Carbon‐based electronic devices are suitable candidates for bioinspired electronics due to their low cost, eco‐friendliness, mechanical flexibility, and compatibility with complementary metal‐oxide‐semiconductor technology. New types of materials such as graphene quantum dots (GQDs) have attracted attention in the search for new applications beyond solar cells and energy harvesting due to their superior properties such as elevated photoluminescence, high chemical inertness, and excellent biocompatibility. In this paper, a biocompatible/organic electronic synapse based on nitrogen‐doped graphene oxide quantum dots (N‐GOQDs) is reported, which exhibits threshold resistive switching via silver cation (Ag+) migration dynamics. In analogy to the calcium (Ca2+) ion dynamics of biological synapses, important biological synapse functions such as short‐term potentiation (STP), paired‐pulse facilitation, and transition from STP to long‐term plasticity behaviors are replicated. Long‐term depression behavior is also evaluated and specific spike‐timing dependent plasticity is assessed. In addition, elaborated switching mechanism of biosimilar Ag+ migration dynamics provides the potential for using N‐GOQD‐based artificial synapse in future biocompatible neuromorphic systems.
A two terminal semiconducting device like a memristor is indispensable to emulate the function of synapse in the working memory. The analog switching characteristics of memristor play a vital role in the emulation of biological synapses. The application of consecutive voltage sweeps or pulses (action potentials) changes the conductivity of the memristor which is considered as the fundamental cause of the synaptic plasticity. In this study, a neuromorphic device using an in-situ growth of sub-tantalum oxide switching layer is fabricated, which exhibits the digital SET and analog RESET switching with an electroforming process without any compliance current (compliance free). The process of electroforming and SET is observed at the positive sweeps of +2.4 V and +0.86 V, respectively, while multilevel RESET is observed with the consecutive negative sweeps in the range of 0 V to −1.2 V. The movement of oxygen vacancies and gradual change in the anatomy of the filament is attributed to digital SET and analog RESET switching characteristics. For the Ti/Ta2O3−x/Pt neuromorphic device, the Ti top and Pt bottom electrodes are considered as counterparts of the pre-synaptic input terminal and a post-synaptic output terminal, respectively.
We
report the dependence of the thickness of amorphous boron nitride
(a-BN) on the characteristics of conductive bridge random access memory
(CBRAM) structured with the Ag/a-BN/Pt stacking sequence. The a-BN
thin film layers of three different thicknesses of 5.5, 11, and 21.5
nm were prepared by the sputtering deposition. Depending on the thickness
of the a-BN layer, the devices are found to be in either low-resistance
state (LRS) or high-resistance state (HRS) prior to any consecutive
switching cycle. All devices with 5.5 nm thick a-BN switching layer
are in LRS as the pristine state, while devices with 21.5 nm thick
a-BN layer are found to be in HRS as the pristine state. To attain
reliable switching cycles, initial RESET and electroforming process
are necessarily required for the devices with 5.5 and 21.5 nm thick
a-BN layer, respectively. However, the devices with the a-BN layer
of thickness between 5.5 and 21.5 nm in pristine states are in either
HRS or LRS. This dependence of the a-BN thickness on different resistance
states in the pristine state can be explained by in situ Ag diffusion
during its sputter deposition to form a top electrode on the a-BN
layer. Our finding shows a detailed investigation and a deep understanding
of the switching mechanism of Ag/a-BN/Pt CBRAM devices with respect
to different a-BN thicknesses for the future computing system.
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