posted on 2016-12-21, 16:20authored byKim D. von Allmen, Henrik Grundmann, Anthony Linden, Greta R. Patzke
The
reaction of the lacunary polyoxometalate precursor Na9[B-α-BiW9O33]·19.5H2O with Cu(II)
ions was explored in search of new economic ways to copper tungstobismuthates
as interesting prototypes for water oxidation and reduction catalysts.
The emerging series of new 0D–3D polyoxometalate architectures
with distinct copper cores was structurally characterized. Na6Rb6[Cu3(H2O)3(BiW9O33)2] (Cu-4) and 3D-K6.56Cu0.43H2.20[(Cu3Cl)(K2.62Cu0.38(H2O)3)(B-α-BiW9O33)2]·13H2O (Cu-5) display a Cu3(H2O)3 core. The 2D representatives Na12[Cu2(H2O)4Cl2(BiW10O35)2] (Cu-1a), Na10[Cu2(H2O)6(BiW10O35)2] (Cu-1b), 2D-Na7K3Cu0.5Cl[Cu2(H2O)4(BiW10O35)2] (Cu-2), and 2D-Na5.5K2.5Cu[Cu2(H2O)4(BiW10O35)2] (Cu-3) contain Cu2(H2O)nW2O4 cores.
Interestingly, the bismuth-free 1D paratungstate B Na4K4Cu[H2W12O42]
(Cu-6) is formed through reassembly of the precursor. Cu-5 displays a disordered transition metal core, implying
the presence of the polyanions [Cu4(H2O)4(BiW9O33)2]10– and [Cu5(H2O)5(BiW9O33)2]8–. The magnetic properties of Cu-5 as
well as its activity as visible-light-driven H2 and O2 evolution catalyst were evaluated.