TY - JOUR
T1 - Elucidating the Role of B-Site Cations toward CO2 Reduction in Perovskite-Based Solid Oxide Electrolysis Cells
AU - Tezel, Elif
AU - Guo, Dezhou
AU - Whitten, Ariel
AU - Yarema, Genevieve
AU - Freire, Maikon
AU - Denecke, Reinhard
AU - McEwen, Jean Sabin
AU - Nikolla, Eranda
N1 - Publisher Copyright:
© 2022 The Electrochemical Society (“ECS”).
PY - 2022/3/1
Y1 - 2022/3/1
N2 - Solid oxide electrolysis cells (SOECs) are promising for the selective electrochemical conversion of CO2, or mixed streams of CO2 and H2O, 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 3d 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.
AB - Solid oxide electrolysis cells (SOECs) are promising for the selective electrochemical conversion of CO2, or mixed streams of CO2 and H2O, 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 3d 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.
UR - http://www.scopus.com/inward/record.url?scp=85128584941&partnerID=8YFLogxK
U2 - 10.1149/1945-7111/ac5e9b
DO - 10.1149/1945-7111/ac5e9b
M3 - Article
AN - SCOPUS:85128584941
SN - 0013-4651
VL - 169
JO - Journal of the Electrochemical Society
JF - Journal of the Electrochemical Society
IS - 3
M1 - 034532
ER -