烧结
催化作用
扩展X射线吸收精细结构
高分辨率透射电子显微镜
氧化物
金属
材料科学
化学工程
无机化学
物理化学
化学
结晶学
纳米技术
冶金
有机化学
透射电子显微镜
吸收光谱法
物理
工程类
量子力学
作者
Donghai Mei,Ja Hun Kwak,Jianzhi Hu,Sung June Cho,János Szanyi,Lawrence F. Allard,Charles H. F. Peden
摘要
γ-Al2O3-supported Pt group catalysts are widely used in many industrially important catalytic processes. However, γ-Al2O3-supported Pt catalysts are prone to deactivation via metal sintering at high temperatures, in oxidative reaction environments, or both. Using a combination of experimental HRTEM and EXAFS measurements and theoretical DFT calculations, we find that pentacoordinated Al3+ sites (Alp) on the γ-Al2O3(100) surface can inhibit Pt sintering both thermodynamically and kinetically because of their strong interactions with atomic Pt or Pt oxide species. The present work suggests a promising approach for stabilizing the size and morphology of supported catalytically active phases.
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