The conversion of sunlight into chemical energy provides a sustainable alternative to fossil fuels that can significantly contribute to the mitigation of climate change. In this regard, water splitting with sunlight using semiconductors coupled with redox catalysts emerges as a potential pathway to generate green hydrogen. Here, the performance of molecular hybrid materials composed of inorganic semiconductors, WO3-BiVO4, combined with molecular water oxidation catalysts based on Cu macrocyclic complexes is described. It is found that the charge transfer from BiVO4 to the molecular catalyst occurs on a similar time scale to the direct interfacial hole transfer to water, with a concomitant 62% decrease in the recombination rate because recombination centers are passivated upon deposition of the Cu molecular catalyst on the WO3-BiVO4 junction. Overall, this results in an improvement of the photocurrent as well as long-term stability of the new hybrid materials generated.
Bellido, C.G., Mazzanti, M., Ranu, K., Piccioni, A., Mazzaro, R., Boscherini, F., et al. (2025). Hybrid Molecular Photoanodes for Water Oxidation Based on Electropolymerized Cu Macrocyclic Complexes on BiVO4‐WO3. ADVANCED ENERGY MATERIALS, 15(40), 1-9 [10.1002/aenm.202500253].
Hybrid Molecular Photoanodes for Water Oxidation Based on Electropolymerized Cu Macrocyclic Complexes on BiVO4‐WO3
Piccioni, Alberto;Mazzaro, Raffaello;Boscherini, Federico;Pasquini, Luca
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2025
Abstract
The conversion of sunlight into chemical energy provides a sustainable alternative to fossil fuels that can significantly contribute to the mitigation of climate change. In this regard, water splitting with sunlight using semiconductors coupled with redox catalysts emerges as a potential pathway to generate green hydrogen. Here, the performance of molecular hybrid materials composed of inorganic semiconductors, WO3-BiVO4, combined with molecular water oxidation catalysts based on Cu macrocyclic complexes is described. It is found that the charge transfer from BiVO4 to the molecular catalyst occurs on a similar time scale to the direct interfacial hole transfer to water, with a concomitant 62% decrease in the recombination rate because recombination centers are passivated upon deposition of the Cu molecular catalyst on the WO3-BiVO4 junction. Overall, this results in an improvement of the photocurrent as well as long-term stability of the new hybrid materials generated.| File | Dimensione | Formato | |
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