Abstract
Depositing a transition-metal hydroxide (TMH) layer on a photoanode has been demonstrated to enhance photoelectrochemical (PEC) water oxidation. However, the controversial understanding for the improvement origin remains a key challenge to unlock the PEC performance. Herein, by taking BiVO4/iron-nickel hydroxide (BVO/FxN4−x-H) as a prototype, we decoupled the PEC process into two processes including charge transfer and surface catalytic reaction. The kinetic information at the BVO/FxN4−x-H and FxN4−x-H/electrolyte interfaces was systematically evaluated by employing scanning photoelectrochemical microscopy (SPECM), intensity modulated photocurrent spectroscopy (IMPS) and oxygen evolution reaction (OER) model. It was found that FxN4−x-H acts as a charge transporter rather than a sole electrocatalyst. PEC performance improvement is mainly ascribed to the efficient suppression of charge recombination by fast hole transfer kinetics at BVO/FxN4−x-H interface.
| Original language | English |
|---|---|
| Pages (from-to) | 3504-3509 |
| Number of pages | 6 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 60 |
| Issue number | 7 |
| DOIs | |
| State | Published - 15 Feb 2021 |
| Externally published | Yes |
Keywords
- charge transfer
- interfaces
- photoelectrochemistry
- surface catalysis
- transition-metal hydroxides