Polymer‐based thermal management materials have many irreplaceable advantages not found in metals or ceramics, such as easy processing, low density, and excellent flexibility. However, their limited thermal conductivity and unsatisfactory resistance to elevated temperatures (<200 °C) still prevent effective heat dissipation during applications with high‐temperature conditions or powerful operation. Therefore, herein highly thermoconductive and thermostable polymer nanocomposite films prepared by engineering 1D aramid nanofiber (ANF) with worm‐like microscopic morphologies into rigid rod‐like structures with 2D boron nitride nanosheets (BNNS) are reported. With no coils or entanglements, the rigid polymer chain enables a well‐packed crystalline structure resulting in a 20‐fold (or greater) increase in axial thermal conductivity. Additionally, strong interfacial interactions between the weaved ANF rod and the stacked BNNS facilitate efficient heat flux through the 1D/2D configuration. Hence, unprecedented in‐plane thermal conductivities as high as 46.7 W m−1 K−1 can be achieved at only 30 wt% BNNS loading, a value of 137% greater than that of a worm‐like ANF/BNNS counterpart. Moreover, the thermally stable nanocomposite films with light weight (28.9 W m−1 K−1/103 (kg m−3)) and high strength (>100 MPa, 450 °C) enable effective thermal management for microelectrodes operating at temperatures beyond 200 °C.

Extracting ubiquitous atmospheric water is a sustainable strategy to enable decentralized access to safely managed water but remains challenging due to its limited daily water output at low relative humidity (≤30% RH). Here, we report super hygroscopic polymer films (SHPFs) composed of renewable biomasses and hygroscopic salt, exhibiting high water uptake of 0.64–0.96 g g−1 at 15–30% RH. Konjac glucomannan facilitates the highly porous structures with enlarged air-polymer interfaces for active moisture capture and water vapor transport. Thermoresponsive hydroxypropyl cellulose enables phase transition at a low temperature to assist the release of collected water via hydrophobic interactions. With rapid sorption-desorption kinetics, SHPFs operate 14–24 cycles per day in arid environments, equivalent to a water yield of 5.8–13.3 L kg−1. Synthesized via a simple casting method using sustainable raw materials, SHPFs highlight the potential for low-cost and scalable atmospheric water harvesting technology to mitigate the global water crisis.

A solar thermoelectric generator (STEG) that generates electricity from sunlight is expected to be a promising technology for harvesting and conversion of clean solar energy. The integration of a phase-change material (PCM) with the STEG even more enables engines to durably generate power in spite of solar radiation flux. However, its photothermal conversion and output electricity is still limited (<15 W/m 2 ) by the PCM's deficient thermal management performance, i.e., restricted thermal conductivity and nonuniform heat-transfer behavior under concentrated sunlight radiation. In this study, a biomimetic phase-change composite, with centrosymmetric and a multidirectionally aligned boron nitride network embedded in polyethylene glycol, is tailored for the STEG via a radial icetemplate assembly and infiltration strategy, which behaves in a highly and multidirectionally thermoconductive way and enables a rapid transfer of heat flux and uniform temperature distribution with respect to even a spot-like heat source. As a consequence, a powerful STEG is tactfully designed via the integration of this high-thermal-management characteristic and maximum collection of solar beams, for durable and real-environment solar−thermal−electric conversion, with its photothermal energy conversion efficiency of up to 85.1% and a high peak power density of 40.28 W/m 2 .

It is still a challenge to fabricate polymer-based composites with excellent thermal conductive property because of the well-known difficulties such as insufficient conductive pathways and inefficient filler-filler contact. To address this issue, a synergistic segregated double network by using two fillers with different dimensions has been designed and prepared by taking graphene nanoplates (GNPs) and multiwalled carbon nanotubes (MWCNT) in polystyrene for example. In this structure, GNPs form the segregated network to largely increase the filler-filler contact areas while MWCNT are embedded within the network to improve the network-density. The segregated network and the randomly dispersed hybrid network by using GNPs and MWCNT together were also prepared for comparison. It was found that the thermal conductivity of segregated double network can achieve almost 1.8-fold as high as that of the randomly dispersed hybrid network, and 2.2-fold as that of the segregated network. Meanwhile, much higher synergistic efficiency (f) of 2 can be obtained, even greater than that of other synergistic systems reported previously. The excellent thermal conductive property and higher f are ascribed to the unique effect of segregated double network: (1) extensive GNPs-GNPs contact areas via overlapped interconnections within segregated GNPs network; (2) efficient synergistic effect between MWCNT network and GNPs network based on bridge effect as well as increasing the network-density.