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[0001] The present invention relates to enhancing process control of plasma based semiconductor manufacturing processes. In particular, at least some embodiments of the present invention relate to modeling and monitoring light spectra emitted by the plasma of a plasma based semiconductor manufacturing process and control the plasma based process based on the light spectra.
[0002] A “plasma based semiconductor process” generally refers to a methodology for fabricating microelectronic devices such as very large scale integration (VLSI) microelectronic chips and/or thin film transistors (TFTs). In particular, plasma based semiconductor processes may be used, for example, in deposition processes (e.g., plasma enhanced chemical vapor deposition, hereinafter “PECVD”) and/or etching processes during the fabrication of microelectronic devices.
[0003] For example, a PECVD run (a particular instance of conducting a PECVD process) includes the following steps: 1) a device to be processed is placed within a chamber; 2) an initial condition is created inside the chamber using control parameters (e.g., RF power, electrode spacing, gas pressure, SiH
[0004] During a PECVD run, diagnosis and proper process control of the PECVD run are desired in order to ensure that microelectronic devices produced by the PECVD run are free of defects. The diagnostics and proper process control may be provided manually or automatically in order to determine when an end point has been reached in order to adjust the control parameters while the PECVD run is in progress.
[0005] A first group of conventional methods for controlling a PECVD run focus on determining when its end point is reached. There are three general techniques in this group of conventional methods: (1) optical end point; (2) interferometric end point; and (3) test wafer measurement.
[0006] The optical end point technique involves determining the end point of a PECVD run by monitoring one or two narrow spectral bands of spectral emission from the plasma of the PECVD run. This technique is generally not predictive. In particular, use of this technique does not adequately permit detection of an approaching end point. Thus, a PECVD run must first come to its end point before the end point is observed by this technique, which almost always causes delays in terminating the PECVD run (which, e.g., can then result in the endpoint being overshot). While these shortcomings may be overlooked in experimental PECVD runs, they may cause unacceptable level of errors should this technique be used in manufacturing processes.
[0007] The interferometric end point technique also attempts to determine the end point, but uses interferometric interference fringes as a measurement. However, a number of different types of material (e.g., metal) do not show the interferometric interference fringes unless the film deposited by the PECVD run is extremely thin. Hence, this technique may not be viable for depositing metal films. In addition, similar to the optical end point technique described above, the interferometric technique does not predict the end points, thereby causing delays in stopping a PECVD run when its end point is reached.
[0008] The test wafer measurement technique involves determination of the quality of microelectronic devices by physically examining one or more microelectronic devices per a batch of manufactured microelectronic devices. Each time a test microelectronic device is examined and passes a minimum standard (e.g., is determined to be within a predetermined range of the end point thickness), it acts as a certification that microelectronic devices of the batch may also meet the minimum standard. However, when a test microelectronic device fails to meet the minimum standard, each and every one of the microelectronic devices of that batch must be discarded or individually tested, which is an expensive process because each microelectronic device may be worth many tens of thousands of dollars. Another drawback of this technique is the fact that many of the quality tests are destructive in nature.
[0009] In addition to the deficiencies mentioned above, the above described conventional techniques of process control cannot detect a PECVD run that has gone out of optimal process specifications (e.g., overshot the optimal thickness of the deposition film) while the process is ongoing. In addition, these techniques do not provide steps that are necessary to correct erroneous processes.
[0010] In order to reduce some of the shortcomings of the above-described techniques, a second group of conventional techniques have also been developed. This group of conventional techniques does not focus on determining when the end points have been reached as in the first conventional techniques. Instead, the second group monitors ongoing processes. An example of such techniques involves monitoring the control parameters. This technique has shown some success in predicting film properties for PECVD runs, but it is still relatively inaccurate in determining the end points because this technique relies only on the control parameters without monitoring the actual PECVD run (e.g., without monitoring the progress of the device being produced).
[0011] Thus, what is needed is a scheme to better control semiconductor processes so that, e.g., the quality of fabricated microelectronic devices will increase.
[0012] Embodiments of the present invention advantageously overcome the above described shortcomings of the aforementioned techniques. In particular, embodiments of the present invention provide a system, method and medium for modeling, monitoring, and/or controlling plasma based semiconductor manufacturing processes. For instance, in at least some embodiments of the present invention, a method of modeling/controlling a plasma based semiconductor manufacturing process includes the steps of conducting a plurality of semiconductor manufacturing process runs by changing at least one of process parameters from its target value, and collecting spectral data indicative of the light emitted by plasma during each of said semiconductor manufacturing process runs. The modeling/controlling also includes the step of formulating a ratio based on a relationship between the collected spectral data and the changes in the at least one of the plurality of process parameters.
