离子液体
X射线光电子能谱
材料科学
催化作用
物理气相沉积
离子键合
薄膜
沉积(地质)
纳米技术
图层(电子)
表面科学
超高真空
化学工程
表面改性
曲面(拓扑)
有机化学
离子
化学
工程类
古生物学
生物
数学
沉积物
几何学
作者
Hans‐Peter Steinrück,Jörg Libuda,Peter Wasserscheid,Till Cremer,Claudia Kolbeck,M. Laurin,Florian Maier,Michal Sobota,Peter S. Schulz,Michael Stark
标识
DOI:10.1002/adma.201100211
摘要
Materials making use of thin ionic liquid (IL) films as support-modifying functional layer open up a variety of new possibilities in heterogeneous catalysis, which range from the tailoring of gas-surface interactions to the immobilization of molecularly defined reactive sites. The present report reviews recent progress towards an understanding of "supported ionic liquid phase (SILP)" and "solid catalysts with ionic liquid layer (SCILL)" materials at the microscopic level, using a surface science and model catalysis type of approach. Thin film IL systems can be prepared not only ex-situ, but also in-situ under ultrahigh vacuum (UHV) conditions using atomically well-defined surfaces as substrates, for example by physical vapor deposition (PVD). Due to their low vapor pressure, these systems can be studied in UHV using the full spectrum of surface science techniques. We discuss general strategies and considerations of this approach and exemplify the information available from complementary methods, specifically photoelectron spectroscopy and surface vibrational spectroscopy.
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