GB2029017A - Control of deposition of thin films - Google Patents
Control of deposition of thin films Download PDFInfo
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- GB2029017A GB2029017A GB7927951A GB7927951A GB2029017A GB 2029017 A GB2029017 A GB 2029017A GB 7927951 A GB7927951 A GB 7927951A GB 7927951 A GB7927951 A GB 7927951A GB 2029017 A GB2029017 A GB 2029017A
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- 239000010409 thin film Substances 0.000 title claims abstract description 11
- 239000010408 film Substances 0.000 claims abstract description 83
- 239000013078 crystal Substances 0.000 claims abstract description 62
- 230000003287 optical effect Effects 0.000 claims abstract description 38
- 239000000758 substrate Substances 0.000 claims abstract description 33
- 230000008859 change Effects 0.000 claims abstract description 32
- 238000002834 transmittance Methods 0.000 claims abstract description 20
- 238000000151 deposition Methods 0.000 claims description 38
- 238000000034 method Methods 0.000 claims description 12
- 238000005259 measurement Methods 0.000 claims description 10
- 238000004544 sputter deposition Methods 0.000 claims description 10
- 238000005137 deposition process Methods 0.000 claims description 8
- 238000001755 magnetron sputter deposition Methods 0.000 claims description 6
- 238000005229 chemical vapour deposition Methods 0.000 claims description 5
- 230000001419 dependent effect Effects 0.000 claims description 5
- 238000005240 physical vapour deposition Methods 0.000 claims description 5
- 239000000463 material Substances 0.000 description 15
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- 238000012544 monitoring process Methods 0.000 description 2
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- 229910052719 titanium Inorganic materials 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/22—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
- C23C14/54—Controlling or regulating the coating process
- C23C14/542—Controlling the film thickness or evaporation rate
- C23C14/545—Controlling the film thickness or evaporation rate using measurement on deposited material
- C23C14/546—Controlling the film thickness or evaporation rate using measurement on deposited material using crystal oscillators
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/22—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
- C23C14/54—Controlling or regulating the coating process
- C23C14/542—Controlling the film thickness or evaporation rate
- C23C14/545—Controlling the film thickness or evaporation rate using measurement on deposited material
- C23C14/547—Controlling the film thickness or evaporation rate using measurement on deposited material using optical methods
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01B—MEASURING LENGTH, THICKNESS OR SIMILAR LINEAR DIMENSIONS; MEASURING ANGLES; MEASURING AREAS; MEASURING IRREGULARITIES OF SURFACES OR CONTOURS
- G01B11/00—Measuring arrangements characterised by the use of optical techniques
- G01B11/02—Measuring arrangements characterised by the use of optical techniques for measuring length, width or thickness
- G01B11/06—Measuring arrangements characterised by the use of optical techniques for measuring length, width or thickness for measuring thickness ; e.g. of sheet material
- G01B11/0616—Measuring arrangements characterised by the use of optical techniques for measuring length, width or thickness for measuring thickness ; e.g. of sheet material of coating
- G01B11/0683—Measuring arrangements characterised by the use of optical techniques for measuring length, width or thickness for measuring thickness ; e.g. of sheet material of coating measurement during deposition or removal of the layer
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01B—MEASURING LENGTH, THICKNESS OR SIMILAR LINEAR DIMENSIONS; MEASURING ANGLES; MEASURING AREAS; MEASURING IRREGULARITIES OF SURFACES OR CONTOURS
- G01B21/00—Measuring arrangements or details thereof, where the measuring technique is not covered by the other groups of this subclass, unspecified or not relevant
- G01B21/02—Measuring arrangements or details thereof, where the measuring technique is not covered by the other groups of this subclass, unspecified or not relevant for measuring length, width, or thickness
- G01B21/08—Measuring arrangements or details thereof, where the measuring technique is not covered by the other groups of this subclass, unspecified or not relevant for measuring length, width, or thickness for measuring thickness
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01B—MEASURING LENGTH, THICKNESS OR SIMILAR LINEAR DIMENSIONS; MEASURING ANGLES; MEASURING AREAS; MEASURING IRREGULARITIES OF SURFACES OR CONTOURS
- G01B7/00—Measuring arrangements characterised by the use of electric or magnetic techniques
- G01B7/02—Measuring arrangements characterised by the use of electric or magnetic techniques for measuring length, width or thickness
- G01B7/06—Measuring arrangements characterised by the use of electric or magnetic techniques for measuring length, width or thickness for measuring thickness
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01B—MEASURING LENGTH, THICKNESS OR SIMILAR LINEAR DIMENSIONS; MEASURING ANGLES; MEASURING AREAS; MEASURING IRREGULARITIES OF SURFACES OR CONTOURS
- G01B7/00—Measuring arrangements characterised by the use of electric or magnetic techniques
- G01B7/02—Measuring arrangements characterised by the use of electric or magnetic techniques for measuring length, width or thickness
