Power Density Research Articles

Investigation of the Single-Particle Scale Structure-Activity Relationship Providing New Insights for the Development of High-Performance Batteries.

As electric vehicles, portable electronic devices and tools have increasingly high requirements for battery energy density and power density, constantly improving battery performance has become a research focus. Accurate measurement of the structure-activity relationship of active materials is the key to advancing the research of high-performance batteries. However, the conventional performance tests of active materials are based on the electrochemical measurement of porous composite electrodes containing active materials, polymer binders, and conductive carbon additives, which cannot establish an accurate structure-activity relationship with the physical characterization of microregions. In this review, in order to promote the accurate measurement and understanding of the structure-activity relationship of materials, the electrochemical measurement and physical characterization of energy storage materials at single-particle scale are reviewed. The potential problems and possible improvement schemes of the single particle electrochemical measurement and physical characterization are proposed. Their potential applications in single particle electrochemical simulation and machine learning are prospected. This review aims to promote the further application of single particle electrochemical measurement and physical characterization in energy storage materials, hoping to achieve three-dimensional unified evaluation of physical characterization, electrochemical measurement, and theoretical simulation at the single particle scale to provide new inspiration for the development of high-performance batteries. This article is protected by copyright. All rights reserved.

Cyanogel-Induced Facile Synthesis of Palladium Hydride for Electrocatalytic Oxygen Reduction.

Palladium hydride (PdHx) is one of the well-known electrocatalytic materials, yet its synthesis is still a challenge through an energy-efficient and straightforward method. Herein, we propose a new and facile cyanogel-assisted synthesis strategy for the preparation of PdH0.649 at a mild environment with NaBH4 as the hydrogen source. Unlike traditional inorganic Pd precursors, the unique Pd-CN-Pd bridge in Pdx[Pd(CN)4]y·aH2O cyanogel offers more favourable spatial sites for insertion of H atoms. The characteristic three-dimensional backbone of cyanogel also acts as a support scaffold resulting in the interconnected network structure of PdH0.649. Due to the incorporation of H atoms and interconnected network structure, the PdH0.649 achieves a high half-wave potential of 0.932 V, a high onset potential of 1.062 V, and a low activation energy, as well as a long-term lifetime for oxygen reduction reaction. Theoretical calculation demonstrates a downshift of the d-band centre of Pd in PdH0.649 owing to the dominant Pd-H incorporation that weakens the binding energies of the *OH intermediate species. Zn-air batteries (ZAB) based on PdH0.649 exhibits high power density, competitive open circuit voltage, and good stability, exceeding that of commercial Pt black.

Seeded Growth of Size-Tunable Au@Ag Core-Shell Nano-Octahedra and Their Yolk-Shell Derivatives for Near Infrared Photothermal Conversion.

Gold-based nanostructures with well-defined morphologies and hollow interiors have significant potential as a versatile platform for various plasmonic applications including biomedical diagnostics and sensing. In this study, we report the synthesis of Au@Ag core-shell nanocrystals with perfect octahedral shapes and tunable edge lengths via seeded growth. These nanocrystals were then oxidatively carved into yolk-shell nanocages with a retained octahedral morphology. The increase in octahedral edge length and volume of the interior hollow cavity synergistically leads to a red-shift of the LSPR peak. As a result, the optimized Au@AuAg yolk-shell octahedral nanocages showed a remarkable temperature increase of 23 °C upon 15 min irradiation of an 808 nm laser at a power density of 1 W cm-2. This study provides a feasible strategy for creating octahedral AuAg nanostructures with tunable sizes and hollow interiors and validates their promising use in NIR photothermal conversion.

Unveiling the Impact of Tailoring Ionic Conductor Characteristics on the Performance of Wearable Triboelectric Nanogenerators.

This work reveals the correlation between the performance of triboelectric nanogenerators (TENGs) and the characteristics of deformable solid-state ionic conductors (referred to as ionogels). For this purpose, we modify ionogel characteristics by incorporating additional plasticizers (propylene carbonate) and solid salts (lithium bis(trifluoromethylsulfonyl)imide) into the ionogels. We conclude that the high capacitance of the ionogel is crucial for achieving a high-performance TENG platform. The optimized ionogel-based TENG (i-TENG) exhibits a power density of ∼372.4 mW·m-2 (based on 95 V and 36 mA·m-2 outputs) with outstanding long-term stability over 2 weeks. Additionally, successful demonstrations of wearable nanogenerators are performed by leveraging the high stretchability (up to ∼1000%) and optical transparency (∼90%) of the ionogels. Overall, the results provide insight into the design of deformable ionic conductors for high-performance, reliable, and wearable TENGs.

