Publications

The low root mean square (RMS) current density generated by triboelectric nanogenerators (TENGs) has significantly hindered their effectiveness in charging lithium batteries. In response, we present a universal energy storage...

Large-scale tactile sensor arrays are of great importance in flexible electronics, human-robot interaction, and medical monitoring. In this paper, a flexible 10 × 10 tribotronic transistor array (TTA) is developed as an active tactile sensing system by incorporating field-effect transistor units and triboelectric nanogenerators into a polyimide substrate. The drain-source current of each tribotronic transistor can be individually modulated by the corresponding external contact, which has induced a local electrostatic potential to act as the conventional gate voltage. By scaling down the pixel size from 5 × 5 to 0.5 × 0.5 mm2, the sensitivities of single pixels are systematically investigated. The pixels of the TTA show excellent durability, independence, and synchronicity, which are suitable for applications in real-time tactile sensing, motion monitoring, and spatial mapping. The integrated tribotronics provides an unconventional route to realize an active tactile sensing system, with prospective applications in wearable electronics, human-machine interfaces, fingerprint identification, and so on.

Ceria (CeO2) based ceramics have been widely used for many applications due to their unique ionic, electronic, and catalytic properties. Here, we report our findings in investigating into the redox processes of undoped and Sm-doped CeO2 ceramics stimulated by high-energy electron beam irradiation within a transmission electron microscope (TEM). The reduced structure with oxygen vacancy ordering has been identified as the CeO1.68 (C-Ce2O3+δ) phase via high-resolution TEM. The reduction of Ce4+ to Ce3+ has been monitored by electron energy-loss spectroscopy. The decreased electronic conductivity of the Sm-doped CeO2 (Sm0.2Ce0.8O1.9, SDC) is revealed by electron holography, as positive electrostatic charges accumulated at the surfaces of SDC grains under electron beam irradiation, but not at CeO2 grains. The formation of the reduced CeO1.68 domains corresponds to lattice expansion compared to the CeO2 matrix. Therefore, the growth of CeO1.68 nuclei builds up strain inside the matrix, causing annihilation of dislocations inside the grains. By using in-situ high-resolution TEM and a fast OneView camera recording system, we investigated dislocation motion inside both CeO2 and SDC grains under electron beam irradiation. The dislocations prefer to dissociate into Shockley partials bounded by stacking faults. Then, the partials can easily glide in the {111} planes to reach the grain surfaces. Even the Lomer-Cottrell lock can be swept away by the phase change induced strain field. Our results revealed the high mobility of dislocations inside CeO2 and SDC grains during their respective redox processes.

Titanium dioxide (TiO(2)) is one of the most widely studied and important materials for catalysis, photovoltaics, and surface science applications, but the ability to consistently control the relative exposure of higher surface energy facets during synthesis remains challenging. Here, we present the repeatable synthesis of highly reactive, rutile {001} or {101} facets on broad, sword-shaped TiO(2) nanostructures rapidly synthesized in minutes. Growth occurs along planes of lower surface energy, repeatedly yielding nanostructures with large, high energy facets. The quantitative photocatalytic reactivity of the nanoswords, demonstrated by the photoreduction of silver, is over an order of magnitude higher than reference low energy TiO(2){110} substrates. Therefore, the higher surface energy dominated TiO(2) nanoswords are ideal structures for characterizing the physicochemical properties of rutile TiO(2), and may be used to enhance a variety of catalytic, optical, and clean-technology applications.

ABSTRACT Technologies for energy harvesting from objects in motion are gaining a continuously increasing interest to directly power wearable electronics, sensors, and wireless transmitters. New networks where things will be uniquely identified and interconnected will require key enabling technologies, particularly cheap, flexible generators of renewable energy, conformable to any solid surface, to power independently individual objects and data transmission. Polymer‐based nanogenerators (PNGs), capable of converting mechanical energy into electricity, have exact features to fulfill these requirements. This article highlights advances in PNGs with focus on material chemistries and geometrical features, device design strategies, and performances. Representative examples of applications which show large‐scale capability are reported. Concluding sections summarize the key challenges and the commercialization perspectives of PNGs for use in real life applications. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135 , 45674.

A simple but practical method to convert the hydroenergy of microfluids into continuous electrical output is reported. Based on the principle of streaming potential/current, a microfluidic generator (MFG) is demonstrated using patterned micropillar arrays as a quasi-porous flow channel. The continuous electrical output makes this MFG particularly suitable as a power source in self-powered systems. Using the proposed MFG to power a single nanowire-based pH sensor, a self-powered fluid sensor system is demonstrated. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.

Wind energy at a high altitude is far more stable and stronger than that near the ground, but it is out of reach of the wind turbine. Herein, we develop an innovative freestanding woven triboelectric nanogenerator flag (WTENG-flag) that can harvest high-altitude wind energy from arbitrary directions. The wind-driven fluttering of the woven unit leads to the current generation by a coupled effect of contact electrification and electrostatic induction. Systematic study is conducted to optimize the structure/material parameters of the WTENG-flag to improve the power output. This 2D WTENG-flag can also be stacked in parallel connections in many layers for a linearly increased output. Finally, a self-powered high-altitude platform with temperature/humidity sensing/telecommunicating capability is demonstrated with the WTENG-flag as a power source. Due to the light weight, low cost, and easy scale-up, this WTENG-flag has great potential for applications in weather/environmental sensing/monitoring systems.

Abstract Shape‐memory polymers (SMPs) are an intriguing class of smart materials possessing reversible shape change and recovery capabilities. Effective routes to shape‐memory porous films (SMPFs) are few and limited in scope owing to the difficulty in manipulating the shape change of pores by conventional methods. Herein we report an unconventional strategy for crafting light‐driven SMPFs by judiciously constructing highly ordered porous films via a facile “breath figure” approach, followed by sequential vapor crosslinking and nondestructive directional light manipulation. Micropores can thus be transformed into other shapes including rectangle, rhombus and size‐reduced micropores at room temperature. The transformed micropores can be reverted to their original shapes by either thermal annealing or UV irradiation. As such, this strategy expands the rich diversity of SMPs accessible.

'Physical Colors' published in 'Encyclopedia of Nanotechnology'