ImageVerifierCode 换一换
格式:PDF , 页数:7 ,大小:138.66KB ,
资源ID:535972      下载积分:5000 积分
快捷下载
登录下载
邮箱/手机:
温馨提示:
如需开发票,请勿充值!快捷下载时,用户名和密码都是您填写的邮箱或者手机号,方便查询和重复下载(系统自动生成)。
如填写123,账号就是123,密码也是123。
特别说明:
请自助下载,系统不会自动发送文件的哦; 如果您已付费,想二次下载,请登录后访问:我的下载记录
支付方式: 支付宝扫码支付 微信扫码支付   
注意:如需开发票,请勿充值!
验证码:   换一换

加入VIP,免费下载
 

温馨提示:由于个人手机设置不同,如果发现不能下载,请复制以下地址【http://www.mydoc123.com/d-535972.html】到电脑端继续下载(重复下载不扣费)。

已注册用户请登录:
账号:
密码:
验证码:   换一换
  忘记密码?
三方登录: 微信登录  

下载须知

1: 本站所有资源如无特殊说明,都需要本地电脑安装OFFICE2007和PDF阅读器。
2: 试题试卷类文档,如果标题没有明确说明有答案则都视为没有答案,请知晓。
3: 文件的所有权益归上传用户所有。
4. 未经权益所有人同意不得将文件中的内容挪作商业或盈利用途。
5. 本站仅提供交流平台,并不能对任何下载内容负责。
6. 下载文件中如有侵权或不适当内容,请与我们联系,我们立即纠正。
7. 本站不保证下载资源的准确性、安全性和完整性, 同时也不承担用户因使用这些下载资源对自己和他人造成任何形式的伤害或损失。

版权提示 | 免责声明

本文(ASTM F1894-1998(2011) Test Method for Quantifying Tungsten Silicide Semiconductor Process Films for Composition and Thickness《定量分析硅化钨半导体加工膜组分和厚度的标准试验方法》.pdf)为本站会员(registerpick115)主动上传,麦多课文库仅提供信息存储空间,仅对用户上传内容的表现方式做保护处理,对上载内容本身不做任何修改或编辑。 若此文所含内容侵犯了您的版权或隐私,请立即通知麦多课文库(发送邮件至master@mydoc123.com或直接QQ联系客服),我们立即给予删除!

ASTM F1894-1998(2011) Test Method for Quantifying Tungsten Silicide Semiconductor Process Films for Composition and Thickness《定量分析硅化钨半导体加工膜组分和厚度的标准试验方法》.pdf

1、Designation: F1894 98 (Reapproved 2011)Test Method forQuantifying Tungsten Silicide Semiconductor Process Filmsfor Composition and Thickness1This standard is issued under the fixed designation F1894; the number immediately following the designation indicates the year oforiginal adoption or, in the c

2、ase of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.1. Scope1.1 This test method covers the quantitative determinationof tungsten and silicon concentrati

3、ons in tungsten/silicon(WSix) semiconductor process films using Rutherford Back-scattering Spectrometry (RBS).2(1) This test method alsocovers the detection and quantification of impurities in themass range from phosphorus (31 atomic mass units (amu) toantimony (122 amu).1.2 This test method can be

4、used for tungsten silicide filmsprepared by any deposition or annealing processes, or both.The film must be a uniform film with an areal coverage greaterthan the incident ion beam (;2.5 mm).1.3 This test method accurately measures the following filmproperties: silicon/tungsten ratio and variations w

5、ith depth,tungsten depth profile throughout film, WSixfilm thickness,argon concentrations (if present), presence of oxide on surfaceof WSixfilms, and transition metal impurities to detectionlimits of 131014atoms/cm2.1.4 This test method can detect absolute differences insilicon and tungsten concentr

6、ations of 63 and 61 atomicpercent, respectively, measured from different samples inseparate analyses. Relative variations in the tungsten concen-tration in depth can be detected to 60.2 atomic percent with adepth resolution of 670.1.5 This test method supports and assists in qualifying WSixfilms by

7、electrical resistivity techniques.1.6 This test method can be performed for WSixfilmsdeposited on conducting or insulating substrates.1.7 This test method is useful for WSixfilms between 20 and400 nm with an areal coverage of greater than 1 by 1 mm2.1.8 This test method is non-destructive to the fil

