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@ARTICLE{Grushko:826830,
      author       = {Grushko, B. and Pavlyuchkov, D. and Mi, S. B. and
                      Balanetskyy, S.},
      title        = {{T}ernary phases forming adjacent to
                      {A}l$_{3}${M}n{A}l$_{4}${M}n in {A}l{M}n{TM} ({TM} = {F}e,
                      {C}o, {N}i, {C}u, {Z}n, {P}d)},
      journal      = {Journal of alloys and compounds},
      volume       = {677},
      issn         = {0925-8388},
      address      = {Lausanne},
      publisher    = {Elsevier},
      reportid     = {FZJ-2017-01047},
      pages        = {148 - 162},
      year         = {2016},
      abstract     = {The Alsingle bondMn alloy system contains complex
                      intermetallics in its Al-rich part, and this was the first
                      system where quasiperiodic structures were recognized. In
                      the present work, the solubility of TMs (TM = Fe, Co, Ni,
                      Cu, Zn and Pd) in the stable binaries, the stabilization
                      effect of these elements on the metastable binaries and the
                      formation of ternary compounds are specified and compared.
                      While the solubility of all these TMs in hexagonal μ-Al4Mn
                      and λ-Al4Mn is low, the high-temperature orthorhombic
                      T-Al3Mn dissolves up to at least 14.5, 12, 16 and 7.5
                      $at.\%$ Fe, Cu, Zn and Pd, respectively. The metastable
                      hexagonal φ-Al10Mn3 is stabilized by Fe, Co and Ni in wide
                      ternary compositional regions, and in Alsingle bondCosingle
                      bondMn such a region propagates up to Al5Co2. In alloys with
                      Fe, Co and Ni, a ternary hexagonal phase isostructural to
                      the Alsingle bondCrsingle bondNi ζ-phase (P63/m, a ≈
                      1.76, c ≈ 1.25 nm) is formed along ∼80 $at.\%$ Al, while
                      in alloys with Cu and Pd the orthorhombic so-called R-phase
                      (Bbmm, a ≈ 2.41, b ≈ 1.25, c ≈ 0.76 nm) was found at
                      similar compositions. This structure is also known in
                      Alsingle bondZnsingle bondMn but at much lower-Al
                      Al68Zn14.5Mn17.5, while in the range of 75–80 $at.\%$ Al a
                      monoclinic phase isostructural to η-Al11Cr2 (C2/c, a ≈
                      1.76, b ≈ 3.04, c ≈ 1.76 nm, β ≈ 90°) is formed. In
                      addition to the stable decagonal D3-phase in Alsingle
                      bondFesingle bondMn and Alsingle bondPdsingle bondMn
                      reported earlier, the stabilization of binary Alsingle
                      bondMn D3-phase was revealed around Al64Cu20Mn16.},
      cin          = {PGI-5},
      ddc          = {670},
      cid          = {I:(DE-Juel1)PGI-5-20110106},
      pnm          = {143 - Controlling Configuration-Based Phenomena (POF3-143)},
      pid          = {G:(DE-HGF)POF3-143},
      typ          = {PUB:(DE-HGF)16},
      UT           = {WOS:000375481100021},
      doi          = {10.1016/j.jallcom.2016.03.220},
      url          = {https://juser.fz-juelich.de/record/826830},
}