Browse
Submit Data
Databases
API
Help

Dataset Information

21 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Magnetic Hysteresis at 10 K in Single Molecule Magnet Self-Assembled on Gold.

ABSTRACT: Tremendous progress in the development of single molecule magnets (SMMs) raises the question of their device integration. On this route, understanding the properties of low-dimensional assemblies of SMMs, in particular in contact with electrodes, is a necessary but difficult step. Here, it is shown that fullerene SMM self-assembled on metal substrate from solution retains magnetic hysteresis up to 10 K. Fullerene-SMM DySc₂N@C₈₀ and Dy₂ScN@C₈₀ are derivatized to introduce a thioacetate group, which is used to graft SMMs on gold. Magnetic properties of grafted SMMs are studied by X-ray magnetic circular dichroism and compared to the films of nonderivatized fullerenes prepared by sublimation. In self-assembled films, the magnetic moments of the Dy ions are preferentially aligned parallel to the surface, which is different from the disordered orientation of endohedral clusters in nonfunctionalized fullerenes. Whereas chemical derivatization reduces the blocking temperature of magnetization and narrows the hysteresis of Dy₂ScN@C₈₀, for DySc₂N@C₈₀ equally broad hysteresis is observed as in the fullerene multilayer. Magnetic bistability in the DySc₂N@C₈₀ grafted on gold is sustained up to 10 K. This study demonstrates that self-assembly of fullerene-SMM derivatives offers a facile solution-based procedure for the preparation of functional magnetic sub-monolayers with excellent SMM performance.

SUBMITTER: Chen CH

PROVIDER: S-EPMC7927621 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Magnetic hysteresis in self-assembled monolayers of Dy-fullerene single molecule magnets on gold.

Project description:Fullerene single molecule magnets (SMMs) DySc2N@C80 and Dy2ScN@C80 are functionalized via a 1,3-dipolar cycloaddition with surface-anchoring thioether groups. The SMM properties of Dy-fullerenes are substantially affected by the cycloaddition. Submonolayers of the physisorbed derivatives exhibit magnetic hysteresis on an Au(111) surface at 2 K as revealed by X-ray magnetic circular dichroism.

| S-EPMC6018719 | biostudies-literature

Ferroelectric Single-Molecule Magnet with Toroidal Magnetic Moments.

Project description:Materials that coexist magnetic and electric properties on the molecular scale in single-molecule magnets (SMMs) with peculiar quantum behaviors have promise in molecular electronics and spintronics. Nevertheless, such molecular materials are limited in potentials because their magnetic signal cannot be transformed into an electrical signal through magnetoresistance or Hall effects for their high insulativity. The discovery of an entirely new material, ferroelectric SMMs (FE SMMs) is reported. This FE SMM also shows single-molecule magnetic behaviors, toroidal magnetic moments, and room-temperature ferroelectricity. The toroidal moment is formed by a vortex distribution of magnetic dipoles in triangular Dy3 clusters. The analysis of ac magnetic susceptibility reveals the coexistence of three distinct magnetic relaxation processes at low temperatures. The ferroelectricity is introduced by incorporating polar alcohol molecules in the structure, which is confirmed by the X-ray diffraction and optical second harmonic generation (SHG) measurements. Moreover, the dielectric measurements reveal a ferroelectric-to-ferroelectric phase transition around 150 K due to the symmetry change from Pc to Pna21 . The coexistence of toroidal moment and ferroelectricity along with quantum magnetism in the rare-earth single-molecule magnets yields a unique class of multiferroics.

| S-EPMC9475528 | biostudies-literature

Partial magnetic ordering in one-dimensional arrays of endofullerene single-molecule magnet peapods.

