Energy Density Research Articles

Rigid structural battery: Progress and outlook

The advancement of high-energy-density batteries is vital for the development of lightweight, durable, and intelligent fully electric mobility systems. Reducing battery weight not only increases energy density but also confers load-bearing properties to the energy storage setup. These integrated batteries, known as rigid structural batteries, effectively encapsulate the concept of structural energy storage. The design of rigid structural batteries follows principles of mechanical/electrochemical decoupling at the microscale, and coupling at the macroscale. Based on achieving mechanical/electrochemical decoupling at different scales, we categorize rigid structural batteries into component-level, unit-level, and material-level rigid structural batteries. This review aims to summarize the progress in this field concerning mechanical/electrochemical decoupling at various scales and discuss fundamental design principles and core issues to address in rigid structural batteries. It also proposes strategies for the expeditious implementation of rigid structural batteries, aiming for long-term breakthroughs to surpass performance bottlenecks.

Nickel-molybdenum bimetallic sulfide decorated biomass derived carbon support for high performance asymmetric supercapacitor application

Biomass - derived carbon electrode material with a porous structure is widely used in supercapacitor applications, which can improve electron transfer and shorter ion diffusion pathways. In this work, the garlic peel biomass carbon (GPBC), NiMo3S4(NMS) and garlic peel biomass carbon decorated with NiMo3S4 (GPBC/NMS) composite were prepared through a in situ two-step hydrothermal method. The synthesized materials were characterized by X-ray diffraction (XRD) and field emission scanning electron microscopy (FE-SEM), energy dispersive x-ray spectroscopy (EDS), Transmission electron microscopy techniques (TEM), Raman spectroscopy and Brunauer-Emmett-Teller (BET) techniques were used to analyze the structure, morphology and specific surface areas and X-ray photoelectron spectroscopy (XPS). The prepared bimetallic metal sulfide on a biomass - derived carbon namely the GPBC/NMS composite is used in supercapacitor application. The GPBC/NMS composite electrode exhibits good cycle performance with high specific capacity of 304C/g at current density of 1 A/g in a 3 M KOH electrolyte solution. The electrochemical performance of the GPBC/NMS//GPBC asymmetric supercapacitor device produces an excellent energy density 45.5 Wh kg−1 at a power density of 1125 W kg−1 in the 1.6 V operating potential window. The GPBC/NMS//GPBC also exhibits 93 % retention of its initial capacitance after the 10,000 GCD cycle performance. The above results demonstrate a new way of developing high performance electrode materials for energy storage applications.

The Effect of Temperature and Film Thickness on Domain Wall Energy Density, Coercivity Force, and Magnetostriction of Galfenol Films

The Effect of Temperature and Film Thickness on Domain Wall Energy Density, Coercivity Force, and Magnetostriction of Galfenol Films

Microstructure and mechanical properties in ultrasonic-magnetic field coaxial hybrid GTAW joints of Ti-6Al-4V

GTAW has less arc energy density and coarse joint microstructure. A novel method of Ultrasonic-Magnetic field coaxial hybrid GTAW (U-M-GTAW) was proposed, which improved upon the traditional GTAW torch. Under 140 A current and 4 mm/s speed, the results indicated that the U-M-GTAW depth-to-width ratio increased by 54.5 % compared to GTAW. Meanwhile, the surface of the joint showed a dense corrugation. The interior of the joints was all composed of martensite α', whose phase transformation obeyed the Burgers orientation relationship. The average martensite length in the U-M-GTAW weld zone was 14.8 μm, which was 33.6 % shorter than GTAW, and the length distribution was more uniform. Additionally, the U-M-GTAW joint orientation shifted from {01−10} to {−12−10}, revealing a higher texture density. The substantial precipitation of martensite in the weld zone resulted in the highest hardness, with an average microhardness of 396.8 ± 9.0 HV, marking a 12.1 % improvement over base metal. Moreover, U-M-GTAW exhibited an elongation of 9.3 %, representing a 10.7 % enhancement compared to GTAW, with deeper dimples in the fracture indicating superior plasticity. Notably, the improvements in microhardness and elongation in U-M-GTAW were primarily attributed to the reduction in martensite length and its uniform distribution under the action of ultrasonic and magnetic fields.

