Search Results (227)

Preceramic polymers, especially silicon oxycarbide (SiOC) and silicon carbonitride (SiCN) ceramics, have gained significant attention due to their wide range of applications in many fields, particularly in energy storage devices beyond conventional lithium-ion batteries (LIBs). This review focuses on the synthesis, structural characteristics, and properties of SiOC and SiCN ceramics as electrodes for battery applications. Furthermore, their promising applications as electrode materials for energy storage systems are explored, along with the most recent advances in the development of such materials and their use in lithium-ion batteries (LIBs), lithium-sulfur batteries (LSBs), potassium-ion batteries (PIBs), sodium-ion batteries (SIBs), and supercapacitors. This review addresses the distinct advantages of SiOC and SiCN ceramics, including high thermal stability, mechanical robustness, and adaptable microstructures. It also examines the challenges associated with the commercialization of these ceramics, including issues related to electronic conductivity and ion transport pathways. Full article

Thermal runaway (TR) remains a critical bottleneck for the safe application of lithium-ion battery (LIB) in large-scale energy storage systems, arising from the instability of battery materials under high temperatures. This review systematically summarizes materials design strategies to suppress TR, focusing on modifications of cathodes, anodes, separators, and electrolytes. For cathodes, surface coating and bulk doping enhance the structural stability and thermal decomposition temperature of high-Ni materials, while nanoscale engineering and carbon networks improve the electronic conductivity and interfacial stability of LiFePO₄ (LFP). For anodes, surface modification of graphite suppresses solid-electrolyte interphase degradation, and nanostructured silicon-based composites mitigate thermal failure caused by volume expansion. Separator functionalization, including ceramic coating, inorganic separators, and thermal shutdown separators, enhances thermo-mechanical stability and enables thermally triggered ion blocking. Flame-retardant electrolytes incorporate phosphorus-based, organosilicon, and halogenated additives that act through combined gas- and condensed-phase mechanisms. The review further discusses challenges in interfacial compatibility, system integration, and trade-offs among multiple performance metrics. Future efforts should focus on integrating intrinsic thermal stability with smart safety functions to achieve both high energy density and inherent safety. This review provides a systematic reference for the design and industrialization of high-safety materials for LIBs. Full article

This study examines the environmental implications of envelope material choices for Nearly-Zero-Energy Building (NZEB) single-family houses in carbon-intensive energy contexts. Using a comparative Life Cycle Assessment (LCA) based on EN 15804+A2, a 100 m² house was analysed over a 50-year lifespan across three archetypes: ceramic masonry (Design 1), solid log (Design 2), and timber–straw (Design 3). By maintaining a common steady-state thermal standard (U ≤ 0.20 W/(m²·K)) across all variants, the study provides a controlled comparison in which differences in GWP and non-renewable primary energy use primarily reflect material choices rather than insulation level. While both biogenic designs achieved negative embodied Global Warming Potential (GWP) in modules A1–A3 due to carbon sequestration, the results also show that structural concept and detailing strongly influence resource efficiency. Design 3 required substantially less timber volume than Design 2 while maintaining a comparable thermal standard and the lowest PENRT_A1–A3. Under the fixed operational assumptions adopted in this comparative study, module B6 remained the dominant single life-cycle contributor in all variants. The timber–straw system is therefore interpreted here as the more resource-efficient envelope strategy, whereas the solid-log solution primarily maximises timber-based carbon storage. Full article

Self-healing materials (SHMs) are a class of bio-inspired materials capable of autonomously repairing damage, similar to how living organisms heal wounds. The core motivation behind SHMs is to extend the service life of components while enhancing safety and reducing maintenance or replacement needs. SHMs can be broadly categorized into intrinsic systems, which rely on reversible internal bonds (dynamic covalent or supramolecular interactions) to heal repeatedly, and extrinsic systems, which embed external healing agents (e.g., microcapsules or vascular networks) that are released upon damage to effect repairs. Researchers have demonstrated self-healing behavior in diverse material families, including polymers, metals, ceramics/cementitious materials, and protective coatings, thereby improving crack resistance, fatigue life, and reliability across aerospace, automotive, civil infrastructure, energy storage, and microelectronics applications. Advances in material design and additive manufacturing have started integrating SHMs into practical structures. However, challenges such as scaling up production, maintaining mechanical performance, and ensuring long-term durability remain. Reported healing efficiencies in self-healing materials typically range from ~50% to near-complete recovery (~100%), depending on material systems and testing conditions, highlighting key trade-offs between healing performance, mechanical integrity, and scalability. Overall, SHMs represent a promising strategy for creating safer and more sustainable engineering systems, with ongoing developments aimed at overcoming current limitations and expanding their capabilities. This review highlights key trade-offs between healing efficiency, mechanical performance, and scalability, providing insights into the design and application of next-generation self-healing materials. Full article

