SnSe crystal has witnessed significant advancements as a promising thermoelectric material over the past decade. Its in-plane direction shows robust mechanical strength for practical thermoelectric applications. Herein, we optimize the in-plane thermoelectric performance of n-type SnSe by crystal symmetry modification. In particular, we find that Te and Mo alloying continuously enhances the crystal symmetry, thereby increasing the carrier mobility to ~ 422 cm²V⁻¹ s⁻¹. Simultaneously, the conduction bands converge with the symmetry modification, further improving the electrical transport. Additionally, the lattice thermal conductivity is limited to ~ 1.1 W m⁻¹ K⁻¹ due to the softness of both acoustic and optical branches. Consequently, we achieve a power factor of ~ 28 μW cm⁻¹ K⁻² and ZT of ~ 0.6 in n-type SnSe at 300 K. The average ZT reaches ~ 0.89 at 300−723 K. The single-leg device based on the obtained n-type SnSe shows a remarkable efficiency of ~ 5.3% under the ΔT of ~ 300 K, which is the highest reported in n-type SnSe. This work demonstrates the substantial potential of SnSe for practical applications of power generation and waste heat recovery.

Studies on the piezoelectric materials capable of efficiently outputting high electrostrains at low electric fields are driven by the demand for precise actuation in a wide range of applications. Large electrostrains of piezoceramics in operation require high driving fields, which limits their practical application due to undesirable nonlinearities and high energy consumption. Herein, a strategy is developed to enhance the electrostrains of piezoceramics while maintaining low hysteresis by incorporating lead magnesium niobate relaxors into lead zirconate titanium at the morphotropic phase boundary. An ultrahigh inverse piezoelectric coefficient \({d}_{33}^{*}\) of 1380 pm/V with a reduced hysteresis of 11.5% is achieved under a low electric field of 1 kV/mm, outperforming the major lead-based piezoelectric materials. In situ synchrotron X-ray diffraction and domain wall dynamics characterization with sub-microsecond temporal resolution reveal that the outstanding performances originate from facilitated domain wall movement, which in turn is due to reduced lattice distortion and miniaturized domain structures. These findings not only address the pending challenges of effective actuation under reduced driving conditions but also lay the foundation for a more systematic approach to exploring the origin of large electrostrains.

This review focuses on the mechanisms of cation–π interactions in high-performance polymeric materials, highlighting advances in mechanical enhancement, energy storage, adsorption, and responsiveness, with prospects in conductivity and catalysis.

Polysiloxanes are versatile polymeric materials with widespread applications in industries ranging from electronics to biomedical devices because of their unique thermal and viscoelastic properties. Accurate molecular simulations of polysiloxanes are essential for understanding their broad applications from a microscopic perspective. However, the accuracy of these simulations is highly dependent on the quality of the force fields used. In this work, we present a comprehensive benchmark and development of force fields tailored for polydimethylsiloxane, which is one of the most widely used polysiloxane materials. Our focus is on their performance in predicting key thermophysical properties including density, heat capacities, isothermal compressibility, and transport properties such as viscosity and thermal conductivity. Experimental measurements are performed in parallel to rigorously validate simulation outcomes. Existing force fields for polydimethylsiloxane, including those derived for organic and inorganic systems, are systematically evaluated against experimental data to identify limitations in accuracy and transferability. Simulation results are compared extensively with experimental observations across a range of temperatures and pressures, revealing the strengths and shortcomings of these commonly utilized force fields for polydimethylsiloxane. Discrepancies between force field predictions and experimental measurements are analyzed in detail for thermodynamic and transport properties of polydimethylsiloxane. This benchmark study serves as a critical assessment of current force fields for polydimethylsiloxane and offers guidelines for their further development, enabling more reliable simulations of polysiloxane-based materials for various industrial applications.