To understand the mechanism for formation of fcc-cobalt nanowires in electrodeposition, we have systematically studied the effect of deposition potential, pH, and deposition temperature on the formation of fcc Co nanowires by X-ray diffraction (XRD), transmission electron microscope (TEM) and scanning electron microscope (SEM). The Co nanowires deposited at the potential of -1.6V are pure hcp phase. When increasing the value of potential to -2.0V, there are hcp Co and fcc Co crystals in the deposited nanowires. The fraction of fcc Co crystals in the nanowires increases with increasing the potential value. At -3.0V, the nanowires are pure fcc Co. The pH of the solution has little effect on formation of fcc Co nanowires. We have also seen that high concentration and low temperature favors fcc phase whereas low concentration and high temperature favors hcp phase. However, at 35°C the co-occurrence of hcp and fcc phases were also observed. These experimental results can be explained by the classical electrochemical nucleation theory. The formation of fcc Co crystals can be attributed to smaller critical clusters formed at a higher potential value since the smaller critical clusters favor formation of fcc nuclei.
Published in | American Journal of Applied Chemistry (Volume 4, Issue 5) |
DOI | 10.11648/j.ajac.20160405.16 |
Page(s) | 192-200 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
Copyright |
Copyright © The Author(s), 2016. Published by Science Publishing Group |
Nanostructure, Electrodeposition, Fcc Cobalt, Crystal Growth
[1] | Nakahara S, Mahajan S. The Influence of Solution p H on Microstructure of Electrodeposited Cobalt. J Electrochem Soc. 1980; 127 283. |
[2] | Cohen-Hyams T, Kaplan WD, Yahalom J. Structure of Electrodeposited Cobalt. Electrochemical and Solid-State Letters. 2002; 5: C75-C8. |
[3] | Vicenzo A, Cavallotti PL. Growth modes of electrodeposited cobalt. Electrochimica Acta 2004; 49: 4079-89. |
[4] | Kersten H. Physics. 1932; 2: 274. |
[5] | Cadorna L, Cavallotti P. Electrochim Metall. 1966; 1: 364. |
[6] | Sard R, Schwartz CD, Weil R. J Electrochem Soc. 1966; 113: 424. |
[7] | Sadana YN. Surf Technol 1977; 5: 97. |
[8] | Wang XW, Fei GT, Tong P, Xu XJ, Zhang LD. Structural control and magnetic properties of electrodeposited Co nanowires. Journal of Crystal Growth. 2007; 300: 421-5. |
[9] | Huang XH, Li L, Luo X, Zhu XG, Li GG. Orientation-Controlled Synthesis and Ferromagnetism of Single Crystalline Co Nanowire Arrays. J Phys Chem C. 2008; 112: 1468-72. |
[10] | Li F, Wang T, Ren L, Sun J. Structure and magnetic properties of Co nanowires in self-assembled arrays. Journal of Physics: Condensed Matter. 2004; 16: 8053. |
[11] | Ramazani A, Kashi MA, Alikhani M, Erfanifam S. Optimized microstructure and magnetic properties in arrays of ac electrodeposited Co nanowires induced by the continuous and pulse electrodeposition. Journal of Physics D: Applied Physics. 2007; 40: 5533. |
[12] | Zhang J, Jones GA, Shen TH, Donnelly SE, Li G. Monocrystalline hexagonal-close-packed and polycrystalline face-centered-cubic Co nanowire arrays fabricated by pulse dc electrodeposition. Journal of Applied Physics. 2007; 101: 054310. |
[13] | Wang XW, Fei GT, Tong P, Xu XJ, Zhang LD. Structural control and magnetic properties of electrodeposited Co nanowires. Journal of Crystal Growth. 2007; 300: 421. |
[14] | Darques M, Encinas A, Vila L, Piraux L. Tailoring of the c -axis orientation and magnetic anisotropy in electrodeposited Co nanowires. Journal of Physics: Condensed Matter. 2004; 16: S2279. |
