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Characteristics of copper/carbon and nickel/carbon composite films produced by microwave plasma-assisted deposition techniques from argon–methane gas mixtures

机译:微波血浆辅助沉积技术从氩甲烷气体混合物中产生的铜/碳和碳复合膜的特性

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Copper/hydrogenated amorphous carbon (a-C:H) and nickel/a-C:H composite films have been deposited on Si substrates by combining sputter-deposition of metal and microwave plasma-assisted chemical vapor deposition of carbon from argon–methane mixtures of various concentrations. The deposition rate of films was found to vary between 10 and 25 nm/min depending on the CH4 concentration in the gas phase. The crystallographic structure of films was identified by X-ray diffraction (XRD) techniques. Diffraction peaks of the face-centered cubic (fcc) Cu phase were always detected in the XRD patterns of Cu/C films. Diffraction peaks of the fcc Ni phase appeared in the XRD patterns of Ni/C films deposited from gas mixtures containing less than 5% of CH4. Diffraction peaks of Ni and Ni3C phases were detectable in the XRD patterns of Ni/C films deposited from a gas phase containing 10% of CH4. For Ni/C films deposited with a CH4 concentration in the range 15–30%, the diffraction peaks in the XRD patterns were only ascribable to the Ni3C phase. Beyond 30% of CH4 in the gas phase, the structure of Ni/C films became progressively amorphous as the CH4 concentration increased. The grain size of Cu, Ni and Ni3C was determined as a function of the CH4 concentration. The residual stresses in Cu/C films were very low and independent of the CH4 concentration in the gas phase (or composition of films). For Ni–C films, the maximum value of compressive residual stresses was0.6 GPa for films deposited with 20% of CH4 in the gas phase (or for Ni/C films containing pure Ni3C phase). The electrical resistivity of films determined by four point probe measurements as well as the hardness and elastic modulus of films deduced from nanoindentation measurements were studied as functions of the CH4 concentration in the gas phase.
机译:通过将金属的溅射沉积与各种浓度的氩甲烷混合物组合,通过组合溅射沉积铜/氢化无定形碳(A-C:H)和镍/ A-C:H复合膜在Si底物上沉积在Si基材上。发现薄膜的沉积速率在10至25nm / min之间根据气相中的CH 4浓度而变化。通过X射线衍射(XRD)技术鉴定薄膜的晶体结构。始终在Cu / C膜的XRD图案中始终检测到面心立立方(FCC)Cu相的衍射峰。 FCC Ni相的衍射峰出现在沉积在含有小于5%CH 4的气体混合物的Ni / C膜的XRD图案中。在沉积在含有10%CH 4的气相的Ni / C膜的XRD图案中检测Ni和Ni3C相的衍射峰。对于沉积在15-30%范围内的CH 4浓度的Ni / C膜,XRD图案中的衍射峰仅易于Ni3C相。在气相中超过30%的CH4,随着CH 4浓度的增加,Ni / C膜的结构变得逐渐是无定形的。 Cu,Ni和Ni3c的晶粒尺寸被确定为CH 4浓度的函数。 Cu / C膜中的残余应力非常低,与气相(或薄膜组成)无关的CH 4浓度。对于Ni-C膜,压缩残余应力的最大值为0.6GPa,用于沉积20%的气相中的CH 4(或含有纯Ni3C相的Ni / C膜)。通过四点探针测量确定的薄膜的电阻率以及从纳米endentation测量中推导的薄膜的硬度和弹性模量作为气相中的CH 4浓度的功能。

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