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        Pigment-Cellulose Nanofibril Composite and Its Application as a Separator-Substrate in Printed Supercapacitors

        Katariina Torvinen,Suvi Lehtimäki,Janne T. Keränen,Jenni Sievänen,Jari Vartiainen,Erkki Hellén,Donald Lupo,Sampo Tuukkanen 대한금속·재료학회 2015 ELECTRONIC MATERIALS LETTERS Vol.11 No.6

        Pigment-cellulose nanofibril (PCN) composites were manufactured in a pilot line and used as a separator-substrate in printed graphene and carbon nanotube supercapacitors. The composites consisted typically of 80% pigment and 20% cellulose nanofibrils (CNF). This composition makes them a cost-effective alternative as a substrate for printed electronics at high temperatures that only very special plastic films can nowadays stand. The properties of these substrates can be varied within a relatively large range by the selection of raw materials and their relative proportions. A semiindustrial scale pilot line was successfully used to produce smooth, flexible, and nanoporous composites, and their performance was tested in a double functional separator-substrate element in supercapacitors. The nanostructural carbon films printed on the composite worked simultaneously as high surface area active electrodes and current collectors. Low-cost supercapacitors made from environmentally friendly materials have significant potential for use in flexible, wearable, and disposable low-end products.

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        New insights into the chemical activation of lignins and tannins using K2CO3—a combined thermoanalytical and structural study

        Guizani Chamseddine,Widsten Petri,Siipola Virpi,Paalijärvi Riina,Berg Jonathan,Pasanen Antti,Kalliola Anna,Torvinen Katariina 한국탄소학회 2024 Carbon Letters Vol.34 No.1

        Engineering of activated carbons (ACs) through chemical activation of organic precursors has been extensively studied for a wide variety of biopolymers, biomasses, wastes and other fossil-based precursors. Despite huge efforts to engineer evermore performant and sustainable ACs, “searching-for-the-best-recipe” type of studies are more the rule than the exception in the published literature. Emerging AC applications related to energy and gas storage require strict control of the AC properties and a better understanding of the fundamentals underlying their engineering. In this study, we provide new insights into the K2CO3 chemical activation of plant-based polyphenols—lignins and tannins—through careful thermoanalytical and structural analyses. We showed for the the first time that the reactivity of polyphenols during K2CO3 chemical activation depends remarkably on their purity and structural properties, such as their content of inorganics, OH functionalities and average molecular weight. We also found that the burn-off level is proportional to the K2CO3/lignin impregnation ratio (IR), but only within a certain range—high impregnation ratios are not needed, unlike often reported in the literature. Furthermore, we showed for the first time that the K2CO3 chemical activation of different carbon surfaces from lignins and tannins can be modelled using simple global solid-state decomposition kinetics. The identified activation energies lay in the range of values reported for heterogenous gas-carbon surface gasification reactions (O2-C, H2O-C, or CO2-C) in which the decomposition of C(O) surface complexes is the common rate-limiting step.

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