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Abstract Kinetical, energetical and solid state considerations were elaborated in a search for suitable electrodes for the oxidation of water with visible light. They led to layer type transition metal dichalcogenides and to the photo-electrochemical utilization of optical d-d-transition which do not break chemical bonds. MoS 2 was selected as a promising compound and it was actually shown to react with water on illumination with light between 400 and 715 nm. At low electrode potentials the liberation of small quantities of molecular oxygen was traced with polarographic techniques. The main portion of the oxidation products of water was, however, found to be lost for the oxydation of crystal bound sulfur to sulfate. An improvement of this situation in favour of an increased rate of oxygen evolution has been accomplished by means of a redox-catalyst, tris (2,2'-bipyridine) -ruthenium (II), which is oxidized through photochemically generated holes from the MoS 2 4 d z ² - valence band and channels them into oxygen-evolution through nucleo-philic addition of hydroxide. A molecular mechanism was elaborated for the photoelectrochemical oxidation of water on MoS 2 and its conclusions tested by investigating the oxidative behaviour of various additional layer-type transition metal compounds. It involves a hole mediated valence change of molybdenum with an intermediate formation of a 5-valent molybdenum hydroxide. A basic kinetical and energetical similarity is suggested with the function of manganese reaction centers in photosynthesis.
H. Tributsch (Thu,) studied this question.