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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Eslava, Salvador
Imperial College London
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (23/23 displayed)
- 2024Activating 2D MoS2 by loading 2D Cu–S nanoplatelets for improved visible light photocatalytic hydrogen evolution, drug degradation, and CO2 reductioncitations
- 2024Ca‐doped PrFeO<sub>3</sub> photocathodes with enhanced photoelectrochemical activitycitations
- 2021Structural Evolution of Iron Forming Iron Oxide in a Deep Eutectic-Solvothermal Reactioncitations
- 2021Silver-Decorated TiO2 Inverse Opal Structure for Visible Light-Induced Photocatalytic Degradation of Organic Pollutants and Hydrogen Evolutioncitations
- 2020Silver-Decorated TiO2 Inverse Opal Structure for Visible Light-Induced Photocatalytic Degradation of Organic Pollutants and Hydrogen Evolutioncitations
- 2020Strategies for the deposition of LaFeO3 photocathodescitations
- 2019Graphite-protected CsPbBr3 perovskite photoanodes functionalised with water oxidation catalyst for oxygen evolution in watercitations
- 2019Enhanced Ceria Nanoflakes using Graphene Oxide as a Sacrificial Template for CO Oxidation and Dry Reforming of Methanecitations
- 2019Inexpensive Metal Free Encapsulation Layers Enable Halide Perovskite Based Photoanodes for Water Splitting
- 2019Enhanced ceria nanoflakes using graphene oxide as a sacrificial template for CO oxidation and dry reforming of methanecitations
- 2019Enhanced ceria nanoflakes using graphene oxide as a sacrificial template for CO oxidation and dry reforming of methanecitations
- 2019Strategies for the deposition of LaFeO3 photocathodes:improving the photocurrent with a polymer templatecitations
- 2018Screen printed carbon CsPbBr3 solar cells with high open-circuit photovoltagecitations
- 2018Enhanced Ceria Nanoflakes using Graphene Oxide as a Sacrificial Template for CO Oxidation and Dry Reforming of Methanecitations
- 2018Efficient hematite photoanodes prepared by hydrochloric acid-treated solutions with amphiphilic graft copolymercitations
- 2017A facile way to produce epoxy nanocomposites having excellent thermal conductivity with low contents of reduced graphene oxidecitations
- 2016Autonomous self-healing structural composites with bio-inspired designcitations
- 2015Printing in Three Dimensions with Graphenecitations
- 2013Metal-organic framework ZIF-8 films as low-κ dielectrics in microelectronicscitations
- 2008Reaction of trimethylchlorosilane in spin-on Silicalite-1 zeolite filmcitations
- 2008Nanoporous organosilicate films prepared in acidic conditions using tetraalkylammonium bromide porogenscitations
- 2007Characterization of a molecular sieve coating using ellipsometric porosimetrycitations
- 2007Profile control of novel non-Si gates using B Cl3 N2 plasmacitations
Places of action
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article
Nanoporous organosilicate films prepared in acidic conditions using tetraalkylammonium bromide porogens
Abstract
Organosilicate films with narrow pore size distribution tunable in the range of 1-3.4 nm were prepared by spin-coating of silicon wafers with sols prepared in acidic conditions using tetraethyl orthosilicate, methyltrimethoxysilane, and tetraalkylammonium bromide (TAABr) porogen. The pore size was defined by the alkyl chain length of the quaternary ammonium molecule and the porogen concentration. The pore network in the films and the hydrophobicity of the pore surfaces were characterized using ellipsometric porosimetry with toluene and water adsorbates. In the absence of TAABr. the pore volume was 9 vol% and the pore size 1 nm. By using TAABr porogens, monomodal pore size distributions were obtained in the range of 1.2-3.5 nm. The pore volume was in the range from 18 vol % at 1.2 nm pore diameter up to 54 vol% at 3.5 nm diameter. The hydrophobicity of the pores was dependent on the pore diameter, with smaller pores being the least hydrophobic. The increase of hydrophobicity with pore size was explained by an increased distance between silanol groups on the curved pore surfaces. The mechanical properties and dielectric constant of these films were comparable to reference materials prepared using more sophisticated porogens reported in the literature.