1. Synergistic effects of MXene support and cobalt salts in dye-sensitized photocatalytic hydrogen generation.
- Author
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Smirnova, Marina, Scheibe, Blazej, Ramírez-Grau, Rubén, García, Hermenegildo, and Lewandowska-Andralojc, Anna
- Subjects
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INTERSTITIAL hydrogen generation , *COBALT catalysts , *X-ray photoelectron spectroscopy , *CATALYST supports , *HYDROGEN production - Abstract
This study introduces an approach to photocatalytic hydrogen production through a dye-sensitized photocatalytic system employing MXene (Ti 3 C 2 T x) and a non-noble cobalt metal catalyst. It was demonstrated that simple integration of eosin Y, Ti 3 C 2 T x and cobalt salt (CoSO 4) significantly enhances the photocatalytic hydrogen evolution, outperforming the corresponding system that does not include Ti 3 C 2 T x. The key to this enhanced performance lies in the unique properties of MXene material, which facilitates effective electron transfer and acts as a support for dye and catalyst. The successful well-dispersed decoration of small (2–3 nm) cobalt-based nanoparticles on the Ti 3 C 2 T x sheet via in situ photodeposition was confirmed by transmission electron microscopy (TEM) and X-ray Photoelectron Spectroscopy (XPS). The optimal hydrogen production rates were achieved with a Co to Ti 3 C 2 T x mass ratio of 15%. This optimized interaction results in a hydrogen evolution rate of 40.1 mmol h−1 g−1 and an apparent quantum efficiency (AQE) of 35.4% at 505 nm. These findings highlight the potential of Ti 3 C 2 T x as a versatile component in photocatalytic systems, particularly effective when paired with economically viable, earth-abundant catalysts like cobalt. [Display omitted] • In situ Co [2]⁺ photodeposition on Ti₃C₂Tₓ nearly triples hydrogen production. • The optimized photocatalytic H 2 efficiency is enhanced to 40.1 mmol h⁻1 g⁻1. • EY/Ti 3 C 2 T x /Co NPs reaches 35.4% AQE at 505 nm. • Enhanced photocatalytic activity due to effective charge separation. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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