Comparative study on the effect of precursors on the morphology and electronic properties of CdS nanoparticles

Cadmium dithiocarbamate and cadmium ethyl xanthate complexes were synthesized and characterized by microanalysis, Fourier transform infrared (FT-IR) spectroscopy and thermogravimetric analyses. The complexes were employed as molecular precursors for the fabrication of CdS nanoparticles in hexadecylamine (HDA) and oleylamine (OLA) at a temperature of 250 degrees C. Spherical and oval shaped particles with sizes ranging from 9.93 +/- 1.89 to 16.74 +/- 2.78 nm were obtained in OLA while spherical, oval and rod shaped particles with sizes ranging from 9.40 +/- 1.65 to 29.90 +/- 5.32 nm were obtained in HDA. Optical properties of the nanoparticles showed blue shifts as compared to the bulk CdS, with the OLA capped nanoparticles slightly more blue shifted than the corresponding HDA capped nanoparticles. Results of crystallinity patterns revealed hexagonal phase of CdS.

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  • BEREMAN RD, 1979, INORG CHEM, V18, P3112, DOI 10.1021/ic50201a031
  • Bruce JC, 2007, NEW J CHEM, V31, P1647, DOI 10.1039/b618254b
  • Byrom C, 2000, POLYHEDRON, V19, P211, DOI 10.1016/S0277-5387(99)00352-6
  • Fan D, 2007, COORDIN CHEM REV, V251, P1878, DOI 10.1016/j.ccr.2007.03.021
  • Green M, 2010, J MATER CHEM, V20, P5797, DOI 10.1039/c0jm00007h
  • Isshiki M, 2017, SPRINGER HDB ELECT P, V1
  • Jen-La Plante I, 2010, J MATER CHEM, V20, P6612, DOI 10.1039/c0jm00439a
  • Jun YW, 2005, J PHYS CHEM B, V109, P14795, DOI 10.1021/jp052257v
  • Ketchemen KIY, 2018, J MATER SCI-MATER EL, V29, P14462, DOI 10.1007/s10854-018-9579-x
  • Klug HP, 1974, XRAY DIFFRACTION PRO, P992
  • Li YC, 2003, J MATER CHEM, V13, P2641, DOI 10.1039/b307594j
  • Lozano G, 2016, LIGHT-SCI APPL, V5, DOI 10.1038/lsa.2016.80
  • Malik MA, 2001, CHEM MATER, V13, P913, DOI 10.1021/cm0011662
  • Mlondo SN, 2009, POLYHEDRON, V28, P2097, DOI 10.1016/j.poly.2009.02.046
  • Mlondo SN, 2005, MAT RES SOC S P E, DOI 10.1557/PROC-879-Z7.6
  • Mlowe S, 2014, NEW J CHEM, V38, P6073, DOI 10.1039/c4nj01201a
  • Mohsennia M, 2015, J NANOPHOTONICS, V9, DOI 10.1117/1.JNP.9.093081
  • Moloto N, 2007, POLYHEDRON, V26, P3947, DOI 10.1016/j.poly.2007.04.015
  • Nair PS, 2002, J MATER CHEM, V12, P2722, DOI 10.1039/b202072f
  • Nyamen LD, 2013, POLYHEDRON, V56, P62, DOI 10.1016/j.poly.2013.03.027
  • Nyamen LD, 2011, NEW J CHEM, V35, P1133, DOI 10.1039/c1nj20069k
  • ONEIL M, 1990, J PHYS CHEM-US, V94, P4356, DOI 10.1021/j100373a089
  • Park M, 2020, RSC ADV, V10, P8261, DOI 10.1039/d0ra00653j
  • Pawar AS, 2016, EUR J INORG CHEM, P366, DOI 10.1002/ejic.201501125
  • Peng ZA, 2002, J AM CHEM SOC, V124, P3343, DOI 10.1021/ja0173167
  • Rahman MF, 2020, APPL PHYS A-MATER, V126, DOI 10.1007/s00339-020-3331-0
  • Revaprasadu N, 1999, CHEM COMMUN, P1573, DOI 10.1039/a901969c
  • SHARMA CP, 1981, J INORG NUCL CHEM, V43, P923, DOI 10.1016/0022-1902(81)80151-0
  • Shombe GB, 2016, MAT SCI SEMICON PROC, V43, P230, DOI 10.1016/j.mssp.2015.11.011
  • SPANHEL L, 1987, J AM CHEM SOC, V109, P5649, DOI 10.1021/ja00253a015
  • Trindade T, 1996, J MATER CHEM, V6, P343, DOI 10.1039/jm9960600343
  • Yan P, 1999, CHEM COMMUN, P1293, DOI 10.1039/a901821b
  • Yin Y, 2005, NATURE, V437, P664, DOI 10.1038/nature04165
  • Yong KT, 2007, J PHYS CHEM C, V111, P2447, DOI 10.1021/jp066392z