Open Voltage Research Articles

6T-8T Hybrid SRAM for Lower-Power Neural-Network Processing by Lowering Operating Voltage

6T-8T Hybrid SRAM for Lower-Power Neural-Network Processing by Lowering Operating Voltage

Wire-to-two-drop plasma thruster: Experimental and numerical investigation of electroaerodynamic jet flow for micro aerial vehicle propulsion

Conventional micro aerial vehicles (MAVs) have primarily relied on complex, flapping-wing mechanisms for propulsion, often exhibiting limitations in terms of reliability and efficiency. To overcome these challenges, this study explores the potential of electroaerodynamic (EAD) thrusters as a novel propulsion system. By accelerating air molecules through ion collisions, EAD jet flow generates thrust, offering advantages such as noiseless operation and zero emissions due to its moving-part-free design. This research presents a comprehensive experimental and numerical investigation of a wire-to-two-drop thruster configuration to elucidate its electromechanical performance, plasma flow dynamics, and EAD jet characteristics. Experimental measurements of key parameters, including current, thrust, power, and effectiveness, were correlated with numerical simulations, demonstrating excellent agreement with a maximum error below 5%. These findings align strongly with established theoretical frameworks, revealing an inverse square root relationship between effectiveness and thrust. To optimize thruster performance, optimal operating voltages were identified at approximately 8.2, 9.4, and 11.6 kV for inter-electrode gap distances of 10, 15, and 20 mm, respectively, achieving a balanced trade-off between thrust and effectiveness. Detailed numerical visualizations of the plasma flow field, including velocity distribution, jet morphology, potential distribution, and electric field lines, provided valuable insights into the thruster's operation. Building upon these insights, a proof-of-concept EAD flier was constructed and tested, incorporating a serrated emitter electrode and lightweight materials. This flier achieved a mass of 0.5 g and generated a thrust of 0.77 g at 15 kV, resulting in a thrust-to-weight ratio of 1.54 and successful liftoff. This demonstration highlights the potential of EAD propulsion for practical MAV applications.

Investigation of distribution system modification using operation voltage unification in order to decrease interruptions in dust climate

Many events in power networks which caused failure and outage of subsystems have root in design and initial selection of equipment and their specification. This concern will be important while the any kind of expanding and acclimation plan need to be executed to strengthen the existing infrastructures in order to provide better condition with regard to satisfied criteria. In Iran one of the most adverse environmental occurrences known Fine Dust, may force several distribution utilities to be changed due to new technical requirements. Medium voltage level regrading in way to decrease or unification of distribution system have been proposed in this paper to reach reduced faults and fast replacement of equipment in damaged situations. Voltage level changing and selection have been investigated in order to increase the network strengthen and reselection of equipment and redesigning critical sections of system against natural events that called fine dust with aim to attain an upgraded distribution utility. Operating of existing 33 kV and 11 kV network in 20 kV level and investigation of changing process have been done for Ahvaz medium voltage distribution system as a case study in these paper's sections. Calculations and results will be contained maximum current capacities in different line conductors, insulation and air clearances assessment, poles acceptable mechanical values, short circuit current and protection coordination for changing voltage level in distribution system.

Cation-inspired polyhedral distortion boosting moisture/electrolyte stability of iron sulfate cathode for durable high-temperature sodium-ion storage