Interface chemical reconstruction with residual lithium compounds on nickel-rich cathode by nonstoichiometrical MoO3-x coating enables high stability

The layered lithium nickel-rich cathodes have become one of the most promising candidates for next-generation lithium-ion batteries with high energy density, However, the nickel-rich cathode suffers from a rapid decay of capacity due to their intrinsic instability and undesirably residual lithium compounds originated from LiNiO2 structural changes on the surface, hindering large-scale commercial application. Herein, a continuous and uniform oxygen vacancy enriched-MoO3-x coating was successfully synthesized and reacted residual lithium compounds as a functional layer on the cathode. Such chemically reconstructed coating (Li2MoO4) strategy endows the 1 wt% MoO3-x coated NCA cathode with a fast Li+ ions transport and enhanced structural stability, leading to an outstanding discharge capacity of 214.0 mAh g−1 at 0.1C (1C = 270 mA g−1), a better capacity retention of 80.3 % after 120 cycles at 0.5C, and an excellent high rate capability of 120 mAh g−1 at 5C cycled in voltage range of 2.75 V–4.3 V. This work provides an effective strategy to modulate surface structure towards advanced Ni-rich cathodes for high-performance lithium-ion batteries.

Layer effects on MXenes electrode and it applied to silicon composite structures

Despite the very high capacity of Si (4200mAh g−1), the widespread application of Si anodes has been hampered by drastic volume changes (up to 300 %) during cycling, leading to electrical contact losses and thus a sharp drop in capacity as the cycle life is shortened. Here we present a class of layered MXene/Si electrodes, which consist of nano-Si embedded in the interlayers of MXene to form a coupling effect, which can inhibit the huge volume change of Si during cycling. Therefore, layered MXene/Si has a highly reversible capacity, much improved cycling performance and excellent mechanical properties. First-principles calculations reveal the excellent electronic conductivity and good diffusion ability of layered MXene/Si, confirming the rapid storage of Li ions. This study provides useful information for the development and production of anode materials with high energy density and good mechanical properties.

Effects of binder content on potato starch-derived porous carbon microspheres for high-performance supercapacitors

Potato starch-based carbon microspheres (PCMs) have successfully synthesized from potato starch by a simple strategy based on (NH4)2HPO4 and KOH activation. The PCMs presents a large specific surface area (SSA) of 2048 m2 g−1. The electrochemical behaviors of the PCMs with different binder content in 6 mol L−1 KOH were studied by impedance spectroscopy, cyclic voltammetry (CV), and galvanostatic charge-discharge (GCD). The results show that PCMs-85 (the binder content is 5 wt%) has a small equivalent series resistance (ESR), high specific capacitance, compacted density, and areal density. PCMs-85 exhibited good cycling durability of 100 % after 10,000 cycles at 1 A g−1 and delivered an energy density of 6.35 Wh L−1 and a volume power density of 167.38 W L−1. The corresponding capacitive performances of PCM-85-based symmetrical two-electrode supercapacitors are investigated in 6 mol L−1 KOH, 1 mol L−1 Na2SO4 and 1 mol L−1 TEA.BF4/AN electrolyte. The PCMs supercapacitor with 6 mol L−1 KOH electrolyte exhibits a mass-specific capacitance of 172 F g−1 with volumetric capacitances of 145 F cm−3 at 1 A g−1.

A sustainable solution: Conversion of distillers' grains waste into high-performance supercapacitor electrode materials for energy storage applications

The development of cost-effective biomass-derived carbon with good electrochemical properties is crucial for advancing energy storage devices sustainably. One feasible approach to producing supercapacitor electrode materials is the conversion of heteroatom-rich biomass waste into heteroatom self-doped hierarchical porous carbons with favorable electrochemical properties. In this study, distillers' grains with abundant crude fiber and protein were utilized as precursors to prepare N, S self-doped hierarchical porous carbon, which presents a high specific surface area of 3642.87 m2 g−1. The N, S doping could improve the interfacial wettability of electrode materials and enhance the pseudocapacitive effect of the materials. In three-electrode system, the carbon delivered a high capacitance of 347 F g−1 at 1 A g−1. Symmetrical capacitors assembled with PVA/KOH gel electrolytes delivered an ultrahigh energy density of 11.29 Wh kg−1 at a power density of 250 W kg−1. This strategy provides a practical, low-cost, and renewable design approach of carbon electrode for high-performance supercapacitors.

