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The fourth state of matter, an ionized gas into which sufficient energy is provided to free electrons from atoms or molecules and to allow neutral molecules, radicals, ions and electrons to coexist. Below is a high level overview of plasma fundamental physics. For a more details look at plasma, see the paper "A Short Introduction to Plasma Physics". Typical Plasma Composition | Neutral Molecules - 10 E16 per cm3
- Do not contribute to the etching process.
| | Radicals - 10 E14 per cm3
- Uncharged atoms with unsatisfied chemical bonds that react with the surface to produce volatile products that are pumped away.
- Form more easily and their lifetime is much longer, resulting in a million times more radicals than ions or electrons.
| | Electrons - 10 E8 per cm3
- Electrons are low mass (9.1 x10-31 kg) and are rapidly accelerated toward the positively charged anode, on the way they collide into other gas molecules creating new species.
| | Positive and Negative Ions - 10 E8 per cm3
- Fast moving, heavy molecules that affect the process through energetic (physical) bombardment of the surface.
- Positive ions are much heavier than electrons (Argon mass 6.6 x10-26 kg), and are accelerated toward the negatively charged cathode.
- Negative ions are short lived and therefore rare in plasma.
| | Collision Processes and the Production of Active Species |
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Electron Excitation - This accounts for the glow. When electrons collide with atoms or molecules, they excite or energize electrons to higher energy levels. When these electrons fall back to lower levels, they emit energy usually in the form of photons of visible light.
- Ar + e- >> Ar + e- + photon
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| Simple Ionization - An electron is completely removed from a gas molecule or atom, to make a positive ion. (Negative ions are rare in plasma)
- Ar + e- >> Ar+ + 2e- (Electron collision with an Argon atom resulting in one positive Ar ion and 2 electrons)
- O2 + e- >> O2+ + 2e- (Electron collision with an Oxygen molecule resulting in one positive Oxygen ion and 2 electrons)
| | Dissociative Ionization - CF4 + e- >> CF3+ + F + 2e- (Electron collision with a CF4 molecule resulting in one CF3 positive ion, one F radical, and two electrons)
| | Dissociative Ionization with Attachment - CF4 + e- >> CF3+ + F- + e- (Electron collision with a CF4 molecule resulting in one CF3 positive ion, one negative F ion, and one electron)
| | Molecular Dissociation, Radical Formation - Electron collisions break up molecules into fragments which as a result have unsatisfied chemical bonding and are chemically reactive. These are called radicals. Radicals have no net charge, and therefore are not accelerated by the field or are not attracted by charged particles.
- CF4 + e- >> CF3 + F + e- (Electron collision with CF4 molecule resulting in on CF3 radical, one F radical, and one electron)
- O2 + e- >> 2O + e- (Electron collision with an Oxygen molecule resulting in two oxygen radicals and an electron)
- CF3Cl + e- >> CF3 + Cl + e- (Electron collision with CF3CL molecule resulting in one CF3 radical, one Cl radical, and one electron)
| | Plasma Loss MechanismsIn a stable plasma, unstable particles are continuously generated and lost. The concentration of ions, radicals, and electrons increase until their loss rate is equal to their generation rate and steady state is reached. | Recombination of Ions and Electrons - Positively charged Ions and negatively charged electrons attract each other, combine, and become neutral atoms and molecules.
| | Recombination of Radicals - Radicals join together creating stable chemical bonds. ( 2O >> O2 )
| | Chemical Reaction - Radicals combine with surface creating volatile byproducts that are pumped away. (example: 4F + Si >> SiF4 )
| | Drift and Diffusion - Electrons are lost and Ions are converted to neutral particles through contact with conductive surfaces. (i.e. chamber walls and electrodes)
| | How is Plasma Made | DC Glow Discharge
| | RF Plasma | |
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Dry Etch Fundamentals
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Dry Etch Material Removal Mechanisms | Reactive Etching - Isotropic process
- High selectivity
- Low etch rate
| Image Modified | Ion Etching - Anisotropic process
- Low selectivity
- Low etch rate
| Image Modified | Reactive Ion Etching - Anisotropic process
- Variable selectivity
- High etch rate (on the order of 5x faster than either reactive etching or ion etching alone)
- Proposed Mechanism 1 - Chemically enhanced sputtering due to fluorinated Si surface versus pure Si surface
- Proposed Mechanism 2 - Lattice damage induced by ion bombardment causes increased chemical reaction rate.
- Proposed Mechanism 3 - Volatile species are ejected from the surface due to ion bombardment increasing reaction rate.
| Image Modified | Dry Etching Equipment Configurations | Capacitive RIE Etch Chamber | Image Modified | Inductive RIE Etch Chamber | Image Modified | Directionality of Etching | Degree of Anisotropy (A) | Image Modified | Vertical Etch
| Image Modified | Anisotropic Etch
| Image Modified | Isotropic Etch | Image Modified |
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Compatibility of Fluorine and Chlorine Etch Chemistry in a Shared Etch Tool
Reactive ion etch processing is known to exhibit significant variability in final etch performance due to wall condition. Previous studies have shown that neutral species transients depend strongly upon chamber seasoning.
