Pulsed anodization of superelastic NiTi alloy in nitric acid electrolyte is a novel surface modification process that enables the formation of an almost Ni-free TiO 2 layer on their surface. The core technology is the modulation of voltage-unapplied state that is necessary for the chemical reaction with an electrolyte. Here, the effect of the adjustment of the voltage-unapplied state on the layer characteristics was investigated. Prolongation of the voltage-unapplied state led to the formation of a thicker

Pulsed anodization allows to form a Ni-free TiO 2 layer on an almost equiatomic NiTi alloy. The surface is then hydrophilized and impedes the release of Ni ions from the alloy. This study aimed to assess the suitability of electrolytes used in the pulsed anodization process with the view of application as a biomaterial. Toward this end, the NiTi alloy was pulsed-anodized in four different aqueous electrolytes, HNO 3 , NH 4 NO 3 , H 2 SO 4 , and (NH 4 ) 2 SO 4 , after which the endothelium cell behavior was compared. The use of H 2 SO 4 as the electrolyte resulted in the formation of a TiO 2 layer with a groove-like structure of several tens of nanometers wide, and this surface inhibited the activity of endothelium cells. The ability to prevent the release of Ni ions was diminished when using the HNO 3 electrolyte, resulted in inferior cell proliferation. The other two electrolytes, NH 4 NO 3 and (NH 4 ) 2 SO 4 , formed a Ni-free TiO 2 layer with a comparatively smooth surface, which more effectively suppressed the release of Ni ions; thus, the cell attachment as well as proliferation were superior to that of the other two electrolytes. The surface smoothness and Ni suppression were thus concluded to be the factors governing the selection of an electrolyte.