posted on 2015-07-15, 00:00authored byHirotaka Horie, Akihide Iwase, Akihiko Kudo
K<sub>4</sub>Nb<sub>6</sub>O<sub>17</sub> (BG: 3.67 eV) and Na<sub>2</sub>W<sub>4</sub>O<sub>13</sub> (BG: 3.12 eV) layered oxide photocatalysts
with wide band gaps were treated with a molten AgNO<sub>3</sub> to
substitute K<sup>+</sup> and Na<sup>+</sup> with Ag<sup>+</sup>, resulting
in red-shifts of absorption edges in diffuse reflectance spectra.
A part of Na<sup>+</sup> ions in the interlayer of Na<sub>2</sub>W<sub>4</sub>O<sub>13</sub> was substituted with Ag<sup>+</sup> ions by
the molten AgNO<sub>3</sub> treatment with keeping the layered structure.
Both Ag(I)-substituted K<sub>4</sub>Nb<sub>6</sub>O<sub>17</sub> and
Na<sub>2</sub>W<sub>4</sub>O<sub>13</sub> showed photocatalytic activities
for O<sub>2</sub> evolution from aqueous solutions containing a sacrificial
reagent utilizing the absorption bands newly formed by the Ag(I)-substitution.
Notably, the Ag(I)-substituted Na<sub>2</sub>W<sub>4</sub>O<sub>13</sub> produced O<sub>2</sub> under visible light irradiation. When ball-milled
Na<sub>2</sub>W<sub>4</sub>O<sub>13</sub> was treated with a molten
AgNO<sub>3</sub>, the Ag(I)-substitution rate increased. The Ag(I)-substituted
Na<sub>2</sub>W<sub>4</sub>O<sub>13</sub> with ball-milling showed
higher photocatalytic activity for O<sub>2</sub> evolution than that
without ball-milling. Z-schematic water splitting proceeded under
visible light irradiation by combining the Ag(I)-substituted Na<sub>2</sub>W<sub>4</sub>O<sub>13</sub> of an O<sub>2</sub>-evolving photocatalyst
with Ru-loaded SrTiO<sub>3</sub> doped with Rh of a H<sub>2</sub>-evolving
photocatalyst.