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Effects of Cl2 and Fluorine Chemistry on Chamber Walls and Etch Parameters | New chamber walls conditioning and cleaning strategies to improve the stability of plasma processes Changes in the chamber wall conditions (e.g. chemical composition) are identified as being one important cause of process drifts such as changes in etch rates, etching profiles, etching selectivity or etching uniformity across the wafer. As the reactor wall conditions are modified due to the deposition or removal of etch products, the plasma chemistry changes, which in turn modifies the process performances. Controlling the reactor wall conditions and their stability is of primary concern when trying to create repeatable processes. In the plot to the right, the first column (a) represents a new, unaltered, Al2O3 chamber wall. In the second column (b), we see the effect of Chlorine etching. There is a clear build up of Silicon Oxychloride layers, as well as, Cl+Br bonded to the wall. The third column (c) represents an 80s fluorine etch following the chlorine etch. We see that the Silicon Oxychloride film and Cl+Br bonds have been removed and we are left with a thin fluorinated aluminum layer. Column (d) represents subsequent fluorine etches totaling 20 minutes of plasma exposure. We see that the fluorinated aluminum layer is building but surface chemistry has not changed. This will lead to several issues including flake off of AlxFy particles on the wafer and process drifts (due both to the progressive growth of AlF material on the SiO2 windows and to the release of F atoms from the chamber walls during the etching process). Plasma chemistry can be used to control the conditioning of the chamber. Transitions from chlorine to fluorine and visa versa require different approaches, see below for details. | Image Modified | Transition from Fluorine to Chlorine etch chemistry |
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Observed Effects Klimecky_JVSTA_wfigs.pdf
A thin film of silicon oxychloride grows on the chamber walls during Chlorine plasma etches. Fluorine etch chemistry will quickly strip away the thin oxychloride film from chamber walls resulting in significant transient effects in plasma density and real-time etch rate when transitioning back to chlorine etch chemistry. The root cause of these transients is assumed to be a result of dynamic oxychloride layer build-up processes at the chamber walls. As shown in the plot to the right, Chlorine etch rate will be lower when transitioning from Fluorine etch back to Chlorine etching. Chlorine etch rate will also be lower when following a chamber mechanical clean as this can also strip the oxychloride film from the chamber walls.
| Image Modified Black trace represents a well seasoned chamber. Green trace represents first Chlorine etch after Fluorine etch. | Proposed Mechanism for Effects The transient effects of oxychloride film buildup persist until it has achieved a steady state creation/loss ratio. At this point the Chlorine etch conditions become constant. In the paper referenced, it is suggested that transient effects are eliminated after approximately 300 seconds of Chlorine etching. The chamber seasoning alters recombination rates at the walls, which affects both the neutral species density and the plasma density as shown in the plot to the right. The plot shows that SiCl4 is low and increasing at the start of first Chlorine etch after a Fluorine etching. SiCl4 is the primary etch product of Si etched in Cl2 chemistry and is a good indicator of real time etch rate.
| Image Modified Black trace represents a well seasoned chamber. Green trace represents first Chlorine etch after Fluorine etch. | Recommended Chlorine Etch Chamber Preparation In our shared facility, it is often difficult to know exactly what has happened in the chamber before you arrived to use the tool. In addition, most users are more concerned with final depth of their etch rather than efficiency of time usage. For these reasons, it is best to return the chamber to a known condition before you begin your processing. Since the transient effects discussed above are consistent and predictable, we can generate a recipe that will bring the chamber to a stable condition before Chlorine etching. Before beginning your Chlorine etch, it is best to strip the oxychloride film from the chamber walls and bring the chamber walls back to a known starting point. Do this by running the clean and coat recipe available at the tool. Once returned to the known starting point, you may proceed with your Chlorine etch as usual. Example Recipe for Panasonic E620 (other tool recipes may vary from this but purpose is the same) 1. Strip and Clean | 800 | 0 | CF4 > 50 | O2 > 40 | 22.5 | 900 | 2. Chamber Purge | 0 | 0 | N2 > 100 | NA | 22.5 | 30 | 3. Grow Oxychloride Film on chamber walls | 400 | 0 | Cl2 > 50 | NA | 22.5 | 300 |
| Image Modified Chlorine etch depth achieved for first three etches after Fluorine etching. Samples etched for 30 seconds each, significant etch rate increase for each sample. This is known as the "First Wafer Effect" in industry. The etch rate is increasing for each run as the wall seasons with oxychloride buildup and the recombination rate goes down. | Transition from Chlorine to Fluorine etch chemistry | Observed Effects During Chlorine plasma etches a thin film of silicon oxychloride grows on the chamber walls. Fluorine etch chemistry will strip away the thin oxychloride film from chamber walls resulting in significant transient effects in plasma density and real-time etch rate when transitioning back to fluorine etch chemistry. The root cause of these transients is assumed to be a result of dynamic oxychloride layer stripping processes at the chamber walls and subsequent build up of Al-F layers. The oxychloride stripping effects of fluorine etch plasma are short lived and typically last less than a minute. The subsequent build up of Al-F layers can take a few minutes to stabilize. | Image Modified Black trace represents a Cl2 seasoned chamber. Green trace represents first Chlorine etch after Fluorine etching, indicating plasma losses due to replacing oxychloride film that was stripped in a 30 second fluorine etch. | Proposed Mechanism for Effects The transient effects of oxychloride film stripping persist until the film has been removed. At this point the fluorine etch conditions become constant. In the paper referenced, it is suggested that transient effects are eliminated after approximately 30 seconds of fluorine etching. The chamber seasoning alters recombination rates at the walls, which affects both the neutral species density and the plasma density as shown in the plot to the right. The plot shows that SiCl4 is low and increasing at the start of first Chlorine etch after a Fluorine etching. SiCl4 is the primary etch product of Si etched in Cl2 chemistry and indicates low etch rate due to plasma losses.
