posted on 2016-12-05, 00:00authored byLorenzo Caccamo, Cristian Fàbrega, Marcel Marschewski, Sönke Fündling, Alaaeldin Gad, Olga Casals, Gerhard Lilienkamp, Oliver Höfft, Joan Daniel Prades, Winfried Daum, Andreas Waag
Understanding the
mechanisms of charge transfer across the semiconductor/liquid
interface is crucial to realize efficient photoelectrochemical devices.
Here, the interfacial charge transfer characteristics of n-type In0.1Ga0.9N photoanodes are investigated and
correlated to their photoactivity properties measured in phosphate
buffered saline solution (pH 7) under illumination conditions. Cyclic
voltammetry measurements show evident photoactivity changes as the
number of cycles increases. In particular, the photocurrent density
reaches its maximum value after 49 voltammetric cycles; meanwhile,
the photocurrent onset potential shifts toward more negative cathodic
potentials. Electrochemical impedance measurements reveal that, first,
the hole transfer process occurs mainly via localized states at the
surface and the photocurrent onset potential is dependent on the energetic
position of those states. Therefore, the observed initial photocurrent
increase and cathodic shift of the photocurrent onset potential can
be attributed to a decrease of the transfer resistance and partial
passivation of the states at the surface. On the other hand, a gradual
oxidation and corrosion of the InGaN surface arises, causing a consequential
decrease of the photocurrent. At this point, the charge transfer process
occurs predominantly from the valence band. This work provides a basic
understanding of the charge transfer mechanisms across the InGaN/liquid
interface which can be used to improve the overall photoanode efficiency.