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Atomic layer deposition of interface control layers for the fabrication of III/V MOS devices

机译:用于制造III / V MOS器件的界面控制层的原子层沉积

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摘要

The continued advancement of metal oxide semiconductor field effect transistor (MOSFET) technology has shifted the focus from Si/SiO2 transistors towards high-κ/III-V transistors for high performance, faster devices. This has been necessary due to the limitations associated with the scaling of the SiO2 thickness below ~1 nm and the associated increased leakage current due to direct electron tunnelling through the gate oxide. The use of these materials exhibiting lower effective charge carrier mass in conjunction with the use of a high-κ gate oxide allows for the continuation of device scaling and increases in the associated MOSFET device performance. The high-κ/III-V interface is a critical challenge to the integration of high-κ dielectrics on III-V channels. The interfacial chemistry of the high-κ/III-V system is more complex than Si, due to the nature of the multitude of potential native oxide chemistries at the surface with the resultant interfacial layer showing poor electrical insulating properties when high-κ dielectrics are deposited directly on these oxides. It is necessary to ensure that a good quality interface is formed in order to reduce leakage and interface state defect density to maximise channel mobility and reduce variability and power dissipation. In this work, the ALD growth of aluminium oxide (Al2O3) and hafnium oxide (HfO2) after various surface pre-treatments was carried out, with the aim of improving the high-κ/III-V interface by reducing the Dit – the density of interface defects caused by imperfections such as dangling bonds, dimers and other unsatisfied bonds at the interfaces of materials. A brief investigation was performed into the structural and electrical properties of Al2O3 films deposited on In0.53Ga0.47As at 200 and 300oC via a novel amidinate precursor. Samples were determined to experience a severe nucleation delay when deposited directly on native oxides, leading to diminished functionality as a gate insulator due to largely reduced growth per cycle. Aluminium oxide MOS capacitors were prepared by ALD and the electrical characteristics of GaAs, In0.53Ga0.47As and InP capacitors which had been exposed to pre-pulse treatments from triethyl gallium and trimethyl indium were examined, to determine if self-cleaning reactions similar to those of trimethyl aluminium occur for other alkyl precursors. An improved C-V characteristic was observed for GaAs devices indicating an improved interface possibly indicating an improvement of the surface upon pre-pulsing with TEG, conversely degraded electrical characteristics observed for In0.53Ga0.47As and InP MOS devices after pre-treatment with triethyl gallium and trimethyl indium respectively. The electrical characteristics of Al2O3/In0.53Ga0.47As MOS capacitors after in-situ H2/Ar plasma treatment or in-situ ammonium sulphide passivation were investigated and estimates of interface Dit calculated. The use of plasma reduced the amount of interface defects as evidenced in the improved C-V characteristics. Samples treated with ammonium sulphide in the ALD chamber were found to display no significant improvement of the high-κ/III-V interface. HfO2 MOS capacitors were fabricated using two different precursors comparing the industry standard hafnium chloride process with deposition from amide precursors incorporating a ~1nm interface control layer of aluminium oxide and the structural and electrical properties investigated. Capacitors furnished from the chloride process exhibited lower hysteresis and improved C-V characteristics as compared to that of hafnium dioxide grown from an amide precursor, an indication that no etching of the film takes place using the chloride precursor in conjunction with a 1nm interlayer. Optimisation of the amide process was carried out and scaled samples electrically characterised in order to determine if reduced bilayer structures display improved electrical characteristics. Samples were determined to exhibit good electrical characteristics with a low midgap Dit indicative of an unpinned Fermi level
机译:金属氧化物半导体场效应晶体管(MOSFET)技术的不断发展已将重点从Si / SiO2晶体管转移到了高性能,更快器件的高κ/ III-V晶体管上。由于与小于约1nm的SiO 2厚度的缩放相关联的限制以及由于直接电子隧穿通过栅极氧化物引起的相关的增加的泄漏电流,因此这是必需的。这些材料的有效电荷载流子质量较低,再加上高κ栅极氧化层的使用,可继续进行器件缩放,并提高相关MOSFET器件的性能。高κ/ III-V界面是在III-V通道上集成高κ电介质的关键挑战。高κ/ III-V系统的界面化学比Si更复杂,这是由于表面上存在大量潜在的天然氧化物化学性质,当高κ介电常数为0时,所得界面层显示出较差的电绝缘性能。直接沉积在这些氧化物上。必须确保形成高质量的接口,以减少泄漏和接口状态缺陷密度,以最大程度地提高通道迁移率并减少可变性和功耗。在这项工作中,进行了各种表面预处理后的氧化铝(Al2O3)和氧化ha(HfO2)的ALD生长,目的是通过降低Dit –密度来改善高κ/ III-V界面缺陷造成的界面缺陷,如材料界面处的悬空键,二聚体和其他不满意的键。对在200和300oC下通过新型a酰胺前体沉积在In0.53Ga0.47As上的Al2O3膜的结构和电学性能进行了简要研究。当样品直接沉积在天然氧化物上时,样品会经历严重的成核延迟,由于每个周期的生长大大降低,导致作为栅极绝缘体的功能降低。通过原子层沉积法制备氧化铝MOS电容器,并检查了已接受三乙基镓和三甲基铟预脉冲处理的GaAs,In0.53Ga0.47As和InP电容器的电学特性,以确定自清洁反应是否类似于三甲基铝的那些存在于其他烷基前体中。观察到GaAs器件的CV特性得到改善,表明界面改善,可能表明在用TEG预脉冲后表面得到了改善,而In0.53Ga0.47As和InP MOS器件经三乙基镓和三氯甲烷预处理后观察到的电特性降低。三甲基铟。研究了原位H2 / Ar等离子体处理或原位硫化铵钝化后的Al2O3 / In0.53Ga0.47As MOS电容器的电学特性,并计算了界面Dit的估计值。等离子体的使用减少了界面缺陷的数量,这在改善的C-V特性中得到了证明。发现在ALD室中用硫化铵处理过的样品没有显示出高κ/ III-V界面的显着改善。 HfO2 MOS电容器是使用两种不同的前体制造的,将工业标准氯化ha工艺与酰胺前体的沉积进行了比较,其中酰胺前体中掺入了约1nm的氧化铝界面控制层,并研究了结构和电性能。与从酰胺前体中生长的二氧化ha相比,由氯化物工艺提供的电容器表现出较低的磁滞现象和改善的C-V特性,这表明使用氯化物前体与1nm中间层结合不会对膜进行蚀刻。进行了酰胺工艺的优化,并对定标的样品进行了电学表征,以确定降低的双层结构是否显示出改善的电学特性。确定样品表现出良好的电特性,并且低中间能隙Dit表示未固定的费米能级

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    Mullins John A.;

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  • 年度 2014
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