Novel sulfur (S) anchoring materials and the corresponding mechanisms for suppressing capacity fading are urgently needed to advance the performance of Li/S batteries. Here, we designed and synthesized a graphene-like oxygenated carbon nitride (OCN) host material that contains tens of micrometer scaled two-dimensional (2D) rippled sheets, micromesopores, and oxygen heteroatoms. N content can reach as high as 20.49 wt %. A sustainable approach of one-step self-supporting solid-state pyrolysis (OSSP) was developed for the low-cost and large-scale production of OCN. The urea in solid sources not only provides self-supporting atmospheres but also produces graphitic carbon nitride (g-C3N4) working as 2D layered templates. The S/OCN cathode can deliver a high specific capacity of 1407.6 mA h g(-1) at C/20 rate with 84% S utilization and retain improved reversible capacity during long-term cycles at high current density. The increasing micropores, graphitic N, ether, and carboxylic O at the large sized OCN sheet favor S utilization and trapping for polysulfides.
A natural self-regeneration step for urea derived graphitic carbon nitride with platinum nanoparticles is found by simply opening the system to air in the dark under ambient conditions, following its solar-driven hydrogen production. The produced peroxides deactivate the graphitic carbon nitride. Release of weakly bound peroxides on the polymeric semiconductor surface is a crucial process for regeneration.
A RGO/CNT hybrid electrode of porous structure is prepared through a surfactant-free solution method to construct a bimorph ionic actuator, showing wide frequency range responsive and highly repeatable (over a million times) and stable bending actuation performance.
Graphitic C3N4 (g-C3N4), as an advanced metal free photocatalyst, is known to be poorly exfoliated and dispersed in water from its powder form which has a layered structure, the intrinsic plane structure is not destroyed, and this has largely limited its application. In this work, we report our progress on successful sonication exfoliation of g-C3N4 nanosheets in graphene oxide (GO) aqueous solution. By making use of the substrate character of GO, g-C3N4 nanosheets of unvaried intrinsic structure were exfoliated and anchored on the GO surface, resulting in a GO/g-C3N4 hybrid. Moreover, the photocurrent of the hybrid was largely reinforced at the optimal weight fraction of GO. As a result, the corresponding photocatalytic performance of the hybrid with optimized photocurrent character was largely improved.
A composite actuator constructed from a carbon nanotube/biopolymer supramolecular structure (see figure) that can be driven by electrical stimulation independently without solution environment support is presented. It is lightweight, constructed from biocompatible components, and exhibits considerable actuation performance at low voltage, making it of great value for biomedical applications.
This paper reports novel electromechanical behavior for a natural biopolymer film due to the incorporation of a conductive carbon nanotube network. Through simple solution blending and casting, high weight fraction single-walled carbon nanotube-chitosan composite films were fabricated and exhibited electromechanical actuation properties with motion controlled by low alternating voltage stimuli in atmospheric conditions. Of particular interest and importance is that the displacement output imitated perfectly the electrical input signal in terms of frequency (<10 Hz) and waveform. Operational reliability was confirmed by stable vibration testing in air for more than 3000 cycles. Proposed electrothermal mechanism considering the alternating current-induced periodic thermal expansion and contraction of the composite film was discussed. The unique actuation performance of the carbon nanotube-biopolymer composite, coupled with ease of fabrication, low driven voltage, tunable vibration, reliable operation, and good biocompatibility, shows great possibility for implementation of dry actuators in artificial muscle and microsystems for biomimetic applications.
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