8、m to theextent of sputtering.1.9 A statistical process control (SPC) of WSixfilms hasbeen monitored since 1993 with reproducibility to 64%.1.10 This test method produces accurate film thicknesses bymodeling the film density of the WSixfilm as WSi2(hexagonal)plus excess elemental Si2. The measured fi

9、lm thickness is alower limit to the actual film thickness with an accuracy lessthan 10 % compared to SEM cross-section measurements (see13.4).1.11 This test method can be used to analyze films on wholewafers up to 300 mm without breaking the wafers. The sitesthat can be analyzed may be restricted to

10、 concentric rings nearthe wafer edges for 200-mm and 300-mm wafers, dependingon system capabilities.1.12 The values stated in SI units are to be regarded asstandard. No other units of measurement are included in thisstandard.1.13 This standard does not purport to address all of thesafety concerns, i

11、f any, associated with its use. It is theresponsibility of the user of this standard to establish appro-priate safety and health practices and determine the applica-bility of regulatory limitations prior to use. The reader isreferenced to Section 8 of this test method for references tosome of the re

12、gulatory, radiation, and safety considerationsinvolved with accelerator operation.2. Referenced Documents2.1 Terminology used in this document is consistent withterms and definitions as used in the Compilation of ASTMStandard Definitions,8thed ASTM, 1994, Philadelphia PA,USA, specifically for terms

13、taken from the following ASTMstandards:2.2 ASTM Standards:3E135 Terminology Relating to Analytical Chemistry forMetals, Ores, and Related MaterialsE673 Terminology Relating to Surface AnalysisE1241 Guide for Conducting Early Life-Stage ToxicityTests with Fishes3. Terminology3.1 Numerous terms specif

14、ic to RBS and ion stopping insolids can be found in the following references (1, 2)2.3.2 Definitions of Terms Specific to This Standard:1This test method is under the jurisdiction of Committee F01 on Electronics ,andis the direct responsibility of Subcommittee F01.17 on Sputter Metallization.Current

15、 edition approved June 1, 2011. Published June 2011. Originallyapproved in 1998. Last previous edition approved in 2003 as F189498 (03). DOI:10.1520/F1894-98R11.2The boldface numbers in parentheses refer to a list of references at the end ofthe text.3For referenced ASTM standards, visit the ASTM web

16、site, www.astm.org, orcontact ASTM Customer Service at serviceastm.org. For Annual Book of ASTMStandards volume information, refer to the standards Document Summary page onthe ASTM website.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United Sta

17、tes.3.2.1 WSixa tungsten silicide film characterized by asilicon/tungsten atomic ratio 2.00.3.2.2 incident ionsHe+or He+ions with energy in therange of 2.25 to 2.30 MeV delivered to a sample surface froman appropriate ion source and accelerator system.3.2.3 backscattered ionsHelium particles (charge

18、d orneutral) recoiling from atoms in a sample structure irradiatedwith a collimated beam of incident ions.3.2.4 RBSRutherford backscattering spectromerty, the en-ergy analysis of backscattered ions for sample composition anddepth profile.3.2.5 normal angle detectora detector situated at an anglebetw

19、een 160 and 180 from the forward trajectory of theincident ion.3.2.6 grazing angle detectora detector situated at an anglebetween 90 to 130 from the forward trajectory of the incidention beam.4. Summary of Test Method4.1 Fig. 1 shows a schematic of the measurement technique.A collimated beam of alph

20、a particles (He+) is incident on thesample surface. A fraction of the incident ions are scattered outof the specimen with backscattered energies corresponding tothe atomic presence of elements in the sample at correspondingdepths.4.2 Spectra of the energy of backscattered ions are acquiredat normal

21、and grazing angle detectors for a measured quantityof integrated ion charge on the sample. The grazing angledetector is movable in order to maintain appropriate depthresolution for films of various thicknesses. The grazing angledetector position is chosen to provide a wide tungsten signal(increasing

