TY - JOUR
T1 - Lattice-Plane-Dependent Distribution of Ce3+ at Pt and CeO2 Interfaces for Pt/CeO2 Catalysts
AU - Hojo, Hajime
AU - Nakashima, Minori
AU - Yoshizaki, Satoru
AU - Einaga, Hisahiro
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/2/13
Y1 - 2024/2/13
N2 - The interaction between a metal and a support, which is known as the metal-support interaction, often plays a determining role in the catalytic properties of supported metal catalysts. Herein, we have developed model Pt/CeO2 catalysts, which enabled us to investigate the interface atomic and electronic structures between Pt and the {001}, {011}, and {111} planes of CeO2 using scanning transmission electron microscopy and electron energy-loss spectroscopy. We found that the number of Ce3+ ions around the Pt nanoparticles followed the order {001} > {011} > {111}, which was the opposite order of the generally accepted stability of low index surfaces of CeO2. Systematic first-principles calculations revealed that the presence of Pt nanoparticles facilitated the formation of oxygen vacancies and that the appearance of the Ptδ+ state was preferred when Pt nanoparticles were in contact with CeO2 {001} planes due to direct charge transfer from Pt to CeO2. These results provide important insights into the nature of the metal-support interaction for a comprehensive understanding of the properties of supported metal catalysts.
AB - The interaction between a metal and a support, which is known as the metal-support interaction, often plays a determining role in the catalytic properties of supported metal catalysts. Herein, we have developed model Pt/CeO2 catalysts, which enabled us to investigate the interface atomic and electronic structures between Pt and the {001}, {011}, and {111} planes of CeO2 using scanning transmission electron microscopy and electron energy-loss spectroscopy. We found that the number of Ce3+ ions around the Pt nanoparticles followed the order {001} > {011} > {111}, which was the opposite order of the generally accepted stability of low index surfaces of CeO2. Systematic first-principles calculations revealed that the presence of Pt nanoparticles facilitated the formation of oxygen vacancies and that the appearance of the Ptδ+ state was preferred when Pt nanoparticles were in contact with CeO2 {001} planes due to direct charge transfer from Pt to CeO2. These results provide important insights into the nature of the metal-support interaction for a comprehensive understanding of the properties of supported metal catalysts.
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U2 - 10.1021/acsnano.3c09092
DO - 10.1021/acsnano.3c09092
M3 - Article
C2 - 38285709
AN - SCOPUS:85184810981
SN - 1936-0851
VL - 18
SP - 4775
EP - 4782
JO - ACS nano
JF - ACS nano
IS - 6
ER -