The rutiles (M,Ru)O-2 (M = Mg, Zn, Co, Ni, Cu) are formed directly under hydrothermal conditions at 240 degrees C from potassium perruthenate and either peroxides of zinc or magnesium or poorly crystalline oxides of cobalt, nickel, or copper. The polycrystalline powders consist of lath-shaped crystallites, tens of nanometres in maximum dimension. Powder neutron diffraction shows that the materials have an expanded a axis and contracted c axis compared to the parent RuO2, but there is no evidence of lowering of symmetry to other AO(2)-type structures, supported by Raman spectroscopy. Rietveld refinement shows no evidence for oxide non-stoichiometry and provides a formula (MxRu1-x)O-2 with 0.14 < x < 0.2, depending on the substituent metal. This is supported by energy-dispersive X-ray analysis on the transmission electron microscope, while Ru K-edge XANES spectroscopy shows that upon inclusion of the substituent the average Ru oxidation state is increased to balance charge. Variable temperature magnetic measurements provide evidence for atomic homogeneity of the mixed metal materials, with suppression of the high temperature antiferromagnetism of RuO2 and increased magnetic moment. The new rutiles all show enhanced electrocatalysis compared to reference RuO2 materials for oxygen evolution in 1 M H2SO4 electrolyte at 60 degrees C, with higher specific and mass activity (per Ru) than a low surface area crystalline RuO2 and with less Ru dissolution over 1000 cycles compared to an RuO2 with a similar surface area. Magnesium substitution provides the optimum balance between stability and activity, despite leaching of the Mg2+ into solution, and this was proved in membrane electrode assemblies.
