The Positional Effect of an Immobilized Re Tricarbonyl Catalyst for CO<sub>2</sub> Reduction
Jeremiah C. Choate, Israel Silva, Po Ching Hsu, Kaylyn Tran, Smaranda C. Marinescu
Abstract
The storage of renewable energy through the conversion of CO 2 to CO provides a viable solution for the intermittent nature of these energy sources. The immobilization of rhenium(I) tricarbonyl molecular complexes is presented through the reductive coupling of bis(diazonium) aryl substituents. The heterogenized complex was characterized through ultra–visible, attenuated total reflectance, infrared reflection absorption spectroscopy, and X-ray photoelectron spectroscopy to probe the electronic structure of the immobilized complex. In addition, studies of cyclic voltammetry, controlled potential electrolysis, and electrochemical impedance spectroscopy were conducted to examine the CO 2 reduction activity. The structure and CO 2 reduction performance were compared with a previously reported immobilized rhenium(I) tricarbonyl molecular complex to probe the effect of varying the tethering of the aryl substituent from the 5,5′-position to the 4,4′-position of the 2,2′-bipyridine backbone. The immobilized complex on carbon cloth at the 4,4′-position provided excellent selectivity (FE CO > 99%) and maximum TON CO and TOF CO values of 3359 and 0.9 s –1, respectively, without the addition of a Bro̷nsted acid source. A nonaqueous flow cell demonstrated the stability of this complex during a 5 h electrolysis. Tethering at the 4,4′-position, compared to the 5,5′-position, yielded lower overall activity for CO 2 reduction and was attributed to the difference in growth morphology and formation of aggregations, due to Re–Re dimer formation and π–π stacking interactions within the metallopolymer matrix. For carbon cloth substrates, an optimized catalyst loading was determined to be 44.6 ± 11 nmol/cm 2 .