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Nanopaiticles

Fig. 2. Histogram showing the size distribution of the silver nanopaiticles corresponding to Fig. 1... Fig. 2. Histogram showing the size distribution of the silver nanopaiticles corresponding to Fig. 1...
Parmon VN. 2007. Thermodynamic analysis of the effect of the nanopaiticle size of the active component on the adsorption equilibrium and the rate of heterogeneous catalytic processes. Dokl Phys Chem 413 42-48. [Pg.562]

Date M, Okumura M, Tsubota S, Haruta M. 2004. Vital role of moisture in the catalytic activity of supported gold nanopaiticles. Angew Chem Int Ed 43 2129-2132. [Pg.588]

The enormous surface area-to-volume ratio of nanopaiticles leads to excess surface free energy that is comparable to the lattice energy leading to structural instabilities. The nanoparticles have to... [Pg.64]

Regarding the mechanism of biomolecules functionalized CNTs entering into cells, endocytosis mechanism may be responsible for the phenomena, a theory model is also suggested (Gao et al., 2005) the optimal size of particles entering into cells is between 20 nm and 700 nm or so, too small nanopaiticles are very difficult to enter into cells because of cellular surface tension force and adhesion. The further mechanism of effects of CNTs on human healthcare and environment is being investigated from the following four scales such as molecular, cellular, animals, and environment levels. [Pg.192]

Figure 6.4 (a) Self-assembly of magnetic FePt nanopaiticles by DNAs and (b) a TEM micro-... [Pg.141]

Fig. 1.3 SEM image of TiO (ST) nanopaiticles (a), and calculated particle size distribution (b)... Fig. 1.3 SEM image of TiO (ST) nanopaiticles (a), and calculated particle size distribution (b)...
Ow, H., D.R. Larson, M. Srivastava, B.A. Baird, W.W. Webb, and U. Wiesner. 2005. Bright and stable core-shell fluorescent silica nanopaiticles. Nano Lett. 5 113-117. [Pg.167]

Figure 8.17 Schematic diagram for detection of three unique DNA sequences via hybridization of target DNA with magnetic bead-conjugated probe DNA followed by hybridization with three different detection probe DNA-modified semiconductor nanopaiticles, ZnS, CdS, and PbS. Dissolution and electrochemical stripping yielded three well-resolved peaks corresponding to the specific metal, and hence, unique DNA sequences detected.76 (Reprinted with permission from J. Wang et aL, J. Am. Chem. Soc. 2003,125, 3214-3215. Copyright 2003 American Chemical Society.) (See color insert.)... Figure 8.17 Schematic diagram for detection of three unique DNA sequences via hybridization of target DNA with magnetic bead-conjugated probe DNA followed by hybridization with three different detection probe DNA-modified semiconductor nanopaiticles, ZnS, CdS, and PbS. Dissolution and electrochemical stripping yielded three well-resolved peaks corresponding to the specific metal, and hence, unique DNA sequences detected.76 (Reprinted with permission from J. Wang et aL, J. Am. Chem. Soc. 2003,125, 3214-3215. Copyright 2003 American Chemical Society.) (See color insert.)...
Figure 13.6 The adsorption of multivalent guest-functionalized dendrimers onto a CD SAM and the subsequent assembly of complementary CD-functionalized nanopaiticles. Figure 13.6 The adsorption of multivalent guest-functionalized dendrimers onto a CD SAM and the subsequent assembly of complementary CD-functionalized nanopaiticles.
Figure 13.12 The preparation of spherically shaped nanoparticle crystals. A chemically patterned SAM with attached droplets of a SiC>2 nanoparticle solution was immersed in decalin. The interfacing between two solutions and shrinkage of the particle droplets resulted in rearrangement of the nanopaiticles to form close-packed spherical particle assemblies. Figure 13.12 The preparation of spherically shaped nanoparticle crystals. A chemically patterned SAM with attached droplets of a SiC>2 nanoparticle solution was immersed in decalin. The interfacing between two solutions and shrinkage of the particle droplets resulted in rearrangement of the nanopaiticles to form close-packed spherical particle assemblies.
Figure 13.14 The use of convective assembly to control the arrangement of nanoparticles on apattemed PDMS stamp and the subsequent printing of the nanopaiticles onto a substrate with single-particle resolution.87... Figure 13.14 The use of convective assembly to control the arrangement of nanoparticles on apattemed PDMS stamp and the subsequent printing of the nanopaiticles onto a substrate with single-particle resolution.87...
Figure 21.1 Block copolymer-nanoparticle co-assemblies as a function of nanoparticle size. The left shows nanoparticles smaller than the root-mean-square end-to-end distance of the block copolymer leading to particle distribution throughout the domain. The right scenario shows much larger nanopaiticles segregating out from the block copolymer.11 (Reprinted with permission from A. Jain and U. Wiesner, Macromolecules 2004, 37, 5665-5670. Copyright 2004 American Chemical Society.)... Figure 21.1 Block copolymer-nanoparticle co-assemblies as a function of nanoparticle size. The left shows nanoparticles smaller than the root-mean-square end-to-end distance of the block copolymer leading to particle distribution throughout the domain. The right scenario shows much larger nanopaiticles segregating out from the block copolymer.11 (Reprinted with permission from A. Jain and U. Wiesner, Macromolecules 2004, 37, 5665-5670. Copyright 2004 American Chemical Society.)...
Castaneda MT Alegret S Merkoci A, Electrochemical sensing of DNA using gold nanopaiticles,... [Pg.701]

