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                                                                    ICP-Mass Spectrometry


                                                                    Author
                                                                    Kenneth Ong
                                                                    PerkinElmer, Inc.
                                                                    Singapore




Determination of
Impurities in                                  Introduction
Semiconductor-Grade                           The making of a semiconductor device comprises
                                              of forming a sacrificial layer on a substrate. Usually,
Sulfuric Acid with the                        a patterned resist layer forms the sacrificial layer
                                              so that ion implantation to the substrate can be
NexION 300S ICP-MS                            performed, after which a wet etching solution is
                                              used to remove the patterned photoresist layer.
     Typically, an etching solution comprises of sulfuric acid (H2SO4) and peroxide (H2O2), known
     as piranha or ozonated sulfuric acid. As with other chemicals used, any metal impurities
     present would have detrimental effect on the reliability of an IC device and thus need to be
     of high purity and quality. SEMI Standard C44-0708 specifies the maximum concentration of
     metal contaminants by element and tier for sulfuric acid.

     Inductively coupled plasma mass spectrometry (ICP-MS) is an indispensable analytical tool for
     quality control because of its superior capability to detect at the ultratrace (ng/L or parts-per-
     trillion) level. Nevertheless, under the conventional plasma conditions, argon ions combine
     with matrix components to generate polyatomic interferences. Some of the interferences in
     sulfuric acid are 32S15N+ on 47Ti+, 32S16O2+ on 64Zn+, ArS+ on 70-74Ge+, 38Ar1H+ on 39K+, 40Ar+ on
     40
        Ca+, 40Ar16O+ on 56Fe+.

     The Dynamic Reaction Cell (DRC™), which uses a quadrupole mass filter to create Dynamic
     Bandpass Tuning (DBT), is a powerful correction technique to remove interferences on
     analytes of interest. Collision cells, using nonreactive gases, have proven to be another
     simple method in reducing specific polyatomic interferences. Both of these techniques
     are available in PerkinElmer’s NexION® 300 ICP-MS through its unique Universal Cell
     Technology™, which allows the use of all three modes (Standard, Collision and Reaction)
     within one analytical method.
This application note demonstrates the ability of the NexION   instrumentation used for this experiment was the NexION
    300 ICP-MS to remove interferences so that trace levels of     300S ICP-MS (PerkinElmer, Shelton, CT USA). Instrumental
    impurities in H2SO4 can be measured under a single set of      parameters and sample introduction components are shown
    hot plasma conditions for all analytes in one analysis.        in Table 1.


    Experimental conditions                                        Results
    Normally, the concentration of H2SO4 is around 98%. In         H2SO4 samples were quantitatively analyzed using additions
    this experiment, a ten-fold dilution is carried out on 98%     calibrations; the calibration curves for Zn, K, Ca, Fe and Ni
    semiconductor-grade H2SO4 from our customer. Standard          are shown in Figures 1–3, indicating good linearity. This is
    solutions were made from a 10 mg/L multi-element standard      possible with all the polyatomic interferences removed by
    (PerkinElmer Pure, PerkinElmer, Shelton, CT USA). The          the reactive NH3 gas in combination with the bandpass.



      Table 1. Instrumental parameters and sample introduction components for the NexION 300S ICP-MS.
      Spray Chamber:	          PFA-Scott	                          Plasma Gas: 	             18 L/min
      Torch:	                  High Efficiency Quartz	             Auxiliary Gas:	           1 L/min
      Torch Injector:	         PFA-Platinum	                       Nebulizer Flow:	          0.96 L/min
      Sampler Cone:	           Platinum	                           RF Power:	                1500 W
      Skimmer Cone:	           Platinum	                           Integration Time:	 1 sec/mass
      Nebulizer:	              PFA-100 (100 µL/min)	               Replicates:	              3




    Figure 1. Zn calibration, with He cell gas flow of 3 mL/min.   Figure 2. Fe calibration, with NH3 cell gas flow of 0.6 mL/min.




                                                                   Figure 3. Ni calibration, with NH3 cell gas flow of 0.3 mL/min.

