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A novel three-dimensional gold catalyst prepared by simple pulse electrodeposition and its high electrochemical performance for hydrogen peroxide reduction

机译:简单脉冲电沉积制备的新型三维金催化剂及其高电化学还原双氧水性能

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摘要

Novel Au nanoparticles (NP), Au pinecones (PC) and Au nanodendrites (ND) supported on carbon coated titanium dioxide (C@TiO2) nanoarrays were successfully obtained through a facile chemical vapor deposition of three-dimensional (3D) C@TiO2 substrate, followed by potential pulse electrodeposition of Au electrocatalysts. The morphology and structure of the open 3D Au-C@TiO2 electrodes was characterized by scanning electron microscopy and X-ray diffractometry. The different morphology of electrodeposited Au can be easily controlled by the applied potential (E-o). Electrochemical methods, including cyclic voltammetry, linear sweep voltammetry and chronoamperometry, were used to examine the catalytic activity of the electrode for H2O2 electroreduction in H2SO4 solution. The Au ND-C@TiO2 electrode exhibited the largest effective specific surface area among the Au-C@TiO2 electrodes, owing to its open nanodendritic structure allowing the full utilization of Au surface active sites. A nearly constant reduction current density of 0.655 A cm(-2) was successfully achieved on the Au ND-C@TiO2 electrode at the potential of 0 V in 2.0 mol L-1 H2O2 + 2.0 mol L-1 H2SO4 solution, which was significantly higher than the catalytic activity of H2O2 electroreduction achieved previously with precious metals as catalysts.
机译:通过在三维(3D)C @ TiO2衬底上进行简便的化学气相沉积,成功获得了负载在碳包覆的二氧化钛(C @ TiO2)纳米阵列上的新型金纳米颗粒(NP),金松果(PC)和金纳米树枝状(ND)。然后电势脉冲沉积Au电催化剂。通过扫描电子显微镜和X射线衍射法对3D Au-C @ TiO2开放电极的形貌和结构进行了表征。电沉积金的不同形态可以通过施加的电势(E-o)轻松控制。电化学方法包括循环伏安法,线性扫描伏安法和计时安培法,用于检查电极对H2SO4溶液中H2O2电还原的催化活性。 Au ND-C @ TiO2电极在Au-C @ TiO2电极中表现出最大的有效比表面积,这是由于其开放的纳米树枝状结构允许充分利用Au表面活性部位。在2.0 mol L-1 H2O2 + 2.0 mol L-1 H2SO4溶液中,Au ND-C @ TiO2电极在0 V电位下成功实现了接近恒定的0.655 A cm(-2)还原电流密度。显着高于以前使用贵金属作为催化剂实现的H2O2电还原的催化活性。

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