TY - JOUR
T1 - La3+-Substituted BaSnO3 Perovskite as a Robust Electrocatalyst for Selective CO2 Reduction to Formate
AU - Zhang, Qian
AU - Gao, Suihan
AU - Yan, Yuehui
AU - Li, Mingtao
AU - Yan, Wei
AU - Huang, Yu
AU - Cao, Jun Ji
N1 - Publisher Copyright:
© 2025 American Chemical Society.
PY - 2025/3/19
Y1 - 2025/3/19
N2 - Rational design of high-performance catalysts for CO2 electroreduction is crucial for achieving carbon neutrality, yet effective modification strategies remain scarce. In this study, we present the microwave heating approach to incorporate La3+ ions into Sn-based perovskite oxides, significantly enhancing their electrocatalytic performance for the reduction of CO2 to formate. Through comprehensive characterization techniques, including X-ray photoelectron spectroscopy, synchrotron radiation X-ray absorption spectroscopy, electrochemical measurements (Tafel analysis and impedance spectroscopy), and density functional theory calculations, we demonstrate that La3+ substitution effectively modulates the Sn-O bond distance in BaSnO3. This structural modification induces local charge density enrichment, facilitates CO2 adsorption, and enhances electron transfer kinetics, resulting in a substantial improvement in the formate Faradaic efficiency. In situ Raman spectroscopic analysis and postreaction XPS characterization confirmed the structural integrity of the perovskite framework and the preservation of Sn valence states under negative potentials. This work provides fundamental insights into the CO2 reduction reaction mechanism on perovskite electrocatalysts and establishes a framework for the design of advanced tin-based electrocatalysts.
AB - Rational design of high-performance catalysts for CO2 electroreduction is crucial for achieving carbon neutrality, yet effective modification strategies remain scarce. In this study, we present the microwave heating approach to incorporate La3+ ions into Sn-based perovskite oxides, significantly enhancing their electrocatalytic performance for the reduction of CO2 to formate. Through comprehensive characterization techniques, including X-ray photoelectron spectroscopy, synchrotron radiation X-ray absorption spectroscopy, electrochemical measurements (Tafel analysis and impedance spectroscopy), and density functional theory calculations, we demonstrate that La3+ substitution effectively modulates the Sn-O bond distance in BaSnO3. This structural modification induces local charge density enrichment, facilitates CO2 adsorption, and enhances electron transfer kinetics, resulting in a substantial improvement in the formate Faradaic efficiency. In situ Raman spectroscopic analysis and postreaction XPS characterization confirmed the structural integrity of the perovskite framework and the preservation of Sn valence states under negative potentials. This work provides fundamental insights into the CO2 reduction reaction mechanism on perovskite electrocatalysts and establishes a framework for the design of advanced tin-based electrocatalysts.
KW - In situ Raman spectroscopy, formate
KW - Sn-based electrocatalysts
KW - carbon utilization
KW - electrochemical reduction
KW - perovskite oxides
UR - https://www.scopus.com/pages/publications/105001060588
U2 - 10.1021/acsami.4c21829
DO - 10.1021/acsami.4c21829
M3 - 文章
C2 - 40051049
AN - SCOPUS:105001060588
SN - 1944-8244
VL - 17
SP - 16881
EP - 16891
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 11
ER -