22、 depth resolution) without causing an overlap of thetungsten and silicon signals. The normal angle detector is heldfixed to provide accuracy and reproducibility over manymonths.4.3 The spectra are analyzed for film composition andthickness using standard software packages. Requirements onthe paramet

23、ers used in software are enumerated in Section 13.5. Significance and Use5.1 This test method can be used to ensure absolute repro-ducibility of WSixfilm deposition systems over the course ofmany months. The time span of measurements is essentiallythe life of many process deposition systems.5.2 This

24、 test method can be used to qualify new WSixdeposition systems to ensure duplicability of existing systems.This test method is essential for the coordination of globalsemiconductor fabrication operations using different analyticalservices. This test method allows samples from various depo-sition sys

25、tems to be analyzed at different sites and times.5.3 This test method is the chosen calibration technique fora variety of analytical techniques, including, but not limited to:5.3.1 Electron spectroscopy for chemical analysis (ESCAorXPS),5.3.2 Auger electron spectroscopy (AES),5.3.3 Fourier transform

26、 infrared red spectroscopy (FTIR),5.3.4 Secondary ion mass spectrometry (SIMS), and5.3.5 Electron dispersive spectrometry (EDS) and particleinduced x-ray emission (PIXE).6. Interferences6.1 Since RBS is a measurement of the energy loss sufferedby energetic helium atoms from atomic masses, the interf

27、er-ence of signals results if two or more atoms in the same layerhave roughly the same atomic number (Z). The separation ofatomic numbers necessary for detectable, independent signalsvaries depending on the mass range of the element in question(1). Masses in the range of 12030 monthsF1894 98 (2011)4

28、NOTE 1Since the values were obtained from various samples with widely varying compositions, the ratios are normalized by originally measured silicon/tungsten ratios.FIG. 4 Running Plot of Measured Silicon/Tungsten Ratios Obtained in an SPC Program.F189498(2011)5generated from the theoretical model i

29、s then produced. Thegrazing angle detector spectrum yields the most precise depthresolution of the tungsten and silicon. The normal angledetector spectrum yields the most accurate layer thicknessesand silicon/tungsten ratios.13.3 For standardization of this test method, it is stronglyrecommended tha

30、t the stopping power coefficients as deter-mined by Ziegler and Chu (3) and reproduced in Table VII ofChu, Mayer, and Nicolet (1) be used in the data reduction of thetungsten and silicon signal heights. This suggestion is madedue to the near-universal recognition of and accessibility to thetext as a

31、n RBS reference. The polynomial fit to the (4) heliumstopping cross-section is reproduced here as follows:5A01 A1E 1 A2E21 A3E31 A4E41 A5E5(1)for tungsten, where the coefficients are:A0= 61.69A1= 156.6A2= 150.9A3= 62.45A4= 12.33, andA5= 0.9421.for silicon, where the coefficients are:A0= 57.97A1= 56.

32、59A2= 77.66A3= 36.41A4= 7.624, andA5= 0.5995.13.4 Subtract the minimum background of the 160 spec-trum between the silicon and tungsten signals. Set the effectivesolid angle of the spectra by normalizing the theoretical modelto the experimental spectrum at the tungsten signal. Determinethe silicon/t

33、ungsten ratio from the 160 spectrum. Determinethe depth profile of the tungsten from the grazing anglespectrum.13.5 The theoretical model assumes that layers in the WSixfilms are comprised of tungsten in WSi2(hexagonal) bonds andexcess elemental silicon. This theoretical approach assumesthat all tun

34、gsten is incorporated into WSi2bonds. The densityof the WSixfilm is then an upper limit on the actual filmdensity and generates a lower limit on the thickness. The RBSformulation arises from the relation that the product of the filmthickness and film density is the fundamental unit of measure-ment (

35、atoms/cm2) in RBS. Film thicknesses determined by thisapproach have demonstrated accuracies to within 10 % com-pared to thicknesses determined from SEM cross-sections (6).14. Report14.1 Report the important experimental parameters with thefollowing results:14.1.1 Sample and laboratory identification

36、,14.1.2 Energy of the incident ion beam,14.1.3 Angle settings of the normal and grazing angledetectors, and14.1.4 Date of measurement (for traceability to SPC re-cords).14.2 Report secondary experimental parameters for archivalpurposes although not critical to presentation of results asfollows:14.2.

