Selective Rapid Thermal Chemical Vapor Deposition of Titanium Disilicide on Silicon and Polysilicon

1997 ◽  
Vol 470 ◽  
Author(s):  
Lixin Nie ◽  
Chad E. Weintraub ◽  
Mehmet C. Öztürk

ABSTRACTSelective rapid thermal chemical vapor deposition (RTCVD) of TiSi2 is a promising alternative to the conventional self-aligned suicide (SALICIDE) process to form low-resistivity contacts to ultra-shallow source/drain junctions of deep submicron MOS transistors. The process makes use of TiCl4 and SiH4 as the Ti and Si source gases in a temperature range of 750 – 825 °C. The primary advantage of the process over the conventional SALICIDE process is that by providing sufficient levels of Si from the gas phase, junction consumption can be eliminated. Furthermore, the process eliminates wet etch and reduces the number of process steps from four to one. For the process to be compatible with CMOS manufacturing, low-resistivity TiSi2 deposition must be achieved on both source/drain junctions as well as the poly cry stalline silicon gate electrode. It is the objective of this paper to compare basic characteristics of the process on these two surfaces. The results indicate that the crystallinity of the surface on which TiSi2 is deposited can impact the nature of the deposited film. Our experimental results indicate enhanced Si consumption on polysilicon, smaller TiSi2 grains and consequently higher sheet resistance. However, the process conditions and TiSi2 thickness can be optimized to achieve consumption free TiSi2 deposition on the junctions with acceptable performance on polysilicon.

1995 ◽  
Vol 387 ◽  
Author(s):  
Xiaowei Ren ◽  
Dannellia B. Gladden ◽  
Mehmet C. Öztürk ◽  
A. Dale Batchelor

AbstractDownscaling of microelectronics devices into the deep submicron regime requires ultrashallow junctions with reliable, low-resistivity contacts. The conventional self-aligned TiSi2 technology exhibits a serious limitation in forming contacts to ultra-shallow junctions due to silicon substrate consumption. Selective chemical vapor deposition of TiSi2 is being investigated because of its potential for overcoming this difficulty. In this process Si and Ti are supplied from the gas phase. The standard source gas for Ti has been TiCl4 while several gases including SiH4, Si2H6 and SiH2Cl2 are available for Si. The reports on this process indicate that optimized process conditions can deliver TiSi2 films without substrate consumption. Although this promise is significant, the deposition has a complicated chemistry involving processes such as silicon etching, silicon consumption or silicon pedestal deposition taking place along with TiSi2 deposition. Although, suppression of Si-substrate etching by excess H2 has been reported previously, a broad quantitative analysis has been lacking up until this reporting. In this work, we have examined silicon etching trends as a function of temperature for different H2:TiCl4 flow ratios using thermodynamic equilibrium calculations. We have also performed experiments in a lamp heated rapid thermal chemical vapor deposition reactor to study substrate etching over the temperature range of 600°C to 800°C and for H2 flows from 0 to 1000 sccm. A silicon conversion efficiency is defined as a measure of the amount of Si converted to TiSi2 relative to total Si used from the substrate and it is evaluated via both thermodynamic calculations and experiments with good agreement between the two. Our calculations suggest that at high temperatures, etching occurs mainly via formation of SiCl2. Addition of H2 into the reaction chemistry encourages formation of HCl reducing the amount of Cl available for SiCl2 formation responsible for substrate etching. Our results show that by optimizing the H2 flow rate and the process temperature silicon substrate etching can be effectively suppressed.


2017 ◽  
Vol 121 (47) ◽  
pp. 26465-26471 ◽  
Author(s):  
Mewlude Imam ◽  
Laurent Souqui ◽  
Jan Herritsch ◽  
Andreas Stegmüller ◽  
Carina Höglund ◽  
...  

2010 ◽  
Vol 133 (3) ◽  
Author(s):  
Myung Gwan Hahm ◽  
Young-Kyun Kwon ◽  
Ahmed Busnaina ◽  
Yung Joon Jung

Due to their unique one-dimensional nanostructure along with excellent mechanical, electrical, and optical properties, carbon nanotubes (CNTs) become a promising material for diverse nanotechnology applications. However, large-scale and structure controlled synthesis of CNTs still have many difficulties due to the lack of understanding of the fundamental growth mechanism of CNTs, as well as the difficulty of controlling atomic-scale physical and chemical reactions during the nanotube growth process. Especially, controlling the number of graphene wall, diameter, and chirality of CNTs are the most important issues that need to be solved to harness the full potential of CNTs. Here we report the large-scale selective synthesis of vertically aligned single walled carbon nanotubes (SWNTs) and double walled carbon nanotubes (DWNTs) by controlling the size of catalyst nanoparticles in the highly effective oxygen assisted thermal chemical vapor deposition (CVD) process. We also demonstrate a simple but powerful strategy for synthesizing ultrahigh density and diameter selected vertically aligned SWNTs through the precise control of carbon flow during a thermal CVD process.


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