Kinetically Controlled Growth of Gold Nanoplates and Nanorods via a One-Step Seed-Mediated Method
Kinetically Controlled Growth of Gold Nanoplates and Nanorods via a One-Step Seed-Mediated Method
Bulletin of the Korean Chemical Society. 2014. Jun, 35(6): 1737-1742
Copyright © 2014, Korea Chemical Society
  • Received : January 28, 2014
  • Accepted : February 17, 2014
  • Published : June 20, 2014
Export by style
Cited by
About the Authors
Soonchang Hong
Department of Chemistry and BK21 School of Chemical Materials Science, Sungkyunkwan University, Suwon 440-746, Korea
Jesus A. I. Acapulco Jr.
Department of Chemistry and BK21 School of Chemical Materials Science, Sungkyunkwan University, Suwon 440-746, Korea
Hee-Jeong Jang
Department of Chemistry and BK21 School of Chemical Materials Science, Sungkyunkwan University, Suwon 440-746, Korea
Akshay S. Kulkarni
Birla Institute of Technology and Sciences, Goa 403-726, India
Sungho Park
Department of Energy Science, BK21 School of Chemical Materials Science, Sungkyunkwan University, Suwon 440-746, Korea

In this research, we further developed the one-step seed mediated method to synthesize gold nanoparticles (GNPs) and control their resulting shapes to obtain hexagonal, triangular, rod-shaped, and spherical gold nanostructures. Our method reveals that the reaction kinetics of formation of GNPs with different shapes can be controlled by the rate of addition of ascorbic acid, because this is the critical factor that dictates the energy barrier that needs to be overcome. This in turn affects the growth mechanism process, which involves the adsorption of growth species to gold nanoseeds. There were also observable trends in the dimensions of the GNPs according to different rates of addition of ascorbic acid. We performed further analyses to investigate and confirm the characteristics of the synthesized GNPs
Metallic nanomaterials, either in pure form 1 2 or mixed with other compounds 3 - 5 and having different geometrical structure 6 possess unique optical, electronic, and catalytic properties. Among the various metallic nanomaterials, gold nanoparticles (GNPs) are widely applied in catalysis, 7 elec-tronics, 8 and diagnostics. 9 Researchers have investigated variously shaped GNPs, especially anisotropic plate-shaped 10 and rod-shaped 11 12 GNPs. However, the mechanism of growth of these anisotropic GNPs is still not yet fully understood, so it remains challenging to synthesize complex GNPs of similar sizes that are homogenous in shape. Seed-mediated, 13 14 photochemical, 15 and biological 16 procedures are commonly used to synthesize GNPs.
Seed-mediated growth, which was pioneered by Natan et al ., 17 Murphy et al ., 18 - 20 and among others, 21 is the funda-mental method used to control the dimensions of GNPs. This method has been used to synthesize gold nanoplates and nanorods. It involves using surfactants to form a template on which growth species assemble, resulting in variously shaped GNPs. 13 14 Usually, production of growth species are controlled by a mild reducing agent, such as ascorbic acid. 12 22 23
Three-step seed-mediated synthesis is a method used to synthesize anisotropic GNPs in aqueous solution; it involves sequentially adding of aliquots one after another from three flasks containing different solutions. Murphy et al. 12 em-ployed this procedure to obtain gold nanorods with an aspect ratio (length/width) greater than 10, while Mirkin et al . 10 extended this method to gold nanoplates and reported pro-duction of gold triangular nanoplates with an average width of 125 nm. Correct and careful use of hand techniques is critical when using the three-step seed-mediated method to successfully produce anisotropic GNPs.
