Common origin of green luminescence in carbon nanodots and graphene quantum dots.

Carbon nanodots (C-dots) synthesized by electrochemical ablation and small molecule carbonization, as well as graphene quantum dots (GQDs) fabricated by solvothermally cutting graphene oxide, are three kinds of typical green fluorescence carbon nanomaterials. Insight into the photoluminescence origin in these fluorescent carbon nanomaterials is one of the important matters of current debates. Here, a common origin of green luminescence in these C-dots and GQDs is unraveled by ultrafast spectroscopy. According to the change of surface functional groups during surface chemical reduction experiments, which are also accompanied by obvious emission-type transform, these common green luminescence emission centers that emerge in these C-dots and GQDs synthesized by bottom-up and top-down methods are unambiguously assigned to special edge states consisting of several carbon atoms on the edge of carbon backbone and functional groups with C═O (carbonyl and carboxyl groups). Our findings further suggest that the competition among various emission centers (bright edge states) and traps dominates the optical properties of these fluorescent carbon nanomaterials.

Direct observation of quantum-confined graphene-like states and novel hybrid states in graphene oxide by transient spectroscopy.

Quantum-confined graphene-like electronic states are directly observed in graphene oxide and photothermally reduced graphene oxide via transient spectroscopy. An unexpected novel hybrid state arising from amorphous carbon-like peripheral structure with high sp(3) /sp(2) carbon ratio in close vicinity of confined graphene-like states is found commonly existent in various carbon nanomaterials, including graphene oxide, graphene quantum dots, and carbon dots.

Controlled fabrication of cross-linked nanoparticles/polymer composite thin films through the combined use of surface-initiated atom transfer radical polymerization and gas/solid reaction.

A promising strategy for the controlled synthesis of inorganic/polymeric nanocomposites may be sustained by fabricating cross-linked PbS nanoparticles/polymer composite thin films through combining surface-initiated atom transfer radical polymerization (ATRP) and gas/solid reaction. The introduction of Pb ions through the extension of surface-initiated ATRP to the monomers containing metal ions provides an opportunity for generating nanoparticles on the substrate.