Paula T. Hammond

High-power lithium batteries from functionalized carbon-nanotube electrodes

Energy storage devices that can deliver high powers have many applications, including hybrid vehicles and renewable energy. Much research has focused on increasing the power output of lithium batteries by reducing lithium-ion diffusion distances, but outputs remain far below those of electrochemical capacitors and below the levels required for many applications. Here, we report an alternative approach based on the redox reactions of functional groups on the surfaces of carbon nanotubes. Layer-by-layer techniques are used to assemble an electrode that consists of additive-free, densely packed and functionalized multiwalled carbon nanotubes. The electrode, which is several micrometres thick, can store lithium up to a reversible gravimetric capacity of approximately 200 mA h g(-1)(electrode) while also delivering 100 kW kg(electrode)(-1) of power and providing lifetimes in excess of thousands of cycles, both of which are comparable to electrochemical capacitor electrodes. A device using the nanotube electrode as the positive electrode and lithium titanium oxide as a negative electrode had a gravimetric energy approximately 5 times higher than conventional electrochemical capacitors and power delivery approximately 10 times higher than conventional lithium-ion batteries.

Carbon Nanotube/Manganese Oxide Ultrathin Film Electrodes for Electrochemical Capacitors

Multiwall carbon nanotube (MWNT)/manganese oxide (MnO2) nanocomposite ultrathin film electrodes have been created via redox deposition of MnO2 on layer-by-layer (LbL)-assembled MWNT films. We demonstrate that these LbL-assembled MWNT (LbL-MWNT)/MnO2 thin films consist of a uniform coating of nanosized MnO2 on the MWNT network structure using SEM and TEM, which is a promising structure for electrochemical capacitor applications. LbL-MWNT/MnO2 electrodes yield a significantly higher volumetric capacitance of 246 F/cm3 with good capacity retention up to 1000 mV/s due to rapid transport of electrons and ions within the electrodes. The electrodes are generated with two simple aqueous deposition processes: the layer-by-layer assembly of MWNTs followed by redox deposition of MnO2 at ambient conditions, thus providing a straightforward approach to the fabrication of high-power and -energy electrochemical capacitors with precise control of electrode thickness at nanometer scales.

Layer-by-layer assembly of all carbon nanotube ultrathin films for electrochemical applications.

All multiwall carbon nanotube (MWNT) thin films are created by layer-by-layer (LBL) assembly of surface functionalized MWNTs. Negatively and positively charged MWNTs were prepared by surface functionalization, allowing the incorporation of MWNTs into highly tunable thin films via the LBL technique. The pH dependent surface charge on the MWNTs gives this system the unique characteristics of LBL assembly of weak polyelectrolytes, controlling thickness and morphology with assembly pH conditions. We demonstrate that these MWNT thin films have randomly oriented interpenetrating network structure with well developed nanopores using AFM and SEM, which is an ideal structure of functional materials for various applications. In particular, electrochemical measurements of these all-MWNT thin film electrodes show high electronic conductivity in comparison with polymer composites with single wall nanotubes, and high capacitive behavior with precise control of capacity.

Recent explorations in electrostatic multilayer thin film assembly

New developments in the area of electrostatic layer-by-layer assembly are reviewed, with emphasis on work in the past two years. Advances in fundamental understanding of polyelectrolyte adsorption is addressed, including the use of new probes and experimental techniques which examine final structure, film interpenetration, and control of thickness. Both theoretical and experimental studies of adsorption of weak polyelectrolytes have been addressed. The role of secondary interactions such as hydrogen bonding or dispersion forces on these parameters is a more recent area of focus. Molecular scale order has been achieved in layered films to produce noncentrosymmetric films; further control of the ordering of molecular side groups in these systems could lead to new and interesting electrical and optical properties. Finally, it has been shown that polyelectrolyte multilayers may be templated onto a number of surfaces; these materials can be patterned onto surfaces to make three dimensional microstructures, or grown on a sacrificial colloidal template to form encapsulant membranes.

