Stable Phase Change Materials Research Articles

Enhanced thermal performance of phase change mortar using multi-scale carbon-based materials

Incorporating phase change material (PCM) into construction materials is an effective method for modifying building energy regulations throughout their service life. However, the effectiveness of PCM is constrained by its low thermal conductivity, highlighting the need for efficient enhancement methods. This study introduces thermally conductive carbon-based additions at both the nano-scale and meso-scale with different shapes, including carbon nano-tube (CNT), carbon black nano-particle (CB), and carbon fibre (CF) in PCM mortar. The mixed hydrated inorganic salt serves as the core PCM, while expanded perlite acts as the supporting material for the stable PCM composite, based on the presented research. The multi-scale additions establish thermal conduction pathways that improve temperature regulation performance. The modified samples exhibited a temperature difference of 2.2 °C and a time lag of up to 20 min under natural cooling conditions. Notably, CB positively influenced thermal conductivity, while CNT demonstrated an unexpected minor reduction. The enhancement in thermal conductivity increased with the content of CB, reaching an optimal enhancement of 18 %, except at a CNT content of 0.5 %. Conversely, both CB and CNT consistently improved thermal diffusivity. Furthermore, the compressive strength of the modified samples was significantly enhanced by up to 24 % compared to PCM mortar without carbon modifications. The modification method proposed in this study significantly improves both the thermal and mechanical properties of PCM mortar.

Evaluation into the effect of lignocellulosic biochar on the thermal properties of shape stable composite phase change materials

Biochar is suitable for preparing shape stable composite phase change materials (sscPCMs) due to the advantages of cost-effective, environmentally, and sustainability. However, the heat properties of biochar-based sscPCMs were not consistent. To investigate how different types of biochar influence the thermal properties of sscPCMs, three types of sscPCMs were successfully prepared using peanut shell biochar (PSC), poplar wood biochar (PWC), and corn straw biochar (CSC) as framework materials and combined with stearic acid (SA). A comprehensive analysis of the thermal properties of three sscPCMs was performed, taking into account thermal conductivity, phase change latent heat, encapsulation efficiency, crystallization rate, and energy storage efficiency. The study indicated that among the three types of sscPCMs, SA/PWC sscPCMs demonstrated excellent comprehensive performance. The phase change latent heat of SA/PWC reached 100.13 J/g, and the thermal conductivity was 0.38 W/mK. Compared to SA/PSC, the phase change latent heat of SA/PWC increased by 45.96 %, with only a 28.30 % reduction in thermal conductivity. In comparison to SA/CSC, the thermal conductivity of SA/PWC improved by 18.75 %, while the phase change latent heat decreased by only 14.02 %. In addition, the proportions of cellulose, hemicellulose, and lignin played a crucial role in determining the thermal properties of sscPCMs. This study clarified the mechanism by which biochar influences the thermal characteristic of sscPCMs, offering valuable insights for choosing biochar framework materials.

Preparation and Properties of Na2HPO4∙12H2O/Silica Aerogel Composite Phase Change Materials for Building Energy Conservation.

In this paper, a morphologically stable composite phase change material (CPCM) suitable for use in the field of building energy conservation was developed using Na2HPO4∙12H2O (DHPD) as the phase change material, Na2SiO3∙9H2O (SSNH) as the nucleating agent, and silica aerogel (SA) as the carrier. The results showed that the incorporation of 25 wt% SA resulted in the as-prepared DHPD-SSNH/SA CPCM with a phase change temperature of 30.4 °C, an enthalpy of 163.4 J/g, and a low supercooling degree of 1.3 °C, which also solved the corrosion problem of reinforcing bars caused by the hydrated salt PCM. Meanwhile, DHPD-SSNH/SA CPCM had good shape stability and low thermal conductivity (0.1507 W/(m·K)). The phase change temperature was basically unchanged, and the enthalpy only decreased by 4.8% after 200 cold-heat cycles. In addition, the thermal performance evaluation of CPCM showed that the indoor thermal comfort time of the testing system loaded with PCM board accounted for 50.75%, which was 43.38% higher than that of the one without PCM board (7.37%). The results suggest that the obtained CPCM had a good energy saving effect and great potential in the field of building energy conservation.

