Search Results (23)

Ultrahigh-temperature ceramic composites based on hafnium diboride have a wide range of applications, including as components for high-speed aircraft and energy generation and storage devices. Consequently, developing methodologies for their fabrication and studying their properties are of paramount importance, in particular in using them as an electrode material for energy storage devices with increased oxidation resistance. This study investigates the behavior of ceramic composites based on the HfB₂-HfO₂-SiC system, obtained using 15 vol% Ti₂AlC MAX-phase as a sintering component, under the influence of subsonic flow of dissociated air. It was determined that incorporating the modifying component (Ti₂AlC) altered the composition of the silicate melt formed on the surface during ceramic oxidation. This modification led to the observation of a protective antioxidant function. Consequently, liquation was observed in the silicate melt layer, resulting in the formation of spherical phase inhomogeneities in its volume with increased content of titanium, aluminum, and hafnium. It is hypothesized that the increase in the high-temperature viscosity of this melt prevents it from being carried away in the form of drops, even at a surface temperature of ~1900–2000 °C. Despite the established temperature, there is no sharp increase in its values above 2400–2500 °C. This is due to the evaporation of silicate melt from the surface. In addition, the electrochemical behavior of the obtained material in a liquid electrolyte medium (KOH, 3 mol/L) was examined, and it was shown that according to the value of electrical conductivity and specific capacitance, it is a promising electrode material for supercapacitors. Full article

Metal–organic frameworks (MOFs), formed by the self-assembly of metal ions/clusters and organic linkers, have attracted considerable attention due to their well-exposed active sites, exceptionally high porosity, and diversified pore architectures. MOF-derived materials obtained through high-temperature pyrolysis or composite structural design not only inherit the porous framework advantages of their precursors but also demonstrate significantly enhanced electrical conductivity and structural stability via the formation of carbon-based frameworks and in situ transformation of metallic species. However, conventional MOF-derived materials struggle to address persistent technical challenges in contemporary energy storage systems, particularly those requiring ultralong cycling stability and ultrahigh-rate capability under practical operating conditions. The integration of MXene, characterized by its abundant surface functional groups (-O, -OH, -F) and exceptional electrical conductivity, with MOF-derived materials presents a viable strategy to address these challenges. Multidimensional nanocomposites constructed through in situ growth and self-assembly techniques synergistically integrate MXene’s conductive network scaffolding effect with the structural tunability of MOF-derived frameworks. This unique architecture enables the following: (i) enhanced exposure of electroactive sites, (ii) optimized ion diffusion kinetics, (iii) mechanical integrity maintenance, collectively boosting the applicability of MXene/MOF hybrids in advanced energy storage systems. This review summarizes the synthesis methods, energy storage performance, and applications of multidimensional nanostructured MXene/MOF-derived composites. Finally, it discusses the opportunities and challenges for MXene/MOF-derived composites in future energy storage applications. Full article

Based on the B-site modification strategy, excellent energy storage properties were achieved in this work by substituting Nb with Ta of the same valence in niobate-based glass ceramics. Ta substitution was found to lead to the transformation of crystal structures, and the space point group evolved from the non-centrosymmetric P4bm to the centrosymmetric P4/mbm, resulting in a transition from relaxor ferroelectric to paraelectric glass ceramics. Furthermore, the addition of Ta led to a significant decrease in grain size and interfacial activation energy, as well as an increase in the optical band gap, resulting in a dramatic increase in BDS from 800 kV/cm to 1300 kV/cm. The KBSN-4.0mol%Ta₂O₅ glass ceramic exhibited optimal energy storage properties, including a discharge energy density of ~5.62 J/cm³ and a superfast discharge rate of ~9.7 ns, resulting in an ultrahigh discharge power density of about ~1296.9 MW/cm³ at 1300 kV/cm. Furthermore, this KBSN-Ta glass ceramic also displayed good thermal stability over a temperature range of 20–120 °C, with the W_d decreasing by 9.0% at 600 kV/cm. B-site modification engineering in glass ceramics has proved to be an important way to effectively optimize energy storage performance. Full article

