Topic
Dysprosium
About: Dysprosium is a research topic. Over the lifetime, 3574 publications have been published within this topic receiving 57626 citations. The topic is also known as: element 66 & 66Dy.
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TL;DR: A dysprosium compound is reported that manifests magnetic hysteresis at temperatures up to 80 kelvin, which overcomes an essential barrier toward the development of nanomagnet devices that function at practical temperatures.
Abstract: Single-molecule magnets (SMMs) containing only one metal center may represent the lower size limit for molecule-based magnetic information storage materials. Their current drawback is that all SMMs require liquid-helium cooling to show magnetic memory effects. We now report a chemical strategy to access the dysprosium metallocene cation [(CpiPr5)Dy(Cp*)]+ (CpiPr5 = penta-iso-propylcyclopentadienyl, Cp* = pentamethylcyclopentadienyl), which displays magnetic hysteresis above liquid-nitrogen temperatures. An effective energy barrier to reversal of the magnetization of Ueff = 1,541 cm–1 is also measured. The magnetic blocking temperature of TB = 80 K for this cation overcomes an essential barrier towards the development of nanomagnet devices that function at practical temperatures.
1,198 citations
TL;DR: The exceptional magnetic axiality of 2Dy is highlighted by computational studies, which reveal this system to be the first lanthanide SMM in which all low-lying Kramers doublets correspond to a well-defined MJ value, with no significant mixing even in the higher doublets.
Abstract: ion of a chloride ligand from the dysprosium metallocene [(Cpttt)2DyCl] (1Dy Cpttt=1,2,4-tri(tert-butyl)cyclopentadienide) by the triethylsilylium cation produces the first base-free rare-earth metallocenium cation [(Cpttt)2Dy]+ (2Dy) as a salt of the non-coordinating [B(C6F5)4]− anion. Magnetic measurements reveal that [2Dy][B(C6F5)4] is an SMM with a record anisotropy barrier up to 1277 cm−1 (1837 K) in zero field and a record magnetic blocking temperature of 60 K, including hysteresis with coercivity. The exceptional magnetic axiality of 2Dy is further highlighted by computational studies, which reveal this system to be the first lanthanide SMM in which all low-lying Kramers doublets correspond to a well-defined MJ value, with no significant mixing even in the higher doublets.
825 citations
TL;DR: In the lanthanide-containing phthalocyanine complexes reported in the literature the ligand environment induces a large splitting of the ground Jmanifold, whereas in SMMs large-spin ground states arising from magnetic interactions between the metal centers of the cluster can enhance the weaker single-ion.
Abstract: The study of paramagnetic metal-ion aggregates has been of increasing interest since the observation that such molecules can exhibit magnetic memory effects. Termed singlemolecule magnets or SMMs, the important factors leading to such properties derive from the combination of a large ground-state spin and a large magnetic anisotropy of the Ising (easy-axis) type. Studies have largely been based on transition-metal compounds since they typically exhibit both of the aforementioned features. The incorporation of lanthanides into these complexes has been investigated to take advantage of the potentially large number of unpaired f-electrons available. However, very little work has been done to date on purely lanthanide-based systems. The origin of SMM behavior in lanthanide-containing compounds is more complicated than that of d-block transition-metal ions since there is likely to be a significant orbital component. In the lanthanide-containing phthalocyanine complexes reported in the literature the ligand environment induces a large splitting of the ground Jmanifold, whereas in SMMs large-spin ground states arising from magnetic interactions between the metal centers of the cluster can enhance the weaker single-ion
770 citations
TL;DR: A monometallic dysprosium complex is reported that shows the largest effective energy barrier to magnetic relaxation of Ueff =1815(1) K, approaching proposed schemes for high-temperature single-molecule magnets (SMMs).
Abstract: We report a monometallic dysprosium complex, [Dy(OtBu)2(py)5][BPh4] (5), that shows the largest effective energy barrier to magnetic relaxation of Ueff=1815(1) K. The massive magnetic anisotropy is due to bis-trans-disposed tert-butoxide ligands with weak equatorial pyridine donors, approaching proposed schemes for high-temperature single-molecule magnets (SMMs). The blocking temperature, TB , is 14 K, defined by zero-field-cooled magnetization experiments, and is the largest for any monometallic complex and equal with the current record for [Tb2N2{N(SiMe3)2}4(THF)2].
721 citations
TL;DR: The Bose-Einstein condensation (BEC) of the most magnetic element, dysprosium is reported and it is observed that stable BEC formation depends on the relative angle of a small polarizing magnetic field to the axis of the oblate trap, a property of trapped condensates only expected in the strongly dipolar regime.
Abstract: We report the Bose-Einstein condensation (BEC) of the most magnetic element, dysprosium. The Dy BEC is the first for an open f-shell lanthanide (rare-earth) element and is produced via forced evaporation in a crossed optical dipole trap loaded by an unusual, blue-detuned and spin-polarized narrowline magneto-optical trap. Nearly pure condensates of 1.5 × 10(4) (164)Dy atoms form below T = 30 nK. We observe that stable BEC formation depends on the relative angle of a small polarizing magnetic field to the axis of the oblate trap, a property of trapped condensates only expected in the strongly dipolar regime. This regime was heretofore only attainable in Cr BECs via a Feshbach resonance accessed at a high-magnetic field.
643 citations