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PII: S0013-4686(15)00522-8
DOI: http://dx.doi.org/doi:10.1016/j.electacta.2015.02.200
Reference: EA 24479
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Carboxymethyl Carrageenan Based Biopolymer Electrolytes
School of Chemical Sciences and Food Technology, Faculty of Science and Technology,
Universiti Kebangsaan Malaysia, 43600, Bangi, Selangor Darul Ehsan, Malaysia
*
Corresponding Author: Tel:60389287262; Fax:60389212115.
Highlights
The paper highlights the potential of carboxymethyl carrageenan based on iota and
kappa to be utilized as host polymer.
The highest conductivity were achieved up to ~10-3 S cm-1 by carboxymethyl
carrageenan without the addition of plasticizer.
The electrochemical stability windows of the films were electrochemically stable up
to 3.0 V.
Abstract
A series of biodegradable carboxymethyl carrageenan based polymer electrolytes, which are
carboxymethyl kappa carrageenan (sulphate per disaccharide) and carboxymethyl iota
carrageenan (two sulphates per disaccharide), have been prepared by a solution casting
technique with different ratios of lithium nitrate (LiNO3) salts. Interestingly, the lithium ions
tended to interact with the carbonyl group in the different modes of symmetry, as observed
from reflection Fourier transform infrared (ATR-FTIR) spectroscopy analysis. In the
carboxymethyl kappa carrageenan electrolytes, as the concentration of LiNO3 increased, the
asymmetric stretching peak of the carbonyl bond became dominant because it can be
observed clearly with the shifting of the peak from 1592 to 1602 cm-1 due to the interaction
between the lithium ion and the carbonyl group, while the broad O-H stretching peak became
sharp and intense. However, for the carboxymethyl iota carrageenan, the asymmetry
stretching mode of the carbonyl group shifted from 1567 to 1599 cm-1, as the salt
concentration increased. The shifting of the C-O-C peak also occurred in the iota-based
electrolytes. However, the changes in the peak that represented SO42- symmetric stretching
were only detected when the ion pair formation was observed. It was proposed that the peak
shifting was due to the presence of the lithium ion pathway, forming a dative bond between
the lithium and oxygen in the carbonyl group. Accordingly, as more peak shifting was
observed, the number of the ion pathways also increased. This hypothesis was supported by
the impedance data, which demonstrated that the ionic conductivity of the 20 wt.% LiNO3
iota-based electrolytes was highly similar with the 30 wt.% LiNO3 kappa-based electrolytes,
with values of 5.85 10-3 S cm-1 and 5.51 x 10-3 S cm-1, respectively. The lithium
transference number for the carboxymethyl kappa carrageenan was higher than for the
carboxymethyl iota carrageenan. Additionally, the carboxymethyl iota carrageenan and
carboxymethyl kappa carrageenan films were electrochemically stable up to ~3.0 and 3.1 V,
respectively, which indicates that these solid biopolymer electrolytes are promising
candidates for utilization in electrochemical devices.
1. Introduction
Carrageenans are a family of anionic polymers that are extracted from certain marine red
algae and that share a common backbone of alternating (1 3)-linked -D-galactopyranose
and (1 4)-linked -D-galactopyranose [1]. There are three primary types of carrageenans:
kappa carrageenan (possesses one sulphate per disaccharide), iota carrageenan (two sulphates
per disaccharide) and lambda (three sulphates per disaccharide) [2]. Carrageenans are
extensively used in the food, pharmaceutical and cosmetic industries as viscosity builders,
gelling agents and stabilizers, [3] especially because carrageenans are regarded as safe
(GRAS) by The Food and Drug Administration in the US [1].
