首页> 外文学位 >Nickel-titanium and nickel-titanium-hafnium shape-memory thin films.
【24h】

Nickel-titanium and nickel-titanium-hafnium shape-memory thin films.

机译:镍钛和镍钛-形状记忆薄膜。

获取原文
获取原文并翻译 | 示例

摘要

Polycrystalline Ti-rich NiTi thin films and (TiHf)-rich NiTiHf thin films containing 9at% Hf were investigated. These films were deposited from single NiTi and NiTiHf targets using a DC magnetron sputtering system. Free-standing film was obtained by using a single crystal silicon substrate. Thickness of these thin films was controlled at around 10–12 μm. In this investigation, the effect of deposition temperature on the microstructure and transformation temperatures of the thin films was studied. Influence of post heat treatment temperature on the properties of the thin films was also investigated. Transformation temperatures of these thin films were determined by differential scanning calorimetry (DSC). Surface and cross-sectional morphology of the films were studied using a scanning electron microscope (SEM). Crystallography is determined using x-ray diffractometry.; Thin films deposited on a hot substrate are crystalline in anture even when the substrate temperatures are as low as 300°C, while the normal crystallization temperature of NiTi-based shape memory alloy is around 500°C. Microstructure of the films deposited on a hot substrate shows a very fine grain size. The grain size increases with increasing substrate temperature during deposition. The effect of post heat treatment on grain size is minimal. For both NiTi and NiTiHf thin films, martensite and austenite transformation temperatures increase with increasing deposition temperature and increasing post heat treatment temperature. R-phase, which was detected only in NiTi thin films, was found to be much less sensitive to the deposition temperature and post heat treatment temperature. No R-phase was observed in the NiTiHf thin films. Miller indices and lattice parameters of different crystal structures were calculated. Thermal hysteresis of above alloys was also analyzed. Thermal hysteresis of NiTi decreases with increasing deposition temperature and post heat treatment temperature. On the contrary, thermal hysteresis of NiTiHf increases. The observed behaviors of NiTi and NiTiHf thin films are a complex influence from internal stresses, internal defects, crystallography and second phases. For example, with elevated deposition temperature and post heat treatment temperature, internal defects are either rearranged or removed and internal stresses decrease. As a result, both martensite and austenite transformation temperatures increase. Besides, with increasing deposition temperature and post heat treatment temperature, more and more second phases precipitate out. This makes the matrix of the films more thermodynamically stable and strengthens the structure of martensite. Consequently, transformation temperature of martensite and austenite increase.
机译:研究了含有9at%Hf的多晶富TiNiTi薄膜和富(TiHf)NiTiHf薄膜。使用直流磁控溅射系统从单个NiTi和NiTiHf靶沉积这些膜。通过使用单晶硅衬底获得自支撑膜。这些薄膜的厚度控制在10–12μm左右。在这项研究中,研究了沉积温度对薄膜的微观结构和转变温度的影响。还研究了后热处理温度对薄膜性能的影响。这些薄膜的转变温度通过差示扫描量热法(DSC)确定。使用扫描电子显微镜(SEM)研究了膜的表面和截面形态。晶体学用X射线衍射法测定。即使当衬底温度低至300°C时,沉积在热衬底上的薄膜仍会结晶,而NiTi基形状记忆合金的正常结晶温度约为500°C。沉积在热基板上的薄膜的微观结构显示出非常细的晶粒尺寸。沉积过程中,晶粒尺寸随基底温度的升高而增加。后热处理对晶粒尺寸的影响最小。对于NiTi和NiTiHf薄膜,马氏体和奥氏体相变温度随着沉积温度的升高和后热处理温度的升高而升高。发现仅在NiTi薄膜中检测到的R相对沉积温度和后热处理温度的敏感度低得多。在NiTiHf薄膜中未观察到R相。计算了不同晶体结构的米勒指数和晶格参数。还分析了上述合金的热滞。 NiTi的热磁滞随沉积温度和后热处理温度的升高而降低。相反,NiTiHf的热磁滞增加。 NiTi和NiTiHf薄膜的观察行为是内部应力,内部缺陷,晶体学和第二相的复杂影响。例如,随着升高的沉积温度和后热处理温度,内部缺陷被重新布置或去除并且内部应力减小。结果,马氏体和奥氏体相变温度均升高。此外,随着沉积温度和后热处理温度的升高,越来越多的第二相析出。这使薄膜的基体在热力学上更稳定,并增强了马氏体的结构。因此,马氏体和奥氏体的相变温度升高。

著录项

  • 作者

    Zhang, Chen.;

  • 作者单位

    Auburn University.;

  • 授予单位 Auburn University.;
  • 学科 Engineering Materials Science.; Engineering Electronics and Electrical.
  • 学位 Ph.D.
  • 年度 2000
  • 页码 172 p.
  • 总页数 172
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 工程材料学;无线电电子学、电信技术;
  • 关键词

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