RESUMEN

Stretchable strain sensors are capable of acquiring data when in contact with human skin or equipment and are widely used in wearable applications. Most strain sensors have tensile properties of less than 20% and have limitations regarding body motion linkage, complex sensor structure, and motion nonreliability. To address these problems, we developed a high tension and high sensitivity sensor with a gauge factor over 40 and tensile stress about 50%. Polydimethylsiloxane (PDMS) was selected as the flexible substrate to ensure tensile strength, and polyaniline (PANI) was used to measure the resistance changes in the sensor. In particular, problems regarding poor uniformity of PANI on PDMS were resolved by surface treatment of the PDMS, wherein PANI polymerization was performed sequentially after forming a self-assembled monolayer (SAM) on the PDMS substrate. O2 plasma and (3-aminopropyl)triethoxysilane were used to form the SAM. It is expected that this sensor can obtain stable characteristics even under high tensile stress through the evenly formed PANI films on the surface-treated PDMS substrate and may be used in various flexible sensor applications.

Asunto(s)

Dimetilpolisiloxanos , Compuestos de Anilina , Dimetilpolisiloxanos/química , Humanos , Polimerizacion , Propilaminas , Silanos

RESUMEN

Research on stretchable strain sensors is actively conducted due to increasing interest in wearable devices. However, typical studies have focused on improving the elasticity of the electrode. Therefore, methods of directly connecting wire or attaching conductive tape to materials to detect deformation have been used to evaluate the performance of strain sensors. Polyaniline (PANI), a p-type semiconductive polymer, has been widely used for stretchable electrodes. However, conventional procedures have limitations in determining an appropriate metal for ohmic contact with PANI. Materials that are generally used for connection with PANI form an undesirable metal-semiconductor junction and have significant contact resistance. Hence, they degrade sensor performance. This study secured ohmic contact by adapting Au thin film as the metal contact layer (the MCL), with lower contact resistance and a larger work function than PANI. Additionally, we presented a buffer layer using hard polydimethylsiloxane (PDMS) and structured it into a dumbbell shape to protect the metal from deformation. As a result, we enhanced steadiness and repeatability up to 50% strain by comparing the gauge factors and the relative resistance changes. Consequently, adapting structural methods (the MCL and the dumbbell shape) to a device can result in strain sensors with promising stability, as well as high stretchability.

RESUMEN

Energy storage characteristics of organic molecules continue to attract attention for supercapacitor applications, as they offer simple processing and can be employed for flexible devices. The current study utilized the ultrasonically driven exfoliation to obtain poly diketo pyrrolopyrrole-thieno thiophene (PDPT) and multiwalled carbon nanotube (CNT) composite, subsequently fabricated a PDPT donor-π-acceptor heterojunction with CNT and investigated energy storage applications. The composite was characterized using series of standard analytical techniques. Morphology indicated well alighted CNT tubes on PDPT polymer nanosheets with an effective interface, providing efficient electrochemical regions, enabling fast charge transfer between PDPT and CNT. We also investigated the PDPT-CNT composite electrochemical behavior, achieving 319.2 and 105.7F.g-1 capacitances for PDPT-CNT and PDPT at 0.5 A.g-1 current density for three electrode configurations; and 126 and 42F.g-1 for symmetric structures, respectively. Experimental results confirmed that PDPT-CNT composite electrodes achieved two fold the capacitance compared with PDPT alone. The hypothesis and synthetic approach provide an excellent candidate for conjugated polymers with carbon nanotubes and energy related devices.

RESUMEN

A large volume of research on lithium-oxygen (Li-O2) batteries (LOBs) has been conducted in the recent decades, inspired by their high energy density and power density. However, these future generation energy-storage devices are still subject to technical limitations, including a squat round-trip efficiency and a deprived rate-capability, due to the slow-moving electrochemical kinetics of both the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) over the surface of the cathode catalyst. Because the electrochemistry of LOBs is rather complex, only a limited range of cathode catalysts has been employed in the past. To understand the catalytic mechanisms involved and improve overall cell performance, the development of new cathode electrocatalysts with enhanced round-trip efficiency is extremely important. In this context, transition metal carbides and nitrides (TMCs and TMNs, respectively) have been explored as potential catalysts to overcome the slow kinetics of electrochemical reactions. To provide an accessible and up-to-date summary for the research community, the present paper reviews the recent advancements of TMCs and TMNs and its applications as active electrocatalysts for LOBs. In particular, significant studies on the rational design of catalysts and the properties of TMC/TMN in LOBs are discussed, and the prospects and challenges facing the continued development of TMC/TMN electrocatalysts and strategies for attaining higher OER/ORR activity in LOBs are presented.