2
The detection limits (DLs) and background equivalent
concentrations (BECs) were both determined in 10%                           Table 2. Detection limits (DLs), background equivalent
H2SO4, while accounting for the sensitivities in 10%                        concentrations (BECs), and 20 ng/L spike recoveries for all
                                                                            analytes in 10% H2SO4.
H2SO4. DLs were calculated by multiplying the standard
deviation by three, and BECs were determined by                             		            Cell Gas Flow*		 DL	 BEC	 20 ppt
                                                                            Analyte	 Mass	 (mL/min)	 RPq	 (ppt)	 (ppt)	 Recovery	 % RSD
measuring the signal intensities. Recoveries were
determined from 20 ng/L spikes. The results are                             Li	        7	            0	     0.25	 0.04	0.04	 102%	 2.7
summarized in Table 2.                                                      Be	        9	            0	     0.25	 0.2	0.03	103%	 3.3
                                                                            B	         11	           0	     0.25	0.9	 11	 100%	 3.2
Stability was determined by continuous introduction
                                                                            Na	        23	           0	     0.25	0.7	 3.3	 103%	 2.1
into the NexION 300S of 10 ng/L spikes in 10% H2SO4
                                                                            Mg	        24	           0	     0.25	0.2	 0.4	 102%	 1.3
(without rinse) for 10 hours. Figures 4 and 5 show
excellent stability, with RSDs of < 3% over 10 hours.                       Al	        27	           0.6	   0.5	 0.7	1.0	 96%	 1.5
The stability results, combined with the spike recovery                     K	         39	           0.6	 0.7	2	 7	113%	1.7
data, highlight the ability of the NexION 300S ICP-MS                       Ca	        40	           1	     0.5	 1	3.2	97%	 1.1
to determine all SEMI-required elements in the H2SO4                        V	         51	           0.6	   0.5	 0.9	ND	103%	 1.3
matrix.
                                                                            Cr	        52	           0.3	   0.5	 5	 155	102%	 1.8
                                                                            Mn	        55	           0.6	   0.7	 0.4	2.2	 98%	 1.3
                                                                            Fe	        56	           0.6	   0.7	 2	 22	113%	 1.5
                                                                            Co	        59	           0.3	   0.65	0.1	 0.3	 106%	 1.4
                                                                            Ni	        60	           0.3	 0.7	1	 2	 99%	 1.8
                                                                            Cu	        63	           0.3	 0.75	1	 2	 103%	 1.9
                                                                            Zn	        68	       3(He)	 0.25	10	 40	 103%	 2.9
                                                                            Ga	        69	           0.6	   0.7	 0.2	0.3	103%	 1.1
                                                                            Ge	        74	           0.3	 0.65	1	 2	 105%	 1.8
                                                                            As	        75	           0	     0.25	0.4	 0.9	 100%	 2.1
Figure 4. Ten-hour long-term stability results at 10 ng/L level for first   Sr	        88	           0	     0.25	0.1	ND	106%	 1.4
group of analytes.
                                                                            Zr	        90	           0	     0.25	0.5	 1.9	 102%	 1.4
                                                                            Nb	        93	           0	     0.25	0.1	ND	100%	 1.2
                                                                            Mo	        98	           0.3	   0.5	 0.9	ND	 98%	 1.8
                                                                            Ru	       102	           0	     0.25	 0.3	0.19	 96%	 1.5
                                                                            Rh	       103	           0	     0.25	0.03	 0.4	 104%	 1.2
                                                                            Pd	       106	           0	     0.25	0.4	ND	102%	 1.8
                                                                            Ag	       107	           0	     0.25	0.4	 0.5	 102%	 1.7
                                                                            Cd	       114	           0	     0.25	0.3	 0.6	 101%	 1.5
                                                                            In	       115	           0	     0.25	0.07	 0.1	 102%	 1.6
                                                                            Sn	       120	           0	     0.25	1	 8	 99%	 1.7

Figure 5. Ten-hour long-term stability results at 10 ng/L level for
                                                                            Sb	       121	           0	     0.25	0.2	ND	103%	 1.6
second group of analytes.                                                   Ba	       138	           0	     0.25	0.07	ND	 101%	 1.3
                                                                            Ta	       181	           0	     0.25	0.2	ND	103%	 2.0
                                                                            W	        184	           0	     0.25	0.3	ND	100%	 1.8
                                                                            Pt	       195	           0	     0.25	0.5	ND	105%	 1.9
                                                                            Au	       197	           0	     0.25	1	ND	93%	 -
                                                                            Tl	       205	           0.6	   0.5	 0.02	ND	 104%	 1.2
                                                                            Pb	       208	           0.6	   0.5	 0.1	ND	102%	 1.5
                                                                            Bi	       209	           0.6	   0.5	 0.02	ND	 103%	 1.8
                                                                            U	        238	           0	     0.25	0.06	ND	 102%	 1.9
                                                                            *Cell gas used is NH3.




                                                                                                                                          3
Conclusion
The NexION 300S ICP-MS is shown to be robust and suitable
for the routine quantification of ultratrace impurities at
the ng/L level in H2SO4. By means of computer-controlled
switching between Standard mode and Reaction mode
in the Universal Cell, interference-free analysis using hot
plasma conditions for all analytes is possible during a single
sample run.


