Harvesting the photoexcited holes on a photocatalytic proton reduction metal–organic framework. (5th July 2017)

• Record Type: Journal Article
• Authors: Santaclara, J. G.; Olivos-Suarez, A. I.; du Fossé, I.; Houtepen, A.; Hunger, J.; Kapteijn, F.; Gascon, J.; van der Veen, M. A.
• Is Part Of: Faraday discussions. Volume 201(2017)
• Page Start: 71
• Page End: 86
• Publication Date: 2017-07-05
• Subjects: Chemistry -- Periodicals; Metallurgy -- Periodicals; Electrochemistry -- Periodicals; 540
• DOI: 10.1039/c7fd00029d
• Languages: English
• ISSNs: 1359-6640

Abstract

Abstract : The highly porous titanium based metal–organic framework NH2 -MIL-125(Ti) has recently attracted significant attention in the field of photocatalysis as a promising material for H + reduction. This work reveals charge transfer upon visible light illumination from this MOF to two different charge acceptors, as an alternative to sacrificial electron donors. Charge transfer is demonstrated through a combined spectroscopic study between this MOF and: (1) 2-(1 H -pyrazol-3-yl)phenol, a molecule that functionally mimics the tyrosine–histidine pair, responsible for shuttling the holes to the oxygen evolving centre in natural photosynthesis, and (2) TEMPO, a well known and stable radical. Charge transfer of the holes from the MOF to these occluded molecules takes place on the picosecond time scale. This work suggests that, by coupling a stable and recyclable charge acceptor to the photogenerated holes, the charges can be utilised for oxidation reactions and, thus, link the reduction to the oxidation reactions in water splitting.