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Nanosized polymeric Janus particles (NPJPs) have important applications in a variety of theoretical and practical research fields. However, the methods that are versatile and can prepare NPJPs highly efficiently are very limited. Herein, we reported a two-step thermodynamically controlled preparation of NPJPs with a high yield using a diblock copolymer as the precursor. At the first step, A--B coassembled in the solution with a partner diblock copolymer C--B to form the mixed shell micelles (MSMs) with B core and A/C mixed shell. Then, intramicellarly covalently cross-linking the A block chains resulted in the complete phase separation of A and C chains in the mixed shell, leading to the direct conversion of the MSMs into NPJPs. The first step, diblock copolymer micellization, is known as a thermodynamically controlled process, and we also made the second step, conversion from MSMs to NPJPs, be thermodynamically controlled due to the application of covalent cross-linking. As the result, the conversion efficiency is close to 100%. Besides, it was further confirmed that the method can be applied to different systems and used to tune the Janus balance. Therefore, this conversion should be very significant for the fabrication and application of the NPJPs.
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http://dx.doi.org/10.1021/acsmacrolett.7b00296 | DOI Listing |
iScience
December 2024
Center for Reproductive Medicine and Obstetrics & Gynecology, Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, Nanjing, China.
Thermodynamic theory suggests that the obvious mechanical behavior caused by temperature and interlayer angle will affect the physical properties of materials, such as mechanical properties and transportation behavior, and it is different from the behavior in three-dimensional bulk materials. We observe an abnormal physical effect of bilayer graphene/hexagonal boron nitride (G/BN)-carbon nanotube (CNT) heterostructures, with a normalized out-of-plane deformation and normalized bond angle percentage to almost several times higher those of pristine G/BN heterostructures (without CNT) at 700-800 K. Our combined finite element theory and molecular dynamics simulations confirmed that the combination of CNT and interlayer angle diverted and bridged the propagating crack and provided a stable crack propagation path and crack tip opening displacement, resulting in the stress fields to be controlled around the CNT at high temperature.
View Article and Find Full Text PDFLangmuir
December 2024
Department of Chemical and Materials Engineering, University of Alberta, Edmonton, AB, Canada T6G 1H9.
We investigated the role of a nanoporous particle on the formation of macroscopic solid in the framework of equilibrium thermodynamics and from the free-energy perspective. The model particle has cylindrical pores with equidistant circular openings on the particle surface. We focused on two potentially limiting steps: (i) the solid nucleation from liquid inside a single pore and (ii) the bridging of multiple pores on the particle surface.
View Article and Find Full Text PDFACS Nanosci Au
December 2024
Department of Materials Science and Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.
Colloidal nanoparticle assembly methods can produce intricate superlattice structures and often use knowledge of atomic crystallization behaviors to guide their design. While this analogy has enabled multiple routes to programming colloidal crystallization thermodynamics, fewer tools or strategies exist to manipulate nanoparticle superlattice growth kinetics in a controlled manner. Here we investigate how small-molecule additives can be used to modulate the thermodynamics and kinetics of supramolecular-chemistry-driven nanoparticle assembly.
View Article and Find Full Text PDFACS Omega
December 2024
School of Earth and Environment, Anhui University of Science and Technology, Huainan 232001, P. R. China.
A strategically designed ternary nanohybrid (TNS-PDA/CNT), consisting of titanate nanosheet (TNS) and polydopamine-modified multiwalled carbon nanotube (PDA/CNT composite), was synthesized by the facile hydrothermal method and wet impregnation method for removal of U(VI) from aqueous solution and were characterized by transmission electron microscopy (TEM), scanning electron microscopy-energy-dispersive X-ray spectroscopy (SEM-EDS), X-ray diffraction (XRD), Fourier transform infrared (FT-IR), thermogravimetric analysis (TGA), Raman spectroscopy, Brunauer-Emmett-Teller (BET), and X-ray photoelectron spectroscopy (XPS). TNSs were introduced into the PDA/CNT composite, which effectively averted the agglomeration of the CNT and further exposed more adsorption sites. PDA thin layer exposing more active sites was conducive to enhance adsorption capacity and kinetic.
View Article and Find Full Text PDFCryst Growth Des
December 2024
Eindhoven Institute of Renewable Energy Systems, Eindhoven University of Technology, PO Box 513, Eindhoven 5600 MB, The Netherlands.
The hydration of salt hydrates is often described as a solution mediated nucleation and growth mechanism, occurring between a reagent and a product in thermodynamic equilibrium with each other. If a system possesses more than one hydrate phase, the kinetic pathway may involve additional mechanisms due to the formation of intermediate hydrate species. We elected CuSO as our model system and analyzed the pathway leading from CuSO·HO (C1H) to CuSO·5HO (C5H), while CuSO·3HO (C3H) being a possible intermediate.
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