- G01B7/06—Measuring arrangements characterised by the use of electric or magnetic techniques for measuring length, width or thickness for measuring thickness
- G01B7/063—Measuring arrangements characterised by the use of electric or magnetic techniques for measuring length, width or thickness for measuring thickness using piezoelectric resonators
- G01B7/066—Measuring arrangements characterised by the use of electric or magnetic techniques for measuring length, width or thickness for measuring thickness using piezoelectric resonators for measuring thickness of coating
-
- G—PHYSICS
- G05—CONTROLLING; REGULATING
- G05D—SYSTEMS FOR CONTROLLING OR REGULATING NON-ELECTRIC VARIABLES
- G05D5/00—Control of dimensions of material
- G05D5/02—Control of dimensions of material of thickness, e.g. of rolled material
- G05D5/03—Control of dimensions of material of thickness, e.g. of rolled material characterised by the use of electric means
Landscapes
- Chemical & Material Sciences (AREA)
- General Physics & Mathematics (AREA)
- Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Automation & Control Theory (AREA)
- Length Measuring Devices By Optical Means (AREA)
- Physical Vapour Deposition (AREA)
Abstract
In apparatus for sensing and controlling the deposition of a thin film on to a substrate (12) from a gas or vapour phase, the optical reflectance or transmittance is sensed, the resonant frequency of a crystal (14) also exposed to the deposition is sensed, and the quotient of the change in each signal over a predetermined time interval is determined. The deposition can be terminated at a suitable thickness, for example a reflectance or transmittance maximum or minimum. instead of an optical property, the electrical resistivity of the film may be sensed and used in the same way. <IMAGE>
Description
SPECIFICATION
Control of deposition of thin films
This invention relates to a method and
apparatus for determining and controlling the
properties of a thin film during deposition of that film. In this specification, the term "thin film" means a film less than about 20 micrometres thick,
and usually about 0.1 micrometres thick, and the words 'optical' and 'light' means electromagnetic
radiation at infra-red visible and ultra-violet wavelengths.
Afllm of this thickness may be referred to as an
optical interference film, because its optical thickness, that is the product of its geometrical thickness and its refractive index, is usually a fraction of the wavelength of light, but may also be up to about three times the magnitude of the wavelength. Optical interference effects may occur due to a phase difference introduced by the film between two light waves reflected respectively at the two film boundaries.
Films of the thickness are often applied to a substrate to alter the reflection properties of the substrate, for example to glass to give an antireflecting surface at visible wavelengths, or to a semi-conducting material to give an anti-reflecting surface at infra-red wavelengths; the films may also be applied to provide beam splitters and broad and narrow band-pass filters at ultra-violet, visible, and infra-red wavelengths, orto give mechanical protection, to a surface orto impart electrical conductivity to it Single layer films may be required, or multiiayer films comprising films of different optical properties. The films may be applied by any physical vapour deposition (PVD) or chemical vapour deposition (CVD) process.In a
PVD process, a material is sputtered or evaporated; examples are d.c. sputtering, radio frequency sputtering, magnetron sputtering; electron beam evaporation; ion plating ; and glow discharge. In a CVD process a material is decomposed by heat, optionaily into a plasma, and optionally an active gas may be added. In some examples of both basic types of decompostion, an ionised atmosphere is generated in the vicinity of the substrate. Materials used vary over a very wide range, and may be elements or compounds, metals, semiconductors, or insulators.
It is usual to monitor the film growth rate and thickness, and to monitor and control the substrate temperature and the constitution and pressure of the atmosphere in the deposition vessel.
Additional variables may be monitored and controlled, depending on the deposition process.
The present invention is applicable to the majority of such films and is largely independent of the material of the film or the method of application.
In the prior art, it is known to monitor indirectly the geometrical film thickness L by use of a high frequency crystal microbalance. A quartz crystal is positioned near the surface to be coated so that the material is deposited at a constant thickness over the surface of the substrate and the crystal. If the deposit is mass m per unit area, and p is the density, then m/p = L; if it is assumed that the film refractive index n and its density are constant during deposition, then the optical thickness nL is proportional to the mass deposited. The mass deposited on the crystal causes a change in resonance frequency; the change in oscillating frequency of the crystal from the original frequency is sensed and this value has beeri used to control the rate of deposition of material.
It is also known to monitor the reflectance R or transmittance T of the deposited film, during the deposition process, by means of a beam photometer, or to monitor the electrical resistivity of an electrically conductive film, and to use such a measured value to determine when a required value of the measured property has been reached; deposition is then terminated.
