Recent Progress in Photoelectrochemical Water Splitting Activity of WO3 Photoanodes

• Published in: Topics in catalysis Vol. 61; no. 9-11; pp. 1043 - 1076
• Main Authors: Kalanur, Shankara S., Duy, Le Thai, Seo, Hyungtak
• Format: Journal Article
• Language: English
• Published: New York Springer US 01.06.2018; Springer Nature B.V
• Subjects: Acidic oxides; Catalysis; Catalytic activity; Characterization and Evaluation of Materials; Charge efficiency; Chemistry; Chemistry and Materials Science; Clean energy; Crystal defects; Crystal structure; Gas evolution; Industrial Chemistry/Chemical Engineering; Lattice vacancies; Morphology; Nanomaterials; Operating temperature; Original Paper; Pharmacy; Photoanodes; Photocatalysis; Physical Chemistry; Solar energy; Substrates; Thin films; Tungsten oxides; Water splitting; Defect states; Electrolyte; Morphology; WO; Crystal facet; Photoelectrochemical water splitting; Tungsten substrate; Crystal structure
• ISSN: 1022-5528; 1572-9028
• DOI: 10.1007/s11244-018-0950-1

Photocatalytic and photoelectrochemical (PEC) water splitting to generate clean fuel H 2 and O 2 from water and solar energy using semiconductor nanomaterials is a green technology which could fulfill the growing energy need of the future and environment concerns. WO x≤3 has received considerable attention in photo-assisted water splitting due to its fascinating advantages such as absorbance in visible region up to ~ 480 nm, low cost, and stability in acidic and oxidative conditions. In this review, an attempt is made to summarize the important efforts made in the literature on the employment of WO 3 for PEC water splitting in the last 5 years. Great milestones in PEC performance of WO 3 have been reached with possible improvements via morphology control, crystal structure/facet, introduction of oxygen vacancy/defects and choice of suitable electrolyte. It is established that, WO 3 nanostructure thin films require annealing, usually between 450 and 550 °C to attain more crystallinity and monoclinic phase of WO x≤3 is the most stable phase at room temperature and demonstrated highest photocatalytic activity when compared to other crystal phases. WO 3 structures that are tightly interconnected and strongly bound to the metal collector substrate result in increased photogenerated charge collection efficiency while increase in PEC operating temperature augments the gas evolution quantity. Finally, we provide possibility for further improvements in WO 3 -based PCE which may be required to enhance its efficiency in water splitting.