In the context of the global energy structure transformation, concentrated solar power (CSP) technology has gained significant attention. Its future trajectory is oriented towards the construction of ultra-high temperature (700–1000 °C) power plants, aiming to enhance thermoelectric conversion efficiency and economic competitiveness. Chloride molten salts, serving as a crucial heat transfer and storage medium in the third-generation CSP system, offer numerous advantages. However, they are highly corrosive to metal materials. This paper provides a comprehensive review of the corrosion behaviors of stainless steels and high-temperature alloys in molten salts. It analyzes the impacts of factors such as temperature and oxygen, and it summarizes various corrosion types, including intergranular corrosion and hot corrosion, along with their underlying mechanisms. Simultaneously, it presents an overview of the types, characteristics, impurity effects, and purification methods of molten salts used for high-temperature heat storage and heat transfer. Moreover, it explores novel technologies such as alternative molten salts, solid particles, gases, liquid metals, and the carbon dioxide Brayton cycle, as well as research directions for improving material performance, like the application of nanoparticles and surface coatings. At present, the corrosion of metal materials in high-temperature molten salts poses a significant bottleneck in the development of CSP. Future research should prioritize the development of commercial alloy materials resistant to chloride molten salt corrosion and conduct in-depth investigations into related influencing factors. This will provide essential support for the advancement of CSP technology. Full article

Nickel hydroxide has ultra-high energy storage capacity in supercapacitors, but poor electrical conductivity limits their further application. The use of graphene to improve its conductivity is an effective measure, but how to suppress the stacking of graphene and improve the overall performance of composite materials has become a new challenge. In this work, a well-designed substrate of N-doped carbon nanowires with reduced graphene oxide (NCNWs/rGO) was fabricated by growing polypyrrole (PPy) nanowires between GO nanosheets layers and then calcining them at high temperatures. This NCNWs/rGO substrate can effectively avoid the stacking of rGO nanosheets, and provides sufficient sites for the subsequent in situ growth of Ni(OH)₂, forming a uniform and stable Ni(OH)₂/NCNWs/rGO composite material. Benefiting from the abundant pores, high specific surface area (107.2 m² g⁻¹), and conductive network throughout the NCNWs/rGO substrate, the deposited Ni(OH)₂ can not only realize an ultra-high loading ratio, but also exposes more active surfaces (221.3 m² g⁻¹). After a comprehensive electrochemical test, it was found that the Ni(OH)₂/NCNWs/rGO positive materials have a high specific capacitance of 2016.6 F g⁻¹ at a scan rate of 1 mV s⁻¹, and exhibit significantly better stability. The assembled Ni(OH)₂/NCNWs/rGO//AC asymmetric supercapacitor could achieve a high energy density of 85.2 Wh kg⁻¹ at power densities of 381 W kg⁻¹. In addition, the asymmetric supercapacitor has excellent stability and could retain 70.1% of initial capacitance after 10,000 cycles. These results demonstrate the feasibility of using NCNWs/rGO substrate to construct high-performance supercapacitor electrode materials, and it is also expected to be promoted in other active composite materials. Full article

The ubiquitous, rising demand for energy storage devices with ultra-high storage capacity and efficiency has drawn tremendous research interest in developing energy storage devices. Dielectric polymers are one of the most suitable materials used to fabricate electrostatic capacitive energy storage devices with thin-film geometry with high power density. In this work, we studied the dielectric properties, electric polarization, and energy density of PMMA/2D Mica nanocomposite capacitors where stratified 2D nanofillers are interfaced between the multiple layers of PMMA thin films using two heterostructure designs of the capacitors, PMMA/2D Mica/PMMA (PMP) and PMMA/2D Mica/PMMA/2D Mica/PMMA (PMPMP). The incorporation of a 2D Mica nanofiller in the low-dielectric-constant PMMA leads to an enhancement in the dielectric constant, with ∆ε ~ 15% and 53% for PMP and PMPMP heterostructures at room temperature. Additionally, a significant improvement in discharged energy density was measured for the PMPMP capacitor (U_d ~ 38 J/cm³ at 825 MV/m) compared to the pristine PMMA (U_d ~ 9.5 J/cm³ at 522 MV/m) and PMP capacitors (U_d ~ 19 J/cm³ at 740 MV/m). This excellent capacitive and energy storage performance of the PMMA/2D Mica heterostructure nanocomposite may inform the fabrication of thin-film, high-density energy storage capacitor devices for potential applications in various platforms. Full article

