Abstract: This paper aims to develop a novel concept for energy harvesting via flexible inverted flags combining photovoltaic cells with piezoelectric flexible films. Using technology currently available, we have designed and fabricated piezo-pyro-photo-electric harvesters made of polyvinylidene fluoride (PVDF) piezoelectric elements combined with mini solar panels made of silicon. Experimental measurements of the motion dynamics and power generation were collected for the flags when subjected to wind, heat, and light sources simultaneously and individually. Results indicate a significant improvement in energy harvesting capability compared to isolated single piezoelectric devices. Thus, we anticipate a substantial impact of piezo- pyro-photo-electric energy harvesting device applications where remote power generation is needed. The Flag uses flexible piezoelectric and pyroelectric strips and flexible photovoltaic cells panel. The piezo-pyro- simultaneously generates power through movement and heat, respectively, while the photovoltaic cells harvest solar energy to produce electric power. The beauty of this Flag is to develop power day and night depending on the energy sources available. The basic concept is presented and validated by laboratory experiments with controlled airflow, light, and infrared heat. The maximum voltage generated was 60 mV when the Flag was simultaneously exposed to low-level wind, thermal and light energies.
more »
« less
Pyroelectric Polyelectrolyte Brushes
Abstract Piezo‐ and pyroelectric materials are of interest, for example, for energy harvesting applications, for the development of tactile sensors, as well as neuromorphic computing. This study reports the observation of pyro‐ and piezoelectricity in thin surface‐attached polymer brushes containing zwitterionic and electrolytic side groups that are prepared via surface‐initiated polymerization. The pyro‐ and piezoelectric properties of the surface‐grafted polyelectrolyte brushes are found to sensitively depend on and can be tuned by variation of the counterion. The observed piezo‐ and pyroelectric properties reflect the structural complexity of polymer brushes, and are attributed to a complex interplay of the non‐uniform segment density within these films, together with a non‐uniform distribution of counterions and specific ion effects. The fabrication of thin pyroelectric films by surface‐initiated polymerization is an important addition to the existing strategies toward such materials. Surface‐initiated polymerization, in particular, allows for facile grafting of polar thin polymer films from a wide range of substrates via a straightforward two‐step protocol that obviates the need for multistep laborious synthetic procedures or thin film deposition protocols. The ability to produce polymer brushes with piezo‐ and pyroelectric properties opens up new avenues of application of these materials, for example, in energy harvesting or biosensing.
more »
« less
- Award ID(s):
- 2204396
- PAR ID:
- 10485133
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Advanced Materials
- ISSN:
- 0935-9648
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
Thin films of poly(arylene ethynylene) conjugated polymers, including low-energy-gap donor–acceptor polymers, can be prepared via stepwise polymerization utilizing surface-confined Sonogashira cross-coupling. This robust and efficient polymerization protocol yields conjugated polymers with a precise molecular structure and with nanometer-level control of the organization and the uniform alignment of the macromolecular chains in the densely packed film. In addition to high stability and predictable and well-defined molecular organization and morphology, the surface-confined conjugated polymer chains experience significant interchain electronic interactions, resulting in dominating intermolecular π-electron delocalization which is primarily responsible for the electronic and spectroscopic properties of polymer films. The fluorescent films demonstrate remarkable performance in chemosensing applications, showing a turn-off fluorescent response on the sub-ppt (part per trillion) level of nitroaromatic explosives in water. This unique sensitivity is likely related to the enhanced exciton mobility in the uniformly aligned and structurally monodisperse polymer films.more » « less
-
ABSTRACT The stability of nonpatterned and nanopatterned strong polyelectrolyte brushes (PEBs) is studied as a function of both brush character and the properties of a contacting liquid. High‐molecular‐weight PEBs of poly(4‐methyl vinylpyridinium iodide) (PMeVP) are synthesized using surface‐initiated radical‐chain polymerization. Nanopatterned brushes (NPBs) line with pattern sizes ranging from 50 to 200 nm are generated by patterning the initiator layer using deep‐ultraviolet photolithography followed by brush growth initiated from the patterned layer. Homogeneous PEBs with different degrees of charging and grafting densities are exposed to water and salt solutions with different temperatures for different periods. The degradation is monitored through dry‐state ellipsometry and atomic force microscopy measurements. Enhanced degrafting for more strongly swollen polymer brushes can be observed in agreement with an “entropic spring” model. Based on the results of the nonpatterned brushes, the NPBs are exposed to water at different temperatures and external salt content for varying periods of time. Counterintuitively, the NPBs show increased degrafting for smaller patterns, which is attributed to different polymer chain dynamics for nanobrushes and microbrushes. We investigate the influence of thermodynamic and kinetic parameters on the stability of (nanopatterned) PEBs and discuss the role of entanglements and formation of complexes in such films. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019, 57, 1283–1295more » « less
-
null (Ed.)Redox-switchable polymerizations of lactide and epoxides were extended to the solid state by anchoring an iron-based polymerization catalyst to TiO 2 nanoparticles. The reactivity of the molecular complexes and their redox-switching characteristics were maintained in the solid-state. These properties resulted in surface-initiated polymerization reactions that produced polymer brushes whose chemical composition is dictated by the oxidation state of the iron-based complex. Depositing the catalyst-functionalized TiO 2 nanoparticles on fluorine-doped tin oxide resulted in an electrically addressable surface that could be used to demonstrate spatial control in redox-switchable polymerization reactions. By using a substrate that contained two electrically isolated domains wherein one domain was exposed to an oxidizing potential, patterns of surface-bound polyesters and polyethers were accessible through sequential application of lactide and cyclohexene oxide. The differentially functionalized surfaces demonstrated distinct physical properties that illustrated the promise for using the method to pattern surfaces with multiple, chemically distinct polymer brushes.more » « less
-
Abstract We present a versatile platform for fabricating two‐photon excitable carbon dot‐based nanocomposite thin films by harnessing the structural versatility of polymer brushes in combination with electron‐beam lithography (EBL). This approach enables the precise spatial organization of carbon dots (CDs) at the nanoscale, facilitating dynamic modulation of their photoluminescent properties in response to environmental stimuli. Three model systems were examined, incorporating pH‐ and thermally responsive polymers, functionalized through covalent and dynamic covalent bonding strategies. By leveraging the spatial control afforded by nanostructured polymer brushes, we achieved precise tuning of optical properties while mitigating aggregation‐induced quenching, a longstanding challenge in solid‐state CD applications. In addition to the advances in controlling optical properties, this work highlights the potential of polymer brush systems to function as optically active, reprogrammable surfaces. The resulting nanoscale‐engineered materials exhibit highly responsive, reconfigurable photonic behavior, offering a scalable pathway for integrating advanced optical interfaces into microchip technologies, biosensing platforms, and multiplexed diagnostic systems. The fusion of polymer brushes, carbon dots, and advanced lithographic techniques marks a substantial advancement in the development of functional materials with nanoscale precision and stimuli‐responsive properties.more » « less