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Polyaniline-based nanocomposites for hydrogen storage             235

           PANI-V 2 O 5 nanocomposite (PANI-VONC). The hydrogen uptake capacities of
           PANI and V 2 O 5 obtained independently were 0.15 and 0.16 wt%, respectively, under
           7 MPa at 77 K. The hydrogen sorption capacity was enhanced appreciably (1.8 wt%)
           for the PANI-VONC, under the same conditions. This improvement in the hydrogen
           sorption capacity of the PANI-V 2 O 5 nanocomposite was due to the increase of
           interlayer spacing between the PANI layer and V 2 O 5 (VO) layer from 1.1 to
           0.72 nm [58].
              Significant hydrogen adsorption capacity was observed for the vanadium
           pentoxide-PANI (V 2 O 5 -PANI) nanocomposite at 473 K. On the other hand, chemi-
           cally modified vanadium pentoxide-PANI-polythiophene composite with nickel
           (V 2 O 5 -PANI-PTH-Ni) was subjected to investigate a hydrogen sorption capacity.
           The existence of nickel improved the uptake at a lower pressure [17]. Senkal et al.
           reported the hydrogen storage applications of PANI modified with boric acid
           (PANI-B) and boron trifluoride (PANI-BF 3 ), and their nanocomposites with PANI-
           B-SWNT (10%), PANI-BF 3 -SWNT (10%), PANI-B-MWNT (10%), and PANI-
           BF 3 -MWNT (10%) were reported at cryogenic temperature under 10 MPa. It was
           noticed that the hydrogen adsorption capacity depends on the nature of CNT used
           and the presence of organic functional groups in the composite. So, the SWNT com-
           posites exhibited higher storage capacity than that of MWNT composites. The
           improvement in adsorption capacity was due to existence of organic functional groups
           (PANI-B and PANI-BF 3 ) and along with the molecular separating property [59].



           8.4   Conclusions


           Hence, this chapter reviewed the hydrogen storage capacity of nonporous and
           nanoporous PANI nanocomposites and its important characteristics. It is evidenced
           that the hydrogen uptake of PANI structures depends on its unique electronic proper-
           ties, surface area, and porous structure of PANI. The measured temperature and hydro-
           gen pressure also play a prominent role in hydrogen storage, and its mechanisms have
           been proposed based on the electronic conducting property and molecular sieving phe-
           nomena (doping-dedoping-redoping process). Further, aromatic ring is the main
           active site for hydrogen adsorption in nanoporous PANI. An electron-donating group
           of the aromatic ring will increase the electron density and results in increasing the
           hydrogen storage capacity of PANI. Among the reported PANI structures, PANI
           nanofibers exhibited maximum hydrogen uptake of 8 wt%. Hence, the PANI struc-
           tures show its potential in hydrogen storage owing to its fast reaction kinetics and
           physisorptive mechanism of hydrogen uptake.


           Acknowledgments


           BS thanks DST-SERB for providing financial support through NPDF scheme (PDF/
           2015/000217). One of the authors (AS) would like to thank CSIR-India for providing financial
           support through Research Associateship (ACK No: 324494/2 K15/1 dt: 31.03.2017).
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