Sanjoy K. Bhattacharia

Dispersions of Non-Covalently Functionalized Graphene with Minimal Stabilizer

We demonstrate that functionalized pyrene derivatives effectively stabilize single- and few-layer graphene flakes in aqueous dispersions. The graphene/stabilizer yield obtained by this method is exceptionally high relative to conventional nanomaterial stabilizers such as surfactants or polymers. The mechanism of stabilization by pyrene derivatives is investigated by studying the effects of various parameters on dispersed graphene concentration and stability; these parameters include stabilizer concentration, initial graphite concentration, solution pH, and type and number of functional groups and counterions. The effectiveness of the pyrene derivatives is pH-tunable, as measured by zeta potential, and is also a function of the number of functional groups, the electronegativity of the functional group, the counterion, the relative polarity between stabilizer and solvent, and the distance from the functional group to the basal plane. Even if the dispersion is destabilized by extreme pH or lyophilization, the graphene does not aggregate because the stabilizer remains adsorbed on the surface. These dispersions also show promise for applications in graphene/polymer nanocomposites (examined in this paper), organic solar cells, conductive films, and inkjet-printed electronic devices.

Rheology and Morphology of Pristine Graphene/Polyacrylamide Gels

Enhancement of toughness in nanomaterial-based hydrogels is a critical metric for many of their engineering applications. Pristine graphene-polyacrylamide (PAM) hydrogels are synthesized via in situ polymerization of acrylamide monomer in PAM-stabilized graphene dispersion. In-situ polymerization leads to the uniform dispersion of the graphene sheets in the hydrogel. The graphene sheets interact with the elastic chains of the hydrogel through physisorption and permit gelation in the absence of any chemical cross-linker. This study represents the first report of pristine graphene as a physical cross-linker in a hydrogel. The properties of the graphene-polymer hydrogel are characterized by rheological measurements and compressive tests, revealing an increase in the storage modulus and toughness of the hydrogels compared to the chemically cross-linked PAM analogues. The physically cross-linked graphene hydrogels also exhibit self-healing properties. These hydrogels prove to be efficient precursors for graphene-PAM aerogels with enhanced electrical conductivity and thermal stability.

Direct laser initiation and improved thermal stability of nitrocellulose/graphene oxide nanocomposites

We report on the enhancement and possible control of both laser ignition and burn rates of Nitrocellulose (NC) microfilms when doped with graphene oxide (GO). A Nd:YAG (1064 nm, 20 ns) laser is used to ignite GO-doped NC films at low temperatures. The effect of GO on the doping concentration of the activation energies of laser ignition and thermal stability of the NC films is studied. The activation energy of laser ignition decreases with increasing GO/NC weight ratio and attains a constant value with higher concentrations. This behavior is accompanied by an increase in the thermal stability.

Adsorption and removal of graphene dispersants

We demonstrate three different techniques (dialysis, vacuum filtration, and spray drying) for removal of dispersants from liquid-exfoliated graphene. We evaluate these techniques for elimination of dispersants from both the bulk liquid phase and from the graphene surface. Thermogravimetric analysis (TGA) confirms dispersant removal by these treatments. Vacuum filtration (driving by convective mass transfer) is the most effective method of dispersant removal, regardless of the type of dispersant, removing up to ∼95 wt.% of the polymeric dispersant with only ∼7.4 wt.% decrease in graphene content. Dialysis also removes a significant fraction (∼70 wt.% for polymeric dispersants) of un-adsorbed dispersants without disturbing the dispersion quality. Spray drying produces re-dispersible, crumpled powder samples and eliminates much of the unabsorbed dispersants. We also show that there is no rapid desorption of dispersants from the graphene surface. In addition, electrical conductivity measurements demonstrate conductivities one order of magnitude lower for graphene drop-cast films (where excess dispersants are present) than for vacuum filtered films, confirming poor inter-sheet connectivity when excess dispersants are present.