An improved seed-mediated method in wet chemistry to synthesize anisotropic GNPs was then reported. This method uses silver ions to reduce the number of required synthesis steps from 3 to 1, and greatly increases the yield of gold nanorods (up to 90%) and has been widely adopted which is referred to as the one-step seed mediated method. However, this method produces GNPs with small dimensions. Gold nanorods with aspect ratios between 1 to 5 were reported by the Oddershede 24 and Murphy 25 research groups. In addition, Chung et al . 26 managed to produce gold nanoprisms with an edge length of 98 ± 17 nm, while Huang et al . 27 reported a one-step seed-mediated method (without silver ions) to synthesize hexagonal and tri-angular gold nanoplates, where the smaller nanoplates were mainly triangular in shape while the larger nanoplates exhibited hexagonal and truncated triangular nanostructures. Although the one-step seed-mediated method can be used to obtain high quality and homogenous gold nanorods and nanoplates, it is still a challenge to pro-duce GNPs with higher dimensions that are of good quality using this method.
To fully control the purity, shape, and size of GNPs, formation kinetics should be understood. Nanosphere homo-geneity and size can be controlled kinetically through cont-rolling the rate of addition of precursor. 28 However, this is only true at some point, because as the nanoparticle’s size increases, so does the deviation value. Most literature reports have focused on temperature variation to kinetically control the morphology of GNP during synthesis. Tsai and colleagues 29 showed that the synthesis of GNPs at elevated room temper-atures was kinetically favored due to instability of the surfactant that served as a template, resulting in the production of icosahedral and plate-like gold nanostructures. Gao et al. 30 also applied the same approach; they were able to restrain the self-nucleation of silver quasi-nanospheres by controll-ing the reaction kinetics through controlling the reaction temperature and the amount of seed; they obtained good homogeneity under these reaction conditions. However, reac-tions carried out at high temperature produced significant amounts of pseudo-spherical nanostructures, because temper-ature is directly proportional to surface diffusion, which affects the Oswald ripening process.
In this paper, we use the one-step seed mediated method, without silver ions at room temperature, to produce high aspect ratio (> 5) gold nanorods. We show that it is possible to specifically tune the size and shape of the gold nanoplates by controlling the reaction kinetics where concentrations, volumes, and temperature are held constant throughout this experiment while the rate of production of monomer was changed by controlling the rate of addition of ascorbic acid. The formation of thermodynamically favorable spheres ap-pears to be unavoidable when synthesizing plate and rod-like gold nanostructures; preventing the production of gold nanospheres therefore still remains a challenge. We eluci-date, for the first time, the kinetic principles underlying the formation of isotropic (spheres) and anisotropic GNPs (plates and rods). We also present the deduced reaction pathway to which the reaction would proceed depending upon the production rate of the monomers that illustrate the energy barrier and final energy differences between isotropic and anisotropic GNPs.
Chemicals. Sodium iodide (NaI), ascorbic acid, and cetyl-trimethylammonium bromide (CTAB) (Fluka) were purchased from Sigma-Aldrich. Gold chloride hydrate (HAuCl 4 ·3H 2 O) was purchased from KOJIMA. Sodium borohydride (NaBH 4 ) was purchased from JUNSEI. Ultra-pure water (18.2 MΩcm −1 ) was used for all experiments.
Seed Preparation. GNP seeds with an average diameter of 5.2 ± 0.6 nm were prepared using the method reported by Millstone et al . 10 A solution containing 18 mL of ultra-pure water and 0.5 mL of 10 mM sodium citrate was used to reduce 0.5 mL of 10 mM HAuCl 4 with 0.5 mL of 100 mM NaBH4 under vigorous stirring. Upon addition of NaBH 4 , the solution turned a reddish orange color and was stirred for an additional minute. The resulting mixture was aged for 2-6 h to allow the hydrolysis of unreacted NaBH4. To confirm the average diameter of GNPs, GNP seeds must exhibit a plasmon resonance peak at 500 nm.