Alluaudite-type iron-based sulfates are prospective positive-electrode active materials for sodium-ion batteries given their low-cost and high operation voltage, yet suffer from poor intrinsic ionic conductivity and (electro)chemical instability at high temperatures. Herein, a cation-modified Na2.466Fe1.724Mg0.043(SO4)3 with micron-sized spherical structure was reported. The substitutive MgO6 octahedron featured stronger covalent bonding interactions and enriched the ion transfer pathways within the crystals, facilitating the ionic kinetics in bulk. Using in situ mass spectrometry and quartz crystal microbalance techniques, Mg cations were demonstrated to lower the electron density around O atoms and surficial nucleophilicity of materials, which effectively suppressed their side reactions with H2O in air and active ester molecule in electrolyte. This interaction enables an inorganic-rich and uniform interphase to stabilize the cathode/electrolyte interface at high voltage (4.5 V vs. Na+/Na). The as-prepared cathode exhibits a high discharge capacity of 102.2 mAh g−1 (voltage platform at 3.74 V), remarkable reaction reversibility (average Coulomb efficiency of 99.3% over 300 cycles) at high loading (9.0 − 9.6 mg cm−2) and temperature (60 °C), as well as long-lasting cyclability (70.8%, 5000 cycles). Its application was verified in assembled sodium-ion full cells with a hard carbon negative electrode, showing a long cycling lifetime over 190 cycles.

A Universal Biocompatible and Multifunctional Solid Electrolyte in p-Type and n-Type Organic Electrochemical Transistors for Complementary Circuits and Bioelectronic Interfaces.

The development of soft and flexible devices for collection of bioelectrical signals is gaining momentum for wearable and implantable applications. Among these devices, organic electrochemical transistors (OECTs) stand out due to their low operating voltage and large signal amplification capable of transducing weak biological signals. While liquid electrolytes have demonstrated efficacy in OECTs, they limit its operating temperature and pose challenges for electronic packaging due to potential leakage. Conversely, solid electrolytes offer advantages such as mechanical flexibility, robustness against environmental factors, and ability to bridge the interface between rigid dry electronics systems and soft wet biological tissues. However, few systems have demonstrated generality and compatibility with a wide range of state-of-the-art organic mixed ionic-electronic conductors (OMIECs). This paper introduces a highly stretchable, flexible, biocompatible, self-healable gelatin-based solid-state electrolyte, compatible with both p- and n-type OMIEC channels while maintaining high performance and excellent stability. Furthermore, this nonvolatile electrolyte is stable up to 120°C and exhibits high ionic conductivity even in dry environment. Additionally, an OECT-based complementary inverter with a record-high normalized-gain of 228 V-1 and a corresponding ultralow static power consumption of 1 nW is demonstrated. These advancements pave the way for versatile applications ranging from bioelectronics to power-efficient implants.

Bipolar Textile Composite Electrodes Enabling Flexible Tandem Solid-State Lithium Metal Batteries.

A majority of flexible and wearable electronics require high operational voltage that is conventionally achieved by serial connection of battery unit cells using external wires. However, this inevitably decreases the energy density of the battery module and may cause additional safety hazards. Herein, a bipolar textile composite electrode (BTCE) that enables internal tandem-stacking configuration to yield high-voltage (6 to 12V class) solid-state lithium metal batteries (SSLMBs) is reported. BTCE is comprised of a nickel-coated poly(ethylene terephthalate) fabric (NiPET) core layer, a cathode coated on one side of the NiPET, and a Li metal anode coated on the other side of the NiPET. Stacking BTCEs with solid-state electrolytes alternatively leads to the extension of output voltage and decreased usage of inert package materials, which in turn significantly boosts the energy density of the battery. More importantly, the BTCE-based SSLMB possesses remarkable capacity retention per cycle of over 99.98% over cycling. The composite structure of BTCE also enables outstanding flexibility; the battery keeps stable charge/discharge characteristics over thousands of bending and folding. BTCE shows great promise for future safe, high-energy-density, and flexible SSLMBs for a wide range of flexible and wearable electronics.

