RESUMO
Energy autonomy is critical for wearable and portable systems and to this end storage devices with high-energy density are needed. This work presents high-energy density flexible supercapacitors (SCs), showing three times the energy density than similar type of SCs reported in the literature. The graphene-graphite polyurethane (GPU) composite based SCs have maximum energy and power densities of 10.22 µWh cm-2 and 11.15 mW cm-2, respectively, at a current density of 10 mA cm-2 and operating voltage of 2.25 V (considering the IR drop). The significant gain in the performance of SCs is due to excellent electroactive surface per unit area (surface roughness 97.6 nm) of GPU composite and high electrical conductivity (0.318 S cm-1). The fabricated SCs show stable response for more than 15 000 charging/discharging cycles at current densities of 10 mA cm-2 and operating voltage of 2.5 V (without considering the IR drop). The developed SCs are tested as energy storage devices for wide applications, namely: a) solar-powered energy-packs to operate 84 light-emitting diodes (LEDs) for more than a minute and to drive the actuators of a prosthetic limb; b) powering high-torque motors; and c) wristband for wearable sensors.
RESUMO
Graphene has great potential for high-performance flexible electronics. Although studied for more than a decade, contacting graphene efficiently, especially for large-area, flexible electronics, is still a challenge. Here, by engineering the graphene-metal van der Waals (vdW) contact, we demonstrate that ultralow contact resistance is achievable via a bottom-contact strategy incorporating a simple transfer process without any harsh thermal treatment (>150 °C). The majority of the fabricated devices show contact resistances below 200 Ω·µm with values as low as 65 Ω·µm achievable. This is on par with the state-of-the-art top- and edge-contacted graphene field-effect transistors. Further, our study reveals that these contacts, despite the presumed weak nature of the vdW interaction, are stable under various bending conditions, thus guaranteeing compatibility with flexible electronics with improved performance. This work illustrates the potential of the previously underestimated vdW contact approach for large-area flexible electronics.
RESUMO
This work reports a temperature-assisted dip-coating method for self-assembly of silica (SiO2) microspheres/nanospheres (SPs) as monolayers over large areas (â¼cm2). The area over which self-assembled monolayers (SAMs) are formed can be controlled by tuning the suspension temperature (Ts), which allows precise control over the meniscus shape. Furthermore, the formation of periodic stripes of SAMs, with excellent dimensional control (stripe width and stripe-to-stripe spacing), is demonstrated using a suitable set of dip-coating parameters. These findings establish the role of Ts, and other parameters such as withdrawal speed (Vw), withdrawal angle (θw), and withdrawal step length (Lw). For Ts ranged between 25 and 80 °C, the morphological analysis of dip-coatings shows layered structures comprising of defective layers (25-60 °C), single layers (70 °C), and multilayers (>70 °C) owing to the variation of SP flux at the meniscus/substrate assembling interface. At Ts = 70 °C, there is an optimum Vw, approximately equal to the downshift speed of the meniscus (Vm = 1.3 µm/s), which allows the SAM formation over areas (2.25 cm2) roughly 10 times larger than reported in the literature using nanospheres. Finally, the large-area SAM is used to demonstrate the enhanced performance of antireflective coatings for photovoltaic cells and to create metal nanomesh for Si nanowire synthesis.
RESUMO
Sensor-laden wearable systems that are capable of providing continuous measurement of key physiological parameters coupled with data storage, drug delivery and feedback therapy have attracted huge interest. Here we report a stretchable wireless system for sweat pH monitoring, which is able to withstand up to 53% uniaxial strain and more than 500 cycles to 30% strain. The stretchability of the pH sensor patch is provided by a pair of serpentine-shaped stretchable interconnects. The pH sensing electrode is made of graphite-polyurethane composite, which is suitable for biosensor application. The sensing patch validated through in-depth electrochemical studies, exhibits a pH sensitivity of 11.13⯱â¯5.8â¯mV/pH with a maximum response time of 8â¯s. Interference study of ions and analyte (Na+, K+ and glucose) in test solutions shows negligible influence on the pH sensor performance. The pH data can be wirelessly and continuously transmitted to smartphone through a stretchable radio-frequency-identification antenna, of which the radiating performance is stable under 20% strain, as proved by vector network analyzer measurement. To evaluate the full system, the pH value of a human sweat equivalent solution has been measured and wirelessly transmitted to a custom-developed smart phone App.
Assuntos
Técnicas Biossensoriais/instrumentação , Suor/química , Tecnologia sem Fio/instrumentação , Elasticidade , Eletrodos , Desenho de Equipamento , Grafite/química , Humanos , Concentração de Íons de Hidrogênio , Poliuretanos/química , Dispositivos Eletrônicos VestíveisRESUMO
In this work, we have developed a contact-printing system to efficiently transfer the bottom-up and top-down semiconductor nanowires (NWs), preserving their as-grown features with a good control over their electronic properties. In the close-loop configuration, the printing system is controlled with parameters such as contact pressure and sliding speed/stroke. Combined with the dry pre-treatment of the receiver substrate, the system prints electronic layers with high NW density (7 NWs/µm for bottom-up ZnO and 3 NWs/µm for top-down Si NWs), NW transfer yield and reproducibility. We observed compactly packed (~115 nm average diameters of NWs, with NW-to-NW spacing ~165 nm) and well-aligned NWs (90% with respect to the printing direction). We have theoretically and experimentally analysed the role of contact force on NW print dynamics to investigate the heterogeneous integration of ZnO and Si NWs over pre-selected areas. Moreover, the contact-printing system was used to fabricate ZnO and Si NW-based ultraviolet (UV) photodetectors (PDs) with Wheatstone bridge (WB) configuration on rigid and flexible substrates. The UV PDs based on the printed ensemble of NWs demonstrate high efficiency, a high photocurrent to dark current ratio (>104) and reduced thermal variations as a result of inherent self-compensation of WB arrangement. Due to statistically lesser dimensional variations in the ensemble of NWs, the UV PDs made from them have exhibited uniform response.