Immunoassay with Single-Walled Carbon Nanotubes as Near-Infrared Fluorescent Labels

The intrinsic photoluminescence of single-walled carbon nanotubes (CNTs) in the near-infrared (NIR) above 1000 nm makes them promising candidates for biological probes owing to low interference by bioorganic molecules and deep tissue penetration. We here demonstrate an immunoassay by using a NIR CNT labels conjugated to immunoglobulin G (IgG) antibodies. Most of the CNT-conjugated IgG was successfully immunoprecipitated with protein G-attached magnetic beads and eluted from them, which was confirmed by the NIR emission of the conjugated CNTs at 1000–1200 nm. The photoluminescence intensity of the CNT labels was strong enough to detect antigens at 600 pM by our simple procedures

Spectroscopic Characterization of Nanohybrids Consisting of Single-walled Carbon Nanotubes and Fullerodendron

<div><p>Hydrogen gas, which can be used in fuel cells to generate electricity, is considered the ultimate clean energy source. Recently, it was reported that a photo-induced electron transfer system consisting of single-walled carbon nanotubes (SWCNTs) and fullerodendrons shows photo-catalytic activity with a very high quantum yield for splitting water under visible light irradiation. However, the mechanism of high efficiency hydrogen generation is not yet clearly understood. We report here the spectroscopic characterizations of the SWCNT-fullerodendron composites. The results indicate two important fundamental properties of the composite system. First, fullerodendrons preferentially interact with the semiconducting SWCNTs instead of with their metallic counterparts. Second, the photo-induced electron transfer process from the C₆₀ moiety of fullerodendrons to SWCNTs occurs more efficiently with an increasing tube diameter.</p> </div

Dimerization-Initiated Preferential Formation of Coronene-Based Graphene Nanoribbons in Carbon Nanotubes

We have investigated the growth mechanism of coronene-derived graphene nanoribbons (GNRs) using two different precursors: coronene and a dimer form of coronene, so-called dicoronylene (C₄₈H₂₀). For both of the precursors, the formation of nanoribbon-like materials inside carbon nanotubes (CNTs) was confirmed by transmission electron microscope observations. Experimental and theoretical Raman analysis reveals that the samples also encapsulated dicoronylene and linearly condensed other coronene oligomers, which can be regarded as analogues to GNRs. Interestingly, it was found that the present doping condition of coronene yields dicoronylene prior to encapsulation due to the thermal dimerization of coronene. These results indicate that the dimerization before the encapsulation drives the preferential formation of the coronene-based GNRs within CNTs