Metal Strip Research Articles

A wideband and low profile dual polarized antenna loaded with artificial magnetic conductor

In this paper, a wideband low profile dual-polarization antenna is proposed based on the in-phase reflection characteristic of artificial magnetic conductor (AMC). The AMC cells are designed as two concentric square metallic rings connected by a ‘*’ shaped metallic strip. Its in-phase reflection bandwidth is 2.12 GHz–3.31 GHz, and input-match bandwidth is 1.56 GHz–2.43 GHz. The relative bandwidth is 43.83% and 43.61%, respectively. In addition, the AMC cells are loaded on the reflector of the proposed dual polarized dipole antenna. The measured results show that the −10 dB reflection coefficient (|S 11|) bandwidth of the antenna is 1.55 GHz to 2.4 GHz (43%), and the height is only 0.136λ 0. Furthermore, the gain and front-to- back ratio of the antenna are increased by about 0.8 and 4 dB respectively due to the action of AMC.

Green Wearable Sensors and Antennas for Bio-Medicine, Green Internet of Things, Energy Harvesting, and Communication Systems.

This paper presents innovations in green electronic and computing technologies. The importance and the status of the main subjects in green electronic and computing technologies are presented in this paper. In the last semicentennial, the planet suffered from rapid changes in climate. The planet is suffering from increasingly wild storms, hurricanes, typhoons, hard droughts, increases in seawater height, floods, seawater acidification, decreases in groundwater reserves, and increases in global temperatures. These climate changes may be irreversible if companies, organizations, governments, and individuals do not act daily and rapidly to save the planet. Unfortunately, the continuous growth in the number of computing devices, cellular devices, smartphones, and other smart devices over the last fifty years has resulted in a rapid increase in climate change. It is severely crucial to design energy-efficient "green" technologies and devices. Toxic waste from computing and cellular devices is rapidly filling up landfills and increasing air and water pollution. This electronic waste contains hazardous and toxic materials that pollute the environment and affect our health. Green computing and electronic engineering are employed to address this climate disaster. The development of green materials, green energy, waste, and recycling are the major objectives in innovation and research in green computing and electronics technologies. Energy-harvesting technologies can be used to produce and store green energy. Wearable active sensors and metamaterial antennas with circular split ring resonators (CSSRs) containing energy-harvesting units are presented in this paper. The measured bandwidth of the matched sensor is around 65% for VSWR, which is better than 3:1. The sensor gain is 14.1 dB at 2.62 GHz. A wideband 0.4 GHz to 6.4 GHz slot antenna with an RF energy-harvesting unit is presented in this paper. The Skyworks Schottky diode, SMS-7630, was used as the rectifier diode in the harvesting unit. If we transmit 20 dBm of RF power from a transmitting antenna that is located 0.2 m from the harvesting slot antenna at 2.4 GHz, the output voltage at the output port of the harvesting unit will be around 1 V. The power conversion efficiency of the metamaterial antenna dipole with metallic strips is around 75%. Wearable sensors with energy-harvesting units provide efficient, low-cost healthcare services that contribute to a green environment and minimize energy consumption. The measurement process and setups of wearable sensors are presented in this paper.

Participation of strong charge-assisted hydrogen bonds in interactions of dissolved organic matter represented by Suwannee River Humic Acid

Terrestrial dissolved organic matter (DOM) plays critical roles in many biotic and abiotic environmental reactions as well as in water treatment. Its structure is therefore of great interest. We examined dissolved Suwannee River Humic Acid (HA) to probe the potential participation of exceptionally strong, negative charge-assisted hydrogen bonds, (−)CAHB, in DOM cohesion and interaction with small weak acids using high performance size exclusion chromatography (HPSEC), transmission electron microscopy, zeta-pH curves, and pH drift experiments. The results support a previously proposed two-tier state of aggregation, in which tightly-knit primary particles (≤ ∼10 kDa) form larger secondary aggregates (up to micrometer in size). Evidence for (−)CAHB is gained through zeta potential changes and pH drift experiments. The primary particles interact with (−)CAHB-capable solutes (simple carboxylic acids and phosphate) but not (−)CAHB-incapable solutes. We identified disruption of intra-segmental and inter-molecular (−)CAHB leading to swelling and disaggregation, as well as formation of nouveau (−)CAHB with free groups on HA. The effects were solute-concentration dependent and greater at pH 5 than pH 6, consistent with CAHB theory. Phosphate induced the greatest shifts in the HPSEC molecular size distribution curves. The shifts were unaffected by prior stripping of innate polyvalent metals. We conclude that the (−)CAHB contributes to the cohesion of DOM, affecting its size and charge, and provides a means by which weak acid pollutants, nutrients, and natural compounds can interact with DOM. Such interactions have implications for the behavior of DOM in the environment, the fate and transport of anthropogenic pollutants, and the roles DOM play in water treatment technologies.