Aqueous zinc-ion batteries (AZIBs) are promising for large-scale grid storage due to inherent safety, low cost, environmental compatibility, high theoretical capacity (820 mAhg⁻¹), and suitable redox potential (−0.763 V vs. SHE). However, practical deployment is hindered by coupled challenges at the zinc anode–hydrogen evolution, dendrite growth, and corrosion/passivation, which severely limit cycle life and coulombic efficiency. This review systematically summarizes key advances in AZIB research. It first elucidates working principles and four cathode energy storage mechanisms: Zn²⁺ insertion/extraction, H⁺/Zn²⁺ co-insertion, chemical conversion, and dissolution/deposition. Second, it examines four mainstream cathodes (manganese-based, vanadium-based, Prussian blue analogs, and organic compounds), analyzing performance bottlenecks and corresponding optimization via structural modification. Third, it explores functional mechanisms of advanced separators (polymer, inorganic/ceramic composite, MOF-based, and cellulose-based) in regulating uniform Zn²⁺ deposition and suppressing dendrites. Fourth, it summarizes anode optimization strategies: artificial protective layers for interface stabilization, electrolyte additives to modulate Zn²⁺ solvation/deposition, and 3D porous structures to reduce local current density and provide nucleation sites. Finally, key scientific challenges and future directions are discussed—multi-strategy synergy, in situ characterization, practical battery construction, and sustainable technological development, offering theoretical guidance for advancing AZIBs toward large-scale applications. This review aims to provide a comprehensive perspective spanning from materials to systems, and from mechanisms to applications. Its core objective is not merely to list the types of cathode materials, but to establish a logical bridge directly connecting “key challenges” to “optimization strategies,” with a particular emphasis on the issues and solutions related to the cathode side. Full article

Ceramic-polymer nanocomposites combine the respective advantages of ceramics and polymers, boasting superior mechanical flexibility, thermal stability, optical transparency, and electrical conductivity, enabling their wide use in cutting-edge fields like medicine, aerospace, optoelectronic devices, and energy storage components. Notably, ceramic-polymer nanocomposites are a promising, widely recognized strategy for developing high-energy-density, low-dielectric-loss, and flexible capacitors, due to the ceramic phase’s intrinsic high dielectric constant, which enhances dielectric capability, and the polymer phase’s high breakdown strength and mechanical flexibility. Ultimately, ceramic-polymer nanocomposites can reach an optimal dielectric performance. In this study, polyvinylidene fluoride (PVDF) was used as the matrix material and barium titanate (BaTiO₃) as the reinforcing phase within the composite structure. The BaTiO₃ ceramic particles were incorporated into PVDF via spin-coating technology, with composite formulations prepared at different concentrations (0.5 wt%, 1.0 wt%, 1.5 wt%, 2.0 wt%, 2.5 wt%, 3.0 wt%). A series of key parameters were measured and compared, such as the dielectric constant, breakdown strength, and energy storage density, of the BT/PVDF nanocomposite. The results indicated that the BT/PVDF nanocomposite with the optimal low BaTiO₃ content demonstrates remarkable performance, achieving a breakdown strength (E_b) of 500 MV/m and an effective energy storage density of 15.5 J/cm³. This represents an improvement over conventional uniformly high-filler films. Full article

