Person:

Shian, Samuel

Focus tunable, adaptive lenses provide several advantages over traditional lens assemblies in terms of compactness, cost, efficiency, and flexibility. To further improve the simplicity and compact nature of adaptive lenses, we present an elastomer-liquid lens system which makes use of an inline, transparent electroactive polymer actuator. The lens requires only a minimal number of components: a frame, a passive membrane, a dielectric elastomer actuator membrane, and a clear liquid. The focal length variation was recorded to be greater than 100% with this system, responding in less than one second. Through the analysis of membrane deformation within geometrical constraints, it is shown that by selecting appropriate lens dimensions, even larger focusing dynamic ranges can be achieved.

Electrically tunable adaptive lenses provide several advantages over traditional lens assemblies in terms of compactness, speed, efficiency, and flexibility. We present an elastomer-liquid lens system which makes use of an in-line, transparent electroactive polymer actuator. The lens has two liquid-filled cavities enclosed within two frames, with two passive outer elastomer membranes and an internal transparent electroactive membrane. Advantages of the lens design over existing systems include large apertures, flexibility in choosing the starting lens curvature, and electrode encapsulation with a dielectric liquid. A lens power change up to 40 diopters, corresponding to focal length variation up to 300%, was recorded during actuation, with a response time on the order of tens of milliseconds.

The thermal conductivity of yttria-stabilized zirconia (YSZ) thermal barrier coatings increases with high-temperature aging. This common observation has been attributed to the densification of the coatings as porosity sinters out and pores and cracks spheroidize to minimize their surface energy. We show that the thermalconductivity of fully-dense 3 mol. % Y({2})O({3}) stabilized zirconia (3YSZ) also increases with high-temperature aging, indicating that densification and pore shape changes alone are not responsible for all the observed increase in thermalconductivity of coatings. Instead, there are also increases due to a combination of phase separation and grain growth. The increase in thermal conductivity can be described by a Larson–Miller parameter. It is also found that the increase in thermal conductivity with aging is greatest when measured at room temperature and decreases with increasing measurement temperature. Measured at 1000 °C, the thermal conductivity of zirconia is almost temperature independent and the changes in thermal conductivity with aging are less than 15%, even after aging for 50 h at 1400 °C.

Dielectric elastomer generators (DEGs) are attractive candidates for harvesting electrical energy from mechanical work since they comprise relatively few moving parts and large elastomer sheets can be mass produced. Successfully demonstrations of the DEG prototypes have been reported from a diverse of energy sources, including ocean waves, wind, flowing water and human movement. The energy densities achieved, however, are still small compared with theoretical predictions. We show that significant improvements in energy density (550 J/kg with an efficiency of 22.1%), can be achieved using an equi-biaxial mechanical loading configuration, one that produces uniform deformation and maximizes the capacitance changes. Analysis of the energy dissipations indicates that mechanical losses, which are caused by the viscous losses both within the acrylic elastomer and within the thread materials used for the load transfer assembly, limits the energy conversion efficiency of the DEG. Addressing these losses is suggested to increase the energy conversion efficiency of the DEG. © (2013) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.

The high-temperature phase transition between the tetragonal (scheelite) and monoclinic (fergusonite) forms of yttrium tantalite (YTaO4 ) has been studied using a combination of first-principles calculations and a Landau free-energy expansion. Calculations of the Gibbs free energies show that the monoclinic phase is stable at room temperature and transforms to the tetragonal phase at 1430 °C, close to the experimental value of 1426±7 °C. Analysis of the phonon modes as a function of temperature indicate that the transformation is driven by softening of transverse acoustic modes with symmetry Eu in the Brillouin zone center rather than the Raman-active Bg mode. Landau free-energy expansions demonstrate that the transition is second order and, based on the fitting to experimental and calculated lattice parameters, it is found that the transition is a proper rather than a pseudoproper type. Together these findings are consistent with the transition being ferroelastic.

Geometrical frustration arises when a local order cannot propagate throughout the space because of geometrical constraints. This phenomenon plays a major role in many systems leading to disordered ground-state configurations. Here, we report a theoretical and experimental study on the behavior of buckling-induced geometrically frustrated triangular cellular structures. To our surprise, we find that buckling induces complex ordered patterns which can be tuned by controlling the porosity of the structures. Our analysis reveals that the connected geometry of the cellular structure plays a crucial role in the generation of ordered states in this frustrated system.

Compositions in the ZrO2-Y2O3-Ta2O5 system are of interest as low thermal conductivity, fracture resistant oxides for the next generation thermal barrier coatings (TBC). Multiple phases occur in the system offering the opportunity to compare the thermal properties of single, two-phase, and three-phase materials. Despite rather large variations in compositions almost all the solid solution compounds had rather similar thermal conductivities and, furthermore, exhibited only relatively small variations with temperature up to 1000oC. These characteristics are attributed to the extensive mass disorder in all the compounds and, in turn, small interfacial Kapitza (thermal) resistances. More complicated behavior, associated with the transformation from the tetragonal to monoclinic phase, occurs on long-term annealing in air of some of the compositions. However, the phases in two of the compositional regions do not change with annealing in air and their thermal conductivities remain unchanged suggesting they may be suitable for further exploration as thermally stable TBC overcoats.

Oxide compositions of equimolar YO1.5 and TaO2.5 in the Y–Ta–Zr–O system have attractive properties for high-temperature applications, including as thermal barrier coatings. The effect of zirconia concentration, from 0 to 20 mol.% cation, on the tetragonal-to-monoclinic phase transition has been studied using high-temperature X-ray diffraction, Raman spectroscopy and electron microscopy. The transformation is reversible and the temperature variation of an order parameter based on the spontaneous strain is consistent with the transformation being ferroelastic, a critical feature for toughening at high temperatures. The presence of twin domains further supports this conclusion. Additionally, stabilization of the tetragonal phase with increasing ZrO2 is evident from the amount of partially retained tetragonal phase at room temperature.

Adaptive optical devices based on electric field induced deformation of dielectricelastomers require transparent and highly compliant electrodes to conform to large shape changes. Electrical, optical, and actuation properties of acrylic elastomerelectrodes fabricated with single-walled carbon nanotubes(SWCNTs) and silver nanowires (AgNWs) have been evaluated. Based on these properties, a figure of merit is introduced for evaluating the overall performance of deformable transparent electrodes. This clearly indicates that SWCNTs outperform AgNWs. Under optimal conditions, optical transparency as high as 91% at 190% maximum actuation strain is readily achievable using SWCNTelectrodes.