To demonstrate the effects of surface atoms on photoluminescence (PL) and photocatalytic activities of luminescent carbon dots (CDs), we design and tailor the surface groups of CDs with heteroatoms by a facile and effective approach. The coexistence of O and N radicals in CDs results in strong PL while CDs containing O and Cl radicals show high photocatalytic activity. This is attributed to the different degrees and directions of energy band bending from inner to surface induced by O, N, and Cl radicals at the surface of CDs. The coexistence of both upward and downward band bending that are caused by the O and Cl radicals, respectively, in CDs is similar to an internal electronic field that facilitates the separation of electron-hole pairs and carrier migration, leading to high photocatalytic activity. These results may also be used for designing and tailoring optical-electronic properties of carbon nanostructures.

We present a facile approach, without the need for external heating and any additional energy input, to produce fluorescent carbon dots (CDs) inexpensively and on a large scale. Fluorescence emission wavelengths from the obtained CDs shift gradually from 630 to 400 nm with reduction in their concentration in solution. This work offers a novel avenue for tuning band gaps in CDs and endowing them with potential for various applications.

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Two-pulse second-order interferometric autocorrelation responses of single Ag nanoparticles are reported. The surface plasmon-enhanced second harmonic generation interferogram for single Ag colloids shows significant broadening with respect to the laser pulse second-order autocorrelation. The interferometric autocorrelation response is described and analyzed with a density matrix formalism that incorporates (phenomenologically) the population and the polarization relaxation of the surface plasmon. The total dephasing time (T 2 ) of the surface plasmon in single Ag colloids is determined to be 10 fs. The present results are compared to previously reported values obtained from ensemble studies of Ag particles and from the line width of the absorption spectrum. Extension of the present ultrafast measurements, the first performed on single nanoparticles, to single molecules studies is discussed.