Thermal Conductive Pathways Research Articles

Synergetic integration of photothermal and self-cleaning features in a composite phase change material based on layered double hydroxides and polypyrrole

Composite phase change materials (PCMs) with photothermal functionality play a crucial role in efficiently storing and utilizing solar energy. However, the challenge of effectively removing of contaminants on photothermal conversion coatings has long puzzled researchers. In this study, we propose a novel approach to enhancing both photothermal conversion performance and self-cleaning properties of wood-based composite phase change materials, ultimately facilitating the sustainable and effective utilization of solar energy. The method utilized metal-organic frameworks (MOFs) as a precursor to form rough layered double hydroxides (LDH) on the wood surface through hydrolysis-induced exchange. Subsequently, polypyrrole (PPy) was deposited through vapor phase onto the LDH, and paraffin wax (PW) is utilized as the phase change material to prepare a novel composite phase change material. This modified wood structure facilitates leak-proof PW encapsulation and effective heat storage (167.6 J/g). PPy acts as a proficient photothermal converter and improves the composite material's heat transfer efficiency by establishing thermal conduction pathways, resulting in an 87.4 % enhancement in thermal conductivity compared to pure PW. The rough surface of LDH promotes multiple light reflections and scattering within the material, leading to increased light absorption by the PPy coating and achieving a photothermal conversion efficiency of up to 96.4 %. Furthermore, the high roughness of the LDH layer combined with the low surface energy of PW imparts superhydrophobic self-cleaning properties to the material, ensuring sustained effectiveness of the photothermal conversion coating over time. This research presents a viable approach for maintaining the cleanliness and efficiency of solar energy systems.

Porous TiO2 microspheres containing MgO nanoparticles/epoxy composite with superior thermal conductivity, EMI shielding, and electrical insulation

With the continuous advancement of electronic devices, the amounts of heat as well as electromagnetic (EM) waves generated have increased. Materials with high thermal conductivity and excellent EM interference shielding effectiveness (EMI SE) can be utilized to address this issue. In this work, we synthesized hollow anatase TiO2 microspheres. Through a reaction, MgO nanoparticles were incorporated into the interior of TiO2 microspheres. (H-TiO2/MgO). The heterostructure of the fillers contributed to performance enhancement. TiO2 and MgO particles formed a dual thermal-conduction pathway. H-TiO2/MgO effectively weakened the energy of EM waves upon contact. Additionally, TiO2, MgO, and epoxy all exhibited hydrophilicity. Consequently, the interfacial compatibility between H-TiO2/MgO and epoxy was excellent. They formed strong interfacial interactions by hydrogen bonding. Because of the excellent electrical insulation properties of H-TiO2 and MgO, the composites exhibited superior insulation performance (over 1010 Ω·cm). Our H-TiO2/MgO/Epoxy composites exhibited a maximum thermal conductivity of 7.52 W/m·K, an EMI SE of 64.92 dB, and a tensile strength of 79.10 MPa. Our composites are expected to effectively manage heat and EM waves generated by electronic devices

Heterogeneous interface engineering of spindle shaped Fe/C through optimizing impedance response for enhanced microwave absorption and thermal conductivity

Heterogeneous interface design is pivotal in creating lightweight, broadband, and high-efficiency electromagnetic wave (EMW) absorption materials. These materials enhance wave absorption by adaptively matching impedance. In this study, spindle-shaped Fe/C nanocomposites with heterogeneous interfaces and diverse surface microtopographies were synthesized by calcining iron-supported metal-organic frameworks (MOFs). During controlled pyrolysis, Fe3+ was reduced by carbon and conversely induced the graphitization of carbon, which is essential for the distribution and appearance of Fe and graphitized carbon as well as for modulating impedance matching. The porous structure of the Fe/C composites and the polarization loss and ferromagnetic resonance from the defective carbon and Fe magnetic particles synergistically enhance the wave absorption performance. The Fe/C-700 nanocomposite achieves a reflection loss (RL) of −55.9 dB at 12.48 GHz with an effective absorption bandwidth (EAB, RL ≤ −10 dB) of 3.9 GHz at 1.8 mm. The Fe/C-900 nanocomposite demonstrates a significant RL of −63.5 dB at 15.8 GHz with an EAB of 4.4 GHz between 13.6 GHz and 18 GHz at 1.5 mm, and an EAB of 5.5 GHz at 1.63 mm. These improvements are attributed to the impedance matching facilitated by the introduction of Fe magnetic particles and graphitized carbon. Additionally, the thermal conduction pathway formed among the Fe/C nanocomposites significantly enhances the thermal conductivity to 0.502 W m−1 K−1. Thus, this work offers a novel approach to the design of advanced wave-absorbing and thermal conductive materials by optimizing impedance through heterogeneous interfaces.

