Covalent functionalization tailors carbon nanotubes for a wide range of applications in varying environments. Its strength and stability of attachment come at the price of degrading the carbon nanotubes sp2 network and destroying the tubes electronic and optoelectronic features. Here we present a non-destructive, covalent, gram-scale functionalization of single-walled carbon nanotubes by a new [2+1] cycloaddition. The reaction rebuilds the extended π-network, thereby retaining the outstanding quantum optoelectronic properties of carbon nanotubes, including bright light emission at high degree of functionalization (1 group per 25 carbon atoms). The conjugation method described here opens the way for advanced tailoring nanotubes as demonstrated for light-triggered reversible doping through photochromic molecular switches and nanoplasmonic gold-nanotube hybrids with enhanced infrared light emission.

Aiming to enhance the luminescence yield of carbon nanotubes, we introduce a new class of hybrid nanoplasmonic colloidal systems (π-hybrids). Nanotubes dispersed in gold nanorod colloidal suspensions yield hybrid structures exhibiting enhanced luminescence up to a factor of 20. The novelty of the proposed enhancement mechanism relies on including metal proximity effects in addition to its localized surface plasmons. This simple, robust and flexible technique enhances the luminescence of nanotubes with chiralities whose enhancement has never reported before, for example the (8,4) tube

Fluorescent nanomaterials are expected to revolutionize medical diagnostic, imaging, and therapeutic tools due to their superior optical and structural properties. Their inefficient water solubility, cell permeability, biodistribution, and high toxicity, however, limit the full potential of their application. To overcome these obstacles, a water-soluble, fluorescent, cytocompatible polymer-single-walled carbon nanotube (SWNT) complex is introduced for bioimaging applications. The supramolecular complex consists of an alkylated polymer conjugated with neutral hydroxylated or charged sulfated dendronized perylene bisimides (PBIs) and SWNTs as a general immobilization platform. The polymer backbone solubilizes the SWNTs, decorates them with fluorescent PBIs, and strongly improves their cytocompatibility by wrapping around the SWNT scaffold. In photophysical measurements and biological in vitro studies, sulfated complexes exhibit superior optical properties, cellular uptake, and intracellular staining over their hydroxylated analogs. A toxicity assay confirms the highly improved cytocompatibility of the polymer-wrapped SWNTs toward surfactant-solubilized SWNTs. In microscopy studies the complexes allow for the direct imaging of the SWNTs' cellular uptake via the PBI and SWNT emission using the 1st and 2nd optical window for bioimaging. These findings render the polymer-SWNT complexes with nanometer size, dual fluorescence, multiple charges, and high cytocompatibility as valuable systems for a broad range of fluorescence bioimaging studies.

We experimentally investigate the effect of the structural and optoelectronic changes carbon nanotubes undergo after covalent functionalization. The carboxylation process alters the crystalline structure and the optical response of the tubes. We analyzed the intensity of disorder modes in the Raman spectra to estimate the structural degradation of the sp 2 network. After functionalization the bands associated with the G and 2D mode shift to higher frequency, indicating a change of the Fermi level DE F $ À0.5 and À0.65 eV in semiconducting and metallic nanotubes. This is also corroborated by the broadening of the semiconducting and narrowing of the metallic G mode phonons. Analysis of the luminescence correlated with absorption spectroscopy suggests that only the large-diameter tubes remain present after the functionalization procedure, whereas the small-diameter (d < 8.2 Å) ones get destroyed in the process. The spectral shifts of the E 11 transition energies indicate uniaxial strain of (e ¼ 0.18%) in the semiconducting nanotubes due to functionalization.

While direct optical excitation of carbon nanotubes activates only the tube species strictly matching the excitation source, excitation energy transfer processes provide a single excitation channel for all the nanotubes species in a sample. The requirement of an overlap between donor emission and acceptor absorption limits the poll of donors able to trasfer their excitation to the tubes, leaving the high-energy part of the solar spectrum excluded from such processes. Here it is shown that the grafting of small metal nanoparticles to the tubes alters those rules, enabling energy transfer process from molecules for which the standard energy transfer process is strongly suppressed. The onset of an energy transfer band in the UV/blue spectral region is demonstrated for an hybrid gold-pyrene-nanotube system, yielding collective emission from all the tubes present in our samples upon excitation of pyrene.

Customized polyglycerol‐based surfactants incorporating different aromatic cores are used to isolate and suspend carbon nanotubes in water. Different cores yield suspension with distinct chiral species distribution. Increasing the number of the phenyl rings connecting head and tail, the dispersion of the semiconducting species becomes sharper toward the nanotubes with bigger family index.

We exploited a non‐covalent approach based on π‐stacking interactions to address the formation of hybrids between pyrene‐functionalized gold nanoparticles (PyAuNPs) and reduced graphene oxide (RGO), in which the former are distributed homogeneously on the surface of the latter with a high degree of coverage. We used water soluble PyAuNPs of two different average dimensions, namely 2 and 8 nm, in which the pendant pyrene moieties were introduced within a mixed monolayer with a choline derivative. The combination with RGO originates highly insoluble materials, in which microscopy evidences a complete adhesion of the PyAuNPs onto the carbon nanomaterial layers in a highly homogeneous fashion, with no traces of free particles, confirming the high affinity between pyrene‐functionalized species and conjugated carbon nanostructure surfaces.

Recently, we introduced a novel hybridization route for carbon nanotubes using gold nanoparticles, whose close proximity neatly enhances their radiative emission. Here we investigate the mechanisms behind the enhancement by monitoring the de-excitation dynamics of our π-hybrids through two-color pump-probe time-resolved spectroscopy. The de-excitation process reveals a fast component and a slow component. We find that the presence of gold prominently affects the fast processes, indicating a stronger influence of the gold nanoparticle on the intra-band non-radiative relaxation than on the inter-band recombination of the single-walled carbon nanotube. By evaluating the de-excitation times, we estimate the balance between near-field pumping and the faster metal-induced de-excitation contributions, proving the enhanced pumping to be the leading mechanism.