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Study of low-temperature direct bonding of (111) and (100) silicon wafers under various ambient and surface conditions

机译:在各种环境和表面条件下对(111)和(100)硅片进行低温直接键合的研究

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Wafer bonding of commercially available (100) and (111) silicon wafers was performed in the range of temperatures from 80℃ to 400℃ in nitrogen, oxygen and low-vacuum atmosphere. Surface preparation with modified RCA cleaning method and hot nitric acid provided extremely clean and hydrophilic surfaces that were later brought into intimate contact. Various combinations of surface terminations such as thin chemical native silicon dioxide and thick thermal silicon dioxide on (111)- and (100)-oriented silicon wafers were prepared and investigated. Bonding quality evaluated by the tensile strength measurements showed the highest values obtained for strengthening in nitrogen atmosphere, reaching 12 MPa. Correlation between prebonding treatment, initial surface roughness and microroughness was made revealing the influence on the bonding energy. Interface imperfections of bonded samples were investigated by infrared transmission imaging revealing bubbles at the bonded interface only in case when bonding was performed in oxygen ambient. Thickness of the chemical native oxide after surface preparation step necessary for good bonding was found to be at least 0.8 nm. Wafers in the (111) orientation exhibited higher bonding abilities compared to (100) in case of bonding wafers with native oxides. This is believed to be due to higher density of available bonding sites as a consequence of enhanced chemical oxide growth rate and its homogeneity on (111) surface. Moreover, it is believed that due to higher positive charge of oxides grown on (111)-oriented silicon compared to (100), desorption of interfacial water is accelerated thus increasing the bonding energy at lower temperature. In conclusion, the best bonding results were obtained by bonding wafers with thick thermal oxide to (111) wafers with native oxide and annealed in nitrogen ambient.
机译:市售的(100)和(111)硅晶圆的晶圆键合是在氮气,氧气和低真空气氛中,在80℃至400℃的温度范围内进行的。使用改进的RCA清洁方法和热硝酸进行的表面处理提供了极其清洁和亲水的表面,随后使它们紧密接触。制备并研究了在(111)和(100)取向的硅片上的各种表面终止剂的组合,例如薄的化学天然二氧化硅和厚的热二氧化硅。通过拉伸强度测量评估的粘合质量显示出在氮气氛中获得的最高强度值,达到12 MPa。进行预粘结处理,初始表面粗糙度和微粗糙度之间的相关性,揭示了对粘结能的影响。通过红外透射成像研究键合样品的界面缺陷,只有在氧气环境中进行键合时,才显示键合界面处有气泡。已经发现,在表面制备步骤之后,对于良好结合而言,化学天然氧化物的厚度至少为0.8nm。与用天然氧化物键合晶片的情况相比,(111)取向的晶片显示出更高的键合能力。据信这是由于提高的化学氧化物生长速率及其在(111)表面上的均质性导致的可用结合位点的更高密度。此外,据信由于与(100)相比,在(111)取向的硅上生长的氧化物具有更高的正电荷,界面水的解吸得以加速,从而在较低温度下增加了键合能。总之,通过将具有厚热氧化物的晶片与具有天然氧化物的(111)晶片粘合并在氮气环境中退火,可以获得最佳的粘合结果。

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