Journal of Alloys and Compounds 527 (2012) 1–4
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Journal of Alloys and Compounds
jou rn al h om epage: www.elsevier.com/locate/jallcom
Letter
Blue shift in band gap and photoluminescence of pulsed laser deposited
SrS:Ce/quartz thin film nanophosphors
Ankush Vij
a,b
, Sanjeev Gautam
a,b
, Ravi Kumar
e
, Amit K. Chawla
c
, Ramesh Chandra
d
,
Nafa Singh
f
, Keun Hwa Chae
a,∗
a
Advanced Analysis Center, Korea Institute of Science and Technology, Seoul 136-791, Republic of Korea
b
Pohang Light Source, San31 Hyojadong, Namgu, Pohang 790-784, Republic of Korea
c
College of Engineering Studies, University of Petroleum and Energy Studies, Dehradun 248-007, India
d
Institute Instrumentation Centre, Indian Institute of Technology, Roorkee 247-666, India
e
Centre for Material Science and Engineering, National Institute of Technology, Hamirpur 177-005, India
f
Department of Physics, Kurukshetra University Kurukshetra, Kurukshetra 136-119, India
a r t i c l e i n f o
Article history:
Received 12 October 2011
Received in revised form 7 February 2012
Accepted 8 February 2012
Available online xxx
Keywords:
SrS:Ce
Thin film nanophosphors
PLD
Photoluminescence
a b s t r a c t
We report on the synthesis of single phase SrS:Ce/quartz thin film nanophosphors at a substrate tempera-
ture of 400
◦
C using pulsed laser deposition. The AFM and FESEM micrographs reveal the island structure
with granular growth of nanophosphors. The average crystallite size (∼ 13 nm using Williamson–Hall
plot), the average grain size (∼ 40 nm using AFM) and the blue shift in band gap confirm the nanostruc-
ture formation. Interestingly, the photoluminescence emission corresponding to 5d-4f transitions in Ce
3+
ion under the cubic crystal field of SrS also exhibits a significant blue shift, which can be explained using
phenomenological crystal field model modified by covalency factor.
© 2012 Elsevier B.V. All rights reserved.
1. Introduction
Rare earth ions doped alkaline earth sulfide (AES) phosphors are
potential candidates for luminescent applications such as optical
storage media, electroluminescent displays, radiation dosimetry,
infrared sensors, ionoluminescence, etc. due to their high lumines-
cence yields [1–5]. SrS, a member of AES family, acts as a good
insulator due to indirect band gap of 4.2 eV in the bulk form. How-
ever, SrS doped with suitable activators such as rare earth ions
exhibits excellent luminescent properties [6,7]. In addition, these
phosphors emit visible light without self absorption.
Generally, thin film phosphors offer several advantages over the
conventional powder phosphor screens, including high resolution,
thermal stability, uniformity, density, and possibly a much lower
susceptibility to charging [8]. There are several reports available
on the synthesis of SrS based thin films on different substrates
using pulsed laser deposition (PLD) [8,9], e-beam evaporation [10],
RF sputtering [11], atomic layer epitaxy [12], etc. Since in low
dimensional systems, electrons and holes are spatially confined
causing quantum confinement effects, energy levels and hence
∗
Corresponding author. Tel.: +82 542791192; fax: +82 542791599.
E-mail address: khchae@kist.re.kr (K.H. Chae).
optical properties become considerably different from their bulk
counterparts [13–15]. This has generated a considerable interest in
exploring nanomaterials both in powder [16–18] and thin film form
[19–21]. Recently SrS based nanophosphors have been investigated
in detail but only in their powder form [7,22,23]. In this letter, we
discuss the hitherto unreported synthesis and characterization of
SrS:Ce thin film nanophosphors. The effect of different substrate
temperatures and subsequent in situ post deposition annealing on
the structure of thin film nanophosphors has been investigated.
2. Experimental details
SrS:Ce thin film nanophosphors were deposited on quartz sub-
strates using PLD. Prior to film deposition, substrates were properly
cleaned in an ultrasonicator using methanol and deionized water.
The source material Ce (0.5 mol%) doped SrS powder for PLD was
synthesized by solid state diffusion method in the presence of thio-
sulfate as a flux [7]. The synthesized powder was hydraulically
pressed into the pellet form and sintered at 1000
◦
C for 4 h in Ar
atmosphere to prevent oxidation. The sintered pellet was used as
the target to deposit thin films by using a PLD chamber (Excel
instruments, Mumbai) and a KrF excimer laser (Lambda Physik,
= 248 nm). The distance from target to substrate was fixed at 3 cm
and the laser energy was adjusted at 250 mJ. The deposition was
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doi:10.1016/j.jallcom.2012.02.063