High-Throughput Combinatorial Analysis of the Spatiotemporal Dynamics of Nanoscale Lithium Metal Plating.

The development of Li metal batteries requires a detailed understanding of complex nucleation and growth processes during electrodeposition. In situ techniques offer a framework to study these phenomena by visualizing structural dynamics that can inform the design of uniform plating morphologies. Herein, we combine scanning electrochemical cell microscopy (SECCM) with in situ interference reflection microscopy (IRM) for a comprehensive investigation of Li nucleation and growth on lithiophilic thin-film gold electrodes. This multimicroscopy approach enables nanoscale spatiotemporal monitoring of Li plating and stripping, along with high-throughput capabilities for screening experimental conditions. We reveal the accumulation of inactive Li nanoparticles in specific electrode regions, yet these regions remain functional in subsequent plating cycles, suggesting that growth does not preferentially occur from particle tips. Optical-electrochemical correlations enabled nanoscale mapping of Coulombic Efficiency (CE), showing that regions prone to inactive Li accumulation require more cycles to achieve higher CE. We demonstrate that electrochemical nucleation time (tnuc) is a lagging indicator of nucleation and introduce an optical method to determine tnuc at earlier stages with nanoscale resolution. Plating at higher current densities yielded smaller Li nanoparticles and increased areal density, and was not affected by heterogeneous topographical features, being potentially beneficial to achieve a more uniform plating at longer time scales. These results enhance the understanding of Li plating on lithiophilic surfaces and offer promising strategies for uniform nucleation and growth. Our multimicroscopy approach has broad applicability to study nanoscale metal plating and stripping phenomena, with relevance in the battery and electroplating fields.

Mathematical Framework to Model Electrodeposition/Stripping in Li-Metal Batteries during Cycling

Li-metal batteries, often heralded as the next frontier in energy storage technology, boast remarkable characteristics such as high energy density. Unlike traditional lithium-ion batteries, Li-metal batteries incorporate a lithium-metal anode, which significantly enhances their energy density. This higher energy density translates to a substantial increase in the amount of energy that can be stored in a given volume or weight, paving the way for more powerful and longer-lasting energy solutions[1–3]. However, significant shortcomings do exist, such as uneven Li-Metal deposition, dendrite formation, dead lithium, etc.[4] These phenomena are different than what are usually observed in Li-ion batteries with intercalation chemistry and lead to issues such as poor cycle life, low coulumbic efficiency, and safety concerns.[3]Mathematical modeling is a promising approach to studying the physicochemical processes involved in the Li-metal batteries to understand the morphology changes during cycling. The plating and stripping of the lithium metal on the anode during cycling can be modeled as a moving boundary problem.[5] Since the process involves a shrinking and expanding electrolyte domain, moving boundary problems call for the fastidious implementation of the model equations and boundary conditions.[6]In this talk, we will show the general mathematical framework involved in modeling Li-metal batteries in 1D systems. It expands upon the importance of carefully implementing boundary conditions to tackle the mass conservation issue that arises while cycling the model. It will also touch upon the additional complexities associated with expanding the model to 2D systems with convection in the electrolyte phase.

Boron-Doped Carbon Scaffold Hosts for Li Metal Batteries

Lithium metal anodes offer the promise of higher energy density batteries. However, the formation of lithium dendrites due to non-uniform plating and stripping of the lithium metal has proven to be a major hurdle for this technology, decreasing the lifetime of the device and causing safety hazards. Utilizing a carbon scaffold host for the lithium metal anode can limit dendrite formation by providing a more uniform electric field and numerous lithium nucleation sites to encourage uniform plating and stripping. In this poster, we present our work developing carbon scaffold hosts for lithium metal anodes. We synthesized scaffolds with various architectures and microstructures using different carbon materials. Our atomistic simulations demonstrated that the addition of boron to the carbon results in stronger binding of lithium to the carbon surface, further improving the lithiophilicity. Therefore, we also prepared boron-doped carbon scaffolds to test this experimentally. Boron was introduced using boric acid and incorporated into the carbon structure during carbonization under nitrogen, and these samples were characterized by XPS, SEM, and BET to try and correlate scaffold properties with performance. In addition, we are investigating other dopants (such as nitrogen), which have also been reported to increase the lithiophilicity of carbon materials. Utilizing these doped carbon scaffolds can help increase the lifetime of lithium metal batteries by improving the cycling uniformity.This work was performed under the auspices of the U.S. Department of Energy by Lawrence Livermore National Laboratory under Contract DE-AC52-07NA27344

