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Hypothetic impact of chemical bonding on the moisture resistance of amorphous SixNyHz by plasma-enhanced chemical vapor deposition

机译:化学键合对等离子体增强化学气相沉积无定形六杆菌耐水湿性的假设影响

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The relationship between the microstructure of silicon nitride and its sensitivity to moisture was studied. The effectiveness of Si-H rich and N-H rich silicon nitride layers was measured under attack from water in vapor and liquid states. For water vapor attack, samples are exposed to vapor at 85 degrees C with a relative humidity of 85% during 1600 hours; for liquid water attack, samples are dipped in water at 60, 85 and 100 degrees C for 200 hours. The water resistance of the Si-H rich and N-H rich silicon nitride layers was evaluated by measuring: (i) the thickness of the silicon dioxide formed after their oxidation with water vapor, (ii) the rate of dissolution of the silicon nitride in liquid water and (iii) the corresponding activation of energy. This evaluation was performed by coupling spectroscopic ellipsometry, infra-red and X-ray photoelectron spectrometry analyses. The results revealed that for Si-H rich layer, 10 nm of silicon dioxide was formed during the water vapor attack; for liquid water attack, a high activation energy (0.88 eV) and a low dissolution rate were observed regardless of the water temperature. For N-H rich layers, approximatively 6 8 nm of silicon dioxide was formed and a low activation energy (0.64 eV) with a high dissolution rate were observed. All of these observations lead to the conclusion that the N-H rich layers could be less resistant to moisture because the isoelectronic relationship between Si2N-H and -H2O facilitated their deterioration in water. Moreover, a higher rate of nanoporosity for N-H rich layers than Si-H rich layer could complete this hypothesis.
机译:研究了氮化硅微观结构与其对水分敏感之间的关系。在蒸汽和液态中的水中测量Si-H富含和N-H富硅氮化硅层的有效性。对于水蒸气攻击,样品在85℃下暴露于蒸汽,在1600小时内相对湿度为85%;对于液体水攻击,样品在60,85和100摄氏度下浸入水中200小时。通过测量:(i)通过水蒸气氧化后形成的二氧化硅的厚度来评价Si-H富含氮氮化硅层的耐水性,(ii)氮化硅氮化硅溶解速率水和(iii)相应的能量激活。通过耦合光谱椭偏针,红外线和X射线光电子光谱分析来进行该评估。结果表明,对于富酸层,在水蒸气攻击期间形成10nm二氧化硅;对于液体水攻击,无论水温如何,观察到高激活能量(0.88eV)和低溶解速率。对于N-H富含层,形成近似68nm二氧化硅,并且观察到具有高溶解速率的低活化能量(0.64eV)。所有这些观察结果都会导致正常的结论是,由于Si2N-H和-H2O之间的等电子关系促进了它们在水中的劣化。此外,对于富含Si-H层的N-H层的纳米孔隙率较高,可以完成该假设。

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