NiCo@EG-based composite PCMs with boosted thermal conductivity and photothermal conversion efficiency for solar energy harvesting

The application of phase change materials (PCMs) in solar energy is hampered by challenges such as insufficient photothermal conversion efficiency, low thermal conductivity and leakage. In this study, a novel composite PCMs based on NiCo@EG were prepared to solve the problems of low thermal conductivity, high leakage rate and inefficient photothermal performance. The NiCo@EG is obtained through calcination of the product of Ni-Co-BTC in-situ on expanded graphite (EG). In the composite PCMs, the octadecanol (OD) acts as a latent heat storage unit, the EG retains its porous network structure as an encapsulating skeleton. The nickel and cobalt nanoparticles derived from Ni-Co-BTC bimetallic organic frameworks are uniformly fixed on the surface of the EG, which could not only construct multiple thermal conduction pathways, but also enhance the photon-trapping ability. Benefiting from the synergy effect of nickel, cobalt metal nanoparticles and EG, the prepared OD/NiCo@EG-550 composite PCMs display high latent heat (168.3 J/g), excellent photothermal conversion efficiency (98.71 %), and improved thermal conductivity of 12.873 W/(m·K). Furthermore, the composite PCMs demonstrate exceptional shape stability, thermal stability, and robust thermal reliability. In summary, the high-efficiency photothermal composite PCMs display significant potential in improving the utilization of solar energy.

Protruding Boron Nitride Nanotubes on the Al2O3 Surface Enabled by Tannic Acid-Assisted Modification to Fabricate a Thermal Conductive Epoxy/Al2O3 Composite.

Over the past few years, the ability to efficiently increase boron nitride nanotube (BNNT) production has opened up ample research possibilities. BNNT has garnered significant attention for diversifying its industrial applications. However, the problem of poor processability resulting from agglomeration and uneven distribution has emerged as a major challenge to integrating BNNT into the polymer matrix for composite material formation. Utilizing noncovalently attached molecules with various reactive sites can be a logical method to enhance the compatibility of BNNT with different polymers. The present study explored a simple approach to protruding BNNT onto the surface of Al2O3 through tannic acid (TA)-assisted generation of alkyl chains (octadecylamine, ODA) to fabricate Al2O3@ODA-BNNT. The subsequent compounding of Al2O3@ODA-BNNT with epoxy polymer generates interconnected thermal conduction pathways, thereby improving the thermal conduction and mechanical performance of the composites. The current research approach allows for the even distribution of BNNT throughout the polymer matrix, as demonstrated by optical characterization, mechanical performance analysis, and isotropic thermal conductivity analysis. The fabricated epoxy composite by incorporating a 2 wt % (BNNT = 1.3 wt % and ODA = 0.7 wt %) ODA-BNNT exhibited 5.117 W/mK thermal conductivity and 7.43 MPa mechanical stress. Thermal conductivity improved by 2528, 76.56, and 54.7%, while mechanical stress enhanced by 270, 221, and 34% compared to neat polymers without BNNT and virgin BNNT epoxy composites, respectively.

Titanium dioxide/graphene oxide synergetic reinforced composite phase change materials with excellent thermal energy storage and photo-thermal performances

The development of advanced composite solid-solid phase change materials (SSPCMs) is urgent to explore for improving solar energy harvesting and storage. Herein, novel composite SSPCMs with synergetic cross-linking structure were fabricated through polymerization using GO and TiO2 constructed on the polyurethane framework skeleton. GO and TiO2 synergetic enhanced polymer framework played a role as skeletal structure to encapsulate PEG in the molecular chains, and provided as highly thermal conductive pathways for the composite SSPCMs. TiO2 nanoparticles performed as extended surface on the skeletal structure for further improvement in thermal conductivity. The composite SSPCMs exhibited a remarkably improved thermal conductivity as high as 0.7 W/(m‧K) and fast thermal response rate. The good light adsorption property of TiO2 enhanced the light absorbance efficiency of the composite SSPCMs by 94.4%. And the photo-thermal conversion efficiency of the composite SSPCMs highly reached 93.5%. Meanwhile, the composite SSPCMs exhibited excellent anti-leakage performance and shape stability under high temperature. Consequently, the as-prepared composite SSPCMs possessed a potential for applications in thermal energy storage and solar energy utilization systems.

