Real time high voltage capacitance for rapid evaluation of dielectric elastomer actuators.

Dielectric elastomer actuators (DEAs) are soft electromechanical transducers that have enabled robotic, haptic, and optical applications. Despite their advantages in high specific energy, large bandwidth, and simple fabrication, their widespread adoption is limited by poor long-term performance. While the mechanical work output has been studied extensively, the electrical energy input has rarely been characterized.

A Wearable Soft Haptic Communicator Based on Dielectric Elastomer Actuators.

Dielectric elastomer actuators exhibit an unusual combination of large displacements, moderate bandwidth, low power consumption, and mechanical impedance comparable with human skin, making them attractive for haptic devices. In this article, we propose a wearable haptic communication device based on a two-by-two array of dielectric elastomer linear actuators. We briefly describe the architecture of the actuators and their mechanical and electrical integration into a wearable armband.

Realizing the potential of dielectric elastomer artificial muscles.

Soft robotics represents a new set of technologies aimed at operating in natural environments and near the human body. To interact with their environment, soft robots require artificial muscles to actuate movement. These artificial muscles need to be as strong, fast, and robust as their natural counterparts.

Multilayer Dielectric Elastomers for Fast, Programmable Actuation without Prestretch.

A novel method for the fabrication of dielectric elastomer actuators (DEAs) combines acrylic polymers and single wall carbon nanotube network electrodes. DEAs made using this technique do not require prestretching, have extremely thin electrodes, and can be actuated at low voltage. The method is applied to create a multimorph device with nine actuation modes based on just four inputs.

Skeletal diversity through radical cyclization of tetrahydropyridine scaffolds.

Suitably functionalized tetrahydropyridines (methyl pipecolates) have been used as conformationally biased templates for radical cyclizations to access benzoisoquinuclidines and linearly fused indenopiperidines. Variation of skeletal types is determined by location of a radical-initiating element.