Graphene Oxide-Grafted
Hybrid Diblock Copolymer Brush
(GO-graft-PEG6k-block-P(MA-POSS)) as Nanofillers for Enhanced Lithium Ion Conductivity
of PEO-Based Nanocomposite Solid Polymer Electrolytes
posted on 2023-02-23, 14:57authored byKhizar
Hayat Khan, Yury Golitsyn, Detlef Reichert, Jörg Kressler, Hazrat Hussain
Nanocomposite solid polymer electrolytes (NSPEs) with
PEO as the
matrix and (i) GO or (ii) GO-graft-PEG6k or (iii) GO-graft-PEG6k-block-P(MA-POSS) as nanofillers have been fabricated to elucidate the
impact of the filler morphology on the lithium ion conductivity. GO-graft-PEG6k was obtained by grafting PEG6k onto GO via esterification. GO-graft-PEG6k-block-P(MA-POSS)
was prepared via surface-initiated atom transfer
radical polymerization. Fourier-transform infrared spectroscopy revealed
enhanced salt dissociation and complexation between the filler and
PEO host that could be attributed to Lewis acid–base interactions.
Electrochemical impedance spectroscopy revealed the improved ion conductivity
of the fabricated NSPEs as compared with the pristine PEO-LiClO4. As an example, at 50 °C, the ion conductivity increased
to 4.01 × 10–5 and 6.31 × 10–5 S cm–1 with 0.3% GO and 0.3% GO-graft-PEG6k, respectively, from 2.36 × 10–5 S cm–1 of PEO-LiClO4, suggesting that
the filler with brush-like architecture (GO-graft-PEG6k) is more efficient in enhancing the ion conductivity.
Further increase in filler content resulted in lowering of the ion
conductivity that could be ascribed to aggregation of the filler.
The most dramatic impact on conductivity was observed with the incorporation
of brush-like GO-graft-PEG6k-block-P(MA-POSS) as a nanofiller (3.0 × 10–4 S
cm–1 at 50 °C with 1.0 wt % filler content).
The increase in ion conductivity in the current systems, as opposed
to the conventional view, could not be correlated with the content
of the amorphous phase of the matrix. The conduction mechanism is
still unclear; nevertheless, it could be assumed that in addition
to the ion conduction through the PEO matrix, the filler forms additional
low-energy ion conducting channels at its interface with the matrix.
The pendent POSS nanocages of GO-graft-PEG6k-block-P(MAPOSS) might probably increase the free
volume at the interface with the matrix that is associated with higher
chain and ion mobility, thus further enhancing the ion conductivity
as compared with GO and GO-graft-PEG6k. The faster ion dynamics in 1.0 wt % GO-graft-PEG6k-block-P(MAPOSS) NSPEs has also been verified
by the dielectric relaxation studies. Thus, integration of both the
PEG and POSS nanocages into GO-grafted brush-like
architecture offers a new tool for tuning the lithium ion conductivity
for potential Li ion battery applications.