Synthesis of Gold Nanoplates and Nanorods. Gold nano-plates were synthesized from 5.2 ± 0.6 nm gold nanoseeds by a one-step seed-mediated method with iodide ions. A 75 mL aliquot of 0.05 M aqueous CTAB solution, 37.5 μL of 0.01 M NaI, 1 mL of 20 mM aqueous HAuCl 4 ·3H 2 O solu-tion, and 40 mL of gold nanoseeds were mixed in a flask. A 30 mL of 0.01 M ascorbic acid was then added at different rates of addition: 0.5 mL/min, 1 mL/min, 2 mL/min, 3 mL/ min, or all at once (abruptly added). Sodium iodide was added for the synthesis of plate-like gold nanostructures, while rod-like nanorods were synthesized in the absence of sodium iodide. Spherical gold nanostructures were obtained regardless of whether sodium iodide was present or not. Synthesized GNPs were obtained by precipitation for 4 hours after synthesis, while the mixture to which ascorbic acid was abruptly added was centrifuged at 9000 rpm for 10 minutes because no precipitate was observed (data not shown).
Instrumentation. A KD Scientific syringe pump was used to control the rate of addition of ascorbic acid. Syn-thesized GNPs were characterized using a JEM-2100F to obtain high-resolution transmission electron microscopy (HRTEM) images. A JEOL 7000F and JEOL 7600F were used to obtain Field emission scanning electron microscopy (FESEM) images and an Ultima IV Rigaku was used to obtain X-ray diffraction (XRD) patterns. UV-vis extinction spectra were acquired using S-3100 Scinco and UV-3600 Shimadzu spectrophotometers.
Results and Discussion
FESEM images of GNPs synthesized in the presence of iodide ions at various rates of addition of ascorbic acid (0.5 mL/min, 1 mL/min, 2 mL/min, 3 mL/min, and abrupt addition) are shown in Figures 1(a)-(e) , respectively. The percent yield of gold nanoplates and spherical gold nanostructures was determined by counting nanostructures in the FESEM images; results are presented in Table 1 . As the rate of addition of ascorbic acid increased from 0.5 to 2 mL/min to abrupt, the shapes of the resulting gold nanostructures chang-ed from hexagonal plates to triangular plates to spherical GNPs, respectively, while addition rates of 1 and 3 mL/min showed the transition to produce the majority of synthesized GNPs. We used UV-vis extinction spectroscopy ( Fig. 1(f) ) to further confirm the homogeneity, shape, and size of the GNPs. We have previously reported the spectra behavior of gold hexagonal nanoplates and our results in Figures 1(a) and (b) are comparable to our previous findings; however, the nanoplates generated in the current study were larger, which may have resulted in unclear peaks. Among the spectra of all the samples, the samples obtained after adding ascorbic acid at 2 mL/min (spectra c) showed the most ideal spectra for gold triangular nanoplates based on the two observable peaks, which were assigned as dipole localized surface plasmon resonance (LSPR) mode located at the near-IR region (1234 nm) and inplane quadrupole LSPR mode at the visible region (784 nm), respectively, in accor-dance with our previous publications. 32 - 34 We assigned the two peaks observed in spectra d, from the acquired GNPs shown in Figure 1(d) , to the LSPR mode mixture of nano-spheres (538 nm) and nanoplates (923 nm), while the syn-thesized GNPs shown in Figure 1(e) (spectra e) only exhibit-ed one peak (530 nm) corresponding to dipolar plasmon resonance of gold nanospheres.
PPT Slide
Lager Image
FESEM images of the synthesized gold nanostructures of plates and spheres with the presence of iodide ions at (A) 0.5 mL/min, (B) 1 mL/min, (C) 2 mL/min, (D) 3 mL/min, and (E) abrupt addition of ascorbic acid. (F) UV-vis extinction spectra a, b, c, d, and e for samples synthesized under conditions A, B, C, D, and E, respectively.
Percent yield at varying addition rate of ascorbic acid in the presence of iodide ion
PPT Slide
Lager Image
Percent yield at varying addition rate of ascorbic acid in the presence of iodide ion
Because precipitation was the only purification method that we used, we were able to compare the weights of the acquired GNPs. Images A, B, and D in Figure 1 show that the acquired GNPs (plates and spheres) had comparable weights. Given that larger GNPs contain more gold atoms than smaller GNPs, our results indicate that the acquired weight is inversely related to the rate of addition of ascorbic acid, as measured from the FESEM images. Image C clearly shows that there was a large difference in weight between the synthesized anisotropic GNPs (plates) and the by-pro-duct isotropic GNPs (spheres), resulting in good homogeneity of the desired product after precipitation.
