This study focuses
on photocatalytic syntheses, in which transition
metal ions (Co2+, Fe2+, or Ni2+),
as the hole scavengers and surface modifiers of partially reduced
graphene oxide, PRGO, were utilized to photoreduce Pt4+. A pulsed UV reactor was used to illuminate the precursors. The
electrostatic interaction between the metal ions (Co2+,
Fe2+, or Ni2+) and the oxygen functional groups
on PRGO was the main parameter, proposed to be the reason controlling
Pt4+ reduction and Pt structure and activity. The alternative
assumption in managing the oxidation states of Pt was the variation
in the oxidation rates of hole scavengers. Pt electrocatalysts’
structural and electrochemical characteristics revealed that utilizing
the cobalt-based hole scavenger caused a dominant growth phase of
Pt particles at preferred positions on PRGO, with metallic states
and improved electrocatalytic activities (ECSA value of 191 m2·g–1 for Co2+ vs 141 m2·g–1 and 127 m2·g–1 for Fe2+ and Ni2+, respectively).
Density functional theory (DFT) calculation, on the other hand, suggested
that the greater affinity of cobalt and iron ions to oxygen groups
could detach more “O” from the graphene plane. Based
on the DFT results, less “O” groups in the vicinity
of Pt particles gave an amorphous morphology to Pt and facilitated
the hydrogen oxidation reaction (HOR).