Polyarylene ether nitrile/boron nitride nanosheets thermally conductive films through heterogeneous multilayer electrostatic spinning

Thermal management materials with excellent thermal conductivity and electrical insulation are highly favorable in the modern integrated electronic areas. In present work, a novel polyarylene ether nitrile (PEN) composite film, integrating thermal conductivity, electrical insulation, and flexibility, was fabricated utilizing a hybrid approach combining heterogeneous multilayer electrostatic spinning with a subsequent hot pressing technique. BNNS acts as a thermally conductive filler which builds a good thermal conduction pathway, and PEN acts as a bonding agent which ensures the flexibility and insulation of the film. Heterogeneous multilayer electrostatic spinning ensures the formation of thermal conduction pathways. Compared to conventional composite film, heterogeneous multilayer film shows excellent thermal conductivity, increases by 83% in-plane, and 71% through-plane, respectively. Therefore, This work will provide a technological reserve for the preparation of thermally conductive and insulating flexible films.

The thermal conductivity of 3D network reinforced polypropylene matrix composites was constructed by the pickering‐like emulsion method

AbstractPolypropylene (PP) has the advantages of corrosion resistance, easy processing, and low dielectric loss, but its low thermal conductivity limits the application of its composites in fields such as electronic packaging. To solve this problem, in this work, composite microspheres with the segregated structure were prepared by coating boron nitride nanosheets (BNNSs) on the PP surface by Pickering‐like emulsion method, and BNNSs@PP composites with three‐dimensional thermal conductivity network were obtained after molding. Due to the high thermal conductivity of BNNSs and the formation of perfect thermal conduction pathways, the thermal conductivity of the composites reached 1.71 W m−1 K−1 when the content of BNNSs was 10.1 wt%, which was a 713% increase in thermal conductivity for that of pure PP. At the same time, the mechanical properties of the composites were ensured. This method provides a simple and effective technique to improve the thermal conductivity of PP‐based thermally conductive composites, which has a wide application potential in electronic packaging.

Improved thermal conductivity of high‐density polyethylene by incorporating hybrid fillers of copper powders and silicon carbide whiskers

AbstractIn this paper, highly electrically and thermally conductive copper powders (Cu) and electrically insulative yet thermally conductive silicon carbide whiskers (SiCw) were selected as functional fillers and high‐density polyethylene (HDPE) was used as the matrix to prepare thermal conductive composites. By controlling the amount of Cu at 30 vol% which is below percolation threshold, the volume resistivity of the composites is maintained above 1014 Ω cm. The results showed that SiCws entered the area which was not occupied by Cu particles and they played a bridging effect among Cu particles, thereby promoting the formation of intact thermal conductive pathways that contributed to improving the thermal conductivity of corresponding composites. The combination of SiCw:Cu = 3:1 at a filler content of 30 vol% resulted in a thermal conductivity as high as 1.921 W/mK, which is 380% higher than pure HDPE.

Consistent Thermal Conductivities of Spring-Like Structured Polydimethylsiloxane Composites under Large Deformation.

Flexible and highly thermally conductive materials with consistent thermal conductivity (λ) during large deformation are urgently required to address the heat accumulation in flexible electronics. In this study, spring-like thermal conduction pathways of silver nanowire (S-AgNW) fabricated by 3D printing are compounded with polydimethylsiloxane (PDMS) to prepare S-AgNW/PDMS composites with excellent and consistent λ during deformation. The S-AgNW/PDMS composites exhibit a λ of 7.63W m-1 K-1 at an AgNW amount of 20 vol%, which is ≈42 times that of PDMS (0.18W m-1 K-1) and higher than that of AgNW/PDMS composites with the same amount and random dispersion of AgNW (R-AgNW/PDMS) (5.37W m-1 K-1). Variations in the λ of 20 vol% S-AgNW/PDMS composites are less than 2% under a deformation of 200% elongation, 50% compression, or 180° bending, which benefits from the large deformation characteristics of S-AgNW. The heat-transfer coefficient (0.29W cm-2 K-1) of 20 vol% S-AgNW/PDMS composites is ≈1.3 times that of the 20 vol% R-AgNW/PDMS composites, which reduces the temperature of a full-stressed central processing unit by 6.8°C compared to that using the 20 vol% R-AgNW/PDMS composites as a thermally conductive material in the central processing unit.

