Over the span of the past decade, carbon dots (CDs) synthesized from renewable organic resources (organic CDs) have gathered a considerable amount of attention for their photoluminescent properties. This review will focus on organic CDs synthesized using clean chemistry and conventional synthetic chemistry from organic sources and their fluorescence mechanisms, such as quantum confinement effect and surface/edge defects, before outlining their performance in electronic applications, including organic photovoltaic devices, organic light-emitting devices, biosensors, supercapacitors, and batteries. The various organic resources and methods of organic CDs synthesis are briefly covered. Many challenges remain before the adoption of CDs can become widespread; their characterization, structure, functionality, and exact photoluminescent mechanism all require additional research. This review aims to summarize the current research outcomes and highlight the area where further research is needed to fully use these materials.
Microfibers of kraft lignin blended with poly(ethylene oxide) (PEO) were produced by electrospinning of the solution of lignin and high molecular weight poly(ethylene oxide) (PEO) in alkaline water. Interactions between lignin and PEO in alkaline aqueous solutions create association complexes, which increases the viscosity of the solution. The effect of polymer concentration, PEO molecular weight, and storage time of solution before spinning on the morphology of the fibers was studied. It showed that after one day the viscosity dropped and fiber diameter decreased. Results from the solutions in alkaline water and N,N-dimethylformamide (DMF) with different polymer concentrations were compared. The 7 wt % of (Lignin/PEO: 95/5 wt/wt) in alkaline aqueous solution was successfully spun and the ratio of PEO in lignin/PEO mixture could be further reduced. In comparison, higher concentrations were needed to prepare a spinning solution in DMF and fiber diameters were in a much smaller range. The final target of spinning lignin is to produce carbonized fibers. Fibers spun from aqueous solutions had lower PEO content, which is a big advantage for the carbonization process as it reduces the challenges regarding melting of the fibers or void creation during carbonization. Furthermore, the larger diameter of these fibers inhibits disintegration of the carbonized fibers, which happens due to the mass loss during the process.
Solution blends of poly(l-lactic acid) (PLLA) and poly(3-hyroxybutyrate-co-3-hydroxyvalerate) (PHBV) in chloroform/DMF were electrospun at room temperature on a stationary collection plate. Polymer blend ratio, PHBV hydroxyvalerate content, solvent ratio, polymer concentration, and electrospinning process parameters were varied to determine optimal electrospinning conditions. The success of each formulation at producing nonwoven mats of continuous submicron diameter fibers was evaluated by optical and scanning electron microscopy. The diameter of the blend fibers was larger than electrospun fibers of either neat electrospun polymer, with a higher PLLA ratio favoring a porous surface morphology and higher PHBV ratios favoring beaded fiber morphology. Differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) were used to analyze the thermal properties of the fibrous mats. The glass transition temperatures of the fibers from blends decreased as the PHBV weight ratio increased. The crystallinity of the PHBV fraction decreased as the ratio of the polymer in the blend decreased, whereas the crystallinity of PLLA was unaffected by the blend ratio. Dynamic mechanical analysis (DMA) indicated that the tensile strength of electrospun PHBV was improved by blending. Porous PLLA/PHBV electrospun fibers have potential for applications that need a high surface to volume ratio such as filtration, biomedical, energy storage devices, etc.
Greenhouse gas emissions and environmental impacts of petroleum-based fuels and materials have necessitated the development of renewable resource-based alternatives. In the process to extract cellulose for converting it to bioethanol (bio-based gasoline) large quantities of lignin are produced as the main byproduct-making it useful for further processing application for sustainable materials. Lignin is the second abundant source of renewable carbon with an aromatic structure which makes it a potential candidate for carbon fiber production. Since lignin can be dissolved in a variety of organic and non-organic solvents, electrospinning has been used to produce precursor fibers for carbon nanofiber production. These carbon nanofibers have been tested as a potentially sustainable alternative for the current non-renewable electrodes in energy storage and conversion devices such as supercapacitors. Using lignin by-products from the fuel energy sector in making devices for electrical energy sector provides a great opportunity for promoting a circular economy from sustainable materials while also contributing to researching alternative sustainable materials in light of a global pandemic. This review presents a summary of the processing conditions for electrospinning different varieties of lignin, characterization of the electrospun fibers and the carbonization conditions for converting fibers. Different techniques that of the structural properties of the precursor fibers, characteristics of carbon nanofibers and their performance in energy storage devices are discussed. Compared to the other published reviews in this field, this review aims to present the current knowledge on material-processing-lignin-carbon fibers properties relationship.
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