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An anisotropically crystallized and nitrogen-doped CuWO4 photoanode for efficient and robust visible-light-driven water oxidation.
- Source :
- Journal of Materials Chemistry A; 11/7/2024, Vol. 12 Issue 41, p28459-28474, 16p
- Publication Year :
- 2024
-
Abstract
- In this work, a nitrogen-doped CuWO<subscript>4</subscript> (N-CuWO<subscript>4</subscript>) photoanode for photoelectrochemical (PEC) water oxidation was synthesized by a mixed metal-imidazole casting (MiMIC) method with 1-butylimidazole (BIm). The N-CuWO<subscript>4</subscript> electrode achieved PEC water oxidation at a wavelength of 540 nm that is longer than that of the film (neat-CuWO<subscript>4</subscript>) prepared without BIm by 40 nm due to the N-doping, which was conscientiously characterized by spectroscopic and theoretical investigations. The N-CuWO<subscript>4</subscript> surface was compactly covered with worm-like particles of 100–500 nm diameter, which is responsible for the rigid adherence of the N-CuWO<subscript>4</subscript> film onto the substrate. The N-CuWO<subscript>4</subscript> film showed anisotropic crystallization of triclinic CuWO<subscript>4</subscript> with predominant growth of the (010) and (100) planes, in contrast to the isotropic crystallization observed for the neat-CuWO<subscript>4</subscript> film. The N-CuWO<subscript>4</subscript> electrode demonstrated superior performance for PEC water oxidation with an incident photon-to-electron conversion efficiency (IPCE) of 5.6% contributed by a charge separation efficiency (η<subscript>sep</subscript>) of 12.3% and a catalytic efficiency (η<subscript>cat</subscript>) of 51.9% (at 420 nm and 1.23 V), a faradaic efficiency (FE<subscript>O<subscript>2</subscript></subscript>) of 97% for O<subscript>2</subscript> evolution, and considerable stability for 40 h, which are advantageously comparable to those of the state-of-the-art CuWO<subscript>4</subscript>-based photoanodes. The water oxidation rate constant (k<subscript>O<subscript>2</subscript></subscript> = 1.6 × 10<superscript>2</superscript> s<superscript>−1</superscript>) at the surface for the N-CuWO<subscript>4</subscript> electrode was higher than that (6.8 s<superscript>−1</superscript>) for the neat-CuWO<subscript>4</subscript> electrode by 2 orders of magnitude, which is responsible for the high IPCE and η<subscript>cat</subscript> of the N-CuWO<subscript>4</subscript> electrode. The higher k<subscript>O<subscript>2</subscript></subscript> value for the N-CuWO<subscript>4</subscript> electrode is ascribed to the higher active site on the (100) facet for water oxidation at the surface. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 20507488
- Volume :
- 12
- Issue :
- 41
- Database :
- Complementary Index
- Journal :
- Journal of Materials Chemistry A
- Publication Type :
- Academic Journal
- Accession number :
- 180411745
- Full Text :
- https://doi.org/10.1039/d4ta04120h