Publications by authors named "Enn Lust"

Article Synopsis
  • This review focuses on how different electrochemical characterization methods affect the assessment of catalyst activity, particularly in the oxygen reduction reaction (ORR) using supported catalysts.
  • The performance of proton exchange membrane fuel cells (PEMFCs) is crucial for enhancing hydrogen use in transportation and energy, and improving ORR catalyst efficiency and durability is a key area for research.
  • While traditional methods like RDE and MEA have limitations, newer techniques such as floating electrodes (FE) and gas diffusion electrodes (GDE) provide better insights into catalyst behavior and efficiency under real operating conditions.
View Article and Find Full Text PDF

Virucidal filter materials were prepared by electrospinning a solution of 28 wt % poly(vinylidene difluoride) in N,N-dimethylacetamide without and with the addition of 0.25 wt %, 0.75 wt %, 2.

View Article and Find Full Text PDF

Highly microporous adsorbents have been under considerable scrutiny for efficient adsorptive storage of H. Of specific interest are sustainable, chemically activated, microporous carbon adsorbents, especially from renewable and organic precursor materials. In this article, six peat-derived microporous carbon materials were synthesized by chemical activation with ZnCl.

View Article and Find Full Text PDF

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 () 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.

View Article and Find Full Text PDF

Influence of electrode potential on the electrochemical behavior of a 1-ethyl-3-methylimidazolium tetrafluoroborate (EMImBF₄) solution containing 5 wt % 1-ethyl-3-methylimidazolium bromide (EMImBr) has been investigated using electrochemical and synchrotron-initiated high-resolution in situ X-ray photoelectron spectroscopy (XPS) methods. Observation of the Br 3d in situ XPS signal, collected in a 5 wt % EMImBr solution at an EMImBF₄⁻vacuum interface, enabled the detection of the start of the electrooxidation process of the Br⁻ anion to Br₃⁻ anion and thereafter to the Br₂ at the micro-mesoporous carbon electrode, polarized continuously at the high fixed positive potentials. A new photoelectron peak, corresponding to B⁻O bond formation in the B 1s in situ XPS spectra at ≤ ⁻1.

View Article and Find Full Text PDF
Article Synopsis
  • Researchers are exploring fluid electrode materials in electrochemical flow capacitors (EFC), which allow for continuous charging and discharging, improving energy storage efficiency compared to traditional solid electrodes.
  • The study presents a new carbonaceous suspension electrode using carboxymethyl cellulose sodium salt (CMC-Na) that enhances electrochemical performance when suspended in aqueous media.
  • Experimental results show that the flow electrode achieved a capacitance of 0.3 F/L, energy density of 7 mWh/kg, and a round trip efficiency of 70%, indicating significant potential for scalable energy storage solutions.
View Article and Find Full Text PDF

The present study introduces a modified melt-electrospinning (MES) method for fabricating the melt-electrospun fibers (MSFs) of a poorly water-soluble drug and carrier polymer. The MES of poorly water-soluble model drug indomethacin (IND) and hydrophilic carrier polymer, Soluplus® (SOL) were prepared at a 1:3 drug-polymer weight ratio. Water was used as an external plasticizer to regulate a MES processing temperature and to improve fiber formation.

View Article and Find Full Text PDF

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.

View Article and Find Full Text PDF

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.

View Article and Find Full Text PDF