Pt Nanoparticles@Photoactive Metal–Organic Frameworks: Efficient Hydrogen Evolution via Synergistic Photoexcitation and Electron Injection

Pt nanoparticles of 2–3 nm and 5–6 nm in diameter were loaded into stable, porous, and phosphorescent metal–organic frameworks (MOFs 1 and 2) built from [Ir(ppy)2(bpy)]+-derived dicarboxylate ligands (L 1 and L 2 ) and Zr6(μ3-O)4(μ3-OH)4(carboxylate)12 secondary building units, via MOF-mediated phot...

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Veröffentlicht in:J. Am. Chem. Soc 2012-05, Vol.134 (17), p.7211-7214
Hauptverfasser: Wang, Cheng, deKrafft, Kathryn E, Lin, Wenbin
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Sprache:eng
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Zusammenfassung:Pt nanoparticles of 2–3 nm and 5–6 nm in diameter were loaded into stable, porous, and phosphorescent metal–organic frameworks (MOFs 1 and 2) built from [Ir(ppy)2(bpy)]+-derived dicarboxylate ligands (L 1 and L 2 ) and Zr6(μ3-O)4(μ3-OH)4(carboxylate)12 secondary building units, via MOF-mediated photoreduction of K2PtCl4. The resulting Pt@MOF assemblies serve as effective photocatalysts for hydrogen evolution by synergistic photoexcitation of the MOF frameworks and electron injection into the Pt nanoparticles. Pt@2 gave a turnover number of 7000, approximately five times the value afforded by the homogeneous control, and could be readily recycled and reused.
ISSN:0002-7863
1520-5126
DOI:10.1021/ja300539p