To enhance the potential of the carboxymethyl derivatives (iota and kappa) for
electrochemical cell applications, such as with lithium batteries, lithium nitrate (LiNO3) will
be introduced as a dopant salt. From the literature, lithium salts, such as lithium perchlorate
(LiClO4) [12], lithium tetrafluoroborate (LiBF4) [13], lithium bis(trifluoromethanesulfonyl)
imide (LiTSFI) [14] and lithium hexafluorophosphate (LiPF6), [15] are among the salts that
have been utilized by other researchers. The potential of LiNO3 was reported by Mohamed et
al. (1995) [16]. They used acetylated chitosan as a polymer host that achieved an electrical
conductivity of 2.7 10-4 S cm-1. Xiong et al. (2012) also demonstrated that the use of LiNO3
was an effective additive that protected the lithium anode [17]. Because lithium-oxygen
batteries are becoming increasingly attractive due to their high theoretical energy densities,
proper cell voltages and utilization of environment-friendly components [18-21], the
selection of lithium nitrate is a great choice. The unique properties of the nitrate electrolyte
allows for it to serve as a secondary source for oxygen at the cathode as well as it providing a
nitrate ion pathway for oxygen reduction [22].
In this work, the effects of the lithium ion on the ionic conductivity and the chemical stability
of carboxymethyl carrageenan will be examined by using Electrochemical Impedance
Spectroscopy (EIS) analysis and Linear Sweep Voltammetry (LSV). This paper will also
investigate the interactions between the targeted functional groups, which are the carboxylate
and sulphate groups, and the lithium ions by using reflection Fourier Transform Infrared
(ATR-FTIR) spectroscopy.
2. Experimental
Carboxymethyl carrageenan was prepared according to the method established by Sun et al.
(2008) [23]. To prepare the polymer electrolyte films, carboxymethyl carrageenan was
dissolved in a 1% acetic acid solution that was continuously stirred with a magnetic bar for
24 hours. Various weight percentages of LiNO3 were dissolved separately in a 1% acetic acid
solution before it was added drop-wise into the carboxymethyl carrageenan solution. The
solutions were further stirred for 24 hours to achieve a homogenous mixture. The solutions
were cast onto petri dishes and allowed to dry completely at room temperature until films
were obtained. The samples were stored in a desiccator for future use.
2.2 Sample characterization
ATR-FTIR analysis was conducted by using a Perkin Elmer Spectrum 2000 for the range
from 4000 to 400 cm1 with a scanning resolution of 4 cm1. This analysis was conducted to
observe the interactions between the polymer matrix and the lithium nitrate salts based upon
the changes in the shapes and the wavenumbers of the peaks. Alternating current (AC)
impedance measurements were conducted by using a high frequency response analyser
(HFRA; Solartron 1260, Schlumberger) and an electrochemical interface (SI 1286) in the
frequency range of 1Hz10 MHz with a 10 mV amplitude at room temperature. The polymer
electrolyte was sandwiched between the stainless steel blocking electrodes with a contact
surface area of 2.0 cm2. The bulk resistance (Rb) was determined from the equivalent circuit
analysis by using the Zview analyser software. The samples were also characterized via
electrical impedance spectroscopy (EIS) using an HIOKI 3532 LCR Hi-Tester that was
interfaced with a computer, and the experiments were conducted in the frequency range
between 50 Hz to 1MHz. The temperature dependence of the AC conductivities for both
systems were recorded between 30 - 65 C with intervals of 5C. The transference number of
lithium ion, tLi+, was determined at 303K by using a Zive mp2 multichannel electrochemical
workstation. The electrolyte was placed between two lithium electrodes. A DC voltage (V=
0.1V) was applied to these two electrodes until the current reached steady-state. The AC
impedance measured the resistance of the polymer electrolyte and the interface before/after
the voltage was applied. The transference number of lithium ion, tLi+, was calculated with the
following formula:
where I0 and IS are the initial and steady-state currents during the polarization, respectively,
and Ri0 and RiS are the interfacial resistances at the initial state and the steady-state,
respectively [24]. The linear sweep voltammetry of the electrolyte films was determined by
the application of a D.C. potential (0.1 V) across the sample using stainless steel electrodes at
303K and a Zive mp2 multichannel electrochemical workstation.
3. Results and Discussion
Fig. 1 shows the physical observations of the carboxymethyl kappa carrageenan and
carboxymethyl iota carrageenan films. It can be observed that the carboxymethyl kappa
carrageenan was more transparent compared to the carboxymethyl iota carrageenan. The
difference in term of colour between kappa carrageenan and iota carrageenan samples were
caused by the source of raw materials. Kappa carrageenan powder which extracted from
Eucheuma cottonii was whiter compared to iota carrageenan powder that extracted from
Eucheuma spinosum.
