首页> 外文期刊>Oxidation of Metals >Surface Analysis of Nickel-Oxide Films Modified by a Reactive Element
【24h】

Surface Analysis of Nickel-Oxide Films Modified by a Reactive Element

机译:反应性元素修饰的氧化镍薄膜的表面分析

获取原文
获取原文并翻译 | 示例
       

摘要

The surface morphology of oxide grown in the temperature range of 873-1173 K on modified high-purity nickel has been observed and quantitatively analyzed by atomic-force microscopy. The modifications included one of two finishing techniques and either CeO_2 sol-gel coatings or Ce-ion implantation. There is an essential difference in the surface morphology and grain size for oxides formed on Ce/CeO_2-modified nickel in comparison to pure NiO. The oxide topography also depends on the substrate-surface-finishing technique and the method of applying the cerium. Both Auger electron spectroscopy and Rutherford backscattering spectrometry were used to evaluate the depth composition of the oxide. In the modified oxide formed on chemically polished substrates the Ce generally appeared to be located close to the outer surface, even after long oxidation times. In oxide grown on mechanically polished substrates Ce was detectable by these techniques only during the very early stages of oxidation. A general correlation exists between the parameters describing the oxide-surface morphology and the Ce-depth distribution, and the reduction of the NiO growth rate achieved by applying the reactive element. Detailed analysis of the oxide surface, internal microstructure, and chemistry gives new insights into the problem of the characterization of thin oxide films and the mechanism of oxide formation.
机译:观察到了在873-1173 K温度范围内在改性高纯镍上生长的氧化物的表面形态,并通过原子力显微镜进行了定量分析。修改包括两种修整技术之一,以及CeO_2溶胶凝胶涂层或Ce离子注入。与纯NiO相比,Ce / CeO_2改性镍上形成的氧化物的表面形态和晶粒尺寸存在本质差异。氧化物的形貌还取决于基底表面修整技术和施加铈的方法。俄歇电子能谱和卢瑟福反向散射能谱均用于评估氧化物的深度组成。在化学抛光的基材上形成的改性氧化物中,即使经过长时间的氧化,铈通常也似乎位于靠近外表面的位置。在机械抛光的基板上生长的氧化物中,只有在氧化的非常早期,才可以通过这些技术检测到Ce。在描述氧化物表面形态和Ce深度分布的参数与通过应用反应性元素实现的NiO增长率降低之间存在普遍的相关性。对氧化物表面,内部微观结构和化学性质的详细分析,为研究薄氧化膜的表征问题和氧化物形成机理提供了新见识。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号