Electrical Properties Research Articles

Crystallographic Pathways to Tailoring Metal-Insulator Transition through Oxygen Transport in VO2.

The metal-insulator (MI) transition of vanadium dioxide (VO2) is effectively modulated by oxygen vacancies, which decrease the transition temperature and insulating resistance. Oxygen vacancies in thin films can be driven by oxygen transport using electrochemical potential. This study delves into the role of crystallographic channels in VO2 in facilitating oxygen transport and the subsequent tuning of electrical properties. A model system is designed with two types of VO2 thin films: (100)- and (001)-oriented, where channels align parallel and perpendicular to the surface, respectively. Growing an oxygen-deficient TiO2 layer on these VO2 films prompted oxygen transport from VO2 to TiO2. Notably, in (001)-VO2 film, where oxygen ions move along the open channels, the oxygen migration deepens the depleted region beyond that in (100)-VO2, leading to more pronounced changes in metal-insulator transition behaviors. The findings emphasize the importance of understanding the intrinsic crystal structure, such as channel pathways, in controlling ionic defects and customizing electrical properties for applications.

Highly flexible yet strain-insensitive conjugated polymer.

Imparting excellent electrical properties, mechanical robustness, suppleness, conduction stability during deformation, and self-healing to intrinsic conducting polymers is a challenging endeavor. The reversibly interlocked macromolecular networks (RILNs) approach is utilized to tackle this problem. Specifically, poly(3,4-ethylenedioxythiophene) (PEDOT) is mixed with flexible polysulfonic acid networks crosslinked by reversible Diels-Alder bonds, while rigid polyaniline networks crosslinked by reversible Schiff base bonds act as molecular staples. Owing to the joint actions of the doping effect of polyaniline on PEDOT, the specific interlocking architecture and synergy between the component materials, the electrical conductivity (59.3-980.5 S cm-1), tensile strength (8.4-81.6 MPa) and elongation at break (44.5-411.0%) of the resultant PEDOT/RILNs films is significantly tunable according to different usage scenarios by adjusting the PEDOT content from 1.48 to 22.24 wt%. More importantly, the electrical resistance of PEDOT/RILNs remains constant during not only a single large extension and deflection but also repeated stretching (up to 1500 cycles) and bending (up to 106 cycles). The built-in reversible covalent bonds enable the PEDOT/RILNs to autonomously restore damaged mechanical and electrical performance. These record-breaking results and the demonstration of self-powered sensor made of PEDOT/RILNs suggest that the proposed approach successfully satisfies various conflicting requirements of flexible electronics regarding the properties of conducting polymers.

Experimental and numerical simulation studies of electrical resistance of cementitious materials under varying temperature history

Many in-service concrete structures are normally exposed to varying temperature condition. The time-dependent and non-uniform temperature distribution in concrete structures could affect the accurate assessment of their electrical properties. Therefore, the influences of temperature change over time and the spatial variation in temperature on the measured electrical resistance of cementitious materials are still in need of investigation. The coupled thermal-electrical responses of two types of cementitious materials under varying temperature history were investigated by a series of thermal and electrical tests in this study. Then a coupled thermal-electrical finite element (FE) model was developed to simulate the coupled thermal-electrical responses. The results show that the input direct current has a minor effect on the measured electrical resistance by embedded four-probe method and the specimen temperature when it is no greater than 3 mA. The relationship between the measured temperature at 10-mm depth of the specimen and the apparent resistance is well captured by a linear equation. The coupled thermal-electrical finite element model can predict well the developments of specimen temperature and apparent electrical resistance under varying temperature history. The FE results reveal that the non-uniform temperature variation results in the redistribution of electrical current within the tested specimen. However, electrical field between the two inner electrodes is always uniform when the embedded four-probe method is used, which is not affected by the non-uniform temperature variation.

Thermal and Mechanical Vibration Response of Auxetic Core Sandwich Smart Nanoplate

This study explores a new nanoplate design's thermal and mechanical properties, including an auxetic core with a negative Poisson ratio. The core is between face plates made of barium–cobalt, which possess magnetoelectroelastic properties. The analysis centers on the parameters θ, β1, and β2 to clarify their influence on the nanoplate's performance. The evaluations of the nanoplate's thermal, electrical, and magnetic properties showcase its remarkable versatility and sensitivity. Incorporating magnetoelectroelastic face plates improves the multifunctionality of the nanoplate, making it a highly promising option for use in smart technologies. The findings offer valuable insights into the distinctive features of auxetic core structures, significantly enhancing the comprehension of these materials. This research emphasizes the potential for creating groundbreaking applications in fields like aerospace engineering and advanced electronics, where versatile and adaptable materials play a vital role. This study contributes to the broader knowledge of auxetic materials and their practical implementation in cutting‐edge technological solutions by exploring the interplay between thermal, mechanical, and magnetoelectroelastic properties.

