Here, a novel design of a mechanical energy harvester combining peak power output competitive with state‐of‐the‐art energy harvester devices is reported, but with a design enabling full transience, or dissolution, of the harvester after 30 min upon triggering in basic water. The harvester incorporates a symmetric cell combining Li
The technological promise of soft devices—wearable electronics, implantables, soft robotics, sensors—has accelerated the demand for deformable energy sources. Devices that can convert mechanical energy to electrical energy can enable self‐powered, tetherless, and sustainable devices. This work presents a completely soft and stretchable (>400% strain) energy harvester based on variable‐area electrical‐double‐layer (EDL) capacitors (≈40 µF cm−2). Mechanically varying the EDL area, and thus the capacitance, disrupts equilibrium and generates a driving force for charge movement through an external circuit. Prior EDL capacitors varied the contact area by depressing water droplets between rigid electrodes. In contrast, here, the harvester consists of liquid‐metal electrodes encased in a hydrogel. Deforming the device by ≈25% strain generates a power density ≈0.5 mW m−2. This unconventional approach is attractive because: (1) it does not need an external voltage supply to provide charge; (2) the electrodes themselves deform; and (3) it can work under various modes of deformation such as pressing, stretching, bending, and twisting. The unique ability of the harvester to operate underwater shows promising applications in wearables that contact sweat, underwater sensing, and blue energy harvesting.
more » « less- PAR ID:
- 10446349
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Advanced Materials
- Volume:
- 33
- Issue:
- 43
- ISSN:
- 0935-9648
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
Abstract x Al alloy electrodes and polyvinyl alcohol packaging that harvests mechanical energy due to the mechanical–electrochemical stress coupling between the electrodes. Prototype harvester devices demonstrate peak output power of 0.208 µW cm−2with continuous energy generation up to 1.76 µJ cm−2at a mechanical input frequency of 0.1 Hz. This work introduces a new class of power systems simultaneously tailored for transience, high‐performance energy harvesting, and operation frequency relevant to wearable technologies. -
Abstract Increasing demand for self-powered wearable sensors has spurred an urgent need to develop energy harvesting systems that can reliably and sufficiently power these devices. Within the last decade, reverse electrowetting-on-dielectric (REWOD)-based mechanical motion energy harvesting has been developed, where an electrolyte is modulated (repeatedly squeezed) between two dissimilar electrodes under an externally applied mechanical force to generate an AC current. In this work, we explored various combinations of electrolyte concentrations, dielectrics, and dielectric thicknesses to generate maximum output power employing REWOD energy harvester. With the objective of implementing a fully self-powered wearable sensor, a “zero applied-bias-voltage” approach was adopted. Three different concentrations of sodium chloride aqueous solutions (NaCl-0.1 M, NaCl-0.5 M, and NaCl-1.0 M) were used as electrolytes. Likewise, electrodes were fabricated with three different dielectric thicknesses (100 nm, 150 nm, and 200 nm) of Al2O3and SiO2with an additional layer of CYTOP for surface hydrophobicity. The REWOD energy harvester and its electrode–electrolyte layers were modeled using lumped components that include a resistor, a capacitor, and a current source representing the harvester. Without using any external bias voltage, AC current generation with a power density of 53.3 nW/cm2was demonstrated at an external excitation frequency of 3 Hz with an optimal external load. The experimental results were analytically verified using the derived theoretical model. Superior performance of the harvester in terms of the figure-of-merit comparing previously reported works is demonstrated. The novelty of this work lies in the combination of an analytical modeling method and experimental validation that together can be used to increase the REWOD harvested power extensively without requiring any external bias voltage.
-
Abstract This paper reports soft and stretchable films of liquid metal particles (LMPs) that offer high surface area and high conductivity. Liquid metals (LM) based on gallium are compelling conductors for soft and stretchable devices, yet it is difficult to make electrodes of LM with high surface area due to the tendency of liquids to minimize their surface area. To form films of percolated particles with high surface area, LMPs are first created by sonicating LM in isopropanol with trace amounts of hydrochloric acid and 1,6‐hexane dithiol to decrease the amount of surface oxide on the LMPs. A film of these particles placed on a tacky substrate is initially insulating but percolate into conductive paths by straining the substrate. The resulting electrode has high conductivity (1.64 × 105S m−1) and high surface area (1257% greater than a bulk LM film with the same areal footprint). Interestingly, these electrodes have nearly strain‐invariant resistance (
R /R 0 = 1.23 at 600% strain). The ability to create high surface area electrodes in such a simple manner may find use in sensing, capacitive storage, batteries, and energy‐harvesting devices. -
Abstract Stretchable polymer semiconductors (PSCs) have seen great advancements alongside the development of soft electronics. But it remains a challenge to simultaneously achieve high charge carrier mobility and stretchability. Herein, we report the finding that stretchable PSC thin films (<100-nm-thick) with high stretchability tend to exhibit multi-modal energy dissipation mechanisms and have a large relative stretchability (
rS ) defined by the ratio of the entropic energy dissipation to the enthalpic energy dissipation under strain. They effectively recovered the original molecular ordering, as well as electrical performance, after strain was released. The highestrS value with a model polymer (P4) exhibited an average charge carrier mobility of 0.2 cm2V−1s−1under 100% biaxial strain, while PSCs with lowrS values showed irreversible morphology changes and rapid degradation of electrical performance under strain. These results suggestrS can be used as a parameter to compare the reliability and reversibility of stretchable PSC thin films. -
Abstract Cutaneous muscles drive the texture‐modulation behavior of cephalopods by protruding several millimeters out of the skin. Inspired by cephalopods, a self‐morphing, stretchable smart skin containing embedded‐printed electrodes and actuated by Twisted Spiral Artificial Muscles (TSAMs) is proposed. Electrothermally actuated TSAMs are manufactured from inexpensive polymer fibers to mimic the papillae muscles of cephalopods. These spirals can produce strains of nearly 2000% using a voltage of only 0.02 V mm−1. Stretchable and low‐resistance liquid metal electrodes are embedded‐printed inside the self‐morphing skin to facilitate the electrothermal actuation of TSAMs. Theoretical and numerical models are proposed to describe the embedded printing of low‐viscosity Newtonian liquid metals as conductive electrodes in a soft elastomeric substrate. Experimental mechanical tests are performed to demonstrate the robustness and electrical stability of the electrodes. Two smart skin prototypes are fabricated to highlight the capabilities of the proposed self‐morphing system, including a texture‐modulating wearable soft glove and a waterproof skin that emulates the texture‐modulation behavior of octopi underwater. The proposed self‐morphing stretchable smart skin can find use in a wide range of applications, such as refreshable Braille displays, haptic feedback devices, turbulence tripping, and antifouling devices for underwater vehicles.