FTIR spectroscopy was utilized to identify the interactions that occurred between the lithium
ions and the oxygen atoms in the chemical structure of the carboxymethyl carrageenan. The
characteristic band regions of hydroxyl stretching, carbonyl and C-O-C stretching were the
main focus in the detection of the ionic interactions. Fig. 2 and 3 show the infrared spectra of
the carboxymethyl kappa carrageenan and the carboxymethyl iota carrageenan at different
weight percentages of salt. As previously reported, the peak that represents the O-H
stretching at 3436 cm-1 shifted to 3386 cm-1 when the powder of the carboxymethyl kappa
carrageenan was dissolved in 1% acetic acid [4]. The shifting of the wavenumber to the lower
frequency was due to the protonation of the hydroxyl group with the addition of acetic acid.
The protonated hydroxyl group will form electrostatic interactions with the acetate ions, as
shown in Scheme 1. However, as the concentration of the lithium nitrate was increased, the
peaks that represented the O-H became more intense. This proved that there were ion dipole
interactions between the oxygen atoms in the hydroxyl groups of the carboxymethyl kappa
carrageenan with the lithium ions, as shown in Scheme 1. These changes were also observed
in the carboxymethyl iota carrageenan- LiNO3 films, as shown in Scheme 2.
The lithium ions also tended to interact with the carbonyl group in the different symmetry
modes, as observed from the ATR-FTIR spectra for both systems. It was observed that the
peak that represented the asymmetric stretching of the carbonyl shifted to a higher
wavenumber, from 1592 to 1602 cm-1 for carboxymethyl kappa carrageenan and from 1562
to 1602 cm-1 for carboxymethyl iota carrageenan. As it is known, asymmetric stretching can
explain the bond stretching in different directions. Because the electrostatic interactions
between the C-O- in the acetate ions and the carboxymethyl ions are stronger compared to the
ion dipole interactions that form between the oxygen atom in C=O with the lithium ion, it
was expected that C=O peak would become shorter, which is shown in Fig. 4. On the other
hand, the symmetric stretching was shifted to lower wavenumbers for both systems.
However, as the concentration of lithium nitrate increased up to 30 wt.% for the
carboxymethyl kappa carrageenan and 20 wt.% for the carboxymethyl iota carrageenan, the
complexation between the lithium ions and the nitrate ions were detected by the appearance
of a new peak at 1630 cm-1. This confirmed that the appearance of ion pairs influenced the
conductivity that was achieved by the system, and the optimum conductivity was achieved by
the carboxymethyl iota carrageenan with 20 wt.% LiNO3.
The asymmetric stretching of the nitrate was also observed when the concentration of lithium
salt increased; this was observed as a shift in the peak from 1379 cm-1 to 1355 cm-1 for the
carboxymethyl kappa carrageenan and by the appearance of new peak at 1358 cm-1 for the
carboxymethyl iota carrageenan. For the carboxymethyl kappa carrageenan, it was also
observed that the peak at 1065 and 1041 cm-1, which represented the C-O-C stretching,
changed in terms of the wavenumber and intensity. The intensity of the peaks at 1065 cm-1
increased while the peak at 1044 cm-1 decreased as the salt concentration increased. Based
upon previous research, the peak at 1044 cm-1 only appeared when the carboxymethyl kappa
carrageenan was dissolved in 1% acetic acid [4]. This finding may be due to the transient
intermolecular hydrogen bonds that were formed between the oxygen atoms (C=O) in the
acetate ions or the carboxylate ions with a hydrogen atom from a protonated hydroxyl group.
However, as the number of lithium ions increased, the interactions between the lithium ions
and the oxygen atoms (C=O) in the acetate ions or the carboxylate ions became more
dominant, and therefore the intensity of the peak at 1044 cm-1 decreased. It was also observed
that the intensity of the hydroxyl peak became sharper as the concentration of the lithium
nitrate increased. For the carboxymethyl iota carrageenan, both peaks at 1069 and 1023 cm-1
decreased in their intensity with the addition of lithium nitrate due to the interactions between
the Li+ cations and the ether oxygen atoms [25]. However, the changes in the wavenumbers
that represent the sulphate stretching peak were only observed for the 25 wt.% LiNO3-
carboxymethyl iota carrageenan and for carboxymethyl kappa carrageenan at 30 wt.%
LiNO3. The appearance of a new peak at 1248 cm-1, which was representative of the
interactions between the lithium ions and the sulphate ions (RSO4- Li+), were detected [26].