These three measurements have been made simultaneously by separate instruments since about 1962, but the output signals of the instruments have never in any way been combined.
It has also been suggested that, to allow precise control of the final film thickness, it would be desirable to measure the differential with
respect to time t of reflectance or transmittance, i.e.
dR dT
or
dt dt
This has the disadvantage that it is assumed that the film optical thickness nL increases linearly with time. In practice this is not the case; for example when a powder source is used, volatilization, may occur as a series of discrete events as particles come into contact with the heat source; this causes fluctuations and instabilities which are undesirable.
From a theoretical point of view, the basic need
is to determine the differential with respect to film optical thickness of the measured variable, for
example
dR
d(nL) and it has been suggested that this can be derived from the differential with respect to time.
However, such a derivation depends on the incorrect assumption that thickness increase is linear. Previously, there have been practical difficulties in directly determining the change in optical thickness, and no method of directly determining the differential with respect to optical thickness has been suggested which eliminates the effect of the temporal variations.
According to the invention, apparatus for sensing and controlling the deposition of a thin film on to a substrate from a gas or vapour phase comprises sensing means arranged to sense the optical reflectance or optical transmittance or electrical resistivity of the deposited film and to provide a first signal having a value representative of the value of the sensed property;
an oscillatable crystal, usually a quartz crystal, arranged adjacent to the substrate with at least one surface of the crystal exposed to the gas or vapour phase;;
and timing and calculating means connected to
the sensing means and to the oscillatable crystal
and arranged to determine the absolute resonace frequency of the oscillatable crystal, to provide a
second signal representative of that frequency, to
determine the quotient of the change in the first
signal and the change in the second signal over a
first predetermined time interval, and to provide
an output signal dependent on said quotient.
The timing and calculating means may be
means such as a computer or microprocessor having a built-in clock. The change in resonance
frequency of the crystal may be determined by a
measurement either of the absolute frequency or of the resonance period. The first predetermined
time interval is conveniently the period of the oscillatabie crystal, which is typically 105 seconds,
It may in some circumstances be desirable to
average the quotient over a second time interval,
usually considerably longer than the first time
interval and typically 1 second. This interval may
be a predetermined time interval chosen so that
the averaged quotient is unaffected by temporal
fluctuations in the deposition rate. Alternatively it
may be a variable time interval, corresponding to a.
predetermined increase in film thickness.
For convenience, the first signal is arranged to
be in the form of a frequency signal, the value of
frequency representing the value of optical
reflectance or transmittance or electrical
resistivity, and the second signal is the output of
the oscillatable crystal. The two frequency signals
can then be digitised and the numbers used to
calculate quotient or averaged quotient.
Also according to the invention, a method of
sensing and controlling the deposition of a thin
film on to a substrate from a gas or vapour phase
comprises:
sensing the optical reflectance or optical
transmittance or electrical resistivity of the
deposited film and providing a first signal having a
value representative of the value of the sensed
property;
arranging an osci!latable crystal adjacent the
substrate with at least one surface of the crystal
exposed to the gas or vapour phase;
determining by timing and calculating means
the absolute resonance frequency of the
oscillatable crystal and deriving a second signal
having a value representative of said resonance
frequency;
determining over a first predetermined interval
of time the quotient of the change in the first
signal and the change in the second signal;
providing an output signal dependent on said
quotient;;
and controlling the variable of the deposition
process in accordance with the output signal.
Referring now to the accompanying drawings,
Figures 1 and 2 are respectively theoretical and typical measured variations of reflectance with increase in film thickness, Figure 3 is an enlarged view of part of Figure 1 and Figure 4 is a typical variation of film electrical resistivity with increase in film thickness. The invention will be described with reference to: Figure 5, which is a schematic sectional drawing of a reactive d.c. sputtering apparatus; and
Figure 6, which is a schematic sectional drawing of a magnetron sputtering apparatus.
Figure 1 shows the theoretical variation of the reflectance R of a film deposited on a glass substrate of refractive index 1.5 as the film thickness increases. Two curves are shown, for films of refractive indices greater (n = 2.0) and lower (n = 1.4) respectively than the substrate.
The curves exhibit maxima and minima at values of the optical thickness nL divided by wavelength of incident light A which correspond to quarterwave intervals; this is due to interference effects within the film. It is assumed that absorption within the film is negligible, but even highly absorbing films show this behaviour until the layer is thick enough to absorb all internally reflected flight. If the refractive index of the film equals the refractive index of the substrate, there will be no variation in reflectance, as indicated by the dotted line for n = 1.5. A plot of transmittance T of the film would give the inverse curves.
