| Literature DB >> 33739590 |
Priti Sharma1, Subodh Kumar1, Ondrej Tomanec1, Martin Petr1, Johnny Zhu Chen2, Jeffrey T Miller2, Rajender S Varma1, Manoj B Gawande1,3, Radek Zbořil1,4.
Abstract
With increasing concerns for global warming, the solar-driven photocatalytic reduction of CO2 into chemical fuels like methanol is a propitious route to enrich energy supplies, with concomitant reduction of the abundant CO2 stockpiles. Herein, a novel single atom-confinement and a strategy are reported toward single ruthenium atoms dispersion over porous carbon nitride surface. Ruthenium single atom character is well confirmed by EXAFS absorption spectrometric analysis unveiling the cationic coordination environment for the single-atomic-site ruthenium center, that is formed by Ru-N/C intercalation in the first coordination shell, attaining synergism in N-Ru-N connection and interfacial carrier transfer. From time resolved fluorescence decay spectra, the average carrier lifetime of the RuSA-mC3 N4 system is found to be higher compared to m-C3 N4 ; the fact uncovering the crucial role of single Ru atoms in promoting photocatalytic reaction system. A high yield of methanol (1500 µmol g-1 cat. after 6 h of the reaction) using water as an electron donor and the reusability of the developed catalyst without any significant change in the efficiency represent the superior aspects for its potential application in real industrial technologies.Entities:
Keywords: carbon nitride; photocatalysts; photocatalytic reduction of carbon dioxide; single atom
Year: 2021 PMID: 33739590 DOI: 10.1002/smll.202006478
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281