Low-Cost Anode-Free Aqueous Batteries Using Permanent Magnets

The rise in portable electronics has created an ever growing demand for more electrochemical energy storage (EES) systems. Lithium-ion batteries have achieved widespread commercial use because of their high energy density, but concerns about their safety and the sustainability of lithium have created a search for alternatives. Aqueous batteries present a much safer option, and they are cheaper both in materials and fabrication. The zinc-ion battery is among the most researched aqueous batteries, but problems remain with the formation of zinc dendrites during plating on the anode. A number of solutions to this problem have been proposed, including the use of a permanent magnet placed behind a zinc-foil anode, which creates uniform zinc deposition via the magnetohydrodynamic (MHD) effect. Herein, we expand this concept to zinc deposition on other substrates for the so-called anode-free configuration, in which an inactive current collector is used for the zinc to plate and strip off of during cycling. This anode-free configuration is a promising way to reduce the cost and increase the energy density of batteries by removing active material and allowing a cheaper, inactive material to serve as the substrate for metal plating and stripping, and the use of a permanent magnet precludes the need for a complicated material or over-engineered solution interface to prevent dendrite growth.

Copper(II)-Tannic Acid@Cu with In Situ Grown Gold Nanoparticles as a Bifunctional Matrix for Facile Construction of Label-Free and Ultrasensitive Electrochemical cTnI Immunosensor.

Sensitive detection of cardiac troponin I (cTnI) is of great significance in the diagnosis of a fatal acute myocardial infarction. A redox-active nanocomposite of copper(II)-tannic acid@Cu (CuTA@Cu) was herein prepared on the surface of a glassy carbon electrode by electrochemical deposition of metallic copper combined with a metal stripping strategy. Then, HAuCl4 was in situ reduced to gold nanoparticles (AuNPs) by strong reductive catechol groups in the TA ligand. The AuNPs/CuTA@Cu composite was further utilized as a bifunctional matrix for the immobilization of the cTnI antibody (anti-cTnI), producing an electrochemical immunosensor. Electrochemical tests show that the immunoreaction between anti-cTnI and target cTnI can cause a significant reduction of the electrochemical signal of CuTA@Cu. It can be attributed to the insulating characteristic of the immunocomplex and its barrier effect to the electrolyte ion diffusion. From the signal changes of CuTA@Cu, cTnI can be analyzed in a wide range from 10 fg mL-1 to 10 ng mL-1, with an ultralow detection limit of 0.65 fg mL-1. The spiked recovery assays show that the immunosensor is reliable for cTnI determination in human serum samples, demonstrating its promising application in the early clinical diagnosis of myocardial infarction.

Release of contraction stress of dental resin composites by water sorption

Polymerization shrinkage of bonded resin composite restorations will result in the development of curing contraction stresses during setting and can cause debonding of the restoration or failure of the surrounding tooth structure. However, the hygroscopic expansion that occurs after exposure of the restorative to the wet oral environment can compensate for this shrinkage. ObjectivesThe purpose of this study was to determine the hygroscopic expansion of six commercial resin composites and relate it to their composition, mechanical properties, shrinkage, and contraction stress development. MethodsShort-term volumetric shrinkage and contraction stress of the different composites were measured by mercury dilatometry and a universal testing machine. The long-term contraction stress was measured by the deflection of a bilayer strip of metal and a resin composite, which were stored dry as well as wet to determine the effect of hygroscopic expansion. The curvature of the strip was measured by profilometry over a period of 3 months. ResultsThe curvature of the strip correlated well (r2 =0.74) with the initial contraction stress, showing that the contraction stress is an important factor in initial deformation. The water sorption in all specimens showed that the initial deformation, within 2–4 weeks after curing, was completely counteracted. A high correlation (r2 =0.90) between deflection and relative water sorption was found, where the relative water sorption is defined as the absolute water sorption corrected for the inorganic filler volume of the composite. SignificanceWithin a period of 2–4 weeks after curing most of the curing contraction stresses of resin composite restoratives will be released by hygroscopic expansion.

