Conventional Metal Electrodes Research Articles

MRI and CT compatible asymmetric bilayer hydrogel electrodes for EEG-based brain activity monitoring

The exploration of multi-dimensional brain activity with high temporal and spatial resolution is of great significance in the diagnosis of neurological disease and the study of brain science. Although the integration of electroencephalogram (EEG) with magnetic resonance imaging (MRI) and computed tomography (CT) provides a potential solution to achieve a brain-functional image with high spatiotemporal resolution, the critical issues of interface stability and magnetic compatibility remain challenging. Therefore, in this research, we proposed a conductive hydrogel EEG electrode with an asymmetrical bilayer structure, which shows the potential to overcome the challenges. Benefiting from the bilayer structure with different moduli, the hydrogel electrode exhibits high biological and mechanical compatibility with the heterogeneous brain-electrode interface. As a result, the impedance can be reduced compared with conventional metal electrodes. In addition, the hydrogel-based ionic conductive electrodes, which are free from metal conductors, are compatible with MRI and CT. Therefore, they can obtain high spatiotemporal resolution multi-dimensional brain information in clinical settings. The research outcome provides a new approach for establishing a platform for early diagnosis of brain diseases and the study of brain science.

Three-dimensional porous SiC/BDD electrode with long-term robustness and enhanced electrochemical degradation performance for refractory organic pollutants

Boron-doped diamond (BDD) electrodes with a three-dimensional (3D) porous network structure can overcome the mass transfer limitations and increase substantially the utilization rate of active oxygen species. Nonetheless, the 3D porous network structure was invariably built using metallic substrates, which inherently have inferior stability because of their non-corrosion resistance and the severe thermal mismatch between BDD films and substrates. Herein, we reported, for the first time, the use of a commercially porous silicon carbide (SiC) as the substrate to construct a 3D SiC/BDD electrode to simultaneously alleviate the problematics of substrate corrosion and thermal mismatch. This novel electrode exhibited a long-term service lifetime of 800 h in 3 M H2SO4 under the current density of 50 mA cm−2, over 500 times longer than the conventional metallic substrate-based BDD electrodes. The optimum p-SiC/BDD electrode exhibited a high oxygen evolution potential of 2.04 V vs. SHE, a low charge transfer resistance of 18.4 Ω, a high mass transfer coefficient of 2.78 × 10−5 m s−1, and a thin diffusion layer thickness of 25.2 μm. The proposed electrode had a threefold larger pseudo-first-order reaction rate constant than a flat BDD electrode, although it consumed just a fourth of the latter’s electric energy. The superior performance was attributable to an increased mass transfer rate confirmed by computational fluid dynamics (CFD) simulations as well as a high yield of reactive oxygen species verified by electron spin resonance (ESR). Furthermore, the proposed SiC/BDD electrode could work effectively under different water matrices in the presence of diverse salt electrolytes, thus paving a new avenue for the structure design of robust non-active anode materials.

Soft-metal bonding-enabled recyclable and anti-interference flexible multilayer piezoelectric sensor for tractor tire strain monitoring

Real-time efficient sensing of machine-soil interactions, especially precise tire-ground contact information, plays a critical role in cultivation, seeding, and harvesting for smart agriculture. However, the complicated agricultural environment poses a considerable challenge to traditional rigid sensors, which cannot suffer from both large deformation and electromagnetic interference. Here, we report a novel soft-metal BiInSn bonding-enabled recyclable and anti-interference flexible multilayer piezoelectric sensor for monitoring tractor tire strain. The printed BiInSn-ink electrode fully wraps the surface fibers of porous BaTiO3/PVDF-HFP electrospun films only through a low pressure at low temperature due to its unique thermal-softening effects, which of the adhesion strength is superior to the intrinsic tension limit of the film. The compact multilayer piezoelectric sensor is thus easily prepared, remarkably increasing the output voltage compared to a single-layer case (up to 300% for three layers). Benefiting from the low melting point of the BiInSn alloy, the sensors are easily recyclable compared to conventional metal electrodes prepared with copper, silver, and gold. In addition, its high electrical conductivity also enables the shielding layer to achieve ultrahigh shielding effectiveness of 2100 dB mm−1. This sensor can be demonstrated for tire strain sensing under complex operating conditions such as plowing, harrowing, and fertilizer application. These findings serve as a foundation for accelerating the development of smart agriculture.

