journal article·2014-02-12

Fabrication of Bifunctional Gold/Gelatin Hybrid Nanocomposites and Their Application

Qianling Cui, Alexey Yashchenok, Lu Zhang, Lidong Li, Admir Masic, Gabriele Wienskol, Helmuth Möhwald, Matias Bargheer

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Abstract

Herein, a facile method is presented to integrate large gold nanoflowers (∼80 nm) and small gold nanoparticles (2-4 nm) into a single entity, exhibiting both surface-enhanced Raman scattering (SERS) and catalytic activity. The as-prepared gold nanoflowers were coated by a gelatin layer, in which the gold precursor was adsorbed and in situ reduced into small gold nanoparticles. The thickness of the gelatin shell is controlled to less than 10 nm, ensuring that the small gold nanoparticles are still in a SERS-active range of the inner Au core. Therefore, the reaction catalyzed by these nanocomposites can be monitored in situ using label-free SERS spectroscopy. In addition, these bifunctional nanocomposites are also attractive candidates for application in SERS monitoring of bioreactions because of their excellent biocompatibility.
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Research context

OpenAlex topics: Gold and Silver Nanoparticles Synthesis and Applications · Nanocluster Synthesis and Applications · Laser-Ablation Synthesis of Nanoparticles

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083, China

Max-Planck Institute of Colloids and Interfaces, Golm-Potsdam 14476, Germany

Institute of Physics and Astronomy, University of Potsdam, Potsdam 14476, Germany

References (21)

Show source-provided references
1. Dieringer J. A. · Faraday Discuss. · 2006 · 132 · 910.1039/B513431P ↗
2. Heck K. N. · J. Am. Chem. Soc. · 2008 · 130 · 1659210.1021/ja803556k ↗
3. Lantman E. M. V. · Nat. Nanotechnol. · 2012 · 7 · 58310.1038/nnano.2012.131 ↗
4. Guerrini L. · Chem. Commun. · 2011 · 47 · 317410.1039/c0cc05013j ↗
5. Min B. K. · Chem. Rev. · 2007 · 107 · 270910.1021/cr050954d ↗
6. Wang A. · J. Am. Chem. Soc. · 2010 · 132 · 953410.1021/ja1024639 ↗
7. Xie W. · J. Am. Chem. Soc. · 2011 · 133 · 1930210.1021/ja208298q ↗
8. Xie W. · J. Am. Chem. Soc. · 2013 · 135 · 165710.1021/ja309074a ↗
9. Ren X. Q. · Phys. Chem. Chem. Phys. · 2013 · 15 · 1419610.1039/c3cp51385h ↗
10. Muralidharan R. · Phys. Chem. Chem. Phys. · 2013 · 15 · 971610.1039/c3cp51128f ↗
11. Tian Z. Q. · Chem. Commun. · 2007 · 351410.1039/b616986d ↗
12. Joseph V. · Angew. Chem., Int. Ed. · 2012 · 51 · 759210.1002/anie.201203526 ↗
13. Xie J. P. · ACS Nano · 2008 · 2 · 247310.1021/nn800442q ↗
14. Cui Q. L. · ACS Appl. Mater. Interfaces · 2013 · 5 · 21310.1021/am302589g ↗
15. Krug J. T. · J. Am. Chem. Soc. · 1999 · 121 · 920810.1021/ja992058n ↗
16. Kiel M. · Langmuir · 2012 · 28 · 480010.1021/la204577m ↗
17. Huang Y. F. · J. Am. Chem. Soc. · 2010 · 132 · 924410.1021/ja101107z ↗
18. Dong B. · J. Raman Spectrosc. · 2011 · 42 · 120510.1002/jrs.2937 ↗
19. Kang L. L. · Chem. Commun. · 2013 · 49 · 338910.1039/c3cc40732b ↗
20. Zhang L. · Opt. Lett. · 2010 · 35 · 329710.1364/OL.35.003297 ↗
21. Orendorff C. J. · Anal. Chem. · 2005 · 77 · 326110.1021/ac048176x ↗