Synthesis of High-Surface-Area Platinum Nanotubes Using a Viral Template
A novel method for the synthesis of high‐active‐surface‐area, platinum–tobacco mosaic virus (Pt–TMV) nanotubes is presented. A platinum salt is reduced to its metallic form on the external surface of a rod‐shaped TMV by methanol, which serves as a solvent and reductant simultaneously. It was found t...
Saved in:
Published in | Advanced functional materials Vol. 20; no. 8; pp. 1295 - 1300 |
---|---|
Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
WILEY-VCH Verlag
23.04.2010
WILEY‐VCH Verlag |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | A novel method for the synthesis of high‐active‐surface‐area, platinum–tobacco mosaic virus (Pt–TMV) nanotubes is presented. A platinum salt is reduced to its metallic form on the external surface of a rod‐shaped TMV by methanol, which serves as a solvent and reductant simultaneously. It was found that for the same Pt loading the Pt–TMV nanotubes had an electrochemically active surface area between 4 to 8 times larger than similarly sized Pt nanoparticles. A Pt–TMV catalyst displays greater stability in acidic conditions than those based on nanoparticles. When used as a catalyst for methanol oxidation, these Pt nanotubes display a 65% increase in catalytic mass activity compared to that based on Pt nanoparticles.
High‐surface‐area Pt–tobacco mosaic virus (Pt–TMV) nanotubes are synthesized using an alcohol reduction method. For the same Pt loading, Pt–TMV nanotubes have an electrochemically active surface area at least 3.7 times larger than Pt nanoparticles. The Pt–TMV system, used as a catalyst for methanol oxidation, shows 65% higher catalytic mass activity than catalyst‐based on Pt nanoparticles. |
---|---|
Bibliography: | University of Leeds ark:/67375/WNG-3G2FQXG4-R istex:D3D516FF799D29FF2101A4C1C211602304D6FE06 ArticleID:ADFM200902196 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1616-301X 1616-3028 1616-3028 |
DOI: | 10.1002/adfm.200902196 |