Intergrowth and Interfacial Structure of Biomimetic Fluorapatite–Gelatin Nanocomposite: A Solid-State NMR Study

The model system fluorapatite–gelatin allows mimicking the formation conditions on a lower level of complexity compared to natural dental and bone tissues. Here, we report on solid-state NMR investigations to examine the structure of fluorapatite–gelatin nanocomposites on a molecular level with particular focus on organic–inorganic interactions. Using ³¹P, ¹⁹F, and ¹H MAS NMR and heteronuclear correlations, we found the nanocomposite to consist of crystalline apatite-like regions (fluorapatite and hydroxyfluorapatite) in close contact with a more dissolved (amorphous) layer containing first motifs of the apatite crystal structure as well as the organic component. A scheme of the intergrowth region in the fluorapatite–gelatin nanocomposite, where mineral domains interact with organic matrix, is presented

Redox Route from Inorganic Precursor Li₂C₂ to Nanopatterned Carbon

We present the synthesis route to carbon with hierarchical morphology on the nanoscale. The structures are generated using crystalline orthorhombic lithium carbide (Li₂C₂) as precursor with nanolamellar organization. Careful treatment by SnI₄ oxidizes carbon at the fairly low temperature of 80 °C to the elemental state and keeps intact the initial crystallite shape, the internal lamellar texture of particles, and the lamellae stacking. The reaction product is amorphous but displays in the microstructure parallel band-like arrangements with diameters in the range of 200–500 nm. These bands exhibit internal fine structure made up by thin strips of about 60 nm width running inclined with respect to the long axis of the band. The stripes of neighboring columns sometimes meet and give rise to arrow-like arrangements in the microstructure. This is an alternative preparation method of nanostructured carbon from an inorganic precursor by a chemical redox route without applying physical methods such as ion implantation, printing, or ablation. The polymerization reaction of the triple bond of acetylide anions gives rise to a network of carbon sp² species with statistically sized and distributed pores with diameters between 2 and 6 Å resembling zeolite structures. The pores show partially paracrystal-like ordering and may indicate the possible formation of carbon species derived from graphitic foams

Synthesis and Three-Dimensional Magnetic Field Mapping of Co₂FeGa Heusler Nanowires at 5 nm Resolution

We present the synthesis of Co₂FeGa Heusler nanowires and the results of our investigations on their three-dimensional (3D) electric and magnetic internal and external fields mapped by electron holographic tomography (EHT). These fields will be of great importance in next-generation nanomagnets integrated in spintronics and memory devices. The Co₂FeGa nanowires with a <i>L2</i>₁ ordered structure are prepared by a SBA-15 silica-assisted method. The magnetic dipole-like stray fields of several Co₂FeGa nanowires are revealed by holographically reconstructed phase images. Based on the measured magnetic phase shifts of an individual nanowire and its 3D reconstruction using EHT, we obtain an internal magnetic induction with a magnitude of 1.15 T and a nonmagnetic surface layer of 10 nm thickness. Furthermore, we also reconstruct the 3D distribution of the electrostatic potential of the same nanowire

Pd@Fe₂O₃ Superparticles with Enhanced Peroxidase Activity by Solution Phase Epitaxial Growth

Compared to conventional deposition techniques for the epitaxial growth of metal oxide structures on a bulk metal substrate, wet-chemical synthesis based on a dispersible template offers advantages such as low cost, high throughput, and the capability to prepare metal/metal oxide nanostructures with controllable size and morphology. However, the synthesis of such organized multicomponent architectures is difficult because the size and morphology of the components are dictated by the interplay of interfacial strain and facet-specific reactivity. Here we show that solution-processable two-dimensional Pd nanotetrahedra and nanoplates can be used to direct the epitaxial growth of γ-Fe₂O₃ nanorods. The interfacial strain at the Pd−γ-Fe₂O₃ interface is minimized by the formation of an Fe_<i>x</i>Pd “buffer phase” facilitating the growth of the nanorods. The γ-Fe₂O₃ nanorods show a (111) orientation on the Pd(111) surface. Importantly, the Pd@γ-Fe₂O₃ hybrid nanomaterials exhibit enhanced peroxidase activity compared to that of isolated Fe₂O₃ nanorods with comparable surface area because of a synergistic effect for the charge separation and electron transport. The metal-templated epitaxial growth of nanostructures via wet-chemical reactions appears to be a promising strategy for the facile and high-yield synthesis of novel functional materials