Mass spectrometric analysis of the anionic products of interaction between bimetallic palladium-copper tetrahydride anions, PdCuH4-, and carbon dioxide, CO2, in a reaction cell shows an efficient generation of the PdCuCO(2)H4(-) intermediate and formate/formic acid complexes. Multiple structures of PdCuH4- and PdCuCO2H4- are identified by a synergy between anion photoelectron spectroscopy and quantum chemical calculations. The higher energy PdCuH4- isomer is shown to drive the catalytic hydrogenation of CO2, emphasizing the importance of accounting for higher energy isomers for cluster catalytic activity. This study represents the first example of CO2 hydrogenation by bimetallic hydride clusters.