We have developed a highly sensitive flexible pressure sensor based on a piezopolymer and silver nanowires (AgNWs) composite. The composite nanofiber webs are made by electrospinning mixed solutions of poly(inylidene fluoride) (PVDF) and Ag NWs in a cosolvent mixture of dimethyl formamide and acetone. The diameter of the fibers ranges from 200 nm to 500 nm, as demonstrated by SEM images. FTIR and XRD results reveal that doping Ag NWs into PVDF greatly enhances the content of β phase in PVDF. This β phase increase can be attributed to interactions between the Ag NWs and the PVDF matrix, which forces the polymer chains to be embedded into the β phase crystalline. The sensitivity of the pressure sensors agrees well with the FTIR and XRD characteristics. In our experiments, the measured sensitivity reached up to 30 pC/N for the nanofiber webs containing 1.5 wt% Ag NWs, which is close to that of poly(vinylidene fluoride-trifluoroethylene) [P(VDF-TrFE), (77/23)]. This study may provide a new method of fabricating high performance flexible sensors at relatively low cost compared with sensors based on [P(VDF-TrFE), (77/23)].
Flexible piezoresistive pressure sensors have been attracted a lot of attention due to their simple mechanism, easy fabrication, and convenient signal acquisition and analysis. Herein, a new flexible piezoresistive sensor based on microstructured electrospun rough polyurethane (PU) nanofibers film is assembled. The microstructured PU film with tiny bumps is prepared in one step via electrospinning technology, which imparts a microstructured rough upper surface and a smooth lower surface. With this unique microstructure, we have made it possible for PU/Ag films to serve as sensing layers for piezoresistive sensors by introducing a silver conductive layer on the surface of electrospun PU film. The fabricated piezoresistive pressure sensor delivers high sensitivity (10.53 kPa−1 in the range of 0–5 kPa and 0.97 kPa−1 in the range of 6–15 kPa), fast response time (60 ms), fast recovery time (30 ms), and long-time stability (over 10,000 cycles). This study presents a fabrication strategy to prepare the microstructured PU nanofiber film using electrospinning technology directly, and the as-developed sensor shows promise in applications such as wrist pulse measurement, finger movement monitoring, etc., proving its great potential for monitoring human activities.
Complementary electrochromic devices (ECDs) composed of WO3 and NiO electrodes have wide applications in smart windows. However, they have poor cycling stability due to ion-trapping and charge mismatch between electrodes, which limits their practical application. In this work, we introduce a partially covered counter electrode (CE) composed of NiO and Pt to achieve good stability and overcome the charge mismatch based on our structure of electrochromic electrode/Redox/catalytic counter electrode (ECM/Redox/CCE). The device is assembled using a NiO-Pt counter electrode with WO3 as the working electrode, and PC/LiClO4 containing a tetramethylthiourea/tetramethylformaminium disulfide (TMTU/TMFDS2+) redox couple as the electrolyte. The partially covered NiO-Pt CE-based ECD exhibits excellent EC performance, including a large optical modulation of 68.2% at 603 nm, rapid switching times of 5.3 s (coloring) and 12.8 s (bleaching), and a high coloration efficiency of 89.6 cm2·C−1. In addition, the ECD achieves a good stability of 10,000 cycles, which is promising for practical application. These findings suggest that the structure of ECC/Redox/CCE could overcome the charge mismatch problem. Moreover, Pt could enhance the Redox couple’s electrochemical activity for achieving high stability. This research provides a promising approach for the design of long-term stable complementary electrochromic devices.
21 September 2015 in Journal of Materials Science: Materials in Electronics
A highly efficient photoanode with a tandem structure of ITO/WO3/Cu2O/CuO produces a photocurrent about 1.4 and 5.5 times the measured values for ITO/WO3/Cu2O and ITO/WO3 ones, respectively.