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Mark Devonport

Publications and source records attributed to Mark Devonport.

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Polarized Neutrons at ISIS: Recent Developments And Highlights

We present two recent projects which aim to improve the performance of polarized neutron scattering experiments using hyperpolarized $^{3}He$ spin filters at ISIS. The first is the optimization of a new compact magnetostatic cavity ("Magic Box") to house the $^{3}He$ spin filters based on an existing design. With a length of only 380 mm, it provides a field gradient relaxation time for the $^{3}He$ cell of 421 h in ambient conditions. It also contains a radiofrequency coil for adiabatic fast passage flipping. The second project is dedicated to the improvement of the $^{3}He$ relaxation time inside the spin filter cell. We have developed a chamber which allows for the deposition of alkali metal coatings on the surface of substrates. This emulates the spin filter cell walls, as well as subsequent heat treatment, thus mimicking the preparation of a new spin filter cell. The chamber is air-tight and has transparent windows, so that the structure resulting from the deposition of alkali metal on the surface of the wafer can be studied by X-ray or neutron reflectometry. We plan to continue this work by performing a systematic study at various conditions, which should help to shed light on the long-standing mystery of how alkali metal coatings help to improve relaxation time of $^{3}He$ cells. The first results are discussed in the text.

physics.ins-det

Molecular Structural Dynamics in Water-Ethanol Mixtures: Spectroscopy with Polarized Neutrons Simultaneously Accessing Collective and Self-Diffusion

Binary mixtures of water with lower alcohols display non-linear phase behaviour upon mixing which are attributed to potential cluster formation at molecular level. Unravelling such elusive structures requires the investigation of hydrogen-bonding sub-nanosecond dynamics. We employ high-resolution neutron time-of-flight spectroscopy with polarization analysis in combination with selective deuteration to study the concentration-dependent structural dynamics, in the water rich part of the phase diagram of water-ethanol mixtures. This method enables the simultaneous access to atomic correlations in space and time, and allows us to separate spatially incoherent scattering probing self-diffusion of the ethanol fraction from the coherent scattering probing collective diffusion of the water network as a whole. Our observations indicate an enhanced rigidity of the hydrogen bond network at mesoscopic lengthscale compared to the intra-molecular scale as the ethanol fraction increases, which is consistent with the hypothesis of clusters.

cond-mat.soft