摘要：Switched photocurrent direction in photoelectrodes is a very interesting phenomenon and has demonstrated their potentials in important applications including photodiodes, phototransistors, light-driven sensors and biosensors. However, the design and mechanism understanding of such photoelectrodes remain challenging to date. Here we report a new phenomenon of sequence-driven the photocurrent direction on a simple bilayer structure of 5 nm thick Au and 10 nm TiO2 under visible-light irradiation. It is found that when Au layer are deposited as the outer layer on TiO2 coated fluorine doped tin oxide (FTO) substrate (designated as FTO/TiO2/Au), anodic photocurrent is obtained due to the band bending formed at the electrode-electrolyte interface. Interestingly, simply swapping the deposition sequence of Au and TiO2 leads to cathodic photocurrent on FTO/Au/TiO2 electrode. Characterization and calculations on the photoelectrode reveals that the photogenerated electrons can be easily trapped in the energy well formed between the band bending and the Schottky contact, which allows electronic tunnelling through the 1.6 nm thick space charge layer, resulting in a unique anodic to cathodic photocurrent conversion. The understanding of this new phenomenon can be important for designing new generation optoelectronic converting devices in a low-cost and facile manner.
