The shape of bright spots from both Ni and Ag maps is the same which indicates that both Ag and Ni are present in particles with alloyed structure. Figure 2 EFTEM maps of Ag 0.9 -Ni 0.1 NPs. (a) Zero-loss image, (b) Ni map, and (c) Ag map [48]. If the ionic PI3K Inhibitor high throughput screening precursors are multivalent and both metals have some probabilities to be reduced by hydrated electrons and radiolytic radicals, the less noble metal ions (M’+) will act as electron donors to the more noble metal ions (M+). Thus, at the first step, monometallic clusters of noble metal (Mn) will be formed. Then, when concentration of M+ ions decreases, M’+ ions

are reduced afterwards at the surface of Mn. The final result is a core-shell cluster where the more noble metal M is coated by the other one M’ [24]. For example, the Cu(core)/Al2O3(shell) nanoparticles were formed when mixed CuCl2 and AlCl3 solution in the presence of PVP was gamma-irradiated [49]. Copper ions have a higher possibility to selleck compound be reduced (higher redox potential, E0(V) = +0.34) than aluminum ions ( E0(V) = -1.66), so the rate of reaction of hydrated electrons in the solution with Cu ions was higher than with Al ions. Thus, when bivalent Cu ions

were irradiated, the reduction occurred until Cu zero-valent content increased. Then in a further step, when Cu2+ ions were depleted, the reduction of Al3+ increased which occurred exclusively at the surface of the Cu particles to form core-shell structure. The core/shell structure of the clusters, as analysed by transmission electron microscopy (TEM; Figure 3), electron diffraction, and XRD, was clearly confirmed [49]. The boundary between the core and shell

was not sharp, since the shells are CuAlO2 and Al2O3 instead of pure Al. Figure 3 TEM images of Cu Adenosine and Cu@CuAlO 2 -Al 2 O 3 nanoparticles. (a) pure Cu nanoparticles and (b) Cu@CuAlO2-Al2O3 nanoparticles in core-shell structure [49]. Under proper conditions, individual nucleation and growth of two kinds of metal atoms can occur separately to form heterostructure. For example, when FePt nanoparticles reacted with AuCl-(PPh3) in the presence of 1,2-dichlorobenzene containing 1-hexadecylamine, the successive growth of Au on to the FePt seeds was observed which resulted in the formation of heterodimers of FePt-Au (Figure 4) [50]. Figure 4 TEM and HRTEM images of FePt-Au heterostructured nanoparticles. (a) TEM image, and (b) HRTEM image of FePt-Au heterodimer nanoparticles reported by Choi et al. [50]. Effects of synthesis parameters The synthesis of metallic nanoparticles by irradiation is governed by a number of experimental parameters such as the choice of solvent and stabilizer, the precursor to stabilizer ratio, pH value during synthesis, and absorbed dose. All of these parameters determine the final ordering, particle size and distribution, and surface area of resultant nanoparticles.