Title :
Preparation and electrochemical performance comparison of titanium electrodes modified with surfactants
Author :
Li, Baohua ; Ge, Hui ; Yin, Zhaoming
Author_Institution :
Xinjiang Ploytechnical Coll., Urumqi, China
Abstract :
Pd/PPy(SDS)/Ti, Pd/PPy(SLS)/Ti, Pd/PPy(SDBS)/Ti and Pd/PPy(CTAB)/Ti electrode were prepared by electrochemical deposition behaviors of composite membrane of surfactants and pyrrole. Electrochemical performance comparison of electrodes was done. The results of CV revealed that Pd/PPy(CTAB)/Ti electrode can get maximal hydrogen adsorption peak of -146.8 mA at -500 mV (vs. Hg/Hg2SO4). Scanning Electron Microscope (SEM) images revealed that Pd was deposited almost homogeneous particles on the PPy composite membrane modified with CTAB. The range of its size is from nanons to a few microns. The surface of tiny particles exhibits a layered structure. This structure has a good spatial extent. The shapes of needle are very dense. ICP-AES showed that, with the surfactants CTAB modification, high electrochemical performance of electrodes was obtained with less loading of Pd on electrode. The results show that Pd/PPy(CTAB)/Ti electrode has great potential applications in the field of electrocatalytic reduction dechlorination.
Keywords :
chemical engineering; composite materials; electrodes; membranes; surfactants; titanium; CTAB; PPy composite membrane; Pd/PPy(CTAB)/Ti electrode; Pd/PPy(SDBS)/Ti electrode; Pd/PPy(SDS)/Ti electrode; Pd/PPy(SLS)/Ti electrode; composite membrane; electrochemical deposition behaviors; electrochemical performance comparison; electrochemical preparation; maximal hydrogen adsorption; pyrrole; scanning electron microscope images; surfactants; titanium electrodes; Electrodes; Films; Mercury (metals); Palladium; Scanning electron microscopy; Sun; Titanium; cyclic voltammetry; electrochemical; electrode; surfactants;
Conference_Titel :
Consumer Electronics, Communications and Networks (CECNet), 2011 International Conference on
Conference_Location :
XianNing
Print_ISBN :
978-1-61284-458-9
DOI :
10.1109/CECNET.2011.5769326