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Rewritable resistive memory effect in poly[N-(3-(9H-carbazol-9-yl)propyl)-methacrylamide] memristor

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61389013%3A_____%2F23%3A00580308" target="_blank" >RIV/61389013:_____/23:00580308 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11320/23:10475361

  • Result on the web

    <a href="https://pubs.rsc.org/en/content/articlelanding/2023/TC/D3TC03394E" target="_blank" >https://pubs.rsc.org/en/content/articlelanding/2023/TC/D3TC03394E</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/D3TC03394E" target="_blank" >10.1039/D3TC03394E</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Rewritable resistive memory effect in poly[N-(3-(9H-carbazol-9-yl)propyl)-methacrylamide] memristor

  • Original language description

    The synthesis of poly[N-(3-(9H-carbazol-9-yl)propyl)methacrylamide] (PCaPMA) is presented, along with its physical, photophysical, and electrical properties, revealing its promising potential for the application in bistable memory devices. The incorporation of the carbazole heterocycle, as a functional charge carrier transporting unit attached to a saturated polymethacryalamide backbone by a flexible alkyl chain, facilitates resistive switching by the applied voltage. Thin films of the polymer, sandwiched between Al or Au and ITO electrodes, exhibit rewriteable flash memory behavior with bistable conductivity with a setting voltage ranging from 2 to 4.5 V, achieving a current ON/OFF ratio exceeding 100. The device demonstrates a remarkable lifetime and remains persistent for more than 104 seconds under a static voltage of 0.5 V. The main physical mechanisms driving the resistive switching have been attributed to the electric field-induced reorientation of heterocycles, which modulates charge transport, and trapping/detrapping of charges in localized states within the bulk of the polymer. Memory persistence is strengthened by the physical crosslinking caused by hydrogen bonds between amide and carbonyl groups in the aliphatic side chains. This physical network further enhances the thermal and mechanical stability of the PCaPMA in comparison to similar polymers highlighting its potential as a suitable material for organic memory devices.

  • 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

    10404 - Polymer science

Result continuities

  • Project

    <a href="/en/project/LTAUSA19066" target="_blank" >LTAUSA19066: A study of polymeric memristors based on methacrylate polymers with pendant carbazole moieties</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2023

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Journal of Materials Chemistry C

  • ISSN

    2050-7526

  • e-ISSN

    2050-7534

  • Volume of the periodical

    11

  • Issue of the periodical within the volume

    48

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    13

  • Pages from-to

    17093-17105

  • UT code for WoS article

    001113938600001

  • EID of the result in the Scopus database

    2-s2.0-85179799203