E structure of your ZnSe C andwas formedC/S heat therapy
E structure with the ZnSe C andwas formedC/S heat treatment at 310 C was to investigate 310 structure from the ZnSe shell ZnSe/ZnS by QDs in which ZnSe for synthesized at for1 h and the ZnS C and ZnSe/ZnS C/S QDs in which ZnSe C was synthesized at for C h along with the ZnS peak was formed the heat therapy at 310agreesynthesized at 310 the 1 for 1 h as well as the ZnS shell was formed C heat therapy at 50 min. As shown in310 XRD pattern, the shell positions of by ZnSe byQDs had been in for 310min. for bulk ZnSethe XRD pattern, the peak positions in the ZnSe C apparent diffraction 50 with 50 min. having a zinc blende structure (Figure 4a-i). positions of your ZnSe C mentC As shown in As shown within the XRD pattern, the peak Three QDs have been in agreeQDs had been in agreement withzinc blende having a zinc blende structure (Figure 4a-i). Three ment positioned at 27.2 45.3 bulk ZnSe structure (Figure 4a-i). Three peaks with the (111), peaks with bulk ZnSe having a and 53.5corresponded for the diffraction clear diffraction apparent diffraction peaks positioned at 27.two , 45.three , and 53.5the diffraction peaks on the (111), peaks situated at 27.2 45.three blende ZnSe, respectively. corresponded to the diffraction (220), and (311) planes of zinc and 53.5corresponded to Following the shelling process (Figpeaks and (311) planes of zinc blendeplanes respectively. Following the respectively. Just after(Figof zinc blende ZnSe, shelling procedure the (220), on the (111), (220), and (311) remained and XRD peaks have been slightly shifted to ure 4a-ii), the zinc blende structure ZnSe, shelling process (Figure 4a-ii), the zinc blende and XRD remained WZ8040 In Vivo andslightly shifted to ure 4a-ii), the zinc blende and 54.1 due to the fact structure peaks lattice XRD peaks had been larger angles (27.six 46.1 structure remained ZnS has smaller have been parameters than slightly angles (27.6 46.1 and (27.6 , because ZnS has since ZnS has smaller sized lattice larger shifted to higher angles 54.1 46.1 , and 54.1 ) smaller lattice parameters than ZnSe [36]. The high degree of crystallinity was also confirmed by high-resolution TEM parameters The higher degreeThecrystallinity was also confirmed also confirmed by highZnSe [36]. than ZnSe [36]. of high degree of crystallinity was by high-resolution TEM resolution TEM (HR-TEM) images, shown in Figure 4b. The HR-TEM images and speedy Fourier transformation (FFT) patterns of the ZnSe C and ZnSe/ZnS C/S QDs are shown in Figure 4b. The lattice fringes had been separated by d = 0.32 nm for the ZnSe C as well as the ZnSe/ZnS C/S QDs, which was consistent together with the lattice spacings involving the (111)Appl. Sci. 2021, 11,(HR-TEM) photos, shown in Figure 4b. The HR-TEM photos a mation (FFT) patterns of your ZnSe C and ZnSe/ZnS C/S QDs are lattice fringes have been separated by d = 0.32 nm for the ZnSe C and six of ten which was consistent together with the lattice spacings among the (11 ZnSe. The synthesized ZnSe/ZnS C/S QDs exhibited a narrow siz planes of zinc blende ZnSe. The synthesized ZnSe/ZnS C/S QDs exhibited a narrow size nm (typical size (typical size deviation). distribution of five.1 0.five nmstandard regular deviation).Figure four. (a) XRD and (b) TEM Methyl jasmonate Epigenetic Reader Domain pictures of (i) ZnSe C QDs and (ii) ZnSe/ZnS C/S QDs. Figure 4. (a) XRD patterns patterns and (b) TEM images of (i) ZnSe C QDs and (ii Decrease insets in(b)show HR-TEM images of (i) ZnSe C of (i) ZnSe C QDs andand the insets in (b) show HR-TEM images QDs and (ii) ZnSe/ZnS C/S QDs (ii) ZnSe/Z upper insets in (b) show FFT patterns for the corresponding HR-TEM photos.insets in (b) show FFT patterns for the cor.