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In this work we study the influence of the thermal contact resistance on the temperature of a typical nanostripe used in current induced magnetic domain wall movement or depinning. The thermal contact resistance arises from an imperfect heat transport across the interface between the metallic ferromagnetic nanostripe and the substrate. We show that this parameter, which is likely non-zero in any experimental device, increases the temperature in the nanostripe considerably. When the current is injected in the nanostripe in nanosecond long pulses, the larger temperature also implies a reduction of the effective current density delivered by the pulse generator. Both the thermal contact resistance and the dynamic response of the pulse generator are usually neglected in theoretical estimations of the influence of spin transfer torque on domain wall displacement and depinning. Here we show that only if the thermal contact resistance and the electric resistivity of the ferromagnetic nanostripe are optimized to the best values reported in the bibliography, the Joule heating may not be so crucial for current densities of the order of 108 A cm−2. Also, the use of physical constrictions (notch) to pin the magnetic domain wall may complicate the interpretation of the results as they always come together with relevant thermal gradients., This work has been partially funded by the Spanish Ministerio de Economía y Competitividad through the projects MAT2014-52477-C5-1-P and MAT2014-52477-C5-3-P and by the Engineering and Physical Sciences Research Council through grant code EPSRC EP/E03389X.

Piezoelectric materials can directly transduce electrical and mechanical energy, making them attractive for applications such as sensors, actuators and energy harvesting devices. The piezoelectric effect is often associated with ceramic materials, yet piezoelectric behaviour is also observed in many polymers. The flexibility, ease of processing and biocompatibility of piezoelectric polymers mean that they are often preferable for certain applications, despite their reduced piezoelectric coefficients. This review will focus on the underlying mechanisms governing piezoelectricity in polymers from both a theoretical and practical perspective, including ways by which the effect can be enhanced through processing and structural modifications, and an outlook on specific areas in biology where piezoelectric polymers can be applied. Given that many biological materials are themselves piezoelectric, there is much interest in studying how artificial piezoelectric materials influence and stimulate cellular function. Understanding and developing piezoelectric polymers is therefore relevant for applications in energy, sensing and biology, as well as for high level, fundamental research in the physical and life sciences.

The requirements for modern electronic devices, particularly those intended for wearable or human health monitoring applications, have rapidly evolved to being both flexible and stretchable. Hence devices, as well as interconnects, need to be capable of retaining functionality even when being mechanically deformed. Most approaches towards achieving this rely on printing or transferring structures onto elastomeric substrates that can withstand stretching. However, the processing involved can often be cumbersome, and the structures themselves tend to suffer from poor fatigue and/or are limited by the mechanical properties of the underlying substrate. Here, we introduce an aerosol-jet printing technique by which fully freestanding functional structures can be built up layer by layer, which are stable and robust upon repeated stretching. The process involves printing a combination of layers of different materials with the desired functionality, onto a substrate coated with a sacrifical film that is subsequently dissolved to release the printed structure. Using this method, we demonstrate freestanding conductive wires can be used as stretchable interconnects/electrodes, and that also function as strain-sensors. We also show that a freestanding capacitive structure functions as a robust, stretchable humidity sensor, paving the way for the development of other multi-layer, multifunctional stretchable devices and sensors.

Semiconducting piezoelectric materials have attracted considerable interest due to their central role in the emerging field of piezotronics, where the development of a piezo-potential in response to stress or strain can be used to tune the band structure of the semiconductor, and hence its electronic properties. This coupling between piezoelectricity and semiconducting properties can be readily exploited for force or pressure sensing using nanowires, where the geometry and unclamped nature of nanowires render them particularly sensitive to small forces. At the same time, piezoelectricity is known to manifest more strongly in nanowires of certain semiconductors. Here, we report the design and fabrication of highly sensitive piezotronic pressure sensors based on GaAs nanowire ensemble sandwiched between two electrodes in a back-to-back diode configuration. We analyse the current–voltage characteristics of these nanowire-based devices in response to mechanical loading in light of the corresponding changes to the device band structure. We observe a high piezotronic sensitivity to pressure, of ~7800 meV MPa−1. We attribute this high sensitivity to the nanowires being fully depleted due to the lack of doping, as well as due to geometrical pressure focusing and current funnelling through polar interfaces.