Trewyn BG Slowing II Giri S Chen HT Lin VSY, Synthesis and functionalization of a mesoporous silica nanopaiticle based on the sol-gel process and applications in controlled release, Acc. Chem. Res., 2007, 40, 846-853. [Pg.703]

Scheme 4 Pt-Nanopaiticle Catalyzed Hydrosilylation of 1, 2-polybutadiene with D DH... Scheme 4 Pt-Nanopaiticle Catalyzed Hydrosilylation of 1, 2-polybutadiene with D DH...
As briefly mentioned in the Introduction the MEF phenomenon is a result of the interactions between the excited states of the fluorophores and the induced surface plasmons of metal nanopaiticles or roughened surfaces. Figure 1.2A depicts our laboratory s interpretation of the processes involved in the interactions of fluorophores with metal nanoparticles in close proximity to one another. There are two main processes thought responsible in MEF 1) non-radiative coupling from the excited state of the fluorescent species to surface plasmons of the metallic... [Pg.15]

Mock, J. J., Smith, D. R. and Schultz, S. (2003). Local refractive index dependence of plasmon resonance spectra from individual nanopaiticles. Nano Lett y. 485-491. [Pg.117]

Jensen, T., Kelly, L., Lazarides, A. and Schatz, G. C. (1999). Electrodynamics of noble metal nanopaiticles and nanoparticle clusters. J. [Pg.117]

Hi quality gold nanocubes can also be prepared by electrochranical methods in the presence of the aiqxopriate surfactant and solvent [86,87]. As illustrated in Figure 11.30 below [87], gold for nanopaiticle growth is supplied through oxidation of a gold anode. Reduction takes place at an inert platinum cathode in the presence of the surfactant. [Pg.325]

Pal, S., Tak, Y. K. and Song, J. M. (2007). Does the antibactmal activity of silver nanopaiticles depend on the shape of the nanoparticle A study of the gram-n ative bacterium Escherichia coli. Appl. Environ. Microbiol 73 1712-1720. [Pg.355]