Silicon carbide (SiC) single crystals have great prospects for high-temperature energy storage due to their robust structural stability, ultrahigh power output, and superior temperature stability. However, energy density is an essential challenge for SiC-based devices. Herein, a facile two-step strategy is proposed for the large-scale synthesis of a unique architecture of SiC nanowires incorporating MnO₂ for enhanced supercapacitors (SCs), arising from the synergy effect between the SiC nanowires as a highly conductive skeleton and the MnO₂ with numerous active sites. The SiC@MnO₂ integrated electrode-based SCs with ionic liquid (IL) electrolytes were assembled and delivered outstanding energy and power density, as well as a great lifespan at 150 °C. This impressive work offers a novel avenue for the practical application of SiC-based electrochemical energy storage devices with high energy density under high temperatures. Full article

One of the most promising and heavily researched energy storage systems due to their high energy density, rate capability and extended cycle life are lithium-ion batteries. Their performance and efficiency are nonetheless strongly dependent on their constituent materials and design, including the current collectors. One attractive approach in this respect is the use of metal foams as an alternative to the conventional current collectors. This concept is therefore intended to increase the current collectors’ specific surface area and therefore load more active material by nominal area while keeping the cell architectures simple and less costly. In the present work, nickel is chosen as a model system for a proof of concept of a novel manufacturing method for nickel foams using a combination of 3D printing, coating and electroplating. The purpose is to create geometrically well-defined hollow structures with high porosity and specific surface area density that can rival and partially outperform the commercially available nickel foams. To this end, a 3D printer is used to create geometrically flexible and well-defined open-pored disks of HIPS (high-impact polystyrene), which are then spray coated with a graphite-based conducting layer and subsequently electroplated with a 5–30 µm thin layer of nickel from an additive-free nickel sulfamate electrolyte. Following the coating process, the support structure is dissolved with toluene, resulting in structures with a unique combination of porosity in the range of 92.3–99.1% and an ultra-high specific surface area density up to 46 m²/kg. Morphological characterization by light and scanning electron microscopy has proven that the temporarily required polymer substrate can be mildly and completely removed by the suggested room temperature dissolution process. Full article

Multilayer graphene–paraffin composites with different contents of graphene (0–10 wt.%) were prepared using an ultra-high shear mixer. The aim is to improve the heat transfer in paraffin wax, which will lead to more-efficient thermal buffering in electronic applications. The multi-layer graphenes obtained by supercritical fluid exfoliation of graphite in alcohol were investigated by Raman spectroscopy, scanning electron microscopy and atomic force microscopy. Interesting morphological features were found to be related to the intercalation of paraffins between the multilayer graphene flakes. Thermal properties were also investigated in terms of phase change transition temperatures, latent heat by differential scanning calorimetry and thermal conductivity. It was found that the addition of graphene resulted in a slight decrease in energy storage capacity but a 150% improvement in thermal conductivity at the highest graphene loading level. This phase-change material is then used as a thermal heat sink for an embedded electronic processor. The temperature of the processor during the execution of a pre-defined programme was used as a performance indicator. The use of materials with multilayer graphene contents of more than 5 wt.% was found to reduce the processor operating temperature by up to 20%. This indicates that the use of such composite materials can significantly improve the performance of processors. Full article