Experimental study and neural network model based prediction of layer thickness influence on LPBF IN625 single track geometry

The performance of interacting metal surfaces having sliding motion is enhanced by fabricating microfeatures on-top of the surfaces. Laser powder bed fusion (LPBF) is used to fabricate the microfeatures of IN625 on-top of a flat surface. In LPBF, geometrical characteristics of microfeatures are based on the energy supplied and the volume of material melted (layer thickness) at that instant of time. There is very few research reported in open literature on the effect of layer thickness on microfeatures geometry during LPBF. In this work, a series of single tracks is fabricated with different combinations of laser power and scanning speed for 75 μm, 100 μm, and 125 μm layer thickness and its effect on single track geometrical characteristics and microstructure was evaluated. It has been found that laser power and scanning speed have a significant influence on the track geometry irrespective of layer thickness. The minimum linear energy density of 2.5 J/mm is considered to fabricate the continuous track formation for investigated layer thickness. From statistical analysis, it is observed that the laser power and scanning speed shows higher contribution on track width and remelting depth, respectively. Whereas, layer thickness shows a higher influence on track height and contact angle of single track as compared to laser power and scanning speed. In 125 μm layer thickness, the volume of material melting is increased which encourages the gravity effect to deform the melt pool and produces larger track width compare to 100 μm layer thickness. Further, the cell spacing is gradually increased with layer thickness resulting increase in the solidification period. The shape controllability of the single track is significantly increased with layer thickness, but as keeps on increasing layer thickness due to the larger volume of molten metal, the melt pool losses ability to maintain convex shapes. An Artificial Neural Network (ANN) model is developed to understand the relationship between the LPBF process parameters and single track geometrical characteristics to predict the responses for a wide range of process parameters. The multiple response neural network model shows excellent agreement with experimental results with R2 value greater than 0.95.

Probing the universe's expansion dynamics: The linear correction scenario perspective on dark energy

In this study, we investigate the cosmological evolution of the universe, focusing on the KMMS models in a model-independent approach, particularly the scenario involving linear correction, given by E2(z)=A(z)+β(1+γB(z)), where A(z)=Ωm0(1+z)3 and B(z)=z. By analyzing recent Cosmic Chronometers (CC) and the Pantheon+ samples, we determine the best-fit values of model parameters using a Markov chain Monte Carlo analysis. Our models exhibit unique dynamics, transitioning from super-exponential to exponential expansion, with a significant shift at redshift zt=0.83−0.10+0.11 and present deceleration parameter q0=−0.69−0.17+0.17. The jerk parameter exceeds 1, indicating a faster change in acceleration than predicted by ΛCDM. The energy density parameter is consistent with Planck observations, and the dark sector evolution follows the expected thermal history. The EoS parameter approaches ωde=−1 over time, with a current value of ωde0=−1.06±0.12, aligning with the phantom phase. Our model presents a new dark energy alternative, emphasizing the importance of considering models like KMMS in understanding cosmic evolution.

Effect of Creep, Fatigue and Random Vibration on the Integrity of Solder Joints in BGA Package

This study employs Finite Element Analysis (FEA) to investigate the effects of creep, fatigue, and random vibration on the integrity of solder joints in BGA packages in electronic modules. Evaluating the response of lead-based Sn63Pb37 and lead-free SnAgCu alloy solders (SAC305, SAC387, SAC396, and SAC405) to induced loads - stress, strain, strain energy density, and displacement in the joints is obtained and studied better to understand the mechanism of the joints' degradation. SAC305 and SAC405 are modelled with linear stress-temperature relationships σ = 3.152T–68.167 and σ = 1.543T–34.983, respectively. The magnitude of the strain energy density in the joints is a key failure driver. SAC387 and SAC396 solder joints display lower values of strain energy density and thus have higher durability. Displacement analysis indicates that SAC305 and Sn63Pb37 are prone to deformation-induced failure. SAC387 exhibits the highest fatigue yield stress at 58 MPa, while SAC405 displays the lowest stress at 22 MPa. Analysis of the results of random vibration shows that Sn63Pb37 developed the highest stress at 34.62 MPa and is thus susceptible to stress-induced failure. The robust stress, strain, and strain energy responses of SAC405 and SAC396 provide key insights into improving the mechanical reliability of future electronic devices towards better sustainability.

