Porous (Ta0.2Nb0.2Ti0.2Zr0.2Hf0.2)C high-entropy ceramics (HEC) with a dual-porosity structure were fabricated by pressureless sintering using a mixture powder of ceramic precursor and SiO2 microspheres. The carbothermal reduction in the ceramic precursor led to the formation of pores with sizes of 0.4–3 μm, while the addition of SiO2 microspheres caused the appearance of pores with sizes of 20–50 μm. The porous HECs exhibit competitive thermal insulation (4.12–1.11 W·m−1 k−1) and extraordinary compressive strength (133.1–41.9 MPa), which can be tailored by the porosity of the ceramics. The excellent properties are ascribed to the high-entropy effects and dual-porosity structures. The severe lattice distortions in the HECs lead to low intrinsic thermal conductivity and high compressive strength. The dual-porosity structure is efficient at phonon scattering and inhabiting crack propagations, which can further improve the thermal insulation and mechanical properties of the porous HECs.

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Construction of Z-scheme heterostructure is of momentous significance for realizing efficient photocatalytic water splitting. However, the consciously modulate of Z-scheme charge transfer is still a great challenge. Herein, interfacial Mo-S bond and internal electric field modulated Z-Scheme heterostructure composed by sulfur vacancies-rich ZnIn2S4 (Vs-ZIS) and MoSe2 was rationally fabricated for efficient photocatalytic hydrogen evolution. Systematic investigations reveal that Mo-S bond and internal electric field induce the Z-scheme charge transfer mechanism as confirmed by the SPS and DMPO spin-trapping EPR spectra. Under the intense synergy among the Mo-S bond, internal electric field and S-vacancies, the optimized photocatalyst exhibits ultrahigh hydrogen evolution rate of 63.21 mmol∙g-1·h-1 with an apparent quantum yield of 76.48% at 420 nm monochromatic light, which is about 18.8-fold of the pristine ZIS. This work affords a new inspiration on consciously modulating Z-scheme charge transfer by atomic-level interface control and internal electric field to signally promote the photocatalytic performance.

The fibres reinforced thin architectural ceramic plates of 900?1800?2.5mm with excellent mechanical properties were prepared by fast-sintering method using a controllable fibre dispersion process. The effects of ball-milling time on dispersity, average length-to-diameter ratio and microstructure of alumina fibres were investigated. Meanwhile, the effects of alumina fibre contents on the bulk density, water absorption, phase transformation and microstructure of the thin ceramic plate were researched. It was found that the two-step ball-milling process can effectively control the average length-to-diameter ratio of alumina fibres, achieving a good dispersion mixture of fibres and ceramic powders. Ceramics bulk density and bending strength increase with fibre contents rise from 0 to 5 wt.% and then decrease with further fibre content addition from 5 to 15wt.%. The in situ formed mullite whiskers via fast-sintering method are beneficial for protecting fibres and fibre/matrix interfaces. The maximum value of bending strength and fracture toughness reach 147MPa for 5 wt.% fibre contents and 2.6MPa?m1/2 for 9 wt.%fibre contents, corresponding to the strengthening of alumina fibres and the formation of mullite whiskers in fibre/matrix interfaces and matrix via fast-sintering process.