Self-powered photodetector based on 1D TiO2-3D CdS mixed dimensional heterostructure fabricated at low temperature

Solution processed photodetectors have garnered great attention in applications such as, machine vision perception, neuromorphic computing and opto-electronic memory storage. Though, such photodetectors offer several advantages such as ease of fabrication, high scalability, low thermal budget and low-cost processing, multi-modal functionality etc. however, they suffer from the major drawback of inferior device performance −as low responsivity and slow rise time, particularly due to the intrinsic poor crystallinity of the photoactive material. In this work, we demonstrate a solution processed photodetector with impressive performance at comparatively low processing temperatures (<150 °C) based on the mixed dimensional heterostructure configuration of 1D TiO2 nanorods and 3D CdS nanoflowers. TiO2 nanorods have been synthesized by hydrothermal technique, whereas their CdS sensitization is done by chemical bath deposition. Low cost carbon paste is used as electrode instead of conventional non-economic noble metal electrodes. X-ray diffraction studies validated excellent crystallinity of the photoactive material even under low temperature processing condition. The type-II Heterojunction (TiO2 and CdS) configuration photodetector shows efficient response at zero bias, thus yielding a self-powered device. The detector shows response in UV and visible region, with excellent responsivity of 110 mA/W (5 V), 563 µA/W (0 V) and a quicker rise time of 81 ms. Albeit the simple fabrication scheme and low processing temperatures, the detector exhibited promising figures-of-merit, which aids in fabrication of novel solution processed photodetectors.

Reversible Transition of Semiconducting PtSe2 and Metallic PtTe2 for Scalable All-2D Edge-Contacted FETs.

Two-dimensional (2D) transition metal dichalcogenide (TMD) layers are highly promising as field-effect transistor (FET) channels in the atomic-scale limit. However, accomplishing this superiority in scaled-up FETs remains challenging due to their van der Waals (vdW) bonding nature with respect to conventional metal electrodes. Herein, we report a scalable approach to fabricate centimeter-scale all-2D FET arrays of platinum diselenide (PtSe2) with in-plane platinum ditelluride (PtTe2) edge contacts, mitigating the aforementioned challenges. We realized a reversible transition between semiconducting PtSe2 and metallic PtTe2 via a low-temperature anion exchange reaction compatible with the back-end-of-line (BEOL) processes. All-2D PtSe2 FETs seamlessly edge-contacted with transited metallic PtTe2 exhibited significant performance improvements compared to those with surface-contacted gold electrodes, e.g., an increase of carrier mobility and on/off ratio by over an order of magnitude, achieving a maximum hole mobility of ∼50.30 cm2 V-1 s-1 at room temperature. This study opens up new opportunities toward atomically thin 2D-TMD-based circuitries with extraordinary functionalities.

Investigations of Charge Transfer Processes on Plasmonic Cathode Electrodes

The establishment of efficient light energy conversion system is an important issue in the field of photoelectrochemical region. For the realization of it, the wide-band semiconductor electrode could be the good candidate. However, semiconductor electrodes often have the limitation to the ultraviolet region because of their band gap energy. Because the sunlight energy mainly consists of visible light, the visible-light induced photoenergy conversion is a challenging issue. As the breakthrough for it, recently, the combination of the plasmonic metal nanostructures with wide semiconductor electrodes has been received much attention because of the addition of visible light response characters. Up to now, the various systems of the anodic reaction controls have been established. Recently, the cathode system which can control the reduction reactions at metal semiconductor interfaces have been reported via the introduction of plasmonic metal nanostructures into the p-type semiconductor electrodes. In our previous study, we have established the plasmonic photocathode by using the Ag nanostructures with the p-type GaP electrode [1]. In this system, it can be considered as the holes excited in the metal structures injected into the valence band of the p-type semiconductor and the remained electron are consumed in the hydrogen evolution reaction. In addition, we have observed the unique pH dependence on the hydrogen evolution which could not be observed on conventional metal electrodes. For understanding the unique reaction selectivity on the plasmonic cathode electrode, the detail understanding about both the charge transfer process and absolute electrochemical potential of generated electrons. In this study, we have attempted to obtain such information through the various chemical reactions using the various types of plasmonic structures. Through the various photoelectrochemical measurements, we have confirmed the changes in the electrochemical potential of excited electrons depending on the optical characters of plasmonic structures. The unique molecular selectivity was also observed. Our current research would provide the novel insight for the accurate design of the high efficient visible light conversion device.[1] H. Minamimoto et al., Chem. Lett., 2020, 49, 806.

