Pulse current electrodeposition of nanocrystalline zinc

被引:128
作者
Saber, K
Koch, CC [1 ]
Fedkiw, PS
机构
[1] N Carolina State Univ, Dept Mat Sci & Engn, Raleigh, NC 27695 USA
[2] N Carolina State Univ, Dept Chem Engn, Raleigh, NC 27695 USA
来源
MATERIALS SCIENCE AND ENGINEERING A-STRUCTURAL MATERIALS PROPERTIES MICROSTRUCTURE AND PROCESSING | 2003年 / 341卷 / 1-2期
关键词
pulse; electrodeposition; zinc; nanocrystalline;
D O I
10.1016/S0921-5093(02)00198-3
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Pulse electrodeposition exhibits marked advantages over direct current electrodeposition in the control of deposit grain size, surface morphology, and preferred orientation. The effect of pulse peak current density (J(p)) on the grain size and surface morphology of zinc deposits with additives (polyacrylamide and thiourea) was studied by scanning electron microscopy and field emission scanning electron microscopy. The preferred orientation of zinc deposits was studied by X-ray diffraction, and microhardness of the deposits was measured by a Knoop microhardness tester. Increasing Jp dramatically changed the surface morphology and decreased the grain size. Nanocrystalline zinc (56 nm) was produced at J(p) = 2 A cm(-2). At J(p) equal to 0.4 A cm(-2,) the preferred orientation of zinc deposits was (1 1 (2) over bar2) and changed to the prismatic (1 1 (2) over bar0) orientation at J(p) equal to 0.8, 1.2, and 1.6 A cm(-2). However, increasing the peak current density to 2 A cm(-2) altered the prismatic (1 1 (2) over bar0) to the random (1 0 (1) over bar1). The microhardness increased to approximately 8 times higher than that of pure polycrystalline zinc (0.29 GPa). Microhardness reached a maximum (2.3 GPa) at 1.6 A cm(-2), then decreased to 1. 5 GPa at 2 A cm(-2). The hardness drop was correlated with the presence of additives and the change in texture from (1 1 (2) over bar0) to the random (1 0 (1) over bar1) with increasing J(p). (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:174 / 181
页数:8
相关论文
共 29 条
[1]   A QUANTITATIVE METHOD OF DETERMINING THE DEGREE OF TEXTURE OF ZINC ELECTRODEPOSITS [J].
BERUBE, LP ;
LESPERANCE, G .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1989, 136 (08) :2314-2315
[2]  
BONINO JP, 1992, PLAT SURF FINISH, V79, P62
[3]  
BROWN H, 1968, PLATING, V55, P1047
[4]  
CHOO RTC, 1995, J APPL ELECTROCHEM, V25, P384, DOI 10.1007/BF00249659
[5]  
Conway B.E., 1961, Electrochim. Acta, V3, P340, DOI DOI 10.1016/0013-4686(61)85009-3
[6]  
Cullity B.D., 1978, Addison-Wesley Series in Metallurgy and Materials, Vsecond
[7]   PULSE PLATING [J].
DEVARAJ, G ;
GURUVIAH, S ;
SESHADRI, SK .
MATERIALS CHEMISTRY AND PHYSICS, 1990, 25 (05) :439-461
[8]   SYNTHESIS OF BULK NANOCRYSTALLINE NICKEL BY PULSED ELECTRODEPOSITION [J].
ELSHERIK, AM ;
ERB, U .
JOURNAL OF MATERIALS SCIENCE, 1995, 30 (22) :5743-5749
[9]  
GADSHOV VI, 1984, METALLOBERFLACHE, V38, P199
[10]   NANOCRYSTALLINE MATERIALS [J].
BIRRINGER, R .
MATERIALS SCIENCE AND ENGINEERING A-STRUCTURAL MATERIALS PROPERTIES MICROSTRUCTURE AND PROCESSING, 1989, 117 :33-43