Related Experiment Video
Updated: Jun 5, 2025

Assembly and Characterization of Biomolecular Memristors Consisting of Ion Channel-doped Lipid Membranes
Published on: March 9, 2019
Exploring the potential of malononitrile functionalized donor-acceptor systems for non-volatile memory device
Ramachandran Gokul1, Ramesh Gayathri1, Predhanekar Mohamed Imran2
1Department of Chemistry, Organic Electronics Division, Central University of Tamil Nadu, Thiruvarur 610 005, India. snagarajan@cutn.ac.in.
Novel organic small molecules were developed for non-volatile resistive switching memory. Triphenylamine-based molecules showed superior performance, offering potential for low-cost electronic device fabrication.
Area of Science:
- Materials Science
- Organic Electronics
- Nanotechnology
Background:
- Organic small molecules are promising for advanced electronic applications.
- Resistive switching memory offers non-volatile data storage solutions.
- Understanding structure-property relationships is key to optimizing molecular design.
Purpose of the Study:
- To design, synthesize, and evaluate novel D-bridge-A organic small molecules for non-volatile resistive switching memory.
- To investigate the structure-property relationships influencing memory performance.
- To explore the potential for low-cost fabrication using these molecules.
Main Methods:
- Synthesis of D-bridge-A organic small molecules incorporating malononitrile units with various donors (dibenzofuran, dibenzothiophene, triphenylamine).
- Photophysical and electrochemical analyses to determine optical band gaps and intramolecular charge transfer.
- Fabrication and testing of memory devices to evaluate resistive switching characteristics (ON/OFF ratio, threshold voltage, retention time).
- Density functional theory (DFT) calculations to visualize molecular orbitals and elucidate switching mechanisms.
Main Results:
- All synthesized compounds demonstrated robust non-volatile resistive switching memory (WORM) with ON/OFF ratios from 10^2 to 10^3.
- Optimal band gaps ranged from 2.20 to 3.10 eV, indicating significant intramolecular charge transfer.
- Triphenylamine-based molecules exhibited superior memory performance.
- Low threshold voltage (-1.25 V) and long retention times (10^3 s) were achieved.
- Good solubility in organic solvents suggests suitability for cost-effective fabrication.
Conclusions:
- Novel D-bridge-A organic small molecules show significant potential for non-volatile WORM memory applications.
- Molecular design, particularly the choice of donor units, critically impacts memory performance.
- The developed molecules are viable for low-cost fabrication techniques, paving the way for practical applications.
- Strategic molecular design with equipotential donors and acceptors is crucial for optimizing device performance and applicability.
More Related Videos
10:40A Fabrication and Measurement Method for a Flexible Ferroelectric Element Based on Van Der Waals Heteroepitaxy
Published on: April 8, 2018
09:49In Situ Transmission Electron Microscopy with Biasing and Fabrication of Asymmetric Crossbars Based on Mixed-Phased a-VOx
Published on: May 13, 2020
Related Concept Videos
Anionic Chain-Growth Polymerization: Overview
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
Diazonium Group Substitution: –OH and –H
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Mechanism
Aldehydes and Ketones with HCN: Cyanohydrin Formation Overview
Nucleophilic Aromatic Substitution of Aryldiazonium Salts: Aromatic SN1
In the Sandmeyer reaction, for example, the diazonio group is replaced by a chloro, bromo,...