Mechanically-Compliant Bioelectronic Interfaces through Fatigue-Resistant Conducting Polymer Hydrogel Coating.

Because of their distinct electrochemical and mechanical properties, conducting polymer hydrogels have been widely exploited as soft, wet, and conducting coatings for conventional metallic electrodes, providing mechanically compliant interfaces and mitigating foreign body responses. However, the long-term viability of these hydrogel coatings is hindered by concerns regarding fatigue crack propagation and/or delamination caused by repetitive volumetric expansion/shrinkage during long-term electrical interfacing. This study reports a general yet reliable approach to achieving a fatigue-resistant conducting polymer hydrogel coating on conventional metallic bioelectrodes by engineering nanocrystalline domains at the interface between the hydrogel and metallic substrates. It demonstrates the efficacy of this robust, biocompatible, and fatigue-resistant conducting hydrogel coating in cardiac pacing, showcasing its ability to effectively reduce the pacing threshold voltage and enhance the long-term reliability of electric stimulation. This study findings highlight the potential of its approach as a promising design and fabrication strategy for the next generation of seamless bioelectronicinterfaces.

Study on SiC UV/EUV Coaxial Photodetector

In this paper, a novel 4H-SiC coaxial p-i-n ultraviolet photodetector with intense photon absorption and high quantum efficiency is studied. The spectral response and electric field distribution of the detector are calculated by TCAD software. The results showed that the innovative 4H-SiC ultraviolet coaxial p-i-n photodetector has a spectral response peak of 0.1998 A/W at 260 nm illumination wavelength and has more than twice response higher than the traditional 4H-SiC p-i-n photodetector, when the illumination wavelength is under 270 nm. The quantum efficiency of the coaxial photodetector reaches 95.3%. Moreover, in the wavelength range of EUV, the 4H-SiC ultraviolet coaxial photodetector shows a relatively high response, while the response is barely observed for the traditional 4H-SiC p-i-n photodetector. For the large area coaxial p-i-n photodetector, the problem of laterally undepleted i layer can be solved by multiple P+-type implanation. The new structure significantly enhances the rate of incident light absorption, prevents the light absorption of the conventional metal electrode and P+ layer, and provides an innovative approach for the construction of ultraviolet photodetectors in the future.

Single-Atom Control of Single-Molecule van der Waals Junctions with Semimetallic Transition Metal Dichalcogenide Electrodes.

Electrodes play an essential role in controlling electrode-molecule coupling. However, conventional metal electrodes require linkers to anchor the molecule. Van der Waals interaction offers a versatile strategy to connect the electrode and molecule without anchor groups. Except for graphene, the potential of other materials as electrodes to fabricate van der Waals molecular junctions remains unexplored. Herein, we utilize semimetallic transition metal dichalcogenides (TMDCs) 1T'-WTe2 as electrodes to fabricate WTe2/metalated tetraphenylporphyrin (M-TPP)/WTe2 junctions via van der Waals interaction. Compared with chemically bonded Au/M-TPP/Au junctions, the conductance of these M-TPP van der Waals molecular junctions is enhanced by ∼736%. More importantly, WTe2/M-TPP/WTe2 junctions exhibit the tunable conductance from 10-3.29 to 10-4.44 G0 (1.15 orders of magnitude) via single-atom control, recording the widest tunable range of conductance for M-TPP molecular junctions. Our work demonstrates the potential of two-dimensional TMDCs for constructing highly tunable and conductive molecular devices.

The high thermal conductivity of graphene prevents ZnO nanorod-graphene interface from degradation

The electrical and thermal properties of the junction between individual ZnO nanorods and conductive electrodes are investigated. It is demonstrated that a stable ohmic contact can be prepared between ZnO nanorods and graphene by eliminating contamination on the graphene surface by local Joule heating. Moreover, it is shown that, for conventional metal electrodes, such as copper, Joule self-heating forms hot spots and subsequently causes thermal damage to the ZnO nanorod near the interface. This issue can be eliminated in graphene contacts because of their excellent thermal conductivity. The experimental results are validated by the numerical modeling of heat dissipation near the ZnO/graphene interface using COMSOL Multiphysics software. To characterize the interface between individual nanorods and graphene, a novel technique was developed using a nanomanipulator in the chamber of the scanning electron microscope. In contrast to conventional approaches, the method eliminates the use of extensive processing chemistry and allows observation of morphological changes in situ when performing electrical characterization.

