Yuan Zhang

Liquid crystals of anisotropic colloids are of great significance in the preparation of their ordered macroscopic materials, for example, in the cases of carbon nanotubes and graphene. Here, we report a facile and scalable spinning process to prepare neat "core-shell" structured graphene aerogel fibers and three-dimensional cylinders with aligned pores from the flowing liquid crystalline graphene oxide (GO) gels. The uniform alignment of graphene sheets, inheriting the lamellar orders from GO liquid crystals, offers the porous fibers high specific tensile strength (188 kN m kg(-1)) and the porous cylinders high compression modulus (3.3 MPa). The porous graphene fibers have high specific surface area up to 884 m(2) g(-1) due to their interconnected pores and exhibit fine electrical conductivity (2.6 × 10(3) to 4.9 × 10(3) S m(-1)) in the wide temperature range of 5-300 K. The decreasing conductivity with decreasing temperature illustrates a typical semiconducting behavior, and the 3D interconnected network of 2D graphene sheets determines a dual 2D and 3D hopping conduction mechanism. The strong mechanical strength, high porosity, and fine electrical conductivity enable this novel material of ordered graphene aerogels to be greatly useful in versatile catalysts, supercapacitors, flexible batteries and cells, lightweight conductive fibers, and functional textiles.

Flexible pressure sensors that have high sensitivity, high linearity, and a wide pressure-response range are highly desired in applications of robotic sensation and human health monitoring. The challenge comes from the incompressibility of soft materials and the stiffening of microstructures in the device interfaces that lead to gradually saturated response. Therefore, the signal is nonlinear and pressure-response range is limited. Here, we show an iontronic flexible pressure sensor that can achieve high sensitivity (49.1 kPa–1), linear response (R2 > 0.995) over a broad pressure range (up to 485 kPa) enabled by graded interlocks of an array of hemispheres with fine pillars in the ionic layer. The high linearity comes from the fact that the pillar deformation can compensate for the effect of structural stiffening. The response-relaxation time of the sensor is <5 ms, allowing the device to detect vibration signals with frequencies up to 200 Hz. Our sensor has been used to recognize objects with different weights based on machine learning during the gripper grasping tasks. This work provides a strategy to make flexible pressure sensors that have combined performances of high sensitivity, high linearity, and wide pressure-response range.

Flexible pressure sensors are one of the vital component units in the next generation of wearable electronics for monitoring human physiological signals. In order to improve the sensing properties of the sensors, we demonstrate flexible, tunably resistive pressure sensors based on elastic microstructured polydimethylsiloxane (PDMS) film via a simple, low-cost colloid self-assembly technology, which uses monodispersed polystyrene (PS) microspheres as monolayer and an ordered sacrificial template. The sensors exhibit high sensitivity of −15 kPa–1 under low pressure (<100 Pa), with fast response time (<100 ms), high stability over 1000 cycles of pressure loading/unloading, low-pressure detection limit of 4 Pa, and wide working pressure regime (<5 kPa) by optimizing the size of PS microspheres. Moreover, the multipixel arrays of the pressure sensor are fabricated to illustrate the sensing ability of space pressure distribution. The developed flexible pressure sensors are successfully used to detect human neck pulse, show great promise for monitoring human body motions, and have potential applications in wearable devices.

Multimodal: Gold nanorods are coated with silica/polymer mutilayers, doped with surface-enhance Raman scattering (SERS) and fluorescence agents as well as photosensitizers. The structural and optical properties are tunable and stable in solutions and in living bodies. A real-time and specific in vivo SERS and fluorescence detection method using this structure is applied for tumor detection and subsequent photodynamic therapy (PDT). Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by 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.