Electrochemically Synthesized Porous Ag Double Layers for Surface-Enhanced Raman Spectroscopy Applications.

Double-layered nanoporous silver is fabricated by dealloying an electrodeposited AgCu double layer with different compositions in each layer. The pore/ligament size and porosity of each layer can be conveniently tailored by controlling the applied voltage profile when electrodepositing the AgCu double-layer precursors. Therefore, nanoporous Ag double layers with a tailor-made porous profile along the film thickness can be easily fabricated. The Ag structures thus obtained are particularly attractive as novel multifunctional enhancement substrates for surface-enhanced Raman spectroscopy (SERS) applications. When a higher porosity is created in the top layer, the double layer can trap more light because of the antireflection effect, enabling stronger SERS enhancement. On the other hand, with smaller pores formed in the top layer, the double layer readily works as a size-screening SERS substrate that can help distinguish SERS signals from a mixture of reagents with different sizes. The theoretical simulation shows good agreement with the experimental observation.

Selective removal of the outer shells of anodic TiO2 nanotubes.

A facile electrochemical method to selectively remove the outer walls of anodic TiO(2) nanotubes by leaving the as-anodized nanotubes in the same electrolyte and applying an electric field parallel to the anodic film for several minutes is reported. The better-separated single-walled TiO(2) nanotubes thus obtained show significantly improved photocatalytic efficiency compared with their non-etched counterparts.

Porous metal-based multilayers for selective thermal emitters.

We report the numerical study of a selective thermal emitter based on a metallic multilayered structure consisting of a graded antireflection top layer, a middle layer with uniform porosity (i.e., volume fraction of voids), and a nonporous substrate layer. Simulation results show that the proposed emitters feature an emission edge in near-IR where the emissivity drops from over 0.9 to below 0.1, for both the TE and TM polarizations. Moreover, these desired emission characteristics persist for a wide range of emission angles with the emission edge nearly nonshifted, making the proposed emitters promising for achieving isotropic thermal emission. The designed emitters are particularly attractive for the thermal-photovoltaic applications by suppressing emission below the photovoltaic material bandgap, which is normally in near-IR.

Mixed-valence Cu(II)Cu(I)15I17 cluster builds up a 3D metal-organic framework with paramagnetic and thermochromic characteristics.

Four cubane-like Cu4I4 units are assembled around an iodine atom to form the giant, mixed-valent Cu(II)Cu(I)15I17 cluster. The Cu(II)Cu(I)15I17 cluster and a bipyrazole linker form a 3D open framework with paramagnetic and thermochromic properties. This paper also touches on the resemblance of this cluster to the self-similar object of a Sierpinski tetrahedron.

Highly stable porous silicon-carbon composites as label-free optical biosensors.

A stable, label-free optical biosensor based on a porous silicon-carbon (pSi-C) composite is demonstrated. The material is prepared by electrochemical anodization of crystalline Si in an HF-containing electrolyte to generate a porous Si template, followed by infiltration of poly(furfuryl) alcohol (PFA) and subsequent carbonization to generate the pSi-C composite as an optically smooth thin film. The pSi-C sensor is significantly more stable toward aqueous buffer solutions (pH 7.4 or 12) compared to thermally oxidized (in air, 800 °C), hydrosilylated (with undecylenic acid), or hydrocarbonized (with acetylene, 700 °C) porous Si samples prepared and tested under similar conditions. Aqueous stability of the pSi-C sensor is comparable to related optical biosensors based on porous TiO(2) or porous Al(2)O(3). Label-free optical interferometric biosensing with the pSi-C composite is demonstrated by detection of rabbit IgG on a protein-A-modified chip and confirmed with control experiments using chicken IgG (which shows no affinity for protein A). The pSi-C sensor binds significantly more of the protein A capture probe than porous TiO(2) or porous Al(2)O(3), and the sensitivity of the protein-A-modified pSi-C sensor to rabbit IgG is found to be ~2× greater than label-free optical biosensors constructed from these other two materials.