Tailoring the physicochemical and dielectric properties of natural polymer using graphene nanoplatelet as filler

AbstractBio‐based flexible dielectric substrates have gained tremendous attention for their potential to reduce environmental risks from nonbiodegradable electronic waste. The present study demonstrates the fabrication of facile, nontoxic, and biodegradable chitosan‐based flexible dielectric substrate using graphene nanoplatelet (GNP) as a nanofiller. The detailed impact of different concentrations of GNP (1, 2, and 3 wt%) into the chitosan (CS) matrix was studied on physicochemical, morphological, mechanical, electrical, and thermal properties. The fabricated CS/GNP composites showed improved mechanical strength, thermal stability, and electrical properties compared with unmodified CS film. The composites exhibited excellent thermal stability (200°C) with a promising biodegradation rate (within 6 days). The mechanical strength of the unmodified CS film was increased unequivocally with 2 wt% GNP loading with tensile strength of 23.56 Mpa. Furthermore, the current–voltage (I–V) characteristic curves for CS/GNP (2%) and CS/GNP (3%) showed similar current conduction and ohmic behavior in flat, bending, and flat‐after‐bending modes. The dielectric measurements revealed that the CS/GNP composite with 2 wt% filler exhibited optimal performance having permittivity (έ) of 32.71 (at 102 Hz) with low dielectric loss of 0.04 (at 106 Hz). These results suggest that the dielectric films offer strong prospects as an eco‐friendly alternative for various applications.Highlights Biodegradable chitosan‐based flexible dielectric films were prepared. Films were made using a simple solvent casting method with 1–3 wt% GNP filler. Optimum physicochemical and electrical properties were seen at 2 wt% GNP. CS/GNP (2%) film exhibited ohmic behavior in both flat and bending modes. Excellent dielectric properties were achieved at 2 wt% GNP filler.

Investigation of Electrical and Dielectrically Properties of a Novel Structure of PANI-PPy--GO-MWCNTs Composite/MnO2/Fe3O4/n-Si Structure

Abstract We investigated here the electrical properties of the novel structure of PANI-PPy-GO-MWCNTs composite/MnO2/Fe3O4/n-Si. This structure has not been addressed in literature before, the manufacture of this novel structure is carried out using a simple technique. So, we introduce here a novel structure with a simple method of manufacture. The imaginary part of modulus M՝՝ has two behaviors, the first behavior at high and low frequency and the second behavior at mid frequency, so the M՝՝ gives two contrarian behaviors, The M՝՝ is a strong function of frequency and we can change the behavior of M՝՝ by change of frequencies. The Col – Col diagram of modulus has ideal figures at some voltages including two semicircles of grains and grain boundaries. The imaginary part of impedance Z՝՝ versus frequency creates peaks, the peaks shift toward the low frequencies. The novel here the Z՝՝ has positive and negative values, despite the Z՝՝ should have negative values only. The real part of impedance Z՝ keeps on without change at high frequencies and splits for all temperatures at low and mid frequencies. Some electrical properties such as barrier height ɸb,Wd the width of the depletion layer, Nss the density of states,

Unveiling GruPol: Predicting Electric and Electrostatic Properties of Macromolecules via the Building Block Approach.

Understanding electrostatics and electric properties of macromolecules is crucial in uncovering the intricacies of their behavior and functionality. The precise knowledge of these properties enhances our ability to manipulate and engineer macromolecules for diverse applications, spanning from drug design to materials science. Having that in mind, we present here the GruPol database approach to characterize and accurately predict dipole moments, static polarizabilities, and electrostatic potential of proteins and their subunits. The method involves partitioning of the electron density, calculated at the M06-HF/aug-cc-pVDZ level of theory, of small peptides into predefined building blocks that are averaged over the database. By manipulating and positioning these building blocks, GruPol enables the description of proteins assembled from over nearly 100 residual entries, allowing for efficient and precise computation of the above-mentioned properties across a broad range of proteins. The database enables the user to include solvent effects as well as define protonation states on the protein's backbone to account for pH variations. The precision of the proposed scheme is benchmarked against experimental data for myoglobin species.

