原子层沉积
材料科学
多孔性
催化作用
化学工程
薄膜
结晶
钯
沉积(地质)
氢氧化物
铝
纳米颗粒
纳米尺度
纳米技术
复合材料
有机化学
化学
工程类
生物
古生物学
沉积物
作者
Cassandra George,Patrick Littlewood,Peter C. Stair
标识
DOI:10.1021/acsami.9b23256
摘要
AlO X thin films deposited by atomic layer deposition (ALD) have previously been used to increase both stability and selectivity of supported palladium catalysts and are known to develop nanoscale porosity upon heating. Understanding the factors that affect ALD thin-film porosity enables future design of layered catalytic structures with tunable nanoscale features on industrially-relevant high-surface-area materials. In this study, porous and nonporous aluminum oxide supports with and without palladium nanoparticles were overcoated with thin films of 2–7 nm AlO X by ALD deposited at temperatures of 100, 200, and 300 °C. Hydroxyl loss and changes in surface chemistry were observed upon heating the films, and changes in surface area and pore volume of the annealed films were correlated to AlO X deposition temperature and the presence of Pd. Crystallization of the overcoat to γ-Al 2 O 3 is shown to occur separately from hydroxyl loss and pore formation. A mechanistic understanding of pore formation in AlO X ALD films is obtained by reference to studies of the structural transformations accompanying the formation of transition aluminas from hydroxide precursors. Additionally, a direct and tunable correlation is established between pore development and the overall hydroxyl content of AlO X ALD coatings.
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