The
roles of hydrogen impurity and oxygen vacancy defects on defining
the conductivity, and hence photoelectrochemical (PEC) performance
characteristics, of monoclinic scheelite bismuth vanadate (BiVO4) are investigated using a combination of experiment and theory.
We find that elemental hydrogen is present as an impurity in as-synthesized
BiVO4 and that increasing its concentration by annealing
in H2 at temperatures up to 290 °C leads to near-complete
elimination of majority carrier transport limitations, a beneficial
shift in the photoanodic current onset potential, and improved fill
factor. Magnetic resonance measurements reveal that hydrogen can be
incorporated in at least two different chemical environments, which
are assigned to interstitial and substitutional sites. Incorporation
of hydrogen leads to a shift of the Fermi level toward the conduction
band edge, indicating that n-type character is correlated with increased
hydrogen content. This finding is in agreement with theory and reveals
that hydrogen acts as a donor in BiVO4. Sub-bandgap photoluminescence
is observed from as-synthesized material and is consistent with deep
electronic states associated with oxygen vacancies. Hydrogen treatment
leads to reduced emission from these states. These findings support
the conclusion that hydrogen, rather than oxygen vacancies, is dominant
in determining the n-type conductivity of BiVO4. These
findings have important implications for controlling the electronic
properties and functional characteristics of this promising photoanode
material.