Solvation behavior of carbonate-based electrolytes in sodium ion batteries.

Sodium ion batteries are on the cusp of being a commercially available technology. Compared to lithium ion batteries, sodium ion batteries can potentially offer an attractive dollar-per-kilowatt-hour value, though at the penalty of reduced energy density. As a materials system, sodium ion batteries present a unique opportunity to apply lessons learned in the study of electrolytes for lithium ion batteries; specifically, the behavior of the sodium ion in an organic carbonate solution and the relationship of ion solvation with electrode surface passivation. In this work the Li+ and Na+-based solvates were characterized using electrospray mass spectrometry, infrared and Raman spectroscopy, 17O, 23Na and pulse field gradient double-stimulated-echo pulse sequence nuclear magnetic resonance (NMR), and conductivity measurements. Spectroscopic evidence demonstrate that the Li+ and Na+ cations share a number of similar ion-solvent interaction trends, such as a preference in the gas and liquid phase for a solvation shell rich in cyclic carbonates over linear carbonates and fluorinated carbonates. However, quite different IR spectra due to the PF6- anion interactions with the Na+ and Li+ cations were observed and were rationalized with the help of density functional theory (DFT) calculations that were also used to examine the relative free energies of solvates using cluster - continuum models. Ion-solvent distances for Na+ were longer than Li+, and Na+ had a greater tendency towards forming contact pairs compared to Li+ in linear carbonate solvents. In tests of hard carbon Na-ion batteries, performance was not well correlated to Na+ solvent preference, leading to the possibility that Na+ solvent preference may play a reduced role in the passivation of anode surfaces and overall Na-ion battery performance.

Removal of copper ions from aqueous solutions via adsorption on carbon nanocomposites.

The development of technologies for water purification is critical to meet the global challenges of insufficient water supply and inadequate sanitation. Among all wastewater treatments, adsorption is globally recognized as the most promising method because of its versatility and economic feasibility. Herein, the removal of copper ions (Cu(II)) from aqueous solutions through adsorption on free-standing hybrid papers comprised of a mixture between graphene and different types of carbon nanotubes (CNTs) was examined. Results indicate that the rate of adsorption and long-time capacity of the metal ions on the nanocomposites significantly exceeds that of activated carbon by a factor of 4. Moreover, the combination of graphene with CNTs endows an increase in the uptake of Cu(II) up to 50% compared to that of CNTs alone, with a maximum adsorption capacity higher than 250 mg·g(-1). The removal of Cu(II) from water is sensitive to solution pH, and the presence of oxygen functional groups on the adsorbent surface promotes higher adsorption rates and capacities than pristine materials. These hybrid nanostructures show great promise for environmental remediation efforts, wastewater treatments, and separation applications, and the results presented in this study have important implications for understanding the interactions of carbonaceous materials at environmental interfaces.

Free-standing carbon nanotube/graphene hybrid papers as next generation adsorbents.

The adsorption of a series of aromatic compounds from aqueous solution onto purified, free-standing single-walled carbon nanotube/graphene nanoplatelet hybrid papers is studied both experimentally and theoretically. Experimental data is obtained via changes in optical absorption spectra of the aqueous solutions and is used to extract all parameters required to implement a semi-empirical mass-transfer model. Agreement between experiment and theory is excellent and data from all compounds can be cast on a universal adsorption curve. Results indicate that the rate of adsorption and long-time capacity of many aromatic compounds on hybrid paper adsorbent significantly exceeds that of activated carbon by at least an order of magnitude. The combination of carbon nanotubes and graphene also promotes on the order of a 25% improvement in adsorption rates and capacities than either component alone. Hybrid nanocomposites show significant promise as adsorption materials used for environmental remediation efforts.

Pair interaction potentials of colloids by extrapolation of confocal microscopy measurements of collective suspension structure.

A method for measuring the pair interaction potential between colloidal particles by extrapolation measurement of collective structure to infinite dilution is presented and explored using simulation and experiment. The method is particularly well suited to systems in which the colloid is fluorescent and refractive index matched with the solvent. The method involves characterizing the potential of mean force between colloidal particles in suspension by measurement of the radial distribution function using 3D direct visualization. The potentials of mean force are extrapolated to infinite dilution to yield an estimate of the pair interaction potential, U(r). We use Monte Carlo simulation to test and establish our methodology as well as to explore the effects of polydispersity on the accuracy. We use poly-12-hydroxystearic acid-stabilized poly(methyl methacrylate) particles dispersed in the solvent dioctyl phthalate to test the method and assess its accuracy for three different repulsive systems for which the range has been manipulated by addition of electrolyte.

Enhanced capacity and rate capability of carbon nanotube based anodes with titanium contacts for lithium ion batteries.

Carbon nanotubes are being considered for adoption in lithium ion batteries as both a current collector support for high-capacity active materials (replacing traditional metal foils) and as free-standing electrodes where they simultaneously store lithium ions. The necessity to establish good electrical contact to these novel electrode designs is critical for success. In this work, application of nickel and titanium as both separable and thin film electrical contacts to free-standing single-wall carbon nanotube (SWCNT) electrodes is shown to dramatically enhance both the reversible lithium ion capacity and rate capability in comparison with stainless steel. Scanning electron microscopy showed that evaporation of Ni and Ti can effectively coat the SWCNT bundles in a bulk electrode which is capable of providing an improved electrical contact. A thin film of titanium emerged as the preferred electrical contact promoting the highest capacity ever measured for a SWCNT free-standing electrode of 1250 mAh/g. In addition, the titanium contacting approach demonstrated a 5-fold improvement in lithium ion capacity at extraction rates greater than 1C for a high-energy density Ge-SWCNT electrode. The overall performance improvement with Ti contacts is attributed to a lower contact resistance, nanoscale "wetting" of SWCNT bundles to improve contact uniformity, and effective electron coupling between Ti and SWCNTs due to work function-energy level alignment. The experimental results provide the basis for a Ragone analysis (power vs energy parameters), whereby Ge-SWCNT-Ti anodes paired with a LiFePO(4) cathode can lead to a 60% improvement over conventional graphite anodes in both power and energy density for a complete battery.

Viscous solvent colloidal system for direct visualization of suspension structure, dynamics and rheology.

We introduce a model colloid system comprised of particles dispersed in a viscous solvent that can be applied to 3D direct visualization studies of suspension structure, dynamics and rheology. The colloids are poly(methyl methacrylate) (PMMA) spheres sterically stabilized by a copolymer of poly(diphenyl-dimethyl) (DPDM) siloxane that matches the refractive index of PMMA. The monodisperse particles, synthesized with mean diameter varying from 0.7 to 1.1 microm, are stably dispersed in a DPDM siloxane solvent, with viscosity varying from 2.2 to 4.3 Pa s at 20 degrees C. As opposed to other classes of PMMA colloids dispersed in organic solvents, this system displays minimal charge interactions. At room temperature, pair potential interactions (measured by extrapolation of pair correlation functions to infinite dilution) are well modeled by a generalized Lennard-Jones alpha-2alpha potential (alpha=10) with dimensionless interaction energy, epsilon/k(B)T=0.6. We use the DPDM-PMMA colloidal system in conjunction with confocal microscopy studies to measure: (i) the radial distribution function in 3D at dilute concentrations and (ii) the colloid self-diffusivity in 3D at dilute concentrations. Both measurements, neither previously reported in uncharged systems, are facilitated by the slow, viscous dynamics of the system. We also show that the viscosity and particle size of the system are such that the high-volume fraction shear thickening transition can be accessed at shear rates amenable to direct visualization.