“…However, nanostructured Te can crystallize in the trigonal phase, and such trigonal Te exhibits high hole mobility (707 cm V −1 s −1 ) [ 17 ], high current density (1 A mm −2 ) [ 18 ], and has tunable energy bandgaps up to 1 eV [ 19 ], opening up additional research fields. Several studies have already shown the possibility of obtaining a variety of nanostructures, such as needle-like nanowires with a tip of 50–70 nm and a base of 150–200 nm [ 20 ], Te nanorods 300–500 nm in diameter and 3 μm in length [ 21 ], nanowires with a base of 200 nm and a conical tip with diameter of 20 nm [ 22 ], tubular nanowires with an inner size of 50 nm and an external size of 500 nm [ 23 ], and finally hexagonal nanowires with tunable dimensions with diameters of 50–3000 nm and lengths of 1–22 μm [ 24 ]. The most common production techniques are based on wet-chemistry processes, while few reports exist on other methods such as chemical vapour deposition (CVD), PVD, or sputtering techniques [ 11 , 20 ].…”