If the film growth rate is constant and the film density and refractive index remain constant with increasing mass, then the abscissa could also be considered to indicate increase with time.
Typically, a deposition run lasts between 2 and 10 or even 20 minutes.
Figure 2 shows a typical curve obtained by
monitoring film growth using a conventional beam photometer and plotting reflectance against time.
The curve irregularities are due to several effects such as instabilities in the deposition rate; for example if a powder is evaporated, volatilization may occur as a series of discrete events as particles come into contact with the heat source; alternatively, during a sputtering process, gas may be released from a target compound, which results in a change in ion density in the gas and a variation in deposition rate. Such instabilities cause changes in the mass growth rate, which affects the rate of increase of geometrical thickness, and may also have secondary effects on the optical thickness if the film density and refractive index are independent on growth rate.
A further contribution to curve irregularities may be made by instrument noise, and the height of the measured maxima may decrease with time due to changes in the refractive index of the deposited film and to absorption.
It will be clear that the measured variation of reflectance with time is only an approximation to the variation of reflectance with the optical density of the deposited film.
It is often a requirement to terminate deposition at a reflectance or transmittance maximum or minimum, corresponding to a quarter-wave thick film, or a multiple thereof. It will be immediately apparent that serious errors can occur because R and T values change by only relatively small amounts near the turning points, and superimposed noise makes it even more difficult to locate the required point with any accuracy, because false maxima and minima may be detected.
These problems could be overcome if the curves of R and T were differentiated with respect to the optical thickness of the film. The quarter wavelength maxima and minima then correspond to zero values. As shown in Figure 3, the differential of the curve at the maximum is zero even if the peak height differs from the theoretical maximum (three peak heights are shown), and the differential at the minimum is zero even if the reflectance of the substrate changes, as indicated by the two dotted lines.
A first embodiment of apparatus which allows such a differentiation to be carried out with optical thickness measured to terms of film mass is shown in Figure 5. A conventional vacuum chamber 10 and its contents are shown in schematic form; a substrate 12 to be coated and a quartz crystal 14 are both exposed to a source of material to be deposited 16, which is connected to a d.c. power supply 1 8 to give reactive d.c.
sputtering. The crystal 14 is driven by an oscillator 15 outside the vacuum chamber. The power supply 1 8 is controlled by a microprocessor 24.
The chamber can be evacuated by a pump 20, and a gas can be supplied through an inlet pipe 22. If the source is a metal and an oxygen atmosphere is provided, then a metal oxide film will be deposited.
The quartz crystal is connected directly to the microprocessor 24.
A light source 26 illuminates the substrate 12 with a collimated beam through a beam splitter 28; reflected light is received via the beam splitter by a reflectance monitor 30, which is connected to the microprocessor; the source 26 and monitor 30 are connected together and to the microprocessor so as to allow operation in synchronism in a pulse mode controlled by the microprocessor. The position of a transmittance monitor 32 is indicated by the dotted line.
The monitors 30 and 32 each comprise a light detector such as a vacuum photocell our a solid state device together with the necessary power supplies. The sensor may provide a voltage or current of a magnitude representing the reflectance or transmittance of the coated substrate.
In operation, the chamber 10 is evacuated and oxygen is supplied to a pressure of between 10-2 and 10-1 torr, and a conventional reactive d.c.
sputtering process is established in which material from the source 1 6 is deposited on both the substrate 12 and the quartz crystal 14, changing the resonant frequency of the crystal; the absolute resonant frequency of the crystal is sensed using the internal clock of the microprocessor 24. The reflectance of the film of material deposited on the substrate 1 2 is sensed by the reflectance monitor, which converts it to a frequency signal, the first signal, and supplies it to the microprocessor. The microprocessor therefore has available two digitised signals, and is arranged to calculate the required quotient over the first time interval.
Conveniently, this first predetermined time interval is the period of the osciliatable crystal, and the change in the frequency of the first signal over this time interval is easily determined from the digitised information.
The average value of the quotient is supplied to a dispiay unit 34 and may be used to supply information to an operator when the apparatus variables are controlled manually. Alternatively, in a fully automatic system, the output signal is used to control the d.c. power supply 1 8. Information relating to a required value or programme of values of the quotient may be stored in the microprocessor, and may include a value at which deposition is to be terminated.
The output of reflectance monitor R is a dimensionless value equivalent to reflected signal/incident signal. If this value is expressed as a frequency, then any change in frequency corresponds to a change S R in R.
Considering now the quartz crystal; for a deposited film such that the film mass is small compared with the mass of the crystal,
ksf
L = pfq2 where L is film thickness, k is a constant is the basic resonant frequency of the quartz crystal and Sf is the change in that frequency, p is the film density, and L = M/p where M is the film mass per unit area. It is also possible to measure the period of oscillation of the crystal, z, where
1
fq when the relation becomes K!AT L =
p where K' isa different constant. This expression is a better approximation at high mass loading.
