There has been active interest to identify new methods to reduce CO2 into usable fuel sources. In this work, we demonstrate two types of photo-electrochemical cells (PECs) that photoreduce CO2 directly to formate in aqueous solutions both in the presence and absence of external bias or additional electron sources. The photocathodes were either a CuFeO2 /CuO electrode or a bilayer of CdTe on NiO, whereas the photoanode was a bilayer of NiOx on CdS. The PECs were characterized by using both electrochemistry and spectroscopy, and the products formed from CO2 reduction were characterized and quantified by using 1 H NMR spectroscopy and ESI-MS. In addition, an organohydride catalyst was tested in conjunction with the PECs, which not only showed a significant gain of 85 times in CO2 reduction (27 μm formate without the catalyst, 2.3 mm formate with it) compared to the NiO/CdTe photocathode system but could also generate methanol under an external bias (10 μm).
Keywords: copper; electrochemistry; nickel; photochemistry; reduction.
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