This finding demonstrated that the lithium ion more favourable interacted with the carboxylic
ions because they were more basic compared to the sulphate ions. Therefore, this finding also
supported the fact that the optimum ionic conductivity was able to be achieved by
carboxymethyl kappa carrageenan at 30 wt.% LiNO3 compared to 20 wt.% LiNO3 for the
carboxymethyl iota carrageenan; this was possible because the carboxymethyl kappa
carrageenan possesses one sulphate per disaccharide and the carboxymethyl iota carrageenan
possesses two sulphates per disaccharide. Schemes 1 and 2 show the proposed mechanism
that explains the interactions between the lithium ions and the electronegativity atoms in the
carboxymethyl carrageenans.
The ionic conductivities of the polymer electrolytes with different concentrations of LiNO3
salts at room temperature for the carboxymethyl kappa carrageenan and carboxymethyl iota
carrageenan are presented in Fig. 5. The recorded conductivity of the carboxymethyl kappa
carrageenan increased with a corresponding increase in the concentration of the LiNO3 salts.
The highest conductivity that was obtained was 5.51 10-3 S cm-1 with a concentration of 30
wt.% of the LiNO3 salt. The ionic conductivity for the carboxymethyl iota carrageenan
increased when up to 20 wt.% of the LiNO3 salt was added.
As seen in the FTIR analysis, interactions occurred between the LiNO3 and the COO- and C-
O-C groups in both host polymers, and these interactions promoted the dissociation of LiNO3
and increased the free charge carriers in the electrolyte systems, which lead to an increase in
the conductivity. This was similar to what had previously been reported in the literature [27],
where it was stated that the increase in the ionic conductivity along with increase in the salt
concentration could be understood in terms of the number density of the charge carriers.
However, as seen from the FTIR spectra, the decrease of the conductivity for the
carboxymethyl iota carrageenan was attributed to the re-association of ions to form ion
clusters. Therefore, there were fewer mobile charge carriers and the larger sized ion clusters
limited the ion mobility. The optimum conductivity for the carboxymethyl iota carrageenan
was achieved at a 20 wt.% salt concentration.
To evaluate the ionic conduction mechanisms, the ionic conductivities of the solid polymer
electrolyte based carboxymethyl kappa carrageenan- 30 wt.% LiNO3 and carboxymethyl iota
carrageenan- 20 wt.% LiNO3 complexes were measured at different temperatures, as shown
in Fig. 5. As illustrated in Fig. 5, typical behaviour for a polymer electrolyte was observed
where the ionic conductivity increased with increasing temperature. Higher temperatures not
only promoted the migration of the carrier ions but also resulted in the expansion of the
polymers [28]. This expansion produced local empty space and increased the free volume,
which promoted the motion of the polymer segments and carrier ions. The highest ionic
conducting samples of the carboxymethyl kappa carrageenan- 30 wt.% LiNO3 and the
carboxymethyl iota carrageenan- 20 wt.% LiNO3 complexes possessed ionic conductivities of
7.42 x 10-3 and 1.51 x 10-2 S cm-1, respectively.
As shown in Fig. 6, the regression values were close to unity, which indicated that the
temperature-dependent ionic conductivities for this SPE system obeyed Arrheniuss rule in
the temperature range between 30 and 60C. Based upon the calculations, the activation
energy for the carboxymethyl kappa carrageenan- 30 wt.% LiNO3 and the carboxymethyl
iota carrageenan- 20 wt.% LiNO3 complexes were 0.18 and 0.38 eV, respectively. The low
activation energy values indicated that a low amount of energy was needed for the formation
of ions [29]. The low apparent activation energies may also be related to the easy
transformation of the polymer conformations [30].
