On generalization for Tribonacci Trigintaduonions

Saini, Kavita; Raj, Kuldip

doi:10.1007/s13226-021-00067-y

Cited by 5 publications

(5 citation statements)

References 10 publications

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“…Compared to pure PET, the diffraction peaks of KH556@PET all shift to higher angles, which indicates that the defects of KH556@PET increase. [47][48][49] This is due to the fact that KH556 can create an organic film layer on the surface of PET, resulting in an increase in the amount of amorphous state on the surface of PET, decreasing the crystallinity of PET. Moreover, the development of organic thin films can prevent PET molecules from being arranged in an orderly fashion on the surface, which will also reduce PET's crystallinity.…”

Section: Resultsmentioning

confidence: 99%

Revamping Triboelectric Output by Deep Trap Construction

Wang,

Liu,

Feng

et al. 2024

Advanced Materials

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High output performance is critical for building triboelectric nanogenerators (TENGs) for future multifunctional applications. Unfortunately, the high triboelectric charge dissipation rate has a significant negative impact on its electrical output performance. Herein, a new tribolayer is designed through introducing self‐assembled molecules with large energy gaps on commercial PET fibric to form carrier deep traps, which improve charge retention while decreasing dissipation rates. The deep trap density of the PET increases by two orders of magnitude, resulting in an 86% reduction in the rate of charge dissipation and a significant increase in the charge density that can be accumulated on tribolayer during physical contact. The key explanation is that increasing the density of deep traps improves the dielectric's ability to store charges, making it more difficult for the triboelectric charges trapped by the tribolayer to escape from the deep traps, lowering the rate of charge dissipation. This TENG has a 1300% increase in output power density as a result of altering the deep trap density, demonstrating a significant improvement. This work describes a simple yet efficient method for building TENGs with ultra‐high electrical output and promotes their practical implementation in the sphere of the Internet of Things.

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Section: Resultsmentioning

confidence: 99%

Revamping Triboelectric Output by Deep Trap Construction

Wang,

Liu,

Feng

et al. 2024

Advanced Materials

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“…This wide range of conductivities is accessible and realized by modifying the dopant, post-treatment time, and redox state of CPs, making this ink formulation useful for applications such as ESD coatings and interfaces. 1,43 While not being the primary focus of this work, Fig. S13 and S14 (ESI †) show that the redox activity of post-treated PANI-PS-FS structures is essentially identical to that of PANI-DNNSA.…”

Section: Conductivity Tuning Via Post-print Processingmentioning

confidence: 96%

Additive manufacturing of polyaniline blends for lightweight structures with tunable conductivity

et al. 2023

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“…Whereas carbon based materials and metals suffer from bleeding, irreproducible results and meager dispersion. Blending conducting polymers with thermoplastics is an excellent solution to this problem because it not only improves conductivity but also adjusts conductivity based on the concentration of the conductive polymer in the blend 2,3 . In this consideration PANI is one of the promising conductive polymer because of its ease of polymerization, high environment stability, reasonably good electrical conductivity, and low cost material.…”

Section: Introductionmentioning

confidence: 99%

Preparation of polyaniline‐poly(ethylene‐vinyl acetate) film: Resistivity in the ESD range

Uppugalla

Srinivasan

2023

J of Applied Polymer Sci

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Films of polyaniline (PANI) salt with poly (ethylene‐vinyl acetate) (EVA) with two different PANI salts, PANI‐methane sulfonic acid (PANI‐MSA) and PANI‐p‐toluene sulfonic acid (PANI‐PTSA) are prepared by solution processing technique for electrostatic discharge (ESD) application. PANI‐MSA/PANI‐PTSA salts were synthesized by emulsion polymerization pathway then dispersed the PANI salt in xylene solvent. EVA was dissolved in xylene solvent. Series of PANI salt/EVA films were prepared by mixing a particular amount of PANI dispersion to a fixed amount of EVA solution and evaporated the solvent. PANI‐EVA films were evaluated by tensile strength, elongation at break and surface resistivity measurements. The results of PANI‐MSA/EVA films are compared with the results of PANI‐PTSA/EVA films. Also, PANI‐MSA/EVA and PANI‐PTSA/EVA solutions are coated on different substrates and measured their electrical resistivity for ESD application. Morphological study and thermal behaviors of PANI‐MSA/EVA films are carried through FE‐SEM and TGA respectively. Sphere morphology of EVA changed to swollen sheet like morphology with the addition of PANI, and the spaces between the sheets increased with the increase in PANI content. The surface resistivity of the EVA‐PANI films are found to be in the range of 104–108 Ω sq−1, which is suitable for ESD application.

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On generalization for Tribonacci Trigintaduonions

Cited by 5 publications

References 10 publications

Revamping Triboelectric Output by Deep Trap Construction

Revamping Triboelectric Output by Deep Trap Construction

Additive manufacturing of polyaniline blends for lightweight structures with tunable conductivity

Preparation of polyaniline‐poly(ethylene‐vinyl acetate) film: Resistivity in the ESD range

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