The Mantid framework is a software solution developed for the analysis and visualization of neutron scattering and muon spin measurements. The framework is jointly developed by software engineers and scientists at the ISIS Neutron and Muon Facility and the Oak Ridge National Laboratory. The objectives, functionality and novel design aspects of Mantid are described.

A search for neutral Higgs bosons has been performed using the full sample of Z 0 decays collected by the OPAL detector at LEP up to 1995. The data were taken at centre-of-mass energies between 88 GeV and 95 GeV and correspond to an integrated luminosity of approximately 160 pb 1. The present search addresses the processes Z 0 !H 0 Z and h 0 Z , where H 0 is the Higgs boson predicted by the Standard Model and h 0 the lightest neutral scalar Higgs boson predicted in the framework of the Minimal Supersymmetric Standard Model. For the virtual Z 0 boson, Z , the following decay c hannels are considered: Z ! , e + e and +. One candidate event

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In this work we explore how an electrolyte additive (fluorinated ethylene carbonate – FEC) mediates the thickness and composition of the solid electrolyte interphase formed over a silicon anode in situ as a function of state-of-charge and cycle. We show the FEC condenses on the surface at open circuit voltage then is reduced to C-O containing polymeric species around 0.9 V (vs. Li/Li+). The resulting film is about 50 Å thick. Upon lithiation the SEI thickens to 70 Å and becomes more organic-like. With delithiation the SEI thins by 13 Å and becomes more inorganic in nature, consistent with the formation of LiF. This thickening/thinning is reversible with cycling and shows the SEI is a dynamic structure. We compare the SEI chemistry and thickness to 280 Å thick SEI layers produced without FEC and provide a mechanism for SEI formation using FEC additives.

With the use of neutron reflectometry, we have determined the thickness and chemistry of the solid-electrolyte interphase (SEI) layer grown on a silicon anode as a function of state of charge and during cycling. We show the chemistry of this SEI layer becomes more LiF like with increasing lithiation and more Li−C−O−F like with delithiation. More importantly, the SEI layer thickness appears to increase (about 250 Å) as the electrode becomes less lithiated and thins to 180 Å with increasing Li content (Li 3.7 Si). We attribute this "breathing" to the continual consumption of electrolyte with cycling.