Electro-thermal actuation in recycled aggregate concrete with rapid self-reinforcement via smart cement-based composites

With the growing call for low-carbon and environmentally friendly materials, recycled aggregate concrete (RAC) holds great promise for sustainable development. Nevertheless, significant challenges exist with respect to the material’s poor flexural carrying capacity. Development of an effective method for improving the flexural carrying capacity of RAC under a specific deflection deformation is important for enhancing the range of its structural applications. In this study, an intelligent structural optimisation strategy for compounding RAC with carbon-fibre (CF) reinforced cement-based composites (CFRCs) to realize rapid self-reinforcement via electro-thermal actuation is proposed. As a smart component, CFRC was first researched to investigate its electrical, mechanical, and microscopic properties. The optimal properties were obtained in specimens incorporating 0.5 vol%, CFRC0.5. CFRC0.5 exhibits an electrical resistivity of approximately 0.39 Ω∙m, accompanied by 65.3 % and 33 % increases in flexural and compressive strengths, respectively, when compared to the control mixture without CF. Furthermore, CFRC0.5 can maintain outstanding stability after multiple electro-thermal cycles. Analysis via microscopic characterisation revealed that a satisfactory conductive network can be formed at 0.5 vol% CF. Furthermore, CFs with excellent dispersity are particularly advantageous in improving the mechanical biting force within the cement matrix and restraining the further formation and expansion of microcracks. Thus CFRC0.5 was designed and fabricated as a pre-stress controller to realise rapid structural self-reinforcement, resulting in a 38.6 % improvement in the flexural carrying capacity of the RAC under specific midspan deflection conditions. Additionally, a response behaviour model for midspan deflection with temperature differential was established, showing an excellent correlation between the experimental results and theoretical simulation. This findings from this study highlight the significance of leveraging intelligent techniques to realise rapid self-reinforcement capabilities in concrete structures, facilitating their potential application in smart and adaptive structures.

Effect of precursor pH on the electrochemically synthesised barium titanium sulphide (BaTiS) material for photovoltaic application

ABSTRACT In this study, we deposited the electrochemically synthesised barium titanium sulphide material for photovoltaic application on FTO glass and studied the effect of precursor pH. The thin films deposited with titanium-doped barium sulphide underwent examination for their optical, structural, electrical, and surface morphological properties. As the wavelength of the photon increased, the absorbance decreased. The Ti-doped CuS thin film had the highest absorbance value (0.79) at pH 4.60 and the lowest value (0.48) at pH 5.10. The films deposited at pH 5.10, 4.90, 4.80, 4.70, and 4.60 yielded data of 0.48, 0.56, 0.62, 0.73, and 0.79. The energy band gaps for the thin films deposited at pH 5.1, 4.9, 4.8, 4.7, and 4.6 were 2.90 eV, 2.87 eV, 2.79 eV, 2.60 eV, and 2.42 eV, respectively. The film’s energy bandgap decreased as the bath pH decreased, as indicated by the results. The X-ray diffraction findings unveiled a cubic structural phase of barium sulphide, with a lattice constant of 6.3748 Å.

How substituents tune quantum interference in meta-OPE3 molecular junctions to control thermoelectric transport.

Quantum interference (QI) can strongly affect electric and thermoelectric properties of molecular junctions (MJs). So far, however, a limited number of experimental studies have explored the influence of QI on thermoelectric transport in MJs. To address this open point, we synthesized derivatives of meta-OPE3 with an electron-withdrawing nitro (-NO2) substituent or an electron-donating N,N-dimethyl amine (-NMe2) substituent, attached at two different positions of the central phenylene ring, and systematically studied the electrical conductance and thermopower of the corresponding gold-molecule-gold junctions. We show that (i) the electrical conductance of MJs depends weakly on the polarity of the substituents but strongly on the substitution position and (ii) MJs with the N,N-dimethyl amine group feature a higher thermopower than MJs with the nitro group. We also present calculations based on first principles, which explain these trends and show that the transport properties are highly sensitive to microscopic details in junctions, exhibiting destructive QI features.

Investigation of the structural, morphological, electrical and dielectric properties of Li2CaGeO4 compound

Investigation of the structural, morphological, electrical and dielectric properties of Li2CaGeO4 compound

High-Performance Organic-Inorganic Hybrid Conductive Hydrogels for Stretchable Elastic All-Hydrogel Supercapacitors and Flexible Self-Powered Integrated Systems.

