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Teng et al. Microstructures 2023;3:2023019  https://dx.doi.org/10.20517/microstructures.2023.07  Page 11 of 29







































                Figure 5. Compounds filling: (A) ACTEM analysis and schematic representation of the PbI @SWCNT. Blue: Pb atoms; yellow: I atoms
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                (Reproduced with permission  . Copyright 2013, Wiley). (B) HRTEM image and corresponding simulation image of an encapsulated
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                bilayer CsSnI  perovskite-like polymeric structure derived from CsSnI  (Reproduced with  permission  . Copyright 2023, Wiley). (C)
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                ACTEM photos, crystal structure, and geometric optimization models of PtS  (Reproduced with  permission  . Copyright 2017, The
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                Royal Society of Chemistry). (D) TEM and ACTEM images of NbSe  single strand in DWCNTs, atomic structure model (red: Se, blue:
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                Nb) (Reproduced with  permission  . Copyright 2018, The American Association for the Advancement of Science). (E) From top to
                bottom are the ADF-STEM images of MTe  single-stranded carbon nanotubes. Illustration below ADF-STEM: ADF-STEM image
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                simulation (left) with the appropriate microscope condition noise added from the structure calculated by the DFT (right) (Reproduced
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                with permission  . Copyright 2021, American Chemical Society).
               Spurred by the novel electronic, optical, magnetic, and structural properties of graphene nanoribbons ,
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               isolating and manipulating ultra-fine nanoribbons of 2D materials (e.g., TMDs) has become popular in
               recent years. However, ultra-fine nanoribbons are difficult to separate and manipulate and may be highly
               air-sensitive due to the abundance of suspended bonds on the edges of the nanoribbons . Encapsulation
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               of metastable materials inside small-diameter nanotubes has emerged as a novel approach to creating new
               quasi-1D nanostructures. Cain et al. reported a gas-phase synthesis method for producing ultra-fine TaS
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               nanoribbons in CNTs . The boundary and number of nanoribbons were limited by the diameter of the
               CNTs. Botos et al. prepared [MS ] @SWCNT (M = Mo or W, average d  = 1.4 nm) by sequentially
                                             2 n
                                                                                NT
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               transforming M(CO)  (M = Mo or W) nanocluster to nanoribbons . Two [MS ]  nanoribbons, well-
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               ordered crystalline hexagonal structures with zigzag edges, grow inward from both ends of SWCNTs. The
               nanoribbon’s width is strictly regulated due to the limitation of the nanotube diameter. Furthermore, the
               nanoribbon is twisted rows in the CNTs due to the edge defect. Similar nanoribbon structures were also
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               exhibited  in  the  WS @MWCNT , MnTe @SWCNT , ReS @SWCNT , HfTe @SWCNT , and
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               PtS @SWCNT [Figure 5C]  heterostructures. Surprisingly, Nagata et al. prepared single MoTe nanowires
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               using CNT as a template and partially oxidized MoTe  as a precursor . They propose that the MoO
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                                                                                                         x
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               oxidizes MoTe  to MoTe and TeO . TEM shows that MoTe nanowires exhibit unusual distortion under the
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               confinement of carbon nanotubes, which may provide the possibility for the application of nanowires.
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