Thus L is proportional to change in frequency or change in period of the crystal. Since refractive index n is essentially constant, the ratio of the change in the first signal over an interval of time to the change in oscillation frequency of the crystal over the same interval of time is an acceptable approximation to the differential of reflectance with respect to the optical thickness of the film.
This differential is not dependent on the assumption that rate of deposition is constant with time and temporal fluctuations are accommodated.
However, if may be preferable in some circumstances, when it is known that temporal fluctuations in deposition will occur within a time interval of the same order as the first predetermined interval, this causing fluctuations in reflectance or in deposition rate, to average the quotient over a second predetermined time interval, longer than the first, so that the effect of actual variations in deposition rate is eliminated.
This second interval of time may be, for example, 0.1 seconds or may be as long as 5 minutes for unusually prolonged deposition process.
Information relating to a required value or programme of values of this averaged quotient may also be stored in the microprocessor, and the source controlled in accordance with the requirement.
Usually, refractive index of a film during deposition is constant, but film materials are known for which refractive index increases or decreases and film density also changes with growth of the film. When such established changes result in a departure from a linear relationship between increase in mass and increase in optical thickness, this can be allowed for when determining the value of the quotient at which deposition is to terminate.
There are further benefits from use of a microprocessor. If a film thickness corresponding to a known number of quarter wavelengths is required, then the microprocessor can be programmed to count the maxima and minima in the reflectance curve, corresponding to the number of zero points in the differential, and to terminate deposition when the required thickness is reached. Termination at a point between a maximum and a minimum is also possible.
Another beneficial aspect of the present invention is illustrated when for some reason the source fails and deposition ceases; a differential with respect to time would then be zero, because there is no temporal change. But the differential with respect to optical thickness remains at a constant value. The microprocessor can be programmed to recognise this condition, to give an alarm signal if required, and, when growth begins again, to continue the calculation of differential from the held value.
If the study or control of the spatial distribution of deposition is required, then additionai quartz crystals, appropriately spaced in the vacuum chamber and each used in conjunction with an optical sensing instrument, can easily be incorporated. This would allow deposition of very uniform films, or films on curved surfaces. The several crystals need not all have the s"ame basic resonance frequency. Also, several sources of material for deposition can be controlled independently by the microprocessor, which can rapidly determine the actual film mass distribution from the monitor crystals during deposition, and determine the independent source emission rates needed to provide a required mass distribution.
The microprocessor can control other variables of the apparatus, such as electron beam current if an electron beam evaporation apparatus is used, or the target and substrate bias potentials in an r.f.
sputtering system, or other variables as appropriate.
Another problem which is met in prior art apparatus and which is overcome by the present invention is that, when deposition takes place in an ionised gas atmosphere (which may occur in either a PVD or a CVD process), the charged particles present may interact with the quartz crystal and cause incorrect readings of thickness of deposited material.
Electrostatic and magnetic shields can provide some protection, but cannot exclude energetic neutrals which can charge the crystal surface on impact by releasing electrons.
An alternative solution is to switch off the exciting discharge and measure the change in frequency of the quartz crystal without exposure to charged or energetic particles, but the time to make such measurements with conventional manually switched instruments is usually long enough, often several seconds, for the film surface to adsorb gases from the environment which become trapped in the film on subsequent growth, giving it an undesirable laminar structure.
In apparatus according to the invention, the microprocessor can be used to switch off the power supply to the exciting discharge for a very short period, such as microsecond or milli-second intervals, and to make a measurement of crystal frequency during that period. The time can be short enough for gas absorption on the film surface to be negligible. Further, such pulsed measurements of thickness can be made at known time intervals so that mass growth rate of the film can be determined.
When the exciting discharge is switched off, deposition of material will continue, because of thermal inertia in a heated container, or relatively slow speed of the shutter conventionally used to terminate deposition; but in apparatus according to the invention deposition in the absence of the discharge can be for such a short period that the properties of the film are essentially not affected.
A similar benefit, when using glow discharge apparatus, is that the pulse operation of the reflectance measurement can be synchronised with the switching-off of the power thus avoiding interference by light from the glow discharge. In this case, the deposition ceases when the power is off.
The invention is particularly applicable to the deposition of materials in which refractive index changes with deposition because the structure changes. The true film thickness then differs from that derived from nL assuming n and film density are constant. Examples of such materials are zirconium and aluminium; respective oxides of these metals are often used in multi-layer antireflection films. Use of the invention will show turning points as the film masses and the optical thickness changes combine to give maximum or minimum reflected energy.
