An
AA′3B4O12-type A-site-ordered
quadruple perovskite oxide AgMn7O12 was prepared
by high-pressure and high-temperature methods. At room temperature,
the compound crystallizes into a cubic Im3̅
symmetry with a charge distribution of AgMn3
3+Mn4
3.5+O12. With the temperature
decreasing to T
CO,OO ≈ 180 K, the
compound undergoes a structural phase transition toward a monoclinic C2/m symmetry, giving rise to a B-site
charge- and orbital-ordered AgMn3
3+Mn2
3+Mn2
4+O12 phase. Moreover,
this charge-/orbital-ordered main phase coexists with the initial
cubic AgMn3
3+Mn4
3.5+O12 phase in the wide temperature range we measured. The charge-/orbital-ordered
phase shows two antiferromagnetic phase transitions near 125 and 90
K, respectively. Short-range ferromagnetic correlations are found
to occur for the initial B-site mixed cubic phase around 35 K. Because
of the robust phase separation, considerable magnetoresistance effects
are observed below T
CO,OO in AgMn7O12.