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Electrochemical oxidation of hydrogen peroxide at a bromine adatom-modified gold electrode in alkaline media

机译:碱性介质中溴原子修饰的金电极上过氧化氢的电化学氧化

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摘要

Bromine (Br)-adatom (Br{sub}(ads)) was in situ fabricated onto polycrystalline gold (Au (poly)) electrode in Br{sub}--containing alkaline media. The surface coverage of Br{sub}(adS) (Г{sub}(Br) varied only in the submonolayer coverage within the investigated potential window under potentiodynamic condition because of the coadsorption of hydroxyl ion (OH{sup}-) in alkaline media. The in situ fabricated Br{sub}(ads)-submonolayer-coated Au (poly) electrode was successfully used for the electrochemical oxidation of hydrogen peroxide (H{sub}2O{sub}2). About five times higher oxidation current was achieved at the modified electrode as compared with the bare electrode. The enhancement of the electrode activity towards the electrochemical oxidation of H{sub}2O{sub}2 was explained based on the enhanced electrostatic attraction between the anionic HO{sub}2{sup}- molecules and Br{sub}(ads)-adlayer-induced positively polarized Au (poly) electrode surface.
机译:在含Br {sub}的碱性介质中,将溴(Br)原子(Br {sub}(ads))原位制作到多晶金(Au(poly))电极上。由于在碱性介质中羟基离子(OH {sup}-)的共吸附,Br {sub}(adS)(Г{sub}(Br)的表面覆盖率仅在电势条件下所研究的电位窗口内的亚单层覆盖率中变化。原位制备的Br {sub}(ads)-亚单层涂层Au(poly)电极成功地用于过氧化氢(H {sub} 2O {sub} 2)的电化学氧化,其氧化电流约为H2的5倍。基于阴离子HO {sub} 2 {sup之间的增强的静电吸引,解释了电极对H {sub} 2O {sub} 2电化学氧化的活性增强。 }-分子和Br {sub}(ads)-层诱导的正极化Au(poly)电极表面。

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