Fig. 7 depicts the lithium transference numbers of the solid polymer electrolytes based upon
carboxymethyl kappa carrageenan and carboxymethyl iota carrageenan. The value of lithium
transference number, tLi+, was calculated from the normalized polarization current versus
time. Based on the graph, the initial total current decreased with time due to the depletion of
the ionic species in the electrolyte, and became constant in the fully depleted situation. At
steady-state, the cell was polarized and the current was allowed to flow because of the
electron migration across the electrolyte and interfaces [31]. The lithium transference
numbers for the studied carboxymethyl kappa carrageenan and carboxymethyl iota
carrageenan complexes were calculated to be 0.54 and 0.42, respectively. These results were
supported by the Ea value, which was lower for the carboxymethyl kappa carrageenan than
for the carboxymethyl iota carrageenan. The lithium transference numbers for these
biopolymers possessed better results compared to the system of polyethylene oxide (PEO)
/LiPBSi, where the calculated lithium transference number was 0.39 [32].
Fig. 8 depicts the linear sweep voltammetry curves for the iota and kappa carboxymethyl
carrageenan. From Fig. 8, a small current was observed through the working electrode until
the applied voltage reached a potential of 3.0 and 3.10 V for carboxymethyl iota carrageenan
and carboxymethyl kappa carrageenan, respectively [33]; this was marked with arrows in Fig.
8. The current increased sharply with the applied voltage, which can be attributed to the
decomposition of the polymer electrolyte. This indicated that the carboxymethyl iota
carrageenan20 wt.% LiNO3 electrolyte was electrochemically stable up to 3.0 V while the
carboxymethyl kappa carrageenan30 wt.% LiNO3 electrolyte was electrochemically stable
up to 3.10 V.
4. Conclusions
The effects of lithium nitrate (LiNO3) salts on the carboxymethyl iota carrageenan and
carboxymethyl kappa carrageenan based solid polymer electrolytes were investigated. The
highest ionic conductivities were achieved for the carboxymethyl kappa and iota carrageenan
were 5.85 10-3 S cm-1 and 5.51 10-3 S cm-1 at 30 wt.% and 20 wt.% of the lithium salts
addition, respectively. FTIR spectra demonstrated that the lithium ion more favourably
interacted with the carbonyl and ether groups compared to the sulphate group. The formation
of the ion pair was observed the appearance of new peaks at 1630 and 1375 cm-1 for 25 wt.%
and 30 wt.% LiNO3 salts, respectively. The ion pair might cause a decrease in the ionic
conductivity for carboxymethyl iota carrageenan. The activation energies for the
carboxymethyl kappa carrageenan and the carboxymethyl iota carrageenan were calculated to
be 0.18 and 0.38 eV, respectively. The activation energy results were supported by the
lithium transference number analysis, where the values were reported as 0.54 and 0.42. From
the LSV analysis, it was demonstrated that both samples were stable up to 3.0 V. These
results indicated that both systems were suitable to be used in lithium-ion battery
applications.
Acknowledgments
The authors would like to thank UKM and the Fisheries Department for the provisions
provided by the grants FRGS/2/2013/TK04/UKM/02/4 and STGL-007-2010, respectively,
and to Syarikat Tacara Sdn Bhd.
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Scheme 1 Interaction between lithium nitrate and the carboxymethyl kappa carrageenan
Scheme 2 Interaction between lithium nitrate and the carboxymethyl iota carrageenan
Fig. 1 Physical observations of A (i) and A (ii) for the carboxymethyl kappa carrageenan at 5
wt.% and 30wt.% LiNO3; B (i) and B (ii) for the carboxymethyl iota carrageenan at 5
wt.% and 25 wt.% LiNO3.
