材料科学
表面改性
纳米孔
堆积
多孔性
球体
聚苯乙烯
纳米技术
化学工程
吸附
复合材料
聚合物
物理化学
核磁共振
物理
工程类
化学
天文
作者
Christhy V. Ruiz M.,Markus Terlinden,Matthias B. Engelhardt,Giulia Magnabosco,Georg Papastavrou,Nicolas Vogel,Matthias Thommes,Julien Bachmann
标识
DOI:10.1002/admi.202300436
摘要
Abstract A geometrically tunable nanoporous system featuring enhanced active surface area by stacking of spheres in cylindrical pores is fabricated. Highly ordered arrays of straight, constricted pores are obtained by anodization of metallic aluminum. Polystyrene (PS) spheres are assembled inside the pores by flowing their suspension through the porous membrane, whereas the construction serves as a filter. After surface functionalization with a noble metal catalyst, these model electrocatalysis systems exhibit functional properties (capacitance in electrochemical impedance spectroscopy) that mirror their geometric parameters. A systematic investigation of the system's geometry as it depends on the surface chemistry of the pores, on the one hand, and the physical parameters of the infiltration procedure, on the other hand, shows that mechanical stacking prevails over surface chemical interactions to determine the stacking density. The highest values of surface area are obtained when PS spheres are put in contact with HfO 2 followed by ZnO according to adsorption measurements. Surface derivatization with organic layers does not improve stacking any further. However, choosing the proper concentration of PS spheres and flow rate are crucial for obtaining densely packed sphere assemblies without clogging of the pore entrance.
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