In the second embodiment the invention is utilised in otherwise conventional apparatus for preparing multilayer interference filters by magnetron sputtering. In magnetron sputtering, metals are sputtered in oxygen-containing atmospheres to deposit oxide films. A reduced pressure of between 10-3 and 10-2 torr is used and a magnetic field is superimposed on the electrode arrangement so that the electrons are trapped in magnetic loops and follow cycloidal paths. Figure 6 shows a vacuum chamber 40 having a central circular cathode support 42 carried by a hollow stem 44 insulated from the chamber baseplate 46.The support 42 is water cooled and the stem has water inlet and outlet pipes 48, 50. A circular array of smali magnets 52 is arranged with their axes radial to the cathode support and their upper surfaces flush with the surface of the support; the loop-shaped magnetic fields are illustrated by the dotted lines. The support is partly shielded by a grounded metal shield 53. The chamber 40 can be evacuated by a pump 55.
A silicon cathode 54 lies on the cathode support; the cathode has a central aperture. A similarly shaped titanium cathode 56 is held by a cathode-changing mechanism 58 operated from outside the vacuum chamber.
The hollow stem 44 of the cathode support is closed at its lower end by a glass window 60 through which a monitoring light beam can pass from a source 62, through a collimating lens 64 up through the hollow stem 44 and through a glass substrate 66 supported (by means not shown) above the aluminium cathode 54. The light beam is then reflected by a plane mirror 68 through a wavelength-selecting filter 70 to a photocell 72.
The electrical signal from the photocell passes through an amplifier 74 to a microprocessor 78, which controls a light chopper 80 which chops the beam from the source 62.
Adjacent the substrate 66 is a high-frequency crystal 82 with a free surface aligned with the surface of the substrate. The crystal is connected through a crystal oscillator 84 to the microprocessor 78. The microprocessor also controls via a servo-motor controlled needle valve 86 the supply to the vacuum chamber 40 of a mixture of argon and oxygen; is connected to the thyristor'power control 88 placed between a power source 90 and a d.c. power supply 92 which is connected to the aluminium cathode 54; and is connected to a visual display unit 94.
In operation, a glow discharge is generated in the vacuum chamber between the cathode 54 and the earthed shield 53 or baseplate 46 and silicon is sputtered from the silicon cathode 54 to be deposited on the surfaces of the glass substrate 66 and the crystal 82 as a film 96 of silicon dioxide. The presence of the magnetic field confines ion bombardment to a narrow annulus on the cathode. This allows a central aperture through which the light beam sensing film transmittance can pass.
In the apparatus shown in Figure 6, the microprocessor 78 combines the quotient of the change in resonant frequency of the crystal 82 and the change in transmittance of the film 96, as in the Figure 5 embodiment, to terminate deposition at a required value. The cathodechanging mechanism 58 is then operated to remove the silicon cathode 54 and place titanium cathode 56 on the electrode support. Titanium oxide film is then deposited as required.
However it is a characteristic of low pressure glow discharges that the sputtering rate can vary for several reasons, even if the discharge current and applied potential are constant. This may occur because the surface condition of the cathode varies, because contaminants are formed on or removed from its surface, or the profile changes as etched tracks form. In apparatus according to the present invention, the derivative of the frequency signal from the crystal 82 can be used to adjust the glow discharge conditions so that the change of resonant frequency with time, and thus the change of film mass with time, is constant. Either the needle valve 86 is adjusted to alter the gas pressure and therefore the glow discharge power input, or the thyristor 88 is adjusted to alter the electrical power input to the discharge.The thyristor, which is a semiconductor rectifier which can be arranged to become conducting for different periods during an a.c. cycle, can conveniently be used to switch off the electrical power supply during periods when the crystal oscillator 84 is energised and frequency measurements are being made. In the magnetron sputtering apparatus, secondary electrons released from the target cathode are bent back towards its surface and trapped by the closed magnetic loops. The measuring crystal 82 is therefore not exposed to the intense electron bombardment characteristic of r.f. and d.c.
sputtering systems operated in the nonmagnetron discharge. A crystal exposed to a magnetron discharge, however, may reach a potential several volts negative with respect to earth unless it is kept earthed during the coating periods. The microprocessor 78 can be programmed to ground the crystal until a frequency measurement is required. Alternatively a separate switch 85 can be provided in the oscillator 84.
The apparatus has been described with particular reference to the measurement of optical reflectance or transmittance of the deposited film.
