Article abstract
Nature Materials 7, 222 - 228 (2008)
Published online: 27 January 2008 | doi:10.1038/nmat2111
Subject Categories: Porous materials | Design synthesis and processing
Direct access to thermally stable and highly crystalline mesoporous transition-metal oxides with uniform pores
Jinwoo Lee1, M. Christopher Orilall1,2, Scott C. Warren1,2, Marleen Kamperman1, Francis J. DiSalvo2 & Ulrich Wiesner1
Abstract
Even after a decade or so of research, the direct synthesis of highly crystalline mesoporous transition-metal oxides that are thermally stable and well ordered still constitutes a major challenge. Although various soft- and hard-templating approaches have been developed in the past, they usually suffer from multiple, tedious steps and often result in poor structure control. For many applications including power generation and energy conversion, however, high crystallinity and controlled mesoporosity are a prerequisite. To this end, here we report on an approach established for group-IV (titanium) and group-V (niobium) oxides, with potential applications to photovoltaic cells and fuel cells, respectively, which overcomes previous limitations. It gives direct access to the desired materials in a 'one-pot' synthesis using block copolymers with an sp2-hybridized carbon-containing hydrophobic block as structure-directing agents which converts to a sturdy, amorphous carbon material under appropriate heating conditions. This in situ carbon is sufficient to act as a rigid support keeping the pores of the oxides intact while crystallizing at temperatures as high as 1,000 °C.
- Department of Materials Science and Engineering, Cornell University, Ithaca, New York 14853, USA
- Department of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853, USA
Correspondence to: Jinwoo Lee1M. Christopher Orilall1,2 These authors contributed equally to this work
Correspondence to: Ulrich Wiesner1 e-mail: ubw1@cornell.edu
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