Staggered-layer-boosted flexible Bi2Te3 films with high thermoelectric performance.

Room-temperature bismuth telluride (Bi2Te3) thermoelectrics are promising candidates for low-grade heat harvesting. However, the brittleness and inflexibility of Bi2Te3 are far reaching and bring about lifelong drawbacks. Here we demonstrate good pliability over 1,000 bending cycles and high power factors of 4.2 (p type) and 4.6 (n type) mW m-1 K-2 in Bi2Te3-based films that were exfoliated from corresponding single crystals. This unprecedented bendability was ascribed to the in situ observed staggered-layer structure that was spontaneously formed during the fabrication to promote stress propagation whilst maintaining good electrical conductivity. Unexpectedly, the donor-like staggered layer rarely affected the carrier transport of the films, thus maintaining its superior thermoelectric performance. Our flexible generator showed a high normalized power density of 321 W m-2 with a temperature difference of 60 K. These high performances in supple thermoelectric films not only offer useful paradigms for wearable electronics, but also provide key insights into structure-property manipulation in inorganic semiconductors.

Physics-guided co-designing flexible thermoelectrics with techno-economic sustainability for low-grade heat harvesting.

Flexible thermoelectric harvesting of omnipresent spatial thermodynamic energy, though promising in low-grade waste heat recovery (<100°C), is still far from industrialization because of its unequivocal cost-ineffectiveness caused by low thermoelectric efficiency and power-cost coupled device topology. Here, we demonstrate unconventional upcycling of low-grade heat via physics-guided rationalized flexible thermoelectrics, without increasing total heat input or tailoring material properties, into electricity with a power-cost ratio (W/US$) enhancement of 25.3% compared to conventional counterparts. The reduced material usage (44%) contributes to device power-cost "decoupling," leading to geometry-dependent optimal electrical matching for output maximization. This offers an energy consumption reduction (19.3%), electricity savings (0.24 kWh W-1), and CO2 emission reduction (0.17 kg W-1) for large-scale industrial production, fundamentally reshaping the R&D route of flexible thermoelectrics for techno-economic sustainable heat harvesting. Our findings highlight a facile yet cost-effective strategy not only for low-grade heat harvesting but also for electronic co-design in heat management/recovery frontiers.

Ice-Templated MXene/Ag-Epoxy Nanocomposites as High-Performance Thermal Management Materials.

High-performance thermal management materials are essential in miniaturized, highly integrated, and high-power modern electronics for heat dissipation. In this context, the large interface thermal resistance (ITR) that occurs between fillers and the organic matrix in polymer-based nanocomposites greatly limits their thermal conductive performance. Herein, through-plane direction aligned three-dimensional (3D) MXene/silver (Ag) aerogels are designed as heat transferring skeletons for epoxy nanocomposites. Ag nanoparticles (NPs) were in situ decorated on exfoliated MXene nanosheets to ensure good contact, and subsequent welding of ice-templated MXene/Ag nanofillers at low temperature of ∼200 °C reduced contact resistance between individual MXene sheets. Monte Carlo simulations suggest that thermal interficial resistance (R0) of the MXene/Ag-epoxy nanocomposite was 4.5 × 10-7 m2 W-1 K-1, which was less than that of the MXene-epoxy nanocomposite (Rc = 5.2 × 10-7 m2 W-1 K-1). Furthermore, a large-scale atomic/molecular massively parallel simulator was employed to calculate the interfacial resistance. It was found that RMXene = 2.4 × 10-9 m2 K W-1, and RMXene-Ag = 2.0 ×10-9 m2 K W-1, respectively, indicating that the Ag NP enhanced the interfacial heat transport. At a relatively low loading of 15.1 vol %, through-plane thermal conductivity reached a value as high as 2.65 W m-1 K-1, which is 1225 % higher than that of pure epoxy resin. Furthermore, MXene/Ag-epoxy nanocomposite film exhibits an impressive thermal conductive property when applied on a Millet 8 and Dell computer for heat dissipation.

Room-Temperature Welding of Silver Telluride Nanowires for High-Performance Thermoelectric Film.

Flexible thermoelectric materials that can harvest waste heat energy have attracted great attention because of the rapid progress of flexible electronics. Ag2Te nanowires (Ag2Te NWs) are considered as promising thermoelectric materials to fabricate flexible thermoelectric film and device because of their high Seebeck coefficient, but poor contact between the Ag2Te NWs results in low electrical conductivity. Generally, hot or cold pressing can increase the electrical conductivity between the Ag2Te NWs. However, these process tend to destroy the initial morphology of the Ag2Te NWs and/or cause only physical contact between the Ag2Te NWs. Herein, we report an approach to the room-temperature welding of Ag2Te NWs to enhance their contacts by facile combination of vacuum filtration and drop-coating methods. The obtained Ag2Te NWs film exhibits excellent Seebeck coefficient of -99.48 µV/K and high electrical conductivity of 15 335.05 S/m at room temperature, which gives the power factor of 151.76 µW m-1 K-2. Surprisingly, an optimal Seebeck coefficient of -154.96 µV/K and electrical conductivity of 14 982.42 S/m can be obtained at 420 K, giving a power factor of 359.76 µW m-1 K-2. Moreover, the electrical resistance of the Ag2Te NWs film was only 1.3 times of the initial electrical resistance after 1000 bending cycles, indicating good flexibility of the film. A finger-touch test is conducted by using the Ag2Te NWs film as thermoelectric power generator, which achieves a stable output voltage of about 0.52 mV, suggesting its great potential applications in self-powered flexible electronic devices.

Highly Compressive Boron Nitride Nanotube Aerogels Reinforced with Reduced Graphene Oxide.

Boron nitride nanotubes (BNNTs), structural analogues of carbon nanotubes, have attracted significant attention due to their superb thermal conductivity, wide bandgap, excellent hydrogen storage capacity, and thermal and chemical stability. Despite considerable progress in the preparation and surface functionalization of BNNTs, it remains a challenge to assemble one-dimensional BNNTs into three-dimensional (3D) architectures (such as aerogels) for practical applications. Here, we report a highly compressive BNNT aerogel reinforced with reduced graphene oxide (rGO) fabricated using a freeze-drying method. The reinforcement effect of rGO and 3D honeycomb-like framework offer the BNNTs/rGO aerogel with a high compression resilience. The BNNTs/rGO aerogels were then infiltrated with polyethylene glycol to prepare a kind of phase change materials. The prepared phase change material composites show zero leakage even at 100 °C and enhanced thermal conductivity, due to the 3D porous structure of the BNNTs/rGO aerogel. This work provides a simple method for the preparation of 3D BNNTs/rGO aerogels for many potential applications, such as high-performance polymer composites.