原子探针
催化作用
纳米颗粒
双金属片
纳米材料
化学
介孔材料
纳米技术
金属
多孔性
Atom(片上系统)
化学工程
氧化物
纳米
材料科学
微观结构
结晶学
有机化学
嵌入式系统
工程类
计算机科学
作者
Florian Zand,Suzanne Hangx,Christopher J. Spiers,Peter J. van den Brink,James T. Burns,Matthew G. Boebinger,Jonathan D. Poplawsky,Matteo Monai,Bert M. Weckhuysen
摘要
Understanding and controlling the structure and composition of nanoparticles in supported metal catalysts are crucial to improve chemical processes. For this, atom probe tomography (APT) is a unique tool, as it allows for spatially resolved three-dimensional chemical imaging of materials with sub-nanometer resolution. However, thus far APT has not been applied for mesoporous oxide-supported metal catalyst materials, due to the size and number of pores resulting in sample fracture during experiments. To overcome these issues, we developed a high-pressure resin impregnation strategy and showcased the applicability to high-porous supported Pd–Ni-based catalyst materials, which are active in CO2 hydrogenation. Within the reconstructed volume of 3 × 105 nm3, we identified over 400 Pd–Ni clusters, with compositions ranging from 0 to 16 atom % Pd and a size distribution of 2.6 ± 1.6 nm. These results illustrate that APT is capable of quantitatively assessing the size, composition, and metal distribution for a large number of nanoparticles at the sub-nm scale in industrial catalysts. Furthermore, we showcase that metal segregation occurred predominately between nanoparticles, shedding light on the mechanism of metal segregation. We envision that the presented methodology expands the capabilities of APT to investigate porous functional nanomaterials, including but not limited to solid catalysts.
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