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Rapid Synthesis of Amino Acid Polyoxometalate Nanotubes by One‐Step Solid‐State Chemical Reaction at Room Temperature
Author(s) -
Wang R.Y.,
Jia D.Z.,
Zhang L.,
Liu L.,
Guo Z.P.,
Li B.Q.,
Wang J.X.
Publication year - 2006
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.200500549
Subject(s) - polyoxometalate , materials science , nanomaterials , magic angle spinning , redox , infrared spectroscopy , keggin structure , sulfonic acid , elemental analysis , scanning electron microscope , transmission electron microscopy , chemical engineering , nanotechnology , inorganic chemistry , catalysis , nuclear magnetic resonance spectroscopy , organic chemistry , polymer chemistry , chemistry , engineering , metallurgy , composite material
Abstract A novel and convenient method—solid‐state chemical reaction at room temperature—is reported for the synthesis of amino acid polyoxometalate nanotubes. As a convenient synthesis method for nanomaterials, it may open up a new pathway for the fabrication of organic–inorganic hybrid materials with nanotubular structure. Here, three novel tyrosine (Tyr) polyoxometalate nanotubes, (HTyr) 3 PMo 12 O 40 · 3H 2 O, (HTyr) 3 PW 12 O 40 · 3H 2 O, and (HTyr) 4 SiW 12 O 40 · 5H 2 O are successfully synthesized via a one‐step solid‐state chemical reaction at room temperature. Elemental analysis confirms the rationality of composition for the samples. Infrared spectroscopy, X‐ray diffraction, and 31 P magic‐angle spinning NMR results prove that the samples still possess Keggin‐type structures. Scanning and transmission electron microscopies suggest that the three samples are comprised of nanotubes with remarkably uniform shape and size, with diameters from 50 to 150 nm and lengths of up to several micrometers. Cyclic voltammograms of samples in 1 mol L –1 H 2 SO 4 indicate that three redox waves correspond to three two‐electron processes resulting from the reduction/oxidation of the heteropoly anion.