Abstract:We have successfully synthesized the coupled spin dimer systems La(x)Ba(3-x)Mn(2)O(8) (x = 0, 0.2, 0.5, 1) and Ba(3)Mn(2-y)V(y)O(8) (y = 0.5, 1.0, 2.0). The magnetic properties have been investigated as a function of magnetic field and temperature down to 2 K. The susceptibility increases and the intradimer spin exchange interaction decreases with increase of La concentration. The most important finding in higher La doped systems reveals hysteresis in magnetization as a function of magnetic field. The substitu… Show more
“…Recently, there have been additional experimental results examining both magnetic and non-magnetic substitution of the Mn 5+ sites for Ba 3 Mn 2 O 8 . 43 The non-magnetic substituted In contrast to many other non-magnetically substituted gapped systems, no evidence for long range order was found in Ba 3 (Mn 1-x V x ) 2 O 8 . Rather, vanadium substitution creates additional quasi-elastic excitations.…”
We present inelastic neutron scattering and thermodynamic measurements characterizing the magnetic excitations in a disordered non-magnetic substituted spin-liquid antiferromagnet. The parent compound Ba 3 Mn 2 O 8 is a dimerized, quasi-two-dimensional geometrically frustrated quantum disordered antiferromagnet. We substitute this compound with non-magnetic vanadium for the S = 1 manganese atoms, Ba 3 (Mn 1-x V x ) 2 O 8 , and find that the singlet-triplet excitations which dominate the spectrum of the parent compound persist for the full range of substitution examined, x = 0.02 to 0.3. We also observe additional low-energy magnetic fluctuations which are enhanced at the greatest substitution values. These excitations may be a precursor to a lowtemperature random singlet phase which may exist in Ba 3 (Mn 1-x V x ) 2 O 8 .
“…Recently, there have been additional experimental results examining both magnetic and non-magnetic substitution of the Mn 5+ sites for Ba 3 Mn 2 O 8 . 43 The non-magnetic substituted In contrast to many other non-magnetically substituted gapped systems, no evidence for long range order was found in Ba 3 (Mn 1-x V x ) 2 O 8 . Rather, vanadium substitution creates additional quasi-elastic excitations.…”
We present inelastic neutron scattering and thermodynamic measurements characterizing the magnetic excitations in a disordered non-magnetic substituted spin-liquid antiferromagnet. The parent compound Ba 3 Mn 2 O 8 is a dimerized, quasi-two-dimensional geometrically frustrated quantum disordered antiferromagnet. We substitute this compound with non-magnetic vanadium for the S = 1 manganese atoms, Ba 3 (Mn 1-x V x ) 2 O 8 , and find that the singlet-triplet excitations which dominate the spectrum of the parent compound persist for the full range of substitution examined, x = 0.02 to 0.3. We also observe additional low-energy magnetic fluctuations which are enhanced at the greatest substitution values. These excitations may be a precursor to a lowtemperature random singlet phase which may exist in Ba 3 (Mn 1-x V x ) 2 O 8 .
“…1 Fig. 1(a)) 19 . For the relevant V concentrations studied here, the data do not suggest clustering of impurities, in which case, for the highest dilution studied, x = 0.046, the probability is 0.64 to find at least one neighboring V ion within 8Å of any given V impurity ( Fig.…”
“…In this respect it should be noted that Sr 4 LiMn 2 O 9 is deep-brown 27 and Ba 3 Mn 2 O 8 is green. 30 The size of the crystals is typical of the powder produced by solid-phase synthesis (1 µm or larger). According to the EDX data, the Ba/Mn ratio was found to be 2.12, i.e.…”
.75 Mn 3.5 O 15.75 is a new hexagonal perovskite whose crystal structure has elements typical for the layered hexagonal perovskites and quasi-one-dimensional oxides, hence representing a new polytype. It has been synthesized via a solid-state microwave route. The crystal structure was solved using a combination of X-ray and neutron diffraction data, which show that Ba 7 Li 1.75 Mn 3.5 O 15.75 crystallizes in a hexagonal unit cell with parameters a = 5.66274(2) Å and c = 16.7467(1) Å (V = 465.063(4) Å 3 ), with one formula unit, and can be described as columns of face-shared octahedra occupied by Mn 4+ and Li + cations and vacancies along the c axis separated in the ab plane by barium atoms. Every sixth layer, the coordination of Mn 5+ and Li + changes to tetrahedral. Additional local ordering of manganese and lithium atoms among cationic sites leading to the formation of a rhombohedral supercell has been observed by scanning transmission electron microscopy.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.