Unconventional Thick Cobalt Telluride Electrodes Enable Homogeneous Ion Flow for High Capacity, Fast and Safe Potassium Storage

The demand for high-energy density, fast-charging, and safe potassium-ion batteries (PIBs) is crucial for large-scale applications in electric vehicles and grid systems. Despite the potential of thick electrode designs by a conventional technique (CTEs) to boost energy density, they often encounter challenges such as reduced capacity, limited cycling lifespan, and localized short circuits. Here, we present a novel cobalt telluride composite anode by a simple tellurization and subsequent heat reduction, featuring Co1.67Te2 nanoparticles uniformly embedded within an N-doped carbon layer on a trace amount of reduced graphene oxide (CT@NC/rGO). By constructing low tortuosity electrodes (LTEs), a homogeneous distribution of potassium ions and current density is achieved, resulting in enhanced potassium storage performance. The CT@NC/rGO LTEs demonstrate excellent discharge capacities: 311.7, 276.5, and 243.7mAh g-1 after 500 cycles at 0.25Ag-1 for mass loadings of 1.4, 1.9, and 2.8mgcm-2, respectively. At a higher current density of 0.5Ag-1, discharge capacities after 650 cycles are 245.3, 175.6, and 159.2mAh g-1 for mass loadings at 1.6, 2.4, and 3.0mgcm-2, respectively. These improvements are attributed to enhanced pseudocapacitive behavior, reduced charge resistance, and accelerated ion diffusion kinetics, as evidenced by experimental and simulation studies. The proposed strategy for synthesizing high-density electrodes holds promise for developing high-performance metallic compound electrodes for PIBs and potentially extending to other types of energy storage systems.

Exploring the application of hydrazine hydrate in protonic ceramic fuel cells: Strategies and performance improvements

Hydrazine hydrate, characterized by its high hydrogen content and eco-friendliness, garners extensive attention in the field of fuels. Its high energy density and rapid decomposition capabilities render it a promising fuel option for Proton-Conductor Solid Oxide Fuel Cells (PCFCs). Given the unique properties of hydrazine hydrate, this study employs a dendritic porous anode structure to facilitate faster fuel transport. Additionally, the influence of operational temperature and concentration of hydrazine hydrate as fuel on cell performance is analyzed. An effective vapor management strategy is implemented to address its decomposition into water vapor, resulting in a significant 23.17 % increase in the maximum power density (MPD) of the cell. To further enhance the performance of hydrazine hydrate fuel in PCFCs, a Pt–Al spherical catalyst is integrated within the anode structure of the cell. This approach notably improves the cell performance, yielding an additional 14.98 % increase in MPD. This design not only augments the electrical output but also effectively mitigates the degradation of the interface between the anode and the electrolyte. These optimization measures significantly improve the lifespan and reliability of the cell. The outcomes of this study demonstrate the practical feasibility of using hydrazine hydrate as a fuel in PCFCs.

Studying the viabilityand growth kinetics of vancomycin-resistant Enterococcus faecalis V583 following femtosecond laser irradiation (420-465 nm).

Enterococcus faecalis is among the most resistant bacteria found in infected root canals. The demand for cutting-edge disinfection methods has rekindled research on photoinactivation with visible light. This study investigated the bactericidal activity of femtosecond laser irradiation against vancomycin-resistant Enterococcus faecalis V583 (VRE). The effect of parameters such as wavelength and energy density on the viability and growth kinetics of VRE was studied to design an optimized laser-based antimicrobial photoinactivation approach without any prior addition of exogenous photosensitizers. The most effective wavelengths were 430nm and 435nm at a fluence of 1000J/cm2, causing a nearly 2-log reduction (98.6% and 98.3% inhibition, respectively) in viable bacterial counts. The colony-forming units and growth rate of the laser-treated cultures were progressively decreased as energy density or light dose increased at 445nm but reached a limit at 1250J/cm2. At a higher fluence of 2000J/cm2, the efficacy was reduced due to a photobleaching phenomenon. Our results highlight the importance of optimizing laser exposure parameters, such as wavelength and fluence, in bacterial photoinactivation experiments. To our knowledge, this is the first study to report an optimized wavelength for the inactivation of VRE using visible femtosecond laser light.

