The
present work reports a solid-state method to synthesize homologous
Ta-doped AgNbO3 with a controllable structure for the reduction
of p-nitrophenol (p-NP). With a
tunable molar ratio of Nb/Ta, the as-synthesized solid solutions exhibit
tunable band gaps, lattice constriction, reduced work functions, and
phase transformation from orthorhombic AgNbO3 to rhombohedral
AgTaO3. All samples were carefully characterized by powder
X-ray diffraction, transmission electron microscopy, UV–vis
diffuse reflectance spectroscopy, and X-ray photoelectron spectroscopy.
It is found that partial Ag+ ions in AgNb1–x
Ta
x
O3 solid
solutions are in situ converted into metallic silver to form a Ag0/AgNb1–x
Ta
x
O3 heterostructure in the presence of
excess NaBH4 during the reduction of p-NP. The doping effects on the crystal, electronic structure, the
work function of AgNb1–x
Ta
x
O3 and the underlying catalytic mechanism
are studied both experimentally and theoretically. It is discovered
that the interfacial charge transfer processes can be regulated by
nonstoichiometric doping. By virtue of well-modulated electronic structures
and overwhelming endurance, the turnover frequency of the AgTaO3 semiconductor for p-NP reduction is estimated
to be 1.09 × 104, approximately 12.5 times larger
than that of AgNbO3.