| Literature DB >> 30510216 |
Marcella Bonchio1, Zois Syrgiannis2,3, Max Burian4, Nadia Marino2, Erica Pizzolato2,3, Konstantin Dirian5, Francesco Rigodanza3, Giulia Alice Volpato2, Giuseppina La Ganga6, Nicola Demitri7, Serena Berardi8, Heinz Amenitsch4, Dirk M Guldi5, Stefano Caramori8, Carlo Alberto Bignozzi8, Andrea Sartorel2, Maurizio Prato9,10,11.
Abstract
The oxygen in Earth's atmosphere is there primarily because of water oxidation performed by photosynthetic organisms using solar light and one specialized protein complex, photosystem II (PSII). High-resolution imaging of the PSII 'core' complex shows the ideal co-localization of multi-chromophore light-harvesting antennas with the functional reaction centre. Man-made systems are still far from replicating the complexity of PSII, as the majority of PSII mimetics have been limited to photocatalytic dyads based on a 1:1 ratio of a light absorber, generally a Ru-polypyridine complex, with a water oxidation catalyst. Here we report the self-assembly of multi-perylene-bisimide chromophores (PBI) shaped to function by interaction with a polyoxometalate water-oxidation catalyst (Ru4POM). The resulting [PBI]5Ru4POM complex shows a robust amphiphilic structure and dynamic aggregation into large two-dimensional paracrystalline domains, a redshifted light-harvesting efficiency of >40% and favourable exciton accumulation, with a peak quantum efficiency using 'green' photons (λ > 500 nm). The modularity of the building blocks and the simplicity of the non-covalent chemistry offer opportunities for innovation in artificial photosynthesis.Entities:
Year: 2018 PMID: 30510216 DOI: 10.1038/s41557-018-0172-y
Source DB: PubMed Journal: Nat Chem ISSN: 1755-4330 Impact factor: 24.427