Phase transition of nanoparticle deposits upon heating The SR-XRD patterns of NP deposits measured from 25°C to 250°C are illustrated in Figure 3. It is apparent that broad and weak (111) diffractions appeared at low temperatures due to the size-broadening effect. Taking the Au GSK1120212 ic50 NPs as example, the quantitative data shown in Figure 4 depict that when the NPs were heated to a critical temperature, the intensity (the maximum peak amplitude)

of the broad peak skyrocketed dramatically, and after that, it increased gradually. Figure 4 also illustrates the peak width (full width at half maximum, FWHM) and thus grain size calculated using Scherrer equation given below [31]. Figure 3 The evolution of (111) diffraction peak of the NP deposits with respect to heating temperature. (a) Au, (b) Au3Ag, (c) AuAg (d) AuAg3, and (e) Ag (the X-ray wavelength λ = 1.5498 Å). Figure 4 The intensity, width and calculated grain size of Au(111) peaks with respect to heating temperature. (Based on the data

obtained from Figure 3a). (1) where D is the grain size, λ is the wavelength of the X-ray, β is the full width at half maximum, and θ is the angle corresponding to the peak. It can be found that the variation in peak width is just opposite to the tendency of increasing intensity. The critical temperature for particle coalescence can be defined as the temperature for the sudden increase in peak intensity, which represents the linking of nanoparticles and www.selleckchem.com/products/incb28060.html a high degree of crystallization [23, 24, 32, 33]. As also indicated in Figure 4, grain growth occurs right after the coalescence of NPs. The coalescence temperature of NP deposits with varying Au/Ag molar ratio are listed in Figure 5. For each sample, the variation in the coalescence temperature was 10 ~ 15°C. The average data show that the coalescence temperature decreased

when the Ag content increased from 0 at% (the Au sample, 160°C) to 50 at% (the AuAg sample, 120°C). After that, the coalescence temperature rose and reached 150°C for the Edoxaban samples of 100 at% Ag (the Ag sample, 150°C). This implies that the coalescence temperatures for alloy nanoparticle deposits were significantly lower than those for pure metals. In addition, with respect to the Ag deposits with a small difference in particle size, the coalescence temperatures did not differ too much. The average values are 153.3°C for bigger Ag NPs (10.7-nm diameter in average) and 146.5°C for those with a smaller size (8.2-nm diameter in average). It was also found that the diffractions tended to shift selleck towards low angles due to thermal expansion. The difference in the lattic constants among the deposits was large at room temperature but was reduced significantly when heated to 250°C (Figure 6a). The lattice constants calculated from the diffraction angles for the as-prepared NP deposits and those after being heated to 250°C are illustrated in Figure 6b.