Chemical reaction of Al-Sm sputtered amorphous electrode for stable encapsulation-free organic electronics

An Al-based amorphous metal alloy (i.e., metallic glass) is fabricated in the form of a thin film electrode for an organic solar cell. The chemical stability of the amorphous alloy thin film is analysed via electrochemical analyses, which reveals that the random atomic arrangement within the electrode suppresses the oxidation reaction upon contact with harsh conditions. Incorporation of an amorphous metal thin film as a top electrode for organic solar cell devices results in considerable enhancement in device stability, as the metallic surface with the amorphous phase hinders the ambient moisture and oxygen from permeating into the underlying organic layers. The electrical parameters of the amorphous electrodes are analysed before and after aging and compared with those of a conventional crystalline metal electrode, which presents the advantage of amorphous electrodes in maintaining high charge transport properties for an extended time.

Fully Flexible MXene-based Gas Sensor on Paper for Highly Sensitive Room-Temperature Nitrogen Dioxide Detection.

Flexible chemiresistive gas sensors have attracted growing interest due to their capability in real-time and rapid detection of gas. However, the performance of gas sensors has long been hindered by the poor charge transfer ability between the conventional metal electrode and gas sensing semiconductors. Herein, for the first time, a fully flexible paper-based gas sensor integrated with the Ti3C2Tx-MXene nonmetallic electrode and the Ti3C2Tx/WS2 gas sensing film was designed to form Ohmic contact and Schottky heterojunction in a single gas sensing channel. Ti3C2Tx/WS2 has outstanding physical and chemical properties for both Ti3C2Tx and WS2 nanoflakes, showing high conductivity, effective charge transfer, and abundant active sites for gas sensing. The response of the gas sensor to NO2 (1 ppm) at room temperature is 15.2%, which is about 3.2 and 76.0 times as high as that of the Au interdigital electrode integrated with the Ti3C2Tx/WS2 sensor (4.8%) and the MXene electrode integrated with the Ti3C2Tx sensor (0.2%), respectively. Besides, this design performed at a limit of detection with 11.0 ppb NO2 gas and displayed excellent stability under high humidities. Based on first-principles density functional theory calculation results, the improvement of the gas sensing performance can be mainly attributed to the heterojunction regulation effect, work function matching, and suppressing metal-induced gap states. This work provides a new approach for the design of flexible gas sensors on paper with MXene-based conductive electrodes and gas sensing materials.

Engineering Electrodes with Robust Conducting Hydrogel Coating for Neural Recording and Modulation.

Coating conventional metallic electrodes with conducting polymers has enabled the essential characteristics required for bioelectronics, such as biocompatibility, electrical conductivity, mechanical compliance, and the capacity for structural and chemical functionalization of the bioelectrodes. However, the fragile interface between the conducting polymer and the electrode in wet physiological environment greatly limits their utility and reliability. Here, a general yet reliable strategy to seamlessly interface conventional electrodes with conducting hydrogel coatings is established, featuring tissue-like modulus, highly-desirable electrochemical properties, robust interface, and long-term reliability. Numerical modeling reveals the role of toughening mechanism, synergy of covalent anchorage of long-chain polymers, and chemical cross-linking, in improving the long-term robustness of the interface. Through in vivo implantation in freely-moving mouse models, it is shown that stable electrophysiological recording can be achieved, while the conducting hydrogel-electrode interface remains robust during the long-term low-voltage electrical stimulation. This simple yet versatile design strategy addresses the long-standing technical challenges in functional bioelectrode engineering, and opens up new avenues for the next-generation diagnostic brain-machineinterfaces.

