FE-SEMField Emission Scanning Electron Microscope
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FE-SEM images of a) [Ag.sub.2]Mo[O.sub.4] crystals, b) ZnO crystals, c-d) [Ag.sub.2]Mo[O.sub.4]/ZnO heterostructure.
Figures 1(a) and 1(b) show FE-SEM micrographs of Sample 1 and Sample 2, respectively.
Acquired by FE-SEM, Figure 6(a) shows a cross-sectional image of the Ti[O.sub.2.sup.m] layer where a very homogeneous structure can be observed throughout the layer thickness.
Figure 3 shows the morphology, by FE-SEM, of the 1D nanostructures obtained after alkaline hydrothermal treatment of the sol-gel Ti[O.sub.2] nanoparticles presented in Figure 1 and Table 1.
TEM (H-7100, Hitachi, Japan) and FE-SEM (JSM-7610F, JEOL, Japan) were used to identify the morphologies of the obtained CBNMs in the CBNFs.
The FE-SEM micrograph of the obtained powders from protocols 3 to 5 are shown in Figure 3.
The larger bend can reduce the crack due to sufficient space or planar behavior at arc having The FE-SEM images of the AAO structures are shown in Fig.
Figure 3(a) was taken as high magnification of the EBSD phase mapping method, with a TSL-OIM system installed in a MIRA II LMH FE-SEM, which was used in depth beam scan mode, with a beam step size of 100 nm.
Bolus microstructure images during mastication were needed to characterize the internal structural changes by field emission scanning electron microscopy (FE-SEM).
In this work, calcium hydroxylapatite [[Ca.sub.5][(P[O.sub.4]).sub.3]OH, Ca-HA] and Zn-substituted hydroxylapatites [[([Z.sub.nx][Ca.sub.1-x]).sub.5][(P[O.sub.4]).sub.3]OH, Zn-Ca-HA] with various Zn/(Zn + Ca) atomic ratios were prepared and the influences of zinc replacement on the hydroxylapatite properties were investigated with XRD, FT-IR, FE-SEM, and FE-TEM instruments.
The thickness was characterized by a JSM-7001F field emission scanning electron microscope (FE-SEM).