Unlocking the potential of Mg-ion batteries: Cu2C MXene anode with ultrahigh storage and energy density with rapid Mg diffusion

Magnesium-ion batteries hold immense promise for the future of electrical energy storage due to the abundant availability of magnesium metal and the efficient energy storage capacity of divalent magnesium ions which has the potential to revolutionize both large-scale stationary applications and portable devices. MXenes, encompassing transition metal carbides/nitrides/carbonitrides, are still considered newcomers in the domain of 2D nanomaterials, especially regarding their utilization in energy storage applications. In this work, we employed first principles based DFT calculations to comprehensively evaluate the electrochemical behavior of 2H phase Cu-based MXene (Cu2C) monolayer as promising anode material for Mg-ion batteries. The stability of the Cu2C monolayer was assessed through calculations of negative cohesive energy, positive phonon frequencies, and AIMD simulations to confirm stability at room temperature along with superior mechanical strength. The simulation outcomes show that strong affinity for Mg ions to the Cu2C monolayer, which is attributed to metallic character, suggesting good electronic conductivity and aslo, the calculated negative adsorption energy of −1.25 eV, indicating a favorable interaction for potential battery applications. The Cu2C monolayer emerges as a compelling candidate for anode materials due to its exceptional combination of high theoretical specific capacity (1541.36 mAh/g) and a low average operating voltage (0.50 V). This translates to a remarkable energy density of 2882.34 mWh/g (referenced against the standard hydrogen electrode potential), making it a strong contender for next-generation battery technologies. Furthermore, our investigation revealed rapid diffusion barriers for Mg-ion migration with exceptional properties with robust compatibility with electrolytes, makes it anode materials for Mg-ion batteries, attracting significant interest in the near future.

Optimum Design of InGaN Blue Laser Diodes with Indium-Tin-Oxide and Dielectric Cladding Layers.

The efficiency of current GaN-based blue laser diodes (LDs) is limited by the high resistance of a thick p-AlGaN cladding layer. To reduce the operation voltage of InGaN blue LDs, we investigated optimum LD structures with an indium tin oxide (ITO) partial cladding layer using numerical simulations of LD device characteristics such as laser power, forward voltage, and wall-plug efficiency (WPE). The wall-plug efficiency of the optimized structure with the ITO layer was found to increase by more than 20% relative to the WPE of conventional LD structures. In the optimum design, the thickness of the p-AlGaN layer decreased from 700 to 150 nm, resulting in a significantly reduced operation voltage and, hence, increased WPE. In addition, we have proposed a new type of GaN-based blue LD structure with a dielectric partial cladding layer to further reduce the optical absorption of a lasing mode. The p-cladding layer of the proposed structure consisted of SiO2, ITO, and p-AlGaN layers. In the optimized structure, the total thickness of the ITO and p-AlGaN layers was less than 100 nm, leading to significantly improved slope efficiency and operation voltage. The WPE of the optimized structure was increased relatively by 25% compared to the WPE of conventional GaN-based LD structures with a p-AlGaN cladding layer. The investigated LD structures employing the ITO and SiO2 cladding layers are expected to significantly enhance the WPE of high-power GaN-based blue LDs.

High-Valent Thiosulfate Redox Electrochemistry for Advanced Sulfur-Based Aqueous Batteries.

Sulfur-based aqueous batteries (SABs) are promising for safe, low-cost, and high-capacity energy storage. However, the low output voltage of sulfur cannot meet the demands of high-energy cathode applications due to its intrinsic negative potential (E0 = -0.51 V vs SHE) of low-valent polysulfide redox (S2-/S0). Here, instead of relying on traditional aqueous polysulfide redox, for the first time, we demonstrate a high-valent thiosulfate redox (S2O32-/S4O62-) electrochemistry, exhibiting positive redox potential (E0 > 0 V vs SHE) and reversible cation storage in aqueous environment. Operando X-ray absorption fine structure spectroscopy, in situ Raman spectroscopy, and density functional theory calculations reveal the high reversibility and dynamic charge transfer process of high-valent thiosulfate redox. Significantly, the aqueous thiosulfate redox exhibits a high operating voltage of approximately 1.4 V, a reversible capacity of 193 Ah L-1, and a long cycling life of over 1000 cycles (99.6% capacity retention). This work provides new insights into the high-valent S-based electrochemistry and opens a new pathway to achieve energetic aqueous batteries.

