Abstract
The titanium-based metal–organic framework MIL-125(Ti) has been widely investigated in photocatalytic carbon dioxide reduction and water splitting, but rarely studied in photocatalytic methane conversion by employing only water as an oxidant under mild conditions. Simultaneously controlling products with high yield and selectivity is highly challenging in methane conversion. Herein, we develop a series of functionalized titanium metal–organic frameworks via a facile organic ligand exchange process. The abundant Ti3+ active sites induced by oxygen vacancies and functionalized ligands synergistically facilitate the adsorption and activation of methane molecules. The carbon monoxide yield over NH2-MIL-125(Ti) increased to 198.6 μmol·gcat−1·h−1 with a high selectivity of 87.1 % under simulated solar illumination. Combined with in-situ characterizations and density functional theoretical calculations, the results confirmed that Ti3+ active sites induced by oxygen vacancies and amino functional groups synergistically enhanced the photocatalytic conversion of methane and elucidate CH4-to-CO conversion mechanism. This study does not only provide insights into the rational design of metal–organic frameworks with copious oxygen vacancies and functional groups, but also provides some significant cognition for photocatalytic methane conversion.
Published Version
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