Project description:Organic phase change materials (PCMs) represent an effective solution to manage intermittent energy sources as the solar thermal energy. This work aims at encapsulating docosane in organosilica shells and at dispersing the produced capsules in epoxy/carbon laminates to manufacture multifunctional structural composites for thermal energy storage (TES). Microcapsules of different sizes were prepared by hydrolysis-condensation of methyltriethoxysilane (MTES) in an oil-in-water emulsion. X-ray diffraction (XRD) highlighted the difference in the crystalline structure of pristine and microencapsulated docosane, and 13C solid-state nuclear magnetic resonance (NMR) evidenced the influence of microcapsules size on the shifts of the representative docosane signals, as a consequence of confinement effects, i.e., reduced chain mobility and interaction with the inner shell walls. A phase change enthalpy up to 143 J/g was determined via differential scanning calorimetry (DSC) on microcapsules, and tests at low scanning speed emphasized the differences in the crystallization behavior and allowed the calculation of the phase change activation energy of docosane, which increased upon encapsulation. Then, the possibility of embedding the microcapsules in an epoxy resin and in an epoxy/carbon laminate to produce a structural TES composite was investigated. The presence of microcapsules agglomerates and the poor capsule-epoxy adhesion, both evidenced by scanning electron microscopy (SEM), led to a decrease in the mechanical properties, as confirmed by three-point bending tests. Dynamic mechanical analysis (DMA) highlighted that the storage modulus decreased by 15% after docosane melting and that the glass transition temperature of the epoxy resin was not influenced by the PCM. The heat storage/release properties of the obtained laminates were proved through DSC and thermal camera imaging tests.
Project description:Latent heat storage using alloys as phase change materials (PCMs) is an attractive option for high-temperature thermal energy storage. Encapsulation of these PCMs is essential for their successful use. However, so far, technology for producing microencapsulated PCMs (MEPCMs) that can be used above 500°C has not been established. Therefore, in this study, we developed Al-Si alloy microsphere MEPCMs covered by α-Al2O3 shells. The MEPCM was prepared in two steps: (1) the formation of an AlOOH shell on the PCM particles using a boehmite treatment, and (2) heat-oxidation treatment in an O2 atmosphere to form a stable α-Al2O3 shell. The MEPCM presented a melting point of 573°C and latent heat of 247 J g(-1). The cycling performance showed good durability. These results indicated the possibility of using MEPCM at high temperatures. The MEPCM developed in this study has great promise in future energy and chemical processes, such as exergy recuperation and process intensification.
Project description:Designing and synthesizing photothermal conversion materials with better storage capacity, long-term stability as well as low temperature energy output capability is still a huge challenge in the area of photothermal storage. In this work, we report a brand new photothermal conversion material obtained by attaching trifluoromethylated azobenzene (AzoF) to reduced graphene oxide (rGO). AzoF-rGO exhibits outstanding heat storage density and power density up to 386.1 kJ·kg-1 and 890.6 W·kg-1, respectively, with a long half-life (87.7 h) because of the H-bonds based on high attachment density. AzoF-rGO also exhibits excellent cycling stability and is equipped with low-temperature energy output capability, which achieves the reversible cycle of photothermal conversion within a closed system. This novel AzoF-rGO complex, which on the one hand exhibits remarkable energy storage performance as well as excellent storage life span, and on the other hand is equipped with the ability to release heat at low temperatures, shows broad prospects in the practical application of actual photothermal storage.
Project description:Long-time thermal batteries with high specific energy are crucial for improving the fast response ability of long-range weapons. Due to its high capacity, safety, and stability, the new sulfide cathode has attracted extensive attention. In this study, an FeS2@CoS2 composite cathode with a core-shell structure was prepared via a combination of hydrothermal and high-temperature vulcanization processes. The novel FeS2@CoS2 cathode not only delivers a high discharge voltage and output capacity, but also has high thermal stability and excellent conductivity. Benefiting from the synergistic effect of FeS2 and CoS2, the as-synthesized cathode yields a high specific capacity. At a large current density of 1 A/cm2, the utilization rate of FeS2@CoS2 cathode material can reach 72.33%, which is 8.23% higher than that of FeS2. Moreover, the maximum output capacity is up to 902 As/g, with a utilization rate of 79.02% at 500 mA/cm2. This novel design strategy holds great promise for the development and application of high-performance thermal batteries in the future.
Project description:A novel type of bi-functional microencapsulated phase change material (MEPCM) microcapsules with thermal energy storage (TES) and carbon dioxide (CO2) photoreduction was designed and fabricated. The polyaniline (PANI)/titanium dioxide (TiO2)/PCN-222(Fe) hybrid shell encloses phase change material (PCM) paraffin by the facile and environment-friendly Pickering emulsion polymerization, in which TiO2 and PCN-222(Fe) nanoparticles (NPs) were used as Pickering stabilizer. Furthermore, a ternary heterojunction of PANI/(TiO2)/PCN-222(Fe) was constructed due to the tight contact of the three components on the hybrid shell. The results indicate that the maximum enthalpy of MEPCMs is 174.7 J·g-1 with encapsulation efficiency of 77.2%, and the thermal properties, chemical composition, and morphological structure were well maintained after 500 high-low temperature cycles test. Besides, the MEPCM was employed to reduce CO2 into carbon monoxide (CO) and methane (CH4) under natural light irradiation. The CO evolution rate reached up to 45.16 μmol g-1 h-1 because of the suitable band gap and efficient charge migration efficiency, which is 5.4, 11, and 62 times higher than pure PCN-222(Fe), PANI, and TiO2, respectively. Moreover, the CO evolution rate decayed inapparently after five CO2 photoreduction cycles. The as-prepared bi-functional MEPCM as the temperature regulating building materials and air purification medium will stimulate a potential application.
