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Viologen‐based reactive mesogen (VRM) is newly designed and synthesized for the development of polarization‐dependent, color‐tunable, and transparent electrochromic (EC) smart windows. By controlling electric field, the color of VRM can be intentionally tuned due to the formation of dication (D state), cation‐radical (C state), and neutral state (N state). Based on the deep understanding of phase transition of VRM, a uniaxially oriented VRM hierarchical nanostructure is successfully constructed on the macroscopic area by simple coating and self‐assembly processes. The subsequent photopolymerization significantly improves thermal, mechanical, and chemical stabilities of the VRM thin film. In addition to the control of color, the transmittance of uniaxially oriented VRM‐based EC smart window can be precisely tuned by rotating a linear polarizer. [ABSTRACT FROM AUTHOR]

To develop smart ionic skins capable of multi‐responsiveness and switchable ionic conductivity, a stimuli‐responsive and ionic conductive azobenzene‐based monomer is newly synthesized, uniaxially oriented, and polymerized for anisotropic liquid crystal elastomers (LCEs). Since the uniaxially oriented monodomain LCE with ionic asymmetric azobenzene monomers (i‐AAM) is prepared by thermal oligomerization, uniaxial stretching, and subsequent photopolymerization, the stimuli‐responsive i‐AAM LCE is thermally contracted by increasing the temperature above TNI as well as is bent along the aligned direction by irradiating it with UV light. In addition to the change of shape, the ionic conductivity of the LCE is reversible in response to heat and light stimuli. Polydomain i‐AAM LCE polymerized without the stretching process exhibits higher ionic conductivity than stretched monodomain LCE due to the initially formed stable ionic pathways. Ionic conductivity can also be switched simultaneously by polarity changes in response to the photoisomerization of i‐AAM, increased mobility from heat, and an elastic mechanoresponse from external stresses. These i‐AAM LCE‐based soft grippers exhibit stimuli‐responsive grasping and releasing actuation and detect ionic conductivity switches finely, suggesting potential as smart skins for advanced soft robots. [ABSTRACT FROM AUTHOR]

Biomass-based functional polymers have received significant attention across various fields, in view of eco-friendly human society and sustainable growth. In this context, there are efforts to functionalize the biomass polymers for next-generation polymer materials. Here, stretchable heat transfer materials are focused on which are essential for stretchable electronics and future robotics. To achieve this goal, natural rubber (NR) is chemically modified with a thiol-terminated phenylnaphthalene (TTP), and then utilized as a thermally conductive NR (TCNR) matrix. Hexagonal boron nitride (h-BN), renowned for its high thermal conductivity and low electrical conductivity, is incorporated as a filler to develop stretchable heat transfer eco-materials. The optimized TCNR/h-BN composite elongates to 140% due to great elasticity of NR, and exhibits excellent dielectric properties (a low dielectric constant of 2.26 and a low dielectric loss of 0.006). Furthermore, synergetic phonon transfer of phenylnaphthalene crystallites and h-BN particles in the composite results in a high thermal conductivity of 0.87 W m -1  K -1 . The outstanding thermal, mechanical, and dielectric properties of the newly developed TCNR/h-BN composite enable the successful demonstration as stretchable and shape-adaptable thermal management materials., (© 2024 Wiley‐VCH GmbH.)