[0013] The detailed description of the present application showing various distinctive features may be best understood when the detailed description is read in reference to the appended drawing in which:
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[0033] Embodiments of the present invention provide proper diagnostics and/or process control to plasma based semiconductor manufacturing processes by conducting one or more of the high-level steps indicated in
[0034] In the modeling step (step
[0035] Detail processes of the modeling step, which includes a number of sub-steps, are described with regard to
[0036] In context of modeling step
[0037] An example modeling run for an optimal SiO
[0038] Another example modeling run is described with regard to
[0039] Table 1 illustrates detailed information on a modeling run similar to the above example modeling run of
TABLE 1 Center Point (CP) values below. Pressure Spacing Power SiH4 N2O 1. Perform chamber conditioning. Obtain CP values. CP 2.70 500 315.0 260 3500 Calculated 10% and 5% values (enter any other value below if calculated value is not desired): +10% 2.97 550 347.0 286 3850 −10% 2.43 450 283.0 234 3150 +5% 2.84 525 331.0 273 3675 −5% 2.57 475 299.0 247 3325 Wafer Pattern Pressure Spacing Power SiH4 N2O 2. Run 46 wafers according to the following 10% recipe. 1 00000 2.70 500 315.0 260 3500 2 000++ 2.70 500 315.0 286 3850 3 0+−00 2.70 550 283.0 260 3500 4 00000 2.70 500 315.0 260 3500 5 00000 2.70 500 315.0 260 3500 6 −+000 2.43 550 315.0 260 3500 7 0−00− 2.70 450 315.0 260 3150 8 −0+00 2.43 500 347.0 260 3500 9 0−+00 2.70 450 347.0 260 3500 10 +000− 2.97 500 315.0 260 3150 11 0+00+ 2.70 550 315.0 260 3850 12 0−−00 2.70 450 283.0 260 3500 13 00000 2.70 500 315.0 260 3500 14 00−0+ 2.70 500 283.0 260 3850 15 −0−00 2.43 500 283.0 260 3500 16 +0+00 2.97 500 347.0 260 3500 17 000−+ 2.70 500 315.0 234 3850 18 0−00+ 2.70 450 315.0 260 3850 19 0+0−0 2.70 550 315.0 234 3500 20 0+0+0 2.70 550 315.0 286 3500 21 +00−0 2.97 500 315.0 234 3500 22 00000 2.70 500 315.0 260 3500 23 +−000 2.97 450 315.0 260 3500 24 0−0+0 2.70 450 315.0 286 3500 25 00−0− 2.70 500 283.0 260 3150 26 000+− 2.70 500 315.0 286 3150 27 +000+ 2.97 500 315.0 260 3850 28 00−+0 2.70 500 283.0 286 3500 29 −00−0 2.43 500 315.0 234 3500 30 −−000 2.43 450 315.0 260 3500 31 ++000 2.97 550 315.0 260 3500 32 00++0 2.70 500 347.0 286 3500 33 +00+0 2.97 500 315.0 286 3500 34 +0−00 2.97 500 283.0 260 3500 35 000−− 2.70 500 315.0 234 3150 36 00+0− 2.70 500 347.0 260 3150 37 00+0+ 2.70 500 347.0 260 3850 38 −000− 2.43 500 315.0 260 3150 39 0+00− 2.70 550 315.0 260 3150 40 00+−0 2.70 500 347.0 234 3500 41 −000+ 2.43 500 315.0 260 3850 42 −00+0 2.43 500 315.0 286 3500 43 00−−0 2.70 500 283.0 234 3500 44 0++00 2.70 550 347.0 260 3500 45 00000 2.70 500 315.0 260 3500 46 0−0−0 2.70 450 315.0 234 3500 3. Run 8 wafers according to the following 5% recipe. 47 +−+−− 2.84 475 331.0 247 3325 48 −−++− 2.57 475 331.0 273 3325 49 −++−+ 2.57 525 331.0 247 3675 50 +−−++ 2.84 475 299.0 273 3675 51 −−−−+ 2.57 475 299.0 247 3675 52 +++++ 2.84 525 331.0 273 3675 53 −+−+− 2.57 525 299.0 273 3325 54 ++−−− 2.84 525 299.0 247 3325 4. Run 10 wafers varying one parameter at a time as follows. 55 +0000 2.97 500 315.0 260 3500 56 −0000 2.43 500 315.0 260 3500 57 0+000 2.70 550 315.0 260 3500 58 0−000 2.70 450 315.0 260 3500 59 00+00 2.70 500 347.0 260 3500 60 00−00 2.70 500 283.0 260 3500 61 000+0 2.70 500 315.0 286 3500 62 000−0 2.70 500 315.0 234 3500 63 0000+ 2.70 500 315.0 260 3850 64 0000− 2.70 500 315.0 260 3150 Run 10 wafers at CP. 65 to 74 00000 2.70 500 315.0 260 3500
[0040] The above described modeling run and the step of collecting spectral data (step
[0041] As shown in
[0042] In at least some embodiments of the present invention, spectrometer
[0043] Once the spectral data for the modeling run has been collected, a preliminary analysis of the spectral data can be conducted (and can be thought of as part of, e.g., step
[0044] In one instance of the preliminary analysis, the collected spectral data may be displayed on a computer display monitor (or used as input for an analysis program) in a number of different ways to provide different perspective of the collected spectral data. Example display methods may include: graphically displaying three-dimensional spectral data (wavelength on the vertical axis vs. time on the horizontal axis vs. intensity displayed as gray level variation,
