臭氧化多晶硅/单晶硅界面多晶硅发射极双极晶体管的研究

S. Niel, C. Hernandez, R. Pantel, I. Sagnes, M. Berenguer, J. Kirtsch, A. Monroy, A. Chantre, G. Vincent
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The HF+dry O3 process thus appears to be a good choice for stable thin poly/mono interfacial oxide preparation, allowing a longer delay time before polysilicon emitter deposition. Fig.1: Diiodomethane contact angle evolution in time for thermal oxide,HF+dryO3, HF+wetO3 Fig.2: Diiodomethane contact angle evolution in time for RCA, HF+dryO3, HF+wetO3 III) Experimental results In our 0.5μm BiCMOS technology the emitter window is opened by dry etching in an oxide layer (800A thickness) (superposition of deposited oxide and thermal oxide). Immediately after the interface preparation (discussed above), the wafers were loaded in the in-situ doped polysilicon reactor. The total thermal budget was 850°C/15min + 1025°C/20sec for the investigated process which had been optimized earlier for an HF interface treatment. Several characterizations were performed after device fabrication: FIB-TEM-EELS, TEM, SIMS. 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引用次数: 1

摘要

本文报道了一种新的多晶硅/单晶硅界面制备技术的发展,以调节双极晶体管的性能。通过对200mm 0.5μm BiCMOS技术的物理表征、静态和动态测量,证明了这项新技术的价值。多/单极界面处的氧对多发射极双极晶体管的性能有显著影响。特别是,众所周知,界面氧化层增加了电流增益和发射极电阻[1]。本文的目的是评价界面氧化形成的新技术。利用两种不同的臭氧化工艺,首次在原位掺杂发射极poly和Si之间的界面上引入了一层薄薄的氧化层。我们讨论了采用200mm 0.5μm准自对准BiCMOS技术制造的器件[2],并集成了臭氧化多/单界面的实验结果。臭氧(O3)的使用有利于硅表面可能存在的烃类残留物的燃烧,有利于硅表面的及时钝化和稳定化。为了测试不同的界面氧化物厚度,开发了两种不同的臭氧处理方法:i)第一种,HF +干O3,对应于众所周知的湿HF最后清洁后的O3气态处理。界面氧化物是在AST机器的气相清洗模块中,在100 hPa的室温下,经过60sec得到的,通过椭偏测量得出其厚度约为0.5-0.7nm[3]。第二,HF +湿O3,对应于经典HF后的湿清洗,O3气体在沉积过程之前在CHAMBER FLOW机器内的水中被稀释。界面层的等效氧化厚度(固定折射率为1.465)是前一种情况(1nm)的两倍。二碘甲烷接触角测量对表面性质很敏感[4],表明在这两种情况下,都存在氧化物生长(与参考热氧化物类似)(图1)。如图1所示,HF+干态O3界面的稳定性与热氧化界面相似,而HF+湿态O3界面的变化速度更快,与常规RCA制备的界面一样(图2)。因此,HF+干O3工艺似乎是制备稳定的薄聚/单界面氧化物的好选择,在多晶硅发射极沉积之前允许更长的延迟时间。图1:热氧化物、HF+dryO3、HF+wetO3的二碘甲烷接触角随时间的变化图2:RCA、HF+dryO3、HF+wetO3的二碘甲烷接触角随时间的变化图III)实验结果在0.5μm BiCMOS技术中,通过在氧化层(800A厚度)(沉积氧化物和热氧化物的叠加)中干刻蚀打开发射极窗口。在界面制备(如上所述)之后,硅片立即加载到原位掺杂多晶硅反应器中。研究过程的总热收支为850°C/15min + 1025°C/20sec,该过程早前针对HF界面处理进行了优化。器件制造后进行了几种表征:FIB-TEM-EELS, TEM, SIMS。图3显示了图4所示TEM横截面三个不同区域记录的EELS (Electron Energy Loss Spectroscopy)光谱。经过背景减除后的信号积分,提供了氧含量的定量评估(由530eV电离阈值识别)。数据表明,界面处的氧含量(3%)确实比多晶硅(0.7%)和单晶硅(0.5%)多。此外,SIMS结果显示臭氧化后界面氧剂量增加(表1),湿O3处理获得的氧剂量最大。P ho to di e C ou nt s Si多晶硅2K 500 550 600能量损耗(eV) 0.7% 500 550 600 Si单晶硅2K能量损耗(eV) 0.5% P ho to di e C ou nt s 2K 4K 500 550 600能量损耗(eV) 3% P ho to di e C ou nt s Ok
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An investigation of polysilicon emitter bipolar transistors with an ozonized polysilicon/monosilicon interface
This paper reports the development of a new polysilicon/monosilicon interface preparation technique to adjust bipolar transistor properties. The interest of this new technique is demonstrated using physical characterizations, static and dynamic measurements on a 200mm 0.5μm BiCMOS technology. I) Introduction Oxygen at the poly/mono interface significantly affects the performances of poly emitter bipolar transistors. In particular, it is well known that an interfacial oxide layer increases the current gain and emitter resistance [1]. The aim of this paper is to evaluate new techniques for interfacial oxide formation. For the first time, a thin oxide layer has been introduced at the interface between in-situ doped emitter poly and Si using two different types of ozonization processes. We discuss the experimental results obtained on devices fabricated in a 200mm 0.5μm quasi self-aligned BiCMOS technology [2], and integrating an ozonized poly/mono interface. II) Interface preparation The use of ozone (O3) is advantageous for the combustion of possible hydrocarbon residues on the silicon surface and for its passivation and stabilization in time. In order to test different interfacial oxide thicknesses, two different ozone processes have been developed: i ) The first, HF + dry O3, corresponds to an O3 gaseous treatment after the well-known wet HF last clean. The interfacial oxide was obtained in the vapor phase cleaning module of an AST machine at room temperature under 100 hPa for 60sec, and its thickness is around 0.5-0.7nm as deduced from ellipsometric measurements [3]. i i ) The second, HF + wet O3, corresponds to a wet cleaning after the classical HF last, the O3 gas being diluted in water inside the CHAMBER FLOW machine before the deposition process. The equivalent oxide thickness (measured with a fixed refraction index of 1.465) of the interfacial layer is twice that of in the previous case (1nm). Diiodomethane contact angle measurements, which are sensitive to surface properties [4], suggest that in both cases, there is oxide growth (by analogy with reference thermal oxide) (Fig.1). As shown in Fig.1, the stability of the HF+dry O3 interface is similar to that of thermal oxide, while the HF+wet O3 changes more rapidly, as does the more conventional RCA prepared interface (Fig.2). The HF+dry O3 process thus appears to be a good choice for stable thin poly/mono interfacial oxide preparation, allowing a longer delay time before polysilicon emitter deposition. Fig.1: Diiodomethane contact angle evolution in time for thermal oxide,HF+dryO3, HF+wetO3 Fig.2: Diiodomethane contact angle evolution in time for RCA, HF+dryO3, HF+wetO3 III) Experimental results In our 0.5μm BiCMOS technology the emitter window is opened by dry etching in an oxide layer (800A thickness) (superposition of deposited oxide and thermal oxide). Immediately after the interface preparation (discussed above), the wafers were loaded in the in-situ doped polysilicon reactor. The total thermal budget was 850°C/15min + 1025°C/20sec for the investigated process which had been optimized earlier for an HF interface treatment. Several characterizations were performed after device fabrication: FIB-TEM-EELS, TEM, SIMS. Fig.3 shows EELS (Electron Energy Loss Spectroscopy) spectra recorded on the three different regions of the TEM cross-section shown in Fig.4. The integral of the signal, after background subtraction, provides a quantitative evaluation of the oxygen content (identified by the 530eV ionization threshold). The data show that there is indeed more oxygen at the interface (3%) than in the poly (0.7%) or in the monosilicon (0.5%). In addition, SIMS results show an increase in the interfacial oxygen dose after ozonization (Table 1), the largest oxygen dose being obtained for the wet O3 treatment. P ho to di od e C ou nt s Si poly 2K 500 550 600 Energy Loss (eV) 0,7% 500 550 600 Si mono 2K Energy Loss (eV) 0,5% P ho to di od e C ou nt s Interface 2K 4K 500 550 600 Energy Loss (eV) 3% P ho to di od e C ou nt s Ok
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