Helical mesoporous silicas are notable from a self-assembly and applications points of view. We report a novel confinement-free synthesis of chloropropyl-functionalized helical mesoporous silica nanofibers (CP-HMSNFs) possessing straight channels at the fiber center surrounded by concentric short-pitch helical channels. The chloropropyl groups are found mainly distributed at the central cylindrical portion of the fibers, allowing the selective inclusion of guest species to fabricate novel nanocomposite fibers. Moreover, the chloropropyl-functionalized nanofibers were applied as a hard template to fabricate helical platinum-cobalt (PtCo) alloy nanowires with small and narrowly distributed radii of gyration. The helical metal nanowires exhibited distinct ferromagnetic properties as compared with their straight counterpart. NPG Asia Materials (2015) 7, e181; doi:10.1038/am.2015.39; published online 22 May 2015
INTRODUCTIONHelical mesoporous silicas 1-11 are analogous to the self-assembled helical biomaterials in nature and have attracted a substantial amount of attention. These helical silicas are also promising hard templates for the preparation of helical nanowires composed of metals [12][13][14][15] or other compositions that may possess unique optical, 16,17 electromagnetic 9,18 or other properties. Efforts to understand the formation mechanism of these helical nanostructures provide additional insights into the interplay of the thermodynamics and kinetics of the assembly of structure-directing surfactants and inorganic silicate species 1,2,19,20 and may also lead to the design and synthesis of additional novel selfassembled nanomaterials with controllable mesostructures and morphologies, allowing for innovative applications. 9,11,21 The first synthesis of helical mesoporous silica materials displaying a MCM-41-like two-dimensional (2D)-hexagonal structure was performed in a static two-phase acidic system. 7 Helical 2D-hexagonal mesoporous silica nanofibers (HMSNFs) or nanorods were then synthesized in single-phase dilute solutions using chiral 5 or achiral 2,20,22 surfactants. The helical formation is mainly driven by a reduction in the free energy of the surface, from straight micellar rods until the free energy is balanced by an increased bending energy. 2,20 Alternatively, HMSNFs can be prepared by evaporation-induced selfassembly (EISA) in porous anodic alumina membranes. 23,24 The confined EISA may result in helical and other thermodynamically more stable mesophases, the former generally being kinetically favored. Notably, materials with mixed mesostructures can also be