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[[Specific_Process_Knowledge/Thin_film_deposition/Sputter_coater#Sputter_coater_03_(Cressington)|Sputter coater 03]] is mainly used for sample preparation before [[Specific_Process_Knowledge/Characterization/SEM: Scanning Electron Microscopy|SEM inspection]]. Usually, [[Specific_Process_Knowledge/Thin_film_deposition/Deposition_of_Gold|Au]] is sputtered on dielectric surfaces to compensate for charge build-up. Alternatively, many other materials can be sputtered if the setup allows (you need to have a turbo pump and Ar gas). Gold can be deposited even in pure oxygen plasma and only with roughing pumps. Fortunately, Sputter Coater 3 located in the basement of building 346, has both a turbo pump and an Ar working gas source. The pressure during the process is measured to be below 0.1 mBar. This page describes deposition of tungsten (W) with this instrument.
[[Specific_Process_Knowledge/Thin_film_deposition/Sputter_coater#Sputter_coater_03_(Cressington)|Sputter coater 03]] is mainly used for sample preparation before [[Specific_Process_Knowledge/Characterization/SEM: Scanning Electron Microscopy|SEM inspection]]. Usually, [[Specific_Process_Knowledge/Thin_film_deposition/Deposition_of_Gold|Au]] is sputtered on dielectric surfaces to compensate for charge build-up. Alternatively, many other materials can be sputtered if the setup allows (you need to have a turbo pump and Ar gas). Gold can be deposited even in pure oxygen plasma and only with roughing pumps. Fortunately, Sputter Coater 3, located in the basement of building 346, has both a turbo pump and an Ar working gas source. The pressure during the process is measured to be below 0.1 mBar. This page describes the deposition of tungsten (W) with this instrument.


The prepared samples were investigated by the [[Specific Process Knowledge/Characterization/XRD/XRD_SmartLab|X-ray Reflectivity (XRR)]], [[Specific_Process_Knowledge/Characterization/SEM: Scanning Electron Microscopy|Scanning Electron Microscopy (SEM)]] and [[Specific Process Knowledge/Characterization/XPS|Photo Electron Spectroscopy (XPS) methods]]. The focus of the study was the deposition conditions.
The prepared samples were investigated by the [[Specific Process Knowledge/Characterization/XRD/XRD_SmartLab|X-ray Reflectivity (XRR)]], [[Specific_Process_Knowledge/Characterization/SEM: Scanning Electron Microscopy|Scanning Electron Microscopy (SEM)]] and [[Specific Process Knowledge/Characterization/XPS|Photo Electron Spectroscopy (XPS) methods]]. The focus of the study was the deposition conditions.
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In summary, the tungsten films produced by Sputter-Coater 3 are of poor quality. The user can install a big (15 cm high glass chamber). In this case, the deposition rate is very low (0.033 nm/s) and the film will contain a high level of oxygen (up to 50%). This can be partially improved by installing a smaller chamber (6.5 cm high). However, this leads to a very bad uniformity disregardless of which current settings are used.  Depositing on small samples (around 1x1 cm) placed in the middle of the chamber will be the most acceptable procedure. Nevertheless, the elevated level of oxygen and rough and porous structure will limit the applicability.
In summary, the tungsten films produced by Sputter-Coater 3 are of poor quality. The user can install a big (15 cm high glass chamber. In this case, the deposition rate is very low (0.033 nm/s), and the film will contain a high level of oxygen (up to 50%). This can be partially improved by installing a smaller chamber (6.5 cm high). However, this leads to very poor uniformity regardless of the current settings used.  Depositing on small samples (approximately 1 cm x 1 cm) placed in the center of the chamber will be the most acceptable procedure. Nevertheless, the elevated level of oxygen and the rough, porous structure will limit its applicability.