2D-on-2D Al-Doped NiCo LDH Nanosheet Arrays for Fabricating High-Energy-Density, Wide Voltage Window, and Ultralong-Lifespan Supercapacitors.

Battery-type electrode materials with high capacity, wide potential windows, and good cyclic stability are crucial to breaking through energy storage limitations and achieving high energy density. Herein, a novel 2D-on-2D Al-doped NiCo layered double hydroxide (NiCoAlx LDH) nanosheet arrays with high-mass-loading are grown on a carbon cloth (CC) substrate via a two-step hydro/solvothermal deposition strategy, and the effect of Al doping is employed to modify the deposition behavior, hierarchical morphology, phase stability, and multi-metallic synergistic effect. The optimized NiCoAl0.1 LDH electrode exhibits capacities of 5.43, 6.52, and 7.25 C cm-2 (9.87, 10.88, and 11.15 F cm-2) under 0-0.55, 0-0.60, and 0-0.65V potential windows, respectively, illustrating clearly the importance of the wide potential window. The differentiated deposition strategy reduces the leaching level of Al3+ cations in alkaline solutions, ensuring excellent cyclic performance (108% capacity retention after 40000 cycles). The as-assembled NiCoAl0.1 LDH//activated carbon cloth (ACC) hybrid supercapacitor delivers 3.11 C cm-2 at 0-2.0V, a large energy density of 0.84 mWh cm-2 at a power density of 10.00mW cm-2, and excellent cyclic stability with ≈135% capacity retention after 150000 cycles.

Standard Response Calculation of Electric Dipole Polarizability and Specific Optical Rotation Power Densities.

A time-dependent method has been developed to solve the standard response equation for the calculation of dynamic molecular property densities, endowed with the characteristic of being origin-invariant, entirely in the atomic orbital basis at both HF and DFT level of theory. The method has been tuned in particular for the calculation of origin-independent electric dipole polarizability density and specific rotation power density. Some demonstrations are given for the hexabenzocoronene molecule and the Tröger base.

Completely Methylene-Free Side Chain Enables Significant Microphase Separation at Medium IECs for Fuel-Cell Anion Exchange Membranes.

The introduction of hydrophobic side chain structures in anion exchange membranes (AEMs) to facilitate ion transport has been widely studied; however, low or moderate hydrophobic hydrocarbon and semifluorinated side chains are insufficient to induce a high degree of microphase separation. Herein, we design and prepare poly(aryl piperidinium) AEMs with completely methylene-free perfluorinated side chains, which can maximize the thermodynamic incompatibility between main- and side chains, thus enhancing microphase separation at medium ion exchange capacities (IECs). According to the molecular dynamics study, the methylene-free perfluorinated side chain leads to better hydration of cations. The hydroxide conductivity of the methylene-free perfluorinated side chain-grafted PAP-pF-1 membrane reaches 124.9 mS cm-1 at 80 °C, and the PAP-sF-1 with semifluorinated side chains and PAP-CH-1 with hydrocarbon side chains show lower conductivity (116.8 and 104.0 mS cm-1). The H2/O2 fuel cell using the PAP-pF-1 membrane demonstrates a remarkable peak power density (1651 mW cm-2 at 80 °C) and durability (greater than 300 h). This work provides a novel insight into enhancing microphase separation in AEMs; it opens up new possibilities for developing high-performance AEMs.