Study on the Single-Event Burnout Effect Mechanism of SiC MOSFETs Induced by Heavy Ions

As a prominent focus in high-voltage power devices, SiC MOSFETs have broad application prospects in the aerospace field. Due to the unique characteristics of the space radiation environment, the reliability of SiC MOSFETs concerning single-event effects (SEEs) has garnered widespread attention. In this study, we employed accelerator-heavy ion irradiation experiments to study the degradation characteristics for SEEs of 1.2 kV SiC MOSFETs under different bias voltages and temperature conditions. The experimental results indicate that when the drain-source voltage (VDS) exceeds 300 V, the device leakage current increases sharply, and even single-event burnout (SEB) occurs. Furthermore, a negative gate bias (VGS) can make SEB more likely via gate damage and Poole–Frenkel emission (PF), reducing the VDS threshold of the device. The radiation degradation behavior of SiC MOSFETs at different temperatures was compared and analyzed, showing that although high temperatures can increase the safe operating voltage of VDS, they can also cause more severe latent gate damage. Through an in-depth analysis of the experimental data, the physical mechanism by which heavy ion irradiation causes gate leakage in SiC MOSFETs was explored. These research findings provide an essential basis for the reliable design of SiC MOSFETs in aerospace applications.

Operating voltage of a W-fuzz cathode arc and the mass/charge composition of the arc plasma depending on the fuzz thickness

The arc operating voltage and the mass/charge composition of the arc plasma were measured for W-fuzz samples with different fuzz thicknesses at different numbers of arc pulses. It was found that the formation of a fuzz structure led to a significant decrease in the arc operating voltage within the first few arc pulses. With an increase in the number of pulses, the operating voltage and the mean charge of tungsten ions in the arc plasma increased to values characteristic of conventional tungsten cathodes. The obtained experimental data were analyzed theoretically using an empirical cohesive energy rule and a magnetohydrodynamic model of the ionization processes occurring in a cathode plasma jet.

Highly Sensitive Biosensors Based on All-PEDOT:PSS Organic Electrochemical Transistors with Laser-Induced Micropatterning.

Recent advances in numerous biological applications have increased the accuracy of monitoring the level of biologically significant analytes in the human body to manage personal nutrition and physiological conditions. However, despite promising reports about costly wearable devices with high sensing performance, there has been a growing demand for inexpensive sensors that can quickly detect biological molecules. Herein, we present highly sensitive biosensors based on organic electrochemical transistors (OECTs), which are types of organic semiconductor-based sensors that operate consistently at low operating voltages in aqueous solutions. Instead of the gold or platinum electrode used in current electrochemical devices, poly(3,4-ethylenedioxythiophene):poly(4-styrenesulfonate) (PEDOT:PSS) was used as both the channel and gate electrodes in the OECT. Additionally, to overcome the patterning resolution limitations of conventional solution processing, we confirmed that the irradiation of a high-power IR laser (λ = 1064 nm) onto the coated PEDOT:PSS film was able to produce spatially resolvable micropatterns in a digital-printing manner. The proposed patterning technique exhibits high suitability for the fabrication of all-PEDOT:PSS OECT devices. The device geometry was optimized by fine-tuning the gate area and the channel-to-gate distance. Consequently, the sensor for detecting ascorbic acid (vitamin C) concentrations in an electrolyte exhibited the best sensitivity of 125 μA dec-1 with a limit of detection of 1.3 μM, which is nearly 2 orders of magnitude higher than previous findings. Subsequently, an all-plastic flexible epidermal biosensor was established by transferring the patterned all-PEDOT:PSS OECT from a glass substrate to a PET substrate, taking full advantage of the flexibility of PEDOT:PSS. The prepared all-plastic sensor device is highly cost-effective and suitable for single-use applications because of its acceptable sensing performance and reliable signal for detecting vitamin C. Additionally, the epidermal sensor successfully obtained the temporal profile of vitamin C in the sweat of a human volunteer after the consumption of vitamin C drinks. We believe that the highly sensitive all-PEDOT:PSS OECT device fabricated using the accurate patterning process exhibits versatile potential as a low-cost and single-use biosensor for emerging bioelectronic applications.