Gold nanoplates are produced primarily due to the prefer-ential adsorption of iodide ions on the (111) facet of gold nanoseeds, because the CTAB bilayer stabilizes the growth of gold nanoseeds, leading to a higher growth rate on the (110) facet than on the (111) facet. 26 We found that it was also possible to produce hexagonal gold nanoplates using the one-step seed-mediated method in contrast to our previ-ous work, 31 where we employed shape transformation of GNPs from triangular to hexagonal gold nanoplates. Shape transformation occurred by selectively etching out the high surface area (vertex) of the triangular nanoplate followed by a ripening process, which yielded hexagonal gold nanoplates. In this study, we were able to directly produce hexagonal gold nanoplates through seed-mediated method by adding ascorbic acid at a low rate.
These findings can also be applied to the synthesis of other GNPs, despite differences in growth mechanism. For example, gold nanorods are synthesized in the absence of iodide ions, and growth involves a “zipping” formation mechanism. 6 We used our developed method to synthesize gold nanorods where we varied the rate of addition of ascorbic acid. We observed similar trends to those we observed for the gold nanoplates, as shown in Figure 2 and Table 2 . In particular, the dimensions of the synthesized gold nanorods decreased as the rate of addition of ascorbic acid increased (measured dimensions displayed in Table 3 ); addition of ascorbic acid at 3 mL/min yielded gold nanorods with an aspect ratio of 6, which was the highest aspect ratio measured among our synthesized gold nanorods. Furthermore, the spectra of gold nanostructures that formed when ascorbic acid was added at 3 mL/min (spectra c in Fig. 2(f) ) showed the typical tran-sverse and longitudinal modes of gold nanorod structures at 522 nm and beyond 1200 nm, respectively, while we assign-ed the peak at 793 nm to longitudinal quadruple surface plasmon resonance. 35 These results indicate that kinetic control during synthesis facilitates the growth of GNPs with various shapes.
PPT Slide
Lager Image
FESEM images of the synthesized rods and spheres gold nanostructures in the absence of iodide ion at (A) 1 mL/min, (B) 2 mL/min, (C) 3 mL/min, (D) 4 mL/min, and (E) abrupt addition of ascorbic acid. (F) UV-vis extinction spectra a, b, c, d, and e for samples synthesized under conditions A, B, C, D, and E, respectively.
Percent yield at varying addition rate of ascorbic acid in the absence of iodide ion
PPT Slide
Lager Image
Percent yield at varying addition rate of ascorbic acid in the absence of iodide ion
The crystallinity of the synthesized plates and rods GNPs was confirmed by HRTEM images and XRD patterns (shown in Fig. 3 ). Both exhibited an ordered crystal lattice. Single crystalline structure of the synthesized gold nanoplates and nanorods was confirmed based on the well-resolved lattice fringe ( Fig. 3(A)-(B) ) with a spacing of 0.236 nm, which is close to the value we reported previously 31 that reflects the forbidden 1/3{422} reflection. Typical FFT patterns of the gold nanostructures of plates and rods were obtained by directing the incident electron beam perpendicular to the {111} facet of the synthesized GNPs. The XRD pattern ( Fig. 3(C) ) of the synthesized gold nanoplate showed {111} and {222} diffraction peaks, corresponding to angles of 38.06° and 81.46°, respectively, implying reflections of face-center-ed cubic (fcc) gold, while for gold nanorods, diffraction peaks were present at {111}, {200}, {220}, {311}, and {222}, consistent with previous studies. 36 37
PPT Slide
Lager Image
HRTEM images of (A) gold nanoplate, and (B) gold nanorod with TEM image and fast Fourier transform (FFT) pattern located at right upper and lower insets, respectively. (C) The X-ray diffraction (XRD) pattern of (a) plate, and (b) rod gold nano-structures.