Fundamental Thermodynamic, Kinetic, and Mechanical Properties of Lithium and Its Alloys.

Lithium alloying reactions are beneficial in promoting uniform plating and stripping of lithium metal in all-solid-state batteries. First-principles calculations are performed to predict thermodynamic, kinetic, and mechanical properties of lithium and several important Li-M alloys (M = Mg, Ag, Zn, Al, Ga, In, Sn, Sb, and Bi). While the Li-Mg binary system forms a solid solution, most other lithium-metal alloys prefer stoichiometric intermetallic compounds with common local motifs that enable fast Li diffusion. Lithium and Li-rich alloys exhibit an unusually flat energy landscape along paths that connect BCC to close-packed structures like FCC and HCP, with important implications for mechanical properties. Very low migration barriers for Li diffusion that rival those of superion conductors are predicted, both in pure Li and in Li-M intermetallics. However, vacancy concentration, which is crucial for substitutional diffusion, is predicted to be low in metallic Li and most Li-M intermetallics. Compounds such as B32 LiAl and LiGa as well as D03 Li3Sb and Li3Bi exhibit structural vacancies at higher ends of their voltage windows, which together with low migration barriers leads to exceptionally high Li mobilities. In the Li-Mg solid solution, the addition of Mg is found to decrease the vacancy tracer diffusion coefficient by an order of magnitude.

Modeling the electro-chemo-mechanical failure at the lithium-solid electrolyte interface: Void evolution and lithium penetration

The solid-solid contact interface is crucial for the reliability of solid-state energy storage systems. The contact condition becomes more complicated when lithium (Li) metal is used as the anode. The contact between solid electrolyte (SE) and Li metal is inferior compared to the liquid/solid interface in conventional Li-ion batteries. Experimental evidence has shown that improper operating conditions of solid-state batteries can lead to electro-chemo-mechanical failures at the Li/SE interface, including the formation of voids and the penetration of Li. In this study, a unified phase-field model is developed to investigate these two mechanisms. The model considers the coupled electro-chemo-mechanical processes including void diffusion, lattice annihilation, stripping and plating reactions, and plastic deformation of Li metal. The study begins with a revisit of the deformation-mechanism map for Li metal under a wide range of temperatures, stress, and deformation rates. This map serves as the basis for the mechanical characterization in the phase-field model. The large inelastic deformation of Li is considered by introducing an advection term into the Allen-Cahn equation, which is used to describe the dynamic evolution of the Li and void phases. The effects of current density and stack pressure on void evolution and Li penetration are studied based on the model predictions. By combining the simulation results with the experimental data from publications, we obtain the stable operation zone of stack pressure and applied current density. In this zone, the Li/SE interface can enable stable stripping and plating of Li metal. The same phase-field modeling framework is transferred to investigate the Li-Mg alloy/SE interface considering Li-Mg alloy is also used as the anode. The fundamental difference between Li/SE and Li-Mg/SE is analyzed accordingly. This study provides a useful tool for the design, manufacturing, and management of next-generation batteries by providing important scientific insights into the electro-chemo-mechanical processes of different anode materials under various operational conditions.

A miniaturized dual wide‐band polarization reconfigurable antenna integrated with artificial magnetic conductor for next‐generation wireless applications

SummaryIn today's intricate wireless communication environment, ensuring system quality demands the use of a reliable and versatile antenna system. This research article introduces a polarization reconfigurable antenna integrated with a 4 × 4 Artificial Magnetic Conductor (AMC) surface. The AMC unit cell exhibits a triple‐band reflection phase response at 1.8GHz, 4.5GHz, and 5.5GHz, demonstrating double negative metamaterial behavior. The antenna features two distinct C‐shaped metal strips connected to two PIN diodes, enabling dynamic current distribution adjustment. Consequently, the proposed antenna offers three reconfigurable states, facilitating seamless switching between dual circular polarization (left and right‐hand circular polarization) and linear polarization. With a frequency coverage ranging from 1.29 to 2.52GHz and 3.59 to 6.15GHz, the antenna boasts a maximum axial ratio (AR) bandwidth of 31.96%. Additionally, it achieves a maximum peak gain of 5.5 dB and maintains front‐to‐back ratio (FBR) values exceeding 25 dB, while recording a minimum specific absorption rate (SAR) value of 0.1059 W/kg. The integration of the AMC surface ensures enhanced performance of the antenna. Experimental results from constructed prototypes closely align with simulation outcomes, validating the effectiveness of the proposed antenna. Consequently, this antenna holds significant promise for next‐generation wireless applications.