A fabric-based electrode for wearable piezoelectric nanogenerators to distinguish sense human motions

To develop a PENG with both good comfort and high performance, we designed a wearable Ag/PEI/Cotton fabric electrode. Herein, PEI was used as a bridge to connect the Ag nanoparticles with cotton fabric by the LbL self-assembly method. The sheet resistance of the Ag/PEI/Cotton fabric electrode reached 1.6 × 10−4 Ω·cm. We found that the Ag/PEI/Cotton fabric electrode was more flexible and had better mechanical properties than the Cu metal electrode. The Ag/PEI/Cotton fabric electrode also showed good antibacterial activity, suggesting that it could be safely used as a fabric in contact with human skin. Since the Ag/PEI/Cotton fabric electrode had a low sheet resistance, it could be used as a replacement for the metal electrode traditionally used in composite PENGs. The output voltage and output current of the BT/PVDF-Ag/PEI/Cotton composite PENG were 1.8 V and 0.37 μA, respectively, and the output voltage was stable after 1500 cycles. The composite PENG prepared with the Ag/PEI/Cotton fabric electrode could sense various types of human motion. Herein, we provide a new method to fabricate a wearable fabric-based electrode, that can replace the conventional metal electrode to prepare composite PENGs. The BT/PVDF-Ag/PEI/Cotton composite PENG has extensive application prospects in motion monitoring and wearable devices.

Dielectric properties of SrTiO3/LaNiO3 composite structure prepared by “sol-gel” method

In this work, Pt/SrTiO3(STO)/LaNiO3(LNO) and Pt/STO/Pt structures were fabricated on Si substrates using sol–gel method. Dielectric tunability characteristics of these two structures are investigated over temperature range of 300–80 K. As temperature decreases, relative dielectric constant and tunability of STO films in both structures increase linearly, while loss tangent (tanẟ) decreases. STO prepared on LNO exhibits better crystallinity and dielectric tunability than that prepared on Pt. Furthermore, LNO top pole array with 0.2 mm diameter was prepared on STO/LNO using photosensitive sol–gel method, resulting in LNO/STO/LNO structure with symmetric electrode. Dielectric tunability tests reveal that, compared with Pt/STO/LNO structure, LNO/STO/LNO structure exhibits similar tunability, lower tanẟ, higher figure-of-merit (FOM) values, and better tunability symmetry. Relative dielectric constant, tunability (350 kV/cm), and FOM are approximately 391, 60%, and 142.6 at 80 K, respectively. Further analysis shows that because of Schottky barrier at Pt/STO interface, the FOM and tunability symmetry of Pt/STO/LNO structure are worse than those of LNO/STO/LNO structure. These results demonstrate that LNO electrode performs better than conventional inert metal electrodes.

Multilayer CVD graphene electrodes using a transfer-free process for the next generation of optically transparent and MRI-compatible neural interfaces.

Multimodal platforms combining electrical neural recording and stimulation, optogenetics, optical imaging, and magnetic resonance (MRI) imaging are emerging as a promising platform to enhance the depth of characterization in neuroscientific research. Electrically conductive, optically transparent, and MRI-compatible electrodes can optimally combine all modalities. Graphene as a suitable electrode candidate material can be grown via chemical vapor deposition (CVD) processes and sandwiched between transparent biocompatible polymers. However, due to the high graphene growth temperature (≥ 900 °C) and the presence of polymers, fabrication is commonly based on a manual transfer process of pre-grown graphene sheets, which causes reliability issues. In this paper, we present CVD-based multilayer graphene electrodes fabricated using a wafer-scale transfer-free process for use in optically transparent and MRI-compatible neural interfaces. Our fabricated electrodes feature very low impedances which are comparable to those of noble metal electrodes of the same size and geometry. They also exhibit the highest charge storage capacity (CSC) reported to date among all previously fabricated CVD graphene electrodes. Our graphene electrodes did not reveal any photo-induced artifact during 10-Hz light pulse illumination. Additionally, we show here, for the first time, that CVD graphene electrodes do not cause any image artifact in a 3T MRI scanner. These results demonstrate that multilayer graphene electrodes are excellent candidates for the next generation of neural interfaces and can substitute the standard conventional metal electrodes. Our fabricated graphene electrodes enable multimodal neural recording, electrical and optogenetic stimulation, while allowing for optical imaging, as well as, artifact-free MRI studies.

