical activity, essential for multiple emerging technologies.
-
Three-dimensional (3D) nanostructures play a crucial role in nanophotonics, lasers, and optical systems. This article reports on the fabrication of 3D nanostructures consisting of opal structures that are spatially aligned to an array of holes defined in the photoresist. The proposed method uses colloidal lithography to pattern a hexagonal array of holes, which are then used to direct the subsequent 3D assembly of colloidal particles. This approach allows the 3D opal structures to be aligned with the 2D array of holes, which can enhance spatial-phase coherence and reduce defects. The polymer patterns can be used as a sacrificial template for atomic layer deposition and create free-standing nanolattices. The final structure consists of a combination of nanolattice, upon which controlled deposition of opal structures is achieved. These structures result in nanostructured materials with high porosity, which is essential to create low-index materials for nanophotonics. A thick layer of titanium oxide with high refractive index is deposited over nanolattices to demonstrate the mechanical stability of underlying structures. These nanolattice structures with precisely controlled height can serve as a low-index layer and can find applications in Bragg reflectors, nanophotonics, and optical multilayers.