Multi‐layer graphene nanosheets bridging binary aluminium oxide for the synergistic enhancement of thermal conductivity and electrical insulation of silicone resin composite

AbstractThe flexible polymer composites usually require high intrinsic thermal conductivity fillers for the applications in thermal management, such as the well‐known graphene, which can, in turn, compromise their electrical insulation properties. Here, the authors developed the silicone resin (SR) composites filled with multi‐layer graphene nanosheets (MGN) and binary alumina (Al2O3), and the microstructure of composites exhibits the dominant skeleton of large‐sized Al2O3 filler and branching of small‐sized Al2O3 fillers features by the size matching effect of optimal binary Al2O3. The introduction of supplementary MGN fillers further increases the face‐to‐face contact probability and bridges the isolated binary Al2O3, which contributes to the high thermal conductivity of 3.0 W·m−1·K−1 under these synergistic effects. The dense and connected ‘Al2O3‐MGN‐Al2O3’ thermal conductive pathway is successfully built, as supported by the numerical simulation and Agari model fitting. Meanwhile, the electrical conductivity caused by MGN can be blocked by the surrounding insulation Al2O3 filler network, exhibiting a high volume resistivity of 1.7 × 1015 Ω · cm. Moreover, the Al2O3/MGN/SR composite films effectively transfer the heat and diminish the hot‐spot temperature by 53.5°C in cooling light emitting diode chip module application.

Broadband sound absorption cellulose/basalt fiber composite paper with excellent thermal insulation and hydrophobic properties

Cellulose-based materials find extensive applications in sound absorption due to their high porosity, biodegradability, and cost-effectiveness. However, these materials also suffer from some limitations such as hydrophilicity and low thermal stability that restrict their applicability and lifespan. Herein, we report a cellulose/basalt fiber (CBF) broadband sound absorption composite paper with excellent thermal insulation and hydrophobic properties fabricated by wet forming and silane vapor treatment. Benefiting from the introduction of eco-friendly basalt fibers, the composite paper has an adjusted pore structure and thermal conduction pathway, leading to enhanced sound absorption and thermal insulation performance. Particularly, the composite paper with 50 wt% basalt fiber shows remarkable sound absorption coefficient (0.71 on average) and ultralow thermal conductivity (0.034 W/m·K). As a novel application of eco-friendly materials for sound absorption, the CBF composite paper is an ideal candidate for indoor architectural decoration.

Interweaved filler network in epoxy resin with reduced interface thermal resistance via in-situ high-temperature “welding” for significantly improved thermal conductivity

For heterogeneous integration in harsh environments, polymeric materials are required to integrate excellent insulating property with significant thermal conductivity. Traditional discrete fillers used in polymeric matrix to create thermal pathways introduce numerous contact interfaces, leading to limited thermal conductivity enhancement efficiency (TCE) and unstable dielectric properties. Here, a distinctive strategy, involving the preparation of an interweaved thermally conductive filler with inherent heat channels through self-templated electrospinning and in-situ high-temperature “interface welding”, is proposed to reduce the interface thermal resistance (ITR). The growth of grains at high temperature facilitates the process of “interface welding”, while self-templated electrospinning establishes intrinsic thermal conduction pathways. Consequently, the epoxy resin fortified with this interweaved filler exhibits an exceptionally TCE of 162.15 % and enhanced in-plane thermal conductivity of 3.75 W m−1 K−1 at ultra-low filler ratio of 7.10 vol%. The combination of high electrical insulation of filler and low filler content results in excellent electrical insulating property (>1017 Ω cm) and stable dielectric properties over a frequency range of 103-106 Hz, enabling the successful implementation of heterogeneous integration in challenging environments. This work has the potential to offer a groundbreaking approach for achieving interconnected functional networks within polymer-based composites.

Highly efficient thermal conductivity of polyarylene ether nitrile composites via the introduction of hybrid fillers and tailored cross-linked structure

