Tracking heterogeneous structural motifs and the redox behaviour of copper–zinc nanocatalysts for the electrocatalytic CO2 reduction using operando time resolved spectroscopy and machine learning. Issue 9 (1st April 2022)

• Record Type: Journal Article
• Authors: Rüscher, Martina; Herzog, Antonia; Timoshenko, Janis; Jeon, Hyo Sang; Frandsen, Wiebke; Kühl, Stefanie; Roldan Cuenya, Beatriz
• Is Part Of: Catalysis science & technology. Volume 12:Issue 9(2022)
• Page Start: 3028
• Page End: 3043
• Publication Date: 2022-04-01
• Subjects: Catalysis -- Periodicals; 541.395
• DOI: 10.1039/d2cy00227b
• Languages: English
• ISSNs: 2044-4753

Abstract

Abstract : Elucidating the role of Zn in bimetallic CuZn nanocatalysts for the electrocatalytic CO2 reduction reaction (CO2 RR), where the greenhouse gas CO2 is converted into valuable industrial chemicals using energy from renewable sources. Abstract : Copper-based catalysts are established catalytic systems for the electrocatalytic CO2 reduction reaction (CO2 RR), where the greenhouse gas CO2 is converted into valuable industrial chemicals, such as energy-dense C2+ products, using energy from renewable sources. However, better control over the catalyst selectivity, especially at industrially relevant high current density conditions, is needed to expedite the economic viability of the CO2 RR. For this purpose, bimetallic materials, where copper is combined with a secondary metal, comprise a promising and a highly tunable catalyst for the CO2 RR. Nevertheless, the synergy between copper and the selected secondary metal species, the evolution of the bimetallic structural motifs under working conditions and the effect of the secondary metal on the kinetics of the Cu redox behavior require careful investigation. Here, we employ operando quick X-ray absorption fine structure (QXAFS) spectroscopy coupled with machine-learning based data analysis and surface-enhanced Raman spectroscopy (SERS) to investigate the time-dependent chemical and structural changes in catalysts derived from shape-selected ZnO/Cu2 O nanocubes under CO2 RR conditions at current densities up to −500 mA cm −2 . We furthermore relate the catalyst transformations observed under working conditions to the catalytic activity and selectivity and correlate potential-dependent surface and subsurface processes. We report that the addition of Zn to a Cu-based catalyst has a crucial impact on the kinetics of subsurface processes, while redox processes of the Cu surface layer remain largely unaffected. Interestingly, the presence of Zn was found to contribute to the stabilization of cationic Cu(i ) species, which is of catalytic relevance since Cu(0)/Cu(i ) interfaces have been reported to be beneficial for efficient electrocatalytic CO2 conversion to complex multicarbon products. At the same time, we attribute the increase of the C2+ product selectivity to the formation of Cu-rich CuZn alloys in samples with low Zn content, while Zn-rich alloy phases result in an increased formation of CO paralleled by an increase of the parasitic hydrogen evolution reaction.