The rate of formation of monomer can be used to control the synthesis of nanoparticles. 38 Because size can influence optical properties, 39 we assigned different reaction rate con-stants based on the addition rate of ascorbic acid, as shown in Figure 4(A) . The slowest addition of ascorbic acid, 0.5 mL/min (k 1 ) for gold nanoplates and 1 mL/min (k 1 ) for gold nanorods, resulted in the formation of anisotropic GNPs with the highest dimensions, while abrupt addition of ascorbic acid, denoted as k 6 , yielded gold nanospheres. Proposed reaction pathway will be discussed later. As commonly observed in other research studies, synthesis of anisotropic GNPs was accompanied by the formation of the by-product of gold nanospheres. 11 37 40 Therefore, these gold nanospheres are competitor GNPs and by plotting the diameter of the by-product as a function of the flow rate of ascorbic acid ( Fig. 4(b) ), we found that the size of the gold nanospheres was inversely proportional to the flow rate, and this relationship also applies to anisotropic GNPs ( Table 3 ). However, as particle dimensions increase, so does the coefficient of varia-tion, because a low rate of addition of ascorbic acid leads to a smaller con-centration of monomer than the minimum concentration required for nucleation, resulting in suppression of the nucleation process and maximization of the growth process, which in turn leads to unequal nucleation distribution to every seed while further growth of randomly-produced gold nuclei is also occurring.
PPT Slide
Lager Image
(a) Schematic diagram of the one-step method to synthesize GNPs showing the obtained result from different reaction rate, and (b) Plot of measured dimension versus flow rate of ascorbic acid with standard deviation.
Summarized measured dimensions of the synthesized GNPs at varying addition rate of ascorbic acid
PPT Slide
Lager Image
Summarized measured dimensions of the synthesized GNPs at varying addition rate of ascorbic acid
In contrast, abrupt addition of ascorbic acid resulted in the synthesis of gold nanospheres regardless of the presence or absence of iodide ions. According to Cao, 44 this can be ex-plained by the rate of nucleation per unit volume and per unit time denoted as RN, as follows:
RN = {C o kT/(3πλ 3 η)}exp(−ΔG * /kT) (1)
where λ is the diameter of the growth species, η is the viscosity of the solution, ΔG * is the minimum energy to form a nuclei, k is the Boltzmann constant, and T is the temperature.
PPT Slide
Lager Image
Proposed schematic diagram of the reaction pathway during the synthesis of kinetically controlled GNPs.
This indicates that a high initial concentration or super-saturation of ascorbic acid (large number of nucleation sites present), low viscosity, and a low critical energy barrier favor the formation of large numbers of nuclei. For a given concentration of solute, a larger number of nuclei means smaller-sized nuclei. The fastest addition rate (k 5 ) resulted in a high initial concentration of ascorbic acid, which in turn led to the production of small homogenous gold nanospheres from a large number of small nuclei during the nucleation process.
Formation of anisotropic (plate- and rod-like) or isotropic (spheres) GNPs can be explained by the Gibbs free energy of the system (y-axis in Scheme 1 ). The solution is at equilibrium state (stable Gibbs free energy) with all species in aqueous ionic state before the addition of ascorbic acid (point x0 in Scheme 1 ). In this state, the nitrogen of CTAB releases bromide to replace the proton of HAuCl 4 . 41 For illustration purposes, we denote negative coordinates (left side) as anisotropic GNPs and positive coordinates (right side) as isotropic GNPs.
The CTA-AuCl 4 formed then serves as a precursor for GNP formation by reduction of Au(III) to Au(I) and finally to Au(0) by deprotonation of ascorbic acid.
