We have used a carbothermal process in the absence of a catalyst or template to prepare two-dimensional (2D) platinum (Pt) nanoplatelets and one-dimensional (1D) Pt nanobelts on sapphire surfaces. This paper describes the first examples of the growth of Pt nanobelts and mesobelts. It appears that the presence of adequate quantities of diamond and Y 2 O 3 powder at a molar ratio was a critical factor controlling the Pt gas species to form nanobelts at a relative low level of supersaturation. When the growth time was 15 h, we obtained ultralong (0.5 mm) mesobelts and microsheets. Electrical measurements indicated that the single-crystal Pt nanobelt had an extremely low resistivity of 16.8 µΩ cm and a failure current density of greater than 1 × 10 7 A cm -2 . These unique Pt nanobelts are potentially attractive nanoscale building blocks for use as interconnects in nanoelectronic devices.Research into noble-metal nanostructures is stimulated by the fascinating size-and shape-dependent properties of these nanomaterials. Because of their unique and tunable properties, they hold promise for various applications in optics, electronics, information storage, biological labeling, and imaging. 1 Platinum (Pt) is one of the most important noble metals, 2-4 especially for its application in the fields of molecular scale electronic devices, 5 biosensors, 6 and catalysts. 7,8 For example, because platinum is inert, highly thermally stable in air, and does not cause contamination of the integrated circuit, it is the most common choice for use in integrated circuit repair and modification and bottom electrode. 9 Also, because of its nice performance toward the detection of hydrogen peroxide, a typical enzymatic product, platinum electrodes, and platinum nanostructure modified electrodes have been widely used for fabrication of biosensors. 10 Because Pt has a face-centered cubic (fcc) structure, there is no crystallographic driving force for anisotropic growth. As a result, Pt atoms generally assemble to form faceted spheres (e.g., singlecrystal cuboctahedrons) 11 and, in particular, few reports exist describing the growth of two-dimensional (2D) and one-dimensional (1D) Pt nanostructures. In spite of that, it is common for other fcc metals (like Ag, Au) to form 2D nanostructures, such as triangular and hexagonal platelets, when transition-metal colloids are prepared in solution through the reduction of metal salts. 12-14 Most reports on the preparation of Pt nanostructures have been limited to the synthesis of nanoparticles (NPs) or polycrystalline nanorods using either solution-phase techniques 15 or template-directed synthesis 16 for examples of synthesized 2D and 1D Pt nanostructures, respectively. Tan et al. prepared 2D Pt NPs by the reduction of their salts with a weak reductant -potassium bitartrate. In their study, Pt NPs have two dominant shape distributions, triangular and square. 17 For an instance of synthesized 1D Pt nanostructures, Zhao et al. synthesized polycrystalline Pt nanowire array electrode by dc electrodeposi...