Tungsten (W) from Sputter Coater 3 is not recommended as a part of sample preparation before SEM inspection. It is better to use Au.
Tungsten (W) from Sputter Coater 3 is not recommended as a part of sample preparation before SEM inspection. It is better to use Au.
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=Big glass configuration (15 cm high)=   
=Big glass configuration (15 cm high)=   


In the beginning, a big glass chamber was installed in the instrument. It was quickly revealed that the deposition rate is very low, so only the highest current setting (80 mA) was used in the experiment.
Initially, a large glass chamber was installed in the instrument. It was quickly revealed that the deposition rate is very low, so only the highest current setting (80 mA) was used in the experiment.


The maximum time the user can select is 300s, so if longer depositions are needed the user has to redo it several times to achieve an expected thickness.
The maximum time the user can select is 300 seconds, so if longer depositions are needed, the user must redo them several times to achieve the expected thickness.


<gallery caption="Big glass chamber setup." widths="500px" heights="500px" perrow="2">
<gallery caption="Big glass chamber setup." widths="500px" heights="500px" perrow="2">
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==SEM Inspection==
==SEM Inspection==


The samples with low aspect ratio Si trenches (500 nm deep, 200 nm wide with a pitch of 400 nm) were used to illustrate the deposition morphology (Instrument: [[Specific_Process_Knowledge/Characterization/SEM_Supra_1|SEM Supra 1]]). To make the result more visible it was deposited <b>twice</b> at the maximum allowed deposition time (2x300s). The SEM results are shown below.
The samples with low aspect ratio Si trenches (500 nm deep, 200 nm wide with a pitch of 400 nm) were used to illustrate the deposition morphology (Instrument: [[Specific_Process_Knowledge/Characterization/SEM_Supra_1|SEM Supra 1]]). To make the result more visible, it was deposited <b>twice</b> at the maximum allowed deposition time (2 × 300 s). The SEM results are shown below.




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X-ray photoelectron spectroscopy (Instrument: [[Specific Process Knowledge/Characterization/XPS/K-Alpha|XPS K-Alpha]]) has been applied to investigate the chemical content and stoichiometry.
X-ray photoelectron spectroscopy (Instrument: [[Specific Process Knowledge/Characterization/XPS/K-Alpha|XPS K-Alpha]]) has been applied to investigate the chemical content and stoichiometry.


The samples used for the XPS analysis were prepared in a big glass chamber with 80mA current and a deposition time of 300s.The pressure is measured to be below 0.1 mBar.
The samples used for the XPS analysis were prepared in a large glass chamber with an 80 mA current and a deposition time of 300 seconds. The pressure is measured to be below 0.1 mBar.


The analysis reveals that the top surface is a native oxide, while the thin layer itself is partially oxidized tungsten. The stoichiometry shows 50%W and 50% O. The stoichiometric tungsten oxide has a form of WO<sub>3</sub>, so the layer itself contains metallic W around 33% mixed with up to 67% oxide. This is not a big surprise since this tool does not have shutter mechanisms or a long well controlled pumping system. The deposition rate is also very low due to the limited power. This also contributes to the elevated oxygen level in the film.
The analysis reveals that the top surface is a native oxide, while the thin layer itself is partially oxidized tungsten. The stoichiometry indicates a 50%W and 50%O composition. The stoichiometric tungsten oxide has a form of WO<sub>3</sub>; therefore, the layer itself contains approximately 33% metallic W, mixed with up to 67% oxide. This is not a big surprise, as this tool lacks shutter mechanisms and a long, well-controlled pumping system. The deposition rate is also very low due to the limited power. This also contributes to the elevated oxygen level in the film.


<gallery caption="XPS depth profile of W thin film. Indicates the presence of native W oxide, the W thin film, and silicon substrate with native oxide." widths="1200px" heights="500px" perrow="1">
<gallery caption="XPS depth profile of W thin film. Indicates the presence of native W oxide, the W thin film, and silicon substrate with native oxide." widths="1200px" heights="500px" perrow="1">
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=Small glass configuration (6.5 cm high)=
=Small glass configuration (6.5 cm high)=


In the next part of the experiment, a small (6.5 cm high) chamber was installed in the instrument. The deposition rate is much higher in this case, so the different current settings (20-80 mA) were employed. The consequence of the higher deposition rate was a very bad uniformity, such as the center of the wafer getting a full thickness, while the edges of the wafer were not covered at all. This deposition mode is better suited for small samples/chips. The produced films revealed high roughness and pronounced porosity revealed by XRR.
In the next part of the experiment, a small (6.5 cm high) chamber was installed in the instrument. The deposition rate is much higher in this case, so the different current settings (20-80 mA) were employed. The consequence of the higher deposition rate was very poor uniformity, with the center of the wafer receiving a full thickness, while the edges remained uncovered. This deposition mode is better suited for small samples/chips. The produced films exhibited high roughness and pronounced porosity, as revealed by XRR.