Project description:The magnetic ordering and bistability of one-dimensional chains of endofullerene Dy2ScN@C80 single-molecule magnets (SMMs) packed inside single-walled carbon nanotubes (SWCNTs) have been studied using high-resolution transmission electron microscopy (HRTEM), X-ray magnetic circular dichroism (XMCD), and ab initio calculations. X-ray absorption measurements reveal that the orientation of the encapsulated endofullerenes differs from the isotropic distribution in the bulk sample, indicating a partial ordering of the endofullerenes inside the SWCNTs. The effect of the one-dimensional packing was further investigated by ab initio calculations, demonstrating that for specific tube diameters, the encapsulation is leading to energetically preferential orientations of the endohedral clusters. Additionally, element-specific magnetization curves reveal a decreased magnetic bistability of the encapsulated Dy2ScN@C80 SMMs compared to the bulk analog.

| S-EPMC6839967 | biostudies-literature

3-Pyridylacetic-Based Lanthanide Complexes Exhibiting Magnetic Entropy Changes, Single-Molecule Magnet, and Fluorescence.

Project description:Four complexes from lanthanides, 3-pyridylacetate, and 1,10-phenanthroline, formulated as [Ln2(3-PAA)2(μ-Cl)2(phen)4](ClO4)2 [Ln = Gd(1), Dy(2), Eu(3), Tb(4), 3-PAA = 3-pyridylacetic acid, phen = 1,10-phenanthroline], were obtained. The four compounds were characterized by IR spectra, thermogravimetric analyses, powder X-ray diffraction, and single-crystal X-ray diffraction. Compounds 1-4 are isomorphous, and they have a dinuclear structure. Magnetic studies reveal that 1 shows the magnetocaloric effect with -ΔS m max = 19.03 J kg-1 K-1 at 2 K for ΔH = 5 T, and 2 displays a field-induced single-molecule magnet with U eff = 19.02 K. The photoluminescent spectra of 3 and 4 exhibit strong characteristic emission, which demonstrate that the ligand-to-EuIII/TbIII energy transfer is efficient.

| S-EPMC8793079 | biostudies-literature

Hysteresis stabilizes dynamic control of self-assembled army ant constructions.

Project description:Biological systems must adjust to changing external conditions, and their resilience depends on their control mechanisms. How is dynamic control implemented in noisy, decentralized systems? Army ants' self-assembled bridges are built on unstable features, like leaves, which frequently move. Using field experiments and simulations, we characterize the bridges' response as the gaps they span change in size, identify the control mechanism, and explore how this emerges from individuals' decisions. For a given gap size, bridges were larger after the gap increased rather than decreased. This hysteresis was best explained by an accumulator model, in which individual decisions to join or leave a bridge depend on the difference between its current and equilibrium state. This produces robust collective structures that adjust to lasting perturbations while ignoring small, momentary shifts. Our field data support separate joining and leaving cues; joining is prompted by high bridge performance and leaving by an excess of ants. This leads to stabilizing hysteresis, an important feature of many biological and engineered systems.

| S-EPMC8897433 | biostudies-literature

Single-Molecule Mechanistic Study of Enzyme Hysteresis.

Project description:Hysteresis is an important feature of enzyme-catalyzed reactions, as it reflects the influence of enzyme regulation in the presence of ligands such as substrates or allosteric molecules. In typical kinetic studies of enzyme activity, hysteretic behavior is observed as a "lag" or "burst" in the time course of the catalyzed reaction. These lags and bursts are due to the relatively slow transition from one state to another state of the enzyme molecule, with different states having different kinetic properties. However, it is difficult to understand the underlying mechanism of hysteresis by observing bulk reactions because the different enzyme molecules in the population behave stochastically. In this work, we studied the hysteretic behavior of mutant ?-glucuronidase (GUS) using a high-throughput single-molecule array platform and investigated the effect of thermal treatment on the hysteresis.

| S-EPMC6813718 | biostudies-literature

Single-Step Organization of Plasmonic Gold Metamaterials with Self-Assembled DNA Nanostructures.

