Molten salt methods have been widely used in the synthesis of high-entropy ceramic powders, yet their scalable production for industrial applications is lacking. In this work, for the first time, a densified microzone molten salt (DMMS) approach was developed for the scale-up preparation of high-entropy ceramic powders, including zirconates, hafnates, silicates, and carbides. The “densified” block of DMMS permitted only trace evaporation of molten salt on surfaces, and the internal “microzone” salt pools significantly promoted the in situ formation of high-entropy phases at relatively low temperatures. Single-phase (La_0.2Nd_0.2Sm_0.2Eu_0.2Gd_0.2)₂Zr₂O₇ (HEZO) powders, as an example, could be synthesized with only ~10 wt% volatilization of NaCl–KCl–NaF salt during 1200 °C treatment, while the resulting powders prepared by the traditional powdery method contained segregation phases with a salt loss as high as ~95 wt%. By simply accommodating the “densified” blocks in a tunnel kiln, scale-up synthesis of high-entropy ceramic powders by DMMS can be realized for industrial production.

Strain engineering offers an effective strategy to break the intrinsic symmetry of two-dimensional (2D) materials, thereby enabling tunable anisotropic responses and broadening their functional versatility. However, achieving novel anisotropic behaviors through strain engineering remains challenging and lacks systematic study. Here, mixed-dimensional 2D/one-dimensional (1D) heterostructures were constructed using monolayer WSe₂ and SiO₂ nanorods, where the diameter of SiO₂ nanorods effectively regulated the strain in monolayer WSe₂ to investigate its anisotropic responses. The WSe₂ at strained interfaces exhibits tunable photoluminescence enhancement, modulated bandgap, and the emergence of polarized photoluminescence by adjusting the diameter of the nanorods. Interestingly, an unexpected in-plane ferroelectricity was observed in monolayer WSe₂ at the heterointerface. Additionally, the heterostructure photodetectors demonstrate outstanding overall performance with a broadband detection range from 375 to 808 nm, a competitive photoswitching ratio of ~ 3200, a high detectivity of 2.4 × 10⁹ Jones and a fast response speed of ~11.3 ms. Another interesting finding is that the photodetectors demonstrate polarization-dependent detection with a tunable dichroic ratio ranging from 1 to 1.51. The heterostructure detectors can reliably capture sequential images of the capital letter “H”. This study provides an effective strategy for tailoring the anisotropic responses of TMDCs and further endowing their diverse functionalities and applications.