3D printing of reversible solid oxide cell stacks for efficient hydrogen production and power generation

Renewable hydrogen offers a promising pathway to address the challenge of large-scale chemical energy storage in the transition to a decarbonized future. The most efficient devices to convert renewable electricity into hydrogen, and vice versa, are reversible solid oxide cells (SOC-s). Despite recent advances in materials performance and durability, conventional ceramic manufacturing technologies strongly limit the huge potential of SOC-s, imposing severe geometrical restrictions that penalize the overall system efficiency. Here we capture the benefits of using previously unexplored complex-shapes by scaling 3D-printed reversible solid oxide cells with improved mechanical properties, higher performance, and embedded functionality. Stacks made of 45 cm2-3D-printed electrolyte-supported solid oxide cells combined with ultrathin flat metallic interconnects were successfully fabricated and operated in fuel cell (SOFC) and electrolysis (SOEC) modes delivering up to 85 L/h of hydrogen production while presenting less than 5 % degradation after more than 500 h of operation. The advances presented here demonstrate the viability of upscaling the process of solid-oxide-cell 3D printing and brings advantageous stack designs aimed for a cost-competitive and customizable hydrogen technologies deployment. In particular, the enhancement by design achieved here provides innovative SOC stacks with volumetric and gravimetric power densities that are three and four times higher, respectively, than their planar counterparts using the same set of materials.

A novel MXene coated liquid crystal display anode derived from a futile computer monitor for microbial fuel cell application

A Ti3C2Tx MXene nanosheet-coated liquid crystal display (LCD) anode is meticulously crafted through precision waterjet cutting, salvaging a discarded LCD monitor. This technique, preserving structural integrity and enhanced electrical conductivity, sets it apart from conventional methods. The resulting MXene-coated LCD anode is well-suited for microbial fuel cell (MFC) applications. Comparative assessments against costlier carbonaceous electrodes like graphite felt and carbon cloth, emphasize that the water-jet cut LCD anode with Ti3C2Tx MXene coating is 3.79 and 2.51 times more cost-effective, with an approximate total cost of $38/m2. Substituting Ti3C2Tx MXene-coated LCD for carbon cloth and graphite felt anodes reduces MFC unit fabrication costs by 19 and 10.45 %, respectively. Notably, the Ti3C2Tx MXene LCD anode-based MFC unit boasts a power density per unit cost of 0.008 W/m2/$, underscoring economic viability. This research highlights waterjet cutting's pivotal role in crafting Ti3C2Tx MXene LCD anodes, opening avenues for scalable, cost-effective electrode production in renewable energy applications.

Photobiomodulation on isolated mitochondria at 810 nm: first results on the efficiency of the energy conversion process

In this paper the photobiomodulation on isolated mitochondria of bovine liver is studied as a thermodynamic process of conversion of energy. This analysis is conducted by considering a particular set-up for the photobiomodulation experiments of interest. It allows, in particular, the computation of the electromagnetic field and the related energetic quantities in the stimulated organelles. The measurements of the excess of biochemical power density produced by the illuminated mitochondria are performed at regular time intervals after the experiments. The calculations and the measurements finally allow us to obtain the first results on the efficiency of the process of conversion of electromagnetic energy into excess of biochemical energy released by the isolated organelles.

Enhancing Performance and Stability of High-Temperature Proton Exchange Membranes through Multiwalled Carbon Nanotube Incorporation into Self-Cross-Linked Fluorenone-Containing Polybenzimidazole.

Addressing critical challenges in enhancing the oxidative stability and proton conductivity of high-temperature proton exchange membranes (HT-PEMs) is pivotal for their commercial viability. This study uncovers the significant capacity of multiwalled carbon nanotubes (MWNTs) to absorb a substantial amount of phosphoric acid (PA). The investigation focuses on incorporating long-range ordered hollow MWNTs into self-cross-linked fluorenone-containing polybenzimidazole (FPBI) membranes. The absorbed PA within MWNTs and FPBI forms dense PA networks within the membrane, effectively enhancing the proton conductivity. Moreover, the exceptional inertness of MWNTs plays a vital role in reinforcing the oxidation resistance of the composite membranes. The proton conductivity of the 1.5% CNT-FPBI membrane is measured at 0.0817 S cm-1 at 160 °C. Under anhydrous conditions at the same temperature, the power density of the 1.5% CNT-FPBI membrane reaches 831.3 mW cm-2. Notably, the power density remains stable even after 200 h of oxidation testing and 250 h of operational stability in a single cell. The achieved power density and long-term stability of the 1.5% CNT-FPBI membrane surpass the recently reported results. This study introduces a straightforward approach for the systematic design of high-performance and robust composite HT-PEMs for fuel cells.