Harvesting energy from ambient mechanical sources in our environment has attracted considerable interest due to its potential to power applications such as ubiquitous wireless sensors and Internet of Things devices. In this context, piezoelectric and/or triboelectric materials offer a relatively simple means of directly converting mechanical energy from ubiquitous ambient vibrating sources into electrical power for microscale/nanoscale device applications. In particular, nanoscale energy harvesters, or nanogenerators, are capable of converting low-level ambient vibrations into electrical energy, thus are vital to the realization of the next generation of self-powered devices. Polymer-based nanogenerators are attractive as they are inherently flexible and robust, making them less prone to mechanical failure which is a key requirement for vibrational energy harvesters. They are also lightweight, easy and cheap to fabricate, lead-free and biocompatible, but in many cases their energy harvesting performance is found lacking in comparison to more commonly studied inorganic materials. Recent advances have been made in developing scalable nanofabrication techniques for flexible and low-cost polymer-based nanogenerators with improved energy conversion efficiency, including the incorporation of high-quality polymer nanowires with enhanced crystallinity, piezoelectric and/or surface charge properties. In this review, we discuss aspects of nanomaterials growth and energy harvester device design, including those involving nanowires of polymers of polyvinylidene fluoride and its co-polymers, Nylon-11, and poly-lactic acid for scalable piezoelectric and triboelectric nanogenerator applications, as well as the design and performance of polymer-ceramic nanocomposite nanogenerators. In particular, we highlight the effects of growth parameters, nanoconfinement, self-poling, surface polarization, crystalline phases, and device assembly on the energy harvesting performance of a range of recently reported nanostructured polymer-based materials and devices.

Triboelectric motion sensors, based on the generation of a voltage across two dissimilar materials sliding across each other as a result of the triboelectric effect, have generated interest due to the relative simplicity of the typical grated device structures and materials required. However, these sensors are often limited by poor spatial and/or temporal resolution of motion due to limitations in achieving the required device feature sizes through conventional lithography or printing techniques. Furthermore, the reliance on metallic components that are relatively straightforward to pattern into fine features limits the possibility to develop transparent sensors. Polymers would allow for transparent devices, but these materials are significantly more difficult to pattern into fine features when compared to metals. Here, we use an aerosol-jet printing (AJP) technique to develop triboelectric sensors using a wide variety of materials, including polymers, which can be directly printed into finely featured grated structures for enhanced sensitivity to displacement and speed of motion. We present a detailed investigation highlighting the role of material selection and feature size in determining the overall resolution of the resulting motion sensor. A 3-channel rotary sensor is also presented, demonstrating the versatility of the AJP technique in developing more complex triboelectric motion sensors.

Thermoelectric generators (TEGs) operate in the presence of a temperature gradient, where the constituent thermoelectric (TE) material converts heat into electricity via the Seebeck effect. However, TE materials are characterised by a thermoelectric figure of merit (ZT) and/or power factor (PF), which often has a strong dependence on temperature. Thus, a single TE material spanning a given temperature range is unlikely to have an optimal ZT or PF across the entire range, leading to inefficient TEG performance. Here, we demonstrate compositionally graded organic-inorganic nanocomposites, where the composition of the TE nanocomposite is systematically tuned along the length of the TEG, in order to optimise the PF along the applied temperature gradient. The nanocomposite composition can be dynamically tuned by an aerosol-jet printing method with controlled in-situ mixing capability, thus enabling the realisation of such compositionally graded thermoelectric composites (CG-TECs). We show how CG-TECs can be realised by varying the loading weight percentage of Bi2Te3 nanoparticles or Sb2Te3 nanoflakes within an organic conducting matrix using bespoke solution-processable inks. The enhanced energy harvesting capability of these CG-TECs from low-grade waste heat (

Perovskite oxides show an amazing diversity of electronic and magnetic properties along with a myriad of structural variants and phase transitions. Large thermal changes may be driven near the ferroic phase transitions in perovskite oxides using magnetic, electric and stress fields to manipulate conjugate order parameters. The ensuing magnetocaloric, electrocaloric and mechanocaloric effects can be utilized for environment-friendly and high-efficiency solid-state cooling applications. Here we describe the details of these caloric effects in perovskite oxides both from a chronological perspective and from the viewpoint of the recent advances in multiple caloric phenomena. We highlight the role of interfaces in oxide thin films for the different caloric effects and address some of the outstanding challenges for the fundamental understanding and practical implementation of perovskite oxides in solid state refrigeration.