Synthesis and characterization of double solid solution (Zr,Ti)2(Al,Sn)C MAX Phase Ceramics

Research output: Contribution to journalArticlepeer-review


Institutes & Expert groups

  • CNRS/IN2P3 - Université Grenoble Alpes - LPSC
  • IPGP - Institut de Physique du Globe de Paris
  • CNRS CEMHTI UPR 3079 - Université d'Orléans
  • DIFFABS Beamline - Soleil Synchrotron
  • UA - Universiteit Antwerpen
  • KUL - Katholieke Universiteit Leuven

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Quasi phase-pure (>98 wt %) MAX phase solid solution ceramics with the (Zr,Ti)2(Al0.5,Sn0.5)C stoichiometry and variable Zr/Ti ratios were synthesized by both reactive hot pressing and pressureless sintering of ZrH2, TiH2, Al, Sn, and C powder mixtures. The influence of the different processing parameters, such as applied pressure and sintering atmosphere, on phase purity and microstructure of the produced ceramics was investigated. The addition of Sn to the (Zr,Ti)2AlC system was the key to achieve phase purity. Its effect on the crystal structure of a 211-type MAX phase was assessed by calculating the distortions of the octahedral M6C and trigonal M6A prisms due to steric effects. The M6A prismatic distortion values were found to be smaller in Sn-containing double solid solutions than in the (Zr,Ti)2AlC MAX phases. The coefficients of thermal expansion along the ⟨a⟩ and ⟨c⟩ directions were measured by means of Rietveld refinement of high-temperature synchrotron X-ray diffraction data of (Zr1−x,Tix)2(Al0.5,Sn0.5)C MAX phase solid solutions with x = 0, 0.3, 0.7, and 1. The thermal expansion coefficient data of the Ti2(Al0.5,Sn0.5)C solid solution were compared with those of the Ti2AlC and Ti2SnC ternary compounds. The thermal expansion anisotropy increased in the (Zr,Ti)2(Al0.5,Sn0.5)C double solid solution MAX phases as compared to the Zr2(Al0.5,Sn0.5)C and Ti2(Al0.5,Sn0.5)C end-members.


Original languageEnglish
Pages (from-to)6669-6683
JournalInorganic Chemistry
Issue number10
Publication statusPublished - 1 May 2019


  • MAX phase, synthesis, pellet, solid solution, Ceramics, XRD analysis

ID: 5253437