Carboxymethyl Cellulose Enhanced Polymeric Form Stable Phase Change Materials with Reversible Transparency for Energy Storage

Carboxymethyl Cellulose Enhanced Polymeric Form Stable Phase Change Materials with Reversible Transparency for Energy Storage

Comparison of UiO-66(Zr) and its derivate in shape stabilized phase change materials: Thermal storage performance and characterizations

In this study, UiO-66(Zr) and its derivative (UiO-66-C) are employed as supports to prepare shape stabilized PCM (U/SA-X and UC /SA-X) for resolving the melting leakage and poor thermal conductivity of stearic acid (SA). Thermal storage performance, including phase change enthalpy, supercooling degree, phase change temperature, thermal conductivity, and shape stability of U/SA-X and UC/SA-X, are compared. Preliminary characterization reveals that the physicochemical property evolution of the support impacts the thermal storage performance of SA. UiO-66 with microporous structure is unfavorable to enhance the shape stability of SA. U/SA-X exhibits low thermal storage efficiency and high supercooling degree owing to nanoconfinement and hydrogen bonding. By contrast, UiO-66-C possesses mesopores and graphitic structure that allows for a remarkable thermal storage performance of UC/SA-X. In detail, UC/SA-50 exhibits an ideal thermal storage performance, where the thermal conductivity (0.531 W/(m·K)) increases by 141 % in comparison to SA with a high phase change enthalpy of 93.6 J/g and low supercooling degree of 0.24 °C. It also shows satisfying thermal reliability that the thermal property of UC/SA-50 maintains stability even after 100 thermal cycles. In addition, the photothermal conversion efficiency of UC/SA-50 is up to 83.06 %.

Thermal conductivity enhancement of polyethylene glycol/NF composite as stabilized phase change materials for thermal energy storage

Polyethylene glycol (PEG) has the advantages of large latent heat of phase transition, a wide range of phase transition, and cheap price, but the application of PEG in the latent thermal energy storage (TES) systems is hindered due to its lower heat transfer rate and leakage. Porous metal foam has excellent thermal conductivity and high strength, which can effectively improve the problems of PEG. In this study, PEG/nickel foam (NF) composite phase change materials (PCM) were prepared by vacuum molten impregnation method using NF as substrate. It was found that PEG had good compatibility with NF, and the highest impregnation rate of PEG6000/NF reached 85.73 %. The thermal conductivity of PEG2000/NF can be increased to 1.58 1.58 W·m−1 K−1, nearly 4 times larger than that of pure PEG. The phase change temperature range of the composite PCM is 51–63 °C, and the phase change enthalpy is 67.8–126.3 J·g−1. Furthermore, the PEG/NF composite demonstrated outstanding photothermal conversion properties and high thermal stability, which can be widely used in the field of building temperature control and device heat dissipation.

Analysis of Freeze-Thaw Damage of Cement Mortars Doped with Polyethylene Glycol-Based Form Stable Phase Change Materials.

The development of construction materials with the integration of phase change materials (PCMs) has been a topic of wide interest in the scientific community, especially in recent years, due to its positive impact on temperature regulation inside buildings. However, little is known about the behavior of materials doped with PCMs when exposed to accidental or severe environments. Currently, a large area of the planet experiences seasonal freeze-thaw effects, which impact the durability and performance of construction materials. Accordingly, the main objective of this study was to evaluate the damage caused by cyclic freeze-thaw actions on the behavior of a cement mortar, including a PEG-based form-stable PCM. An experimental methodology was developed based on the physical and mechanical characterization of mortars under normal operating conditions and after being subjected to freeze-thaw cycles. The results indicated that, under normal exposure conditions, the incorporation of aggregate functionalized with PCM led to a decrease in the mortar's water absorption capacity, compressive strength, and adhesion. However, its applicability has not been compromised. Exposure to freeze-thaw cycles caused a loss of mass in the specimens and a decrease in the compressive strength and adhesion capability of the mortar.

Confined Crystallization Polyether-Based Flexible Phase Change Film for Thermal Management.

Phase change materials (PCMs) possess the potential to regulate temperature by utilizing their thermal properties to absorb and release heat. Nevertheless, the application of PCMs in thermal management is constrained by issues such as liquid leakage and limited flexibility. In this study, we propose a novel approach to address these challenges by incorporating a pore structure within nanofibers to confine the crystallization of phase change molecules, thereby enhancing the flexibility of the composite material. Additionally, inspired by the adaptive mechanisms observed in plants, we have developed a form stable PCM based on polyether, which effectively mitigates the issue of liquid leakage at higher temperatures. Despite being a solid-liquid PCM at its core, this material exhibits molecular-scale flow and macroscopic shape stability as a result of intermolecular forces. The composite film material possesses remarkable flexibility, efficient thermal management capabilities, adjustable phase transition temperature, and the ability to undergo repeated processing and utilization. Consequently, it holds promising potential for applications in personal thermal energy management.

