Templating against currently existing nanowires (or rods, belts) provides a straightforward and powerful route to greatly expand the diversity of materials that can be processed as uniform, one-dimensional (1D) nanostructures.[1] In one approach, the surfaces of nanowires could be directly coated (using a range of different methods) with conformal sheaths made of a different material to generate coaxial nanocables.[2]Subsequent removal of the nanowires would lead to the formation of nanotubes with well-controlled dimensions. In another approach, it has been demonstrated that single crystalline nanowires could serve as substrates for the epitaxial growth of another material to obtain coaxial, bilayer nanotapes characterized by sharp structural and compositional interfaces. [3] By carefully modulating the composition of reactant in sequential steps, it is also possible to fabricate semiconductor multiple-sheath nanowire heterostructures via epitaxial growth. [4] In a third approach (or the so-called template-engaged process), nanowires had been partially (e.g., on the surface only) or completely converted to other materials without changing the 1D morphology when they were reacted with appropriate chemical reagents under carefully controlled conditions.[5] The concept of this method was originally demonstrated by Lieber and co-workers, where they found that highly crystalline nanorods of metal carbides could be formed by reacting carbon nanotubes with the vapors of metal oxides or halides at elevated temperatures.[5a] A similar procedure (including the use of both vapor-and solution-phase reactions) was later exploited by many research groups to generate 1D nanostructures from a wealth of solid materials. These studies have also made it possible to incorporate a number of functions (e.g., luminescent, ferromagnetic, ferroelectric, piezoelectric, and superconducting) into an individual nanowire that will find applications in various areas. Here, we would like to add another example to this list, where uniform nanowires of t-Se were employed as chemical templates to generate Se@CdSe nanocables and then CdSe nanotubes. Figure 1 shows a schematic outline of the approach. The first step involved the synthesis of single-crystalline nanowires of t-Se via a sonochemical process.[ Note that the solubility of CdSeO 3 is sufficiently high at the refluxing temperature that it would not inhibit the formation of a dense CdSe sheath around each t-Se template via processes such as co-precipitation with CdSe. As the reaction was cooled down to room temperature, CdSeO 3 did precipitate out as nanoparticles decorating the surfaces of Se@CdSe nanocables. Fortunately, this unwanted byproduct could be effectively removed by washing the as-synthesized sample with hot water in the setting of filtration. Due to the relatively low melting point of t-Se (~217 C) as compared with CdSe nanoparticles, [8] the unreacted core of t-Se could be conveniently removed through evaporation (by heating at~230 C for a few minutes) to obtain the nanotube ...