| Literature DB >> 32989272 |
Md Asmaul Hoque1, Marcos Gil-Sepulcre1, Adiran de Aguirre1, Johannes A A W Elemans2, Dooshaye Moonshiram3, Roc Matheu1, Yuanyuan Shi1,4, Jordi Benet-Buchholz1, Xavier Sala5, Marc Malfois6, Eduardo Solano6, Joohyun Lim7, Alba Garzón-Manjón7, Christina Scheu7, Mario Lanza8, Feliu Maseras9,10, Carolina Gimbert-Suriñach11, Antoni Llobet12,13.
Abstract
Photoelectrochemical cells that utilize water as a source of electrons are one of the most attractive solutions for the replacement of fossil fuels by clean and sustainable solar fuels. To achieve this, heterogeneous water oxidation catalysis needs to be mastered and properly understood. The search continues for a catalyst that is stable at the surface of electro(photo)anodes and can efficiently perform this reaction at the desired neutral pH. Here, we show how oligomeric Ru complexes can be anchored on the surfaces of graphitic materials through CH-π interactions between the auxiliary ligands bonded to Ru and the hexagonal rings of the graphitic surfaces, providing control of their molecular coverage. These hybrid molecular materials behave as molecular electroanodes that catalyse water oxidation to dioxygen at pH 7 with high current densities. This strategy for the anchoring of molecular catalysts on graphitic surfaces can potentially be extended to other transition metals and other catalytic reactions.Entities:
Year: 2020 PMID: 32989272 DOI: 10.1038/s41557-020-0548-7
Source DB: PubMed Journal: Nat Chem ISSN: 1755-4330 Impact factor: 24.427