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Surface Plasma Resonance of Gold-coated Iron-oxide Nanoparticles

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Surface Plasma Resonance of Gold-coated Iron-oxide Nanoparticles

Yousaf Iqbal · Hongsub Bae · Ilsu Rhee

Department of Physics, Kyungpook National University, Daegu 702-701, Korea

Sungwook Hong

Division of Science Education, Daegu University, Gyeongsan 712-714, Korea (Received 9 December 2014 : revised 23 February 2015 : accepted 23 February 2015)

Gold-coated iron-oxide nanoparticles were synthesized by using chemical reactions. The X-Ray diffraction (XRD) confirmed the crystallinity of the cubic spinel structure. Transmission electron microscope (TEM) images showed that the gold-coated iron-oxide nanoparticles were spherical in shape with an average diameter of 15.5 nm. The binding of the gold to the surface of the iron- oxide nanoparticles was revealed by using measurements made with Fourier transform infrared (FTIR) spectrometer. The vibrating sample magnetometer (VSM) results showed no hysteresis, indicating that the nanoparticles were superparamagnetic with a single domain. A surface plasma resonance was observed in an aqueous solution of the gold-coated iron-oxide nanoparticles, which provided direct evidence that the gold was well bound to the surfaces of the iron-oxide nanoparticles.

The wavelength of the surface plasma resonance of the gold-coated iron-oxide nanoparticles was compared with those of gold nanoparticles. We observed a red-shifted surface plasma wavelength for the gold-coated iron-oxide nanoparticles, which was another piece of evidence for gold being well bound on the surfaces of the iron-oxide nanoparticles.

PACS numbers: 81.05.Ni, 76.60.Es, 61.46.Df, 87.61.-c

Keywords: Iron-oxide nanoparticles, Gold coating, Surface plasma resonance, Superparamagnetic

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This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License

(http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any

medium, provided the original work is properly cited.

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Fig. 1. (Color online) (a) TEM image of the gold-coated iron oxide nanoparticles (b) Particle size distributions for one hundred particles obtained from a TEM image.

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Fig. 2. (Color online) XRD patterns of the gold-coated iron oxide nanoparticles. The indices of the crystal plane in the figure match with those of cubic spinel structure.

Fig. 3. (Color online) FTIR spectra of the gold and gold- coated iron oxide nanoparticles.

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Fig. 4. (Color online) Hysteresis curve of the gold- coated iron oxide nanoparticles at room temperature.

The blown-up figure near zero magnetic field is shown in the inset.

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Fig. 5. (Color online) UV-VIS spectra of the gold-coated iron oxide nanoparticles and gold nanoparticles with an average diameter of 14 nm [15]. The size dependence of the surface plasma resonance wavelength is shown in the inset for the gold and gold-coated iron oxide nanoparti- cles.

÷ &# Q e ” “ ¦, F K Ü ¼– Ð  ïh A ) a í ß – o^ o =  ” ¸{ 9   15.5 nm“   F

K  ” ¸{ 9  _  ³ ð€   e  ¦  Ý ¼  / B N" î  © œõ  { 9 u  Ù ¼– Ð, s

  H F K s  í ß – o^ o = ³ ð€  \  ¸ ú ˜  ҂ à Ì÷ &# Q e ” 6 £ §`  ¦ ~ ½ Ó7 £ x ô  Ç .

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‰ “  ½ + É Ã º e ” % 3  . FTIR`  ¦ s 6   x # Œ F K _  í ß – o^ o =  ” ¸ { 9

 _  ³ ð€  \ _   ҂ à Ì © œI \  ¦ · ú ˜ ˜ Ѐ Œ ¤ . VMS\  ¦ : Ÿ x K 



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f ˜ Ð § 4 s  \ O % 3 Ü ¼ 9, s   H  ” ¸{ 9    H é ß – ½ ¨ (single domain) – Ð" f œ í © œ $ í e ” `  ¦   ? /  H   õ s  . UV-VIS 8

£ ¤& ñ \ " f ³ ð€   e  ¦  Ý ¼  / B N" î ‰ & ³ © œ`  ¦ ˜ Ð% i Ü ¼ 9, s  / B N" î

 © œ`  ¦ l ” > r _  F K  ” ¸{ 9  _  / B N" î  © œõ  q “ § % i  .

f ”

 â _  ß ¼l \          H / B N" î  © œ\ " f      H

&

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Ò  o¼ # s \  ¦ ^  ¦ à º e ” % 3  . s   H F K s  í ß – o^ o =  ” ¸{ 9   ³ ð

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 \  ¸ ú ˜  ҂ à Ì÷ &% 3    H  כ `  ¦ ç ß –] X & h Ü ¼– Ð ˜ Ð# ŒÅ ҍ  H   õ  s

 .

(5)

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c p 8 ý ò k >

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REFERENCES

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수치

Figure 2 \   H XRD z  ´+ « &gt;u  Å Ò# Q4 R e ”  . Õ ªa Ë &gt;\ &#34; f
Fig. 4. (Color online) Hysteresis curve of the gold- gold-coated iron oxide nanoparticles at room temperature.

참조

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