Conductive polymer hydrogels exhibit unique electrical, electrochemical, and mechanical properties, making them highly competitive electrode materials for stretchable high-capacity energy storage devices for cutting-edge wearable electronics. However, it remains extremely challenging to simultaneously achieve large mechanical stretchability, high electrical conductivity, and excellent electrochemical properties in conductive polymer hydrogels because introducing soft insulating networks for improving stretchability inevitably deteriorates the connectivity of rigid conductive domain and decreases the conductivity and electrochemical activity. This work proposes a distinct confinement self-assembly and multiple crosslinking strategy to develop a new type of organic-inorganic hybrid conductive hydrogels with biphase interpenetrating cross-linked networks. The hydrogels simultaneously exhibit high conductivity (2000 S m-1), large stretchability (200%), and high electrochemical activity, outperforming existing conductive hydrogels. The inherent mechanisms for the unparalleled comprehensive performances are thoroughly investigated. Elastic all-hydrogel supercapacitors are prepared based on the hydrogels, showing high specific capacitance (212.5 mF cm-2), excellent energy density (18.89 µWh cm-2), and large deformability. Moreover, flexible self-powered luminescent integrated systems are constructed based on the supercapacitors, which can spontaneously shine anytime and anywhere without extra power. This work provides new insights and feasible avenues for developing high-performance stretchable electrode materials and energy storage devices for wearable electronics.

Study on the Aging Characteristics of a ±500 kV Composite Dead-End Insulator in Longtime Service

Composite insulators have been widely used in power grids due to their excellent electrical-external-insulation performance. Long-term operation at high voltage levels accelerates the aging of composite insulators; however, there is a scarcity of research on aged composite insulators operating at 500 kV for over ten years. In this paper, the mechanical, electrical, and microscopic properties were tested on different sheds along a 500 kV composite insulator that had been running for 18 years. Additionally, the results were compared with a new insulator and the standards for live insulator operation. The results showed that the aging of the high-voltage end of composite insulators was the most serious. The results of the physical properties test indicated that the insulator’s hardness was compliant but its tensile strength and break elongation did not meet standards. Under wet conditions, the pollution flashover voltage decreases by about 50% compared to the new insulator. Combined with the microscopic test results, the shed skeleton structure could be damaged and the filler might be lost during the aging process of polydimethylsiloxane (PDMS). The hardness of the insulator would increase by the precipitation of inorganic silicon; however, inorganic silicon might destroy the hydrophobicity and other properties of insulator sheds. These results can provide theoretical references for insulator life prediction and operation protection.

Pressure tuning of superconductivity in TiN thin films

Abstract Titanium nitride (TiN) thin films are used for the fabrication of superconducting devices due to their chemical stability against oxidization and high quality at interfaces. The high-pressure technique serves as a useful tool to understand the mechanical and electrical properties of materials, which is crucial for practical applications. However, high-pressure transport measurements of thin films are extremely difficult due to the limited sample space of high-pressure cells and the fragility of thin films. Here, we successfully carried out high-pressure electrical transport and Raman measurements on TiN films up to ~50 GPa. The superconducting transition temperature gradually decreases with increasing pressure, which can be attributed to the decrease of electron -phonon coupling and is consistent with our first-principles calculations. In addition, the coexistence of a symmetry-enforced Dirac nodal chain and a nodal box is revealed by our calculations in TiN. Our work provides a promising way to study the physical properties of thin films at high pressure, which would broaden the high-pressure research field.

Experimental Investigations of the AC-Conductivity in NaTaO3 Ceramic Materials Doped with Cu and Al Metal Ions

Two ceramic samples of sodium tantalate (NaTaO3), doped with metal ions of copper (Cu; sample S1) or aluminum (Al; sample S2), were obtained by the sol-gel method. Complex impedance measurements in the frequency range (200 Hz–2 MHz) and at temperatures between 30 °C and 90 °C allowed identification of a transition temperature from semiconductor-type behavior to conductor-type behavior for each sample (52 °C for sample S1 and 54 °C for sample S2). In the temperature range with semiconductor behavior, the activation energy of each sample was determined. Based on the Mott’s variable-range hopping (VRH) model, the density of localized states at the Fermi level, N(EF), the hopping distance (R) and the hopping energy (W) were determined, for the first time, on NaTaO3 samples doped with Cu or Al metal ions. The increase in N(EF) of sample S2 compared to N(EF) of sample S1 was explained by the decrease in the hopping distance of charge carriers in sample S2 compared to that in sample S1. Additionally, using the correlated barrier hopping (CBH) model, the energy band gap (Wm) and the hopping (crossover) frequency (ωh) at various temperatures were determined. Knowledge of these electrical properties is very important for explaining the electrical conduction mechanisms in metal ion-doped compounds, with perovskite structure being of interest for the use of these materials in the conversion of thermoelectric energy, photocatalytic applications, electronics or other applications.

