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Ultrathin films and hollow shells with pillared architectures fabricated via layer-by-layer self-assembly of Titania nanosheets and aluminum Keggin ions

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JOURNAL OF PHYSICAL CHEMISTRY B
卷 108, 期 14, 页码 4283-4288

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AMER CHEMICAL SOC
DOI: 10.1021/jp035818w

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Inorganic multilayer films and hollow shells with pillared architectures have been fabricated layer-by-layer on spherical poly(methyl methacrylate) (PMMA) templates as well as flat substrates through the electrostatic self-assembly technique. Positively charged polyoxocations of aluminum Keggin ions were employed both as inorganic binder and as pillaring agent in electrostatic self-assembly with exfoliated unilamellar crystallites of Ti0.9O2, yielding new types of ultrathin films and core-shell composites. Ultraviolet-visible absorption spectra revealed progressive enhancement of absorbance with increasing deposition cycles, indicating the regular growth of multilayer assemblies of titania nanosheets and aluminum polyoxocations. Evolution of a Bragg peak with a periodicity of ca. 1.5 nm and its enhancement also supported the formation of nanostructured multilayer films and shells, accommodating aluminum polyoxocations in the nanosheet gallery. Depth X-ray photoelectron spectra confirmed their inorganic nature. Calcination at 400 T produced ultrathin films and hollow shells with alumina pillars between the titania sheets. N-2 adsorption results revealed a high specific surface area of 260 m(2) g(-1) and nanoporous feature for the pillared hollow spheres.

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