Elucidating the Role of B-Site Cations toward CO2 Reduction in Perovskite-Based Solid Oxide Electrolysis Cells. Issue 3 (1st March 2022)

• Record Type: Journal Article
• Authors: Tezel, Elif; Guo, Dezhou; Whitten, Ariel; Yarema, Genevieve; Freire, Maikon; Denecke, Reinhard; McEwen, Jean-Sabin; Nikolla, Eranda
• Is Part Of: Journal of the Electrochemical Society. Volume 169:Issue 3(2022)
• Publication Date: 2022-03-01
• Subjects: Electrochemistry -- Periodicals; 541.3705
• DOI: 10.1149/1945-7111/ac5e9b
• Languages: English
• ISSNs: 0013-4651

Abstract

Abstract : Solid oxide electrolysis cells (SOECs) are promising for the selective electrochemical conversion of CO2, or mixed streams of CO2 and H2 O, into high energy products such as CO and H2 . However, these systems are limited by the poor redox stability of the state-of-the-art Ni-based cathode electrocatalysts. Due to their favorable redox properties, mixed ionic-electronic conducting (MIEC) oxides have been considered as promising alternatives. However, improvement of the electrochemical performance of MIEC-based SOEC electrocatalysts is needed and requires an understanding of the factors that govern their activity. Herein, we investigate the effect of B-site 3 d metal cations (Cr, Fe, Co, Ni) of LaBO3 perovskites on their CO2 electrochemical reduction activity in SOECs. We find that their electrochemical performance is highly dependent on the nature of the B-site cation and trends as LaFeO3 > LaCoO3 > LaNiO3 > LaCrO3 . Among these perovskites, LaNiO3 is the least stable and decomposes under electrochemical conditions. In situ characterization and ab initio theoretical calculations suggest that both the nature of the B-site cation and the presence of oxygen surface vacancies impact the energetics of CO2 adsorption and reduction. These studies provide fundamental insights critical toward devising ways to improve the performance of MIEC-based SOEC cathodes for CO2 electroreduction.