Effects of strain and ferromagnetic metal stripe on the electron transport properties in a graphene

Effects of strain and ferromagnetic metal stripe on the electron transport properties in a graphene

Real-time coloration control of gallium-based strips through cold rolling.

Cold rolling has been used as a real-time surface oxidation control method to create colored strips on flexible substrates. By controlling the extrusion rate in real time, a variety of colored strips have been fabricated on Ga-based liquid metal (LM) strips. X-ray photoelectron spectroscopy (XPS) analysis shows that the surfaces of the colored strips, which were obtained through extrusion rate control of LM-Al, consist primarily of metal oxide composites, including Ga2O3, Ga2O, Al2O3, SnO2, and In2O3. The colors of the strip surfaces are directly correlated with the oxide film thickness. Additionally, these cold-rolled colored thin strips demonstrate high conductivity and have significant potential for use as conductive flexible components with indicator functions in the flexible electronics realm.

Exploring the Application of Terahertz Metamaterials Based on Metallic Strip Structures in Detection of Reverse Micelles.

Terahertz spectroscopy has unique advantages in the study of biological molecules in aqueous solutions. However, water has a strong absorption capability in the terahertz region. Reducing the amount of liquid could decrease interference with the terahertz wave, which may, however, affect the measurement accuracy. Therefore, it is particularly important to balance the amount and water content of liquid samples. In this work, a terahertz metamaterial sensor based on metallic strips is designed, fabricated, and used to detect reverse micelles. An aqueous confinement environment in reverse micelles can improve the signal-to-noise ratio of the terahertz response. Due to "water pool" trapped in reverse micelles, the DOPC (1,2-dioleoyl-sn-glycero-3-phosphocholine) solution and DOPC emulsion can successfully be identified in intensity by terahertz spectroscopy. Combined with the metamaterial sensor, an obvious frequency shift of 30 GHz can be achieved to distinguish the DOPC emulsion (5%) from the DOPC solution. This approach may provide a potential way for improving the sensitivity of detecting trace elements in a buffer solution, thus offering a valuable toolkit toward bioanalytical applications.

Analysis of two-dimensional planar gratings and metasurfaces in the quasi-static approximation

Currently, composite materials based on metal gratings with a period D much smaller than the wavelength l are widely used. With the use of such materials, it is possible to control the amplitude, phase and polarization of an electromagnetic wave, which opens wide possibilities for the creation of new types of antennas, radio-absorbing coatings, etc. This paper considers gratings of metallic strip or patches on the surface of a thin metal-backed dielectric slab to control the phase of the reflected wave. In the quasi-static approximation, the input impedance of such materials can be calculated using simple analytical formulas. This paper investigates the accuracy of the quasi-static approximation at different angles of incidence of the electromagnetic wave on two-dimensional gratings. Using the equivalent circuits method, analytical expressions for the input impedance of metasurfaces are obtained. The dispersion properties of composite materials “inductive or capacitive grating on the surface of a thin metal-backed dielectric slab” are investigated, and a technique for determining the resonant frequency, which corresponds to the maximum of the input impedance of the metasurface, is presented. The obtained results show that at any angle of incidence, it is possible to evaluate the condition of the quasi-static approximation applicability for two-dimensional gratings and for metasurfaces based on such gratings. If this condition is satisfied, that simple analytical expressions can be used to calculate the input impedance. The use of these expressions allows us to determine the frequency at which the input impedance reaches its maximum. It is established that for inductive and capacitive gratings the impedance boundary condition of M.A. Leontovich is equivalent to the averaged boundary condition of M.I. Kontorovich. It is obtained that for grating in free space, quasi-static approximation corresponds to the M.A. Leontovich impedance condition. The dispersion properties of composite materials “inductive or capacitive grating on a thin metal-backed dielectric slab” are investigated. It is shown that the phase transition of the reflection coefficient through zero occurs at maximum values of the input impedance. Using the considered method of equivalent circuits, the presented results can be easily generalized to any type of multilayer metasurfaces.

