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SEMI M1-0305 © SEMI 1978, 2005 48 R2-7.14 Site Flatness is generally determined by SEM I MF1530 (see Not e 1, above). The m ost commonly used site flatness parameter is SFQR; other site flatness paramet ers are discussed…

SEMI M1-0305 © SEMI 1978, 2005 47
R2-7.2 Flat Length should be determined by SEMI MF671. If flat diameter is specified instead of flat length, it can
be determined by ¶6.2.1 of DIN 50441/4 or by a dial gauge method as agreed upon between the supplier and
customer. Both SEMI MF671 and DIN 50441/4 take account of the possibility that the ends of the flat might be
rounded.
R2-7.3 Notch Dimensions should be determined by SEMI MF1152 (see Figure 5).
R2-7.4 Flat Orientation can be confirmed by SEMI MF847. There is no standardized method for determining the
crystallographic orientation of the diameter that bisects the notch.
R2-7.5 Edge Profile is usually determined by using one of the two templates (see Figure 6) with Method B of SEMI
MF928 or Procedure 2 of DIN 50441/2, both of which are nondestructive. The other two procedures in these
methods are destructive and not so widely used.
R2-7.6 Thickness is usually determined at the center point of the wafer with the use of SEMI MF1530, an
automated technique. Manual techniques originally used in the industry include SEMI MF533, JIS H 0611, and
DIN 50441/1.
NOTE 2: Test methods SEMI MF1530 (for thickness, thickness variation, and flatness), SEMI MF1451 (for sori), and SEMI
MF1390 (for warp) may not be suitable for use on large diameter wafers with polished back surfaces. New standardized test
methods for measuring these parameters on such wafers are under development.
R2-7.7 Total Thickness Variation (TTV) was originally determined with the use of manual 5-point techniques
covered in SEMI MF533, JIS H 0611, and DIN 50441/1. JIS H 0611 differs from SEMI MF533 and DIN 50441/1,
in that the measurements in JIS H 0611 are taken at the center and at 5 mm from the edge on diameters parallel and
perpendicular to the primary flat or notch bisector, while the measurements in SEMI MF533 and DIN 50441/1 are
taken at the center and at 6 mm from the edge on diameters 30 degrees and 120 degrees counterclockwise from the
bisector to the primary flat or notch (with the wafer facing front surface up). TTV can also be determined with the
use of SEMI MF657, which involves a continuous scan pattern over a portion of the wafer surface. Currently,
however, it is most frequently determined using SEMI MF1530, which involves an automated continuous scan
pattern over the entire wafer surface. In this case, the quantity determined is equal to the global flatness GBIR (see
Appendix 1 and Note 1, above).
R2-7.8 Surface Orientation can be determined by the x-ray methods of SEMI MF26, JEITA EM-3501, or DIN
50433/1, the optical method of SEMI MF26 or DIN 50433/2, or the Laue method of DIN 50433/3.
R2-7.9 For off-orientation {111} wafers, the orthogonal misorientation is specified for each of the wafer categories
in Tables 4 through 9. There is no standardized measurement method for this property so it should be determined by
a method agreed upon between supplier and customer.
R2-7.10 Bow can be determined with the manual methods SEMI MF534 and JIS H 0611. Currently, bow is not as
widely used a parameter as warp.
R2-7.11 Warp is currently most often measured with the use of SEMI MF1390, which is an automated method with
full surface scan and correction for gravitational sag. It can also be measured with the use of the contactless manual
method SEMI MF657, in which the prescribed scan pattern covers only a portion of the wafer surface in which there
is no correction for gravitational sag. As noted in Appendix 2, different reference planes are used for the two
methods. Because SEMI MF657 employs a back surface reference plane, the measured warp may include
contributions from thickness variation of the wafer. SEMI MF1390 employs a median surface reference plane and
is not susceptible to interferences from thickness variations. In general, the latter is preferred, especially for wafers
150 mm in diameter and larger (see Note 1, above).
R2-7.12 Sori , which is sometimes specified in lieu of bow or warp or both, can be determined by SEMI MF1451
(see Note 1, above).
R2-7.13 Global Flatness can be determined by either capacitance measurements, as in SEMI MF1530, or by
multiple beam interference, as in DIN 50441/3. Generally, the former is considered to be more reliable, especially
as the need increases for measuring smaller flatness deviation (see Note 1, above). As noted in ¶R2-7.7, GBIR is the
same as TTV; other global flatness parameters are discussed in Appendix 1.