[15] | Pan H, Liu B, Yi J, Poh C, Lim S, Ding J, et al. Growth of Single-Crystalline Ni and Co Nanowires via Electrochemical Deposition and Their Magnetic Properties. The Journal of Physical Chemistry B. 2005; 109: 3094-8. |
[16] | Han X, Liu Q, Wang J, Li S, Ren Y, Liu R, et al. Influence of crystal orientation on magnetic properties of hcp Co nanowire arrays. Journal of Physics D: Applied Physics. 2009; 42: 095005. |
[17] | Wang XW FG, Xu XJ, Jin Z, Zhang LD. Size-dependent orientation growth of large-area ordered Ni nanowire arrays. J Phys Chem B. 2005; 109: 24326-30. |
[18] | Granqvist CG, Buhrman RA. Ultrafine metal particles. J Appl Phys. 1976; 47: 2200. |
[19] | Kitakami O, Sato H, Shimada Y, Sato F, Tanaka M. Size effect on the crystal phase of cobalt fine particles. Physical Review B. 1997; 56: 13849. |
[20] | Gangopadhyay S, Hadjipanayis GC, Sorensen CM, Klabunde KJ. IEEE Trans Magn 1992; 28: 3174. |
[21] | Kimoto K, Kamiya Y, Nonoyama M, Ueda R. Jpn J Appl Phys. 1963; 2: 702. |
[22] | Sato H, Kitakami O, Sakurai T, Shimada Y. Structure and magnetism of hcp-Co fine particles. J Appl Phys 1997; 81: 1858. |
[23] | Tan M, Chen XQ. Growth Mechanism of Single Crystal Nanowires of fcc Metals (Ag, Cu, Ni) and hcp Metal (Co) Electrodeposited. Journal of The Electrochemical Society. 2012; 159: K15. |
[24] | Williams DB, Carter CB. Transmission Electron Microscopy, A Textbook for Materials Science. New York Springer 2009. |
[25] | Cho JU, Wu JH, Min JH, Ko SP, Soh JY, Liu QX, et al. Control of magnetic anisotropy of Co nanowires. Journal of Magnetism and Magnetic Materials 2006; 303: e281. |
[26] | Huang, Li L, Luo X, Zhu, Li. Orientation-Controlled Synthesis and Ferromagnetism of Single Crystalline Co Nanowire Arrays. The Journal of Physical Chemistry C. 2008; 112: 1468-72. |
[27] | Nishiyama Z. Martensitic Transformation. New York: Academic; 1978. |
[28] | Miedema AR, Nieuwenhuys BE. Surf Sci. 1981; 104: 491. |
[29] | Alden M, Mirbt S, Skriver HL, Rosengaard NM, Johansson B. Phys Rev B 1992; 46: 6303. |
[30] | Troiano AR, Tokich JL. Trans Metall Soc AIME. 1948; 195: 728. |
[31] | Owen EA, Jones DM. Proc R Soc London, Ser B. 1954; 67: 456. |
[32] | Isaev VA, Grishenkova OV. Electrochemistry Communications. 2001; 3: 500. |
[33] | Paunovic M, Schlesinger M. Fundamentals of Electrochemical Deposition. New York: Wiley; 1998. |
[34] | Krause A, Uhlemann M, Gebert A, Schultz L. A study of nucleation, growth, texture and phase formation of electrodeposited cobalt layers and the influence of magnetic fields. Thin Solid Films. 2006; 515: 1694. |
[35] | WINAND R. Fundamentals and Practice of Aqueous ElectrometallurgyÕÕ (short course) (The Metallurgical Society of CIM, Montreal, PQ, Canada). 1990: 7. |
APA Style
Tahir Mehmood, Aiman Mukhtar, Babar Shahzad Khan, Wu Kaiming. (2016). How Deposition Parameters Affect Phase Formation in Metals. American Journal of Applied Chemistry, 4(5), 192-200. https://doi.org/10.11648/j.ajac.20160405.16
ACS Style
Tahir Mehmood; Aiman Mukhtar; Babar Shahzad Khan; Wu Kaiming. How Deposition Parameters Affect Phase Formation in Metals. Am. J. Appl. Chem. 2016, 4(5), 192-200. doi: 10.11648/j.ajac.20160405.16
AMA Style
Tahir Mehmood, Aiman Mukhtar, Babar Shahzad Khan, Wu Kaiming. How Deposition Parameters Affect Phase Formation in Metals. Am J Appl Chem. 2016;4(5):192-200. doi: 10.11648/j.ajac.20160405.16
@article{10.11648/j.ajac.20160405.16, author = {Tahir Mehmood and Aiman Mukhtar and Babar Shahzad Khan and Wu Kaiming}, title = {How Deposition Parameters Affect Phase Formation in Metals}, journal = {American Journal of Applied Chemistry}, volume = {4}, number = {5}, pages = {192-200}, doi = {10.11648/j.ajac.20160405.16}, url = {https://doi.org/10.11648/j.ajac.20160405.16}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajac.20160405.16}, abstract = {To understand the mechanism for formation of fcc-cobalt nanowires in electrodeposition, we have systematically studied the effect of deposition potential, pH, and deposition temperature on the formation of fcc Co nanowires by X-ray diffraction (XRD), transmission electron microscope (TEM) and scanning electron microscope (SEM). The Co nanowires deposited at the potential of -1.6V are pure hcp phase. When increasing the value of potential to -2.0V, there are hcp Co and fcc Co crystals in the deposited nanowires. The fraction of fcc Co crystals in the nanowires increases with increasing the potential value. At -3.0V, the nanowires are pure fcc Co. The pH of the solution has little effect on formation of fcc Co nanowires. We have also seen that high concentration and low temperature favors fcc phase whereas low concentration and high temperature favors hcp phase. However, at 35°C the co-occurrence of hcp and fcc phases were also observed. These experimental results can be explained by the classical electrochemical nucleation theory. The formation of fcc Co crystals can be attributed to smaller critical clusters formed at a higher potential value since the smaller critical clusters favor formation of fcc nuclei.}, year = {2016} }
TY - JOUR T1 - How Deposition Parameters Affect Phase Formation in Metals AU - Tahir Mehmood AU - Aiman Mukhtar AU - Babar Shahzad Khan AU - Wu Kaiming Y1 - 2016/10/13 PY - 2016 N1 - https://doi.org/10.11648/j.ajac.20160405.16 DO - 10.11648/j.ajac.20160405.16 T2 - American Journal of Applied Chemistry JF - American Journal of Applied Chemistry JO - American Journal of Applied Chemistry SP - 192 EP - 200 PB - Science Publishing Group SN - 2330-8745 UR - https://doi.org/10.11648/j.ajac.20160405.16 AB - To understand the mechanism for formation of fcc-cobalt nanowires in electrodeposition, we have systematically studied the effect of deposition potential, pH, and deposition temperature on the formation of fcc Co nanowires by X-ray diffraction (XRD), transmission electron microscope (TEM) and scanning electron microscope (SEM). The Co nanowires deposited at the potential of -1.6V are pure hcp phase. When increasing the value of potential to -2.0V, there are hcp Co and fcc Co crystals in the deposited nanowires. The fraction of fcc Co crystals in the nanowires increases with increasing the potential value. At -3.0V, the nanowires are pure fcc Co. The pH of the solution has little effect on formation of fcc Co nanowires. We have also seen that high concentration and low temperature favors fcc phase whereas low concentration and high temperature favors hcp phase. However, at 35°C the co-occurrence of hcp and fcc phases were also observed. These experimental results can be explained by the classical electrochemical nucleation theory. The formation of fcc Co crystals can be attributed to smaller critical clusters formed at a higher potential value since the smaller critical clusters favor formation of fcc nuclei. VL - 4 IS - 5 ER -