Because the amount of ascorbic acid is greater than the amount of CTA-AuCl 4 , CTA-AuCl 4 is the limiting reactant, resulting in complete reduction of Au(III) to Au(I). An excess amount of ascorbic acid will further reduce Au(I) to Au(0), favoring the formation of GNPs. However, the major factor that dictates the resulting shape of GNPs is the addi-tion rate of ascorbic acid. As mentioned earlier, there are two directions that the reaction can proceed after the addition of ascorbic acid; to the right to produce gold nanospheres, or to the left to produce anisotropic GNPs. The reaction will proceed to the right at high reaction rates, while it will proceed to the left at low reaction rates. When ascorbic acid is added, the solution will exceed its equilibrium solubility; in other words, the solution is supersaturated and has high Gibbs free energy. The supersaturated solution will tend to reduce the overall Gibbs free energy of the system to acquire equilibrium (point –x2 or point x2) and to attain this, the solution will form a solid phase (colloids) in the form of GNPs. Ascorbic acid will be converted into dehydroascorbic acid, reducing the gold ions (AuCl 2 and [Au(OH) 2 ] ) to metallic gold. 40 41 The formation of gold nanospheres is due to the lower energy barrier (point x1) required to form iso-tropic spheres than anisotropic GNPs (point –x1). Another factor that causes the formation of isotropic spheres is the nucleation process. Because synthesis of nanoparticles involves two processes, namely nucleation and growth, one must con-trol the nucleation process to obtain pure non-spherical GNPs. Growth of GNPs then proceeds; however, the number of final particles is limited by the abstruse balance between the rates of nucleation and growth. 42 43 That is why seed-mediated growth is preferred. To decrease the probability of gold nano-sphere formation, the concentration of the growth species must be less than the minimum concentration of nucleation so that nucleation process stops and growth process continues. Since the concentration of the growth species is highly dependent on ascorbic acid, decreasing the addition rate of ascorbic acid will reduce the concentration of the growth species compared to the minimum concentration for nuclea-tion. In addition, we believe that the increase and decrease yield of anisotropic GNPs as the addition rate of ascorbic acid is increased are due to the atomic addition of gold on the seed. That is, at low and high addition rate of ascorbic acid, monomers are thermodynamically driven favoring the formation of nanospheres.
As stated above, we controlled the reaction rate by controlling the rate of addition of ascorbic acid. Hence, the activation energy for anisotropic GNPs, Ea(a), was greater than the activation energy for gold nanospheres, Ea(i), based on the reaction rate given by the Arrhenius equation.
Scheme 1 shows that the change in Gibbs free energy of anisotropic GNPs, ΔG(a), was lower than the change in Gibbs free energy of isotropic GNPs. This is because isotropic GNPs are thermodynamically favored, resulting in a low and stable energy profile compared to that of anisotropic GNPs.
In summary, we were able to control the homogeneity, shape, and size of gold nanoplates, nanorods, and nano-spheres by controlling the rate of addition of ascorbic acid. By controlling this rate, we were able to control the kinetics of reaction for the formation of GNPs. We found that as the addition rate of ascorbic acid decreased, large dimension of GNPs were produced, regardless of the mechanism of formation. Moreover, abrupt addition of ascorbic acid favor-ed the formation of gold nanospheres with small diameters regardless of whether iodide ions were present or absent. Our method offers a direct process to produce GNPs with large dimensions and to tune these dimensions for further applications. Lastly, we described the synthesis of GNPs in terms of energy as a function of the rate of addition of ascorbic acid. The activation energy for the formation of anisotropic GNPs was higher than the activation energy for isotropic GNPs. Other parameters and conditions of the methodology presented here can be developed further to gain a better understanding of the mechanisms of formation of nanoparticles.
This work was supported by the National Research Foundation of Korea (National Leading Research Lab: 2012R1A2A1A03670370) and the Human Resources Development program (no. 20124010203270) of the Korea Institute of Energy Technology Evaluation and Planning (KETEP) grant funded by the Korea Government Ministry of Trade, Industry and Energy.
