We present experiments involving oscillating droplets in aqueous cyclodextrin-surfactant solutions. In these experiments, α-cyclodextrin (αCD) and anionic surfactants exhibit remarkable viscoelasticity at the liquid/air interface, with dilatational modulus varying across orders of magnitude. This rheological response depends on the concentrations of different complexes in the solution, particularly of the 2 : 1 inclusion complexes formed by two αCD molecules (αCD), and one surfactant (S). We propose a model that describes the distribution of these complexes on the droplet surface using a free energy approach, accounting for dipole-dipole interactions. The results of the model reproduce the interfacial behavior of the viscoelastic modulus and phase shift in excellent agreement with the data, clearly indicating that dipole-dipole interactions determine and control the viscoelastic properties of the drops.
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http://dx.doi.org/10.1039/d4sm01007h | DOI Listing |
Nanomaterials (Basel)
December 2024
College of Science, Inner Mongolia University of Technology, Hohhot 010051, China.
Relaxor ferroelectric film capacitors exhibit high power density with ultra-fast charge and discharge rates, making them highly advantageous for consumer electronics and advanced pulse power supplies. The Aurivillius-phase bismuth layered ferroelectric films can effectively achieve a high breakdown electric field due to their unique insulating layer ((BiO) layer)). However, designing and fabricating Aurivillius-phase bismuth layer relaxor ferroelectric films with optimal energy storage characteristics is challenging due to their inherently stable ferroelectric properties.
View Article and Find Full Text PDFGels
December 2024
Research Institute of Smart Medicine and Biological Engineering, Health Science Center, Ningbo University, Ningbo 315211, China.
Many tissues exhibit structural anisotropy, which imparts orientation-specific properties and functions. However, recapitulating the cellular patterns found in anisotropic tissues presents a remarkable challenge, particularly when using soft and wet hydrogels. Herein, we develop self-assembled anisotropic magnetic FeO micropatterns on polyethylene glycol hydrogels utilizing dipole-dipole interactions.
View Article and Find Full Text PDFNano Lett
December 2024
Anhui Province Key Laboratory of Low-Energy Quantum Materials and Devices, High Magnetic Field Laboratory, HFIPS, Chinese Academy of Sciences, Hefei, 230031, China.
We report deterministic operations on single dipolar skyrmions confined in nanostructured cuboids by using in-plane currents. We achieve highly reversible writing and deleting of skyrmions in a simple cuboid without any artificial defects or pinning sites. The current-induced creation of skyrmions is well-understood through the spin-transfer torque acting on surface spin twists of the spontaneous 3D ferromagnetic state, caused by the magnetic dipole-dipole interaction of the uniaxial FeSn magnet with a low-quality factor.
View Article and Find Full Text PDFACS Nano
December 2024
Department of Materials Science and Engineering, Technion - Israel Institute of Technology, Haifa 32000, Israel.
Collective optical properties can emerge from an ordered ensemble of emitters due to interactions between the individual units. Superlattices of halide perovskite nanocrystals exhibit collective light emission, influenced by dipole-dipole interactions between simultaneously excited nanocrystals. This coupling changes both the emission energy and rate compared to the emission of uncoupled nanocrystals.
View Article and Find Full Text PDFJ Sep Sci
December 2024
Department of Chromatography and Mass Spectrometry, Institute of Horticulture, Dobele, Latvia.
Silica-based monoliths offer higher separation efficiency per unit pressure drop compared to particle-packed columns. Their application is limited by the commercial availability of different column chemistries. Pentafluorophenyl ligands enable hydrogen bonding, dipole-dipole, π-π, and hydrophobic interactions, facilitating the separation of various compounds.
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