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Versatile control over size and spacing of small mesopores in metal oxide films and catalytic coatings viatemplating with hyperbranched core-multishell polymers

Controlling the pore structure of metal oxide films and supported catalysts is an essential requirement for tuning their functionality and long-term stability. Typical synthesis concepts such as "Evaporation Induced Self Assembly" rely on micelle formation and self assembly. These processe...

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Published in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2014-07, Vol.2 (32), p.13075-13082
Main Authors: Bernsmeier, Denis, Ortel, Erik, Polte, Jorg, Eckhardt, Bjorn, Nowag, Sabrina, Haag, Rainer, Kraehnert, Ralph
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container_issue 32
container_start_page 13075
container_title Journal of materials chemistry. A, Materials for energy and sustainability
container_volume 2
creator Bernsmeier, Denis
Ortel, Erik
Polte, Jorg
Eckhardt, Bjorn
Nowag, Sabrina
Haag, Rainer
Kraehnert, Ralph
description Controlling the pore structure of metal oxide films and supported catalysts is an essential requirement for tuning their functionality and long-term stability. Typical synthesis concepts such as "Evaporation Induced Self Assembly" rely on micelle formation and self assembly. These processes are dynamic in nature and therefore strongly influenced by even slight variations in the synthesis conditions. Moreover, the synthesis of very small mesopores (2-5 nm) and independent control over the thickness of pore walls are very difficult to realize with micelle-based approaches. In this contribution, we present a novel approach for the synthesis of mesoporous metal oxide films and catalytic coatings with ordered porosity that decouples template formation and film deposition by use of hyperbranched core-multishell polymers as templates. The approach enables independent control of pore size, wall thickness and the content of catalytically active metal particles. Moreover, dual templating with a combination of hyperbranched core-multishell polymers and micelles provides facile access to hierarchical bimodal porosity. The developed approach is illustrated by synthesizing one of the most common metal oxides (TiO sub(2)) and a typical supported catalyst (PdNP/TiO sub(2)). Superior catalyst performance is shown for the gas-phase hydrogenation of butadiene. The concept provides a versatile and general platform for the rational optimization of catalysts based e.g. on computational prediction of optimal pore structures and catalyst compositions.
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title Versatile control over size and spacing of small mesopores in metal oxide films and catalytic coatings viatemplating with hyperbranched core-multishell polymers
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