<gallery caption="Small glass chamber setup." widths="500px" heights="500px" perrow="2">
<gallery caption="Small glass chamber setup." widths="400px" heights="350px" perrow="2">
image:eves_W_sputter_coater_3_small_glass_01_20220914.png| Small glass configuration.
image:eves_W_sputter_coater_3_small_glass_01_20220914.png| Small glass configuration.
image:eves_W_sputter_coater_3_small_glass_02_20220914.png| Glow discharge in the deposition chamber.
image:eves_W_sputter_coater_3_small_glass_02_20220914.png| Glow discharge in the deposition chamber.
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==SEM Inspection==
==SEM Inspection==


<gallery caption="Small glass chamber setup. Flat films deposited on a Si wafers at different current settings." widths="300px" heights="300px" perrow="4">
<gallery caption="Small glass chamber setup. Flat films deposited on a Si wafer at different current settings." widths="190px" heights="150px" perrow="4">
image:eves_W_sputter_coater_3_small_glass_flat_20mA_300s_20220915.png| 20mA, 300s deposition time.
image:eves_W_sputter_coater_3_small_glass_flat_20mA_300s_20220915.png| 20mA, 300s deposition time.
image:eves_W_sputter_coater_3_small_glass_flat_40mA_300s_20220915.png| 40mA, 300s deposition time.
image:eves_W_sputter_coater_3_small_glass_flat_40mA_300s_20220915.png| 40mA, 300s deposition time.
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==Deposition rate and Uniformity==
==Deposition rate and Uniformity==


<gallery caption="Small glass chamber setup. Flat films deposted on a Si wafers at different current settings." widths="300px" heights="300px" perrow="4">
<gallery caption="Small glass chamber setup. Flat films deposited on Si wafers at different current settings." widths="190px" heights="150px" perrow="4">
image:eves_W_sputter_coater_3_small_glass_uniformity_20mA_300s_20220915.png| 20mA, 300s deposition time.
image:eves_W_sputter_coater_3_small_glass_uniformity_20mA_300s_20220915.png| 20mA, 300s deposition time.
image:eves_W_sputter_coater_3_small_glass_uniformity_40mA_300s_20220915.png| 40mA, 300s deposition time.
image:eves_W_sputter_coater_3_small_glass_uniformity_40mA_300s_20220915.png| 40mA, 300s deposition time.
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To measure the deposition rate the samples were cleaved, and only the center part was inspected, as the edges almost do not have a layer.
To measure the deposition rate the samples were cleaved, and only the center part was inspected, as the edges almost do not have a layer.


<gallery caption="Small glass chamber setup. Deposition rate as a function of current." widths="500px" heights="400px" perrow="2">
<gallery caption="Small glass chamber setup. Deposition rate as a function of current." widths="400px" heights="350px" perrow="2">
image:eves_W_sputter_coater_3_small_glass_dep_rate_1_20220918.png| Thickness as a function of current. Measured after 300s deposition, in the middle of the sample.
image:eves_W_sputter_coater_3_small_glass_dep_rate_1_20220918.png| Thickness as a function of current. Measured after 300s deposition, in the middle of the sample.
image:eves_W_sputter_coater_3_small_glass_dep_rate_2_20220918.png| Deposition rate as a function of current. Measured after 300s deposition, in the middle of the sample.
image:eves_W_sputter_coater_3_small_glass_dep_rate_2_20220918.png| Deposition rate as a function of current. Measured after 300s deposition, in the middle of the sample.
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==X-ray reflectivity==
==X-ray reflectivity==


Deposition of W in Sputter Coater 3 using a small glass (6.5cm high) glass chamber configuration is fast, but the resulting coatings are still expected to have a significant fraction of oxygen. Although XPS measurements were not performed on these films, the sheet resistance values were very high if compared with pure tungsten layers.  
The deposition of W in Sputter Coater 3 using a small glass chamber (6.5 cm high) configuration is fast, but the resulting coatings are still expected to contain a significant fraction of oxygen. Although XPS measurements were not performed on these films, the sheet resistance values were significantly higher compared to pure tungsten layers.  




