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Papers, presented at NANO-2015
Investigation on structural and photoluminescence properties of ($\mathrm{Co}$, $\mathrm{Al}$) $\mathrm{Co}$-doped $\mathrm{SnO}_2$ nanoparticles
P. Venkateswara Reddya,
S. Venkatramana Reddya,
B. Sankara Reddyb,
R. P. Vijayalakshmia a Department of Physics, Sri Venkateswara University, Tirupati-517
502, A.P., India
b Visweswaraiah Institutes of Science and Technology, Angallu, Madana Palli, A.P., India
Аннотация:
Pure and (
$\mathrm{Co}$,
$\mathrm{Al}$) co-doped (
$\mathrm{Co}=1,3,5$ mol %, and
$\mathrm{Al}=5$ mol % as constant)
$\mathrm{SnO}_2$ nanoparticles were synthesized in aqueous solution by the chemical coprecipitation method using polyethylene glycol (PEG) as a stabilizer. The effects of structural and photoluminescence of (
$\mathrm{Co}$,
$\mathrm{Al}$) co-doped
$\mathrm{SnO}_2$ nanoparticles are investigated. The XRD pattern reveals that the samples are in a single phase rutile type tetragonal crystalline structure of
$\mathrm{SnO}_2$. The peak positions with
$\mathrm{Co}$ concentration are slightly shifted to lower
$2\theta$ values and size of particles from XRD calculations are in between
$20$ –
$30$ nm. The Raman studies of the samples reveal that the Raman peaks are shifted towards lower wave numbers, when compared to those of pure
$\mathrm{SnO}_2$ at
$150$ cm
$^{-1}$,
$303$ cm
$^{-1}$,
$476$ cm
$^{-1}$,
$630$ cm
$^{-1}$, and
$765$ cm
$^{-1}$ respectively. Photoluminescence studies show that pure
$\mathrm{SnO}_2$ has an emission peak at
$444$ nm and (
$\mathrm{Co}$,
$\mathrm{Al}$) co-doped samples show emission peaks at
$417$ nm,
$433$ nm and
$485$ nm with exciting wave length
$320$ nm. The PL intensity increases and broadening of peaks for co-doped samples with increase of
$\mathrm{Co}$ concentration indicates the decrease of size of the crystallinity. The UV absorption spectrum exhibits absorption at
$310$ nm, and is in agreement with the emission spectra.
Ключевые слова:
EDAX, co-precipitation method, PL, UV-Absorption.
PACS:
81.07.Bc,
81.07.Nb Поступила в редакцию: 23.01.2016
Язык публикации: английский
DOI:
10.17586/2220-8054-2016-7-3-494-498