Fig. 2 FTIR spectra of the carboxymethyl kappa carrageenan at different weight percentages
of lithium nitrate salts where (a) is the hydroxyl band region, (b) is the carbonyl
stretching and (c) is the C-O-C band region
Fig. 3 FTIR spectra of the carboxymethyl iota carrageenan at different weight percents of
lithium nitrate salts where (a) is the hydroxyl band region, (b) is the carbonyl stretching and
(c) is the C-O-C band region
Fig. 4 Modes of the carbonyl bond stretching: (A) Symmetric stretching (B) Asymmetric
Stretching
Fig. 5 Ionic conductivities of the solid polymer electrolytes based upon carboxymethyl
carrageenan at ambient temperature
Fig. 6 Effect of the temperature on the ionic conductivities of the solid polymer electrolytes
based upon carboxymethyl carrageenan
Fig. 7 Normalized current using Li metal as the electrode for the solid polymer electrolytes
based upon carboxymethyl carrageenan
H2C C O
6
OSO3 O
6'
5 O
4' 5' O O 1
1' O 3
2' 4 2
3'
O O
O
H H n
NO3
Li+
Li+
+Li
H2C C O
6
OSO3 O
6'
5 O
4' 5' O O 1
1' O 3
2' 4 2
3'
O O
H O
H H n
H
(iii)
(i)
Li +
CH3CH2(O)O
CH 3C(O)O
Li +
(ii)
H
n H H H
O
O 3' O
2 4 2'
3
O 1'
1 5' 4'
O O
O Li+
5
6'
O O3SO
6
O C CH2
Li+
Scheme 1
HOOCH 2C
O
O
OSO3- C H O
2
O O
O
O
H OSO3-
Li+ NO3-
+Li
NO3-
Li+
O(O)HCH2C Li+
O Li+
O
OSO3- CH O
2
O O
Li+
O
O
H
H OSO3-
n
(ii)
CH3C(O)O
+Li
LI+
(i)
n
OSO3- H H
O
O
O O
O C2H OSO3-
O
O
CH2C(O)O
Scheme 2
A A (ii)
(i)
B
B (ii)
(i)
Fig. 1
100
100
100
90 90
90
80 80 80
%T
%T
%T
70 70 70
60 60 60
5% LiNO3
5% LiNO3 5% LiNO3
10% LiNO3 10% LiNO3 10% LiNO3
50 15% LiNO3 50 15% LiNO3 50 15% LiNO3
20% LiNO3 20% LiNO3 20% LiNO3
25% LiNO3 25% LiNO3 25% LiNO3
30% LiNO3 30% LiNO3 30% LiNO3
40 40 40
4000 3600 3200 2800 1600 1500 1400 1300
1200 1100 1000
-1 -1
-1 Wavenumber/cm
Wavenumber/cm Wavenumber/cm
Fig. 2
100 100 100
90
90 90
80
80 80
%T
%T
%T
70
70 70
60
60
60
0% LiNO3 50
0% LiNO3
5% LiNO3 0% LiNO3
5% LiNO3
10% LiNO3 5% LiNO3
50 10% LiNO3
50 15% LiNO3 10% LiNO3
15% LiNO3
20% LiNO3 40 15% LiNO3
20% LiNO3
25% LiNO3 20% LiNO3
25% LiNO3
30% LiNO3 25% LiNO3
40 30% LiNO3
30% LiNO3
40 30
4000 3500 3000 1700 1600 1500 1400 1300
1200 1100 1000
-1 -1
Wavenumber/cm Wavenumber/cm -1
Wavenumber/cm
Fig. 3
Li+
A) B)
Li+
O
O
C O-
C O-
H3C
H3C
Fig. 4 Modes of the carbonyl bond stretching: (A) Symmetric stretching (B) Asymmetric
Stretching
-2.0
-2.5
log(conductivity/S cm )
-1
-3.0
-3.5
-4.0
carboxymethyl iota carrageenan
carboxymethyl kappa carrageenan
-4.5
0 5 10 15 20 25 30 35
Fig. 5
-1.6
-2.2
y= -0.9496x +0.69
-2.4 2
r =0.923
-2.6
3.00 3.05 3.10 3.15 3.20 3.25 3.30
(1000/T)/K-1
Fig. 6
1.2
0.8
Current /A
0.6
0.4
0.2
0.0
time/s
Fig. 7
0.10
0.08
30% LiNO3-carboxymethyl kappa carrageenan
20% LiNO3-carboxymethyl iota carrageenan
0.06
0.04
Current/A
0.02
0.00
-0.02
-0.04
-2 -1 0 1 2 3
Applied potential/V
3.0 V
Fig. 8 3.1 V