Ionomer nanocomposites provide a promising solution to address ion crossover issues inherent to traditional ion-containing membranes used in batteries for grid-scale energy storage (e.g., vanadium redox flow batteries). Herein, we investigate the impact of nanoparticle surface chemistry on nanoparticle dispersion, membrane morphology, and vanadium ion permeability in a series of Nafion nanocomposites. Specifically, silica nanoparticles (SiNPs) were functionalized with various chemical moieties, seven in total, that electrostatically interact, either attractively or repulsively, with the sulfonic acid groups that coalesce to form the ionic network within Nafion. As seen from electron microscopy analysis of the nanocomposites, SiNPs with sulfonic acid end-functionality were, on average, well dispersed within the ionomer membrane, though increased vanadium ion permeability, as compared to pristine (or unmodified) Nafion, was observed and attributed to changes in the Donnan potential of the system. In contrast, SiNPs with amine end-functionality were, on average, observed to form large aggregates within the ionomer membrane. Surprisingly, nanocomposites containing a higher degree of nanoparticle aggregation demonstrated the lowest vanadium ion permeability. Fractal analysis of the low-Q small-angle neutron scattering data suggests that the interface between the ionomer and the SiNP surface transitions from rough to smooth when the nanoparticle surface is changed from sulfonic acid-functionalized to amine-functionalized.

Perfluorosulfonic acid (PFSA) ionomers are ubiquitous as proton-exchange membranes (PEMs) in vanadium redox flow batteries (VRFBs), as they provide high proton conductivity and robust chemical stability. However, traditional PFSA ionomers suffer from high vanadium ion crossover, i.e., low ion selectivity, which reduces the efficiency and lifetime of the battery. Herein, a novel method to fabricate PFSA nanocomposites containing fluorocarbon-decorated silica nanoparticles is presented. These composite ionomers exhibit drastically reduced vanadium ion permeability and an almost two orders of magnitude increase in proton selectivity when compared to the current benchmark commercial ionomer. Small-angle neutron scattering data suggest that the nanostructures of these nanocomposites are drastically different from their pristine counterpart, where the periodic spacing of the hydrophobic domains is significantly reduced, while changes to the ionic structure were seen to be minimal. This work suggests that composite PEMs containing a secondary phase that alters the hydrophobic, nonion-conducting phase of the ionomer may prove to be a fruitful fabrication route to produce ionomer membranes with enhanced performance for use in VRFBs.

Herein, we present a systematic investigation of the impact of silica nanoparticle (SiNP) size and surface chemistry on the nanoparticle dispersion state and the resulting morphology and vanadium ion permeability...

Perfluorosulfonic acid (PFSA) ionomer nanocomposites are a promising solution to address the poor ion selectivity of current membranes utilized in vanadium redox flow batteries. Herein, we investigate the impact of a casting substrate on the nanostructure and vanadium ion transport in bulk ionomer and ionomer nanocomposite membranes (i.e., films with thicknesses of ∼100 μm). Specifically, solution-cast ionomer nanocomposite membranes, containing either unfunctionalized (hydroxyl groups), amine-functionalized, or sulfonic acid-functionalized silica nanoparticles (SiNPs), were fabricated by casting on either a polished quartz or polytetrafluoroethylene (PTFE) substrates. Surprisingly, the choice of the casting substrate was seen to affect the bulk morphology of the PFSA ionomers, resulting in substrate-specific vanadium ion transport, where suppressed ion transport was observed for membranes cast on the polished quartz, when compared to their PTFE-cast counterparts. Additionally, the chemical composition of the substrate-adjacent surface was a function of both the substrate and the surface functionality of the SiNPs. Moreover, it was observed that both the chemical composition of the membrane surface and the substrate-induced changes to the bulk ionomer morphology governed vanadyl ion transport through the PFSA ionomers. Results from this work have direct implications for the design of next-generation ionomer nanocomposites, as the casting substrate used to fabricate these materials, and the orientation of these membranes inside the operating flow battery, can significantly influence transport of vanadium ions.