Flexible supercapacitors (SCs) with compact configuration are ideal energy storage devices for portable electronics, owing to their original advantages (e.g., fast charging/discharging). To effectively reduce the volume of SCs, an integrated electrode of free-standing polyaniline (PANI)/single-wall carbon nanotube (SWCNT) film with high performance has been developed via a facile solution deposition method, which can be employed as current collector and active material in the meantime. Thanks to the strong π-π interactions between PANI and CNTs, an efficient conductive network with ordered PANI molecular chains is formed in this hybrid film electrode, which is beneficial for the ion diffusion process and fast redox reaction resulting in a high capacitance of 446 F g and outstanding cycling stability, achieving 98% retention over 13 000 cycles. Predictably, solid-state SCs constructed by this free-standing PANI/SWCNT film electrode exhibited remarkable mechanical stability and flexibility in a compact configuration, let alone its excellent capacitive performance (218 F g). Moreover, the highest energy density of flexible solid-state SC reached 19.45 Wh kg at a power density of 320.5 W kg, further indicating a good potential as an energy storage device. This work would inspire other simple process techniques for high-performance flexible SCs, catering to the demand of portable electronic devices.
Structural colors of high purity and brightness are desired in various applications. This study presents a general strategy of selecting the appropriate material and thickness of each layer to create high‐purity reflective colors in a classic asymmetric Fabry–Pérot cavity structure based on a dielectric–absorber–dielectric–metal multilayered configuration. Guided by the derived complex refractive index of the ideal absorber layer, an effective absorbing bilayer medium consisting of two ultrathin lossy films is used to improve the color purity of reflective colors by suppressing the reflection of its complementary colors with the enhanced optical absorption. Highly pure red, green, and blue reflective colors are designed and experimentally demonstrated employing different effective bilayer absorbers. Due to the high refractive index of the dielectric material, the colored structures exhibit great angle‐robust appearance (blue and red colors are up to ±60°, and green color is up to ±45°). The generalized design principles and the proposed method of using effective bilayer absorbers open up new avenues for realizing high‐purity thin‐film structural colors with more materials selections.
Plants have evolved an array of adaptive responses to cope with phosphate (Pi) starvation. These responses are mainly controlled at the transcriptional level. In Arabidopsis, PHR1, a member of the MYB-CC transcription factor family, is a key component of the central regulatory system controlling plant transcriptional responses to Pi starvation. Its homologs in the MYB-CC family, PHL1 (PHR1-LIKE 1), PHL2, and perhaps also PHL3, act redundantly with PHR1 to regulate plant Pi starvation responses. The functions of PHR1’s closest homolog in this family, PHL4, however, have not been characterized due to the lack of its null mutant. In this work, we generated two phl4 null mutants using the CRISPR/Cas9 technique and investigated the functions of PHL4 in plant responses to Pi starvation. The results indicated that the major developmental, physiological, and molecular responses of the phl4 mutants to Pi starvation did not significantly differ from those of the wild type. By comparing the phenotypes of the phr1 single mutant and phr1phl1 and phr1phl4 double mutants, we found that PHL4 also acts redundantly with PHR1 to regulate plant Pi responses, but that its effects are weaker than those of PHL1. We also found that the overexpression of PHL4 suppresses plant development under both Pi-sufficient and -deficient conditions. Taken together, the results indicate that PHL4 has only a minor role in the regulation of plant responses to Pi starvation and is a negative regulator of plant development.
International audienceCathode structure plays a vital role in lithium-air battery for that it can provide space for discharged products accommodation and free path for oxygen, e− and Li+ transport. However, pore blockage, cathode passivation and degradation all result in low discharge rates and poor cycling capability. To get rid of these predicaments, a novel highly conductive dual pore carbon aerogel based air cathode is fabricated to construct a lithium-air battery, which exhibits 18 to 525 cycles in the LiTFSI/sulfolane electrolyte at a current density varying from 1.00 mA cm−2 to 0.05 mA cm−2, accompanied by a high energy efficiency of 78.32%. We postulate that the essence lies in that the as-prepared air cathode inventively create a suitable tri-phase boundary reaction zone, facilitating oxygen and Li+ diffusion in two independant pore channels, thus realizing a relative higher discharge rate capability, lower pore blockage and cathode passivation. Further, pore structure, carbon loading, rate capability, discharge depth and the air's effect are exploited and coordinated, targeting for a high power and reversible lithium-air battery. Such nano-porous carbon aerogel air cathode of novel dual pore structure and material design is expected to be an attractive alternative for lithium-air batteries and other lithium based batteries
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