Md. H. R. acknowledges CSIR, India for providing a Fellowship. This research was supported by the grants from CSIR, New Delhi, India. Thanks are also due to the partial support from the Nanoscience and Technology Initiatives, DST, New Delhi. Supporting Information is available online from Wiley InterScience or from the authors.
Full Paper
Templateless Synthesis of Polygonal Gold Nanoparticles: An Unsupported and Reusable Catalyst with Superior Activity†
Article first published online: 21 JUL 2008
DOI: 10.1002/adfm.200800085
Copyright © 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Rashid, M. H. and Mandal, T. K. (2008), Templateless Synthesis of Polygonal Gold Nanoparticles: An Unsupported and Reusable Catalyst with Superior Activity. Advanced Functional Materials, 18: 2261–2271. doi: 10.1002/adfm.200800085
- †
Publication History
- Issue published online: 6 AUG 2008
- Article first published online: 21 JUL 2008
- Manuscript Revised: 17 MAR 2008
- Manuscript Received: 17 JAN 2008
Funded by
- CSIR, New Delhi, India
Keywords:
- catalysts;
- gold nanoparticles;
- hexoses;
- nitrophenols;
- polygonal
Graphical Abstract

Polygonal gold nanoparticles (GNPs) are synthesized by an in-situ templateless reduction technique (see figure) using ferric ammonium citrate. These polygonal GNPs act as a highly active unsupported catalyst for the borohydride reduction of three isomeric nitrophenols and also for the aerobic oxidation of different D-hexoses. The catalytic activity of these polygonal GNPs is much higher (ca. 300–1000 times) than their spherical counterparts and they can be reused several times for nitrophenol reduction.
Abstract
We report the synthesis of polygonal gold nanoparticles (GNPs) by an in situ reduction technique using ferric ammonium citrate as reducing agent in absence of any surfactant or polymeric template. Transmission electron microscopic analysis and selected area electron diffraction patterns confirmed the formation of well-crystalline polygonal GNPs grown preferentially along the (111) direction, which is consistent with the results of X-ray diffractometry analysis. The results of control experiments of HAuCl4 with tri-ammonium citrate in presence of different externally added metal ions like Fe3+, Ni2+, Cu2+, Zn2+, and Al3+ suggested the ion-induced growth mechanism in the formation of polygonal GNPs. The purified polygonal GNPs were then successfully used as catalyst in the borohydride reduction of three isomeric nitrophenols and also in the aerobic oxidation of different D-hexoses (e.g., D-glucose, D-mannose, D-fructose). The catalytic activity of these polygonal GNPs is higher by a factor of 300–1000, depending on the GNP's sample type, in nitrophenol reduction compared to that of spherical GNPs. Similar activity enhancement was also observed in the aerobic oxidation of different D-hexoses. These polygonal GNPs catalyst are very stable and could be reused several times in the borohydride reduction of nitrophenols without much losing in their virgin catalytic activity.

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