Nature-based solutions (NBSs), such as green roofs, are among the most effective ways to manage urban stormwater, improve building energy efficiency, and adapt to climate change. However, conventional green roofs confront several restrictions related to stormwater drainage, retention capacity, irrigation demand, and pressure on urban water networks during dry periods. This study proposes and experimentally validates a novel system applicable to green roofs and other NBS, including streetside planting systems and vegetated sports grounds. The novelty of the proposed system lies in a double-layer design, the integration of filters within soil substrate to enhance short-term stormwater retention and controlled drainage, and passive subsurface capillary irrigation with cords to improve irrigation efficiency. Infiltration tests showed that filter hydraulic conductivity strongly depends on pore size, with measured infiltration rates ranging from 0.01 mm/min (ceramic, 0.1 μm) to 20 mm/min (polypropylene, 50 μm). The results showed that filter material and pore size significantly influence infiltration behaviour and short-term storage capacity. When integrated with the soil substrate, the combined system exhibited infiltration rates of 0.8–2.0 mm/min, decreasing as hydraulic head declined. Capillary rise experiments demonstrated a maximum vertical rise of 32 cm and horizontal rise of 39 cm for polyester cords (6 mm width), confirming the feasibility of passive subsurface irrigation through stored runoff reuse without external energy. The experiments were conducted at a laboratory scale (25 × 25 cm) as a proof-of-concept validation. Finally, the study results demonstrate the feasibility of the proposed system as a multifunctional NBS solution that enhances stormwater retention while enabling passive irrigation using retained runoff. Full article

Porous ceramic oxides have gained significant interest as components in a wide variety of energy storage devices. Their use, however, is limited by long and high-temperature processing methods. We recently demonstrated Porogen-integrated Rapid Oxidation (PiRO) as a new method to manufacture porous aluminum oxide in significantly shorter times and with substantial manufacturing cost savings, but challenges remain with the resultant porous matrices. First, carbonaceous residue remains in the films after the combustion event, which is necessary to minimize for electronic applications. Second, the porous structure is not stable at elevated temperatures (>250 °C), which are often required for nanocomposite applications of the matrices where filling with a second phase is achieved through high-temperature annealing. Here, we address these challenges by using post-processing treatments, including UV/Ozone, high-temperature nitrogen oven anneals, and oxygen plasma. First, we characterize the treatments’ efficacy in carbon removal using FTIR and measure bulk carbon removal with XPS. Second, we characterize the matrices’ thickness collapse and porosity changes after treatments with ellipsometry. Finally, we use nanoindentation to understand changes in stiffness resulting from the various treatments. By understanding the treatments’ roles in removing carbon from the films and stabilizing the matrix structure, we are able to select optimal post-processing treatments for designing a stable platform for further applications of the mesoporous oxide. Full article

Lithium-ion batteries are widely used in electrochemical energy storage due to their advantages such as fast response and good scalability, but they are prone to thermal runaway (TR) under abusive conditions. Liquid nitrogen has been proven effective in suppressing lithium-ion cell TR in previous studies owing to its excellent cooling capacity. To further enhance the suppression capability of liquid nitrogen on lithium-ion cell TR, a method combining liquid nitrogen with fire-resistant materials was proposed. All experiments were conducted under strictly controlled conditions to ensure result comparability. Experiments on the synergistic suppression of lithium-ion cell TR propagation were conducted with the type and thickness of the fire-resistant materials as variables. The results demonstrated that installing porous fire-resistant materials inside the lithium-ion battery module significantly enhanced the efficacy of liquid nitrogen in suppressing TR propagation. The maximum rebound temperature of the cell after nitrogen injection cessation was reduced by up to 32.7% compared to the condition without fire-resistant materials. Both material characteristics and thickness influenced the heat exchange process—ceramic fiber aerogel, with its low thermal conductivity, achieved a maximum cooling rate of 2.45 °C/s on the TR cell surface, exhibiting the optimal enhancement effect; as the material thickness increased, the synergistic fire suppression performance was further enhanced with increasing material thickness, with the 9 mm thick ceramic fiber aerogel performing better than the thinner (6 mm and 3 mm) variants. The research findings provide a valuable reference for module-level thermal runaway suppression in energy storage systems. Full article

