The Crystal Structure of Bornite Cu5FeS4: Ordered Fe and Split Cu

The crystal structure of bornite with ideal formula Cu5FeS4 from the Saishitang skarn copper deposit in Qinghai Province, along with bornite from the Yushui spouting hydrothermal copper deposit in Guangdong Province and the Bofang sandstone copper deposit in Hunan Province, has been refined by single-crystal X-ray diffraction with R1 = 0.0259–0.0483 (I > 2σ) and 0.0338–0.1067 for 2732 to 3273 unique reflections. As represented by the Saishitang sample, it is orthorhombic with a Pbca space group and unit cell parameters a = 10.97016(18) Å, b = 21.8803(4) Å, c = 10.9637(2) Å, V = 2631.61(8) Å3 and Z = 16. The structure is composed of sulfur layers parallel to the (0 1 0) lattice plane with interstices occupied by metal atoms. The Fe atoms occupy two tetrahedral sites with full occupancy, but the Cu atoms are all partially distributed over 20 paired sites, split from 10 sites with a distance ranging from 0.24 Å to 0.54 Å. The Fe-S tetrahedra are not split with Fe-S lengths from 2.2609 Å to 2.3286 Å (average 2.2997 Å). The Cu-S lengths in pyramidal triangles are from 2.218 Å to 2.397 Å (average 2.288 Å), whereas the Cu-S tetrahedra are strongly distorted, with great variations in Cu-S lengths from 2.224 Å to 2.604 Å (average 2.391 Å). The orthorhombic unit cell is stacked from 16 1a-type (5.5 Å) cubes; each cube has one tetrahedrally-coordinated Fe atom, five split from 3- to 4-coordinated Cu atoms, and two vacancies, i.e., 5CuIII–IV+FeIV+2[]+4S. The phenomenon of site-splitting of Cu atoms may provide for a more accurate structure of bornite, allowing for a better understanding of its magnetic properties and ore-formation conditions.

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