Lattice distortion induced internal electric field in TiO<sub>2</sub> photoelectrode for efficient charge separation and transfer.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 32358565.
- Also identified by DOI 10.1038/s41467-020-15993-4 and PMC identifier 7195485.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Providing sufficient driving force for charge separation and transfer (CST) is a critical issue in photoelectrochemical (PEC) energy conversion. Normally, the driving force is derived mainly from band bending at the photoelectrode/electrolyte interface but negligible in the bulk. To boost the bulky driving force, we report a rational strategy to create effective electric field via controllable lattice distortion in the bulk of a semiconductor film. This concept is verified by the lithiation of a classic TiO<sub>2</sub> (Li-TiO<sub>2</sub>) photoelectrode, which leads to significant distortion of the TiO<sub>6</sub> unit cells in the bulk with well-aligned dipole moment. A remarkable internal built-in electric field of ~2.1 × 10<sup>2</sup> V m<sup>-1</sup> throughout the Li-TiO<sub>2</sub> film is created to provide strong driving force for bulky CST. The photoelectrode demonstrates an over 750% improvement of photocurrent density and 100 mV negative shift of onset potential upon the lithiation compared to that of pristine TiO<sub>2</sub> film.