The chemical and morphological surface transformations accompanying the deposition of Pt from
normalH2PtCl6
solutions onto hydrogen-terminated
normaln
-Si(111) surfaces were investigated in Part I [ J. Electrochem. Soc. , 155 , D527 (2008) ]. In this second part, an analysis of the nucleation and growth mechanisms of Pt islands is presented. Oxidized surface atoms act as preferential sites for the nucleation of nanoislands, introducing surface states that facilitate the electron transfer. A potential-independent hole injection into the valence band drives surface etching, which leads to an increasing number of nucleation sites. The energy level of the surface states above the redox level of the hydrogen evolution leads to a strong hydrogen evolution accompanying the nucleation and growth of Pt particles at low nucleation overpotentials.