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Novel Anion Exchange Method for Exact Antimony Doping Control of Stannic Oxide Nanocrystal Powder
Author(s) -
Zhang Xuejun,
Liang Hongbo,
Gan Fuxing
Publication year - 2006
Publication title -
journal of the american ceramic society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.9
H-Index - 196
eISSN - 1551-2916
pISSN - 0002-7820
DOI - 10.1111/j.1551-2916.2005.00793.x
Subject(s) - inorganic chemistry , antimony , hydrolysis , doping , nanocrystal , chlorine , materials science , ion exchange , nanocrystalline material , oxide , chemistry , nuclear chemistry , ion , nanotechnology , organic chemistry , optoelectronics
There are major problems associated with the preparation of nanometer‐sized antimony‐doped stannic oxide using the current sol–gel processes, such as difficulties in removing chlorine, in accurate doping of antimony, and in the repeatability of doping. This paper presents a novel solution method of doping, which involves a precipitation–condensation process with non‐aqueous ion exchange for removal of chlorine. This involved hydrolysis of SnCl 4 ·5H 2 O and SbCl 3 in an ethanol–ammonia anion‐exchange resin mixture at pH=6–8. The removal of chlorine ion and the hydrolysis are conducted at the same time. The short duration of hydrolysis prevents the formation of high condensates. The use of ion‐exchange resin saves a great deal of solvent and allows all the hydrolysis products to be recovered by distillation. This ensured that the doping is exact. The determination of antimony within the dry hydrolysate on an atomic absorption spectrometer confirmed the doping accuracy and the repeatability of the method. The proportion of Sb to Sn was found to be between 0.0528 and 0.0550 molar fraction at the optimum conductivity of the nanocrystalline SnO 2 doped with Sb. TEM pictures and XRD patterns showed that nanocrystallites fired from the powder were small and had a narrow size range of 10±5 nm at 650°C.