Sensing and Stimulating Electrodes for Electroceuticals

Electroceuticals is an emerging field that combines the technology in conductive materials with their ability to interface with biological systems. The development of highly conductive electrodes to monitor human health in real-time while simultaneously delivering stimulation promises to revolutionize medical science. Aspects to consider during development include the desired shape, electrode material properties, number of active sites, carriers used, and methods of deployment and activation. Novel organic-conductor based electrode compositions offer properties unattainable with conventional metal electrodes. Emerging innovative deployment strategies communicate directly with target tissues while minimizing damage to the surrounding biological environment. Here we highlight the recent reported technology on platinized graphene fibers (sutrode), a high performance electrode, capable of recording electrophysiological signals from small autonomic nerves, which could bring us closer to the ultimate goal: modulating the activity of individual organs with high selectivity and precision for a therapeutic medical outcome. An in-depth understanding of electrode materials and methods of fabrication and deployment can provide unprecedented opportunities for electroceutical research.

Direct measurement of nanoscale filamentary hot spots in resistive memory devices.

Resistive random access memory (RRAM) is an important candidate for both digital, high-density data storage and for analog, neuromorphic computing. RRAM operation relies on the formation and rupture of nanoscale conductive filaments that carry enormous current densities and whose behavior lies at the heart of this technology. Here, we directly measure the temperature of these filaments in realistic RRAM with nanoscale resolution using scanning thermal microscopy. We use both conventional metal and ultrathin graphene electrodes, which enable the most thermally intimate measurement to date. Filaments can reach 1300°C during steady-state operation, but electrode temperatures seldom exceed 350°C because of thermal interface resistance. These results reveal the importance of thermal engineering for nanoscale RRAM toward ultradense data storage or neuromorphic operation.

All-Ceramic Passive Wireless Temperature Sensor Realized by Tin-Doped Indium Oxide (ITO) Electrodes for Harsh Environment Applications.

In this work, an all-ceramic passive wireless inductor–capacitor (LC) resonator was presented for stable temperature sensing up to 1200 °C in air. Instead of using conventional metallic electrodes, the LC resonators are modeled and fabricated with thermally stable and highly electroconductive ceramic oxide. The LC resonator was modeled in ANSYS HFSS to operate in a low-frequency region (50 MHz) within 50 × 50 mm geometry using the actual material properties of the circuit elements. The LC resonator was composed of a parallel plate capacitor coupled with a planar inductor deposited on an Al2O3 substrate using screen-printing, and the ceramic pattern was sintered at 1250 °C for 4 h in an ambient atmosphere. The sensitivity (average change in resonant frequency with respect to temperature) from 200–1200 °C was ~170 kHz/°C. The temperature-dependent electrical conductivity of the tin-doped indium oxide (ITO, 10% SnO2 doping) on the quality factor showed an increase of Qf from 36 to 43 between 200 °C and 1200 °C. The proposed ITO electrodes displayed improved sensitivity and quality factor at elevated temperatures, proving them to be an excellent candidate for temperature sensing in harsh environments. The microstructural analysis of the co-sintered LC resonator was performed using a scanning electron microscope (SEM) which showed that there are no cross-sectional and topographical defects after several thermal treatments.

Low-voltage, self-powered and broadband photodetector with Ohmic, transparent and cost-effective AZO electrodes on vertical aligned MoS2 flakes

The transparent Ohmic electrodes are the extreme necessity to develop cutting-edge broadband photodetectors. Conventional metal electrodes reflect incident light and diminish overall performance of photodetector. Here, we report cost-effective, transparent Ohmic Al-doped ZnO (AZO) electrodes to develop self-powered, highly responsive photodetectors from visible to near-infrared regions using vertically-aligned MoS2 (VA- MoS2) flakes. The MoS2 photodetector with AZO electrode (AZO-MoS2) shows a high responsivity of 40.67 A/W at 800 nm at low biasing voltage of 0.5 V. The self-driven behavior is observed in a broad range from 400 to 1100 nm with high responsivity of 38.18 mA/W at 800 nm. Moreover, AZO-MoS2 device has fast rise and decay time. To understand impact of Ohmic AZO electrode in comparison to traditional metal electrodes, we have also investigated conventional Au-MoS2 PDs fabricated under identical dimensions. The AZO-MoS2 PD demonstrated 100 times higher responsivity than conventional Au-MoS2 PD at 800 nm. We have investigated band-alignment between AZO and MoS2 using ultraviolet spectroscopy (UPS) and confirmed ohmic nature between the AZO and MoS2. These results indicate superior performance of AZO-MoS2 PD device in comparison to traditional metal electrodes.