Hydrogen-Bonding Layer-by-Layer-Assembled Biodegradable Polymeric Micelles as Drug Delivery Vehicles from Surfaces

We present the integration of amphiphilic block copolymer micelles as nanometer-sized vehicles for hydrophobic drugs within layer-by-layer (LbL) films using alternating hydrogen bond interactions as the driving force for assembly for the first time, thus enabling the incorporation of drugs and pH-sensitive release. The film was constructed based on the hydrogen bonding between poly(acrylic acid) (PAA) as an H-bond donor and biodegradable poly(ethylene oxide)-block-poly(epsilon-caprolactone) (PEO-b-PCL) micelles as the H-bond acceptor when assembled under acidic conditions. By taking advantage of the weak interactions of the hydrogen-bonded film on hydrophobic surfaces, it is possible to generate flexible free-standing films of these materials. A free-standing micelle LbL film of (PEO-b-PCL/PAA)60 with a thickness of 3.1 microm was isolated, allowing further characterization of the bulk film properties, including morphology and phase transitions, using transmission electron microscopy and differential scanning calorimetry. Because of the sensitive nature of the hydrogen bonding employed to build the multilayers, the film can be rapidly deconstructed to release micelles upon exposure to physiological conditions. However, we could also successfully control the rate of film deconstruction by cross-linking carboxylic acid groups in PAA through thermally induced anhydride linkages, which retard the drug release to the surrounding medium to enable sustained release over multiple days. To demonstrate efficacy in delivering active therapeutics, in vitro Kirby-Bauer assays against Staphylococcus aureus were used to illustrate that the drug-loaded micelle LbL film can release significant amounts of an active antibacterial drug, triclosan, to inhibit the growth of bacteria. Because the micellar encapsulation of hydrophobic therapeutics does not require specific chemical interactions, we believe this noncovalent approach provides a new route to integrating active small, uncharged, and hydrophobic therapeutics into LbL thin films for biological and biomedical coatings.

Facilitated Ion Transport in All-Solid-State Flexible Supercapacitors

The realization of highly flexible and all-solid-state energy-storage devices strongly depends on both the electrical properties and mechanical integrity of the constitutive materials and the controlled assembly of electrode and solid electrolyte. Herein we report the preparation of all-solid-state flexible supercapacitors (SCs) through the easy assembly of functionalized reduced graphene oxide (f-RGO) thin films (as electrode) and solvent-cast Nafion electrolyte membranes (as electrolyte and separator). In particular, the f-RGO-based SCs (f-RGO-SCs) showed a 2-fold higher specific capacitance (118.5 F/g at 1 A/g) and rate capability (90% retention at 30 A/g) compared to those of all-solid-state graphene SCs (62.3 F/g at 1A/g and 48% retention at 30 A/g). As proven by the 4-fold faster relaxation of the f-RGO-SCs than that of the RGO-SCs and more capacitive behavior of the former at the low-frequency region, these results were attributed to the facilitated ionic transport at the electrical double layer by means of the interfacial engineering of RGO by Nafion. Moreover, the superiority of all-solid-state flexible f-RGO-SCs was demonstrated by the good performance durability under the 1000 cycles of charging and discharging due to the mechanical integrity as a consequence of the interconnected networking structures. Therefore, this research provides new insight into the rational design and fabrication of all-solid-state flexible energy-storage devices as well as the fundamental understanding of ion and charge transport at the interface.

Virus-templated self-assembled single-walled carbon nanotubes for highly efficient electron collection in photovoltaic devices

The performance of photovoltaic devices could be improved by using rationally designed nanocomposites with high electron mobility to efficiently collect photo-generated electrons. Single-walled carbon nanotubes exhibit very high electron mobility, but the incorporation of such nanotubes into nanocomposites to create efficient photovoltaic devices is challenging. Here, we report the synthesis of single-walled carbon nanotube-TiO(2) nanocrystal core-shell nanocomposites using a genetically engineered M13 virus as a template. By using the nanocomposites as photoanodes in dye-sensitized solar cells, we demonstrate that even small fractions of nanotubes improve the power conversion efficiency by increasing the electron collection efficiency. We also show that both the electronic type and degree of bundling of the nanotubes in the nanotube/TiO(2) complex are critical factors in determining device performance. With our approach, we achieve a power conversion efficiency in the dye-sensitized solar cells of 10.6%.