Stabilized Nickel‐Rich‐Layered Oxide Electrodes for High‐Performance Lithium‐Ion Batteries

Next‐generation Li‐ion batteries are expected to exhibit superior energy and power density, along with extended cycle life. Ni‐rich high‐capacity layered nickel manganese cobalt oxide electrode materials (NMC) hold promise in achieving these objectives, despite facing challenges such as capacity fade due to various degradation modes. Crack formation within NMC‐based cathode secondary particles, leading to parasitic reactions and the formation of inactive crystal structures, is a critical degradation mechanism. Mechanical and chemical degradation further deteriorate capacity and lifetime. To mitigate these issues, an artificial cathode electrolyte interphase can be applied to the active material before battery cycling. While atomic layer deposition (ALD) has been extensively explored for active material coatings, molecular layer deposition (MLD) offers a complementary approach. When combined with ALD, MLD enables the deposition of flexible hybrid coatings that can accommodate electrode material volume changes during battery operation. This study focuses on depositing ‐titanium terephthalate thin films on a electrode via ALD‐MLD. The electrochemical evaluation demonstrates favorable lithium‐ion kinetics and reduced electrolyte decomposition. Overall, the films deposited through ALD‐MLD exhibit promising features as flexible and protective coatings for high‐energy lithium‐ion battery electrodes, offering potential contributions to the enhancement of advanced battery technologies and supporting the growth of the EV and stationary battery industries.

Microwave synthesis of magnesium phosphate-rGO as an effective electrode for supercapacitor application

Abstract Transition metal phosphate based materials is being used for energy storage because of P–O covalent bond which facilitates more storage compared to other transition metals and this covalent bond enhanced the electrochemical performance for supercapacitor applications. Pure magnesium phosphate (Mg3(PO4)2) were synthesized via microwave synthesis as the composite varies with rGO (MgPO-XrGO) X=25,50,75,100mg. The prepared composite materials were examined employing XRD, Raman, FT-IR, SEM and XPS studies. Electrochemical studies (CV, EIS, GCD) of three electrode system for the prepared electrodes were performed using Biologic SP-150 with 2M (H2SO4) as electrolyte. From the XRD results, triclinic structured MgPO was confirmed (JCPDS card #35–0329) and rGO has enhanced the crystallinity of MgPO composite. From Raman analyses, the well graphitization nature of rGO in composite MgPO was identified and from XPS analysis chemical composition of the elements was analyzed. The FT-IR fundamental modes of vibrations of PO 4 3 − ${\text{PO}}_{4}^{3-}$ (γ 1,γ 3,γ 4) were obtained. The electrochemical analysis of the prepared material such as pure and composite materials showed better performance. The high specific capacitance was obtained for MgPO-50rGO because MgPO has high coordination with rGO. As Mg2+ oxidation state has high chemical reactivity compared to other earth metals and other advantage is P–O covalent bond that enhanced the performance of the electrode. By facilitating these advantages, rGO is included as composite to develop the electrode to favor the practical applications. By using the optimum level rGO composite with MgPO4-50rGO a better new candidate was successfully developed for supercapacitor applications. The fabricated MgPO-50rGO//Activate carbon full cell set up exhibited the specific capacitance 61 Fg−1 at 1 Ag−1, 21.7 Wh kg−1 energy density and 790.0 W kg−1 power densities and explored outstanding capacitive retention in 2 electrode full cell setup cyclic stability of 99.1 % over the 5000 cycles.

Overvoltage Avoidance Control Strategy for Braking Process of Brushless DC Motor Drives with Small DC-Link Capacitance

Single-phase input rectifier brushless DC motor drives with a small film capacitor have many advantages, such as high power density and high reliability. However, when the motor system operates in regenerative braking mode, the dc-link capacitor with reduced capacitance may suffer from overvoltage without adding additional hardware circuits. At the same time, the braking torque control of the motor will be affected by speed variations. In order to ensure smooth and reliable operation of the motor system, an anti-overvoltage braking torque control method is proposed in this article. The relationship among the dc-link capacitance, the dc-link capacitor voltage, and the speed during regenerative braking is analyzed quantitatively, and the speed at which the regenerative braking is switched to the plug braking is obtained, which in turn consumes the capacitor energy to avoid dc-link overvoltage. Additionally, based on the relationship between the controllability of the braking torque and the speed, a reference value of the braking current that matches the speed is designed. The proposed method makes use of the capacitor’s energy storage during regenerative braking. Meanwhile, it mitigates the impact of motor speed on braking torque. Finally, the effectiveness of the proposed method is verified on a motor platform equipped with the dc-link film capacitor.