Comparative study of sodium and potassium compounds as promoters for growth of monolayer MoS2 with high crystal quality on SiO2/Si substrate

Abstract Monolayer MoS2 is promising candidate for fabrication of optoelectronic devices due to its direct bandgap nature and high carrier mobility. Alkali metal compounds have been demonstrated to be helpful promoters for the growth of large single crystal monolayer MoS2 on SiO2/Si substrate. However, the catalytic mechanism of alkali metal compounds is still under debate. Herein, we compared the surface morphology, optical properties, and electrical properties of monolayer MoS2 flakes grown on SiO2/Si substrate assisted by promoters containing potassium or sodium cations and halogen (chlorine) or non-halogen (hydroxide) anions, i.e., NaCl, NaOH, KCl and KOH. Based on the analysis of existing growth mechanism, we proposed that the alkali metal cation, plays a dominant role in promoting the lateral growth of monolayer MoS2 and obtaining high crystal quality. Furthermore, potassium has a greater promoting effect than sodium. By optimizing growth conditions, monolayer triangular MoS2 flakes with large lateral size over 160 µm were grown assisted by KCl promoter. Raman and PL spectra verified excellent crystal quality of the flakes, with typical electron mobilities of 2.98 and 20 cm2·V-1·s-1 for the back-gated filed effect transistors fabricated on as-grown and fresh SiO2/Si substrates, respectively.

High-Performance Tin Oxide Thin-Film Transistors Realized by Codoping and Their Application in Logic Circuits.

Tin oxide is a promising channel material, offering the advantages of being low-cost and environmentally friendly and having a wide band gap. However, despite the high electron mobility of SnO2 in bulk, the corresponding thin-film transistors (TFTs) generally exhibit moderate performance, hindering their widespread application. Herein, we proposed a codoping strategy to improve both the electrical property and the stability of SnO2 TFTs. A comparative analysis between doped and undoped SnO2 was conducted. It is observed that taking advantage of the difference in ionic radii between two dopants (indium and gallium) and the tin ions in the host lattice can effectively reduce impurity-induced strain. Additionally, we investigated the effect of codoping content on SnO2 TFTs. The optimal codoped SnO2 (TIGO) TFTs demonstrate high performance, featuring a field-effect mobility of 15.9 cm2/V·s, a threshold voltage of 0.2 V, a subthreshold swing of 0.5 V/decade, and an on-to-off current ratio of 2.2 × 107. Furthermore, the devices show high stability under both positive and negative bias stress conditions with a small threshold voltage shift of 1.8 and -1.2 V, respectively. Utilizing the TIGO TFTs, we successfully constructed a resistor-loaded unipolar inverter with a high gain of 10.76. This study highlights the potential of codoped SnO2 TFTs for advanced applications in electronic devices.

Evidence for Morphology Control by Polyelectrolyte Templating in PEDT:PSSH

AbstractDespite decades of research, the fundamental question of structure and morphology of the poly(3,‐4‐ethylenedioxythiophene):poly(styrene sulfonate) complex (PEDT: PSS) electrically conducting polymer remains open. Here, through a systematic study of the polymerization of 3,4‐ethylenedioxythiophene (EDT) on two series of sulfonated polystyrenes, i.e., PS‐co‐SSH and PS‐co‐SSNa, with per cent sulfonation 24 ≲ x ≲ 100, this study shows that the substrate polyelectrolyte not only affords charge compensation and processability, but also templates the morphology of the growing PEDT chain—whether extended, coiled or collapsed. This determines the electrical, electronic and optical properties of the resultant PEDT: PSS interpolyelectrolyte complexes, including their work function. This study calls this the Polyelectrolyte Template model. The PEDT: PSS complex retains memory of its polymerization morphology even after subsequent ion‐exchange, for example, to the same acid form. Electrical conductivity decreases sharply with decreasing x, and depends on whether the polymerization is templated with the H+ or Na+ form of the polyelectrolyte. The work function is less sensitive to x, but exhibits a transition from low to high work function (5.2–5.3 eV) when x exceeds a threshold, which indicates formation of a polar surface driven by molecular‐scale segregation of the PSS counteranion. This surface segregation also affects the ability of these complexes to inject holes into very large‐ionization‐energy semiconductors.

