Enhancing catalytic performance and hot electron generation through engineering metal-oxide and oxide-oxide interfaces

被引:3
|
作者
Song, Kyoungjae [1 ]
Kim, Jihun [2 ]
Kim, Daeho [1 ]
Hong, Seunghwa [1 ]
Kim, Ki-jeong [3 ]
An, Kwangjin [2 ]
Park, Jeong Young [1 ]
机构
[1] Korea Adv Inst Sci & Technol KAIST, Dept Chem, Daejeon 34141, South Korea
[2] Ulsan Natl Inst Sci & Technol UNIST, Sch Energy & Chem Engn, Ulsan 44919, South Korea
[3] Pohang Accelerator Lab, Beamline Res Div, Pohang 37674, South Korea
基金
新加坡国家研究基金会;
关键词
Hot electrons; Selectivity; Metal-oxide interfaces; Oxide-oxide interfaces; Methanol oxidation; In-situ NAP-XPS analysis; SURFACE-CHEMISTRY; GOLD CATALYSTS; METHANOL; OXIDATION; SUPPORT; NANOPARTICLES; HYDROGEN; EXCITATIONS; SELECTIVITY; CRYSTAL;
D O I
10.1016/j.cattod.2023.114306
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Interfaces are of utmost importance in catalytic reactions, influencing reaction kinetics and electron transfer processes. However, investigations in combined interfaces of metal-oxide and oxide-oxide at heterogeneous catalysts still have challenges due to their complex structure. Herein, we synthesized well-defined Co3O4 and CeO2 cubes with distinct facets and investigated their catalytic performance when deposited on a Pt-thin film, focusing on the influence of metal-oxide and oxide-oxide interfaces. Catalytic measurements demonstrated that the CeO2/Pt interface significantly enhanced turnover frequency (TOF) and selectivity for partial methanol oxidation compared to Co3O4/Pt and bare Pt. Notably, the CeO2/Co3O4/Pt nanodevice exhibited improved partial oxidation selectivity, highlighting the role of the CeO2/Co3O4 interface in methyl formate production. Chemicurrent measurements demonstrate enhanced hot electron generation due to increased overall TOF and partial oxidation production. We also conducted near ambient pressure X-ray photoelectron spectroscopy (NAPXPS) analysis, revealing a higher concentration of Ce3+ ions and increased oxygen vacancies in the CeO2/Co3O4/ Pt catalyst, suggesting oxygen migration from CeO2 to Co3O4, leading to methoxy species stabilization and promoting methyl formate formation.
引用
收藏
页数:11
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