Characterization of manufacturing material and carbon nanohybrid for renewable energy and storage systems

Scientists are exploring advanced energy alternatives to compete with rising fossil fuel consumption and CO2 emissions due to population growth and technological advancements. Supercapacitors are highly efficient systems for storing energy due to their specific capacitance and power density, meeting modern energy storage demands. Perovskite and carbon-based materials have emerged as the most effective materials in this respect. In this work, SrSnO3/rGO nanohybrid is chosen as the supercapacitor electrode material for the very first time and a range of characterization techniques are employed to ascertain the structural and textural characteristics of the composite. The physicochemical properties of the SrSnO3 included rGO are shown to have a greater surface area, excellent electrical conductivity and a lower resistance. It is demonstrated that the rGO improved quicker ion diffusion channels for the increased redox performance in the SrSnO3/rGO nanohybrid. Additionally at 1 A/g, the SrSnO3/rGO nanohybrid has an elevated specific capacitance of 1385 F/g along with energy and power density of 66 Wh/kg and 293 W/kg, respectively in a three-electrode system. During the two electrode observations, the revealed Cs of SrSnO3/rGO nanohybrid was 122 F/g at 1 A/g with 66 Wh/kg and 293 W/kg of energy density and power density, respectively. The SrSnO3/rGO nanohybrid has exceptional functionality, as demonstrated by its 65 h stability examination via chronoamperometry and a modest drop in its CV polarization curve area after the 5000th cycle of the CV stability analysis. These evaluated results point to the nanohybrid's promising future.

Printed flexible solid-state microsupercapacitor with highly-stable aqueous cobalt-based inks

Cobalt-based nanomaterials are among the most noticed candidates for manufacturing supercapacitive electrodes. Inkjet-printing is an emerging technique for fabricating miniaturized devices. In this work, highly flexible microsupercapacitors (MSCs) are manufactured, using a pseudocapacitive (C = 900 F‌ g−1 at 1 A g−1) Co-oxide-hydroxide water-based and ultra-stable (up to 12 months) ink on paper. The synthesized capacitive active material consists of cobalt-oxide nanocubes and cobalt-hydroxide hexagonal nanoflakes. Conductive (Rs = 13 Ω/□) silver nanowire networks serve as current collectors, and the morphology of cobalt oxide-hydroxide structures and the developed ink features, allow for printing well-detailed and homogeneous patterns. The inkjet-printed symmetric and asymmetric devices show notable areal specific capacitances of 35.68 mF cm−2 and 23.60 mF cm−2 at a current density of 0.1 mA cm−2, respectively. The asymmetric devices deliver impressive energy and power densities of 2.76 μW h cm−2 (4.10 W h kg−1) and 646 μW cm−2 (959 W kg−1), respectively. A thorough study on the cyclic and mechanical stability of the flexible devices resulted in perfect capacitance maintenance of 94.3 % after 10,000 charge and discharge cycles and retention of over 80 % even after 1000 cycles of successive bending and folding. The extensive study of capacitance retention following folding under various obtuse and reflex angles, which can be regarded as an important step toward characterizing flexible devices suitable for being utilized in wearable electronics, is carried out for the first time to the best of our knowledge. The findings of this study clearly illustrate the prospects of using the inkjet-printing technique to fabricate high-performance MSC devices appropriate for integration with flexible and wearable electronics.

Laser-Scribed Battery Electrodes for Ultrafast Zinc-Ion Energy Storage.

Aqueous Zn batteries are promising for large-scale energy storage applications but are plagued by the lack of high-performance cathode materials that enable high specific capacity, ultrafast charging, and outstanding cycling stability. In this work, we design a laser-scribed nano-vanadium oxide (LNVO) cathode that can simultaneously achieve these properties. Our material stores charge through Faradaic redox reactions on/near the surface at fast rates owing to the small grain size (2-6nm) of vanadium oxide and interpenetrating three-dimensional (3D) graphene network, displaying a surface-controlled capacity contribution (90%-98%). Multiple characterization techniques unambiguously reveal that zinc and hydronium ions co-insert with minimal LNVO lattice change upon cycling. As a result, we demonstrate that a high specific capacity of 553 mAh g-1 can be achieved by the LNVO/Zn system at 0.1 A g-1 , and an impressive 264 mAh g-1 capacity can be retained at 100 A g-1 with a 10 s charge/discharge cycle, showing excellent rate capability. The LNVO/Zn is also capable of reaching >90% capacity retention after 3,000 cycles at a high rate of 30 A g-1, as well as achieving both high energy (369Wh kg-1) and power densities (56,306W kg-1). Moreover, the LNVO cathode retains its excellent cycling performance when integrated into quasi-solid-state pouch cells, further demonstrating mechanical stability and its potential for practical application in wearable and grid-scale applications. This article is protected by copyright. All rights reserved.