Anisotropy of Electrical and Thermal Conductivity in High-Density Graphite Foils

Flexible graphite foils with varying thicknesses (S = 282 ± 5 μm, M = 494 ± 7 μm, L = 746 ± 8 μm) and an initial density of 0.70 g/cm3 were obtained using the nitrate method. The specific electrical and thermal conductivity of these foils were investigated. As the density increased from 0.70 g/cm3 to 1.75 g/cm3, the specific electrical conductivity increased from 69 to 192 kS/m and the thermal conductivity increased from 109 to 326 W/(m·K) due to the rolling of graphite foils. The study showed that conductivity and anisotropy depend on the shape, orientation, and contact area of thermally expanded graphite (TEG) mesoparticles (mesostructural factor), and the crystal structure of nanocrystallites (nanostructural factor). A proposed mesostructural model explained these increases, with denser foils showing elongated, narrowed TEG particles and larger contact areas, confirmed by electron microscopy results. For graphite foils 200 and 750 μm thick, increased density led to a larger coherent scattering region, likely due to the rotation of graphite mesoparticles under mechanical action, while thinner foils (<200 μm) with densities > 1.7 g/cm3 showed increased plastic deformation, indicated by a sharp reduction in the coherent scattering region size. This was also evident from the decrease in misorientation angles with increasing density. Rolling reduced nanocrystallite misorientation angles along the rolling direction compared to the transverse direction (TD) (for 1.75 g/cm3 density ΔMA = 1.2° (S), 2.6° (M), and 2.4° (L)), explaining the observed anisotropy in the electrical and mechanical properties of the rolled graphite foils. X-ray analysis confirmed the preferred nanocrystallite orientation and anisotropy coefficients (A) using Kearns parameters, which aligned well with experimental measurements (for L series foils calculated as: A0.70 = 1.05, A1.30 = 1.10, and A1.75 = 1.16). These calculated values corresponded well with the experimental measurements of specific electrical conductivity, where the anisotropy coefficient changed from 1.00 to 1.16 and mechanical properties varied from 0.98 to 1.13.

P/N-Type Conversion of 2D MoTe2 Controlled by Top Gate Engineering for Logic Circuits.

Two-dimensional (2D) transition-metal dichalcogenides (TMDCs) are regarded as promising materials for next-generation logic circuits. Top gate field-effect transistors (FETs) have independent gate control ability and can be fabricated directly on TMDC materials without a transfer process. Therefore, it has the merits of device reliability and complementary metal-oxide semiconductor (CMOS) process compatibility, which are demanded in practical circuit-level integration. However, the fabrication of the top gate FET involves depositing an insulating dielectric layer and a gate electrode in sequence on the TMDC channel material, which may affect the device performance. Insightfully investigating the influences of different top-gate-deposition methods on the electrical properties of the TMDC channel and further harnessing these influences to realize a homogeneous CMOS device on an identical 2D TMDC platform are with practice significance. In this work, p/n-type controllable top gate FET arrays based on 2H-MoTe2 are fabricated by using different top-gate-deposition methods. The electron-beam evaporation (EBE) of top metal gate exhibits an obvious n-doping effect on the 2H-MoTe2 channel and converts it from p-type to n-type, whereas the thermal evaporation of top gate affects little to the channel. High-resolution transmission electron microscopy (HR-TEM) analysis reveals that the high-energy metal atoms from the EBE process can penetrate through the 30 nm gate dielectric layers (including 10 nm Al2O3 seeding layer), leading to multiple atomic defects in both MoTe2 and the interface between MoTe2 and Al2O3. Furthermore, by utilizing the top gate engineering, a large-scale double-top-gate MoTe2 homogeneous CMOS inverter array is fabricated. The CMOS inverters exhibit clear logic swing, negligible hysteresis, and high device yield (∼93%), indicating high device reliability and stability. Notably, the fabrication process is facile, free from transfer procedure, and compatible with traditional silicon technology. This work promotes the application of 2D TMDCs in nanoelectronics integration.