Xu B. S. , Tanaka S. I. 2001 Scripta Mater. 44 (8-9) 2051 - 2054    DOI : 10.1016/S1359-6462(01)00862-4
Yan J. F. , Zou G. S. , Wu A. P. , Ren J. L. , Yan J. C. , Hu A. M. , Zhou Y. 2012 Scripta Mater. 66 (8) 582 - 585    DOI : 10.1016/j.scriptamat.2012.01.007
Mahl D. , Diendorf J. , Ristig S. , Greulich C. , Li Z. A. , Farle M. , Koller M. , Epple M. 2012 J. Nanopart. Res. 14 (10) 1 - 13
Terzi F. , Zanardi C. , Daolio S. , Fabrizio M. , Seeber R. 2011 Electrochim. Acta 56 (10) 3673 - 3678    DOI : 10.1016/j.electacta.2010.10.038
Mott D. , Luo J. , Smith A. , Njoki P. N. , Wang L. Y. , Zhong C. J. 2007 Nanoscale Res. Lett. 2 (1) 12 - 16    DOI : 10.1007/s11671-006-9022-8
Gao J. X. , Bender C. M. , Murphy C. J. 2003 Langmuir 19 (21) 9065 - 9070    DOI : 10.1021/la034919i
Thompson D. T. 2007 Nano Today 2 (4) 40 - 43
Huang D. , Liao F. , Molesa S. , Redinger D. , Subramanian V. 2003 J. Electrochem. Soc. 150 (7) G412 - G417    DOI : 10.1149/1.1582466
Peng G. , Tisch U. , Adams O. , Hakim M. , Shehada N. , Broza Y. Y. , Billan S. , Abdah-Bortnyak R. , Kuten A. , Haick H. 2009 Nat. Nanotechnol. 4 (10) 669 - 673    DOI : 10.1038/nnano.2009.235
Millstone J. E. , Wei W. , Jones M. R. , Yoo H. J. , Mirkin C. A. 2008 Nano Lett. 8 (8) 2526 - 2529    DOI : 10.1021/nl8016253
Millstone J. E. , Metraux G. S. , Mirkin C. A. 2006 Adv. Funct. Mater. 16 (9) 1209 - 1214    DOI : 10.1002/adfm.200600066
Gole A. , Murphy C. 2004 J. Chem. Mater. 16 (19) 3633 - 3640    DOI : 10.1021/cm0492336
Johnson C. J. , Dujardin E. , Davis S. A. , Murphy C. J. , Mann S. 2002 J. Mater. Chem. 12 (6) 1765 - 1770    DOI : 10.1039/b200953f
Sau T. K. , Murphy C. J. 2004 J. Am. Chem. Soc. 126 (28) 8648 - 8649    DOI : 10.1021/ja047846d
Kim F. , Song J. H. , Yang P. D. 2002 J. Am. Chem. Soc. 124 (48) 14316 - 14317    DOI : 10.1021/ja028110o
Shankar S. S. , Rai A. , Ankamwar B. , Singh A. , Ahmad A. , Sastry M. 2004 Nat. Mater. 3 (7) 482 - 488    DOI : 10.1038/nmat1152
Brown K. R. , Walter D. G. , Natan M. 2000 Chem. Mater. 12 (2) 306 - 313    DOI : 10.1021/cm980065p
Jana N. R. , Gearheart L. , Murphy C. 2001 J. Adv. Mater. 13 (18) 1389 - 1393    DOI : 10.1002/1521-4095(200109)13:18<1389::AID-ADMA1389>3.0.CO;2-F
Jana N. R. , Gearheart L. , Murphy C. J. 2001 J. Phys. Chem. B 105 (19) 4065 - 4067
Jana N. R. , Gearheart L. , Murphy C. 2001 J. Langmuir 17 (22) 6782 - 6786    DOI : 10.1021/la0104323
Lohse S. E. , Murphy C. J. 2013 Chem. Mater. 25 (8) 1250 - 1261    DOI : 10.1021/cm303708p
Goia D. V. , Matijevic E. 1999 Colloids and Surfaces A 146 (1-3) 139 - 152    DOI : 10.1016/S0927-7757(98)00790-0