Harnessing Green Electricity from Food: A Split Black Gram-Based Triboelectric Nanogenerator for a Self-Powered Autonomous Lighting System and Portable Electronics.

Triboelectric nanogenerators (TENGs) represent a promising solution to mounting environmental concerns associated with battery disposal amid the escalating demand for portable electronics. However, prevailing TENG fabrication predominantly relies on nonbiodegradable, nonbiocompatible, and synthetic materials, posing a grave ecological threat. To mitigate this, there is a pressing need to develop eco-friendly and green TENGs leveraging sustainable, naturally occurring materials. This study pioneers the use of split black gram (SBG) as a tribo-positive material for TENGs. SBG's effectiveness as a tribo-positive material stems from its abundance of oxygen-containing functional groups, as confirmed by FTIR analysis, facilitating electron donation during the triboelectric process. SBG offers compelling advantages, including widespread availability, cost-effectiveness, biodegradability, and hydrophobic and adhesive properties due to its richness in starch and protein, positioning it as an optimal choice for eco-conscious TENG manufacturing. The fabrication process of an SBG-TENG is not only economical and facile but also solvent-free, requiring no specialized tools. Demonstrating commendable performance, the SBG-TENG achieves a maximum power density of 15.36 μW/cm2 at 1 MΩ, with an open circuit voltage of 84 V and short circuit current of 28 μA, comparable to recent studies. In practical applications, the SBG-TENG seamlessly integrates with LEDs and portable electronic devices via a full bridge rectifier, successfully powering them postcapacitor charging. Moreover, an autonomous lighting system is developed by embedding the SBG-TENG in a foot mat, enabling wireless light control through human stepping on the mat, introducing power-saving functionality for residential and office environments. In essence, the introduction of the SBG-TENG not only delivers cost-effectiveness but also minimizes the environmental impact by harnessing sustainable energy from food sources.

Enhancing motor impedance measurements: broadening the spectrum from low to high frequencies

Three-phase induction motors serve as critical parts in various industrial applications, lauded for their high energy efficiency and notable power density. Obtaining their broadband impedance information is paramount for analyzing conducted emissions, evaluating overvoltage ringing, and assessing motor health status. Nonetheless, conventional methods for motor impedance measurements typically rely on Kelvin clip leads or extension cables, which are effective only in a relatively low-frequency region (i.e. below 1 MHz). This paper presents an improved approach to extend the measurable spectrum from low to high frequencies, up to 120 MHz. The proposed method develops a series of fixture adapters to enable seamless interconnection between the terminals of an induction motor and the coaxial ports of an impedance analyzer. The parasitics introduced by these adapters are identified using boundary-element analysis, and their impacts are minimized based on the de-embedding concept. Experimental results affirm the accuracy and effectiveness of the proposed method for four types of motor impedances (i.e. single-phase, phase-to-ground, common-mode, and differential-mode) across a broad frequency range from 100 Hz to 120 MHz. Moreover, the inaccuracy of motor impedance measurements at high frequencies (i.e. above 1 MHz) using conventional methods, including Kelvin clip leads and extension cables, is also demonstrated.

Crystalline-Amorphous Heterophase PdMoCrW Tetrametallene: Highly Efficient Oxygen Reduction Electrocatalysts for a Long-Term Zn-Air Battery.

