铂金
催化作用
材料科学
铂纳米粒子
X射线吸收精细结构
扫描透射电子显微镜
铈
纳米颗粒
氧化铈
金属
吸收光谱法
无机化学
光化学
化学工程
透射电子显微镜
光谱学
氧化物
纳米技术
化学
冶金
工程类
生物化学
物理
量子力学
作者
Suresh Gatla,Daniel Aubert,Giovanni Agostini,Olivier Mathon,S. Pascarelli,Thomas Lunkenbein,Marc Georg Willinger,Helena Kaper
标识
DOI:10.1021/acscatal.6b00677
摘要
Platinum nanoparticles dispersed on nanosized ceria are active for CO oxidation at room temperature after hydrogen pretreatment. High angular annular dark field scanning transmission electron microscopy (HAADF-STEM) analysis of the reduced catalyst shows spreading of the 1 nm sized platinum particles under the electron beam, characteristic for a two-dimensional strong metal–support interaction. In situ X-ray absorption fluorescence spectroscopy (XAFS) reveals a Pt–O distance of 2.1 Å, which is significantly longer than the Pt–O distance in PtO2 (2.0 Å). This elongated Pt–O distance can be related to interaction of the platinum species with cerium oxide in the form of a low-temperature active species–support interaction. These findings contribute to the general understanding of catalytic systems operating at low temperature.
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