Fabrication of Non-volatile Charge Storage Memory Device by Novel doped ZnO nanoparticles with 4.79 eV bandgap
SOUDIP SINHA ROY
Quantumorbit Synthesis Pvt. Ltd., India
Nowadays, the drastic participation of the nanosized materials in technology have been implicated with various applications which mainly aims the performance optimization, dimensional downscaling, ultra-low power consumption etc. to overcome the fundamental limits of the microscale devices. It is the requisite stage to familiarize a convenient alternative of the traditional large-scale technologies in the purpose of accelerating the flow of the applied science for mankind. This article presents two novel non-volatile device structures which are fabricated by layer by a layer deposition method. I-V measurements for both the samples justify the device characteristic as p-type –insulator–n-type configuration. The measurements confirm that the successful fabrication of those devices and proves the high-density charge capacity with an improved lifetime of the carriers compared to erstwhile reports. The measured the threshold voltage for this device is 0.939V.
Diode characteristic of the fabricated device
Keys: Zinc oxide, charge storage devices, quantum physics, nanotechnology
To unfold the hidden mysteries of the molecules and their applications the nanoscience have been presented plenty of its morphism in order to rapid performance scale up with drastic dimensional down scaling. Manipulation of the molecular information technology has numerous existing approaches for instance molecular non-volatile memory, electron spin devices, nano-memorister, quantum dot island based devices, capacitive devices etc. which have proven their superior activities in binary logic and storage device applications. Nowadays, the utility of the hard storage has become quite crucial and instantaneous which claims to be tinier and fastest to meet the present requirements of the mankind. The fabrication of the non-volatile charge storage devices opens a convenient way with millions charge storing capacity in a few nanometer areas. In this letter the ZnO nanoparticle-based non-volatile memory device has reported which provides a better optimization to the device efficiency. To fabricate this device three major materials have involved those are PMMA, Ag NPs, ZnO NPs. In another type of the device is fabricated by using Nafion which exhibits a benchmarking of the p-i-n diode. The PMMA layer is used as the tunneling barrier for the electrons that provides a path to the electrons to be tunnelled during the biasing application but resistance during cutoff state. It also acts as the high impedance to the electrons during cutoff state that resists from the discharging by defending the reverse tunnelling. To fabricate this device the ZnO and Ag doped ZnO NPs are utilized and specifically sputtered on the surface of the ITO. Two different types of devices have been walked through firstly ITO/PMMA/Nafion has been examined and next is ITO/PMMA /ZnO-NPs doped with Ag NPs. The reduced bandgap of the doped ZnO layer works as the electron hopping state and allows to operate it at ultra-low power input.
2. Background of Non-volatile Memory Devices
Since the last twenty years of the 19th century, the advancement of the nanotechnology has bequeathed a lot of novel applications to the current technology to accelerate its current flow over its fundamental limits. The molecular technology has eliminated various complications in the device fabrication and operation for instance impurity inconsistency, thermal carrier diffusion, elevated outlay of photolithography etc. which genuinely overcomes the unwanted faults in circuit and strictly shrinks the number of superposition states. In the recently published article it is reported that [1,2] the tunneling current depends on the barrier resistivity which tunneling get violated dynamically due to the operating temperature variation. Therefore, the temperature stability is also a key point which rights to be high to opt the ultimate device performance.
The synthesis of the non-volatile memory devices through the molecular thin film technology has already been taken care of before a couple of years. The floating gate MOS devices also acceptable performances in charge storing but those have the less storage density and lower speed of operation. The involvement of the nanoparticles induce a high surface area with the wide bandgap that imposes to store high density data and optimized operating speed with ultralow power consumption and minute faults.exhibits
between the ITO and the Ag NPs layer. Another report communicates that the structure ITO/a-C/ZnO/a-C/Al contact also exhibits very high optimization in switching rate and the charge storage capability where two a-C has incorporated which acts ITO/PMMA/Ag NPs based device has already been reported previously which exhibits superior performance adaptability . The ON/OFF ratio (switching rate) has also improved drastically due to the incorporation of the PMMA layer as a typical insulator .