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Another issue is the pronounced roughness. The attempt to perform XRR on the film (which is expected to be in the range of 120-130nm) reveals a very clear rough layer profile, where all oscillations were canceled, and a smooth curve of reflected intensity was observed. These findings support the conclusion that produced films are porous and partially oxidized.
Another issue is the pronounced roughness. The attempt to perform XRR on the film (which is expected to be in the range of 120-130 nm) reveals a very clear rough layer profile, where all oscillations are canceled, and a smooth curve of reflected intensity is observed. These findings support the conclusion that produced films are porous and partially oxidized.

Revision as of 14:33, 28 July 2025

Feedback to this page: click here

This page is written by Evgeniy Shkondin @DTU Nanolab if nothing else is stated.
All images and photos on this page belongs to DTU Nanolab.
The fabrication and characterization described below were conducted in 2022 by Evgeniy Shkondin, DTU Nanolab.


Sputter coater 03 is mainly used for sample preparation before SEM inspection. Usually, Au is sputtered on dielectric surfaces to compensate for charge build-up. Alternatively, many other materials can be sputtered if the setup allows (you need to have a turbo pump and Ar gas). Gold can be deposited even in pure oxygen plasma and only with roughing pumps. Fortunately, Sputter Coater 3, located in the basement of building 346, has both a turbo pump and an Ar working gas source. The pressure during the process is measured to be below 0.1 mBar. This page describes the deposition of tungsten (W) with this instrument.

The prepared samples were investigated by the X-ray Reflectivity (XRR), Scanning Electron Microscopy (SEM) and Photo Electron Spectroscopy (XPS) methods. The focus of the study was the deposition conditions.


It is recommended to clean the target with fine sandpaper to remove the native oxide if the target was not used for a long time.


In summary, the tungsten films produced by Sputter-Coater 3 are of poor quality. The user can install a big (15 cm high glass chamber. In this case, the deposition rate is very low (0.033 nm/s), and the film will contain a high level of oxygen (up to 50%). This can be partially improved by installing a smaller chamber (6.5 cm high). However, this leads to very poor uniformity regardless of the current settings used. Depositing on small samples (approximately 1 cm x 1 cm) placed in the center of the chamber will be the most acceptable procedure. Nevertheless, the elevated level of oxygen and the rough, porous structure will limit its applicability.

Tungsten (W) from Sputter Coater 3 is not recommended as a part of sample preparation before SEM inspection. It is better to use Au.


Big glass configuration (15 cm high)

Initially, a large glass chamber was installed in the instrument. It was quickly revealed that the deposition rate is very low, so only the highest current setting (80 mA) was used in the experiment.

The maximum time the user can select is 300 seconds, so if longer depositions are needed, the user must redo them several times to achieve the expected thickness.


SEM Inspection

The samples with low aspect ratio Si trenches (500 nm deep, 200 nm wide with a pitch of 400 nm) were used to illustrate the deposition morphology (Instrument: SEM Supra 1). To make the result more visible, it was deposited twice at the maximum allowed deposition time (2 × 300 s). The SEM results are shown below.


X-ray Photoelectron Spectroscopy

X-ray photoelectron spectroscopy (Instrument: XPS K-Alpha) has been applied to investigate the chemical content and stoichiometry.

The samples used for the XPS analysis were prepared in a large glass chamber with an 80 mA current and a deposition time of 300 seconds. The pressure is measured to be below 0.1 mBar.