Exploring the Fundamental Spatial Limits of Magnetic All-Optical Switching.

All-optical switching (AOS) results in ultrafast and deterministic magnetization reversal upon single laser pulse excitation, potentially supporting faster and more energy-efficient data storage. To explore the fundamental limits of achievable bit densities in AOS, we have used soft X-ray transient grating spectroscopy to study the ultrafast magnetic response of a GdFe alloy after a spatially structured excitation with a periodicity of 17 nm. The ultrafast spatial evolution of the magnetization in combination with atomistic spin dynamics and microscopic temperature model calculations allows us to derive a detailed phase diagram of AOS as a function of both the absorbed energy density and the nanoscale excitation period. Our results suggest that the minimum size for AOS in GdFe alloys, induced by a nanoscale periodic excitation, is around 25 nm and that this limit is governed by ultrafast lateral electron diffusion and by the threshold for optical damage.

Assessment of the Potential for Increasing the Energy Efficiency in the Cooling Sector

Cooling supply to ensure the indoor microclimate is becoming more important as global average air temperatures rise. With growing societal demands for higher thermal comfort and increasing individual cooling solutions in the building sector, global energy consumption for cooling is increasing accordingly. Scientific literature and studies estimate that the demand for cooling energy will have a significant impact on global energy demand in the future. In compliance with the European Union goal of achieving climate neutrality by 2050, it is essential to find solutions for reducing energy consumption in the building sector, which is already among the largest energy consumers and greenhouse gas emission producers. Replacing individual cooling solutions with district cooling in urban areas where higher energy density can be reached is one of the solutions for decarbonizing the building sector. To spatially assess the feasibility of district cooling in certain areas, energy demand mapping can be performed. Within this research mapping is carried out using a geographical information system (GIS) tool. The purpose of the mapping is to identify the places in the city of Riga with the highest district cooling potential. Spatial assessment using a GIS tool can be done in different ways – mostly it depends on the available data. The spatial data (buildings) of the cadastral information system and additional detailed information about buildings were obtained from the Latvian open data portal. Information on the type of use of the building, indoor area and the age of building was attached to each building on the map. Then building energy certificate data containing information on specific energy consumption for cooling (kWh/m2 per year) was obtained from the same portal. By processing the data of energy certificates of buildings, excluding outliers, a specific index was obtained for different types of buildings. For the residential sector, the age of the building is also used. Using cadastral data on the indoor area of buildings and the type of building use, the theoretical cooling demand in Riga is calculated and results are quantified and displayed visually. By visualizing the results with the GIS tool, hot spots with the highest cooling energy demand were detected. Results can be further used to calculate the technical and economic justification for the district cooling solutions in specific areas as well as assess the energy efficiency that would be provided by implementation of district cooling solutions.

Single Step Synthesis of gem-Dinitro Methyl-1,2,4-triazole and Its Hydroxylamine Salt: An Alternative to the FOX-7 and Other Benchmark Explosives.

gem-Dinitro methyl based high-energy-density material 5-(dinitromethylene)-4,5-dihydro-1H-1,2,4-triazole (2) and its hydroxylamine salt (4) were synthesized for the first time in a single step and characterized. Further, the structure of 2 was confirmed by single-crystal X-ray diffraction (SCXRD) studies. Interestengly, both the compounds show excellent density (> 1.83 g cm-3), detonation velocity (> 8700 m s-1), pressure (> 30 GPa) and are insensitive toward mechanical stimuli such as impact and friction sensitivity. Considering their synthetic fesibility and balanced energetic performance, compounds 2 and 4 show future prospects as potential next-generation energetic materials for the replacenent of many presently used benchmark high energy density materials such as RDX, FOX-7 and highly insensitive H-FOX.