Dependence of superconducting properties of (Ca,RE)(Fe,TM)As2 [(Ca,RE)112, TM: Co, Ni)] on RE elements (RE = La-Gd) was systematically investigated. Improvement of superconducting properties by Co or Ni co-doping was observed for all (Ca,RE)112, whic
h is similar to Co-co-doped (Ca,La)112 or (Ca,Pr)112. Tc of Co-co-doped samples decreased from 38 K for RE = La to 29 K for RE = Gd with decreasing ionic radii of RE3+. However, Co-co-doped (Ca,Eu)112 showed exceptionally low Tc = 21 K probably due to the co-existence of Eu3+ and Eu2+ suggested by longer interlayer distance dFe-Fe of (Ca,Eu)112 than other (Ca,RE)112.
Superconducting properties of Co-co-doped (Ca,RE)FeAs2 ((Ca,RE)112: RE = La, Pr) were investigated. Co-co-doping increased Tc of (Ca,Pr)112 while Mn-co-doping suppressed superconductivity of (Ca,RE)112. Co-co-doped (Ca,La)112 showed large diamagnetic
screening and sharper superconducting transition than Co-free (Ca,La)112. Tczero observed in resistivity measurements increased from 14 K to 30 K by Co-co-doping, while Tconset was not increased. The critical current density (Jc) of Co-co-doped (Ca,La)112 were approximately 2.1 x 104 Acm-2 and 3.2 x 103 Acm-2 at 2 K and 25 K, respectively, near zero field. These relatively high Jcs and large diamagnetic screening observed in susceptibility measurement as for polycrystalline bulks suggest bulk superconductivity of Co-co-doped (Ca,RE)112 compounds.
Synthesis of a series of layered iron arsenides Ca1-xRExFeAs2 (112) was attempted by heating at 1000 C under a high-pressure of 2 GPa. The 112 phase successfully forms with RE = La, Ce, Nd, Sm, Eu and Gd, while Tb, Dy and Ho substituted and RE free s
amples does not contain the 112 phase. The Ce, Nd, Sm, Eu and Gd doped Ca1-xRExFeAs2 are new compounds. All of them exhibit superconducting transition except for the Ce doped sample. The behaviour of the critical temperature, with the RE ionic radii have been investigated.
