Benjamin Boesl

Oxidative Unzipping and Transformation of High Aspect Ratio Boron Nitride Nanotubes into “White Graphene Oxide” Platelets

Morphological and chemical transformations in boron nitride nanotubes under high temperature atmospheric conditions is probed in this study. We report atmospheric oxygen induced cleavage of boron nitride nanotubes at temperatures exceeding 750 °C for the first time. Unzipping is then followed by coalescence of these densely clustered multiple uncurled ribbons to form stacks of 2D sheets. FTIR and EDS analysis suggest these 2D platelets to be Boron Nitride Oxide platelets, with analogous structure to Graphene Oxide, and therefore we term them as “White Graphene Oxide” (WGO). However, not all BNNTs deteriorate even at temperatures as high as 1000 °C. This leads to the formation of a hybrid nanomaterial system comprising of 1D BN nanotubes and 2D BN oxide platelets, potentially having advanced high temperature sensing, radiation shielding, mechanical strengthening, electron emission and thermal management applications due to synergistic improvement of multi-plane transport and mechanical properties. This is the first report on transformation of BNNT bundles to a continuous array of White Graphene Oxide nanoplatelet stacks.

Harnessing Three Dimensional Anatomy of Graphene Foam to Induce Superior Damping in Hierarchical Polyimide Nanostructures

Graphene foam-based hierarchical polyimide composites with nanoengineered interface are fabricated in this study. Damping behavior of graphene foam is probed for the first time. Multiscale mechanisms contribute to highly impressive damping in graphene foam. Rippling, spring-like interlayer van der Waals interactions and flexing of graphene foam branches are believed to be responsible for damping at the intrinsic, interlayer and anatomical scales, respectively. Merely 1.5 wt% graphene foam addition to the polyimide matrix leads to as high as ≈300% improvement in loss tangent. Graphene nanoplatelets are employed to improve polymer-foam interfacial adhesion by arresting polymer shrinkage during imidization and π-π interactions between nanoplatelets and foam walls. As a result, damping behavior is further improved due to effective stress transfer from the polymer matrix to the foam. Thermo-oxidative stability of these nanocomposites is investigated by exposing the specimens to glass transition temperature of the polyimide (≈400 °C). The composites are found to retain their damping characteristics even after being subjected to such extreme temperature, attesting their suitability in high temperature structural applications. Their unique hierarchical nanostructure provides colossal opportunity to engineer and program material properties.

Three-Dimensional Graphene Foam Induces Multifunctionality in Epoxy Nanocomposites by Simultaneous Improvement in Mechanical, Thermal, and Electrical Properties

Three-dimensional (3D) macroporous graphene foam based multifunctional epoxy composites are developed in this study. Facile dip-coating and mold-casting techniques are employed to engineer microstructures with tailorable thermal, mechanical, and electrical properties. These processing techniques allow capillarity-induced equilibrium filling of graphene foam branches, creating epoxy/graphene interfaces with minimal separation. Addition of 2 wt % graphene foam enhances the glass transition temperature of epoxy from 106 to 162 °C, improving the thermal stability of the polymer composite. Graphene foam aids in load-bearing, increasing the ultimate tensile strength by 12% by merely 0.13 wt % graphene foam in an epoxy matrix. Digital image correlation (DIC) analysis revealed that the graphene foam cells restrict and confine the deformation of the polymer matrix, thereby enhancing the load-bearing capability of the composite. Addition of 0.6 wt % graphene foam also enhances the flexural strength of the pure epoxy by 10%. A 3D network of graphene branches is found to suppress and deflect the cracks, arresting mechanical failure. Dynamic mechanical analysis (DMA) of the composites demonstrated their vibration damping capability, as the loss tangent (tan δ) jumps from 0.1 for the pure epoxy to 0.24 for ∼2 wt % graphene foam-epoxy composite. Graphene foam branches also provide seamless pathways for electron transfer, which induces electrical conductivity exceeding 450 S/m in an otherwise insulator epoxy matrix. The epoxy-graphene foam composite exhibits a gauge factor as high as 4.1, which is twice the typical gauge factor for the most common metals. Simultaneous improvement in thermal, mechanical, and electrical properties of epoxy due to 3D graphene foam makes epoxy-graphene foam composite a promising lightweight and multifunctional material for aiding load-bearing, electrical transport, and motion sensing in aerospace, automotive, robotics, and smart device structures.

Three-Dimensional Graphene Foam–Polymer Composite with Superior Deicing Efficiency and Strength

The adhesion of ice severely compromises the aerodynamic performance of aircrafts operating under critically low-temperature conditions to their surfaces. In this study, highly thermally and electrically conductive graphene foam (GrF) polymer composite is fabricated. GrF-polydimethylsiloxane (PDMS) deicing composite exhibits superior deicing efficiency of 477% and electrical conductivities of 500 S m-1 with only 0.1 vol % graphene foam addition as compared to other nanocarbon-based deicing systems. The three-dimensional interconnected architecture of GrF allows the effective deicing of surfaces by employing low power densities (0.2 W cm-2). Electrothermal stability of the GrF-PDMS composite was proven after enduring 100 cycles of the dc loading-unloading current. Moreover, multifunctional GrF-PDMS deicing composite provides simultaneous mechanical reinforcement by the effective transfer and absorption of loads resulting in a 23% and 18% increase in elastic modulus and tensile strength, respectively, as compared to pure PDMS. The enhanced efficiency of the GrF-PDMS deicing composite is a novel alternative to current high-power consumption deicing systems.

Multiscale characterization and experimentation on particulate reinforced composites

The addition of particulate additives has long been used as a method to adjust and design material systems for specific loading conditions. The transfer of loading to particulate additives can result in added toughness and can change ductility, among other properties. These changes are a function of many factors including the size, concentration, mechanical properties, interaction strength and dispersion of the particles. Recent advancements in scientific knowledge and manufacturing techniques have guided research towards the inclusion of particles with characteristic lengths measuring less than 100 nm and a renewed interested in particulate reinforced materials. This reduction in particle size can provide a drastic increase in the surface area between particle and matrix, which can theoretically provide increased load transfer and increased toughening. The reduction in particle size does result in a series of additional manufacturing and analysis challenges, namely the dispersing of particles for optimum load transfer and bulk response and the imaging of the particles in a representative and repeatable manner. In addition, the large surface area interactions tend to cause the particles to agglomerate, creating areas of high stress concentration and a reduction in bulk properties. Three novel characterization techniques will be presented in this article to discuss the effects of ZnO nanoparticle reinforcement of polymer materials and discussion over varying length scales.