Citation:
Abstract:
In the field of electrochemical reduction of CO2 (CO2ER) Cu and oxide derived OD-Cu electrocatalysts have been widely studied due to their unique capability to produce high added value products, such as CO, hydrocarbons and alcohols, albeit with relatively low selectivity.1 Cu-M bimetallic catalysts are a promising approach to break scaling relations among key intermediates and modulate the CO2ER selectivity. In the past 5 years, several studies on the CO2ER activity of Cu-Sn bimetallic catalysts have demonstrated remarkably high selectivities towards CO2,3 or formate.4,5In general, comparison of several studies employing various Cu-Sn stoichiometries shows that Sn-poor catalysts are typically selective towards CO production, while Sn-rich catalysts favor formate (HCOO⁻). However, the specific optimal compositions leading to high activity towards CO or formate vary significantly among reports. 6–8 Furthermore, the mechanistic origins of the selectivity differences among Cu-Sn catalysts remains a topic of debate.
Trends in product selectivity have been ascribed to aspects including composition, lattice effects,7charge redistribution among metals in alloy structures,9 oxidation states,4,8 and the resulting effects on adsorption strength of key intermediates (e.g. *COOH, *OCHO, *CO, *H) directing selectivity among H2, CO and HCOO⁻. A comparison of the relevant literature has allowed us to establish common trends in CO2ER activity of Cu-Sn of various morphologies, synthetic procedures and speciation (Oxide derived vs Alloy materials) and identify points of controversy and key open questions that might help unifying the understanding of the activation of CO2 on Cu-Sn bimetallics. At the center of the debate is the persistence of oxidized metal sites during CO2ER and the precise nature of the active site. A major challenge in this regard, is the complex dependence of catalyst structure and composition with applied electrochemical bias.
In this context, we explore X-ray spectroscopies as powerful tools to investigate the chemical environment and oxidation state of metal sites Sn and Cu in bimetallic electrocatalysts. By correlating diverse X-ray spectroscopy methods (soft and hard X-ray absorption (XAS) techniques, as well as X-ray photoelectron spectroscopy (XPS)), complementary information can be obtained on the chemical environment of metal sites in an electrocatalyst bulk and surface. We report our study on the dependence of structure and composition on applied electrochemical potential in Sn-functionalized Cu catalysts, achieved by combining in situ hard XAS, ex situ soft-XAS and XPS toward building a more complete picture of this model catalyst system.
