2012
DOI: 10.1016/j.mseb.2012.02.006
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Optical properties of SnO2 nanostructures prepared via one-step thermal decomposition of tin (II) chloride dihydrate

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Cited by 39 publications
(17 citation statements)
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“…S2 in Supporting Information) in CPPC 0.2 , STEPC 0.2 , and STUWEPC 0.2 indicates SnCl 2 ·2H 2 O decomposition to Sn 4 (OH) 6 Cl 2 and HCl and H 2 O release . Additionally, CPPC 0.2 , STEPC 0.2 , and STUWEPC 0.2 showed a weight loss between 200–300 °C owing to the conversion of Sn 4 (OH) 6 Cl 2 to liquid Sn and SnOCl 2 . The formed intermediates between 300–400 °C for all three catalysts were further decomposed to SnO 2 nanoparticles.…”
Section: Resultsmentioning
confidence: 99%
“…S2 in Supporting Information) in CPPC 0.2 , STEPC 0.2 , and STUWEPC 0.2 indicates SnCl 2 ·2H 2 O decomposition to Sn 4 (OH) 6 Cl 2 and HCl and H 2 O release . Additionally, CPPC 0.2 , STEPC 0.2 , and STUWEPC 0.2 showed a weight loss between 200–300 °C owing to the conversion of Sn 4 (OH) 6 Cl 2 to liquid Sn and SnOCl 2 . The formed intermediates between 300–400 °C for all three catalysts were further decomposed to SnO 2 nanoparticles.…”
Section: Resultsmentioning
confidence: 99%
“…The loss of chlorine as Cl2 or some oxychlorine is also occurring in the process. Tin oxychlorines could be the intermediates forming and evaporating during the heating, as discussed by others [27,28] for the heating of the divalent tin salt SnCl22H2O.…”
Section: Sncl45h2omentioning
confidence: 92%
“…The evaporation is ended by an exothermic reaction (F), most probably the formation of tin oxide. Tin oxychlorine species have been proposed to form and evaporate during the oxide formation process [27,28]. Assuming SnO2 as the only product, the deposition efficiency (ηeff) was 23 % which is almost double that of the tetrachloride salt.…”
Section: Sncl22h2omentioning
confidence: 99%
“…6.The band gap energy of ZnO without PVP modification was found to bẽ 3.22 eV which decreased from 3.20 eV (b-ZnO-Nanowalls) to 3.14 eV (c-ZnO-Nanorods) as a result of increasing concentration of PVP, depicted in Table 3. We believe that the observed difference of the optical band gap may be related to the variation of the stoichiometry of ZnO samples and the concentration of the point defects associated with them [32]. Dutta et al [33] have reported a significant change in optical band gap of ZnO due to defects with discrete states or increase localized energy levels within the band gap [34].…”
Section: Uv-vis Absorption Spectroscopymentioning
confidence: 92%