This work presents the design, modeling, and experimental validation of an innovative, highly autonomous, and economically viable photovoltaic solar cooker, integrating a robust battery storage system. The system combines 1200 Wp photovoltaic panels, a control block with DC/DC power converters and digital control for intelligent energy management, and a thermally insulated heating plate equipped with two resistors. The objective of the system is to reduce dependence on conventional fuels while overcoming the limitations of existing solar cookers, particularly insufficient cooking temperatures, the need for continuous solar orientation, and significant thermal losses. The optimization of thermal insulation using a ceramic fiber and glass wool configuration significantly reduces heat losses and increases the thermal efficiency to 64%, nearly double that of the non-insulated case (34%). This improvement enables cooking temperatures of 100–122 °C, heating element surface temperatures of 185–464 °C, and fast cooking times ranging from 20 to 58 min, depending on the prepared dish. Thermal modeling takes into account sheet metal, strengths, and food. The experimental results show excellent agreement between simulation and measurements (deviation < 5%), and high converter efficiencies (84–97%). The integration of the batteries guarantees an autonomy of 6 to 12 days and a very low depth of discharge (1–3%), allowing continuous cooking even without direct solar radiation. Crucially, the techno-economic analysis confirmed the system’s strong market competitiveness. Despite an Initial Investment Cost (CAPEX) of USD 1141.2, the high performance and low operational expenditure lead to a highly favorable Return on Investment (ROI) of only 4.31 years. Compared to existing conventional and solar cookers, the developed system offers superior energy efficiency and optimized cooking times, and demonstrates rapid profitability. This makes it a sustainable, reliable, and energy-efficient home solution, representing a major technological leap for domestic cooking in rural areas. Full article

The consumption of energy and sports drinks is on the rise globally, exposing dental restorations to more frequent low-pH challenges, which affect degradation. This in vitro study simulated the combined effect of energy drink exposure and cyclic fatigue loading on the fatigue survival rate and flexural strength of three direct dental resin restorative materials with distinct chemistries: a bioactive ionic resin (Activa Presto), a giomer (Beautifil Flow Plus F00) and a conventional nano-hybrid composite (Tetric Ceram). Bar-shaped specimens (25 × 2 × 2 mm) were fabricated according to ISO 4049 and stored for 24 h in either distilled water or 0.2 M citric acid (pH ≈ 2.5), simulating an energy drink (n = 10/group). The samples then underwent chewing simulation (40 N, 100,000 cycles, 1.6 Hz) using a steel antagonist; surviving specimens were tested via three-point bending to determine their flexural strength. All the materials were affected by storage conditions: Activa Presto showed the lowest fatigue survival (20% in water; 0% in citric acid), Tetric N-Ceram moderate survival (40% in both solutions) and Beautifil Flow Plus F00 the highest and most stable survival (90% in water; 40% in citric acid). Among the surviving specimens, Tetric Ceram exhibited the highest flexural strength, followed by Beautifil Flow Plus F00 and then Activa Presto. Citric acid exposure and cyclic loading adversely affected the mechanical performance of all the materials within the limitations of this study. Full article

A novel strategy was adopted to enhance the energy storage properties of materials through constructing a vacancy defect. BaTi_1−xCu_xO_3−x (abbreviated as BTCx, x = 0–0.05) ceramics were prepared. The influences of Cu doping on structure and electrical properties were systematically investigated in this study. The result reveals that the oxygen vacancies in BTCx ceramics can inhibit grain growth and improve breakdown strength. Notably, as Cu content increases, the abundance of oxygen vacancies of the BTCx ceramics intensifies the relaxor behavior and induces double hysteresis loops with high energy storage performance. The excellent energy storage density of 1.34 J/cm³ and efficiency of 90.1% were achieved for BTC3 ceramics at 180 kV/cm, which indicates that the outstanding energy storage properties of BTCx ceramics make them have broad application prospects in advanced pulse power capacitors. Full article

