Abstract

Kaatialaite mineral Fe[AsO2(OH)2]5H2O from Jáchymov, Czech Republic forms white aggregates of needle-shaped crystals with micrometric size. Its structure at ambient temperature has already been reported but hydrogen atoms could not be identified from single-crystal X-ray diffraction. An analysis using 3D electron diffraction at low temperature brings to light the hydrogen positions and the existence of hydrogen disorder. At 100 K, kaatialaite is described in a monoclinic unit cell of a = 15.46, b = 19.996, c = 4.808 Å, β = 91.64° and V = 1485.64 Å3 with space group P21/n. The hydrogen sites were revealed after refinements both considering the dynamical effects and ignoring them. The possibility to access most of the hydrogen positions, including partially occupied ones among heavy atoms, from the kinematical refinement is due to the recent developments in the analysis of 3D electron data. The hydrogen bonding observed in kaatialaite provides examples of H2O configurations that have not been observed before in the structures of oxysalts with the presence of unusual inverse transformer H2O groups.

Highlights

  • MATERIALS j COMPUTATIONHydrogen disorder in kaatialaite Fe[AsO2(OH)2]5H2O from Jachymov, Czech Republic: determination from low-temperature 3D electron diffraction

  • Kaatialaite is an environmentally crucial acidic ferric arsenate with the formula FeIII[AsO2(OH)2]3(H2O)n, where n ranges from 3 to 5 (Boudjada & Guitel, 1981; Raade et al, 1984)

  • The structure of synthetic kaatialaite has been described by Boudjada & Guitel (1981); the positions of the hydrogen atoms remained undetected from X-ray single-crystal data

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Summary

MATERIALS j COMPUTATION

Hydrogen disorder in kaatialaite Fe[AsO2(OH)2]5H2O from Jachymov, Czech Republic: determination from low-temperature 3D electron diffraction. Kaatialaite mineral Fe[AsO2(OH)2]5H2O from Jachymov, Czech Republic forms white aggregates of needle-shaped crystals with micrometric size. Its structure at ambient temperature has already been reported but hydrogen atoms could not be identified from single-crystal X-ray diffraction. An analysis using 3D electron diffraction at low temperature brings to light the hydrogen positions and the existence of hydrogen disorder. The possibility to access most of the hydrogen positions, including partially occupied ones among heavy atoms, from the kinematical refinement is due to the recent developments in the analysis of 3D electron data. The hydrogen bonding observed in kaatialaite provides examples of H2O configurations that have not been observed before in the structures of oxysalts with the presence of unusual inverse transformer H2O groups

Introduction
Method
Findings
Limiting Miller indices
Full Text
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