Design and analysis of ultra-wideband miniaturized metamaterial absorbers for radiation suppression

This paper presents a novel miniaturized ultra-wideband metamaterial absorber with a thickness of 0.069λ L thick, engineered to suppress electromagnetic radiation in high-frequency chip packaging. The absorber’s bandwidth is enhanced through the incorporation of lumped resistors and patterned metal strips. Simulation results reveal an absorption efficiency exceeding 90% across the frequency range of 17.3–33.5 GHz, while maintaining polarization insensitivity and angular stability. The absorption mechanism is investigated using equivalent circuit theory and the S-parameter inversion method, which demonstrate consistent impedance matching and advantageous loss characteristics throughout the wide band. Relevant objects were meticulously prepared and tested, yielding a high correlation between the measured and simulated results. The proposed absorber, when integrated into package chips and patch antennas, significantly reduces the far-field electric field amplitude in both applications. Specifically, the packaged chip shows up to 19.7 dB of electromagnetic radiation suppression and the patch antenna structure achieves over 10 dB of radiation suppression in the 24.2 GHz–30.4 GHz range post-integration. These results affirm the absorber’s efficacy in effectively reducing unwanted electromagnetic radiation in specified frequency bands within complex electromagnetic environments. The absorber’s demonstrated effectiveness provides a promising approach to address the increasing issue of electromagnetic radiation in progressively miniaturized electronic devices.

Piperazinium Poly(Ionic Liquid)s as Solid Electrolytes for Lithium Batteries.

Poly(ionic liquid)s combine the unique properties of ionic liquids (ILs) within ionic polymers holding significant promise for energy storage applications. It is reported here the synthesis and characterization of a new family of poly(ionic liquid)s synthesized from cationic piperazinium ionic liquid monomers. The cationic poly(acrylamide piperazinium) in combination with sulfonamide anions like bis(trifluoromethanesulfonyl) imide (TFSI) and bis(fluorosulfonyl) imide (FSI) are characterized as solid polymer electrolytes. The polymer electrolytes in combination with pyrrolidonium ILs and LiFSI show high ionic conductivity, 5×10-3 S cm-1 at 100 °C. Piperazinium polymer electrolytes show excellent compatibility with lithium metal reversible plating and stripping at high current density and low temperature 40 °C.

A Spoof Surface Plasmon Polaritons Filter with Controllable Negative Slope Equalization Based on Surface Resistance

This paper presents a novel spoof surface plasmon polariton (SSPP) filter integrated with controllable negative slope equalization. Different from traditional microwave filters, two microwave functions - amplitude compensation and interference suppression - are integrated into one device by depositing a lossy indium tin oxide (ITO) film on the rectangular corrugated stub of the SSPP unit. The key point of negative slope equalization benefits from the surface resistance of the ITO film, and the circuit model and behavior are analyzed in detail. Based on the principle, a prototype of a SSPP filter operating from S to C band is designed and fabricated. The measurement results show that the attenuation in the passband increases almost linearly from 3.5 GHz (−4.8 dB) to 6.9 GHz (−15.4 dB), indicating that −10.6 dB equalization is achieved. The improved S21 is attributed to the good impedance matching by sputtering the ITO film on the rectangular metal strip rather than the central strip. Due to the natural low-pass property of SSPPs, the high-order parasitic band is suppressed above the cut-off frequency of 8.5 GHz. The analyses, simulations and measurements show that the proposed SSPP filter is provided with an additional ability to compensate for positive amplitude fluctuation in wideband antennas.

Metal Strip Implanted Tunneling Field-Effect Transistor Biosensor as a Label-Free Biosensor.

In this study, we design and simulate a metal implanted dielectrically modulated tunneling field-effect transistor (MI-DMTFET). In the ambipolar conduction state, the proposed structure works as an efficient sensor for the detection of a wide range of biomolecules. A metal strip (MS) is implanted above the drain-channel junction in the gate dielectric to improve the alignment of band gaps. Therefore, with the help of implanted metal work function engineering, the tunneling barrier gets lowered, which in turn increases the ambipolar current. An optimum metal-strip implant work function of 4.85 eV and a length of 1.5 nm have resulted in significantly improved performance of the proposed device. It has been observed that when the biomolecules with varying dielectric constants and charge densities are captured in the nanogap cavity, the ambipolar current of the biosensor changes, resulting in the detection of the biomolecules. Quantitative and comprehensive analyses of device parameters such as surface potential, electric field, band-to-band tunneling, subthreshold slope, and ION/IOFF ratio analysis have been performed. Rigorous comparative analyses of key performance-measuring parameters have been performed with a conventional sensor device. It has been found that the proposed device offers maximum sensitivity of 1220 under an ambipolar state at k = 12.