Converting a low-cost industrial polymer into organic cathodes for high mass-loading aqueous zinc-ion batteries

Aqueous zinc-ion batteries (AZIBs) using organic cathodes have emerged as a sustainable energy storage technology benefitting from high safety, low cost, and abundant feedstocks. However, most organic cathodes are n-type polyaromatic compounds and conjugated polymers, which require sophisticated synthesis, provide a low operational voltage and slow Zn2+ diffusion kinetics. Herein, we report access to p-type radical polymer cathodes from a commercially available poly(methyl vinyl ether-alt-maleic anhydride) (poly(MVE-alt-MA)) polymer. The modification of poly(MVE-alt-MA) with 4-amino-TEMPO produces radical polymers (PTEMPO) that are easily scalable to tens of grams. The corresponding polymer AZIBs deliver a capacity of 92 mAh g-1 at 10 C with 95 % capacity retention over 1000 cycles. Importantly, the electrode composites and battery assembly procedure are optimised so that no fluoro-containing electrolytes and binders are needed, and cheap carbon additives can be used. We assemble the Swagelok batteries, small pouch, and large pouch batteries with a high mass-loading of 7.8 to 50 mg cm-2, demonstrating nearly 100 % Coulombic efficiency. The pouch battery with 0.8–0.9 g of active polymer displayed a 60-mAh capacity with 1.5 V operational voltage. This work paves the way for simple and practical implementation of polymer AZIBs for real-world applications.

Mechanical and electric friction properties of Poly(methyl methacrylate) – Nitrocellulose blend polymer for triboelectric nanogenerators

In this study, nitrocellulose - polymethyl methacrylate (NC/PMMA) blend film as a positive triboelectric material for triboelectric nanogenerator (TENG) with controlled flexibility was successfully synthesized by varying the PMMA content in the polymer blend. The combination of NC and PMMA reduced the limitations of the individual component materials with improved mechanical properties such as tensile strength, elastic modulus and elongation at breaking point. The TENG fabricated from NC/PMMA as a positive friction layer paired with fluorinated ethylene propylene (FEP) or polytetrafluoroethylene (PTFE) as a negative friction layer demonstrates a high peak to peak voltage output of 234 V at low frequency and with an actuation force of 10~N. The open circuit triboelectric voltage value maintains 91% durability after 26200 click-release cycles. This work provides a potential approach to simultaneously improve the electrical and mechanical properties of triboelectric materials, promoting the possibility of practical applications of TENG.

N‐Doped Carbon Coated Bimetallic CoFe2O4 Nanomembranes as An Enhanced Negative Electrode for Asymmetric Supercapacitors

AbstractIn‐suit nitrogen‐doped carbon layer coated on CoFe2O4 nanomembrane (NC−CoFe2O4) directly grown on carbon cloth was successfully fabricated. The electrochemical performance was conveniently manipulated by regulating the molar ration of Co2+ : Fe3+ (molar ration=1 : 2, CoFe2O4 nanomembrane, 2.9 F cm−2). Nitrogen‐doped (N‐doped) carbon coating strategy on CoFe2O4 nanomembrane (NC−CoFe2O4) via annealing of polypyrrole (PPy) was presented and NC−CoFe2O4 nanomembranes displayed a prominent capacitance of 12.1 F cm−2 (2563.8 F g−1) at 5 mA cm−2. More important, the composite demonstrated more stable microstructure and showed long‐term cycling stability (16.0 % decrease after 7000 cycles), which was significantly better than the unmodified CoFe2O4 (55.8 % decrease after 1000 cycles). To verify the practicability of the materials, an aqueous asymmetric supercapacitor has been fabricated using NC−CoFe2O4 composite anode and MnO2/CNTs cathode, and the device has a remarkable wide operating voltage range of 1.9 V. In addition, the assembled device has an exceptional specific capacity of 1.3 F cm−2 at 10 mA cm−2, high energy density (43.3 Wh kg−1 at a power density of 642.9 W kg−1), and also with a good capacity retention rate of 84.9 % after 1000 cycles.