3. Preparation of respective nanoparticles
The following nanoparticles are used in the device fabrication process. The process of synthesis of that nanomaterial is very easy, cheaper and time efficient. The involved chemicals have easy commercial availability. The list of chemicals is as follows.
Sodium Borohydrate (NaBH4); AgNO3; PVP; Zinc Acetate-dihydrate (Zn(COOCH3)2.2H2O);
Isopropyl Alcohol (CH3CH2CH2OH); Ethanolamine (C2H7NO).
3.1. ZnO NP preperation method
As a precursor commercially available Zinc Acetate-dihydrate (Zn(COOCH3)2.2H2O) salt was used and dissolved into Isopropyl Alcohol (CH3CH2CH2OH) having molar mass 60.09 g/mol. The final obtained solution was 0.5M. Afterwards, the solution was put in stirring and the Ethanolamine (C2H7NO) was added drop-wise during stirring at constant 80 C temperature until the gel is formed. After obtaining the gel the sample was dried at 35C until the solvent is completely evaporated out. However, the organic solvent evaporates faster in rate even at room temperature.
3.2. Ag NP preparation method
With the 60ml of distill water, the 0.004M NaBH4 was dissolved and kept for 30 min at continuous stirring in an ice bath. During stirring gently add 4ml of 0.002M AgNO3 dropwise until the colour of the solution is converted into light yellow. Once the desired colour is achieved 0.3% PVP as the capping agent was gently added. Afterwards, store the prepared solution immediately in dark space to avoid the particle agglomeration.
3.3. Ag-doped ZnO nanopowder preperation method
As a precursor commercially available Zinc Acetate-dihydrate (Zn(COOCH3)2.2H2O) salt was used and dissolved into Isopropyl Alcohol (CH3CH2CH2OH) having molar mass 60.09 g/mol. The final obtained solution was 0.5M. Afterwards, the solution was put in stirring and the Ethanolamine (C2H7NO) was added drop-wise during stirring at constant 80 C temperature until the gel is formed. After the ZnO gel formation, the 5% concentric AgNO3 was added dropwise while stirring at 6000 rpm inside an ice bath. Once the doping is successful then by centrifuging the sample and washing by MEA several times bright white coloured Ag-doped ZnO nanopowder was obtained.
Figure 1 | (a) UV-vis measurement for the pure ZnO NPs (50nm), (b) Zoomed view for further clarification
As the UV visible optical bandgap approximation asserts that B.G.= 1240/lamda eV.
Therefore, the calculate B.G. of this above ZnO sample is given by 1240/258.40= 4.79 eV.
The bandgap for a pure ZnO nanoparticle is at around ~3.2eV which response to 380nm UV wavelength. But in this case the bandgap is found with an unexpected increment which responded at 258.40 nm UV wavelength. In the next context this reason will be revealed out. Research is going on, on this topic.
4. Device Fabrication
The fabrication is the ultimate step for providing a physical aspect to any theoretical substance. In this case, two different types of devices have been fabricated fig. 2 is the ITO/PMMA/ZnO NPs based device. This device operates with the basic fundamental process of the charge trapping and hopping states. But the second device fig. 3 operates with the reduced bandgap of the ZnO through Ag doping and results in the ultra-low power operating with optimized ON/OFF ratio.
4.1. ITO/PMMA/Naffion structured device
The chemical formula of the nafion is C7HF13O5SC2F4·. Initially, the ITO was repeatedly cleaned by the concentric ethanol and the acetone in the ultrasonicator then it was dried at an hour at room temperature. After that, the ITO was exposed to the PMMA by a suitable spin coater and kept for 24 hrs. at room temperature for drying purpose. The grown thickness in 40nm. Once the drying is completed then highly purified nafion was drop casted onto the dried PMMA surface of the ITO and dried for 24 hrs. at room temperature.