Kim F. , Sohn K. , Wu J. S. , Huang J. X. 2008 J. Am. Chem. Soc. 130 (44) 14442 - 14443    DOI : 10.1021/ja806759v
Selhuber-Unkel C. , Zins I. , Schubert O. , Sonnichsen C. 2008 Nano Lett. 8 (9) 2998 - 3003    DOI : 10.1021/nl802053h
Gou L. F. , Murphy C. 2005 J. Chem. Mater. 17 (14) 3668 - 3672    DOI : 10.1021/cm050525w
Ha T. H. , Koo H. J. , Chung B. H. 2007 J. Phys. Chem. C 111 (3) 1123 - 1130
Chu H. C. , Kuo C. H. , Huang M. H. 2006 Inorg. Chem. 45 (2) 808 - 813    DOI : 10.1021/ic051758s
Schwartzberg A. M. , Olson T. Y. , Talley C. E. , Zhang J. Z. 2006 J. Phys. Chem. B 110 (40) 19935 - 19944    DOI : 10.1021/jp062136a
Min-Chen H. , Liu R. S. , Tsai D. P. 2009 Cryst. Growth Des. 9 (5) 2079 - 2087    DOI : 10.1021/cg800396t
Liu X. X. , Yin Y. D. , Gao C. B. 2013 Langmuir 29 (33) 10559 - 10565    DOI : 10.1021/la402147f
Hong S. , Shuford K. L. , Park S. 2011 Chem. Mater. 23 (8) 2011 - 2013    DOI : 10.1021/cm103273c
Baik H. J. , Hong S. , Park S. 2011 J. Colloid Interf. Sci. 358 (2) 317 - 322    DOI : 10.1016/j.jcis.2011.03.041
Hong S. , Choi Y. , Park S. 2011 Chem. Mater. 23 (24) 5375 - 5378    DOI : 10.1021/cm2021966
Kim J. , Hong S. , Jang H. J. , Choi Y. , Park S. 2013 J. Colloid Interf. Sci. 389 71 - 76    DOI : 10.1016/j.jcis.2012.09.007
Hong S. , Shuford K. L. , Park S. 2013 Chem-Asian J. 8 (6) 1259 - 1264    DOI : 10.1002/asia.201300004
Sun J. H. , Guan M. Y. , Shang T. M. , Gao C. L. , Xu Z. 2010 Sci. China Chem. 53 (9) 2033 - 2038    DOI : 10.1007/s11426-010-4053-5
Guo Z. R. , Zhang Y. , DuanMu Y. , Xu L. , Xie S. L. , Gu N. 2006 Colloid Surface A 278 (1-3) 33 - 38    DOI : 10.1016/j.colsurfa.2005.11.075
Abecassis B. , Testard F. , Kong Q. Y. , Francois B. , Spalla O. 2010 Langmuir 26 (17) 13847 - 13854    DOI : 10.1021/la1020274
Nikoobakht B. , El-Sayed M. A. 2003 Chem. Mater. 15 (10) 1957 - 1962    DOI : 10.1021/cm020732l
Wu H. Y. , Liu M. , Huang M. H. 2006 J. Phys. Chem. B 110 (39) 19291 - 19294    DOI : 10.1021/jp063711d
Khan Z. , Singh T. , Hussain J. I. , Hashmi A. A. 2013 Colloid Surface B 104 11 - 17    DOI : 10.1016/j.colsurfb.2012.11.017
van Embden J. , Sader J. E. , Davidson M. , Mulvaney P. 2009 J. Phys. Chem. C 113 (37) 16342 - 16355    DOI : 10.1021/jp9027673
Shevchenko E. V. , Talapin D. V. , Schnablegger H. , Kornowski A. , Festin O. , Svedlindh P. , Haase M. , Weller H. 2003 J. Am. Chem. Soc. 125 (30) 9090 - 9101    DOI : 10.1021/ja029937l
Cao G. 2004 Nanostructures & Nanomaterials; Synthesis, Properties & Applications Imperial College Press