Issue 1, 2025

Exploring the potential of malononitrile functionalized donor–acceptor systems for non-volatile memory device applications

Abstract

A novel series of D-bridge-A type organic small molecules has been designed, synthesized, and evaluated for non-volatile resistive switching write-once read-many (WORM) memory application. This study explores structure–property relationships by coupling electron-deficient malononitrile units with donors such as dibenzofuran, dibenzothiophene, and triphenylamine. Photophysical investigations revealed significant intramolecular charge transfer interaction, while electrochemical analyses demonstrated optimal band gaps ranging from 2.20 to 3.10 eV. All synthesized compounds exhibited robust, non-volatile, resistive switching memory capabilities, with ON/OFF ratios spanning 102 to 103. The lowest recorded threshold voltage was −1.25 V, and devices demonstrated substantial stability with retention times of 103 s. Notably, triphenylamine-based compounds displayed superior memory performance compared to their counterparts. The solubility of the compounds in common organic solvents suggests that they are viable for cheap fabrication techniques. Density functional theory calculations were used to visualize the key molecular orbitals and support the proposed mechanisms for resistive switching. The strategic implementation of equipotential donors and acceptors is highly desirable. This well-rounded approach guarantees optimal performance and fosters broader applicability of these devices.

Graphical abstract: Exploring the potential of malononitrile functionalized donor–acceptor systems for non-volatile memory device applications

Supplementary files

Article information

Article type
Paper
Submitted
24 Aug 2024
Accepted
27 Nov 2024
First published
27 Nov 2024

Phys. Chem. Chem. Phys., 2025,27, 129-137

Exploring the potential of malononitrile functionalized donor–acceptor systems for non-volatile memory device applications

R. Gokul, R. Gayathri, P. M. Imran, N. S. P. Bhuvanesh and S. Nagarajan, Phys. Chem. Chem. Phys., 2025, 27, 129 DOI: 10.1039/D4CP03313B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements