Fabrication & characterization of macroporous CdSe nanostructure via colloidal crystal templating with electrodeposition method

Springer Science and Business Media LLC - Tập 13 - Trang 281-285 - 2006
S. H. Yeo1, L. K. Teh1, C. C. Wong1
1School of Materials Science and Engineering, Nanyang Technological University, Singapore

Tóm tắt

Large area ordered arrays of macroporous Cadmium Selenide (CdSe) nanostructure, which possesses high refractive index and negligible absorption in the visible spectrum critical for the realization of photonic band gaps, was prepared via colloidal templating by galvanostatic electrodeposition. This work investigates the effect of electrodeposition parameters on the macroporous CdSe nanostructure. Field Emission Scanning Electron Microscope (FESEM) images showed two and three dimensional porous structures, consisting of interconnected close-packed arrays of pores. For CdSe thin film of thickness less than 1/3 of the diameter of a polystyrene sphere, it showed a monolayer of circular pores. As for film thickness close to the diameter of the sphere, the pores adopted irregular rounded triangular shapes. When the film thickness was more than one layer of the colloidal polystyrene template, the pores were spherical and had the same diameter as the polystyrene spheres. X-ray Diffraction (XRD) showed that the CdSe films prepared had a cubic structure with nanometer grain size, which was smaller than the diameter of the template spheres as well as the diameter of the interconnected channels. A range of 45–70 nm thick CdSe films with > 90% optical transmittance showed that there was negligible absorption at wavelength of 750 nm. In addition, the CdSe thin film exhibited a band gap energy of 2.07 eV, blue-shifted from the characteristic 1.7 eV of CdSe. This blue-shift characteristic of the deposited CdSe film further indicated that it was nanocrystalline which is potentially useful in photonic applications.

Tài liệu tham khảo

E. Yablonovitch, Phys. Rev. Lett. 58, 2059 (1987). S. John, Phys. Rev. Lett. 58, 2846 (1987). J.D. Joannopoulos, P.R. Villeneuve, and S. Fan, Nature 386, 143 (1997). S.Y. Lin, J.G. Fleming, D.L. Hetherington, B.K. Smith, R. Biswas, K.-M. Ho, M.M. Sigalas, W. Zubrzycki, S.R. Kurtz, and J. Bur, Nature 394, 251 (1998). Yu.V. Miklyaev, D.C. Meisel, A. Blanco, G. von Freymanna, K. Busch, W. Koch, C. Enkrich, M. Deubel, and M. Wegener, Appl. Phys. Lett. 82, 1284 (2003). A. Van Blaaderen, R. Ruel, and P. Wiltzius, Nature, 385, 321 (1997). R. Biswas, M.M. Sigalas, G. Subramania, C.M. Soukoulis, and K.-M. Ho, Phys. Rev. B 61, 4549 (2000). A. Stein and R. C. Schroden, Curr. Opin. Solid State Mater. Sci. 5, 553 (2001). D. Hahn, K.K. Mishra, and K.K. Rajeshwar, J. Electrochem. Soc. 138, 100 (1991). K.K. Mishra and K.K. Rajeshwar, J. Electroanal. Chem. 273, 169 (1989). S.N. Sarangi and S.N. Sahu, Physica E 23, 159 (2004). P.V. Braun and P. Wiltzius, Nature 402, 603 (1999). R.G. Gilbert, Emulsion Polymerization: a mechanistic approach (Academic Press, London, 1995), p. 161. G. Hodes, Electrochemistry of Nanomaterials (Wiley-VCH, Weinheim, 2001), p. 29.