Phase change materials (PCMs) offer a promising solution to address the challenges posed by intermittency and fluctuations in solar thermal utilization. However, for organic solid–liquid PCMs, issues such as leakage, low thermal conductivity, lack of efficient solar-thermal media, and flammability have constrained their broad applications. Herein, we present an innovative class of versatile composite phase change materials (CPCMs) developed through a facile and environmentally friendly synthesis approach, leveraging the inherent anisotropy and unidirectional porosity of wood aerogel (nanowood) to support polyethylene glycol (PEG). The wood modification process involves the incorporation of phytic acid (PA) and MXene hybrid structure through an evaporation-induced assembly method, which could impart non-leaking PEG filling while concurrently facilitating thermal conduction, light absorption, and flame-retardant. Consequently, the as-prepared wood-based CPCMs showcase enhanced thermal conductivity (0.82 W m⁻¹ K⁻¹, about 4.6 times than PEG) as well as high latent heat of 135.5 kJ kg⁻¹ (91.5% encapsulation) with thermal durability and stability throughout at least 200 heating and cooling cycles, featuring dramatic solar-thermal conversion efficiency up to 98.58%. In addition, with the synergistic effect of phytic acid and MXene, the flame-retardant performance of the CPCMs has been significantly enhanced, showing a self-extinguishing behavior. Moreover, the excellent electromagnetic shielding of 44.45 dB was endowed to the CPCMs, relieving contemporary health hazards associated with electromagnetic waves. Overall, we capitalize on the exquisite wood cell structure with unidirectional transport inherent in the development of multifunctional CPCMs, showcasing the operational principle through a proof-of-concept prototype system.

The growing demand for sustainable energy storage solutions has underscored the importance of phase change materials (PCMs) for thermal energy management. However, traditional PCMs are always inherently constrained by issues such as leakage, poor thermal conductivity, and lack of solar energy conversion capacity. Herein, a multifunctional composite phase change material (CPCM) is developed using a balsa-derived morphology genetic scaffold, engineered via bionic catechol surface chemistry. The scaffold undergoes selective delignification, followed by a simple, room-temperature polydopamine (PDA) modification to deposit Ag nanoparticles (Ag NPs) and graft octadecyl chains, resulting in a superhydrophobic hierarchical structure. This superhydrophobicity plays a critical role in preventing PCM leakage and enhancing environmental adaptability, ensuring long-term stability under diverse conditions. Encapsulating stearic acid (SA) as the PCM, the CPCM exhibits exceptional stability, achieving a high latent heat of 175.5 J g⁻¹ and an energy storage efficiency of 87.7%. In addition, the thermal conductivity of the CPCM is significantly enhanced along the longitudinal direction, a 2.1-fold increase compared to pure SA, due to the integration of Ag NPs and the unidirectional wood architecture. This synergy also drives efficient photothermal conversion via π-π stacking interactions of PDA and the surface plasmon effects of Ag NPs, enabling rapid solar-to-thermal energy conversion. Moreover, the CPCM demonstrates remarkable water resistance, self-cleaning ability, and long-term thermal reliability, retaining its functionality through 100 heating–cooling cycles. This multifunctional balsa-based CPCM represents a breakthrough in integrating phase-change behavior with advanced environmental adaptability, offering promising applications in solar–thermal energy systems.

Wood, a renewable and abundant biomass resource, holds substantial promise as an encapsulation matrix for thermal energy storage (TES) applications involving phase change materials (PCMs). However, practical implementations often reveal a disparity between observed and theoretical phase change enthalpy values of wood-derived composite PCMs (CPCMs). This study systematically explores the confinement behavior of organic PCMs encapsulated in a delignified balsa wood matrix with morphology genetic nanostructure, characterized by a specific surface area of 25.4 ± 1.1 m²/g and nanoscale pores averaging 2.2 nm. Detailed thermal performance evaluations uncover distinct phase change behaviors among various organic PCMs, influenced by the unique characteristics of functional groups and carbon chain lengths. The encapsulation mechanism is primarily dictated by host–guest interactions, which modulate PCM molecular mobility through hydrogen bonding and spatial constraints imposed by the hierarchical pore structure of the wood. Notably, results demonstrate a progressive enhancement of nanoconfinement effects, evidencing a transition from octadecane to stearic acid, further supported by density functional theory (DFT) calculations. This research significantly advances the understanding of nanoconfinement mechanisms in wood-derived matrices, paving the way for the development of high-performance, shape-stabilized composite PCMs that are essential for sustainable thermal energy storage solutions.