The energy storage performances of supercapacitors are expected to be enhanced by the use of nanostructured hierarchically micro/mesoporous hollow carbon materials based on their ultra-high specific surface areas and rapid diffusion of electrolyte ions through the interconnected channels of their mesoporous structures. In this work, we report the electrochemical supercapacitance properties of hollow carbon spheres prepared by high-temperature carbonization of self-assembled fullerene-ethylenediamine hollow spheres (FE-HS). FE-HS, having an average external diameter of 290 nm, an internal diameter of 65 nm, and a wall thickness of 225 nm, were prepared by using the dynamic liquid-liquid interfacial precipitation (DLLIP) method at ambient conditions of temperature and pressure. High temperature carbonization (at 700, 900, and 1100 °C) of the FE-HS yielded nanoporous (micro/mesoporous) hollow carbon spheres with large surface areas (612 to 1616 m² g⁻¹) and large pore volumes (0.925 to 1.346 cm³ g⁻¹) dependent on the temperature applied. The sample obtained by carbonization of FE-HS at 900 °C (FE-HS_900) displayed optimum surface area and exhibited remarkable electrochemical electrical double-layer capacitance properties in aq. 1 M sulfuric acid due to its well-developed porosity, interconnected pore structure, and large surface area. For a three-electrode cell setup, a specific capacitance of 293 F g⁻¹ at a 1 A g⁻¹ current density, which is approximately 4 times greater than the specific capacitance of the starting material, FE-HS. The symmetric supercapacitor cell was assembled using FE-HS_900 and attained 164 F g⁻¹ at 1 A g⁻¹ with sustained 50% capacitance at 10 A g⁻¹ accompanied by 96% cycle life and 98% coulombic efficiency after 10,000 consecutive charge/discharge cycles. The results demonstrate the excellent potential of these fullerene assemblies in the fabrication of nanoporous carbon materials with the extensive surface areas required for high-performance energy storage supercapacitor applications. Full article

Smart hydrogels with high electrical conductivity, which can be a real source of power while also collecting and storing the diverse sources of energy with ultrahigh stretchability, strong self-healability, low-temperature tolerance, and excellent mechanical properties, are great value for tailored wearable cloths. Considerable effort has been dedicated in both scientific and technological developments of electroconductive hydrogels for supercapacitor applications in the past few decades. The key to realize those functionalities depends on the processing of hydrogels with desirable electrochemical properties. The various hydrogel materials with such properties are now emerging and investigated by various scholars. The last decade has witnessed the development of high-performance supercapacitors using hydrogels. Here, in this review, the current status of different hydrogels for the production of flexible supercapacitors has been discussed. The electrochemical properties such as capacitance, energy density and cycling ability has been given attention. Diverse hydrogels, with their composites such as carbon-based hydrogels, cellulose-based hydrogels, conductive-polymer-based hydrogels and other hydrogels with excellent electromechanical properties are summarized. One could argue that hydrogels have played a central, starring role for the assembly of flexible supercapacitors for energy storage applications. This work stresses the importance of producing flexible supercapacitors for wearable clothing applications and the current challenges of hydrogel-based supercapacitors. The results of the review depicted that hydrogels are the next materials for the production of the flexible supercapacitor in a more sustainable way. Full article

Sodium–ion batteries (SIBs) are essential for large–scale energy storage attributed to the high abundance of sodium. Polyanion Na₃V₂(PO₄)₃ (NVP) is a dominant cathode candidate for SIBs because of its high-voltage and sodium superionic conductor (NASICON) framework. However, the electrochemical performance of NVP is hindered by the inherently poor electronic conductivity, especially for extreme fast charging and long-duration cycling. Herein, we develop a facile one-step in-situ polycondensation method to synthesize the three-dimensional (3D) Na₃V₂(PO₄)₃/holey-carbon frameworks (NVP@C) by using melamine as carbon source. In this architecture, NVP crystals intergrown with the 3D holey-carbon frameworks provide rapid transport pathways for ion/electron transmission to increase the ultrahigh rate ability and cycle capability. Consequently, the NVP@C cathode possesses a high reversible capacity of 113.9 mAh g⁻¹ at 100 mA g⁻¹ and delivers an outstanding high–rate capability of 75.3 mAh g⁻¹ at 6000 mA g⁻¹. Moreover, it shows that the NVP@C cathode is able to display a volumetric energy density of 54 Wh L⁻¹ at 6000 mA g⁻¹ (31 Wh L⁻¹ for NVP bulk), as well as excellent cycling performance of 65.4 mAh g⁻¹ after 1000 cycles at 2000 mA g⁻¹. Furthermore, the NVP@C exhibits remarkable reversible capabilities of 81.9 mAh g⁻¹ at a current density of 100 mA g⁻¹ and 60.2 mAh g⁻¹ at 1000 mA g⁻¹ even at a low temperature of −15 °C. The structure of porous carbon frameworks combined with single crystal materials by in-situ polycondensation offers general guidelines for the design of sodium, lithium and potassium energy storage materials. Full article