Polymer dielectrics with high thermal conductivity (λ) and excellent insulating properties are of interest in miniaturized and integrated electronic devices. However, most polymers are unable to fulfill this need due to their inherent structure. In this work, a polymer alloy with balanced thermal conductive and dielectric properties was successfully prepared by polyarylene ether nitrile(PEN), bisphthalonitrile-microsphere@boron nitride nanosheets(Bm@BNNS), and silicon carbide whisker (SiCws) at different scales. Specifically, introduction of Bm@BNNS fillers with core-shell structure into PEN resins results in heterogeneous interfaces, which effectively reduces the agglomeration and dosage of BNNS and synergistically improves the λ and dielectric performance. Besides, it has high breakdown strength (Eb) and high energy storage density (242.26 kV/mm, 1.66J/cm3) when filled with only 4.37 vol% BNNS compared to pure PEN. Furthermore, effects of one-dimensional SiCws at different scales on formation of heat-conduction pathways and electrical insulation properties of PEN/Bm@BNNS composites were investigated. The findings display that PEN/Bm@BNNS/SiCws composites with large size SiCws (7.81 vol%) achieved a high λ of 2.376 W/m.K, which was 135.24 % and 87.09 % higher than pure PEN and PEN/Bm@BNNS composites, respectively. Thus, the thermal conductive pathways are constructed by line-plate structure (SiCws-BNNS), and insulating performance primarily on the core-shell structure (Bm@BNNS). Besides, the novel PEN/Bm@BNNS/SiCws hybrid materials are together with a low coefficient of thermal expansion of 38–89 ppm/°C and high Tg of 220 °C. Thus, it gives a promising insight to achieve highly λ polymer-based insulating film materials used for high-temperature-resistant fields.

Sizing agent induces the oriented attachment of 2D nanosheets for preparing high-performance carbon fiber composites

Inducing highly oriented 2D nanosheets to create a mussel-inspired interface phase on the carbon fiber (CF) surface to enhance its composites’ strength and toughness has become a great challenge. In this study, a novel coating was synthesized to induce the graphene oxide (GO) oriented distributed on the CF surface while constructing a biomimetic "Brick-and-Mortar" structural interface phase, which simultaneously promoted the strength and toughness of CF composites. Acting as a sizing agent, di-pyrene terminated PEG (py-PEG-py) facilitates abundant π-π* stacking interactions, and enables flexible chain segment motion during interface fracture of composites, as well as effectively improving the toughness of composites. Eventually, the formation of a superior mechanism on the CF surface results in remarkable properties for composites, including an interfacial shear strength (IFSS) of 99.3 MPa, interlaminar shear strength of 93.2 MPa, and flexural strength of 1430 MPa. The tensile strength and toughness increased to 1777 MPa and 45.0 MJm−3, respectively. Simultaneously, the continuous thermal conduction pathway produced by the oriented attachment of GO on the CF surface increased in-plane thermal conductivity. The reinforcing mechanisms of the unique mussel-inspired coating were systematically investigated. This work opens up an effective and scalability avenue for obtaining high-performance CF composites.

High performance composite phase change materials enhanced via evaporation-induced hydrogen bond network refactoring

Composite phase change materials (CPCMs) with real-time thermal harvesting are in high demand in the solar-thermal energy conversion industry. However, poor heat conduction, lack of strength and leakage problem severely restrict its availability. In this study, we develop an evaporation-inspired, facile, and versatile strategy for manufacturing shape stable CPCMs from organohydrogels with enhanced thermal performances for advanced thermal energy storage and management. Organohyodrogels contained with graphene nanoplatelets (GNPs) served as the template. By oven-drying the organohydrogel, hydrogen bonding reconstruction would assist in the formation of a dense polymer layer to encapsulate PCMs, forming the non-leakage CPCMs. The strong capillary force generated during the oven-drying process would induce the alignment of GNPs, forming thermal conduction pathways. The as-prepared composite exhibits a high thermal conductivity (1.25 W m-1K−1), satisfactory latent heat storage (171.5 J g−1) and excellent Young’s modulus (8.3 MPa). When subjected to solar radiation, solar energy is converted to heat and stored inside the material, with a conversion efficiency as high as 95.8 %. The robust composite with high performance is expected to be an efficient and reliable thermal management material in solar-thermal energy conversion.

In situ three-roll mill exfoliation approach for fabricating asphalt/graphite nanoplatelet composites as thermal interface materials