Experimental dynamic thermal properties determination of EPDM/NBR panels with a shape stabilized Phase Change Material based on summer daily temperatures of four cities in Italy

In this work, the evaluation of E-PCM panels based on an elastomeric matrix containing a shape-stabilized paraffinic phase change material with a melting point of 28 °C was carried in a climatic chamber, simulating the summer daily temperature profile of four geographical locations in Italy at different latitudes. The characterization, carried out on testing boxes insulated using the E-PCM panels, allowed the determination of the delay (time lag) and of the dampening (decrement factor) in the propagation of the heat wave when passing from the outer to the inner surface of the walls; the results were correlated to two important parameters, the characteristic admittance and the heat capacity. From the difference between the heat fluxes on the outer and inner surface of the panels it was also possible to quantify the amount of stored energy and to do a comparison with a reference insulating panel (aerogel). Aerogel panels, despite the low thermal conductivity but due to the limited heat capacity and characteristic admittance, were unable to provide an effective insulation during summer conditions while E-PCM panels led to excellent outcomes. Results showed that with a peak of 33 °C in the external temperature, the phase change material limited the internal one at 27 °C with a maximum delay in the peak temperature of 6 h, an overall decrement factor of 0.4, time lag of 3 h and stored energy of 740 kJ/m2 per day. Finally, also the influence of the testing speed on the response of the E-PCM was evaluated through repetition of heating/cooling cycles in the temperature range 19–35 °C, highlighting the necessity of improving the thermal conductivity of the system in case of fast-response applications (cycle length < 3.5 h) and/or to optimize the PCM amount in the panel depending on the energy to be absorbed.

Evaluation of carbonized cotton stalk for development of novel form stable composite phase change materials for solar thermal energy storage

Generating energy from the renewable sources is a pathway to attain sustainable energy systems. Utilizing bio-char produced from pyrolysis process as porous material would not only add great value to the waste discards, but also contributes towards enhancing the thermal properties. This work is focussed on the development of form stable phase change material (FSPCM) through a facile impregnation method by introducing cotton stalk biochar (CSB) as porous matrix along with polyethylene glycol having molar mass 10000 g/mol (PEG10000) as PCM. Cotton stalk is an agriculture waste material and biochar was produced by intermediate pyrolysis method at 550 °C. Thermal, chemical and surface characterization tests were executed on seepage free FSPCM (BCPCM4) as it showed no leakage at 60 °C. XRD, FTIR, FESEM, TGA, DSC, Raman spectroscopy and BET analysis were carried out to characterize thermal, chemical and surface properties of BCPCM4. The microporous structure of CSB was able to accommodate 80 wt% of PEG10000. Surface characterization tests demonstrated that adequate amount of PEG10000 was absorbed into the pores of CSB and the crystal structure of PEG10000 was not modified. The results of TGA illustrated that BCPCM4 was thermally stable. Additionally, cotton stalk derived FSPCM displayed high heat transfer rate which indicates an increase in thermal conductivity. To substantiate thermal reliability, 500 thermal cycles were run on BCPCM4 and about 1 % variation in latent heat has been noticed with meagre change in chemical properties. Therefore, biochar derived FSPCMs would serve as promising materials to accommodate solar thermal energy.

The preparation and selection process for a new form stable phase change material (FSPCM) intended for use as thermal storage in applications at intermediate temperatures

There is a greater focus on solar energy since the food processing business requires a lot of thermal energy to remove moisture from agricultural products. This study thoroughly explains how to choose Phase Change Materials (PCMs) within a specific temperature range. The best PCM is selected from the Multiple Criteria Decision Making (MCDM) procedures based on a few characteristics. Based on the results of the MCDM method, the eutectic of paraffin and palmitic acid is chosen. PCM is bound, and FSPCM is formed using clay. The method of preparation of Clay-based FSPCM is described in detail. The amount of clay materials and different clay percentage combinations are chosen from the leakage experiment. Kaolin has the least amount of leakage out of all the clay materials tested. Kaolin-based FSPCM Exhibits improvement in thermal conductivity compared to Pure PCM.

