2D Monoelements. Группа авторов
surface were flatter than on Sb2Te3 (111) surface due to the larger lattice constants of Bi2Te3 (111) substrate. The interfacial strain and charge transfer induced a change in band dispersions. This work is a milestone in this kind of study, which is critical for the understanding of the electrical structure of antimonene.
Subsequently, monolayer-to-multilayer antimonene were successfully grown on 2D substrates by the MBE method, such as PdTe2, MoS2, WTe2, and graphene [29–32]. Wu et al. grew large-area monolayer antimonene on a freshly cleaved PdTe2 substrate in an ultrahigh vacuum (UHV) MBE chamber (2 × 10−10 mbar), and the schematic of growth process was shown in Figure 2.6a [29]. 2D PdTe2 was chosen as a suitable substrate in the growth of antimonene, because of its small mismatch of crystal periodicity with free-standing antimonene and chemically stable surface. From the topological scanning tunneling microscopy (STM) image shown in Figure 2.6b, it is observed that an atomically smooth antimonene film was obtained with no obvious defects or domain boundaries. According to the LEED pattern in the inset of Figure 2.6b, this film is a well-ordered single crystalline with a commensurate (1 × 1) lattice periodicity. The height of this film is about 2.8 Å, which is consistent with that of a monolayer antimonene (Figure 2.6c). Figure 2.6d shows an atomic-resolution STM image of antimonene, it is clearly seen that this epitaxial film has a buckled honeycomb lattice with a periodicity of 4.13 ± 0.02 Å. It is noted that monolayer antimonene grown on PdTe2 was chemically inert to the air. This work first unveils the atomic-scale morphology of epitaxial monolayer β-antimonene.
Figure 2.6 (a) Schematic of growth process of monolayer antimonene on 2D PdTe2 substrate. (b) Topographic STM image of large-area antimonene on PdTe2. Inset: LEED pattern of monolayer antimonene on PdTe2 substrate. (c) A height profile of antimonene taken along the red line in panel (b). (d) Atomic-resolution STM image of antimonene. (e) Schematic diagram of epitaxial α-antimonene on 2D Td-WTe2 substrate. (f) Topographic STM image of monolayer α-antimonene on WTe2. The area is 120 × 120 nm2. (g) A line-scan profile of antimonene along the green line in panel (f). (h) Atomic-resolution STM image taken at U = +300 mV, It = 100 pA. The area is 8 × 8 nm2. Inset: the unit cells of √2 × √2 lattice and original 1 × 1 lattice. (i) Schematic of the evolution processes from initial Sb atoms to final antimonene on Cu (111) substrates. Topographic STM images of 0.5 monolayer antimonene deposition on Cu (111) surface before (j) and (k) after annealing at 700 K. (l) High-resolution STM image of antimonene. (a–d) Reproduced with permission [29]. Copyright 2017, Wiley-VCH. (e–h) Reproduced with permission [30]. Copyright 2019, Wiley-VCH. (i–l) Reproduced with permission [36]. Copyright 2019, Wiley-VCH.
Interestingly, besides the usual β-antimonene, α-phase antimonene can also be obtained on the 2D substrate by using MBE. Shi et al. controllably synthesized micro-sized monolayer α-antimonene on the 2D Td-WTe2 substrate [30]. Due to the inert surface and the compatibility with α-antimonene, Td-WTe2 was considered as a suitable substrate to achieve the freestanding epitaxial growth of monolayer α-antimonene. As illustrated in Figure 2.6e, α-antimonene takes a BP-like puckered honeycomb structure, which is different from a buckled honeycomb structure of β-antimonene. Figure 2.6f shows the topographic STM image of α-antimonene, it can be seen that Sb forms atomically flat islands on the Td-WTe2 with no apparent defects, and the height of the Sb island is around 0.78 nm (Figure 2.6g). The atomic-resolution STM image (Figure 2.6h) revealed a reconstructed √2 √2 lattice of α-antimonene with lattice constants of 0.62 × 0.63 nm. Monolayer α-antimonene possesses a linearly dispersed metallic band crossing the Fermi level, resulting in a high electrical conductivity. Large-scale multilayer antimonene was also grown by controlling the amount of Sb, which showed ultrahigh stability in air.
In the meantime, MBE was employed to grow antimonene on different metal substrates as well, including Ge (111), Ag (111), Pd (111), Cu (110), and Cu (111) [33–36]. Niu et al. fabricated single-crystalline monolayer antimonene on Cu (111) and Cu (110) substrates via MBE [36]. When Sb atoms were deposited on two substrates at low coverage, surface alloys were first formed, including √3 × √3 R30°-Sb on Cu (111) and c (2 × 2)-Sb on Cu (110). After increasing the coverage to 1 monolayer followed by postannealing, two atomic types of monolayer antimonene were then formed. Schematic of epitaxial growth of Sb atoms on Cu (111) substrates was shown in Figure 2.6i, where Sb atoms were evaporated from a Knudsen cell onto clean Cu (111) surfaces held at room temperature in an UHV chamber (2 × 10−10 mbar). The topographic STM image of 0.5 monolayer antimonene illustrated that Cu (111) surface was covered by short-range ordered single Sb atoms and their small clusters (Figure 2.6j). After annealing at 700 K, a variety of patches with dark holes (missing atoms) and black lines (misalignment of neighboring domains) were generated (Figure 2.6k). When increasing the coverage and postannealing, well-ordered monolayer antimonene was formed, showing a buckled honeycomb lattice and a larger lattice constant than the free-standing antimonene because of a 7.5% tensile strain (Figure 2.6l). But unlike the result of Cu (111) surface, threefold symmetric antimonene was formed on the twofold symmetric c (2 × 2) Sb-Cu (110) surface, inducing a 6.8% compressive strain. The generation of strain also caused the changes of band gaps of antimonene on two substrates.
2.3.4 Other Methods
In addition to the above three common synthesis methods, there are other methods can also be used to synthesize few- or multilayer antimonene nanosheets, nanoribbons, flakes, or Sb films [37–40]. Few-layer β-antimonene nanosheets were successfully prepared by the solution-phase synthesis method, where SbCl3 solutions as the Sb source were reduced by oleylamine [37]. In this anisotropic growth, both dodecylthiol (DDT) and halide ions played an important role in the formation of β-antimonene. The synthesized β-antimonene nanosheets were single-crystalline with lateral size of 0.5–1.5 μm and thickness of 5–30 nm. Besides, multilayer antimonene nanoribbons were synthesized by the plasma-assisted process, where InSb (001) was selected as the substrates and provided Sb source for the formation of antimonene [38]. During the growth process, the indium at the surface of InSb occurred preferentially the nitridation under