Thermal interface materials (TIMs) are vital to dissipate excess heat generated by electronic components with ever-growing power density to ensure their reliability and performance. However, the limited dispersibility of nano-sized thermal conductive fillers hinders further enhancement of thermal conductivity in TIMs. It remains challenging to manufacture high-performance TIMs with simultaneous high thermal conductivity, low cost, and capability of large-scale production. Herein, a solvent-free and scalable approach was adopted to fabricate asphalt/graphite nanoplatelets (GNPs) composites by in situ exfoliating graphite in asphalt melt using a three-roll mill. During exfoliation, asphalt was adsorbed onto the surface of GNPs via π-π interaction and improved their dispersibility. Hence, GNPs formed integrated thermal conductive pathways with reduced interfacial thermal resistance, which significantly improved the thermal conductivity of asphalt/GNP composites. At 25 vol% loading, the asphalt/GNP composite displayed a thermal conductivity of 1.95 W m−1 K−1, showing a 114 % increase compared to the asphalt/commercial GNP (c-GNP) composite prepared by conventional mechanical mixing. Moreover, the heat-resistant and mechanical properties of the asphalt/GNP composites were also enhanced due to the improved filler dispersion and filler-matrix interactions. Thus, the asphalt/GNP composites fabricated by in situ three-roll milling possessed remarkable advantages as TIMs compared with asphalt/c-GNP composites and commercial silicone rubber thermal pads.

Radial assembly of graphene nanoplates via ice-template method to construct 3D thermally conductive phase change materials

Phase change material (PCM) with the capacity to store and release substantial thermal energy, has drawn significant attention. However, its large-scale application is still hindered by inadequate thermal management capacity and unsatisfactory thermal conductivity. In this study, graphene nanoplates were assembled into a 3D thermally conductive scaffold using a specialized ice template method. By virtue of the unique growth of ice crystals in radial pattern, a series of multidirectional thermal conduction pathways were successfully constructed within PCM, which has provided microscopically interconnected pathways for thermal transport. Consequently, a remarkable 5.2-fold increment in thermal conductivity (1.365 W m−1 K−1) in comparison to pure paraffin was achieved by incorporating a mere 6 vol% of GNP, which therefore enables excellent thermal cycling stability, remarkable latent heat storage capacity exceeding 175 J/g, together with leak-proof properties even under extended high-temperature conditions. Moreover, the solar-to-thermal energy storage efficiency is up to 85.8 % due to its efficient photothermal effect. This work presents an innovative approach to design PCMs with enhanced thermal conductivity and photothermal efficiency, offering promising applications in advanced thermal storage.

Compressible thermal interface materials with high through-plane thermal conductivity from vertically oriented carbon fibers

The mechanical properties especially the compression performance are very important for thermal interface materials (TIMs) to mitigate warpage failure caused by stress concentration and reduce contact resistance in practical applications. However, high thermal conductivity and excellent mechanical properties are generally incompatible in traditional TIMs. Herein, we fabricate a high-performance carbon fiber-based TIM by using an extrusion method based on the flow shearing effect. The vertically oriented composite shows a through-plane thermal conductivity up to 18.5 W·m−1·K−1 at 20 wt% carbon fiber content, which is 92.7 times that of pure matrix and 6.3 times that of the random structure. Moreover, the as-prepared material exhibits low hardness of 56 (Shore 00) and outstanding elastic compression performance of 51.4% compression under a pressure of 45 psi. These excellent properties are primarily attributed to the high orientation of the carbon fibers (CFs), thereby establishing a direct and effective thermal conductivity path in the vertical direction. In addition, the synergistic effect of carbon fibers and alumina particles is also beneficial for building thermal conduction pathways. Our work provides an insight to further research in fabricating high-performance flexible TIMs as a promising candidate for applying in advanced thermal management fields.

Bioinspired Thermal Conductive Cellulose Nanofibers/Boron Nitride Coating Enabled by Co-Exfoliation and Interfacial Engineering.

Thermal conductive coating materials with combination of mechanical robustness, good adhesion and electrical insulation are in high demand in the electronics industry. However, very few progresses have been achieved in constructing a highly thermal conductive composites coating that can conformably coat on desired subjects for efficient thermal dissipation, due to their lack of materials design and structure control. Herein, we report a bioinspired thermal conductive coating material from cellulose nanofibers (CNFs), boron nitride (BN), and polydopamine (PDA) by mimicking the layered structure of nacre. Owing to the strong interfacial strength, mechanical robustness, and high thermal conductivity of CNFs, they do not only enhance the exfoliation and dispersion of BN nanoplates, but also bridge BN nanoplates to achieve superior thermal and mechanical performance. The resulting composites coating exhibits a high thermal conductivity of 13.8 W/(m·K) that surpasses most of the reported thermal conductive composites coating owing to the formation of an efficient thermal conductive pathway in the layered structure. Additionally, the coating material has good interface adhesion to conformably wrap around various substrates by scalable spray coating, combined with good mechanical robustness, sustainability, electrical insulation, low-cost, and easy processability, which makes our materials attractive for electronic packaging applications.