Applied Surface Science 258 (2012) 5858–5862
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Applied Surface Science
jou rn al h om epa g e: www.elsevier.com/locate/apsusc
Synthesis and photocatalytic property of lead molybdate dendrites with exposed
(0 0 1) facet
Muhammad Hashim, Chenguo Hu
∗
, Xue Wang, Xiaoyan Li, Donglin Guo
Department of Applied Physics, Chongqing University, Chongqing 400044, PR China
a r t i c l e i n f o
Article history:
Received 12 February 2012
Accepted 22 February 2012
Available online 3 March 2012
Keywords:
Lead molybdate
Composite molten salt method
Photocatalytic property
a b s t r a c t
PbMoO
4
dendrites have been synthesized by the composite molten salt method at 180
◦
C. The dendritic
plane is exposed on (0 0 1) facet. PbMoO
4
dendritic crystals exhibited high photocatalytic activity through
the degradation of rhodamine B under the irradiation of the simulated sunlight, mainly due to the exposed
facet (0 0 1). The (0 0 1) facet is assumed to provide more multi-atomic centers (PbMo
4
), which are the
origin of the active sites for hydrophilicity and adsorption of O
2
and the cause of the high photocat-
alytic activity. The photocatalytic activity of the PbMoO
4
dendrites was also compared with those of the
conventional catalysts, P25 (21 nm) and TiO
2
nanoparticles (50–200 nm).
© 2012 Elsevier B.V. All rights reserved.
1. Introduction
The properties of nanocrystals depend not only on their com-
position, but also on their structure, phase, shape, size and
crystallization [1–4]. Varied morphologies, such as nanoparti-
cles, nanorods, nanospheres, nanoneedles, nanosheets, nanowires,
nanotubes, nanobelts or nanoribbons, nanofibers, and dendrites
have been presented [5–12]. The surface characteristics of pho-
tocatalysts have much impact on their photocatalytic efficiency.
Recent investigations have proved that exposed facets of semi-
conductor oxide photocatalysts can remarkably improve their
photocatalytic activity because of their higher surface energy, more
oxygen defects and intraplane vacancies [13–15]. Normally, TiO
2
catalyst with exposed (0 0 1) facet exhibits better photocatalysis
due to its higher surface activity than that of other low index
facets [16,17]. Recently, Shen et al. [13] demonstrated that the
PbMoO
4
microcrystals with preferentially exposed (0 0 1) facet
exhibit higher catalytic activity than that of (1 0 0) facet. Simi-
larly, Xi and Ye found that the m-BiVO
4
nanoplates synthesized
by a hydrothermal method with preferentially exposed (0 4 0)
facet exhibit greatly enhanced activity for the photodegradation
of organic contaminants and the photooxidation of water for O
2
production [15].
Anyhow, it is a great challenge to synthesize the photocat-
alysts which possess both high photocatalytic activity and fast
and low cost recyclability with stable catalytic activity. Herein,
we reported the synthesis of lead molybdate (PbMoO
4
) dendritic
∗
Corresponding author. Tel.: +86 23 65678362; fax: +86 23 65678362.
E-mail address: hucg@cqu.edu.cn (C. Hu).
nanocrystals with preferentially exposed (0 0 1) facet by a facile
composite molten salt (CMS) method without using any surfac-
tant or capping agent, which is a new strategy for the synthesis
of nanomaterials using two salts as solvent [10,18,19]. The pho-
tocatalytic activity of the PbMoO
4
dendrites with preferentially
exposed (0 0 1) facet is evaluated by the degradation of rhodamine
B (RhB) dye under the simulated sunlight irradiation and the results
were compared with common commercial catalysts, P25 and TiO
2
nanoparticles. The well recyclability with a stable catalytic activ-
ity of the PbMoO
4
dendrite catalyst has been verified through RhB
degradation.
2. Experimental
2.1. Synthesis of PbMoO
4
dendritic nanocrystals
All chemicals purchased from Chongqing Chemical Company
were analytically pure and used without further purification.
PbMoO
4
dendritic nanocrystals have been synthesized by the CMS
method. Typically, 3 g of LiNO
3
and KNO
3
with mass ratio of 1:2
were mixed in a Teflon vessel of 25 mL capacity. Then, 1 mmol of
Pb(NO
3
)
2
and H
2
MoO
4
and 4 mL ammonia solution (pH 9) were
added in the Teflon vessel. After reacting at 180
◦
C for 23 h in a
furnace, the vessel was taken out and allowed to cool at room tem-
perature naturally. Finally, the sample was obtained after washing
the product several times with distilled water and absolute ethanol.
2.2. Characterization
The crystal phase of the sample was characterized by
X-ray diffractometer (XRD, BDX320) equipped with graphite
0169-4332/$ – see front matter © 2012 Elsevier B.V. All rights reserved.
doi:10.1016/j.apsusc.2012.02.116