“…This material was chosen because substitution by Pr, which is the largest trivalent rare-earth ion, except for Ce which does not form the YBCO structure 29 , results in the emergence of hybridization between the Pr 4 f orbitals and planar CuO 2 states 30 that yields an electronically relevant, hybridized orbital 31 with spatial extension in three dimensions, in stark contrast to the planar Cu 3 orbitals that dominate the physics of the parent compound. Unlike substitution by other rare-earth elements, such as Dy, which do not significantly alter the parent YBCO phase diagram 32 , increasing Pr substitution in the Pr x Y 1− x Ba 2 Cu 3 O 7 system continually reduces the superconducting T c , yielding a pseudogap regime 30 , 33 , 34 and eventually an antiferromagnetic insulating phase 30 , 35 – 40 . Furthermore, the in- and out-of-plane zero-temperature superconducting coherence lengths are substantially longer in Pr-YBCO than in YBCO and increase monotonically with Pr concentration 41 – 43 .…”