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Received June 10, 2008
Accepted December 17, 2008
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Size-selective Pd nanoparticles stabilized by dialkylmorpholinium ionic liquids
Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology, 335 Gwahangno, Yuseong-gu, Daejeon 305-701, Korea 1Department of Chemical and Biological Engineering, Chungju National University, 72 Daehangno, ChungCheongbuk-do, Chungju 380-702, Korea
h_lee@kaist.ac.kr
Korean Journal of Chemical Engineering, May 2009, 26(3), 760-764(5), 10.1007/s11814-009-0127-5
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Abstract
We have successfully synthesized palladium (Pd) nanoparticles (NPs) protected by dialkylmorpholinium ionic liquids (ILs) via chemical reduction. ATR-FTIR, UV, and NMR spectroscopies and transmission electron microscopy (TEM) were employed for characterization of the Pd NPs. The ILs effectively stabilized the Pd NPs, and the particle sizes were precisely controlled by the alkyl chain length of the cation in the ILs. The produced particles had a highly crystalline structure with a face-centered cubic (fcc) lattice. Broadening of the (111) plane in the X-ray diffraction (XRD) patterns was observed and the particle sizes calculated by Scherrer’s equation were in good agreement with the TEM results. Additionally, UV, IR, and NMR spectra indicated that nano-sized particles were produced and ILs were bound to the surface of the NPs, thereby protecting the particles from aggregation.
References
Kim KS, Choi S, Demberelnyamba D, Lee H, Oh J, Lee BB, Mun SJ, Chem. Commun., 828 (2004)
Kim KS, Park SY, Yeon SH, Lee H, Electrochim. Acta, 50(28), 5673 (2005)
Yeon SH, Kim KS, Choi S, Lee H, Kim HS, Kim H, Electrochim. Acta, 50(27), 5399 (2005)
Kim KS, Shin BK, Lee H, Ziegler F, Fluid Phase Equilib., 218(2), 215 (2004)
Welton T, Chem. Rev., 99(8), 2071 (1999)
Marsh KN, Deev A, Wu ACT, Tran E, Klamt A, Korean J. Chem. Eng., 19(3), 357 (2002)
Seddon KR, Stark A, Torres MJ, Pure Appl. Chem., 72, 2275 (2000)
Dupont J, Fonseca GS, Umpierre AP, Fichtner PFP, Teixeira SR, J. Am. Chem. Soc., 124(16), 4228 (2002)
Huang J, Jiang T, Han B, Gao H, Chang Y, Zhao G, Wu W, Chem. Commun., 1654 (2003)
Zhu YJ, Wang WW, Qi RJ, Hu XL, Angew. Chem. Int. Ed., 43, 1410 (2004)
Kim KS, Choi S, Cha JH, Yeon SH, Lee H, J. Mater. Chem., 16, 1315 (2006)
Parnham ER, Morris RE, J. Am. Chem. Soc., 128(7), 2204 (2006)
Ding KL, Miao ZJ, Liu ZM, Zhang ZF, Han BX, An GM, Miao SD, Xie Y, J. Am. Chem. Soc., 129(20), 6362 (2007)
Shimano S, Zhou H, Honma I, Chem. Mater., 19, 5216 (2007)
Tang Z, Kotov NA, Giersig M, Science, 297, 237 (2002)
Tang ZY, Ozturk B, Wang Y, Kotov NA, J. Phys. Chem. B, 108(22), 6927 (2004)
Kim KS, Demberelnyamba D, Lee H, Langmuir, 20(3), 556 (2004)
Kim KS, Demberelnyamba ND, Yeon SW, Choi S, Cha JH, Lee H, Korean J. Chem. Eng., 22(5), 717 (2005)
Cha JH, Kim KS, Choi S, Yeon SH, Lee H, Lee CS, Shim JJ, Korean J. Chem. Eng., 24(6), 1089 (2007)
Creighton JA, Eadon DS, J. Chem. Soc. Faraday Trans., 87, 3881 (1991)
1H-NMR (500 MHz; Acetone; TMS) 4.15-4.09 (m, 4H), 3.89-3.82 (q, 4H), 3.73-3.70 (t, 3H), 3.45 (s, 2H), 1.50-1.46(m, 3H)
Teranishi T, Miyake M, Chem. Mater., 10, 594 (1998)
Kim KS, Park SY, Yeon SH, Lee H, Electrochim. Acta, 50(28), 5673 (2005)
Yeon SH, Kim KS, Choi S, Lee H, Kim HS, Kim H, Electrochim. Acta, 50(27), 5399 (2005)
Kim KS, Shin BK, Lee H, Ziegler F, Fluid Phase Equilib., 218(2), 215 (2004)
Welton T, Chem. Rev., 99(8), 2071 (1999)
Marsh KN, Deev A, Wu ACT, Tran E, Klamt A, Korean J. Chem. Eng., 19(3), 357 (2002)
Seddon KR, Stark A, Torres MJ, Pure Appl. Chem., 72, 2275 (2000)
Dupont J, Fonseca GS, Umpierre AP, Fichtner PFP, Teixeira SR, J. Am. Chem. Soc., 124(16), 4228 (2002)
Huang J, Jiang T, Han B, Gao H, Chang Y, Zhao G, Wu W, Chem. Commun., 1654 (2003)
Zhu YJ, Wang WW, Qi RJ, Hu XL, Angew. Chem. Int. Ed., 43, 1410 (2004)
Kim KS, Choi S, Cha JH, Yeon SH, Lee H, J. Mater. Chem., 16, 1315 (2006)
Parnham ER, Morris RE, J. Am. Chem. Soc., 128(7), 2204 (2006)
Ding KL, Miao ZJ, Liu ZM, Zhang ZF, Han BX, An GM, Miao SD, Xie Y, J. Am. Chem. Soc., 129(20), 6362 (2007)
Shimano S, Zhou H, Honma I, Chem. Mater., 19, 5216 (2007)
Tang Z, Kotov NA, Giersig M, Science, 297, 237 (2002)
Tang ZY, Ozturk B, Wang Y, Kotov NA, J. Phys. Chem. B, 108(22), 6927 (2004)
Kim KS, Demberelnyamba D, Lee H, Langmuir, 20(3), 556 (2004)
Kim KS, Demberelnyamba ND, Yeon SW, Choi S, Cha JH, Lee H, Korean J. Chem. Eng., 22(5), 717 (2005)
Cha JH, Kim KS, Choi S, Yeon SH, Lee H, Lee CS, Shim JJ, Korean J. Chem. Eng., 24(6), 1089 (2007)
Creighton JA, Eadon DS, J. Chem. Soc. Faraday Trans., 87, 3881 (1991)
1H-NMR (500 MHz; Acetone; TMS) 4.15-4.09 (m, 4H), 3.89-3.82 (q, 4H), 3.73-3.70 (t, 3H), 3.45 (s, 2H), 1.50-1.46(m, 3H)
Teranishi T, Miyake M, Chem. Mater., 10, 594 (1998)