3 research outputs found
Nanoporous carbons from hydrothermally treated biomass as anode materials for lithium ion batteries
Biomass is transformed to carbon nanoparticles with surface-end groups called ‘hydrochar’ (HC) by an efficient and green hydrothermal carbonization (HTC) method. Three different approaches are used to introduce porosity to the HC: sole heat treatment, traditional potassium hydroxide (KOH) activation,
and environmentally benign magnesium oxide (MgO) templating. All the resulting microporous materials are tested as Li-ion intercalation hosts in lithium cells by using an 1 M LiPF6 in EC/DMC electrolyte solution. They all show stable reversible capacities at elevated current rates (1C), closely comparable to the maximum theoretical capacity of graphite. Among all the materials studied, the HC-MA with a surface area of 150 m2 g1 and obtained by MgO templating of the hydrochar shows the best cycling performance in lithium cell at room temperature (307 mAh g1 at cycle 100 at 1C). The HC-600 with the highest degree of aromaticity/order, lowest content of oxygen functional groups and surface area of 250 m2 g1, obtained by heating the hydrochar at 600 C under inert atmosphere, shows the best power and overall performance with its ability to sustain high discharge/charge rates (1C, 2C, 5C, 10C, 20C). These electrochemical performances attained with materials of reasonable specific surface areas – obtained by green, low cost and practical strategies – can address the space limitations in Li-ion battery applications by improving
volumetric energy densities
Dual-polymer electrochromic film characterization using bipotentiostatic control
We report an analytical method which allows the systematic variation of color states of pairs of electrochromic conjugated conducting polymers with simultaneous spectroelectrochemical and colorimetric characterization of the resulting color summation. This method measures colors by transmitting light through two polymer films stacked together in electrolyte and under separate potentiostatic control. The polymers that were used in this work are poly(3,4-ethylenedioxythiophene) (PEDOT), poly(3,4-propylenedioxypyrrole) (PProDOP), and dihexyl substituted poly(3,4-propylenedioxythiophene) (PProDOT-Hx2). These are all cathodically coloring polymers, PEDOT switching from a transmissive sky blue to a deep blue, PProDOP switching from a highly transmissive gray/blue to a brown and then to an orange, and PProDOT-Hx2 switching from a transmissive sky blue to a deep blue-purple color upon reduction. Coupling these polymers logically by the dual-polymer electrochromic film characterization technique led us to obtain new colors which were not observed when these polymers studied separately. For example; coupling PEDOT and PProDOP films in their neutral state resulted in a new red/brown color (L*=59 a*=25 b*=50) which is different from the original colors these polymers show in their neutral states, deep blue (L*=64 a*=-5 b*=-38) and orange (L*=76 a*=31 b*=75), respectively. A full palette of colors is accessible by coupling existing electrochromic polymers by this new bipotentiostatic technique