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Ultrasound electrodeposition pulse

Reisee et al. [52] first described a pulsed electrodeposition and pulsed out-of-phase ultrasound to prepare copper nanopowders. Such an electrochemical method has since then employed to synthesize a variety of nanoparticles. Mancier et al. [53] have prepared Cu20 nanopowders (8 nm) with very high specific surface area of 2,000 m2/g by pulsed ultrasound assisted-electrochemistry. [Pg.203]

Reisse and co-workers [147-149] were the first to describe a novel device for the production of metal powders using pulsed sonoelectrochemical reduction. This device exposes only the flat circular area at the end of the sonic tip to the electrodeposition solution. The exposed area acts as both cathode and ultrasound emitter, named by Reisse et al. as sonoelectrode . A pulse of electric current produces a high density of fine metal nuclei. This is immediately followed by a burst of ultrasonic energy that removes the metal particles from the cathode, cleans the surface of the cathode, and replenishes the double layer with metal cations by stirring the solution. In [145], a list is given of chemically pure fine crystalline powders, mostly metals or metallic alloys, prepared by this method, with particle sizes varying between 10 and 1000 run depending on deposition conditions. [Pg.149]

Sonoelectrochemical synthesis has recently been used for the preparation of semiconductor nanocrystalline powders. In the sonoelectrochemical method, the ultrasound horn acts as both cathode and ultrasound emitter. This technique was used for preparing metal powders [65] and was extended to CdTe, although details of the CdTe particle size were not given [66]. CdSe nanocrystalline powders have been prepared by pulsed sonoelectrochemical reduction from an aqueous selenosulfate solution. The crystal size could be varied from X-ray amorphous up to 9 nm (sphalerite phase) by controlling the various electrodeposition and sonic parameters [67]. Crystal size was smaller for lower preparation temperatures, higher ultrasound intensity, and shorter current pulse width. These dependencies could be explained based on a pulse of electric... [Pg.182]


See other pages where Ultrasound electrodeposition pulse is mentioned: [Pg.124]    [Pg.77]    [Pg.119]    [Pg.119]    [Pg.120]    [Pg.121]    [Pg.322]    [Pg.1337]   
See also in sourсe #XX -- [ Pg.124 ]




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