With the development of electronic technology, there is an increasing demand for high-temperature dielectric energy storage devices based on polyimides for a wide range of applications. However, the current nanofillers/PI nanocomposites are used for energy harvesting at no more than 200 °C, which does not satisfy the applications in the oil and gas, aerospace, and power transmission industries that require an operating temperature of 250–300 °C. Therefore, we introduced a nanocomposite based on nonsolid TiO₂ nanoparticles and polyimide (PI) with high energy storage performance at an ultrahigh temperature of 300 °C. The synergy of excellent dielectric properties and a high breakdown strength endowed the nanocomposite with a low loading content of 1 wt% and a high energy storage density of 5.09 J cm⁻³. Furthermore, we found that the nanocomposite could stably operate at 300 °C with an outstanding energy storage capability (2.20 J cm⁻³). Additionally, finite element simulations demonstrated that the partially hollow nanostructures of the nanofillers avoided the evolution of breakdown paths, which optimized the breakdown strength and energy storage performance of the related nanocomposites. This paper provides an avenue to broaden the application areas of PI-based nanocomposites as ultrahigh-temperature energy-storage devices. Full article

Photovoltaics and wind power are expected to account for a large share of power generation in the carbon-neutral era. A gas turbine combined cycle (GTCC) with an industrial gas turbine as the main engine has the ability to rapidly start up and can follow up to load fluctuations to smooth out fluctuations in power generation from renewable energy sources. Simultaneously, the system must be more efficient than today’s state-of-the-art GTCCs because it will use either Carbon dioxide Capture and Storage (CCS) when burning natural gas or hydrogen/ammonia as fuel, which is more expensive than natural gas. This paper describes the trend of cooled turbine rotor blades used in large industrial gas turbines that are carbon neutral. First, the evolution of cooled turbine stationary vanes and rotor blades is traced. Then, the current status of heat transfer technology, blade material technology, and thermal barrier coating technology that will lead to the realization of future ultra-high-temperature industrial gas turbines is surveyed. Based on these technologies, this paper introduces turbine vane and blade cooling technologies applicable to ultra-high-temperature industrial gas turbines for GTCC in the carbon-neutral era. Full article

Accelerator scientists have high demands on photocathodes possessing high quantum efficiency (QE) and long operational lifetime. p-GaN, as a new photocathode type, has recently gained more and more interest because of its ability to form a negative electron affinity (NEA) surface. Being activated with a thin layer of cesium, p-GaN:Cs photocathodes promise higher QE and better stability than the known photocathodes. In our study, p-GaN samples grown on sapphire or silicon were wet chemically cleaned and transferred into an ultra-high vacuum (UHV) chamber, where they underwent a subsequent thermal cleaning. The cleaned p-GaN samples were activated with cesium to obtain p-GaN:Cs photocathodes, and their performance was monitored with respect to their quality, especially their QE and storage lifetime. The surface topography and morphology were examined by atomic force microscopy (AFM) and scanning electron microscopy (SEM) in combination with energy dispersive X-ray (EDX) spectroscopy. We have shown that p-GaN could be efficiently reactivated with cesium several times. This paper systematically compares the influence of wet chemical cleaning as well as thermal cleaning at various temperatures on the QE, storage lifetime and surface morphology of p-GaN. As expected, the cleaning strongly influences the cathodes’ quality. We show that high QE and long storage lifetime are achievable at lower cleaning temperatures in our UHV chamber. Full article