Lithium Niobate MEMS Antisymmetric Lamb Wave Resonators with Support Structures.

The piezoelectric thin film composed of single-crystal lithium niobate (LiNbO3) exhibits a remarkably high electromechanical coupling coefficient and minimal intrinsic losses, making it an optimal material for fabricating bulk acoustic wave resonators. However, contemporary first-order antisymmetric (A1) Lamb mode resonators based on LiNbO3 thin films face specific challenges, such as inadequate mechanical stability, limited power capacity, and the presence of multiple spurious modes, which restrict their applicability in a broader context. In this paper, we present an innovative design for A1 Lamb mode resonators that incorporates a support-pillar structure. Integration of support pillars enables the dissipation of spurious wave energy to the substrate, effectively mitigating unwanted spurious modes. Additionally, this novel approach involves anchoring the piezoelectric thin film to a supportive framework, consequently enhancing mechanical stability while simultaneously improving the heat dissipation capabilities of the core.

Broadband Photoluminescence in 2D Organic-Inorganic Hybrid Perovskites: (C7H18N2)PbBr4 and (C9H22N2)PbBr4.

Organic-inorganic hybrid perovskites have aroused intense research interest because of their excellent physical performance and potential for use in optoelectronic field. Herein, we report two new 2D hybrid lead bromides, (C7H18N2)PbBr4 [C7H18N2 is 1,7-diaminoheptane] and (C9H22N2)PbBr4 [C9H22N2 is 1,9-diaminononane], both of which possess ⟨100⟩-oriented inorganic layers consisting of corner-sharing octahedra. The optical bandgaps are experimentally determined to be 2.76 eV for (C7H18N2)PbBr4 and 2.78 eV for (C9H22N2)PbBr4. Upon 390 nm excitation, (C7H18N2)PbBr4 exhibits white-light emission centered at 600 nm, and (C9H22N2)PbBr4 exhibits red-light emission centered at 620 nm. These broad photoluminescent spectra originate from the synergistic emission of free excitons (FEs) and self-trapped excitons (STEs). This work provides a strategy for realizing single-component white-light emission and efficient red-light emission in two-dimensional perovskites, demonstrating the vast application prospects of 2D perovskites in photoelectric devices.

Lead-Free Broadband Orange-Emitting Zero-Dimensional Hybrid (PMA)3InBr6 with Direct Band Gap.

Low-dimensional organic-inorganic hybrid metal halides have emerged as broadband light emitters for phosphor-converted white light-emitting diodes (WLEDs). Herein, we report a new zero-dimensional (0-D) lead-free metal halide (PMA)3InBr6 [PMA+: (C6H5CH2NH3)+] that crystallizes in the monoclinic system with P21/c space group. The structure consists of slightly distorted [InBr6]3- octahedra surrounded by organic PMA+ cations. The direct band gap characteristic of (PMA)3InBr6 was demonstrated by density functional theory calculation, and its relatively wide band gap of 3.78 eV was experimentally determined. Upon 365 nm ultraviolet light excitation, (PMA)3InBr6 exhibited strong broadband orange luminescence with a full-width at half-maximum of ∼132 nm resulting from self-trapped exciton emission, and the photoluminescence quantum yield was determined to be ∼35%. A WLED fabricated by combining the orange-emitting (PMA)3InBr6, a green phosphor Ba2SiO4:Eu2+, and a blue phosphor BaMgAl10O17:Eu2+ exhibited a high color-rendering index of 87.0. Our findings indicate that the organic-inorganic hybrid (PMA)3InBr6 may have potential for luminescence-based applications.