(Fe, Mg) distribution in olivine effects of data collection and refinement strategies

Abstract

Determination of cation distributions in minerals is crucial for any thermodynamic application. In order to explore to what extent the choice of X-ray data collection, reduction, and structure refinement procedures might influence obtained site occupancies, a methodological and interlaboratory study was undertaken. Two single crystals of olivine (Fo 90 and Fo 45 ) were used to collect diffraction data up to 2𝛉 = 110° (Mo K α) in three Italian laboratories with different single-crystal diffractometers (Sℐℰℳℰ𝒩𝒮 Aℰ𝒟II, Pℋℐℒ𝒫𝒮 PW1100, K𝒰ℳ𝒜 KM4). In each laboratory, several data collections (12 and 10 for samples Fo 90 and Fo 45 , respectively) were carried out for each crystal, changing crystal mounting and measurement strategies for every experiment. All data were refined using the Strucsy, Orfls and Shelxl-93 programs with various refinement models, refinement strategies and weighting schemes, for a total number of 240 and 204 refinements for samples Fo 90 and Fo 45 , respectively. The main results are as follows. Atomic coordinates obtained by refining data sets at various resolutions with different refinement programs and crystal mountings do not change significantly. The structural geometry is therefore not affected by either resolution or refinement strategy. When refining a single set of data with different programs, the differences obtained for M1 and M2 site occupancies are up to 0.02 and 0.03 for both Fo 90 and Fo 45 crystals due to changing refinement models (valence states, extinction correction) and refinement strategy. When all the data sets collected in the three laboratories were refined with the same program (Shelxl-93), the results only suffered from different crystal mountings and experimental apparatus, and showed differences in M1 and M2 site occupancies up to 0.017. Considering both cases b and c, we observed differences which are approximately ten times the e.s.d.’s of the single values. The use of scattering curves with no pre-established ionization for Si and O led to better agreement between crystallographic site occupancies and chemical data.