All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

Volumetric Double-Layer Charge Storage in Composites Based on Conducting Polymer PEDOT and Cellulose

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216305%3A26620%2F21%3APU142123" target="_blank" >RIV/00216305:26620/21:PU142123 - isvavai.cz</a>

  • Result on the web

    <a href="https://pubs.acs.org/doi/10.1021/acsaem.1c01850" target="_blank" >https://pubs.acs.org/doi/10.1021/acsaem.1c01850</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/acsaem.1c01850" target="_blank" >10.1021/acsaem.1c01850</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Volumetric Double-Layer Charge Storage in Composites Based on Conducting Polymer PEDOT and Cellulose

  • Original language description

    Energy storage technology incorporating conducting polymers as the active component in electrode structures, in part based on natural materials, is a promising strategy toward a sustainable future. Electronic and ionic charge transport in poly(3,4-ethylenedioxythiophene) (PEDOT) provides fundamentals for energy storage, governed by volumetric PEDOT:counterion double layers. Despite extensive experimental investigations, a solid understanding of the capacitance in PEDOT-based nanocomposites remains unsatisfactory. Here, we report on the charge storage mechanism in PEDOT composited with cellulose nanofibrils (termed as "power paper") from three different perspectives: experimental measurements, density functional theory atomistic simulations, and device-scale simulations based on the NernstPlanck-Poisson equations. The capacitance of the power paper was investigated by varying the film thickness, charging currents, and electrolyte ion concentrations. We show that the volumetric capacitance of the power paper originates from electrostatic molecular double layers defined at atomistic scales, formed between holes, localized in the PEDOT backbone, and their counterions. Experimental galvanostatic cycling characteristics of the power paper is well reproduced within the electrostatic Nernst-PlanckPoisson model. The difference between the specific capacitance and the intrinsic volumetric capacitance is also outlined. Substantial oxygen reduction reactions were identified and recorded in situ in the vicinity of the power paper surface at negative potentials. Purging of dissolved oxygen from the electrolyte leads to the elimination of currents originating from the oxygen reduction reactions and allows us to obtain well-defined electrostatic-capacitive behavior (box-shaped cyclic voltammetry and triangular galvanostatic charge-discharge characteristics) at a large operational potential window from -0.6 V to +0.6 V. The obtained results reveal that the fundamental charge storage

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10405 - Electrochemistry (dry cells, batteries, fuel cells, corrosion metals, electrolysis)

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2021

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    ACS APPLIED ENERGY MATERIALS

  • ISSN

    2574-0962

  • e-ISSN

  • Volume of the periodical

    4

  • Issue of the periodical within the volume

    8

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    12

  • Pages from-to

    8629-8640

  • UT code for WoS article

    000688250200124

  • EID of the result in the Scopus database

    2-s2.0-85113764612