| 1. |
- Edberg, Richard, et al.
(författare)
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Dipolar spin ice under uniaxial pressure
- 2019
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Ingår i: Physical Review B. - : American Physical Society. - 2469-9950 .- 2469-9969. ; 100:14
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Tidskriftsartikel (refereegranskat)abstract
- 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 of the neutron structure factor of Ho2Ti2O7 under pressure and compare the experimental results to the predictions of our theoretical model.
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| 2. |
- Sandberg, L. o., et al.
(författare)
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Design, calibration, and performance of a uniaxial pressure cell for neutron scattering studies of quantum magnetism
- 2023
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Ingår i: Review of Scientific Instruments. - : AIP Publishing. - 0034-6748 .- 1089-7623. ; 94:10
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Tidskriftsartikel (refereegranskat)abstract
- We provide an overview of a pressure cell designed to apply uniaxial pressure to single crystals for the study, by neutron scattering techniques, of strongly correlated magnetic systems and, in particular, quantum magnets. A detailed overview of the pressure cell components, their requirements, and links to the scientific and technical specifications are presented. The pressure cell is able to accommodate a 200 mm(3) single crystal that can be pressurized up to 2 GPa at cryogenic temperatures. The pressure cell is consistent with the requirements of inelastic neutron scattering and, importantly, neutron polarization analysis. A particular strength of the uniaxial pressure cell is the highly uniform and low background for a wide scattering angle of 360(degrees) horizontally and +/- 20(degrees) vertically. We show the performance of the uniaxial pressure cell using a relevant neutron scattering instrument, the polarized diffuse scattering instrument, D7. The experiments confirm that the cell complies with the scientific and technical requirements. This uniaxial pressure cell will provide a useful additional tool in the sample environment suite available for the study of quantum magnetism.
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| 3. |
- Edberg, Richard, et al.
(författare)
-
Effects of uniaxial pressure on the spin ice Ho2Ti2O7
- 2020
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Ingår i: Physical Review B. - : American Physical Society. - 2469-9950 .- 2469-9969. ; 102:18
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Tidskriftsartikel (refereegranskat)abstract
- The spin ice materials Ho2Ti2O7 and Dy2Ti2O7 are experimental and theoretical exemplars of highly frustrated magnetic materials. However, the effects of applied uniaxial pressure are not well studied, and here we report magnetization measurements of Ho2Ti2O7 under uniaxial pressure applied in the [001], [111], and [110] crystalline directions. The basic features are captured by an extension of the dipolar spin ice model. We find a good match between our model and measurements with pressures applied along two of the three directions, and we extend the framework to discuss the influence of crystal misalignment for the third direction. The parameters determined from the magnetization measurements reproduce neutron scattering measurements that we perform under uniaxial pressure applied along the [110] crystalline direction. In the detailed analysis, we include the recently verified susceptibility dependence of the demagnetizing factor. Our work demonstrates the application of a moderate applied pressure to modify the magnetic interaction parameters. The knowledge can be used to predict critical pressures needed to induce new phases and transitions in frustrated materials, and in the case of Ho2Ti2O7 we expect a transition to a ferromagnetic ground state for uniaxial pressures above 3.3 GPa.
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| 4. |
- Markmann, Verena, et al.
(författare)
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Real-time structural dynamics of the ultrafast solvation process around photo-excited aqueous halides
- 2024
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Ingår i: CHEMICAL SCIENCE. - 2041-6520 .- 2041-6539. ; 15:29, s. 11391-11401
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Tidskriftsartikel (refereegranskat)abstract
- This work investigates and describes the structural dynamics taking place following charge-transfer-to-solvent photo-abstraction of electrons from I- and Br- ions in aqueous solution following single- and 2-photon excitation at 202 nm and 400 nm, respectively. A Time-Resolved X-ray Solution Scattering (TR-XSS) approach with direct sensitivity to the structure of the surrounding solvent as the water molecules adopt a new equilibrium configuration following the electron-abstraction process is utilized to investigate the structural dynamics of solvent shell expansion and restructuring in real-time. The structural sensitivity of the scattering data enables a quantitative evaluation of competing models for the interaction between the nascent neutral species and surrounding water molecules. Taking the I0-O distance as the reaction coordinate, we find that the structural reorganization is delayed by 0.1 ps with respect to the photoexcitation and completes on a time scale of 0.5-1 ps. On longer time scales we determine from the evolution of the TR-XSS difference signal that I0: e- recombination takes place on two distinct time scales of similar to 20 ps and 100 s of picoseconds. These dynamics are well captured by a simple model of diffusive evolution of the initial photo-abstracted electron population where the charge-transfer-to-solvent process gives rise to a broad distribution of electron ejection distances, a significant fraction of which are in the close vicinity of the nascent halogen atoms and recombine on short time scales. Time-resolved X-ray solution scattering with a 1-photon and 2-photon pump qualitatively confirms the similar to 0.5 & Aring; increase in the nearest-neighbour halide-oxygen distances of iodide and bromide solvated in water.
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