Electrochimica Acta 85 (2012) 256–262
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Electrochimica Acta
jou rn al h om epa ge: www.elsevier.com/locate/electacta
Porous nickel oxide microflowers synthesized by calcination of coordination
microflowers and their applications as glutathione electrochemical sensor
and supercapacitors
Huan Pang
a,b,c,∗
, Yunfeng Shi
a
, Jimin Du
a
, Yahui Ma
a
, Guochang Li
a
, Jing Chen
a
, Jiangshan Zhang
a
,
Honghe Zheng
b,∗
, Baiqing Yuan
a,∗
a
College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang, 455000, Henan, PR China
b
School of Energy, Soochow University, Suzhou, 215006, Jiangsu, PR China
c
State Key Laboratory of Coordination Chemistry, Nanjing University, Nanjing, 210093, Jiangsu, PR China
a r t i c l e i n f o
Article history:
Received 26 June 2012
Received in revised form 10 August 2012
Accepted 15 August 2012
Available online 23 August 2012
Keywords:
Porous NiO microflowers
Glutathione electrochemical sensor
Electrochemical supercapacitors
a b s t r a c t
Porous nickel oxide (NiO) microflowers have been successfully synthesized by calcining a coordina-
tion microflower without any hard template, seed or using soft template. More importantly, porous
NiO microflowers have been applied as effective electrochemical sensor of the tripeptide glutathione
(GSH) and electrochemical supercapacitors. The effectively electrochemical GSH sensor of porous NiO
microflowers in 0.1 M HAc–NaAc (pH 5.0) solution was the first time evaluated. Moreover, the specific
capacitance of porous NiO microflower was up to 1678.4 F g
-1
at current density of 0.625 A g
-1
, and
maintained about 99.7% at 6.25 A g
-1
after 1000 cycles.
© 2012 Elsevier Ltd. All rights reserved.
1. Introduction
Thiols are very important to living organisms as they provide
regulatory intracellular and extracellular functions. The tripeptide
glutathione (Glu-Cys-Gly, GSH) is pivotal for reducing oxidative
stress in cells and maintaining redox homeostasis that is cru-
cial for cell growth [1–3]. Electrochemical methods have proven
as very useful for determination of thiols as they are sensitive,
selective, with very good linear range and rapid response times.
The oxidation of thiols on carbon based electrodes exhibits rela-
tively low heterogeneous electron transfer rates. In the past, the
electrode materials used for the determination of thiols consisted
of mercury, edge plane pyrolytic graphite, boron doped diamond
electrode, fullerenes and carbon nanotubes [4–9]. The electro-
catalytic enhancement of biologically related thiol detection was
sought and PtFeNi [10] or PtNiCo [11] catalysts were employed.
Recently, Martin Pumera have successfully discovered that NiO
nanoparticles significantly enhance the signal of glutathione dur-
ing cyclic voltammetry measurements [12,13]. As the development
of nanoscience, precisely control of the morphology of NiO
∗
Corresponding authors at: College of Chemistry and Chemical Engineering,
Anyang Normal University, Anyang, 455000, Henan, PR China.
E-mail addresses: huanpangchem@hotmail.com (H. Pang),
hhzheng@suda.edu.cn (H. Zheng), baiqingyuan1981@126.com (B. Yuan).
nanomaterials would serve to maximize the performance of using
inexpensive NiO for enhanced detection of regulatory peptides glu-
tathione.
Transition metal oxides such as ruthenium oxide, manganese
oxide, cobalt oxide, and nickel oxide are qualified to be electro-
chemical capacitor materials. Among these materials, NiO is of
great significance, and the theoretical capacitance of NiO can be
ca. 2573 F g
-1
within 0.5 V. With the development of nanoscience,
many groups found that nanomaterials generally exhibit many
size and shape dependent properties, and the specific capacitance
of NiO nanomaterials is depended on the synthesis method and
morphology [14–27]. In particular, there have been considerable
research efforts devoted to the use of nickel oxide for super-
capacitors, due to its good pseudocapacitive behavior, practical
availability, environmentally begin nature and low cost compared
to the state-of-the-art supercapacitor material RuO
2
[16–24].
The interaction between metal ions and ligands has been widely
investigated in materials science and chemistry during the past
few decades [28,29]. Recently, a growing number of studies are
now dedicated to the synthesis of nanostructured metal–organic
complexes [30]. Coordination complexes have been used as a
nanostructured precursor to prepare mesoporous metal oxides in
our previous work [31–33]. The coordination complex precursor
always has a micro or nanostructure due to the growth mechanism
of the polymer complex precursor, and such unique nanostruc-
ture may bring on an exciting performance of utility in many
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http://dx.doi.org/10.1016/j.electacta.2012.08.057