SEMI M1-0305 © SEMI 1978, 2005 48
R2-7.14 Site Flatness is generally determined by SEMI MF1530 (see Note 1, above). The most commonly used
site flatness parameter is SFQR; other site flatness parameters are discussed in Appendix 1. Although it is not
widely used, the scanning site flatness parameter SFSR was recently introduced. For this parameter, use a subsite
width, Wss, equal to 8 mm and orient the wafer so the effective scan direction is along the wafer’s y-axis as defined
in SEMI M20.
R2-7.14.1 SEMI M49 is a guide for specifying test equipment for use in determining thickness, shape, and flatness
parameters on wafers intended to be used to fabricate advanced integrated circuits.
R2-7.15 Nanotopography should be determined by SEMI M43. This guide gives a variety of options that can be
used, so it is essential to specify the various conditions that are desired in any given case. The conditions chosen
should be agreed upon between supplier and customer.
R2-8 Front Surface Chemistry
R2-8.1 Surface Metal Contaminants
R2-8.1.1 Sodium, aluminum, potassium, and iron can be measured by secondary ion mass spectrometry (SIMS),
inductively coupled plasma mass spectrometry (ICP/MS), or atomic absorption spectroscopy (AAS). SIMS has
been standardized as SEMI MF1617. The latter two methods are frequently combined with vapor phase
decomposition (VPD), but they have not yet been standardized.
R2-8.1.2 Potassium, chromium, iron, nickel, copper, and zinc can be measured by Total Reflection X-Ray
Fluorescence Spectroscopy (TXRF), ICP/MS, and AAS. TXRF has been standardized both with (SEMI M33 and
ISO 17706) and without (ISO 14706) use of VPD to preconcentrate the surface metal contaminants.
R2-8.1.2.1 VPD is chemical preconcentration of the surface metals using vapor phase HF to decompose the surface
native oxide and a water (or acid-spiked water) droplet to scan across the wafer dissolving the surface metals. The
recovery rate of this preconcentration method is dependent upon the chemistry of the surface metals and upon the
chemistry used for the preconcentration. An alternative preconcentration method to VPD is to scan an acid droplet
across the wafer surface.
R2-8.1.2.2 VPD/AAS is a single-element technique which is widely used in Japan. It is element-specific and very
sensitive. VPD/ICP-MS is a rapid multi-element technique which is a more recent development. It is also very
sensitive, but its reproducibility is dependent upon the injection process into the ICP-MS. VPD/TXRF is an even
more recently developed multi-element technique. It is also very sensitive, but its reproducibility is dependent on
the residue-drying process.
R2-8.2 Surface Organics can be measured by SEMI MF1982. This standard describes two methods; the method to
be utilized should be agreed upon between supplier and customer.
R2-9 Surface Inspection Characteristics
R2-9.1 Visual Inspection of either the front or back surface of wafers can be carried out in accordance with SEMI
MF523 or JIS H 0614. The following conditions should be used for examination under high intensity illumination:
Background light intensity: 8 ± 2 fc (86 ± 22 lux),
Angle (alpha): 45 ± 10, and
Angle (beta): 90 ± 10.
See ¶6.8 for a discussion of which artifacts on the surface should be considered as defects. SEMI MF154 is a useful
guide for identifying structures and contaminants seen on silicon surfaces.
R2-9.1.1 Scratches—In inspecting for scratches, it is important to note that while macro-scratches can be seen under
both high intensity and diffuse illumination, micro-scratches can be seen only under high intensity illumination.
Therefore, to separate the two kinds of scratches, it is necessary to count the scratches observed under both kinds of
illumination. The count of scratches seen under diffuse illumination is the number of macro-scratches while the
difference of the counts seen under high intensity illumination and diffuse illumination is the number of micro-
scratches. Of course, if the total requirement is for no scratches of either kind, then examination under high
intensity illumination only is adequate.

SEMI M1-0305 © SEMI 1978, 2005 49
R2-9.2 X-ray Topography (DIN 50443/1) can also be used to test for defects in silicon wafers. This method may
see defects that do not intersect the surface, and can also be used to examine for bulk defects in the wafer (see
Section 2.4.10 of Table 1).
R2-9.3 Automated Surface Inspection by Light Scattering can also be used to detect many surface defects,
especially on polished surfaces. These techniques have not been fully standardized but there is a group of standards
that assist in making certain that the instruments are performing correctly. These include SEMI M52 for
determining if surface scanning inspection systems (SSIS) have suitable characteristics for the desired use, SEMI
M53 for calibrating SSISs, SEMI M58 for assuring that the calibration artifacts meet the desired requirements,
SEMI M50 for determining capture rate characteristics of SSISs and SEMI M35 for discriminating among various
surface features with an SSIS. Because of the lack of complete standardization, the testing conditions for use of
SSISs should be agreed upon between supplier and customer.
R2-9.3.1 Localized Light Scatterers — SSISs are particularly appropriate for inspecting polished surfaces for the
presence of particles and other localized light scatterers (LLS). In this case, it is essential to define the size ranges
(in units of latex sphere equivalents, LSE) as well as the maximum permissible counts, usually in terms of counts
per wafer, but occasionally in terms of counts per unit area.
R2-9.4 Surface Roughness affects the size of particle or other LLS that can be detected on a surface. SEMI M40
provides guidance on how to measure and report surface roughness on planar surfaces. Surface microroughness can
be determined with SSISs, through the use of the power spectral density as described in SEMI MF1811, or with an
atomic force microscope, which can be calibrated with the use of JEITA EM-3505. Other documents useful in
connection with surface microroughness measurements include ISO 4287/1 and ANSI/ASME B46.1. Because of
the lack of standardization, the testing conditions for surface microroughness measurements should be agreed upon
between supplier and customer.
R2-9.5 Back Surface Finish of 300 mm diameter wafers is specified as “polished.” The standard quantitative test
for the polish finish, which is not a smooth as the mirror polished front surface, is gloss. The general techniques for
determining gloss are given in ASTM Test Method D 523 and JIS Z 8741. However, for measuring gloss of silicon
surfaces, visible illumination at a 60 angle of incidence is referenced to a mirror polished silicon front surface.
Surface microroughness measurements (see ¶R2-9.4) can also be used as a quantitative test for back surface finish,
especially when it is necessary to observe particles or other LLSs smaller than 0.25 m LSE on the surface.
NOTICE: SEMI makes no warranties or representations as to the suitability of the standards set forth herein for any
particular application. The determination of the suitability of the standard is solely the responsibility of the user.
Users are cautioned to refer to manufacturer's instructions, product labels, product data sheets, and other relevant
literature, respecting any materials or equipment mentioned herein. These standards are subject to change without
notice.
By publication of this standard, Semiconductor Equipment and Materials International (SEMI) takes no position
respecting the validity of any patent rights or copyrights asserted in connection with any items mentioned in this
standard. Users of this standard are expressly advised that determination of any such patent rights or copyrights, and
the risk of infringement of such rights are entirely their own responsibility.