Searcharxiv⌕ Search

arXiv subjects

J. L. Manson

Publications and source records attributed to J. L. Manson.

23 records · Page 2Linked to original sources

Isotope effect in quasi-two-dimensional metal-organic antiferromagnets

Although the isotope effect in superconducting materials is well-documented, changes in the magnetic properties of antiferromagnets due to isotopic substitution are seldom discussed and remain poorly understood. This is perhaps surprising given the possible link between the quasi-two-dimensional (Q2D) antiferromagnetic and superconducting phases of the layered cuprates. Here we report the experimental observation of shifts in the Néel temperature and critical magnetic fields ($ΔT_{\rm N}/T_{\rm N}\approx 4%$; $ΔB_{\rm c}/B_{\rm c}\approx 4%$) in a Q2D organic molecular antiferromagnets on substitution of hydrogen for deuterium. These compounds are characterized by strong hydrogen bonds through which the dominant superexchange is mediated. We evaluate how the in-plane and inter-plane exchange energies evolve as the hydrogens on different ligands are substituted, and suggest a possible mechanism for this effect in terms of the relative exchange efficiency of hydrogen and deuterium bonds.

cond-mat.str-el↗

Exchange parameters of copper-based quasi-two-dimensional Heisenberg magnets measured using high magnetic fields and muon-spin rotation

Pulsed-field magnetization experiments (fields $B$ of up to 85 T and temperatures $T$ down to 0.4 K) are reported on nine organic Cu-based two-dimensional (2D) Heisenberg magnets. All compounds show a low-$T$ magnetization that is concave as a function of $B$, with a sharp ``elbow'' transition to a constant value at a field $B_{\rm c}$. Monte-Carlo simulations including a finite interlayer exchange energy $J_{\perp}$ quantitatively reproduce the data; the concavity indicates the effective dimensionality and $B_{\rm c}$ is an accurate measure of the in-plane exchange energy $J$. Using these values and Neél temperatures measured by muon-spin rotation, it is also possible to obtain a quantitative estimate of $|J_{\perp}/J|$. In the light of these results, it is suggested that in magnets of the form [Cu(HF$_2$)(pyz)$_2$]X, where X is an anion, the sizes of $J$ and $J_{\perp}$ are controlled by the tilting of the pyrazine (pyz) molecule with respect to the 2D planes.

cond-mat.str-el↗

Muon-fluorine entangled states in molecular magnets

The information accessible from a muon-spin relaxation experiment is often limited since we lack knowledge of the precise muon stopping site. We demonstrate here the possibility of localizing a spin polarized muon in a known stopping state in a molecular material containing fluorine. The muon-spin precession that results from the entangled nature of the muon-spin and surrounding nuclear spins is sensitive to the nature of the stopping site and we use this property to identify three classes of site. We are also able to describe the extent to which the muon distorts its surroundings.

cond-mat.str-el↗

Magnetic order in the S=1/2 two-dimensional molecular antiferromagnet, copper pyrazine perchlorate Cu(Pz)_2(ClO_4)_2

We present an investigation of magnetic ordering in the two-dimensional S=1/2 quantum magnet Cu(Pz)_2(ClO_4)_2 using specific heat and zero field muon-spin relaxation (μ^+SR). The magnetic contribution to the specific heat is consistent with an exchange strength of 17.7(3) K. We find unambiguous evidence for a transition to a state of three-dimensional long range order below a critical temperature T_N=4.21(1) K using μ^+SR even though there is no feature in the specific heat at that temperature. The absence of a specific heat anomaly at T_N is consistent with recent theoretical predictions. The ratio of T_N/J=0.24 corresponds to a ratio of intralayer to interlayer exchange constants of |J'/J|=6.8x10^-4, indicative of excellent two-dimensional isolation. The scaled magnetic specific heat of [Cu(Pz)_2(HF_2)]BF_4, a compound with an analogous structure, is essentially identical to that of Cu(Pz)_2(ClO_4)_2 although both differ slightly from the predicted value for an ideal 2D S=1/2 Heisenberg antiferromagnet.

cond-mat.str-el↗

Magnetic order in the quasi-one-dimensional spin 1/2 chain, copper pyrazine dinitrate

We present the first evidence of magnetic order in the quasi-one-dimensional spin 1/2 molecular chain compound, copper pyrazine dinitrate Cu(C4H4N2)(NO3)2}. Zero field muon-spin relaxation measurements made at dilution refrigerator temperatures show oscillations in the measured asymmetry, characteristic of a quasistatic magnetic field at the muon sites. Our measurements provide convincing evidence for long range magnetic order below a temperature T_N=107(1) mK. This leads to an estimate of the interchain coupling constant of |J'|/k_B=0.046 K and to a ratio |J'/J| = 4.4 x 10^-3.

cond-mat.str-el↗