High-pressure X-ray study of LiCrSi₂O₆ clinopyroxene and the general compressibility trends for Li-clinopyroxenes

High-pressure single-crystal X-ray diffraction measurements of synthetic LiCrSi₂O₆ clinopyroxene (with space group P2₁/c) were performed in a diamond-anvil cell up to 7.970 GPa. No phase transition has been observed within the pressure range investigated, but the elastic behavior at lower pressures (up to ∝2.5 GPa) is affected by an anomalous softening due to the proximity of the phase transition to the HT-C2/c phase at 330 K and at ambient pressure. A third-order Birch-Murnaghan equation of state fitted to the compression data above 2.5 GPa yields a bulk modulus K_T0 = 93(2) GPa and its first derivative K' = 8.8(6). The structural data measured up to 7.970 GPa confirm that the space group P2₁/c is maintained throughout the whole pressure range investigated. The atomic parameters, obtained from the integrated diffraction intensities, suggest that the Li coordination polyhedron changes its coordination number from 5 to 6 at 6-7 GPa by means of the approach of the bridging O atom, related to the increased kinking of the B tetrahedral chain. Furthermore, at higher pressures, the structural evolution of LiCrSi₂O₆ provides evidence in the variation of kinking angles and bond lengths of a potential phase transition above 8 GPa to the HP-C2/c space group. A comparison of the Li-clinopyroxenes (M1 = Cr, Al, Sc, Ga, Mg + Fe) previously investigated and our sample shows that their elastic behavior and structural mechanisms of compression are analogous. (orig.)