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Demonstration of a novel rotating cylindrical electrode in growth of oxide films with spatially controlled microstructural variation on al 6061

机译:在Al 6061上演示了一种新型的旋转圆柱电极在氧化膜生长中的空间控制的微观结构变化

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We report growth and characterization of oxide films with spatiallycontrolled microstructure on Al 6061 using a coaxial rotating, axially translating electrochemical reactor (CRATER). The instrument allows oxide film growth with spatially controlled microstructure on a single working electrode (WE) under well-defined conditions of mass transfer, electrode potential, and residence time. This is achieved by restricting electro-oxidation to a "window" of narrow axial extent just below the free surface of an electrolyte whose coaxial inner and outer boundaries are a rotating counterelectrode and an axially translating WE, respectively. Axial variation of oxide microstructure on the WE reported here corresponds to temporal variation of potential during WE ascent, with remarkable monodispersity and azimuthal uniformity of pore size distribution. Continuous scanning of process variables in a single experiment by this approach allows identification of desirable microstructures in narrow ranges of operating conditions. Application of CRATER methodology to electrodissolution and electrodeposition is discussed.
机译:我们报告了使用同轴旋转,轴向平移电化学反应器(CRATER)在Al 6061上具有空间可控的微观结构的氧化膜的生长和表征。该仪器可以在传质,电极电势和停留时间的明确条件下,在单个工作电极(WE)上以具有空间可控的微观结构的氧化物膜生长。这是通过将电氧化限制在紧靠电解质自由表面正下方的狭窄轴向范围的“窗口”来实现的,电解质的自由内表面的同轴内,外边界分别是旋转的反电极和轴向平移的WE。此处报道的WE上的氧化物微观结构的轴向变化与WE上升期间电位的时间变化相对应,具有明显的单分散性和孔径分布的方位均匀性。通过这种方法在单个实验中连续扫描过程变量,可以在狭窄的操作条件范围内识别出所需的微结构。讨论了CRATER方法在电溶解和电沉积中的应用。

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