Abstract

Along with TiO_2, ZnO is the main photocatalyst for a wide class of redox reactions used to convert light energy into chemical and for environmental cleanup. It has been shown that the creation in ZnO of surface intrinsic defects in ZnO i.e. vacancies in the anionic and cationic sublattices (F-type and V-type centers) - makes it possible to create long-lived (up to 10^3 s) photocatalysis centers and thus fundamentally (tens of times) to increase the quantum yield of reactions. Slow surface states — photocatalysis centers — are created by the diffusion of electrons and holes generated during interband transitions in the volume of the photoactivated sample. However, the transfer efficiency is sharply reduced due to carrier recombination and losses when overcoming the Schottky surface barrier. In this work, In order to reduce these losses during energy transfer to the surface, we used in this work neutral energy carriers — excitons. The high (60 meV) exciton binding energy in ZnO allows it to move at room temperature without decay. The radiation loss of the exciton energy in our experiments is effectively reduced by the formation of a surface 2D structure. The results obtained confirm the high efficiency of the exciton channel for the formation of surface long-lived F and V centers of photocatalysis in the processes of oxygen photoadsorption and photodesorption, imitating the full cycle of the redox photocatalytic reaction.

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