High-efficiency, lead-free dielectrics are sought for pulsed-power capacitors, yet pristine Bi_0.5Na_0.5TiO₃ (BNT) suffers from large remanence, high coercivity, and limited breakdown strength. Here, we report (1 − x)Bi_0.5Na_0.5Ti_0.97Nb_0.03O₃-xSr_0.85Ba_0.15Ta_0.5+0.02xAl_0.5−0.02xO₃ (BNTNb–SBTA, x = 0–0.15) ceramics synthesized via solid-state reaction, achieving enhanced relaxor ferroelectric behavior through multi-cation substitution at A- and B-sites. X-ray diffraction confirms a pure perovskite solid solution, while scanning electron microscopy reveals grain refinement, suppressing oxygen vacancies and boosting the breakdown strength. Raman and dielectric analyses evidence strengthened relaxor behavior, accompanied by loop slimming and a systematic rise in breakdown strength. The composition x = 0.10 achieves the best trade-off, delivering W_rec = 3.357 J cm⁻³ and η = 90.5% at E_b = 240 kV cm⁻¹. Robust operational stability is demonstrated with small variations of W_rec/η over 0.1–200 Hz, 25–175 °C, and 10⁶ cycles. Pulsed tests show fast discharge (∼26 ns) with W_d = 0.826 J cm⁻³ at ∼90% efficiency under moderate fields. These results indicate that synergistic A/B-site disorder (Sr/Ba on A-site; Ta/Al with Nb on B-site), combined with microstructural densification, effectively minimizes P_r while elevating E_b, enabling high-efficiency energy storage under practical operating conditions. Full article

This work presents a comparative study on the structural, microstructural, and functional properties of a novel lead-free solid solution based on (1−x)(0.95(Bi_0.5Na_0.5)TiO₃–0.05BaTiO₃)–x(0.5Ba_0.7Ca_0.3TiO₃–0.5BaTi_0.8Zr_0.2O₃), abbreviated as (1−x)(BNT–5BT)–xBCZT, with x values ranging from 0 to 0.20. Two different synthesis routes were evaluated: a direct route, where all raw materials were mixed and processed in a single step, and an indirect route, where BNT–5BT and BCZT were pre-synthesized separately and later combined. X-ray diffraction (XRD) and Raman spectroscopy confirmed the formation of single-phase perovskite structures, with progressively increasing tetragonality as x increased. Field-emission scanning electron microscopy (FE-SEM/EDS) revealed dense microstructures and secondary rod-like phases whose morphology and amount evolved with composition. Dielectric measurements indicated an enhanced relaxor behavior with increasing BCZT content, evidenced by a shift in the T_F–R with frequency. The direct route resulted in more efficient dopant incorporation, leading to stronger dielectric relaxation, reduced hysteresis losses, and improved energy storage performance. The maximum energy efficiency (η) reached 43.7% for x = 0.075 via the direct route, compared to 38.0% for the same composition prepared by the indirect route. The maximum recoverable energy density (W_rec) reached 0.42 J·cm⁻³ for x = 0.075 via the direct route (vs. 0.40 J·cm⁻³ for the indirect route), with corresponding peak energy efficiencies of 43.7% and 38.0%, respectively. These findings demonstrate that (1−x)(BNT–5BT)–xBCZT ceramics synthesized via the direct route constitute a promising and scalable approach for high-efficiency, lead-free dielectric capacitors. Full article

The investigation of environmentally friendly, Pb-free ceramic dielectric materials with excellent energy storage capability represents a fundamental yet challenging research direction for the development of next-generation high-power capacitors. In this study, linear dielectric Ca_0.7La_0.2(Mg_1/3Nb_2/3)O₃ was added into [0.65BaTiO₃–0.35(Na_0.5Bi_0.5)TiO₃] to form a solid solution. The introduction of Ca_0.7La_0.2(Mg_1/3Nb_2/3)O₃ modified the crystal structure, enhanced insulation performance and breakdown strength, and reduced hysteresis loss. These improvements collectively contributed to higher energy storage density and efficiency (η). The ceramic pellet with the optimal 10 mol% Ca_0.7La_0.2(Mg_1/3Nb_2/3)O₃ demonstrated a higher retrievable energy density (~3.40 J cm⁻³) and efficiency (~81%) at a breakdown strength of 340 kV cm⁻¹ compared to BaTiO₃-based ferroelectric ceramics. The sample also exhibited good stability across a temperature range of 30–90 °C and a frequency range of 0.5–300 Hz. Thus, the as-prepared ceramics sample exhibited significant potential for pulsed power device applications. Full article