화학공학소재연구정보센터
Journal of the American Chemical Society, Vol.131, No.8, 2986-2992, 2009
Response of Superconductivity and Crystal Structure of LiFeAs to Hydrostatic Pressure
On the application of hydrostatic pressures of up to 1.3 GPa, the superconducting transition temperatures (T-c) of samples of LiFeAs are lowered approximately monotonically at approximately -2 K GPa(-1). Measurements of the X-ray powder diffraction pattern at hydrostatic pressures of up to 17 GPa applied by a He gas pressure medium in a diamond anvil cell reveal a bulk modulus for LiFeAs of 57.3(6) GPa which is much smaller than that of other layered arsenide and oxyarsenide superconductors. LiFeAs also exhibits much more isotropic compression than other layered iron arsenide superconductors. The higher and more isotropic compressibility is presumably a consequence of the small size of the lithium ion. At ambient pressure the FeAs4 tetrahedra are the most compressed in the basal plane of those in any of the superconducting iron arsenides. On increasing the pressure the Fe-Fe distance contracts more rapidly than the Fe-As distance so that the FeAs4 tetrahedra become even more distorted from the ideal tetrahedral shape. The decrease in T-c with applied pressure is therefore consistent with the observations that in the iron arsenides and related materials investigated thus tar, T. is maximized for a particular electron count when the FeAs4 tetrahedra are close to regular.