Journal of Chemistry, Vol. 42 (2), P. 236 - 240, 2004<br />
<br />
<br />
<br />
Nickel-Nanoclusters-Containing Polyaniline<br />
Composites Having Structure Layer-by-Layer<br />
Part I - the Development of Concept and Structural<br />
Morphology<br />
Received 17-4-2003<br />
Tran Trung, Tran Huu Trung<br />
Department of Electrochemical Technology and Metal Protection,<br />
Faculty of Chemical Technology, Hanoi University of Technology<br />
<br />
<br />
Abstract<br />
The development of concept in structural morphology lets description the location of<br />
nickel nanoclusters in conductive organic polymers, which may be a new kind of structure in<br />
conductive organic polymer composites family. As a new route, such the development was<br />
supported by electrochemical two-pot process, on which polianiline containing nanoclusters<br />
of nickel incorporated in layer by layer were prepared, in H2SO4 0.1 M solutions. The<br />
presence of nickel nanoclusters in polymer matrix and the changes in morphology were<br />
confirmed by SEM/EDS.<br />
<br />
<br />
I – Develo`pment of concept [1 - 3], or by incorporation of immobilized organic<br />
anions [4 - 6].<br />
Electropolymerization, an interesting method,<br />
On the other way, very small size particles,<br />
has been widely used to prepare conjugated<br />
in micron or submicron scale, of transition metal<br />
polymers, such as polypyrrole, polythiophen,<br />
oxides including MnO2, LiMn2O4, WO3, RuO2<br />
polyaniline [1 - 3]. Such all conjugated polymers<br />
etc. and inorganic polyanions used as dopants for<br />
with spatially extended -bonding system found doping conjugated polymers [1, 7 - 10]. In some<br />
exhibit unique physical and electrochemical cases, microparticles and submicro-particles<br />
properties unobtainable for conventional such as MnO2 and LiMn2O4 can be oxidized<br />
polymers. And it is very well known that during electrosynthesis, and manganese atoms in<br />
depending on the potential value at the end of low oxidative states will transform into high<br />
the electrosynthesis, the polymers have been in oxidative state Mn+6. In consequences, a strongly<br />
various the oxidative states, therefore leading to hybrid between d-unfilled orbitals of manganese<br />
the different physical and electrochemical atom and -electron of polymer chains or/and<br />
properties. lone-pair electrons of nitrogen was formed [1]. It<br />
To improve physical and electrochemical is unobtainable and quite different from<br />
properties, conjugated polymers have been chemically way used to prepare such organic<br />
modified by incorporation of small size ions, Cl-, conductive polymer composites. Metal nanopar-<br />
Br-, BF4-, NO3-, ClO4-, SO22- etc. that can be ticles, such as Pt and Pd nanoparticles [11, 12],<br />
diffusion into and diffusion out polymer matrix and metal complexes [13] have been already<br />
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236<br />
electrochemically incorporated into polyaniline (PANI).<br />
<br />
PANI Films<br />
A B<br />
<br />
<br />
<br />
PANI layer Nickel-enriched PANI layer<br />
<br />
Aspects of the interconnection of metal nanoclusters and polymer fibrils<br />
Nanoclusters of nickel Polymer fibrils<br />
<br />
<br />
<br />
<br />
Figure 1: Schematic representation of the layer-by layer structured polymer composite film (A)<br />
and polymer composite film in which particles dispersed in to the whole of the<br />
polymer matrix (B), and of several aspects of the interconnection of metal<br />
nanoclusters and polymer fibrils<br />
In all cases mentioned above such dopants This study attempt to find a route, by using<br />
were electrochemically homogeneously disper- electrochemical approach, on which we can<br />
sed into the whole of conjugated polymer film overcome such problems and can control the<br />
(Fig. 1b). In this work, a new concept in distribution of particulates in the whole of<br />
structural morphology, the metal-nanoclusters- polymer matrix or in an alternatively layer<br />
containing conductive organic polymers having structured polymer film, as shown in figure 1. In<br />
structure layer-by-layer was suggested and such composites there exist several aspects of<br />
developed. The success of preparation of nickel- interconnect of nanoclusters of metal and<br />
nanoclusters-containing polyaniline is obviously polymer fibrils (Fig. 1c).<br />
