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Real Time Tracking of Nanoconfined Water-Assisted Ion Transfer in Functionalized Graphene Derivatives Supercapacitor Electrodes

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216305%3A26620%2F24%3APU152401" target="_blank" >RIV/00216305:26620/24:PU152401 - isvavai.cz</a>

  • Alternative codes found

    RIV/61989592:15640/24:73626051 RIV/61989100:27240/24:10255271 RIV/61989100:27640/24:10255271 RIV/61989100:27740/24:10255271

  • Result on the web

    <a href="https://onlinelibrary.wiley.com/doi/10.1002/advs.202307583" target="_blank" >https://onlinelibrary.wiley.com/doi/10.1002/advs.202307583</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/advs.202307583" target="_blank" >10.1002/advs.202307583</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Real Time Tracking of Nanoconfined Water-Assisted Ion Transfer in Functionalized Graphene Derivatives Supercapacitor Electrodes

  • Original language description

    Water molecules confined in nanoscale spaces of 2D graphene layers have fascinated researchers worldwide for the past several years, especially in the context of energy storage applications. The water molecules exchanged along with ions during the electrochemical process can aid in wetting and stabilizing the layered materials resulting in an anomalous enhancement in the performance of supercapacitor electrodes. Engineering of 2D carbon electrode materials with various functionalities (oxygen (& horbar;O), fluorine (& horbar;F), nitrile (& horbar;C equivalent to N), carboxylic (& horbar;COOH), carbonyl (& horbar;C & boxH;O), nitrogen (& horbar;N)) can alter the ion/water organization in graphene derivatives, and eventually their inherent ion storage ability. Thus, in the current study, a comparative set of functionalized graphene derivatives-fluorine-doped cyanographene (G-F-CN), cyanographene (G-CN), graphene acid (G-COOH), oxidized graphene acid (G-COOH (O)) and nitrogen superdoped graphene (G-N) is systematically evaluated toward charge storage in various aqueous-based electrolyte systems. Differences in functionalization on graphene derivatives influence the electrochemical properties, and the real-time mass exchange during the electrochemical process is monitored by electrochemical quartz crystal microbalance (EQCM). Electrogravimetric assessment revealed that oxidized 2D acid derivatives (G-COOH (O)) are shown to exhibit high ion storage performance along with maximum water transfer during the electrochemical process. The complex understanding of the processes gained during supercapacitor electrode charging in aqueous electrolytes paves the way toward the rational utilization of graphene derivatives in forefront energy storage applications. Covalent functionalization and doping of graphene surfaces -featuring groups such as oxygen, cyano-, carbon-fluorine, carboxyl groups, and nitrogen heteroatoms- significantly affects water-assisted ion transfer as monitored

  • 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

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2024

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Advanced Science

  • ISSN

    2198-3844

  • e-ISSN

  • Volume of the periodical

    11

  • Issue of the periodical within the volume

    39

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    18

  • Pages from-to

    „“-„“

  • UT code for WoS article

    001284575600001

  • EID of the result in the Scopus database

    2-s2.0-85200452763