Insights into effect of lignocellulosic biomass framework types on bio-based shape stable composite phase change materials

The utilization of biomass waste as framework materials to inhibit the leakage of phase change material (PCMs) has gained widespread attention. In this work, three new kinds of shape stable composite phase change materials (sscPCMs) were prepared which combined with stearic acid (SA) and peanut shell powders (PSP), poplar wood powders (PWP), and corn straw powders (CSP), respectively. The influence of lignocellulosic biomass types on the thermal energy storage performance of sscPCMs was studied by comparing three types of sscPCMs. The research results indicated that SA/CSP exhibited superior properties in terms of load capacity and thermal energy storage performance. According to leakage experiments the load capacity of SA/PSP, SA/PWP and SA/CSP was 31.67 %, 44.69 %, and 50.09 %, respectively. The phase change latent heat of SA/PSP, SA/PWP, and SA/CSP was 55.78, 84.27 and 98.47 J/g, respectively. In addition, the relationship between biomass component content and load rates was studied. The results showed that there was a positive correlation between the loading rates of SA and the ratio of holocellulose (cellulose + hemicellulose) to lignin. The results provided a promising approach for the selection of lignocellulosic biomass framework materials.

Physical-Entanglements-Supported Polymeric Form Stable Phase Change Materials with Ultrahigh Melting Enthalpy.

With the rapid development of new energy and the upgrading of electronic devices, structurally stable phase change materials (PCMs) have attracted widespread attentions from both academia and industries. Traditional cross-linking, composites, or microencapsulation methods for preparation of form stable PCMs usually sacrifice part of the phase change enthalpy and recyclability. Based on the basic polymer viscoelasticity and crystallization theories, here, a kind of novel recyclable polymeric PCM is developed by simple solution mixing ultrahigh molecular weight of polyethylene oxide (UHMWPEO) with its chemical identical oligomer polyethylene glycol (PEG). Rheological and leakage-proof experiments confirm that, even containing 90% of phase change fraction PEG oligomers, long-term of structure stability of PCMs can be achieved when the molecular weight of UHMWPEO is higher than 7000kg mol-1 due to their ultralong terminal relaxation time and large number of entanglements per chain. Furthermore, because of the reduced overall entanglement concentration, phase change enthalpy of PCMs can be greatly promoted, even reaching to ≈185 J g-1, which is larger than any PEG-based form stable PCMs in literatures. This work provides a new strategy and mechanism for designing physical-entanglements-supported form stable PCMs with ultrahigh phase change enthalpies.

Development and preparation of novel nano-enhanced organic eutectic phase change materials for low-temperature solar thermal applications

ABSTRACT Thermally reliable and stable eco-friendly Phase change materials are of significant aid in thermal energy storage technology, leading to improved energy utilization and reliability of the system. This study develops two novel organic eutectic PCM of Lauric acid – Margaric acid (LM) and Myristic acid – Margaric acid (MM), which are chemically stable and thermally compatible for latent heat energy storage. LM eutectic mixture had a melting temperature of 52.66°C with a latent heat of 163.68 J/g, and MM eutectic mixture had its melting temperature at 44.79°C and a latent heat of 197.31 J/g. The phase change temperatures were favorable for low temperature solar thermal applications with good latent heat capacity. The thermal characteristics of these eutectic mixtures are further enhanced with the dispersion of highly conductive Multi walled carbon nanotubes (MWCNT) at three different mass fractions (.5%, 1% and 1.5% by weight). Nano enhancement could achieve exceptional thermal conductivity enhancement in MM eutectic mixture by 110.6% and 83.73% in LM eutectic mixture. Thermogravimetric analysis and Fourier-transform infrared spectroscopy analysis ensured the thermal and chemical stability of the eutectic mixtures. The optical absorption characteristics were extensively enhanced with nano particle addition, which is highly preferable in solar thermal applications.

Harnessing leather waste in polymer matrix for sustainable smart shape‐stable phase change materials

AbstractThe utilization of leather waste (LW) in a polyurethane (PU) matrix makes a smart and novel shape stable phase change material (SSPCM). This is essential for sustainability as it reduces landfill waste after use. The PU is synthesized in bulk with a 90% yield, using biodegradable polycaprolactone diol and bio‐based polyol (castor oil), along with tolylene‐2,4‐diisocyanate. PL and PLG composites are prepared by blending of constituent components PU (P), LW (L), and poly(glycidyl methacrylate) (PGMA, G), as specified by their code names. Role of LW (hydrogen bonding and chemical crosslinking) and morphology are elucidated by FTIR and SEM, respectively. Self‐healing time (2 h), shape fixity ratios (Rf) (PL: 60–80% and PLG: 60–70%) and shape recovery ratios (Rr) (100% for both) are determined at 60°C. PLG displays faster shape recovery in water (&lt;30 s) compared to air (&gt;300 s). Shape stability and thermal properties of the SSPCM are examined using the temperature responsive leakage study, TGA, and DSC. This research introduces a new approach for using leather waste (LW) in SSPCM, with self‐healing and 100% Rr. This material may find application where SSPCM with high durability and flexibility is essential such as textile and footwear materials.

