Relative roles of H2O2 and glycine in CMP of copper studied with impedance spectroscopy

被引:83
作者
Lu, J [1 ]
Garland, JE
Pettit, CM
Babu, SV
Roy, D
机构
[1] Clarkson Univ, Ctr Adv Mat Proc, Potsdam, NY 13699 USA
[2] Clarkson Univ, Dept Phys, Potsdam, NY 13699 USA
关键词
D O I
10.1149/1.1795256
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Peroxide-based slurries are commonly used in chemical mechanical polishing (CMP) of copper. When glycine is included in such a slurry, the planarization efficiency of Cu-CMP is considerably enhanced. In this work, we investigate the selective and collective chemical effects of H2O2 and glycine that promote favorable conditions for CMP of Cu. A number of surface reactions contribute to metal removal in this system by forming soluble surface complexes that can be easily removed by mechanical abrasion. We use Fourier transform electrochemical impedance spectroscopy (FT-EIS) to probe these reactions. The FT-EIS results provide detailed circuit models of the chemically active Cu interface. Simple analyses of the voltage-dependent kinetic (circuit) parameters of these models allow us to propose and examine the reaction steps for Cu-glycine complex formation on oxidized Cu. (C) 2004, The Electrochemical Society.
引用
收藏
页码:G717 / G722
页数:6
相关论文
共 35 条
[1]   The role of glycine in the chemical mechanical planarization of copper [J].
Aksu, S ;
Doyle, FM .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2002, 149 (06) :G352-G361
[2]   Electrochemistry of copper in aqueous glycine solutions [J].
Aksu, S ;
Doyle, FM .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2001, 148 (01) :B51-B57
[3]  
BABU SV, 2001, CHEM MECH POLISHING
[4]   Determination of the local structure of glycine adsorbed on Cu(110) [J].
Booth, NA ;
Woodruff, DP ;
Schaff, O ;
Giessel, T ;
Lindsay, R ;
Baumgartel, P ;
Bradshaw, AM .
SURFACE SCIENCE, 1998, 397 (1-3) :258-269
[6]   Electrochemical characterization of copper chemical mechanical polishing [J].
Du, TB ;
Tamboli, D ;
Desai, V .
MICROELECTRONIC ENGINEERING, 2003, 69 (01) :1-9
[7]   STARK SHIFT OF AN INTERBAND TRANSITION IN CU DETERMINED BY SURFACE-CHARGE MEASUREMENTS [J].
GAO, R ;
HEWITT, TD ;
ROY, D .
JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS, 1993, 54 (06) :685-690
[8]   Analysis of experimental constraints and. variables for time resolved detection of Fourier transform electrochemical impedance spectra [J].
Garland, JE ;
Pettit, CM ;
Roy, D .
ELECTROCHIMICA ACTA, 2004, 49 (16) :2623-2635
[9]   Kinetic analysis of electrosorption using fast Fourier transform electrochemical impedance spectroscopy:: underpotential deposition of Bi3+ in the presence of coadsorbing ClO4- on gold [J].
Garland, JE ;
Assiongbon, KA ;
Pettit, CM ;
Emery, SB ;
Roy, D .
ELECTROCHIMICA ACTA, 2002, 47 (25) :4113-4124
[10]   Analysis of potentiostatic current transients at metal/liquid interfaces: resolving the effects of a finite step interval [J].
Garland, JE ;
Pettit, CM ;
Walters, MJ ;
Roy, D .
SURFACE AND INTERFACE ANALYSIS, 2001, 31 (06) :492-503