Electrochemical metal deposition on atomically nearly-flat silicon surfaces accompanied by nano-hole formation

被引:16
作者
Morisawa, K [1 ]
Ishida, M [1 ]
Yae, S [1 ]
Nakato, Y [1 ]
机构
[1] Osaka Univ, Grad Sch Engn Sci, Dept Chem, Osaka 5608531, Japan
关键词
electrodeposition; semiconductor; nano-holes; reductive dissolution; SPM;
D O I
10.1016/S0013-4686(99)00077-8
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A number of nanometer-sized holes, 20-80 nm wide and 0.6-0.7 nm deep, were produced at NH4F-etched, atomically nearly-flat n-Si(111) surfaces while platinum was electrochemically deposited at -0.40 V vs SCE in 5.0 x 10(-3) M H2PtCl6 + 0.5 M Na2SO4 of pH 2.9. The nano-holes were produced only during the Pt deposition at potentials more negative than -0.35 V. Experiments have shown that hole injection (or extraction of valence-band electrons) by H2PtCl6 plays no important role in the nano-hole formation. When the n-Si(111) surfaces were kept at -0.4 V in 0.18 M H2SO4 which has the same pH as the 5.0 x 10(-3) M H2PtCl6 + 0.5 M Na2SO4, much smaller nano-holes than the above case were produced, suggesting that electrochemical reductive dissolution of Si occurs in acidic solutions. It is proposed as a possible mechanism that deposited Pt atoms, while migrating along the n-Si surface, act as a catalyst for the reductive dissolution of Si, leading to acceleration of nano-hole formation. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:3725 / 3729
页数:5
相关论文
共 23 条
[1]   ETCHING OF SILICON IN NAOH SOLUTIONS .2. ELECTROCHEMICAL STUDIES OF N-SI(111) AND N-SI(100) AND MECHANISM OF THE DISSOLUTION [J].
ALLONGUE, P ;
COSTAKIELING, V ;
GERISCHER, H .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1993, 140 (04) :1018-1026
[2]   Electrochemical and radiochemical study of copper contamination mechanism from HF solutions onto silicon substrates [J].
Bertagna, V ;
Rouelle, F ;
Revel, G ;
Chemla, M .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1997, 144 (12) :4175-4182
[3]  
GRAEF D, 1989, J VAC SCI TECHNOL A, V7, P808
[4]  
GRUNDNER M, 1988, AIP C P, V167, P329
[5]   STEP-FLOW MECHANISM VERSUS PIT CORROSION - SCANNING-TUNNELING MICROSCOPY OBSERVATIONS ON WET ETCHING OF SI(111) BY HF SOLUTIONS [J].
HESSEL, HE ;
FELTZ, A ;
REITER, M ;
MEMMERT, U ;
BEHM, RJ .
CHEMICAL PHYSICS LETTERS, 1991, 186 (2-3) :275-280
[6]   IDEAL HYDROGEN TERMINATION OF THE SI-(111) SURFACE [J].
HIGASHI, GS ;
CHABAL, YJ ;
TRUCKS, GW ;
RAGHAVACHARI, K .
APPLIED PHYSICS LETTERS, 1990, 56 (07) :656-658
[7]   ATOMIC RESOLUTION IMAGES OF H-TERMINATED SI(111) SURFACES IN AQUEOUS-SOLUTIONS [J].
ITAYA, K ;
SUGAWARA, R ;
MORITA, Y ;
TOKUMOTO, H .
APPLIED PHYSICS LETTERS, 1992, 60 (20) :2534-2536
[8]   CHEMICAL ETCHING OF VICINAL SI(111) - DEPENDENCE OF THE SURFACE-STRUCTURE AND THE HYDROGEN TERMINATION ON THE PH OF THE ETCHING SOLUTIONS [J].
JAKOB, P ;
CHABAL, YJ .
JOURNAL OF CHEMICAL PHYSICS, 1991, 95 (04) :2897-2909
[9]   ATOMIC-SCALE ETCHING PROCESSES OF N-SI(111) IN NH4F SOLUTIONS - IN-SITU SCANNING-TUNNELING-MICROSCOPY [J].
KAJI, K ;
YAU, SL ;
ITAYA, K .
JOURNAL OF APPLIED PHYSICS, 1995, 78 (09) :5727-5733
[10]   CHEMICALLY ETCHED SILICON SURFACES VIEWED AT THE ATOMIC LEVEL BY FORCE MICROSCOPY [J].
KIM, Y ;
LIEBER, CM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (06) :2333-2335