Photosensitizing units have already been applied to enable light-driven catalytic reduction of CO 2 with mononuclear rhenium complexes. However, dinuclear catalytic systems that are able to activate CO 2 in a cooperative bimetallic fashion have only rarely been combined with photosensitizers. We here present detailed studies on the influence of additional photosensitizers on the catalytic performance of a dirhenium complex (Re 2 Cl 2 ) and present correlations with spectroscopic measurements, which shed light on the reaction mechanism. The use of [Ir(dFppy) 3 ] (Ir, dFppy = 2-(4,6-difluorophenyl)pyridine)) resulted in considerably faster CO 2 to CO transformation than [Cu-(xant)(bcp)]PF 6 (Cu, xant = xantphos, bcp = bathocuproine). Emission quenching studies, transient absorption as well as IR spectroscopy provide information about the electron transfer paths of the intermolecular systems. It turned out that formation of double reduced species [Re 2 Cl 2 ] 2À along with an intermediate with a ReÀ Re bond ([ReRe]) can be taken as an indication of multi-electron storage capacity. Furthermore, under catalytic conditions a CO 2 -bridged intermediate was identified.