Project description:Phase change materials (PCMs), which can absorb and release large amounts of latent heat during phase change, have been extensively studied for heat storage and thermal management. However, technical bottlenecks regarding low thermal conductivity and leakage have hindered practical applications of PCMs. In this paper, a simple, economical, and scalable absorption polymerization technique is proposed to prepare the polymethyl methacrylate/propyl palmitate/expanded graphite (MPCM/EG) phase change composites by constructing the microencapsulated phase change materials (polymethyl methacrylate/propyl palmitate, MPCM) with core-shell structures in the three-dimensional (3D) EG networks, taking propyl palmitate as the PCM core, polymethyl methacrylate (PMMA) as the shell, and long-chain "worm-like" EG as the thermally conductive networks. This technique proved to be a more appropriate combinatorial pathway than direct absorption of MPCM via EG. The MPCM/EG composites with high thermal conductivity, high enthalpy, excellent thermal stability, low leakage, and good thermal cycle reliability were prepared. The results showed that the MPCM-80/EG-10 composite demonstrated a high thermal conductivity of 3.38 W/(m·K), a phase change enthalpy up to 152.0 J/g, an encapsulation ratio of 90.3%, outstanding thermal stability performance, and long-term thermal cycle reliability when the EG loading is 10% and propyl palmitate is 80%. This research offers an easy and efficient approach for designing and fabricating phase change composites with promising applications in diverse energy-saving fields, such as renewable energy collection, building energy conservation, and microelectronic devices thermal protection.
Project description:Dielectric capacitors are highly desired for electronic systems owing to their high-power density and ultrafast charge/discharge capability. However, the current dielectric capacitors suffer severely from the thermal instabilities, with sharp deterioration of energy storage performance at elevated temperatures. Here, guided by phase-field simulations, we conceived and fabricated the self-assembled metadielectric nanostructure with HfO2 as second-phase in BaHf0.17Ti0.83O3 relaxor ferroelectric matrix. The metadielectric structure can not only effectively increase breakdown strength, but also broaden the working temperature to 400 oC due to the enhanced relaxation behavior and substantially reduced conduction loss. The energy storage density of the metadielectric film capacitors can achieve to 85 joules per cubic centimeter with energy efficiency exceeding 81% in the temperature range from 25 °C to 400 °C. This work shows the fabrication of capacitors with potential applications in high-temperature electric power systems and provides a strategy for designing advanced electrostatic capacitors through a metadielectric strategy.
Project description:Stoichiometric salt hydrates can be inexpensive and provide higher volumetric energy density relative to other near-room-temperature phase change materials (PCMs), but few salt hydrates exhibit congruent melting behavior between 0 and 30 °C. Eutectic salt hydrates offer a strategy to design bespoke PCMs with tailored application-specific eutectic melting temperatures. However, the general solidification behavior and stability of eutectic salt hydrate systems remain unclear, as metastable solidification in eutectic salt hydrates may introduce opportunities for phase segregation. Here, we present a new family of low-cost zinc-nitrate-hexahydrate-based eutectics: Zn(NO3)2·6(H2O)-NaNO3 (Teu = 32.7 ± 0.3 °C; ΔHeu = 151 ± 6 J·g-1), Zn(NO3)2·6(H2O)-KNO3 (Teu = 22.1 ± 0.3 °C; ΔHeu = 140 ± 6 J·g-1), Zn(NO3)2·6(H2O)-NH4NO3 (Teu = 11.2 ± 0.3 °C; ΔHeu = 137 ± 5 J·g-1). While the tendency to undercool varies greatly between different eutectics in the family, the geologic mineral talc has been identified as an active and stable phase that dramatically reduces undercooling in Zn(NO3)2·6(H2O) and all related eutectics. Zn(NO3)2·6(H2O) and its related eutectics have shown stability for over a hundred thermal cycles in mL scale volumes, suggesting that they are capable of serving as robust and stable media for near-room-temperature thermal energy storage applications in buildings.
Project description:High-temperature infrared (IR) camouflage is crucial to the effective concealment of high-temperature objects but remains a challenging issue, as the thermal radiation of an object is proportional to the fourth power of temperature (T 4). Here, we experimentally demonstrate high-temperature IR camouflage with efficient thermal management. By combining a silica aerogel for thermal insulation and a Ge/ZnS multilayer wavelength-selective emitter for simultaneous radiative cooling (high emittance in the 5-8 μm non-atmospheric window) and IR camouflage (low emittance in the 8-14 μm atmospheric window), the surface temperature of an object is reduced from 873 to 410 K. The IR camouflage is demonstrated by indoor/outdoor (with/without earthshine) radiation temperatures of 310/248 K for an object at 873/623 K and a 78% reduction in with-earthshine lock-on range. This scheme may introduce opportunities for high-temperature thermal management and infrared signal processing.