TY - JOUR
T1 - Robust Cathode for Efficient CO2 Electrolysis Driven by Entropy Engineering in Solid Oxide Electrolysis Cells
AU - Yang, Meiting
AU - Liu, Shuai
AU - Shen, Xinran
AU - Xu, Ruijia
AU - Feng, Jiangyuan
AU - Luo, Zhixin
AU - Yang, Guangming
AU - Liu, Yu
AU - Ran, Ran
AU - Zhou, Wei
AU - Shao, Zongping
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/8/9
Y1 - 2024/8/9
N2 - Herein, we introduce an innovative approach of entropy engineering to design high-performance and durable electrodes. A series of perovskite oxides with varying configurational entropy (Sconfig) based on Pr1/2Ba1/2FeO3−δ (PBF) matrix are synthesized, and their physicochemical properties and electrochemical performances in CO2 reduction reaction process are explored via manipulating Sconfig. Notably, a high-entropy perovskite, Pr1/6La1/6Sm1/6Ba1/6Sr1/6Ca1/6FeO3−δ (PLSBSCF), with an Sconfig of 1.79 R, exhibits significant lattice distortion due to homogeneous distributed A-site elements. It demonstrates a high concentration of oxygen vacancies, good CO2 adsorption capability, and rapid O2-/e- conductions. Compared to bare PBF perovskite, PLSBSCF offers a greater number of active sites for CO2RR, and the corresponding cell achieves remarkably high current densities of 2.86 A cm-2 at 850 °C (1.5 V) during direct CO2 electrolysis, while maintaining good thermal stability and operational durability. Density Functional Theory calculations also confirm the good CO2 reduction activity of PLSBSCF perovskite.
AB - Herein, we introduce an innovative approach of entropy engineering to design high-performance and durable electrodes. A series of perovskite oxides with varying configurational entropy (Sconfig) based on Pr1/2Ba1/2FeO3−δ (PBF) matrix are synthesized, and their physicochemical properties and electrochemical performances in CO2 reduction reaction process are explored via manipulating Sconfig. Notably, a high-entropy perovskite, Pr1/6La1/6Sm1/6Ba1/6Sr1/6Ca1/6FeO3−δ (PLSBSCF), with an Sconfig of 1.79 R, exhibits significant lattice distortion due to homogeneous distributed A-site elements. It demonstrates a high concentration of oxygen vacancies, good CO2 adsorption capability, and rapid O2-/e- conductions. Compared to bare PBF perovskite, PLSBSCF offers a greater number of active sites for CO2RR, and the corresponding cell achieves remarkably high current densities of 2.86 A cm-2 at 850 °C (1.5 V) during direct CO2 electrolysis, while maintaining good thermal stability and operational durability. Density Functional Theory calculations also confirm the good CO2 reduction activity of PLSBSCF perovskite.
UR - http://www.scopus.com/inward/record.url?scp=85198538636&partnerID=8YFLogxK
U2 - 10.1021/acsenergylett.4c01447
DO - 10.1021/acsenergylett.4c01447
M3 - 文章
AN - SCOPUS:85198538636
SN - 2380-8195
VL - 9
SP - 3818
EP - 3827
JO - ACS Energy Letters
JF - ACS Energy Letters
IS - 8
ER -