evidence to support the development. The<br />
location of nickel nanocluster, as bridging II - Experimental<br />
nanocluster between polymers fibrils, in polymer<br />
matrix was also suggested (Fig. 2). Another Polyaniline composites containing nanoclus-<br />
striking point in such the preparation is that ters of nickel were electrochemically prepared<br />
different from the electrochemically dispersion by two-pot process and structured layer-by-layer.<br />
of Pd and Pt microparticles into PANI film, the The controlled electropolymerization system for<br />
dispersion of nanoclusters of metals, for preparation of aniline or the controlled electro-<br />
example nickel and iron (their standard redox deposition system for incorporating nanoclusters<br />
potentials are very negative vs. Ag/AgCl of nickel into PANI film were composed of a<br />
electrode), into organic conductive polymers has potentiostat, the EG&E Priceton Applied<br />
met a problem. It is due to the big difference Research model 362 with program Ecuniv-HH5,<br />
between the redox potential of such a metal connected with a standard three electrodes cell<br />
and the potentials, usually ranging from 0.2 V to containing an aqueous solution of 0.1 M aniline<br />
1.2 V vs. Ag/AgCl electrode, used to electro- monomer or of 0.5 M nickel sulfate, respectively.<br />
polymerize of aniline, pyrrole and thiophen The potential applied on the PANI composite<br />
monomers by potential sweep. Oppositely, the films, which was electrodeposited onto platinum<br />
electro-deposition of metal ions conducted at electrode (S = 1 cm2), was vs. Ag/AgCl reference<br />
potentials very negative to Ag/AgCl electrode. electrode for all electrochemical measurements<br />
<br />
237<br />
and a platinum sheet was serving as auxiliary The presence of nickel in the obtained PANI<br />
electrode. composite films was confirmed by energy<br />
All chemicals used are in AR grade and dispersion X-ray spectroscopy (EDXS, the<br />
supplied by Merck. To deoxygenate doubly incident angle kept constantly at 35o) equipped<br />
distilled water, for preparation of solutions, and with a scanning electron microscope (SEM)<br />
the electrolyte solution, nitrogen gas was model JEOL JSM-5410LV, which was used to<br />
bubbled before and during experiments. investigate the surface morphology of the films.<br />
<br />
<br />
<br />
<br />
Figure 2: Schematic representation of the structures involving in the generation of principle<br />
forms and charge carriers of PANI as well as of illustration of the role of<br />
nanoclusters of nickel<br />
<br />
III - Structural morphology of form commonly called leucoemeraldine, the<br />
nickel nanoclusters containing fully oxidized form termed pernigraniline, and<br />
the half-oxidized form, emeraldine. The<br />
polyaniline<br />
oxidation state of a PANI film onto the working<br />
As the known well, the PANI film electro- electrode immersed in aqueous acidified solution<br />
oxidized during potential sweep in voltammetry depends on the applied potential and the<br />
can be existed in a variety of form, which differs presence of dopants (Fig. 3). The presence of<br />
in their oxidative level. Principle neutral forms nickel nanoclusters incorporated into PANI<br />
of PANI were consisting of the most reduced matrix leads to the changes in the density of<br />
<br />
238<br />
charge carriers, consequently leading the shift of during electropolymerization of aniline, the<br />
anodic waves of cyclic voltammetry, as shown in branched PANI chains were performed and<br />
figure 3. Like cyclic voltammograms in aqueous twisted together to form the branched PANI<br />
acidified solution, the cyclic voltammograms of fibrils as observed by SEM studies (Fig. 4). As<br />
PANI film conducted in 0.1 M H2SO4 solution, at seen there is quite difference in structural surface<br />
potential scanning rate of 50 mV.s-1 consists of morphology between PANI film and PANI film<br />
two main peaks of oxidation (Fig. 3d). The first containing nanoclusters of nickel (PANI-Ni).<br />
one maximum at 0.2 V vs. Ag/AgCl reference PANI-Ni film seems just structured of a number<br />
electrode corresponds to the oxidization of leuco- of the coral-like branched polymer matrix<br />
emeraldine to emeraldine, and the second one consisting of twisted polymer fibrils. Meanwhile,<br />
maximum at a higher potential of 0.7 V attribu- PANI film shows its structural surface<br />
