2 research outputs found

    Peptide-Decorated Tunable-Fluorescence Graphene Quantum Dots

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    We report here the synthesis of graphene quantum dots with tunable size, surface chemistry, and fluorescence properties. In the size regime 15–35 nm, these quantum dots maintain strong visible light fluorescence (mean quantum yield of 0.64) and a high two-photon absorption (TPA) cross section (6500 Göppert–Mayer units). Furthermore, through noncovalent tailoring of the chemistry of these quantum dots, we obtain water-stable quantum dots. For example, quantum dots with lysine groups bind strongly to DNA in solution and inhibit polymerase-based DNA strand synthesis. Finally, by virtue of their mesoscopic size, the quantum dots exhibit good cell permeability into living epithelial cells, but they do not enter the cell nucleus

    Silver Nanoparticles with Surface-Bonded Oxygen for Highly Selective CO<sub>2</sub> Reduction

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    The surface electronic structures of catalysts need to be carefully engineered in CO<sub>2</sub> reduction reaction (CO<sub>2</sub>RR), where the hydrogen evolution side reaction usually takes over under a significant overpotential, and thus dramatically lowers the reaction selectivity. Surface oxides can play a critical role in tuning the surface oxidation state of metal catalysts for a proper binding with CO<sub>2</sub>RR reaction intermediates, which may significantly improve the catalytic activity and selectivity. Here, we demonstrate the importance of surface-bonded oxygen on silver nanoparticles in altering the reaction pathways and improving the CO<sub>2</sub>RR performances. A comparative investigation on air-annealed Ag (Air-Ag) catalyst with or without the post-treatment of H<sub>2</sub> thermal annealing (H<sub>2</sub>-Ag) was performed. In Air-Ag, the subsurface chemically bonded O species (O–Ag<sup>δ+</sup>) was identified by angle resolved X-ray photoelectron spectroscopy and X-ray absorption spectroscopy techniques, and contributed to the improved CO selectivity rather than H<sub>2</sub> in CO<sub>2</sub>RR electrolysis. As a result, though the maximal CO Faradaic efficiency of H<sub>2</sub>-Ag is at ∼30%, the Air-Ag catalyst presented a high CO selectivity of more than 90% under a current density of ∼21 mA/cm<sup>2</sup>
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