Solution-processable homoleptic aluminum(III) catecholaldimine complex as an active material for RRAM switching
Vivek Sharma1, Anupam Chetia2, Rishabh Raj Upadhyay2
1Department of Chemistry, Indian Institute of Technology Jodhpur, Rajasthan-342030, India. rkmetre@iitj.ac.in.
Abstract:
In this paper, we report the synthesis and structural characterization of a new mononuclear aluminum complex 1, containing a redox-active hydrazine based catecholaldimine ligand (4,6-di-tert-butyl-2,3-dihydroxybenzylidene)furan-2-carbohydrazide (LH3). Complex 1 was readily obtained by refluxing (LH3) and Al(NO3)3·9H2O in a 2 : 1 molar ratio in the presence of triethylamine in a methanolic solution. Single-crystal X-ray diffraction analysis of complex 1 shows that catecholaldimine ligands bind through octahedral coordination to the Al(III) center. Complex 1 was also further characterized by various techniques such as HRMS, UV-vis, FTIR, TGA and CHN analysis. Complex 1 was found to exhibit absorption bands at 225 and 354 nm in dichloromethane (DCM) solution assigned to ligand-based electronic transitions, which is in quite good agreement with absorption bands calculated by TD-DFT theoretically. The electrochemical characterization of complex 1 was done by cyclic voltammetry in DCM solution, which showed several quasi-reversible and irreversible oxidation-reduction peaks. The solution processable mononuclear aluminum complex 1 was further employed as an active material to fabricate a resistive switching memory device. Interestingly, the device exhibits distinct bipolar resistive switching with a maximum ON/OFF ratio of almost 103. The device also shows stable resistive switching behaviour for 102 iterations with negligible loss of resistance ratio and stability of both resistive states (LRS and HRS) for 3300 s, demonstrating its promising potential for non-volatile memory applications. This work offers a new direction for the rational design and fabrication of high-performance resistive memory devices based on Earth-abundant aluminum metal-based molecular complexes with a new diverse redox-active ligand backbone.
More Related Videos
Related Concept Videos
Acid Halides to Alcohols: LiAlH4 Reduction
The mechanism proceeds in three steps. First, the nucleophilic hydride ion attacks the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs as a leaving group, generating an aldehyde. A second nucleophilic attack by the hydride yields an alkoxide ion, which, upon protonation, gives a primary alcohol as...
MOS Capacitor
The metal gate is typically made from highly conductive materials such as aluminum or polysilicon. Beneath the metal gate lies a thin layer of...