37、1 Energy per channel calibration,14.2.2 Surface elemental markers (channel numbers) forrelevant elements,14.2.3 Software name and version, and14.2.4 Operator.15. Precision and Bias15.1 PrecisionThe precision of this test method is deter-mined from step heights observed in the tungsten signal fromnum

38、erous films. The accuracy of this test method is reinforcedfrom the measurement of the bismuth implant “standard” (4, 5)and the stringency of the SPC program.15.2 The accuracy of film thicknesses is based on compari-son to SEM cleave and cross-section measurements (6). TheSEM instrument is calibrate

39、d to NIST standards and providesbasis for accuracy (see Annex A1 for details on the thicknessdetermination).16. Keywords16.1 analysis of tungsten silicide; backscattering analysis;composition; metallization films; quantitative analysis; RBS;WSixANNEX(Mandatory Information)A1. EQUATIONS GOVERNING DEN

40、SITY CALCULATION OF WSixFILMSA1.1 The atomic density (in units of atoms/cm3)ofaWSixfilm is calculated by assuming that the film is comprised ofWSi2plus excess elemental silicon. The equation used tocalculate the film density from the atomic concentration ofeach layer is as follows:DWSix5 3 3 fw3 DWS

41、i21 fSi2 2 3 fW! 3 DSi5 fWSi23 DWSi21 fSi3 DSi. (A1.1)A1.2 The density of a layer is related to the thickness of alayer because the product yields the areal concentration (inunits of atoms/cm2) of the elemental signals. The areal con-centration is the fundamental unit measured in an RBSanalysis.A1.3

42、 It is assumed that all tungsten is incorporated intoWSi2unit cell. Thus, thicknesses determined from Eq A1.1 is alower limit on the actual film thickness.F1894 98 (2011)6REFERENCES(1) Chu, W. K., Mayer, Nicolet, Backscattering Spectrometry, AcademicPress, New York, 1978.(2) Handbook of Modern Ion B

43、eam Materials Analysis, Ed. J.R. Tesmerand M. Nastasi, Materials Research Society, Pittsburgh, PA 15237USA, 1995.(3) Ziegler, J.F., and Chu, W.K. Atomic Data Nuclear Data Tables,Vol13, 1974, p. 483.(4) Cohen, C., Davies, J.A., Drigo A.V., and Jackman, T.E. Nucl. Inst.Meth, Vol 218, 1983, p.147.(5) D

44、avies, J.A., Jackman, T.E., Eschbach, H.L., Domba, W., Watjen, U.,and Chivers, D. Nucl. Inst. Meth, Vol B15, p. 238.(6) “Determination of Accurate Metal Silicide Layer Thickness by RBS”,Kirchhoff, J.F., Baumann, S. M., Evans, C., Ward, I., Conveney, P.,Nucl. Instr. Meth Vol B 99 pp. 476-478.ASTM Int

45、ernational takes no position respecting the validity of any patent rights asserted in connection with any item mentionedin this standard. Users of this standard are expressly advised that determination of the validity of any such patent rights, and the riskof infringement of such rights, are entirel

46、y their own responsibility.This standard is subject to revision at any time by the responsible technical committee and must be reviewed every five years andif not revised, either reapproved or withdrawn. Your comments are invited either for revision of this standard or for additional standardsand sh

47、ould be addressed to ASTM International Headquarters. Your comments will receive careful consideration at a meeting of theresponsible technical committee, which you may attend. If you feel that your comments have not received a fair hearing you shouldmake your views known to the ASTM Committee on St

48、andards, at the address shown below.This standard is copyrighted by ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959,United States. Individual reprints (single or multiple copies) of this standard may be obtained by contacting ASTM at the aboveaddress or at 610-832-9585 (phone), 610-832-9555 (fax), or serviceastm.org (e-mail); or through the ASTM website(www.astm.org). Permission rights to photocopy the standard may also be secured from the ASTM website (www.astm.org/COPYRIGHT/).F1894 98 (2011)7

copyright@ 2008-2019 麦多课文库(www.mydoc123.com)网站版权所有
备案/许可证编号:苏ICP备17064731号-1