Project description:Self-assembled DNA nanostructures hold great promise as nanoscale templates for organizing nanoparticles (NPs) with near-atomistic resolution. However, large-scale organization of NPs with high yield is highly desirable for nanoelectronics and nanophotonic applications. Here, we design five-strand DNA tiles that can readily self-assemble into well-organized micrometer-scale DNA nanostructures. By organizing gold nanoparticles (AuNPs) on these self-assembled DNA nanostructures, we realize the fabrication of one- and two-dimensional Au nanostructures in single steps. We further demonstrate the one-pot synthesis of Au metamaterials for highly amplified surface-enhanced Raman Scattering (SERS). This single-step and high-yield strategy thus holds great potential for fabricating plasmonic metamaterials.

| S-EPMC6750079 | biostudies-literature

Modulated self-reversed magnetic hysteresis in iron oxides.

Project description:The steadfast rule of a ferromagnetic hysteresis loop claims its saturation positioned within the first and third quadrants, whereas its saturation positioned in the second and fourth quadrants (named as self-reversed magnetic hysteresis) is usually taken as an experimental artifact and is always intentionally ignored. In this report, a new insight in this unique hysteresis phenomenon and its modulation were discussed in depth. Different iron oxides (magnetite, maghemite and hematite) with varying dimensions were soaked in FeCl3 aqueous solution and absorbed Fe3+ cations due to their negative enough surface zeta potentials. These iron oxides@Fe3+ core-shell products exhibit well pronounced self-reversed magnetic hysteresis which concurrently have typical diamagnetic characteristics and essential ferromagnetic features. The presence of pre-magnetized Fe3+ shell and its negatively magnetic exchange coupling with post-magnetized iron-oxide core is the root cause for the observed phenomena. More strikingly, this self-reversed magnetic hysteresis can be readily modulated by changing the core size or by simply controlling Fe3+ concentration in aqueous solution. It is anticipated that this work will shed new light on the development of spintronics, magnetic recording and other magnetically-relevant fields.

| S-EPMC5318991 | biostudies-literature

Analysis of the Magnetic Coupling in a Mn(II)-U(V)-Mn(II) Single Molecule Magnet.

Project description:[{Mn(TPA)I}{UO2(Mesaldien)}{Mn(TPA)I}]I formula (here TPA=tris(2-pyridylmethyl)amine and Mesaldien=N,N'-(2-aminomethyl)diethylenebis(salicylidene imine)) reported by Mazzanti and coworkers (Chatelain et al. Angew. Chem. Int. Ed. 2014, 53, 13434) is so far the best Single Molecule Magnet (SMM) in the {3d-5f} class of molecules exhibiting barrier height of magnetization reversal as high as 81.0 K. In this work, we have employed a combination of ab initio CAS and DFT methods to fully characterize this compound and to extract the relevant spin Hamiltonian parameters. We show that the signs of the magnetic coupling and of the g-factors of the monomers are interconnected. The central magnetic unit [UV O2 ]+ is described by a Kramers Doublet (KD) with negative g-factors, due to a large orbital contribution. The magnetic coupling for the {Mn(II)-U(V)} pair is modeled by an anisotropic exchange Hamiltonian: all components are ferromagnetic in terms of spin moments, the parallel component JZ twice larger as the perpendicular one J⊥ . The spin density distribution suggests that spin polarization on the U(V) center favors the ferromagnetic coupling. Further, the JZ /J⊥ ratio, which is related to the barrier height, was found to correlate to the corresponding spin contribution of the g-factors of the U(V) center. This correlation established for the first time offers a direct way to estimate this important ratio from the corresponding gS -values, which can be obtained using traditional ab initio packages and hence has a wider application to other {3d-5f} magnets. It is finally shown that the magnetization barrier height is tuned by the splitting of the [UV O2 ]+ 5 f orbitals.

| S-EPMC10092672 | biostudies-literature

A Gadolinium(III) Complex Based on Pyridoxine Molecule with Single-Ion Magnet and Magnetic Resonance Imaging Properties

Project description: Not available

| S-EPMC10889197 | biostudies-literature