References
1.	SEMI Standard C44-0708, SEMI Standards, http://www.
   semi.org/en/index.htm




PerkinElmer, Inc.
940 Winter Street
Waltham, MA 02451 USA	
P: (800) 762-4000 or
(+1) 203-925-4602
www.perkinelmer.com



For a complete listing of our global offices, visit www.perkinelmer.com/ContactUs

Copyright ©2012, PerkinElmer, Inc. All rights reserved. PerkinElmer® is a registered trademark of PerkinElmer, Inc. All other trademarks are the property of their respective owners.

010282_01

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Application Note: Determination of Impurities in Semiconductor-Grade Sulfuric Acid with the NexION 300S ICP-MS

  • 1. a p p l i c at i o n N o t e ICP-Mass Spectrometry Author Kenneth Ong PerkinElmer, Inc. Singapore Determination of Impurities in Introduction Semiconductor-Grade The making of a semiconductor device comprises of forming a sacrificial layer on a substrate. Usually, Sulfuric Acid with the a patterned resist layer forms the sacrificial layer so that ion implantation to the substrate can be NexION 300S ICP-MS performed, after which a wet etching solution is used to remove the patterned photoresist layer. Typically, an etching solution comprises of sulfuric acid (H2SO4) and peroxide (H2O2), known as piranha or ozonated sulfuric acid. As with other chemicals used, any metal impurities present would have detrimental effect on the reliability of an IC device and thus need to be of high purity and quality. SEMI Standard C44-0708 specifies the maximum concentration of metal contaminants by element and tier for sulfuric acid. Inductively coupled plasma mass spectrometry (ICP-MS) is an indispensable analytical tool for quality control because of its superior capability to detect at the ultratrace (ng/L or parts-per- trillion) level. Nevertheless, under the conventional plasma conditions, argon ions combine with matrix components to generate polyatomic interferences. Some of the interferences in sulfuric acid are 32S15N+ on 47Ti+, 32S16O2+ on 64Zn+, ArS+ on 70-74Ge+, 38Ar1H+ on 39K+, 40Ar+ on 40 Ca+, 40Ar16O+ on 56Fe+. The Dynamic Reaction Cell (DRC™), which uses a quadrupole mass filter to create Dynamic Bandpass Tuning (DBT), is a powerful correction technique to remove interferences on analytes of interest. Collision cells, using nonreactive gases, have proven to be another simple method in reducing specific polyatomic interferences. Both of these techniques are available in PerkinElmer’s NexION® 300 ICP-MS through its unique Universal Cell Technology™, which allows the use of all three modes (Standard, Collision and Reaction) within one analytical method.
  • 2. This application note demonstrates the ability of the NexION instrumentation used for this experiment was the NexION 300 ICP-MS to remove interferences so that trace levels of 300S ICP-MS (PerkinElmer, Shelton, CT USA). Instrumental impurities in H2SO4 can be measured under a single set of parameters and sample introduction components are shown hot plasma conditions for all analytes in one analysis. in Table 1. Experimental conditions Results Normally, the concentration of H2SO4 is around 98%. In H2SO4 samples were quantitatively analyzed using additions this experiment, a ten-fold dilution is carried out on 98% calibrations; the calibration curves for Zn, K, Ca, Fe and Ni semiconductor-grade H2SO4 from our customer. Standard are shown in Figures 1–3, indicating good linearity. This is solutions were made from a 10 mg/L multi-element standard possible with all the polyatomic interferences removed by (PerkinElmer Pure, PerkinElmer, Shelton, CT USA). The the reactive NH3 gas in combination with the bandpass. Table 1. Instrumental parameters and sample introduction components for the NexION 300S ICP-MS. Spray Chamber: PFA-Scott Plasma Gas: 18 L/min Torch: High Efficiency Quartz Auxiliary Gas: 1 L/min Torch Injector: PFA-Platinum Nebulizer Flow: 0.96 L/min Sampler Cone: Platinum RF Power: 1500 W Skimmer Cone: Platinum Integration Time: 1 sec/mass Nebulizer: PFA-100 (100 µL/min) Replicates: 3 Figure 1. Zn calibration, with He cell gas flow of 3 mL/min. Figure 2. Fe calibration, with NH3 cell gas flow of 0.6 mL/min. Figure 3. Ni calibration, with NH3 cell gas flow of 0.3 mL/min. 2