Highly Efficient Plasmon-Enhanced Dye-Sensitized Solar Cells through Metal@Oxide Core–Shell Nanostructure

We have investigated the effects of localized surface plasmons (LSPs) on the performance of dye-sensitized solar cells (DSSCs). The LSPs from Ag nanoparticles (NPs) increase the absorption of the dye molecules, allowing us to decrease the thickness of photoanodes, which improves electron collection and device performance. The plasmon-enhanced DSSCs became feasible through incorporating core-shell Ag@TiO(2) NPs into conventional TiO(2) photoanodes. The thin shell keeps the photoelectrons from recombining on the surface of metal NPs with dye and electrolyte and improves the stability of metal NPs. With 0.6 wt % Ag@TiO(2) NPs, the power conversion efficiency of DSSCs with thin photoanodes (1.5 μm) increases from 3.1% to 4.4%. Moreover, a small amount of Ag@TiO(2) NPs (0.1 wt %) improves efficiency from 7.8% to 9.0% while decreasing photoanode thickness by 25% for improved electron collection. In addition, plasmon-enhanced DSSCs require 62% less material to maintain the same efficiency as conventional DSSCs.

Nanostructured carbon-based electrodes: bridging the gap between thin-film lithium-ion batteries and electrochemical capacitors

The fast evolution of portable electronic devices and micro-electro-mechanical systems (MEMS) requires multi-functional microscale energy sources that have high power, high energy, long cycle life, and the adaptability to various substrates. Nanostructured thin-film lithium-ion batteries and electrochemical capacitors (ECs) are among the most promising energy storage devices that can meet these demands. This perspective presents an overview of recent progresses and challenges associated with the development of binder-free, carbon-based nanostructured electrodes prepared from layer-by-layer (LbL) electrostatic assembly, which provide enhanced gravimetric and volumetric energy for ECs and enhanced power capabilities for batteries. Based on promising findings for thin electrodes of several microns in thickness, LbL-based electrodes could also potentially be envisioned for portable electronics, electrified transportation, and load-leveling applications if successful scale-up to tens or hundreds of microns can be achieved.

Layer-by-Layer Nanoparticles for Systemic Codelivery of an Anticancer Drug and siRNA for Potential Triple-Negative Breast Cancer Treatment

A single nanoparticle platform has been developed through the modular and controlled layer-by-layer process to codeliver siRNA that knocks down a drug-resistance pathway in tumor cells and a chemotherapy drug to challenge a highly aggressive form of triple-negative breast cancer. Layer-by-layer films were formed on nanoparticles by alternately depositing siRNA and poly-l-arginine; a single bilayer on the nanoparticle surface could effectively load up to 3500 siRNA molecules, and the resulting LbL nanoparticles exhibit an extended serum half-life of 28 h. In animal models, one dose via intravenous administration significantly reduced the target gene expression in the tumors by almost 80%. By generating the siRNA-loaded film atop a doxorubicin-loaded liposome, we identified an effective combination therapy with siRNA targeting multidrug resistance protein 1, which significantly enhanced doxorubicin efficacy by 4 fold in vitro and led to up to an 8-fold decrease in tumor volume compared to the control treatments with no observed toxicity. The results indicate that the use of layer-by-layer films to modify a simple liposomal doxorubicin delivery construct with a synergistic siRNA can lead to significant tumor reduction in the cancers that are otherwise nonresponsive to treatment with Doxil or other common chemotherapy drugs. This approach provides a potential strategy to treat aggressive and resistant cancers, and a modular platform for a broad range of controlled multidrug therapies customizable to the cancer type in a singular nanoparticle delivery system.