A graphene-CuNWs@PAMPS mixed aerogel for composite phase change materials with high thermal conductivity and excellent solar-thermal to electrical conversion

Phase change materials could store and release heat energy through phase change. However, the shortcomings of low thermal conductivity in the photothermal conversion process and easy leakage in the solid-liquid conversion seriously hinder the application of heat energy utilization. Graphene had high thermal conductivity, and it was an ideal material for improving the solar absorption, solar energy conversion and thermal conductivity of phase change materials. In this paper, a graphene aerogel composed of copper nanowires (CuNWs)/2-acrylamide-2-methylpropanesulfonic acid (AMPS) was designed. The thermal conductivity and shape stability of phase change materials for solar-thermal-electrical conversion applications were enhanced by composite CuNWs. Furthermore, PAMPS was coated on the surface of copper nanowires to avoid the oxidation of copper nanowires, and the sulfonic acid group of PAMPS was used to induce CuNWs to disperse uniformLy on the graphene sheets, which further constructed a good conductive network. After vacuum impregnation of PW, the best thermal conductivity phase change composite (PW-CuNWs@PAMPS-GA(1:1)) was obtained. The PCC loaded with CuNWs with the same graphene content achieved a thermal conductivity of 1.46 W/(m·K) and a high latent heat of 206.8 J/g. The latent heat retention rate was as high as 99.57 %. The photothermal conversion efficiency of PW-CuNWs@PAMPS-GA(1:1) was remarkable at 96.4 %. Due to its excellent solar-thermal-electrical conversion efficiency, the output voltage and output current were 800.8 mV and 85.8 mA, respectively, at a solar analog intensity of 5 kW/m2. Even after the sunlight was stopped, the voltage output could be maintained for a while by releasing the heat energy stored in the phase change composite.

Nanoscale Stabilization Mechanism of Sodium Sulfate Decahydrate at Polyelectrolyte Interfaces.

Sodium sulfate decahydrate (SSD) is a low-cost phase-change material (PCM) for thermal energy storage applications that offers substantial melting enthalpy and a suitable temperature range for near-ambient applications. However, SSD's consistent phase separation with decreased melting enthalpy over repeated thermal cycles limits its application as a PCM. Sulfonated polyelectrolytes, such as dextran sulfate sodium (DSS), have shown great effectiveness in preventing phase separation in SSD. However, there is limited understanding of the stabilization mechanism of SSD by DSS at the atomic length and time scales. In this work, we investigate SSD stabilization via DSS using neutron scattering and molecular dynamics (MD) simulations. Neutron scattering and pair distribution function analysis revealed the structural evolution of the PCM samples below and above the phase change temperatures. MD simulations revealed that water from the hydrate structure migrates from the hydrate crystal to the SSD-DSS interfacial region upon melting. The water is stabilized at this interface by aggregation around the hydrophilic sulfonic acid groups attached to the backbone of the polyelectrolyte. This architecture retains water near the dehydrated sodium sulfate, preventing phase separation and, consequently, stabilizing SSD rehydration. This work provides atomistic insight into selecting and designing stable and high-performance PCMs for heating and cooling applications in building technologies.

Recent trends on energy-efficient solar dryers for food and agricultural products drying: a review

AbstractThe energy efficiency enhancement of solar dryers has attracted the attention of researchers worldwide because of the need for energy storage in solar drying applications, which arises primarily from the irregular nature of solar energy that leads to improper drying which will reduce the quality of the products being dried. This work comprehensively reviews the state-of-the-art research carried out on solar dryers for energy efficiency enhancement using various alternative strategies, including hybrid solar dryers that use auxiliary heating sources, such as electric heaters or biomass heaters, solar-assisted heat pump dryer, use of desiccant materials, and heat storage systems that use both sensible and latent heat storage. The advent of phase change materials (PCM), such as thermally and chemically stable PCMs, for long-term storage, bio-degradable and bio-compatible PCM materials to alleviate the negative environmental impact of conventional PCMs is also presented. The performance parameters considered for evaluating dryers include the maximum temperature attained inside the drying chamber, drying time and efficiency, specific moisture extraction rate (SMER), energy and exergy efficiency and CO2 mitigation effect. The factors considered to analyze the PCMs application in solar dryers include cost and sustainability of PCMs, and both energy and exergy analyses of dryers using PCMs. The gaps in current knowledge and future scope for further improvement of solar dryers are also elucidated. Graphical abstract

