We report the single crystal growth and characterization of the highest T c ironbased superconductor SmFeAsO 1−x H x . Some sub-millimeter-sized crystals were grown using the mixture flux of Na 3 As + 3NaH + As at 3.0 GPa and 1473 K. The chemical composition analyses confirmed 10% substitution of hydrogen for the oxygen site (x = 0.10), however, the structural analyses suggested that the obtained crystal forms a multidomain structure. By using the FIB technique we fabricated the single domain SmFeAsO 0.9 H 0.10 crystal with the T c of 42 K, and revealed the metallic conduction in in-plane (ρ ab ), while semiconducting in the out-of-plane (ρ c ). From the in-plane Hall coefficient measurements, we confirmed that the dominant carrier of SmFeAsO 0.9 H 0.10 crystal is an electron, and the hydride ion occupied at the site of the oxygen ion effectively supplies a carrier electron per iron following the equation: O 2− → H − + e − . S. Iimura et al., Particularly, the iron pnictides family consists of various structures by inserting alkali metal cation, alkaline earth metal cation, positively charged PbO-type layer, or perovskite-type block between the FePn layers to compensate the neutrality. A prototypical REFeAsO-type (RE = rare earth) material, abbreviated as 1111-type, crystallizes in a tetragonal lattice at room temperature (space group P4/nmm, a ~ 4 Å, c ~ 8-9 Å, and Z = 2), in which the conducting [FeAs] − and insulating [REO] + layers stack alternately along the crystallographic c axis (Fig. 1a). On cooling, they undergo a tetragonal-orthorhombic transition at T ~ 150 K, accompanying a paramagneticantiferromagnetic (PM-AFM) transition just below the structural transition temperature [4,5]. Superconductivity appears if the AFM is suppressed by doping carriers or applying pressure (see x = 0 in Fig. 1b).Carrier doping mode in 1111-type is categorized into four from a view of doping site and carrier polarity. Substitution for the site in conducting layer is called "direct doping", while that in insulating layer is called "indirect doping". Among those methods, the indirect electron doping has intensively been studied because it induces