Alternatively, electrical resistivity of a conducting orsemiconducting film can be measured; such a curve does not show interference maxima and minima, but can be used to control thickness precisely. The two alternatives are not mutually exclusive, some conducting films also show optical interference effects.
instead of instructing the microprocessor to provide values of the quotient averaged over a predetermined time interval, it could also be averaged over a variable time interval, each
interval corresponding to a predetermined change
in the second signal, that is, a predetermined
increase in film thickness.
As an alternative to a microprocessor, a
computer or microcomputer can be used, or any
other calculating device having an internal clock or
timing device which can be used to measure the
absolute oscillation frequency of the quartz
crystal.
Claims (11)
1. Apparatus for sensing and controlling the
deposition of a thin film on to a substrate from a
gas or vapour phase comprises sensing means
arranged to sense the optical reflectance or optical
transmittance or electrical resistivity of the
deposited film and to provide a first signal having
a value representative of the value of the sensed
property.
an oscillatable crystal arranged adjacent to the
substrate with at least one surface of the crystal
exposed to the gas or vapour phase;
and timing and calculating means connected to
the sensing means and to the oscillatable crystal
and arranged to determine the absolute resonance frequency of the oscillatable crystal, to provide a
second signal representative of that frequency, to
determine the quotient of the change in the first
signal and the change in the second signal over a first predetermined time interval, and to provide
an output signal dependent on said quotient
2. Apparatus according to Claim 1 in which the first predetermined time interval is the period of the oscillatable crystal.
3. Apparatus according to Claim 1 or Claim 2 further comprising means to average the quotient over a second predetermined time interval.
4. Apparatus according to any preceding claim in which the first signal is in the form of a frequency signal, the value of frequency representing the value of optical reflectance or transmittance or electrical resistivity, and in which the second signal is the output of the oscillatable crystal.
5. Apparatus according to any preceding claim in which the deposition process is such that an ionised gas atmosphere is generated further comprising switching means controlled by the timing and calculating means and arranged to terminate the generation of the ionised gas atmosphere intermittently, the measurement of crystal frequency being made only while the ionised gas atmosphere is absent.
6. Apparatus according to Claim 5 in which the deposition process is a reactive d.c. sputtering apparatus or a magnetron sputtering apparatus.
7. Apparatus according to Claim 5 or Claim 6 in which the generation of the ionised gas atmosphere is terminated intermittently for periods each less than 0.01 seconds.
8. Apparatus for depositing a thin film on to a substrate by physical vapour deposition or chemical vapour deposition comprising a substrate support; means to generate a gas or vapour phase in the vicinity of the substrate support; sensing means arranged to sense the optical reflectance or optical transmittance or electrical resistivity of the deposited film and to provide a first signal having a value representative of the value of the sensed property;
an oscillatable crystal ananged adjacent to the substrate with at least one surface of the crystal exposed to the gas or vapour phase;;
and timing and calculating means connected to the sensing means and to the oscillatable crystal and arranged to determine the absolute resonance frequency of the oscillatable crystal, to provide a second signal representative of that frequency, to determine the quotient of the change in the first signal and the change in the second signal over a first predetermined time interval, and to control the means to generate the gas or vapour phase in accordance with said quotient.
9. A method of sensing and controlling the deposition of a thin film on to a substrate form a gas or vapour phase comprising:- sensing the optical refiectance or optical transmittance or electrical resistivity of the deposited film and providing a first signal having a value representative of the value of the sensed property;
arranging an oscillatable crystal adjacent the substrate with at least one surfce of the crystal exposed to the gas or vapour phase;
determining by timing and calculating means the absolute resonance frequency of the oscillatable crystal and deriving a second signal having a value representative of said resonance frequency;
determining over a first predetermined interval of time the quotient of the change in the first signal and the change in the second signal; ;
providing an output signal dependent on said quotient;
and controlling a variable of the deposition process in accordance with the output signal;
10. A method according to Claim 9 in which the optical reflectance or optical transmittance is sensed, and the deposition process is terminated at a reflectance or transmittance maximum or minimum.