  • 3. The detection limits (DLs) and background equivalent concentrations (BECs) were both determined in 10% Table 2. Detection limits (DLs), background equivalent H2SO4, while accounting for the sensitivities in 10% concentrations (BECs), and 20 ng/L spike recoveries for all analytes in 10% H2SO4. H2SO4. DLs were calculated by multiplying the standard deviation by three, and BECs were determined by Cell Gas Flow* DL BEC 20 ppt Analyte Mass (mL/min) RPq (ppt) (ppt) Recovery % RSD measuring the signal intensities. Recoveries were determined from 20 ng/L spikes. The results are Li 7 0 0.25 0.04 0.04 102% 2.7 summarized in Table 2. Be 9 0 0.25 0.2 0.03 103% 3.3 B 11 0 0.25 0.9 11 100% 3.2 Stability was determined by continuous introduction Na 23 0 0.25 0.7 3.3 103% 2.1 into the NexION 300S of 10 ng/L spikes in 10% H2SO4 Mg 24 0 0.25 0.2 0.4 102% 1.3 (without rinse) for 10 hours. Figures 4 and 5 show excellent stability, with RSDs of < 3% over 10 hours. Al 27 0.6 0.5 0.7 1.0 96% 1.5 The stability results, combined with the spike recovery K 39 0.6 0.7 2 7 113% 1.7 data, highlight the ability of the NexION 300S ICP-MS Ca 40 1 0.5 1 3.2 97% 1.1 to determine all SEMI-required elements in the H2SO4 V 51 0.6 0.5 0.9 ND 103% 1.3 matrix. Cr 52 0.3 0.5 5 155 102% 1.8 Mn 55 0.6 0.7 0.4 2.2 98% 1.3 Fe 56 0.6 0.7 2 22 113% 1.5 Co 59 0.3 0.65 0.1 0.3 106% 1.4 Ni 60 0.3 0.7 1 2 99% 1.8 Cu 63 0.3 0.75 1 2 103% 1.9 Zn 68 3(He) 0.25 10 40 103% 2.9 Ga 69 0.6 0.7 0.2 0.3 103% 1.1 Ge 74 0.3 0.65 1 2 105% 1.8 As 75 0 0.25 0.4 0.9 100% 2.1 Figure 4. Ten-hour long-term stability results at 10 ng/L level for first Sr 88 0 0.25 0.1 ND 106% 1.4 group of analytes. Zr 90 0 0.25 0.5 1.9 102% 1.4 Nb 93 0 0.25 0.1 ND 100% 1.2 Mo 98 0.3 0.5 0.9 ND 98% 1.8 Ru 102 0 0.25 0.3 0.19 96% 1.5 Rh 103 0 0.25 0.03 0.4 104% 1.2 Pd 106 0 0.25 0.4 ND 102% 1.8 Ag 107 0 0.25 0.4 0.5 102% 1.7 Cd 114 0 0.25 0.3 0.6 101% 1.5 In 115 0 0.25 0.07 0.1 102% 1.6 Sn 120 0 0.25 1 8 99% 1.7 Figure 5. Ten-hour long-term stability results at 10 ng/L level for Sb 121 0 0.25 0.2 ND 103% 1.6 second group of analytes. Ba 138 0 0.25 0.07 ND 101% 1.3 Ta 181 0 0.25 0.2 ND 103% 2.0 W 184 0 0.25 0.3 ND 100% 1.8 Pt 195 0 0.25 0.5 ND 105% 1.9 Au 197 0 0.25 1 ND 93% - Tl 205 0.6 0.5 0.02 ND 104% 1.2 Pb 208 0.6 0.5 0.1 ND 102% 1.5 Bi 209 0.6 0.5 0.02 ND 103% 1.8 U 238 0 0.25 0.06 ND 102% 1.9 *Cell gas used is NH3. 3
  • 4. Conclusion The NexION 300S ICP-MS is shown to be robust and suitable for the routine quantification of ultratrace impurities at the ng/L level in H2SO4. By means of computer-controlled switching between Standard mode and Reaction mode in the Universal Cell, interference-free analysis using hot plasma conditions for all analytes is possible during a single sample run. References 1. SEMI Standard C44-0708, SEMI Standards, http://www. semi.org/en/index.htm PerkinElmer, Inc. 940 Winter Street Waltham, MA 02451 USA P: (800) 762-4000 or (+1) 203-925-4602 www.perkinelmer.com For a complete listing of our global offices, visit www.perkinelmer.com/ContactUs Copyright ©2012, PerkinElmer, Inc. All rights reserved. PerkinElmer® is a registered trademark of PerkinElmer, Inc. All other trademarks are the property of their respective owners. 010282_01