Publications

Abstract As an emerging branch of energy conversion technologies, the triboelectric nanogenerator (TENG) pioneers a brand‐new path to effectively harness varieties of mechanical energies for the purpose of powering and/or sensing. Since its invention in 2012, the TENG has experienced a booming and revolutionary development in every respect, ranging from materials synthesis and modification, architecture design to performance optimization, power management, and application exploration. In comparison to the organic solar cell and organic light‐emitting diodes, TENG is a unique technique that opens the venue of using polymer materials (PMs) for harvesting mechanical energy. So far, by virtue of superior charge transfer and capturing capabilities during friction, various kinds of PMs have been developed and used as triboelectric materials in order to achieve high‐performance TENGs. Here, this work focuses on the utilization and development of PMs for the TENGs technology and first gives a summary of main PMs that are frequently adopted in currently reported energy‐harvesting TENGs. Second, several kinds of PMs used lately in a few novel TENGs for special or specific energy‐harvesting circumstances are introduced and highlighted. Finally, the perspectives on and challenges in developing high‐performance PMs toward TENGs technology are conceived and expected to be instructive to future research.

Flexible and stretchable physical sensors capable of both energy harvesting and self-powered sensing are vital to the rapid advancements in wearable electronics. Even so, there exist few studies that can integrate energy harvesting and self-powered sensing into a single electronic skin. Here, a stretchable and washable skin-inspired triboelectric nanogenerator (SI-TENG) is developed for both biomechanical energy harvesting and versatile pressure sensing. A planar and designable conductive yarn network constructed from a three-ply-twisted silver-coated nylon yarn is embedded into flexible elastomer, endowing the SI-TENG with desired stretchability, good sensitivity, high detection precision, fast responsivity, and excellent mechanical stability. With a maximum average power density of 230 mW m-2 , the SI-TENG is able to light up 170 light-emitting diodes, charge various capacitors, and drive miniature electronic products. As a self-powered multifunctional sensor, the SI-TENG is adopted to monitor human physiological signals, such as arterial pulse and voice vibrations. Furthermore, an intelligent prosthetic hand, a self-powered pedometer/speedometer, a flexible digital keyboard, and a proof-of-concept pressure-sensor array with 8 × 8 sensing pixels are successively demonstrated to further confirm its versatile application prospects. Based on these merits, the developed SI-TENG has promising applications in wearable powering technology, physiological monitoring, intelligent prostheses, and human-machine interfaces.

Lidocaine was the commonly used local anesthetic. The present study aimed to compare the pharmacokinetics of intravenous and topical lidocaine in patients undergoing thoracoscopic pulmonary resection.

Mechanosensation electronics (or Electronic skin, e-skin) consists of mechanically flexible and stretchable sensor networks that can detect and quantify various stimuli to mimic the human somatosensory system, with the sensations of touch, heat/cold, and pain in skin through various sensory receptors and neural pathways. Here we present a skin-inspired highly stretchable and conformable matrix network (SCMN) that successfully expands the e-skin sensing functionality including but not limited to temperature, in-plane strain, humidity, light, magnetic field, pressure, and proximity. The actualized specific expandable sensor units integrated on a structured polyimide network, potentially in three-dimensional (3D) integration scheme, can also fulfill simultaneous multi-stimulus sensing and achieve an adjustable sensing range and large-area expandability. We further construct a personalized intelligent prosthesis and demonstrate its use in real-time spatial pressure mapping and temperature estimation. Looking forward, this SCMN has broader applications in humanoid robotics, new prosthetics, human-machine interfaces, and health-monitoring technologies.

It is known that the suspended liquid droplets in clouds can generate electrostatic charges, which finally results in the lightning. However, the detailed mechanism related to the contact-electrification process on the liquid-gas (L-G) interfaces is still poorly understood. Here, by introducing an acoustic levitation method for levitating a liquid droplet, we have studied the electrification mechanism at the L-G interface. The tribo-motion between water droplets and air induced by the ultrasound wave leads to the generation of positive charges on the surface of the droplets, and the charge amount of water droplets (20 μL) gradually reaches saturation within 30 s. The mixed solid particles in droplets can increase the amount of transferred charge, whereas the increase of ion concentration in the droplet can suppress the charge generation. This charge transfer phenomenon at L-G interfaces and the related analysis can be a guidance for the study in many fields, including anti-static, harvesting rainy energy, micro/nano fluidics, triboelectric power generator, surface engineering, and so on. Moreover, the surface charge generation due to L-G electrification is an inevitable effect during ultrasonic levitation, and thus, this study can also work for the applications of the ultrasonic technique.

Polymers are commonly used to fabricate triboelectric nanogenerators (TENGs). Here, several polymer films with similar main chains but different functional groups on the side chain are employed to clarify the contributions of each functional group to contact electrification (CE). The results show that the electron-withdrawing (EW) ability and density of these functional groups on the main chain can determine both the polarity and density of CE-induced surface charges. Similar results are obtained for CE in both the polymer-polymer and polymer-liquid modes. A theoretical mechanism involving electron cloud overlap is proposed to explain all of these results. More importantly, the unsaturated groups on poly(tetrafluoroethylene) molecular chain are proved to have a much stronger EW ability than the saturated groups. The density of these unsaturated groups can be increased using a sputtering technique, suggesting that this is a facile and effective method of enhancing the performance of TENGs. These results clarify the correlation between the molecular structure and macroscopic electrification behavior of polymers.