11. Apparatus for depositing a thin film on to a substrate from a gas or vapour phase substantially as hereinbefore described with reference to Figure 5 or Figure 6 of the accompanying drawings.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB7927951A GB2029017B (en) | 1978-08-18 | 1979-08-10 | Control of deposition of thin films |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB7833927 | 1978-08-18 | ||
| GB7927951A GB2029017B (en) | 1978-08-18 | 1979-08-10 | Control of deposition of thin films |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| GB2029017A true GB2029017A (en) | 1980-03-12 |
| GB2029017B GB2029017B (en) | 1982-10-13 |
Family
ID=26268606
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB7927951A Expired GB2029017B (en) | 1978-08-18 | 1979-08-10 | Control of deposition of thin films |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB2029017B (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4367044A (en) * | 1980-12-31 | 1983-01-04 | International Business Machines Corp. | Situ rate and depth monitor for silicon etching |
| FR2531774A1 (en) * | 1982-08-12 | 1984-02-17 | Cit Alcatel | DEVICE FOR CONTROLLING THE THICKNESS OF LOWLY ABSORBENT THIN LAYERS |
| US4676883A (en) * | 1986-03-03 | 1987-06-30 | Sierracin Corporation | Optical disk transmission monitor for deposited films |
| EP0290657A1 (en) * | 1987-05-15 | 1988-11-17 | KSB Aktiengesellschaft | Method and device for measuring the optical properties of thin layers |
| EP0407298A1 (en) * | 1989-07-06 | 1991-01-09 | France Telecom | Method for monitoring the thickness of an antireflection layer and apparatus for carrying out the same |
| DE3925536A1 (en) * | 1989-08-02 | 1991-02-07 | Leybold Ag | ARRANGEMENT FOR THICKNESSING OF THICK FILMS |
| GB2240179A (en) * | 1990-01-12 | 1991-07-24 | Leybold Inficon Inc | Control circuitry for quartz crystal deposition monitor |
| GB2242523A (en) * | 1990-03-30 | 1991-10-02 | Leybold Inficon Inc | Measuring and controlling deposition on a piezoelectric monitor crystal |
| EP1094341A3 (en) * | 1999-10-15 | 2002-08-28 | Sony Corporation | Apparatus and method for producing optical component |
| EP1602919A1 (en) * | 2004-06-01 | 2005-12-07 | Applied Films GmbH & Co. KG | Measuring device for the survey of the transmittance of a coating |
-
1979
- 1979-08-10 GB GB7927951A patent/GB2029017B/en not_active Expired
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4367044A (en) * | 1980-12-31 | 1983-01-04 | International Business Machines Corp. | Situ rate and depth monitor for silicon etching |
| FR2531774A1 (en) * | 1982-08-12 | 1984-02-17 | Cit Alcatel | DEVICE FOR CONTROLLING THE THICKNESS OF LOWLY ABSORBENT THIN LAYERS |
| EP0101049A1 (en) * | 1982-08-12 | 1984-02-22 | Alcatel | Device for monitoring the thickness of thin, hardly absorbing films |
| US4676883A (en) * | 1986-03-03 | 1987-06-30 | Sierracin Corporation | Optical disk transmission monitor for deposited films |
| EP0290657A1 (en) * | 1987-05-15 | 1988-11-17 | KSB Aktiengesellschaft | Method and device for measuring the optical properties of thin layers |
| US5024853A (en) * | 1989-07-06 | 1991-06-18 | Etat Francais Represente Par Le Ministre | Method to control the thickness of an antireflection coating and implementation installation |
| FR2649419A1 (en) * | 1989-07-06 | 1991-01-11 | France Etat | METHOD FOR CONTROLLING THE THICKNESS OF AN ANTIREFLECTION LAYER AND INSTALLATION FOR IMPLEMENTING THE SAME |
| EP0407298A1 (en) * | 1989-07-06 | 1991-01-09 | France Telecom | Method for monitoring the thickness of an antireflection layer and apparatus for carrying out the same |
| DE3925536A1 (en) * | 1989-08-02 | 1991-02-07 | Leybold Ag | ARRANGEMENT FOR THICKNESSING OF THICK FILMS |
| GB2240179A (en) * | 1990-01-12 | 1991-07-24 | Leybold Inficon Inc | Control circuitry for quartz crystal deposition monitor |
| GB2242523A (en) * | 1990-03-30 | 1991-10-02 | Leybold Inficon Inc | Measuring and controlling deposition on a piezoelectric monitor crystal |
| GB2242523B (en) * | 1990-03-30 | 1993-10-27 | Leybold Inficon Inc | Measuring and controlling deposition on a piezoelectric monitor crystal |
| EP1094341A3 (en) * | 1999-10-15 | 2002-08-28 | Sony Corporation | Apparatus and method for producing optical component |
| US6733821B1 (en) | 1999-10-15 | 2004-05-11 | Sony Corporation | Method for forming an optical component |
| EP1602919A1 (en) * | 2004-06-01 | 2005-12-07 | Applied Films GmbH & Co. KG | Measuring device for the survey of the transmittance of a coating |
| US7414738B2 (en) | 2004-06-01 | 2008-08-19 | Applied Materials Gmbh & Co. Kg. | Measuring device for measuring the degree of transmission of a coating |
Also Published As
| Publication number | Publication date |
|---|---|
| GB2029017B (en) | 1982-10-13 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 732 | Registration of transactions, instruments or events in the register (sect. 32/1977) | ||
| PCNP | Patent ceased through non-payment of renewal fee |