Abstract
Nanostructured molybdenum oxide (α-MoO3) thin film photoelectrodes were synthesised by anodisation. Upon band gap-excitation by light illumination, α-MoO3 is able to store a portion of the excited charges in its layered structure with the simultaneous intercalation of alkali cations. The stored electrons can be discharged from α-MoO3 for utilisation under dark conditions, and α-MoO3 is able to recharge itself with successive illuminations to behave as a 'self-photo-rechargeable' alkali-ion battery. The alteration of the anodisation pH allowed the crystal structure and oxygen vacancy concentrations of α-MoO3 to be modulated to achieve (i) a distorted MoO6 octahedra for enhanced charge separation and storage, (ii) a layered structure with a greater exposed (010) crystal face for rich and reversible ion intercalation and (iii) a highly crystalline thin film that suppresses electron-hole pair recombination. Overall, the larger MoO6 octahedral distortion in α-MoO3 at a higher pH favours charge storage, whereas smaller octahedral distortion at a lower pH leads to anodic photocurrent enhancement.
| Original language | English |
|---|---|
| Pages (from-to) | 1934-1941 |
| Journal | ChemSusChem |
| Volume | 7 |
| Issue number | 7 |
| Online published | 8 May 2014 |
| DOIs | |
| Publication status | Published - Jul 2014 |
| Externally published | Yes |
Research Keywords
- electrochemistry
- energy conversion
- intercalations
- molybdenum
- thin films
Policy Impact
- Cited in Policy Documents
Fingerprint
Dive into the research topics of 'Harvesting, storing and utilising solar energy using MoO3: modulating structural distortion through pH adjustment'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver