Peat-derived hard carbon electrodes with superior capacity for sodium-ion batteries.

Herein we demonstrate how peat, abundant and cheap biomass, can be successfully used as a precursor to synthesize peat-derived hard carbons (PDCs), applicable as electrode materials for sodium-ion batteries (SIB). The PDCs were obtained by pre-pyrolysing peat at 300-800 °C, removing impurities with base-acid solution treatment and thereafter post-pyrolysing the materials at temperatures (T) from 1000 to 1500 °C. By modification of pre- and post-pyrolysis temperatures we obtained hard carbons with low surface areas, optimal carbonization degree and high electrochemical Na+ storage capacity in SIB half-cells. The best results were obtained when pre-pyrolysing peat at 450 °C, washing out the impurities with KOH and HCl solutions and then post-pyrolysing the obtained carbon-rich material at 1400 °C. All hard carbons were electrochemically characterized in half-cells (vs. Na/Na+) and capacities as high as 350 mA h g-1 at 1.5 V and 250 mA h g-1 in the plateau region (E < 0.2 V) were achieved at charging current density of 25 mA g-1 with an initial coulombic efficiency of 80%.

Low concentrated carbonaceous suspensions assisted with carboxymethyl cellulose as electrode for electrochemical flow capacitor.

The search for efficient energy storage devices has recently led to the introduction of a fluid electrode material employing electrochemical flow capacitors (EFC). Unlike the classical solid electrode film containing capacitors, where the electrode material is fixed to the current collectors and capacitance is therefore limited with an active surface area of porous electrode, the flow electrodes offer new design opportunities which enable fully continuous charging/discharging processes as well as easily scalable systems. Here we describe the successful incorporation of the carboxymethyl cellulose sodium salt (CMC-Na) assisted carbonaceous suspension electrode in aqueous media for the electrochemical flow capacitor concept and demonstrate the electrochemical charge storage in flowable electrodes using a cation conductive membrane as separator in a double-pipe flow-electrode module. Experimental results were combined with computer simulations (FEM) to specify limiting processes EFC charging. The flow-electrode slurry is based on 0.1 M Na2SO4, 3 wt% CMC-Na and activated carbon powder suspended in water. During continuous operation of the system, the capacitance of the flow electrode reached to 0.3 F/L providing the energy and current densities of 7 mWh/kg and 56 mW/L, respectively. Additionally, we report a 70% round trip efficiency calculated during charging and discharging of the cell between 0 V and +0.75 V, while applying the current density of 1.6 mA/kg. The double-pipe flow-electrode module is easily expandable for transportation of large volumes of electrode material.

In situ hydrodynamic spectroscopy for structure characterization of porous energy storage electrodes.

A primary atomic-scale effect accompanying Li-ion insertion into rechargeable battery electrodes is a significant intercalation-induced change of the unit cell volume of the crystalline material. This generates a variety of secondary multiscale dimensional changes and causes a deterioration in the energy storage performance stability. Although traditional in situ height-sensing techniques (atomic force microscopy or electrochemical dilatometry) are able to sense electrode thickness changes at a nanometre scale, they are much less informative concerning intercalation-induced changes of the porous electrode structure at a mesoscopic scale. Based on a electrochemical quartz-crystal microbalance with dissipation monitoring on multiple overtone orders, herein we introduce an in situ hydrodynamic spectroscopic method for porous electrode structure characterization. This new method will enable future developments and applications in the fields of battery and supercapacitor research, especially for diagnostics of viscoelastic properties of binders for composite electrodes and probing the micromechanical stability of their internal electrode porous structure and interfaces.

Microporous and mesoporous carbide-derived carbons for strain modification of electromechanical actuators.

Low-voltage stimuli-responsive actuators based on carbide-derived carbon (CDC) porous structures were demonstrated. Bending actuators showed a differential electromechanical response defined by the porosity of the CDC used in the electrode layer. Highly porous CDCs prepared from TiC (mainly microporous), B4C (micromesoporous), and Mo2C (mainly mesoporous) precursors were selected to demonstrate the influence of porosity parameters on the electromechanical performance of actuators. CDC-based bending-type actuators showed a porosity-driven displacement response over a frequency range of 200 to 0.005 Hz at an applied excitation voltage of ±2 V. The displacement response of the CDC actuators increased with an increasing number of mesopores in the electrode layer, and the generated strain of the bending actuators was proportional to the total porosity (micropores and mesopores) of the CDC. The modifiable electromechanical response that arises from the precise porosity control attained through tailoring the CDC architecture demonstrates that these actuators hold great promise for smart, low-voltage-driven actuation devices.