Deciphering the Degradation Mechanisms and Realize High-Voltage Stability of A3V2(PO4)3 (A=Li+, Na+) in Aqueous Dual-Ion Batteries.

Polyanionic A3V2(PO4)3 (A=Li+, Na+) with open channels have been extensively utilized as cathode materials for aqueous zinc-metal batteries (AZMBs), whereas suffering from severe capacity fading and rapid operation voltage decay during cycling. when used as In this work, it is disclosed that the rapid degradation is induced by an irreversible phase change from electrochemical active Li3V2(PO4)3 to nonactive monoclinic LiZnPO4, as well as active Na3V2(PO4)3 to nonactive rhombic Zn3(PO4)2(H2O)4. Subsequently, a rational dual-cation (Al-Fe) doping strategy is proposed to suppress these detrimental transformations. Such dual-cation doping entails stronger P-O and V-O bonds, thus stabilizing the initial polyanionic structures. Consequently, the optimized member of Li3V1.775Al0.075Fe0.225(PO4)3 (LVAFP) exhibits desirable cycling stability (1000 cycles, 68.5% capacity retention) and notable rate capability (92.1% of the initial capacity at 10 C). Moreover, the dual-cation doping methodology is successfully extended to improve the stability of Na3V2(PO4)3 cathode in aqueous dual-ion batteries, signifying the versatility and feasibility of this strategy. The comprehensive identification of local structural evolution in these polyanions will broaden the scope of designing high-performance alkali-vanadyl-phosphates for multivalent aqueous batteries.

Understanding the Role of Mn Substitution for Boosting High-Voltage Na4Fe3-xMnx(PO4)2P2O7 Cathode in Sodium-Ion Batteries.

Na4Fe3(PO4)2P2O7 is regarded as the most promising polyanionic cathode for sodium-ion batteries (SIBs) due to its superior structural stability, cost-effectiveness, and environmental benignity. However, the low operating voltage inevitably weakens its competitiveness in energy density. Previous works have tried to enhance its operating voltage by Mn doping, which draws on the design idea of LiFexMn1-xPO4 cathode for lithium-ion batteries, but with little success. In this context, uncovering the role of Mn substitution in Na4Fe3-xMnx(PO4)2P2O7 (NFMxPP) cathode is urgently needed. This work discloses the effect of Mn contents on the structure, sodium storage property, and reaction mechanism of NFMxPP cathode for the first time. Introducing a moderate amount of Mn (0.6 ≤ x ≤ 1.2) into NFMxPP can weaken the Fe-O bonding interaction, thus leading to the full utilization of Mn3+/Mn2+ redox couple. As the representative, NFM1.2PP cathode exhibited a high operating voltage of ≈3.3V with a reversible capacity of 109.2 mAh g-1. Note that a Hard carbon||NFM1.2PP full battery manifests considerably high-capacity retention of 92.3% over 1600 cycles. It is believed that an understanding of the role of Mn substitution in this work will promote the practical application of high voltage NFMxPP cathodes for SIBs.