Metallenes have received sustained attention owing to their unique microstructure characteristics and compelling catalytic applications, but the synthesis of multielement crystalline-amorphous metallenes remains a formidable challenge. Herein, we report a one-step wet chemical reduction method to synthesize composition-tunable crystalline-amorphous heterophase PdMoCrW tetrametallene. As-synthesized PdMoCrW tetrametallene is composed of approximately six to seven atomic layers and has flexible crimpiness, a crystalline-amorphous heterophase structure, and high-valence metal species. Time-dependent experiments show that PdMoCrW tetrametallene follows a three-step growth mechanism that includes nucleation, lateral growth, and atom diffusion, respectively. The novel ultrathin structure, optimized Pd electronic structure, and hydrophilic surface together greatly promote the activity and stability of PdMoCrW tetrametallene in the alkaline oxygen reduction reaction. Pd75.9Mo9.4Cr8.9W5.8/C exhibits excellent mass and specific activities of 2.81 A mgPd-1 and 4.05 mA cm-2, which are 20.07/14.46 and 23.42/16.20 times higher than those of commercial Pt/C and Pd/C, respectively. Furthermore, a Zn-air battery assembled using Pd75.9Mo9.4Cr8.9W5.8/C as a cathode catalyst achieves a peak power density of 156 mW cm-2 and an ultralong durability of 329 h. This study reports an effective strategy for constructing crystalline-amorphous quaternary metallenes to advance non-Pt electrocatalysts toward oxygen reduction reaction (ORR) performance and for a Zn-air battery.

Understanding of multi-way heat extraction using peripheral diamond in AlGaN/GaN HEMT by electrothermal simulations

Abstract High power operation of high electron mobility transistors (HEMTs) is limited due to a variety of thermal resistances in the HEMT device causing self-heating effects (SHEs) in the device. To reduce the SHEs, diamond heat spreaders integrated to the device have proven efficient for heat extraction from the device. In this report using electro-thermal TCAD simulations, we demonstrate an understanding of multiway heat extraction utilizing diamond heat spreaders for improving HEMT thermal performance at high DC output power density
(~40 W/mm). The impact of each heat extraction pathway is understood while considering the thermal boundary resistance between Diamond/GaN hetero-interface and optimization of the GaN buffer layer thickness. Using these findings, we simulated an AlGaN/GaN HEMT device operating at 40 W/mm DC output power while maintaining device temperature at approximately 470 - 500 K.

Dynamics and Energetics of Ion Adsorption at the Interface between a Pure Ionic Liquid and Carbon Electrodes.

Molecular dynamics simulations have been used extensively to determine equilibrium properties of the electrode-electrolyte interface in supercapacitors held at various potentials. While such studies are essential to understand and optimize the performance of such energy storage systems, investigation of the dynamics of adsorption during the charge of the supercapacitors is also necessary. Dynamical properties are especially important to get an insight into the power density of supercapacitors, one of their main assets. In this work, we propose a new method to coarse-grain simulations of all-atom systems and compute effective Lennard-Jones and Coulomb parameters, allowing subsequently to analyze the trajectories of adsorbing ions. We focus on pure 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide in contact with planar carbon electrodes. We characterize the evolution of the ion orientation and ion-electrode distance during adsorption and show that ions reorientate as they adsorb. We then determine the forces experienced by the adsorbing ions and demonstrate that Coulomb forces are dominant at a long range while van der Waals forces are dominant at a short range. We also show that there is an almost equal contribution from the two forces at an intermediate distance, explaining the peak of ion density close to the electrode surface.

Nanostructured binary transition-metal-sulfides and nanocomposites as high-performance electrodes for hybrid supercapacitors

Supercapacitors (SCs) are attractive as promising energy storage devices because of their distinctive attributes, such as high power density, good current charge/discharge ability, excellent cyclic stability, reasonable safety, and low cost. Electrode materials play key roles in achieving excellent performance of these SCs. Among them, binary transition metal sulfides (BTMSs) have received significant attention, attributed to their high conductivity, abundant active sites, and excellent electrochemical properties. This topic review aims to summarize recent advances in principles, design, and evaluation of the electrochemical performance for nanostructured BTMSs (including nickel–cobalt sulfides, zinc–cobalt sulfides, and copper–cobalt sulfides.) and their nanocomposites (including those carbon nanomaterials, transition metal oxides, binary transition metal oxides, transition metal sulfides, and polymers). Nanostructuring of these BTMSs and nanocomposites as well as their effects on the performance were discussed, including nanoparticles, nanospheres, nanosheets, nanowires, nanorods, nanotubes, nanoarrays, and hierarchitectured nanostructures. Their electrochemical performance has further been reviewed including specific capacitance, conductivity, rate capability, and cycling stability. In addition, the performance of hybrid supercapacitors (HSCs) assembled using the nanostructured BTMSs as the cathodes also have been summarized and compared. Finally, challenges and further prospects in the HSCs-based BTMS electrodes are presented.