Solar Gas-Phase CO<sub>2</sub> Hydrogenation by Multifunctional UiO-66 Photocatalysts
Celia M. Rueda‐Navarro, Zahraa Abou Khalil, Arianna Melillo, Belén Ferrer, Raúl Montero, Asier Longarte, Marco Daturi, Ignacio Vayá, Mohamad El-Roz, Virginia Martínez‐Martínez, Herme G. Baldoví, Sergio Navalón
Abstract
High Resolution Image Download MS PowerPoint Slide Solar-assisted CO 2 conversion into fuels and chemical products involves a range of technologies aimed at driving industrial decarbonization methods. In this work, we report on the development of a series of multifunctional metal–organic frameworks (MOFs) based on nitro- or amino-functionalized UiO-66(M) (M: Zr or Zr/Ti) supported RuO x NPs as photocatalysts, having different energy band level diagrams, for CO 2 hydrogenation under simulated concentrated sunlight irradiation. RuO x (1 wt %; 2.2 ± 0.9 nm)@UiO-66(Zr/Ti)-NO 2 was found to be a reusable photocatalyst, to be selective for CO 2 methanation (5.03 mmol g –1 after 22 h;, apparent quantum yield at 350, 400, and 600 nm of 1.67, 0.25, and 0.01%, respectively), and to show about 3–6 times activity compared with previous investigations. The photocatalysts were characterized by advanced spectroscopic techniques like femto- and nanosecond transient absorption, spin electron resonance, and photoluminescence spectroscopies together with (photo)electrochemical measurements. The photocatalytic CO 2 methanation mechanism was assessed by operando FTIR spectroscopy. The results indicate that the most active photocatalyst operates under a dual photochemical and photothermal mechanism. This investigation shows the potential of multifunctional MOFs as photocatalysts for solar-driven CO 2 recycling.