Protecting effect of mass transport during electrochemical reduction of oxygenated carbon dioxide feedstocks. Issue 5 (26th March 2019)

• Record Type: Journal Article
• Authors: Williams, Kindle; Corbin, Nathan; Zeng, Joy; Lazouski, Nikifar; Yang, Deng-Tao; Manthiram, Karthish
• Is Part Of: Sustainable energy & fuels. Volume 3:Issue 5(2019)
• Page Start: 1225
• Page End: 1232
• Publication Date: 2019-03-26
• Subjects: Renewable energy sources -- Periodicals; Fuel cells -- Periodicals; Electric batteries -- Periodicals; Electrochemistry -- Periodicals; 660.297
• DOI: 10.1039/c9se00024k
• Languages: English
• ISSNs: 2398-4902

Abstract

Abstract : This work elucidates fundamental transport and kinetic phenomena underlying oxygen gas feed impurity behavior during CO2 electroreduction. Abstract : Electrochemical CO2 reduction is a promising path toward mitigating carbon emissions while also monetizing waste gas through chemicals production and storage of surplus renewable energy. However, deploying such a technology for use on industrial CO2 sources requires an understanding of the effects that gas feed impurities have upon CO2 reduction reaction (CO2 RR). In this work, we elucidate the impact of molecular oxygen on the network of reactions occurring in a CO2 reduction system. Our findings indicate that for a planar, polycrystalline Au electrode in an aqueous environment, oxygen reduction current is limited by the transport characteristics specific to the cell geometry and solvent; as a result, mass transport confers a protective effect by mitigating the otherwise thermodynamically and kinetically favorable reduction of oxygen. The presence of oxygen does not appear to have a significant impact on either CO2 RR or hydrogen evolution partial currents, indicating that the mechanisms of reduction reactions involving oxygen are independent of CO2 RR and hydrogen evolution. Further, an electrokinetic mechanistic analysis indicates many feasible candidates for the rate-determining step of CO2 RR; there is no indication that the CO2 RR mechanism at P CO2 = 0.5 atm is altered by the presence of oxygen, as the Tafel slopes (59 mV dec −1 ) and reaction orders with respect to bicarbonate (0), CO2 (∼1.5), and protons (0 from lack of KIE) are consistent between systems with P O2 = 0 atm and those with P O2 = 0.5 atm. While this is promising for the robustness of CO2 RR to oxygen impurities in gas feeds, the ultimate design tradeoff when utilizing CO2 sources containing oxygen is between the cost of separation processes and the corresponding cost of power inefficiency as a result of electrons lost to oxygen reduction. This represents a first step in understanding kinetic and transport considerations in the design of gas-impurity-tolerant CO2 reduction systems.