纳米氧化铬包埋镍薄膜的微观结构演变

Hagit Barda, L. Klinger, E. Rabkin
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引用次数: 1

摘要

研究了一种陶瓷纳米颗粒增强金属基复合薄膜的制备方法。为此,我们在蓝宝石衬底上沉积了20nm Ni /超薄cr -氧化物层/ 20nm Ni三层,并在700℃的温度下退火样品。研究发现,退火10 min后,cr -氧化物层团聚成单晶或双晶切面Cr2O3纳米颗粒,其取向关系为(11¯)Ni∥(0006)Cr2O3和[112]Ni∥[12¯10]Cr2O3与Ni基体的取向关系为(11¯)Ni∥(0006)Cr2O3。我们发现,相对于氧化铬层的初始位置,氧化铬颗粒的质心出现了令人惊讶的垂直扩散。我们建立了颗粒形状演变及其垂直漂移的动力学模型,从而可以估计Ni-Cr2O3界面的有效扩散系数(d1 = 7.4·10−19 m 2 s)。虽然比Ni中的晶界扩散慢得多,但这种界面扩散使超薄cr -氧化物层快速转变为嵌入Ni膜中的孤立的cr2o3纳米颗粒阵列。在本工作中获得的对系统动力学的深入了解为金属薄膜的颗粒增强设计铺平了道路,并精确控制了颗粒的空间位置。
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Microstructure Evolution of Thin Nickel Films with Embedded Chromium Oxide Nanoparticles
Abstract We developed a fabrication method of thin metal matrix composite films reinforced with ceramic nanoparticles. To this end, we deposited a 20 nm Ni / ultrathin Cr-oxide layer / 20 nm Ni tri-layer on a sapphire substrate, and annealed the sample at the temperature of 700°C. We found that after annealing for 10 min the Cr-oxide layer agglomerates into single- or bi-crystalline faceted Cr2O3 nanoparticles, with the orientation relationship of ( 11 1 ¯ ) N i ∥ ( 0006 ) C r 2 O 3 and [ 112 ] N i ∥ [ 1 2 ¯ 10 ] C r 2 O 3 to the Ni matrix. We encountered a surprising vertical spread of the centers of mass of the Cr-oxide particles with respect to the initial position of the Cr-oxide layer. We developed a kinetic model of the evolution of particles shape and of their vertical drift, which enabled an estimate of the effective diffusion coefficient of the Ni-Cr2O3 interface ( D i = 7.4 · 10 − 19 m 2 s ). Though much slower than grain boundary diffusion in Ni, this interface diffusion enables fast transformation of ultra-thin Cr-oxide layer into an array of isolated Cr2O3nanoparticles embedded in the Ni film. The insight into the kinetics of the system obtained in the present work paves the way for the design of particle reinforcement of thin metal films with a precise control over the spatial positions of the particles.
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