[0045] The above-described spectral data can be collected using various techniques. One collection technique contemplated by at least some embodiments of the present invention is described below in connection with the collection of three-dimensional (intensity vs. wavelength vs. time) spectral data. Such data may be collected by spectrometer
[0046] As can be appreciated by the previous discussions, another part of the preliminary analysis as contemplated by at least some embodiments of the present invention includes analyzing the spectral data collected during the center point runs. This analysis establishes a baseline against which changes observed in the spectral data of the various non-center point recipes can be compared. This analysis may begin with characterization of the time-dependent behavior of the total emission (the sum of the intensities recorded in the 2048 CCD pixels each second,
[0047] The characterization of the time dependent behavior of the total emission may involve measuring the magnitude of the total emission observed as a function of time and noting any structure in the spectral data.
[0048] In addition, the characterization of the time-dependent behavior of the center point runs may involve the characterization of the time-dependent behavior of individual spectral bands.
[0049] The first behavior is the ±1% periodic oscillation of the spectral data. This behavior is consistent with interference fringes arising from the interaction of light reflecting from the substrate of the wafer undergoing the PECVD runs and the surface of the growing film during the PECVD run. As the film grows, the increasing thickness of the film causes the reflected light to add alternatively (e.g., constructively and destructively) as a function of time, giving rise to the fringe pattern. It follows that the light received by spectrometer
[0050] The second behavior noted in the wavelength traces is that the values of the spectral data decay for the first 30 seconds of the runs and then plateau for the final 30 seconds. This behavior may result because the light is reflected from two components. As noted above, the first component is the light that is reflected from the substrate and the second component is the light that is reflected from the surface of the growing film. If the substrate is more reflective than the film, the intensity of the reflected component of the light may decrease with time as the film grows. When the film becomes sufficiently thick, the values of the spectral data plateau because the component reflected from the substrate is minimized. A prediction of this model is that the interference fringes should disappear as the light reflected from the substrate is minimized. Therefore, it is expected that all traces decrease by about the same amount if the chamber and process conditions are equivalent for each run.
[0051] The above-described characterizations of the preliminary analysis are provided only as examples. Other observations and characterizations within the skill set of one of ordinary skill in the art are also contemplated within embodiments of the present invention.
[0052] After the preliminary analysis (or after collecting the spectral data without performing the preliminary analysis), a number of spectral bands are formed by combining the collected spectral data from a range of wavelengths (step
TABLE 2 λ λ(initial) λ(final) N/A 250 300 314 310 317 337 331 342 350 347 354 357 355 360 367 363 372 374 372 377 380 377 383 390 387 395 398 396 401 404 401 408 414 410 416 418 416 421 426 421 430 434 430 437 442 438 444 448 444 451 456 451 460 465 460 469 472 469 474 483 477 488 547 532 563 655 620 691 752 720 784
[0053] Once spectral bands are determined, spectral data corresponding to each formed spectral band is calculated, categorized, and analyzed (steps
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[0055] ↑ increase in band intensity
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[0059] ↓ decrease in band intensity
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[0061] It should be noted that, although Table 3 shows only qualitative measurements, using precise quantitative numbers is also contemplated within at least some embodiments of the present invention.
TABLE 3 Spectral Pressure Spacing Power SiH N Band (nm) Hi Lo Hi Lo Hi Lo Hi Lo Hi Lo 310-317
332-338.5
347.5-354.5
354.6-360
362.5-372.5
372.5-376.8
376.8-382
386-392.5
392.5-395
395-401.5
401.5-408
410-416