The recent booming development of wearable electronics urgently calls for high-performance flexible strain sensors. To date, it is still a challenge to manufacture flexible strain sensors with superb sensitivity and a large workable strain range simultaneously. Herein, a facile, quick, cost-effective, and scalable strategy is adopted to fabricate novel strain sensors based on reduced graphene oxide woven fabrics (GWF). By pyrolyzing commercial cotton bandages coated with graphene oxide (GO) sheets in an ethanol flame, the reduction of GO and the pyrolysis of the cotton bandage template can be synchronously completed in tens of seconds. Due to the unique hierarchical structure of the GWF, the strain sensor based on GWF exhibits large stretchability (57% strain) with high sensitivity, inconspicuous drift, and durability. The GWF strain sensor is successfully used to monitor full-range (both subtle and vigorous) human activities or physical vibrational signals of the local environment. The present work offers an effective strategy to rapidly prepare low-cost flexible strain sensors with potential applications in the fields of wearable electronics, artificial intelligence devices, and so forth.

No abstract

A honeycomb‐like 3D N/S co‐doped porous carbon‐coated cobalt sulfide (CoS, Co9S8, and Co1– xS) composite (CS@PC) is successfully prepared using polyacrylonitrile (PAN) as the nitrogen‐containing carbon source through a facile solvothermal method and subsequent in situ conversion. As an anode for lithium‐ion batteries (LIBs), the CS@PC composite exhibits excellent electrochemical performance, including high reversible capacity, good rate capability, and cyclic stability. The composite electrode delivers specific capacities of 781.2 and 466.0 mAh g−1 at 0.1 and 5 A g−1, respectively. When cycled at a current density of 1 A g−1, it displays a high reversible capacity of 717.0 mAh g−1 after 500 cycles. The ability to provide this level of performance is attributed to the unique 3D multi‐level porous architecture with large electrode–electrolyte contact area, bicontinuous electron/ion transport pathways, and attractive structure stability. Such micro‐/nanoscale design and engineering strategies may also be used to explore other nanocomposites to boost their energy storage performance.

No abstract

Numerous studies have reported that the enhancement of rate capability of carbonaceous anode by heteroatom doping is due to the increased diffusion‐controlled capacity induced by expanding interlayer spacing. However, percentage of diffusion‐controlled capacity is less than 30% as scan rate is larger than 1 mV s−1, suggesting there is inaccuracy in recognizing principle of improving rate capability of carbonaceous anode. In this paper, it is found that the heteroatom doping has little impact on interlayer spacing of carbon in bulk phase, meaning that diffusion‐controlled capacity is hard to be enhanced by doping. After synergizing with tensile stress, however, the interlayer spacing in subsurface region is obviously expanded to 0.40 nm, which will increase the thickness of accessible subsurface region at high current density. So SRNDC‐700 electrodes display a high specific capacity of 160.6 and 69.5 mAh g−1 at 20 and 50 A g−1, respectively. Additionally, the high reversibility of carbon structure insures ultralong cycling stability and hence attenuation of SRNDC‐700 is only 0.0025% per cycle even at 10 A g−1 for 6000 cycles. This report sheds new insight into mechanism of improving electrochemical performance of carbonaceous anode by doping and provides a novel design concept for doping carbon.