Adsorption experiments and density functional theory (DFT) simulations indicated that Cu(acac) 2 is chemisorbed on the monoclinic sheelite (ms)-BiVO 4 surface to form an O 2 -bridged binuclear complex (OBBC/BiVO 4 ) like hemocyanin. Multi-electron reduction of O 2 is induced by the visiblelight irradiation of the OBBC/BiVO 4 in the same manner as a blue Cu enzyme. The drastic enhancement of the O 2 reduction renders ms-BiVO 4 to work as a good visible-light photocatalyst without any sacrificial reagents. As a model reaction, we show that this biomimetic hybrid photocatalyst exhibits a high level of activity for the aerobic oxidation of amines to aldehydes in aqueous solution and imines in THF solution at 25 8C giving selectivities above 99 % under visiblelight irradiation.In industry, approximately 30 % of fine chemicals are produced by oxidation processes.[1] The development of "green" oxidative synthetic routes utilizing the sunlight and O 2 in the air as the energy source and oxidizing agent, respectively, is crucial for reducing CO 2 emissions and saving energy. O 2 reduction is the key process in photocatalytic reactions as well as in fuel cells and biological energy conversion. Among a variety of visible-light photocatalysts developed so far, [2] metal oxide semiconductors represented by BiVO 4 [3] are very attractive because of the moderate oxidation ability and the good physicochemical stability. Since the solar spectrum peaks at around 500 nm, the metal oxide should possess an absorption edge longer than 500 nm or a band gap (E g ) smaller than 2.5 eV for an efficient use of the sunlight. However, there is a trade-off between the visiblelight absorptivity and the driving force for O 2 reduction, i.e., the decrease in the band gap necessarily lowers the conduction band (CB) minimum or the reducing ability of the excited electrons, because the valence band (VB) maximum, mainly consisting of O2p orbitals, is almost constant (+ 2.94 V vs. standard hydrogen electrode, SHE).[4] Thus, the CB minimum for the metal oxide semiconductors with E g < 2.5 eV is located below + 0. [5] If metal oxide semiconductors with E g < 2.5 eV can be endowed with electrocatalytic activity for the multi-electron O 2 reduction, the method would be accessible for efficient and selective oxidative chemical transformation processes. A fascinating approach is the hybridization of metal oxide semiconductors exhibiting a strong absorption in the wide spectral range and molecular metal complexes with highly efficient and selective electrocatalytic activity. [6,7] Although this type of hybrid photocatalysts has recently attracted much interest for H 2 generation, [8] CO 2 reduction, [9,10] and environmental purification, [11]