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Hydrogenation during thermal nitridation of silicon dioxide

机译:二氧化硅热氮化过程中的氢化

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The incorporation of nitrogen and hydrogen during nitridation of SiO2 was studied over the temperature range of 800–1000 °C and for ammonia pressures of 1, 5, and 10 atm. The nitrogen content of the nitrided films was determined with Rutherford‐backscattering spectrometry and elastic‐recoil detection. Nitrogen in‐depth profiles were obtained applying Auger analysis combined with ion sputtering. Hydrogen profiles in the films were measured using nuclear‐reaction analysis. Both the nitrogen and hydrogen incorporation were found to increase with temperature in this range. A higher ammonia pressure primarily increases nitridation of the bulk of the oxide films. Depending on the nitridation conditions, up to 10 at.% of hydrogen may be incorporated. As distinct from the nitrogen profiles, the hydrogen in‐depth profiles are essentially flat. The concentration of hydrogen in the films, however, was always found to be smaller than that of nitrogen: measured H/N ratios varied between 0.25 and 0.85, the smaller values being obtained for the thinner oxides and higher nitridation temperatures. The model previously postulated to explain the nitrogen incorporation during atmospheric nitridation of SiO2 proves to be valid at higher pressures as well. By considering the role of OH as a reaction product of the nitridation process, the hydrogen results can be accommodated within the same concept. The model predicts a low H/N‐incorporation ratio for a thin surface and interface layer and a substantially larger ratio for the bulk of the film. If this prediction is correct, which seems to be indicated by the etch‐rate behavior of the nitrided oxides, then this would have considerable importance for the electrical properties of this material.
机译:研究了在800–1000 temperatureC的温度范围内以及在1、5和10 atm的氨气压力下SiO2氮化过程中氮和氢的结合。氮化膜的氮含量通过卢瑟福反向散射光谱法和弹性反冲检测法测定。使用俄歇分析结合离子溅射获得了氮的深度分布图。使用核反应分析法测量薄膜中的氢分布。发现在该范围内,氮和氢的掺入均随温度增加。较高的氨压力主要增加了大部分氧化膜的氮化作用。取决于氮化条件,最多可掺入10 at。%的氢。与氮剖面不同,氢深度剖面基本上是平坦的。然而,总发现薄膜中的氢浓度小于氮浓度:测得的H / N比在0.25至0.85之间变化,对于更薄的氧化物和更高的氮化温度而言,值较小。先前推测用来解释SiO2大气氮化过程中氮掺入的模型也被证明在较高压力下也是有效的。通过考虑OH作为氮化过程的反应产物的作用,可以将氢的结果纳入同一概念。该模型预测,薄的表面和界面层的H / N掺入率低,而大部分薄膜的H / N掺入率则大得多。如果这种预测是正确的,这似乎是由氮化氧化物的蚀刻速率行为所表明的,那么这对于这种材料的电性能将具有相当重要的意义。

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    《Journal of Applied Physics》 |1986年第8期|P.2765-2772|共8页
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  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
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