Photocatalytic Hydrogen Generation from Water with Iron Carbonyl Phosphine Complexes: Improved Water Reduction Catalysts and Mechanistic Insights

An extended study of a novel visible‐light‐driven water reduction system containing an iridium photosensitizer, an in situ iron(0) phosphine water reduction catalyst (WRC), and triethylamine as sacrificial reductant is described. The influences of solvent composition, ligand, ligand‐to‐metal ratio,...

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Published inChemistry : a European journal Vol. 17; no. 23; pp. 6425 - 6436
Main Authors Gärtner, Felix, Boddien, Albert, Barsch, Enrico, Fumino, Koichi, Losse, Sebastian, Junge, Henrik, Hollmann, Dirk, Brückner, Angelika, Ludwig, Ralf, Beller, Matthias
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 27.05.2011
WILEY‐VCH Verlag
Wiley Subscription Services, Inc
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Summary:An extended study of a novel visible‐light‐driven water reduction system containing an iridium photosensitizer, an in situ iron(0) phosphine water reduction catalyst (WRC), and triethylamine as sacrificial reductant is described. The influences of solvent composition, ligand, ligand‐to‐metal ratio, and pH were studied. The use of monodentate phosphine ligands led to improved activity of the WRC. By applying a WRC generated in situ from Fe3(CO)12 and tris[3,5‐bis(trifluoromethyl)phenyl]phosphine (P[C6H3(CF3)2]3, Fe3(CO)12/PR3=1:1.5), a catalyst turnover number of more than 1500 was obtained, which constitutes the highest activity reported for any Fe WRC. The maximum incident photon to hydrogen efficiency obtained was 13.4 % (440 nm). It is demonstrated that the evolved H2 flow (0.23 mmol H2 h−1 mg−1 Fe3(CO)12) is sufficient to be used in polymer electrolyte membrane fuel cells, which generate electricity directly from water with visible light. Mechanistic studies by NMR spectroscopy, in situ IR spectroscopy, and DFT calculations allow for an improved understanding of the mechanism. With respect to the Fe WRC, the complex [HNEt3]+[HFe3(CO)11]− was identified as the key intermediate during the catalytic cycle, which led to light‐driven hydrogen generation from water. Reduced circumstances: Turnover numbers of up to 1600 and an incident photon‐to‐hydrogen efficiency of 13.4 % were achieved with an iron‐based water‐reduction catalyst combined with an iridium photosensitizer (see picture). Mechanistic investigations were carried out by NMR and in situ FTIR spectroscopy and DFT calculations. [HFe3(CO)11]− was identified as the active iron species during photocatalytic hydrogen evolution from water.
Bibliography:BMBF
istex:2D27B853054280775EC34FAF0F1C2E30CFE4F65E
ark:/67375/WNG-D0M1TM07-X
DFG
Fonds der Chemischen Industrie
State of Mecklenburg-Vorpommern
ArticleID:CHEM201003564
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0947-6539
1521-3765
DOI:10.1002/chem.201003564