This journal is © The Royal Society of Chemistry 2014 Chem. Commun.
Cite this: DOI: 10.1039/c3cc48773c
Facile synthesis of nanostructured CuCo
2
O
4
as a novel electrode material for high-rate
supercapacitors†
Afshin Pendashteh,
a
Mohammad S. Rahmanifar,
b
Richard B. Kaner
c
and
Mir F. Mousavi*
ac
CuCo
2
O
4
nanostructures were synthesized through a facile solution
combustion method. Electrochemical investigations demonstrate a novel
electrode material for supercapacitors with remarkable performance
including high-rate capability, high-power density (22.11 kW kg
À1
) and
desirable cycling stability at di fferent current densities.
With demand growing every day for electric energy storage for
electrical vehicles and portable devices, electrochemical capacitors
or supercapacitors (SCs) have stimulated extensive research interest
due to their high-power density, high-rate capability and long cycle
life.
1
The charge storage mechanism in SCs is based on either non-
Faradaic electrochemical double layer capacitance (EDLC) or fast,
reversible Faradaic redox reactions (pseudocapacitance).
2
Transi-
tion metal oxides have been extensively investigated as pseudo-
capacitive materials due to their potentially higher capacitance
compared to EDLCs, mainly ascribed to their multiple oxidation
states.
3
However, they suffer from intrinsically low electrical con-
ductivity and the fact that fast Faradaic reactions only occur at the
surface of the electrode.
4
These disadvantages hinder their applica-
tion in high-rate supercapacitors. Therefore, novel materials or
strategies to improve the performance of the electrode materials for
high-power applications, including fabrication of nano-engineered
structures or utilizing synergistic effects of hybrid materials, are
needed.
5,6
Among the many transition metal oxides, Co
3
O
4
has
been widely studied in pseudocapacitors, and has demonstrated
promising performance.
7
Complete or partial substitution of Co
with low-cost and benign elements to form the spinel structure
could prove to be even better.
8
Recently, CuCo
2
O
4
nanostructures
have been investigated as an anode material in Li-ion batteries,
showing high Li-ion storage capacities,
8,9
suggesting that they can
offer high-charge storage capacity through redox reactions.
In this communication, a simple urea combustion method
is combined with a post annealing process to synthesize
nanostructured CuCo
2
O
4
particles in the shape of cauliflower-
like structures. The electrochemical behavior of the sample as a
novel material for supercapacitor electrodes was evaluated using
different electrochemical techniques including cyclic voltammetry
(CV), chronopotentiometry (CP), and electrochemical impedance
spectroscopy (EIS).
CuCo
2
O
4
nanostructures were synthesized via a combustion
route using the corresponding nitrate salts as precursors and urea
as fuel. The detailed preparation procedure can be found in the
ESI. † Moreover, a sample comprised of CuCo
2
O
4
microparticles
was also synthesized via the co-precipitation method (see ESI†).
The as-prepared samples were structurally characterized by
means of powder X-ray diffraction (XRD). The XRD patterns of
both samples can be entirely indexed to a cubic spinel copper
cobaltite structure with the lattice parameter a = 8.039 Å, belonging
to the Fd3m space group (Fig. 1a, and Fig. S4A, ESI†), which is well
matched with the JCPDS file no. 001-1155. These features are also in
good agreement with previous reports.
8,9
For clarity, the hkl lines are
ascribed to the corresponding peaks. Broadened di ffracted peaks for
the nanostructured sample illuminate the fine crystalline size of the
Fig. 1 XRD pattern (a), and FESEM of CuCo
2
O
4
nanostructures magnified
30 000Â (b) and 100 000Â (c).
a
Department of Chemistry, Tarbiat Modares University, Tehran, Iran
b
Faculty of Basic Sciences, Shahed University, Tehran, Iran
c
Department of Chemistry and Biochemistry and California NanoSystems Institute,
University of California, Los Angeles (UCLA), Los Angeles, CA 90095, USA.
E-mail: mousavim@modares.ac.ir, mousavi@chem.ucla.edu
† Electronic supplementary information (ESI) available: Details of the experi-
mental procedure. See DOI: 10.1039/c3cc48773c
Received 17th November 2013,
Accepted 16th December 2013
DOI: 10.1039/c3cc48773c
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