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Polymer nanocomposite materials in energy storage: Properties and applications  251

           chemical degradation in the presence of nonaqueous electrolytes [140]. Wu et al.
           synthesized a composite 3,4,9,10-perylenetetracarboxylic dianhydride/carbon nano-
           tube (PDTA/CNT) and its corresponding polymer nanocomposite, poly(3,4,9,10-
           perylenetetracarboxylic dianhydride ethylene diamine)/carbon nanotube (PI/CNT),
           by closed-tube polymerization. These two composites were used as organic cathode
           materials for lithium-ion batteries. Compared with PTCDA, PTCDA/CNT exhibited
           an enhanced rate capability, and the capacity was increased from 10 to 115 mAh g  1
           at 2 C. Polymerization increased the cycling stability of organic cathode materials.
           The capacity of the polymer nanocomposite PI/CNT remained at 93% after 300 cycles
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           under a current of 100 mA g , while the capacity of PTCDA/CNT was only 74%
           after 300 cycles. The improved electrochemical properties of these materials were
           ascribed to increased electronic conductivity of PTCDA due to the formation of com-
           posites with CNTs and their decreased solubility in the electrolyte due to polymeri-
           zation [24,141]. Sun et al. [142] used conjugated poly(1,5-diaminoanthraquinone)
           (PDAA) as a redox organic polymer to make nanocomposite with graphene
           nanosheets (GNS). The GNS provide self-supporting porous graphene foam, which
           is intriguing and highly favored due to large accessible surface and integrated conduc-
           tive network [85].
              The 3D porous framework not only efficiently prevents the restacking of graphene
           sheets but also endows them with high-rate transportation of electrons and electrolyte
           ions [31,143]. The well-ordered graphene nanosheets/acid-treated multiwalled
           carbon nanotube (GNS/aMWCNT)-supported 1,5-diaminoanthraquinone (DAA)
           organic foams (oGCTF(DAA)) were attained by organic solvent displacement
           method (forming graphene oxide/carbon nanotube organic colloids with DAA mono-
           mers) followed by solvothermal reaction. Afterward, promising GNS/aMWCNT
           organic foam-supported PDAA (oGCTF@PDAA) nanocomposites were obtained
           by electrochemical polymerization based on oGCTF(DAA). Three-dimensional
           porous GNS/aMWCNT organic foam-supported poly(1,5-diaminoanthraquinone)
           (oGCTF@PDAA) nanocomposites showed a discharge capacity of 289 mAh g  1  at
                                                                              1
           30 mA g  1  current, whereas in the rapid charge/discharge conditions of 10 A g ,
                                        1
           it shows a capacity of 122 mAh g . It showed tremendous cyclic stability as even
           after 2000 cycles, it could maintain 85.2% of its initial capacity even under high dis-
                                1
           charge condition (10 A g )(Table 9.1).
              Apart from the abovementioned materials, important polymer nanocomposite
           materials have been prepared and tested for their suitability as cathode material for
           lithium [148–151]. Some very recent results have been summarized by Pitchai
           et al. [117],Xuetal. [118], and Myung et al. [90].


           9.3.1.3 PNCs as anode material for the Li ion batteries
           Since the first commercialization of the Li-ion battery in the 1990s, tremendous
           amount of research efforts has been devoted to the development of novel materials
           to function as anode, the negative electrode, for the Li-ion batteries. It is very well
           known that the anode material primarily dictates the energy density, the power den-
           sity, and the cycle life of the battery. State-of-the-art material for anode for Li-ion
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