Spin–glass magnetism in RFeTi2O7 (R=Lu and Tb) compounds

20th International Conference on Magnetism.The compounds RFeTi2O7 (R=Lu and Tb) crystallize at room temperature in centrosymmetric orthorhombic space group Pcnb. There are five non-equivalent positions of the iron ions: the two positions, Fe’ and Fe”, in the octahedron consisting of the Fe’ tetrahedron and Fe” five-vertex polyhedron and the three positions, Fe1, Fe2 and Fe3 in the mixed Fe-Ti octahedra [1]. The populations of the mixed Fe-Ti sites are different. The crystal structure features lead to atomic disorder in the distribution of the magnetic ions in this compound. From low temperature heat capacity, magnetization and frequency dependent ac susceptibility we conclude that both compounds undergo a spin glass transition at TSG=4.5 and 6 K for R =Lu and Tb, respectively. Since Lu is not magnetic, in RFeTi2O7 the spin glass behavior is caused by the disordered distribution of the magnetic Fe3+ ions in the different crystallographic positions. The substitution of the magnetic and highly anisotropic Tb ion instead of Lu increases TSG because of the additional Tb-Fe exchange interaction, while the critical exponent of the frequency dependence on temperature hardly varies. The spin glass behavior in these crystalline compounds is caused by the presence of competitive interactions that lead to frustration.The financial support of the Spanish MINECO MAT2011-23791, MAT2014-53921-R and Aragonese DGA-IMANA E34 projects is acknowledged.Peer Reviewe

Roles of moisture and cyclic loading in microstructures and their effects on mechanical properties for typical Chinese bituminous coals

This work aimed at studying the roles of moisture and cyclic loading in microstructures and their effects on mechanical properties for typical Chinese bituminous coals. Different relative moisture contents (100%, 75%, 50%, 25%, and 0%) for Shenmu coal (SM), Hongshaquan coal (HSQ), and Wucaiwan coal (WCW) were chosen to study the effects of moisture. The raw SM was then further selected to investigate the effects of cyclic loading. Images of coals surfaces and mechanical properties during simulated crushing process were recorded and combined to be analyzed. The results showed that the moisture possessed significant effects on coal mechanical properties, which strongly depended on their porosities. As for low porosity coal (SM), the adsorption of moisture can soften and lubricate the microstructures, weakening mechanical properties. While the drying process would destroy the microstructures and decease mechanical properties for high porosity coals (HSQ and WCW). Under the cyclic loading process, the cumulative effects of strain showed a step-up state and the first cyclic loading can typically cause the biggest change of microstructures and produce the largest strain under different stress levels. Finally, a normalized quantitative relationship ([fórmula]) between the relative fractal dimension and relative stress was built

Heteronuclear {TbxEu1-x} furoate 1D polymers presenting luminescent properties and SMM behavior

We report the synthesis, crystal structure and photo-magnetic properties of novel Tb/Eu polymeric complexes of general formula {TbxEu1-x(a-fur)3(H2O)3}n, supported by 2-furancarboxilic acid: the homonuclear Tb(iii) complex {Tb} (1), four heterodinuclear complexes, {Tb0.8Eu0.2} (2), {Tb0.7Eu0.3} (3), {Tb0.3Eu0.7} (4), and {Tb0.1Eu0.9} (5), and the homonuclear Eu(iii)-only complex {Eu} (6). X-ray diffraction experiments show that the a-furoate ligands, acting in bridging mode, consolidate the 1D polymeric chains along the c-axis. Luminescence studies show the sensitization capability of the furoic acid ligand. Color tuning from green to red can be successfully achieved through the heterodinuclear strategy. We have measured Eu emission by direct excitation at the resonant 7F0 ¿ 5L6 (395 nm), and indirectly, by excitation of the non-resonant wavelength (280 nm) which provokes ligand ¿ Tb ¿ Eu energy transfer. Besides, ac susceptibility measurements under varying frequencies and temperatures reveal that mixed {TbxEu1-x} complexes exhibit field-induced slow relaxation dynamics, with extremely slow relaxation times, owing to direct processes affected by the bottleneck effect. Thus, the {TbxEu1-x} complexes represent interesting low-dimensional multifunctional materials combining both luminescent and SMM magnetic properties

Antiferromagnetic single-chain magnet slow relaxation in the {Tb(α-fur)3}n polymer with non-Kramers ions

We report the synthesis, crystal structure and magnetic properties of a new molecular complex based on a Tb(iii) ion supported by 2-furancarboxylic molecules: {Tb(α-fur)(HO)} (α-fur = CHOCOO). Two slightly different Tb sites (A and B) exist depending on the position of one of the dangling ligands. Ab initio calculations predict that, for both sites, the magnetic ground state is highly anisotropic (g∗ = 17.8) and consists of a quasi-doublet with a small gap, well isolated from the next excited state. The α-fur ligand forms 1D polymeric chains of Tb ions of the same type (either A or B) running along the c-axis. The crystal structure is formed by the supramolecular stacking along the a-axis of 2D layers containing parallel chains of the same type. Static magnetization and heat capacity measurements show that, magnetically, the system can be modeled as an ensemble of Ising chains of non-Kramers Tb ions with effective spin S∗ = 1/2, antiferromagnetically (AF) coupled by a weak intrachain interaction (J∗/k = -0.135 K). At very low temperatures, the static susceptibility reflects the presence of a 2-4% concentration of defects in the chains. Ac susceptibility measurements at H = 0 performed down to mK temperatures have enabled us to observe the slow relaxation of magnetization through two different pathways. They are assigned to Single-Chain-Magnet (SCM) behavior in two different types of AF chains (A and B), triggered by the existence of defects breaking the chains into segments with short-range order. At temperatures below 0.1 K this mechanism is replaced by individual relaxation of the ions through direct processes. Under the application of a magnetic field the system slowly relaxes by two distinct direct processes, strongly affected by a phonon bottleneck effect.This work has been financed by MECOM Projects MAT11/23791 and MAT11/27233-C02-02, MAT2015-68204-R, MAT2014-53921-R, DGA IMANA E34 and MOLCHIP E98 Projects. Consolider Nanoselect (CSD2007-00041) and by a grant of the Ministry of National Education, CNCS – UEFISCDI, project number PN-II-ID-PCE-2012-4-0261. D. P. thanks the Alexander von Humboldt (AvH) Foundation for financial support.Peer Reviewe

