Publications by authors named "Otavio Augusto Titton Dias"

The synergistic effect of single-crystal structure and dual doping in Li-rich cobalt-free cathode materials was thoroughly investigated. Lithium-ion pouch cells employing Sb/Sn doped LiMnNiO and graphite exhibited a specific capacity of 191.01 mA h g at 1C rate and exceptionally stable performance upon cycling, with capacity retention of 87.

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Lithium-sulfur batteries (LSBs) show promise for achieving a high energy density of 500 W h kg, despite challenges such as poor cycle life and low energy efficiency due to sluggish redox kinetics of lithium polysulfides (LiPSs) and sulfur's electronic insulating nature. We present a novel 2D TiC Mxene on a 2D graphitic carbon nitride (g-CN) heterostructure designed to enhance LiPS conversion kinetics and adsorption capacity. In a pouch cell configuration with lean electrolyte conditions (∼5 μL mg), the g-CN-Mx/S cathode exhibited excellent rate performance, delivering ∼1061 mA h g at C/8 and retaining ∼773 mA h g after 190 cycles with a Coulombic efficiency (CE) of 92.

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Regioselectively substituted nanocellulose was synthesized by protecting the primary hydroxyl group. Herein, we took advantage of the different reactivities of primary and secondary hydroxyl groups to graft large capping structures. This study mainly focuses on regioselective installation of trityl protecting groups on nanocellulose chains.

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The design and high-throughput manufacturing of thin renewable energy devices with high structural and atomic configurational stability are crucial for the fabrication of green electronics. Yet, this concept is still in its infancy. In this work, we report the extraordinary durability of thin molecular interlayered organic flexible energy devices based on chemically tuned cellulose nanofiber transparent films that outperform glass by decreasing the substrate weight by 50%.

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Photoresponsive functionalized nanofilms were prepared via radical polymerization of carbazole units on a nanofibrillated cellulose (NFC) backbone via one-pot procedure. Herein, NFC was functionalized with active carbazole units as pendant organic moieties. The nanofilms were characterized by UV-vis and fluorescence spectroscopy, Fourier transformed infrared (FTIR) and Raman spectroscopy, C NMR and proton NMR spectra, contact angle analysis, mechanical testing, and scanning electron microscopy (SEM).

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This research work is the first to report thermal stability, heat deformation resistance, and crystallization behavior of a Polyethylene (PE)-based biphasic polyolefin system reinforced with Reduced Graphene Oxide (RGO), which was obtained through Graphene Oxide (GO) chemical reduction. Polypropylene (PP) represented the polymeric dispersed phase. A strategic PE/PP/RGO manufacturing procedure was employed to thermodynamically localize RGO at the PE/PP interface, as confirmed by Transmission Electron Microscopy (TEM), bringing a uniform micro phase dispersion into the macro phase.

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Novel and unique applications of nanocellulose are largely driven by the functional attributes governed by its structural and physicochemical features including excellent mechanical properties and biocompatibility. In recent years, thousands of groundbreaking works have helped in the development of targeted functional nanocellulose for conductive, optical, luminescent materials, and other applications. The growing demand for sustainable and renewable materials has led to the rapid development of greener methods for the design and fabrication of high-performance green nanomaterials with multiple features, and consequently new challenges and opportunities.

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Industrial ecology, sustainable manufacturing, and green chemistry have been considered platform-based approaches to the reduction of the environmental footprint. Recently, nanofibrillated cellulose (NFC) has gained significant interest due to its mechanical properties, biodegradability, and availability. These outstanding properties of NFC have encouraged the development of a more sustainable substrate for electronics.

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