ted to the oxidization of emeraldine to pernigra- morphology like a “fishing-net” with unit cells<br />
niline. Except for just mentioned there also exist covered by slab of PANI. Especially, the PANI<br />
an obtuse peak (a shoulder) in the middle. The polymers in coil shape, present in PANI film,<br />
obtuse peak formed in combination of middle however seem disappeared in PANI-Ni film. It<br />
peaks in the cyclic voltammetry of PANI reported may be consisted with the presence of<br />
in [14]. It signifies that there is coexistence of nanoclusters of nickel in PANI-Ni film. The<br />
reactions between nitronium aniline cation mentioned changes show the change in popula-<br />
(C4H5NH+) and the nitronium in PANI matrix tion of charge carriers in PANI-Ni film in<br />
( C6H4N+ ), and of reaction between PANI comparing with those in PANI film. It is a main<br />
chains itself, through the substitution of a reason to cause the broadening and shift of the<br />
nitronium cation in another PANI chain. On the first anodic wave in cyclic voltammogram, and<br />
other words, the transform from emeraldine to the second peak seems shifted to the higher<br />
pernigraniline occurred simultaneously with the potential, which is out of the studying potential<br />
formation of charge carriers of PANI consisting range (Fig. 3 a - c). Further studies in order to<br />
of polaron and bipolaron forms delocalized on elucidate the influence of nickel in PANI-Ni film<br />
PANI chains. By such cross-linking reactions are going to show in the next paper.<br />
<br />
<br />
<br />
<br />
Figure 3: Multi-cyclic voltammograms of PANI-Ni films consisting of a layer of<br />
nanoclusters of nickel (a), of two layer of nanoclusters of nickel (b) and<br />
three (c), and of no layer of nanoclusters of nickel (d)<br />
<br />
239<br />
A B<br />
<br />
<br />
<br />
<br />
Figure 4: SEM photographs of PANI films in magnification of 10,000 (A), and of<br />
PANI-Ni film in magnification of 10,000 (B)<br />
<br />
IV - ConclusionS R. M. Hirohashi. J. Electroanal. Chem.,<br />
Vol. 426, P. 97 (1997).<br />
A new concept in structural morphology<br />
4. M. Zhou, J. J. Xu, H. Y. Chen, and H. Q.<br />
was suggested and developed for conductive<br />
Fang. Electroanalysis, Vol. 9, P. 1185 (1997).<br />
organic polymer composites containing nano-<br />
clusters of metals and nanoparticles. The 5. N. Oyama, J. M. Pope, T. Tatsuma, O.<br />
success of the preparation of PANI-Ni films Hatazaki, F. Matsumoto, Q. J. Chi, S. C.<br />
having structure layer-by-layer, by using Paulson, and M. Iwaku. Macromol. Symp.,<br />
electrochemical two-pot process was obviously Vol. 13, P. 103 (1998).<br />
evidence to support the mentioned develop- 6. J. Huang and M. Wan. Solid State Communi-<br />
ment. cation, Vol. 108, P. 255 (1998).<br />
The presence of nanoclusters of nickel in 7. N. Endo, Y. Miho, and K. Ogura. J. Mol.<br />
PANI-Ni films is main reason to cause the Catal. A: Chem., Vol. 127, P. 49 (1997).<br />
changes in the density of charge carriers and<br />
8. K. Pielichowski and M. Hasik. Synth. Met.,<br />
the broadening, as well as the shift of the first<br />
Vol. 89, P. 1999 (1997).<br />
anodic waves. Followed that the flow of<br />
electrons delivered through metal substrate 9. P. Wang and Y. F. Li. J. Electroanal. Chem.,<br />
electrode increases significantly (Fig. 3). The Vol. 408, P. 77 (1996).<br />
further works on such the composite polymers 10. M. Barth, M. Lapkowski, W. Turek, J.<br />
will focus on the mechanism of processes Muszynski, and S. Lefrant. Synth. Met., Vol.<br />
coexisted during electrooxidation and on 84, P. 111 (1997).<br />
possible applications of those.<br />
11. C. H. Yang and T. C. Wen. Electrochim.<br />
Acta, Vol. 44, P. 207 (1998).<br />
References<br />
12. H. Kim and W. Chang. Synth. Met. Vol. 101,<br />
1. T. Tran and V. T. Nguyen. Functional P. 150 (1999).<br />
Materials (Proceedings of EUROMAT'99), 13. C. Coutanceau, P. Crouigneau, J. M. LÐger,<br />
Ed. by VCH-Wiley, P. 309 (2000). and C. Lamy. J. Electroanal. Chem., Vol.<br />
2. V. Aboutanos, J. N. Barisci, L. A. P. Kane- 379, P. 389 (1994).<br />
Maguire, and G. G. Wallace. Synth. Met., 14. E. M. GeniÌs, M. Lapkowski, and J. E.<br />
Vol. 106, P. 89 (1999). Penneau. J. Electroanal. Chem., Vol. 249, P. 97<br />
3. K. Teshima, K. Yamada, N. Kobayashi, and (1988).<br />
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