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Electrocatalytic oxidation of nitric oxide at TiO2-Au nanocomposite film electrodes

机译:TiO2-Au纳米复合膜电极上一氧化氮的电催化氧化

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摘要

Structured films of TiO2 (anatase) nanoparticles (ca. 6 nm diameter) and gold nanoparticles (nominal 20 nm diameter) are formed via a layer-by-layer deposition procedure. TiO2 nanoparticles are deposited with a Nafion polyelectrolyte binder followed by calcination to give a mesoporous thin film electrode. Gold nanoparticles are incorporated into this film employing a poly(diallyldimethylammonium chloride) polyclectrolyte binder followed by calcination to give a stable mesoporous TiO2-gold nanocomposite. This methodology allows well-defined and structured films to be formed which are re-usable after a 500 degrees C heat treatment in air. Electrochemical experiments are performed in aqueous KCl and buffer solutions and for the oxidation of nitric oxide, NO, and nitrite in phosphate buffer solution. It is shown that the NO oxidation occurs as a highly effective electrocatalytically amplified process at the surface of the gold nanocomposite probably with co-evolution of oxygen, O-2. In Contrast, the oxidation of nitrite to nitrate occurs at the same potential but without oxygen evolution. A mechanistic scheme for the amplified NO detection process is proposed. (c) 2006 Elsevier B.V. All rights reserved.
机译:TiO2(锐钛矿)纳米颗粒(直径约6 nm)和金纳米颗粒(标称直径20 nm)的结构膜是通过逐层沉积程序形成的。用Nafion聚电解质粘合剂沉积TiO2纳米颗粒,然后煅烧以提供中孔薄膜电极。使用聚(二烯丙基二甲基氯化铵)聚电解质粘合剂将金纳米颗粒掺入该膜中,然后煅烧以得到稳定的介孔TiO 2-金纳米复合材料。这种方法可以形成轮廓分明的结构化薄膜,在空气中进行500摄氏度的热处理后可以重复使用。电化学实验是在氯化钾水溶液和缓冲溶液中进行的,用于氧化磷酸盐缓冲溶液中的一氧化氮,一氧化氮和亚硝酸盐。结果表明,NO氧化作为一种​​高效的电催化放大过程在金纳米复合材料表面发生,可能与氧O-2共同释放。相反,亚硝酸盐氧化成硝酸盐的电势相同,但没有氧气析出。提出了一种放大NO检测过程的机理方案。 (c)2006 Elsevier B.V.保留所有权利。

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