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Experimental and Theoretical Study of SbPO4 under Compression.

André Luis de Jesus PereiraDavid Santamaría-PérezRosário VilaplanaDaniel ErrandoneaCatalin PopescuEstelina Lora da SilvaJuan Angel SansJuan Rodríguez-CarvajalAlfonso MunozPlacida Rodriguez-HernandezAndres MujicaSilvana Elena RadescuArmando BeltránAlberto Otero-de-la-RozaMarcelo NalinMiguel MollarFrancisco Javier Manjón
Published in: Inorganic chemistry (2019)
SbPO4 is a complex monoclinic layered material characterized by a strong activity of the nonbonding lone electron pair (LEP) of Sb. The strong cation LEP leads to the formation of layers piled up along the a axis and linked by weak Sb-O electrostatic interactions. In fact, Sb has 4-fold coordination with O similarly to what occurs with the P-O coordination, despite the large difference in ionic radii and electronegativity between both elements. Here we report a joint experimental and theoretical study of the structural and vibrational properties of SbPO4 at high pressure. We show that SbPO4 is not only one of the most compressible phosphates but also one of the most compressible compounds of the ABO4 family. Moreover, it has a considerable anisotropic compression behavior, with the largest compression occurring along a direction close to the a axis and governed by the compression of the LEP and the weak interlayer Sb-O bonds. The strong compression along the a axis leads to a subtle modification of the monoclinic crystal structure above 3 GPa, leading from a 2D to a 3D material. Moreover, the onset of a reversible pressure-induced phase transition is observed above 9 GPa, which is completed above 20 GPa. We propose that the high-pressure phase is a triclinic distortion of the original monoclinic phase. The understanding of the compression mechanism of SbPO4 can aid to improve the ion intercalation and catalytic properties of this layered compound.
Keyphrases
  • crystal structure
  • molecular dynamics simulations
  • ionic liquid
  • diabetic rats
  • oxidative stress
  • quantum dots
  • solid state
  • raman spectroscopy