Heteronuclear {TbxEu1-x} furoate 1D polymers presenting luminiscent properties and SMM behavior

We report the synthesis, crystal structure and photo-magnetic properties of novel Tb/Eu polymeric complexes of general formula {TbxEu1−x(α-fur)3(H2O)3}n, supported by 2-furancarboxilic acid: the homonuclear Tb(III) complex {Tb} (1), four heterodinuclear complexes, {Tb0.8Eu0.2} (2), {Tb0.7Eu0.3} (3), {Tb0.3Eu0.7} (4), and {Tb0.1Eu0.9} (5), and the homonuclear Eu(III)-only complex {Eu} (6). X-ray diffraction experiments show that the α-furoate ligands, acting in bridging mode, consolidate the 1D polymeric chains along the c-axis. Luminescence studies show the sensitization capability of the furoic acid ligand. Color tuning from green to red can be successfully achieved through the heterodinuclear strategy. We have measured Eu emission by direct excitation at the resonant 7F0 → 5L6 (395 nm), and indirectly, by excitation of the non-resonant wavelength (280 nm) which provokes ligand → Tb → Eu energy transfer. Besides, ac susceptibility measurements under varying frequencies and temperatures reveal that mixed {TbxEu1−x} complexes exhibit field-induced slow relaxation dynamics, with extremely slow relaxation times, owing to direct processes affected by the bottleneck effect. Thus, the {TbxEu1−x} complexes represent interesting low-dimensional multifunctional materials combining both luminescent and SMM magnetic properties

Heteronuclear {TbxEu1−x} furoate 1D polymers presenting luminescent properties and SMM behavior

We report the synthesis, crystal structure and photo-magnetic properties of novel Tb/Eu polymeric complexes of general formula {TbxEu1−x(α-fur)3(H2O)3}n, supported by 2-furancarboxilic acid: the homonuclear Tb(III) complex {Tb} (1), four heterodinuclear complexes, {Tb0.8Eu0.2} (2), {Tb0.7Eu0.3} (3), {Tb0.3Eu0.7} (4), and {Tb0.1Eu0.9} (5), and the homonuclear Eu(III)-only complex {Eu} (6). X-ray diffraction experiments show that the α-furoate ligands, acting in bridging mode, consolidate the 1D polymeric chains along the c-axis. Luminescence studies show the sensitization capability of the furoic acid ligand. Color tuning from green to red can be successfully achieved through the heterodinuclear strategy. We have measured Eu emission by direct excitation at the resonant 7F0 → 5L6 (395 nm), and indirectly, by excitation of the non-resonant wavelength (280 nm) which provokes ligand → Tb → Eu energy transfer. Besides, ac susceptibility measurements under varying frequencies and temperatures reveal that mixed {TbxEu1−x} complexes exhibit field-induced slow relaxation dynamics, with extremely slow relaxation times, owing to direct processes affected by the bottleneck effect. Thus, the {TbxEu1−x} complexes represent interesting low-dimensional multifunctional materials combining both luminescent and SMM magnetic properties

Genetic Algorithm to Evolve Ensembles of Rules for On-Line Scheduling on Single Machine with Variable Capacity

International Work-Conference on the Interplay Between Natural and Artificial Computation, IWINAC (8th . 2019. Almería, Spain

Luminiscent and Magnetic Tb-MOF Flakes Deposited on Silica

The synthesis of a terbium-based 2D metal-organic framework (MOF), of formula [Tb(MeCOO)(PhCOO)2] (1), a crystalline material formed by neutral nanosheets held together by Van der Waals interactions, is presented. The material can be easily exfoliated by sonication and deposited onto different substrates. Uniform distributions of Tb-2D MOF flakes onto silicon were obtained by spin-coating. We report the luminescent and magnetic properties of the deposited flakes compared with those of the bulk. Complex 1 is luminescent in the visible and has a sizeable quantum yield of QY = 61% upon excitation at 280 nm. Photoluminescence measurements performed using a micro-Raman set up allowed us to characterize the luminescent spectra of individual flakes on silicon. Magnetization measurements of flakes-on-silicon with the applied magnetic field in-plane and out-of-plane display anisotropy. Ac susceptibility measurements show that 1 in bulk exhibits field-induced slow relaxation of the magnetization through two relaxation paths and the slowest one, with a relaxation time of tlf ⇡ 0.5 s, is assigned to a direct process mechanism. The reported exfoliation of lanthanide 2D-MOFs onto substrates is an attractive approach for the development of multifunctional materials and devices for different applications