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Mesoporous Tungsten Trioxide Photoanodes Modified with Nitrogen-Doped Carbon Quantum Dots for Enhanced Oxygen Evolution Photo-Reaction

Nanostructured photoanodes are attractive materials for hydrogen production via water photo-electrolysis process. This study focused on the incorporation of carbon quantum dots doped with nitrogen as a photosensitizer into mesoporous tungsten trioxide photoanodes (N-CQD/meso-WO(3)) using a surfactan...

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Detalles Bibliográficos
Autores principales: Amer, Mabrook S., Arunachalam, Prabhakarn, Al-Mayouf, Abdullah M., Prasad, Saradh, Alshalwi, Matar N., Ghanem, Mohamed A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6836200/
https://www.ncbi.nlm.nih.gov/pubmed/31652537
http://dx.doi.org/10.3390/nano9101502
Descripción
Sumario:Nanostructured photoanodes are attractive materials for hydrogen production via water photo-electrolysis process. This study focused on the incorporation of carbon quantum dots doped with nitrogen as a photosensitizer into mesoporous tungsten trioxide photoanodes (N-CQD/meso-WO(3)) using a surfactant self-assembly template approach. The crystal structure, composition, and morphology of pure and N-CQD- modified mesoporous WO(3) photoanodes were investigated using scanning electron and transmission microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. Due to their high surface area, enhanced optical absorption, and charge-carrier separation and transfer, the resulting N-CQD/meso-WO(3) photoanodes exhibited a significantly enhanced photocurrent density of 1.45 mA cm(−2) at 1.23 V vs. RHE under AM 1.5 G illumination in 0.5 M Na(2)SO(4) without any co-catalysts or sacrificial reagent, which was about 2.23 times greater than its corresponding pure meso-WO(3). Moreover, the oxygen evolution onset potential of the N-CQD/meso-WO(3) photoanodes exhibited a negative shift of 95 mV, signifying that both the charge-carrier separation and transfer processes were promoted.