| Image Modified Black trace represents a Cl2 seasoned chamber. Green trace represents first Chlorine etch after Fluorine etching, indicating low etch product due to replacing oxychloride film that was stripped in a 30 second fluorine etch.
| Recommended Fluorine Etch Chamber Preparation In our shared facility, it is often difficult to know exactly what has happened in the chamber before you arrived to use the tool. In addition, most users are more concerned with final depth of their etch rather than efficiency of time usage. For these reasons, it is best to return the chamber to a known condition before you begin your processing. Since the transient effects discussed above are consistent and predictable, we can generate a recipe that will bring the chamber to a stable condition before fluorine etching. Before beginning your fluorine etch, it is best to strip the oxychloride film from the chamber walls and bring the chamber walls back to a known starting point. Do this by running the chamber clean recipe available at the tool. Once returned to the known starting point, you may proceed with your fluorine etch as usual. Example Recipe for Panasonic E620 (other tool recipes may vary from this but purpose is the same) 1. Initial Step | 700 | 0 | CF4 > 50 | O2 > 40 | 37.5 | 5 | 2. Strip and Clean | 700 | 0 | CF4 > 50 | O2 > 40 | 37.5 | 30 | 3. N2 Purge | 100 | 0 | N2 > 100 | NA | 18.8 | 10 |
| Image Modified Chlorine etch depth achieved for first three etches after Fluorine etching. The etch rate is increasing for each run as the wall seasons with oxychloride buildup and the recombination rate goes down, indicating previous fluorine etch stripped oxychloride film. |
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References
Introduction to Plasma Etching_Lecture_102417_Day2_sntzd.pdf
BookDry etch for semiconductors _Nojiri.pdf
Purdue Etchers - 1.xlsx
Oxford Plama Etching Media Center
Materials
Aluminum Oxide
General - Will it etch
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Materials can generally be etched in the RIEs as long as they form volatile byproducts, or products for which the vapor pressure (at the temperature of the etch) is higher than the pressure of the chamber. Etching is very complicated and this will be massive oversimplification...but generally volatile byproducts can be determined from literature, or as a fallback, the CRC Handbook of Chemistry and Physics Online, (4) Properties of the Elements & Inorganics, Physical Constants of Inorganic Compounds: https://hbcp.chemnetbase.com/faces/documents/04_02/04_02_0001.xhtml. From there, click "Go to Interactive Table", and find products that may be formed (i.e. chloride, fluorides, oxides, depending on the gasses). A compound is deemed volatile if it has a boiling point at a reasonable temperature range for the temperature and pressure of the system. Note that at lower pressures, boiling points decrease, so these are just a good staring point reference. As a VERY general rule of thumb, anything with a boiling point (tbp) < 185 C will be volatile in the ICP RIEs. As an example, aluminum chloride is volatile, and aluminum fluoride and aluminum are not. Image Modified Image Modified Image Modified Image Modified Neither Copper chloride or copper fluoride is volatile, which is why it is not allowed in any chamber: Image Modified Image Modified Image Modified Image Modified Image Modified Image Modified Byproducts of silicon are very volatile: Image Modified Image Modified Many times different fluorides/chlorides of the same material will have drastically different boiling points. It's important to research which will be formed in the plasma. Titanium is a good example of this, with TiCl2 and TiCl3 being non-volatile, and TiCl4 being volatile: Image Modified Image Modified Image Modified |
Mounting
Small samples may be mounted to carrier wafers with Crystalbond 555 HMP. More info here: A09_18.pdf and 821-1-2-3-4-6-TN.pdf
Basic Procedure: Attaching a Sample to a Carrier Wafer Using Crystalbond.pdf
Detailed Paper on Attaching Samples from Stanford: https://snfexfab.stanford.edu/docs/process/attaching-samples-to-carrier-wafers-for-etching-or-deposition