Multi-objective economic operation of smart distribution network with renewable-flexible virtual power plants considering voltage security index

This paper discusses the simultaneous management of active and reactive power of a flexible renewable energy-based virtual power plant placed in a smart distribution system, based on the economic, operational, and voltage security objectives of the distribution system operator. The formulated problem aims to specify the minimum weighted sum of energy cost, energy loss, and voltage security index, considering the optimal power flow model, voltage security formulation, and the operating model of the virtual power plant. The virtual unit includes renewable sources, like wind systems, photovoltaic, and bio-waste units. Flexibility resources include electric vehicle parking lot and price-based demand response. In the mentioned scheme, parameters of load, renewable sources, electric vehicles, and energy prices are uncertain. This paper utilizes the Unscented Transformation method for modeling uncertainties. Fuzzy decision-making is utilized to extract a compromised solution. The suggested approach innovatively considers the simultaneous management of active and reactive power of a virtual unit with electric vehicles and price-based demand response. This is performed to promote economic, operational, and network security objectives. According to numerical results, the approach with optimal power management of renewable virtual units is capable of boosting the economic, operation, and voltage security status of the network by approximately 43%, 47–62%, and 26.9%, respectively, to power flow studies. Only price-based demand response can improve the voltage security, operation, and economic states of the network by about 19.5%, 35–47%, and 44%, respectively, compared to the power flow model.

Improvement of an ionic wind blower’s flow characteristic by auxiliary electrodes for thermal management of light-emitting diodes

Electronic device advancements in power, size reduction, and integration have resulted in increased heat flux and operating temperatures, negatively impacting the reliability of electronics. Ionic wind cooling is a new, environmentally friendly, and energy-efficient thermal management approach that effectively cools high heat flux local heat sources. However, enhancing ionic wind strength continuously can be challenging. In this study, an ionic wind blower consisting of an emitting electrode, a collecting electrode, and auxiliary electrodes is constructed. The experimental verification confirms the supplemental acceleration capacity of the auxiliary electrodes. When determining the optimal operating voltage applied to the auxiliary electrodes, the power consumption of the system and the intensity of the output ionic wind are taken into consideration. Theblower’s operational and structural factors, such as the emitter structure, discharge gap, and distance between the auxiliary electrodes and collectors, are optimized according to how they affect the device’s functional qualities. The improved blower’s heat dissipation ability is evaluated by cooling an LED chip. The results demonstrate that the system performs optimally with an emitter having seven needles, a discharge gap of 5 mm, and 9 mm between the auxiliary electrodes and the collector. The wind speed reaches 2.47 m/s, while the power consumption is only 1.6 W. Compared to the absence of auxiliary electrodes (47.7 W/(m2∙K)), the system’s mean convective heat transfer coefficient can reach 61.12 W/(m2∙K), resulting in a temperature reduction of the LED chip by up to 41.6 °C. With increasing voltage, the heat transfer enhancement ratio improves, enabling a blower with auxiliary electrodes to provide significant cooling while consuming less power.

A Compact V-Band Transit Time Oscillator with Reflective Modulation Cavity

Improving compactness is essential for high-power microwave (HPM) sources. In this paper, a novel reflective modulation cavity is proposed and investigated in a V-band relativistic coaxial transit-time oscillator (RCTTO). The cold cavity analyses and particle-in-cell simulations show that the reflective modulation cavity has larger reflection coefficients of TEM mode and stronger electron beam modulation capability when compared with a uniform modulation cavity. When the input diode voltage is 391 kV, the beam current is 4.91 kA, and when the guiding magnetic field is 0.6 T, the compact V-band RCTTO produces an output microwave power of 518 MW (conversion efficiency of 27.0%). Compared with the original RCTTO, the compact V-band RCTTO featuring a reflective modulation cavity exhibits a 24.8% increase in output power and a 5.4% improvement in efficiency, and the axial length of the magnetic field uniform region is reduced by 24.2%. The compact V-band RCTTO also demonstrates a broad operation voltage range, indicating potential for stable operation with voltage fluctuations in experiments. Furthermore, the reflective modulation cavity can be integrated into other high-frequency O-type HPM devices to enhance compactness, thereby diminishing the demands on the magnetic field region, which is advantageous for the future permanent packaging of HPM sources.