Carbon dots (C-dots) with sulfur-doped (S-doped) was synthesized using a simple and straightforward hydrothermal method. The as-prepared S-doped C-dots exhibit significant high fluorescence quantum yield (67%) and unique emission property. The form spherical shaped S-doped C-dots have average diameter 4.6 nm and the fluorescence of S-doped C-dots can be effectively and selectively quenched by 10

Collisions of several kinds of metal or metal oxide single nanoparticles (NPs) with a less catalytic electrode surface have been observed through amplification of the current by electrocatalysis. Two general types of current response, a current staircase or a current blip (or spike) are seen with particle collisions. The current responses were caused by random individual events as a function of time rather than the usual continuous current caused by an ensemble of a large number of events. The treatment of stochastic electrochemistry like single NP collisions is different from the usual model for ensemble-based electrochemical behaviour. Models for the observed responses are discussed, including simulations, and the frequency of the steps or blips investigated for several systems experimentally.

Environmentally friendly synthetic methodologies have gradually been implemented as viable techniques in the synthesis of a range of nanostructures. In this work, we focus on the application of green-chemistry principles to the synthesis of complex metal oxide and fluoride nanostructures. In particular, we describe advances in the use of the molten-salt synthetic methods, hydrothermal protocols, and template-directed techniques as environmentally sound, socially responsible, and cost-effective methodologies that allow us to generate nanomaterials without the need to sacrifice sample quality, purity, and crystallinity, while allowing control over size, shape, and morphology.

Recent experiments on the observation of collisions of single nanoparticles (NPs) with an electrode through amplification of the current by electrocatalysis are described. Systems in which the particles adhere to the electrode upon collision produce a step and staircase response, while those in which particles only interact for a short time with the electrode produce a spike or blip, with little change in the steady state current. Examples of both behaviors, e. g., Pt NPs on a Au electrode for hydrazine oxidation (staircase response) and IrOx NPs on a Pt electrode for water oxidation (blip response) are shown. Controlling the nature of the electrode surface is important in generating useful responses, for example, in the case of gold NPs on an oxidized Pt electrode for borohydride oxidation.

ZnO nanowires, CuO nanowires, and alpha-Fe(2)O(3) nanotubes as well as their corresponding arrays have been successfully synthesized via a low cost, generalizable, and simplistic template method. Diameters of one-dimensional (1-D) metal oxide nanostructures ( approximately 60-260 nm), measuring micrometers in length, can be reliably and reproducibly controlled by the template pore channel dimensions. Associated vertically aligned arrays have been attached to the surfaces of a number of geometrically significant substrates, such as curved plastic and glass rod motifs. The methodology reported herein relies on the initial formation of an insoluble metal hydroxide precursor, initially resulting from the reaction of the corresponding metal solution and sodium hydroxide, and its subsequent transformation under mild conditions into the desired metal oxide nanostructures. Size- and shape-dependent optical, magnetic, and catalytic properties of as-prepared 1-D metal oxides were investigated and noted to be mainly comparable to or better than the associated properties of the corresponding bulk oxides. A plausible mechanism for as-observed wire and tube-like motifs is also discussed.

Single nanoparticle (NP) collisions were successfully observed by a potentiometric measurement. The open circuit potential (OCP) of a measuring Au ultramicroelectrode (UME) changes when Pt NPs collide with the UME in a hydrazine solution. The OCP change is related to the redox processes, the concentration of particles, particle size, and electrode size. Compared with the amperometric technique, this approach has several advantages: higher sensitivity, simpler apparatus, fewer problems with NP decomposition, and contamination.

After growing a thin layer of oxide (PtO x ) by anodization of a Pt electrode, it changed from catalytically active for electrochemical NaBH4 oxidation into an inactive electrode. When held at a potential where the oxide film was maintained, collisions of individual 14 nm diameter Au nanoparticles (NPs) that catalyzed NaBH4 oxidation were successfully observed as discrete current pulses (spikes or blips) for each NP interaction with the modified Pt electrode via amplification from NaBH4 oxidation. The current response is affected by NP concentration and the applied potential.

Quantum dots, derived from two-dimensional (2D) materials, have shown promising applications in bioimaging, photocatalysis, biosensors and white light emission devices (W-LEDs).