The analysis reveals that the top surface is a native oxide, while the thin layer itself is partially oxidized tungsten. The stoichiometry indicates a 50%W and 50%O composition. The stoichiometric tungsten oxide has a form of WO3; therefore, the layer itself contains approximately 33% metallic W, mixed with up to 67% oxide. This is not a big surprise, as this tool lacks shutter mechanisms and a long, well-controlled pumping system. The deposition rate is also very low due to the limited power. This also contributes to the elevated oxygen level in the film.

X-ray Reflectivity

The samples used for X-ray analysis (Instrument: XRD SmartLab) were prepared in a large glass chamber with an 80 mA current and a deposition time of 300 seconds.

X-ray reflectivity (XRR) profiles for W films at two different positions on a 100 mm wafer have been obtained using the Rigaku XRD SmartLab equipment. The voltage and current settings for the Cu X-ray tube were standard: 40 kV and 30 mA. The incident optics contained an IPS (incident parallel slit) adapter with a 5 ° Soller slit. Other slits: IS=0.03mm, RS1=0.03mm, and RS2=0.075mm. Step size: 0.01 and measurement time - 5s for each point. The fitting procedure was performed using the commercial GlobalFit software, assuming a model based on a Si substrate with native oxide, followed by the deposited W film with thin oxides and moisture-sensitive surfaces. The results are summarized in a table below.


X-ray analysis result (100mm Si wafer)
Center point
Layer name Thickness (nm) Density (g/cm3) Rougness (nm) Delta Beta
Moisture/WO3 0.98 2.75 1.04 8.8007e-6 2.0437e-7
W

10.14

5.70 0.81 1.8574e-5 4.3131e-7
SiO2 (native oxide) 1.52 2.18 0.30 7.0883e-6 9.2376e-8
Si (wafer) 2.328 0.00 7.5795e-6 1.7601e-7
Edge point
Layer name Thickness (nm) Density (g/cm3) Rougness (nm) Delta Beta
Moisture/WO3 2.22 2.63 1.17 8.5746e-6 1.9912e-7
W

6.53

8.10 0.81 2.6387e-5 6.1274e-7
SiO2 (native oxide) 2.23 2.12 0.37 6.8799e-6 8.9659e-8
Si (wafer) 2.328 0.00 7.5795e-6 1.7601e-7



The fitted value of the tungsten density (5-8 g/cm3) is much less than the bulk value of pure W, which is 19.25 g/cm3. This low value is very similar to the density of stoichiometric tungsten oxide WO3, which is 7.16 g/cm3. XPS, however, reveals that 67% of the film consists of tungsten oxide and 33% W, so this low density cannot be explained solely by the oxidation event. The most logical explanation is to assume that the layer is not very dense. It contains numerous nanopores, grain imperfections, and other defects.

Deposition rate and Uniformity

  • Deposition rate of W at 80 mA in a big glass (15 cm high) configuration is 0.033 nm/s. The uniformity variation across a 100 mm wafer is up to 50%. The pressure is measured to be below 0.1 mBar.



Small glass configuration (6.5 cm high)

In the next part of the experiment, a small (6.5 cm high) chamber was installed in the instrument. The deposition rate is much higher in this case, so the different current settings (20-80 mA) were employed. The consequence of the higher deposition rate was very poor uniformity, with the center of the wafer receiving a full thickness, while the edges remained uncovered. This deposition mode is better suited for small samples/chips. The produced films exhibited high roughness and pronounced porosity, as revealed by XRR.



SEM Inspection

Deposition rate and Uniformity

To measure the deposition rate the samples were cleaved, and only the center part was inspected, as the edges almost do not have a layer.

X-ray reflectivity

The deposition of W in Sputter Coater 3 using a small glass chamber (6.5 cm high) configuration is fast, but the resulting coatings are still expected to contain a significant fraction of oxygen. Although XPS measurements were not performed on these films, the sheet resistance values were significantly higher compared to pure tungsten layers.



Another issue is the pronounced roughness. The attempt to perform XRR on the film (which is expected to be in the range of 120-130 nm) reveals a very clear rough layer profile, where all oscillations are canceled, and a smooth curve of reflected intensity is observed. These findings support the conclusion that produced films are porous and partially oxidized.