Journal of Power Sources 195 (2010) 6977–6981
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Journal of Power Sources
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Short Communication
Capacitance decay of nanoporous nickel hydroxide
Guangxia Hu
a
, Chunxiang Li
b
, Hao Gong
a,∗
a
Department of Materials Science & Engineering, National University of Singapore, 10 Kent Ridge Crescent, Singapore 119260, Singapore
b
Advanced Materials Technology Centre, Singapore Polytechnic, 500 Dover Road, Singapore 139651, Singapore
article info
Article history:
Received 17 February 2010
Received in revised form 16 March 2010
Accepted 22 March 2010
Available online 3 April 2010
Keywords:
Nanoporous nickel hydroxide
Capacitance decay
High current density
Supercapacitor
Phase change
abstract
Nanoporous nickel hydroxide Ni(OH)
2
coated on nickel foam by using a chemical bath deposition method
shows a high specific capacitance of 2200 F g
-1
at a discharging current density of 1 Ag
-1
. After 500
charge–discharge cycles, the specific capacitance is stabilized at 1470 Fg
-1
, and there is only a 5% fall in
specific capacitance during the following 1500 cycles. The relationship between the capacitance decay
and changes in the microstructure and morphology of nanoporous Ni(OH)
2
is investigated. The results
show that phase transformation and the growth of particle/crystal size, rather than the formerly proposed
flaking off of Ni(OH)
2
, are the major factors contributing to the capacitance decay.
© 2010 Published by Elsevier B.V.
1. Introduction
Nickel hydroxide (Ni(OH)
2
) has been used for many decades
as an active material for the positive electrode of batteries. These
nickel-based batteries can perform well at relatively low discharge
rates (0.1–1 C). At very high discharge rates (>10 C), however, only
a few percent of the storage capacity can be used [1]. At high dis-
charge rates/current densities, the best energy-storage device is
the supercapacitor. Well-developed carbon-based supercapacitors
(electric double-layer capacitors) have very high discharge current
densities, but they suffer from a low energy density or a low specific
capacitance of about 200 F g
-1
[2].
In recent years, nanosized Ni(OH)
2
, which can function well
at high discharge current densities, has been identified as a
very promising material for supercapacitors [3–10]. Two types of
energy-storage mechanism play a role in a supercapacitor, namely,
non-faradic charging as in electric double-layer capacitors and
Faradaic charging similar to the processes in batteries. Studies
[11,12] show that high current density discharge performance is
improved greatly by using nanostructured Ni(OH)
2
because of the
high specific surface area, fast redox reaction and shortened diffu-
sion path in the solid phase. Cheng et al. [8] reported a specific
capacitance of ∼696 F g
-1
for sol–gel-derived Ni(OH)
2
xerogels,
i.e., a performance that is significantly higher than that of well-
developed carbon-based materials. Yuan et al. [13] reported a
specific capacitance of ∼710 F g
-1
for spherical superstructured
∗
Corresponding author. Tel.: +65 65164632; fax: +65 68742081.
E-mail address: msegongh@nus.edu.sg (H. Gong).
Ni(OH)
2
. Lang et al. [5] and Yang et al. [14] further reported
a higher specific capacitance (>2000 F g
-1
) for loosely packed,
nanoflake Ni(OH)
2
structures. Although a high specific capacitance
is achieved, nanostructured Ni(OH)
2
suffers from significant capac-
itance decay during charge–discharge cycles and thereby prevents
it from industry applications such as electrical vehicles and hybrid
electrical vehicles. Some researchers propose that the capacitance
decay may be due to the flaking off of Ni(OH)
2
[14]. There is
no strong evidence to support this view, however, and no other
possible reasons have been advanced, according to the best of
our knowledge. A systematic investigation is needed to alleviate
the ambiguities for a better understanding of this important phe-
nomenon and thus pave the way to industrial applications of high
capacitance Ni(OH)
2
supercapacitors.
In this work, a Ni(OH)
2
film with interconnected nanoflakes is
deposited directly on a nickel foam substrate, and a high specific
capacitance of up to 2200 F g
-1
is achieved. The decay in capaci-
tance during charge–discharge cycles is studied systematically by
means of multi-characterization techniques including XRD, SEM,
TEM, and electrochemical methods. Capacitance decay behaviour
under different current regimes is also examined.
2. Experimental details
The solution for chemical bath deposition (CBD) was prepared
by mixing 40 mL of 1 M nickel sulfate, 30 mL of 0.25 M potassium
persulfate, 10 mL of aqueous ammonia (22–24% NH
3
), and 20 mL of
deionized water in a 250 mL Pyrex beaker at room temperature. The
Ni foam substrate was chemically cleaned with acetone, methanol,
0378-7753/$ – see front matter © 2010 Published by Elsevier B.V.
doi:10.1016/j.jpowsour.2010.03.093