Figure 20.16 Fluorescence spectra of HSC 3 cells incubated with nanosphere solution. = 280 nm. Overall, gold nanospheres decrease the fluorescence of cells however, in some samples an increase in fluorescence is observed. The data is similar for all three cell lines (HaCat, HOC 313, and HSC 3) when the nanopaiticles were incubated with cells. Cited from reference 52. Figure 20.16 Fluorescence spectra of HSC 3 cells incubated with nanosphere solution. = 280 nm. Overall, gold nanospheres decrease the fluorescence of cells however, in some samples an increase in fluorescence is observed. The data is similar for all three cell lines (HaCat, HOC 313, and HSC 3) when the nanopaiticles were incubated with cells. Cited from reference 52.
Figure 7.1 (A) Schematic representation of the Metal-Enhanced Fluorescence phenomena (B) FDTD calculations for two silver nanoparticle arrays (d = 100 nm). (C) Wavelength-dependent calculated Ej maximum intensity for silver nanoparticle arrays (d = 100 nm). Geometries and incident field polarization [p-polarized) and propagation direction are shown in the insets. The gap between the nanopaiticles was assumed to be 2 nm in the calculations. (D) Calculated field enhancement as a function of distance for a single silver nanoparticle (d = 100 nm).The inset shows these results as an FDTD E image above the nanoparticle. Figure 7.1 (A) Schematic representation of the Metal-Enhanced Fluorescence phenomena (B) FDTD calculations for two silver nanoparticle arrays (d = 100 nm). (C) Wavelength-dependent calculated Ej maximum intensity for silver nanoparticle arrays (d = 100 nm). Geometries and incident field polarization [p-polarized) and propagation direction are shown in the insets. The gap between the nanopaiticles was assumed to be 2 nm in the calculations. (D) Calculated field enhancement as a function of distance for a single silver nanoparticle (d = 100 nm).The inset shows these results as an FDTD E image above the nanoparticle.
In the panicle synthesis, metal atoms produced by the heating collide with the inert gas atoms to decrease the diffusion rate of the atoms from the source region. The collisions also cool the atoms to induce the formation of small clusters of fairly homogeneous size. The clusters grow mainly by cluster-cluster condensation to give nanopaiticles with a broader size distribution. A convective flow of the inen gas between the warm region near the vapour source and the cold surface carries the nanopanicles to the cooled finger, where they are let to deposit. The inen gas pressure, the evaporation rate, and the gas composition can control the characteristics... [Pg.79]

Figure 47.1. Types of naiiocaniers for dmg delivery. A liposomes B nanopaiticles C nanospheres D nanosuspensions E polymer micelles F- nanogel G block ionomer complexes H nanofibers and nanot ... Figure 47.1. Types of naiiocaniers for dmg delivery. A liposomes B nanopaiticles C nanospheres D nanosuspensions E polymer micelles F- nanogel G block ionomer complexes H nanofibers and nanot ...
Panyam J, Labhasetwai V (2003) Biodegradable nanopaiticles for dmg and gene delivery to cells and tissue. Adv Dmg DeHv Rev 55 329—347. [Pg.706]

Figure 3. (a) TEM image of Ge layers in Si sandwiched layers and (b and c) HRTEM images of nanopaiticles in the layers after 800°C annealing, (d) a typical diffraction pattern with rin indicating randomly oriented dbmond Ge crystals. [Pg.80]

Simultaneous account for local field and local density of photon states enhancements in close proximity to a silver ellipsoidal nanopaiticle is found to provide up to 10 -fold Raman scattering cross-section rise up. A model of the so-called hot points in surface enhanced spectroscopy has been elaborated as local areas with high Q-factor at incident and scattered (emitted) light frequencies. Further experiments are proposed towards verification of the model in terms of transient Raman experiments to clarify incident field enhancement and scanning near-field optical mapping of local density of photon states. [Pg.164]

Strong enhancement of light absorption over the spectral range of the copper localized surface plasmon resonance has been observed at two-layer planar systems of copper and silver nanopaiticles made with the use of successive vacuum evaporation. The result obtained is treated with taking into account strong near-fieid coupling at a close-packed array of silver and copper nanoparticles. [Pg.180]


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See also in sourсe #XX -- [ Pg.26 , Pg.28 , Pg.29 , Pg.65 , Pg.254 , Pg.255 , Pg.263 , Pg.279 , Pg.280 , Pg.401 ]




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