A novel cement mortar comprising natural zeolite/dodecyl alcohol shape stable composite phase change material for energy effective buildings

Investigations into Phase Change Materials (PCMs) for heat storage in facilities have gained significance, contributing to indoor temperature regulation, decreased energy usage, and improved building efficiency, thereby supporting sustainability initiatives. However, the issue of PCM leakage during the heating phase has constrained its thermal energy storage (TES) prospective at large scaled-practices. Addressing this concern, the present study emphases on elimination of the leakage problem of dodecyl alcohol (DA) as a PCM with appropriate melting temperature for building TES request by its impregnating into the natural zeolite (NZ) as a low cost host matrix. In the second stage of the work, using the developed shape stable-NZ/DA (SS-NZ/DA) composite PCM in cement mortar instead of sand, novel cementitious mortars with enhanced thermal properties were created by incorporating different weight percentages (25 %, 50 %, 75 %, and 100 %) compared to the mortar comprising NZ. Experimental works were carried out to analyze the shape-stability, TES features, cycling TES stability and thermal endurance of the SS-NZ/DA composite as well the physical properties, mechanical strength, and solar temperature regulation performance of the SS-NZ/DA included mortars. The SS-NZ/DA demonstrated the melting enthalpy of 107.5 J/g at 19.47 °C and a freezing enthalpy of 106.1 J/g at 19.86 °C. The performance test results obtained under real weather conditions indicated that the integration of SS-NZ/DA into mortar presented maximum drop of 10 % and 9.26 % in peak indoor temperature at the SS-CPCM slab surface and the center of SS-CPCM slab-cabin, respectively, accompanied by an approximate 3-hour time delay. Mortars with SS-NZ/DA composite PCM exhibited a decreased dry unit weight (1189 kg/m3) and thermal conductivity (0.394 W/mK) while experiencing a moderate strength loss (4.5 MPa). These favorable physico-mechanical properties, TES characteristics and thermal management capability make the novel cementitious mortar containing composite PCM as an energy-efficient material for creating thermo-regulative building components. In this study, the natural, economical, and environmentally friendly nature of the NZ material used for PCM impregnation, its ability to contain a high percentage of PCM (up to 45 %) without any leakage issues, is the most fundamental and important characteristic of the composite used. The most unique feature of this composite mortar is the ability to achieve sufficient mechanical and thermal properties in cementitious mortars produced using this composite material without any leakage problems.

Phase change materials encapsulated in a novel hybrid carbon skeleton for high-efficiency solar-thermal conversion and energy storage

Phase change materials (PCMs) with high energy density and stationary transition temperature are now considered promising solar energy storage mediums. However, their intrinsic poor light absorption, thermal conductivity and stability severely impede their potential applications. In this study, a novel carbonized hybrid aerogel (CHA) structure was firstly constructed by incorporating MXene and carbon nanofibers (CNFs) into a continuous phase polyamic acid salt (PAAS) aqueous solution, followed by directional freezing, vacuum drying, imidization, and carbonization processes. Finally, the composite PCMs (CPCMs) were fabricated by vacuum impregnation of PCMs into the CHAs. The CPCM, of which CHA consists of 20 wt% MXene and 10 wt% CNF@PDA, demonstrates high solar-thermal conversion efficiency (>91 %), improved thermal conductivity of 0.40 W·m−1·K−1, great thermal stability (enthalpy loss < 0.19 % after 100 cycling tests with no obvious leakage). The introduction of MXene and CNFs endows PCM with broader light absorption spectrum range. The skeleton matrix embedded with bonded MXene sheets and CNFs provides more thermal pathways, light absorption sites and carrying capacity, improves the thermal conductivity, solar-thermal conversion property and stability of PCM. In addition, CPCM also exhibits outstanding EMI SE (95 dB). The multifunctional and high-performance CPCMs shows potential to realize the effective capture and utilization of solar energy. This work provides a new strategy to construct stable and multifunctional hybrid carbon skeleton for high-efficiency solar-thermal conversion and energy storage.