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Magnetocaloric Study of Spin Relaxation in `Frozen Dipolar Spin Ice Dy2Ti2O7

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 Added by Erik Cizmar
 Publication date 2006
  fields Physics
and research's language is English




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The magnetocaloric effect of polycrystalline samples of pure and Y-doped dipolar spin ice Dy2Ti2O7 was investigated at temperatures from nominally 0.3 K to 6 K and in magnetic fields of up to 2 T. As well as being of intrinsic interest, it is proposed that the magnetocaloric effect may be used as an appropriate tool for the qualitative study of slow relaxation processes in the spin ice regime. In the high temperature regime the temperature change on adiabatic demagnetization was found to be consistent with previously published entropy versus temperature curves. At low temperatures (T < 0.4 K) cooling by adiabatic demagnetization was followed by an irreversible rise in temperature that persisted after the removal of the applied field. The relaxation time derived from this temperature rise was found to increase rapidly down to 0.3 K. The data near to 0.3 K indicated a transition into a metastable state with much slower relaxation, supporting recent neutron scattering results. In addition, magnetic dilution of 50 % concentration was found to significantly prolong the dynamical response in the milikelvin temperature range, in contrast with results reported for higher temperatures at which the spin correlations are suppressed. These observations are discussed in terms of defects and loop correlations in the spin ice state.



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While sources of magnetic fields - magnetic monopoles - have so far proven elusive as elementary particles, several scenarios have been proposed recently in condensed matter physics of emergent quasiparticles resembling monopoles. A particularly simple proposition pertains to spin ice on the highly frustrated pyrochlore lattice. The spin ice state is argued to be well-described by networks of aligned dipoles resembling solenoidal tubes - classical, and observabl
Dy2Ti2O7 has been advanced as an ideal spin ice. We present a neutron scattering investigation of a sample of 162Dy2Ti2O7. The scattering intensity has been mapped in zero applied field in the hhl and hk0 planes at temperatures between 0.05 K and 20 K. The measured diffuse scattering (in the static approximation) has been compared to that predicted by the dipolar spin ice model. The comparison is good, except at the Brillouin zone boundaries where extra scattering appears in the experimental data. It is concluded that the dipolar spin ice model provides a successful basis for understanding Dy2Ti2O7, but that there are issues which remain to be clarified.
112 - Yishu Wang , T. Reeder , Y. Karaki 2020
When degenerate states are separated by large energy barriers, the approach to thermal equilibrium can be slow enough that physical properties are defined by the thermalization process rather than the equilibrium. The exploration of thermalization pushes experimental boundaries and provides refreshing insights into atomic scale correlations and processes that impact steady state dynamics and prospects for realizing solid state quantum entanglement. We present a comprehensive study of magnetic relaxation in Ho$_2$Ti$_2$O$_7$ based on frequency-dependent susceptibility measurements and neutron diffraction studies of the real-time atomic-scale response to field quenches. Covering nearly ten decades in time scales, these experiments uncover two distinct relaxation processes that dominate in different temperature regimes. At low temperatures (0.6K<T<1K) magnetic relaxation is associated with monopole motion along the applied field direction through the spin-ice vacuum. The increase of the relaxation time upon cooling indicates reduced monopole conductivity driven by decreasing monopole concentration and mobility as in a semiconductor. At higher temperatures (1K<T<2K) magnetic relaxation is associated with the reorientation of monopolar bound states as the system approaches the single-spin tunneling regime. Spin fractionalization is thus directly exposed in the relaxation dynamics.
Spin ices, frustrated magnetic materials analogous to common water ice, are exemplars of high frustration in three dimensions. Recent experimental studies of the low-temperature properties of the paradigmatic Dy$_2$Ti$_2$O$_7$ spin ice material, in particular whether the predicted transition to long-range order occurs, raise questions as per the currently accepted microscopic model of this system. In this work, we combine Monte Carlo simulations and mean-field theory calculations to analyze data from magnetization, elastic neutron scattering and specific heat measurements on Dy$_2$Ti$_2$O$_7$. We also reconsider the possible importance of the nuclear specific heat, $C_{rm nuc}$, in Dy$_2$Ti$_2$O$_7$. We find that $C_{rm nuc}$ is not entirely negligible below a temperature $sim 0.5$ K and must be taken into account in a quantitative analysis of the calorimetric data of this compound below that temperature. We find that small effective exchange interactions compete with the magnetostatic dipolar interaction responsible for the main spin ice phenomenology. This causes an unexpected refrustration of the long-range order that would be expected from the incompletely self-screened dipolar interaction and which positions the material at the boundary between two competing classical long-range ordered ground states. This allows for the manifestation of new physical low-temperature phenomena in Dy$_2$Ti$_2$O$_7$, as exposed by recent specific heat measurements. We show that among the four most likely causes for the observed upturn of the specific heat at low temperature -- an exchange-induced transition to long-range order, quantum non-Ising (transverse) terms in the effective spin Hamiltonian, the nuclear hyperfine contribution and random disorder -- only the last appears to be reasonably able to explain the calorimetric data.
The magnetically frustrated spin ice family of materials is host to numerous exotic phenomena such as magnetic monopole excitations and macroscopic residual entropy extending to low temperature. A finite-temperature ordering transition in the absence of applied fields has not been experimentally observed in the classical spin ice materials Dy2Ti2O7 and Ho2Ti2O7. Such a transition could be induced by the application of pressure, and in this work we consider the effects of uniaxial pressure on classical spin ice systems. Theoretically we find that the pressure induced ordering transition in Dy2Ti2O7 is strongly affected by the dipolar interaction. We also report measurements on the neutron structure factor of Ho2Ti2O7 under pressure, and compare the experimental results to the predictions of our theoretical model.
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