Praseodymium oxides present redox properties analogous to those of Ce-based systems and have been proposed for catalytic applications in combination with CeO
2, ZrO
2, or both. However, uncertainties remain concerning the nature and redox behavior of Pr-rich mixtures, especially with ZrO
2. Here we study the eutectic composites of the ZrO
2–PrO
x system, focusing on the sensitivity of their microstructure, phase symmetry, and composition to variations of the processing atmosphere from oxidizing to reducing. Mixed oxides have been produced by a laser-assisted directional solidification technique in O
2, air, N
2, or 5%H
2(Ar) environment, and the resulting materials have been analyzed by scanning electron microscopy/energy-dispersive X-ray spectroscopy, X-ray diffraction, Raman spectroscopy, and magnetic susceptibility. In air, N
2, or 5%H
2(Ar) atmosphere, a lamellar, eutectic-like microstructure forms, the major phase being the one with less Pr content. Both the Pr concentration in each phase as the PrO
x molar percentage of the eutectic composites decrease as the atmosphere becomes more reducing. Both eutectic phases are fluorite-like when processing in air, whereas in N
2 or 5%H
2(Ar), the phase with high Pr content is of the A-R
2O
3 type, and the phase with low Pr content can be described as a fluorite phase containing C-R
2O
3-like short-range-ordered regions. The results obtained for samples processed in O
2 suggest that for high enough pO
2 no eutectic forms, in analogy with the ZrO
2–CeO
2 system. The evolution of the phase composition and symmetry is discussed in terms of the limited stability of the phases found in the ZrO
2–Pr
2O
3 system, namely, A- or C-R
2O
3-like, beyond a certain Pr oxidation degree and oxygen content.
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