Copper oxide coupled with photon upconversion for solar water splitting

Photoelectrochemical water splitting is a promising solution for harnessing solar radiation for hydrogen production. Copper oxide semiconductors, particularly materials based on cuprous oxide, have attracted attention due to their abundant elemental availability and scalable synthesis methods. To im...

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Veröffentlicht in:Communications materials 2024-07, Vol.5 (1), p.126-8, Article 126
Hauptverfasser: Magazov, Yerbolat, Kudryashov, Vladislav, Moldabekov, Kuanysh, Amze, Magzhan, Nurmanova, Aiisha, Aliyev, Asset, Nuraje, Nurxat
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Sprache:eng
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Zusammenfassung:Photoelectrochemical water splitting is a promising solution for harnessing solar radiation for hydrogen production. Copper oxide semiconductors, particularly materials based on cuprous oxide, have attracted attention due to their abundant elemental availability and scalable synthesis methods. To improve the generated photocurrent of the photoelectrode system, photon upconversion materials can be implemented into water-splitting devices. Here, we demonstrate the potential application of triplet-triplet annihilation-based upconversion in solar-assisted water splitting and highlight the significance of photonic designs to improve the light-harnessing properties of photoactive materials. The triplet-triplet annihilation mechanism is particularly suitable due to its efficient conversion at low photon intensity, namely under 1-sun illumination. Our results show that Cu 2 O coupled with an upconverter outperforms bare Cu 2 O by 56% in terms of produced photocurrent density. We construct a hybrid water-splitting device with an extended absorption range by utilizing a semi-transparent 600 nm Cu 2 O film with a 5 nm Au underlayer. Photoelectrochemical water splitting uses solar radiation for hydrogen production. Here, triplet-triplet annihilation-based upconversion is integrated into a water-splitting device which improves the light-harnessing properties of the photoactive materials
ISSN:2662-4443
2662-4443
DOI:10.1038/s43246-024-00574-5