Guohong Zhou

This study utilized tetramethylammonium hydroxide (TMAH) as a substitute for traditional catalysts and successfully incorporated platinum octaethylporphyrin (PtOEP) into SiO₂ nanoparticles (PtOEP@SiO₂) via the Stöber method. Methyl silicone resin was employed as the matrix material, and a drop-coating technique was applied to fabricate thin films of PtOEP@SiO₂ particles for dissolved oxygen (DO) sensing in seawater. By optimizing the concentrations of TMAH and PtOEP, a highly sensitive oxygen-sensing film with a quenching ratio (I₀/I₁₀₀) of 28 was ultimately developed, with a wide linear detection range (0~20 mg/L, R² = 0.994). Stability tests revealed no significant performance degradation during five oxygen–nitrogen cycle tests. After 30 days of immersion in East China Sea seawater, the quenching ratio decreased by only 6%, confirming its long-term stability and excellent resistance to ion interference. This research provides a novel strategy for developing highly reliable in situ marine DO sensors.

The integration, miniaturization, and high frequency of microwave vacuum electronics put forward higher requirements for heat-conducting and wave-absorbing integrated materials. However, these materials must balance the dispersion and isolation of wave-absorbing components to optimize absorption while maintaining the continuity of thermal conductivity pathways with low defect rates and minimal interfaces. This presents a significant challenge in achieving both high thermal conductivity and efficient wave absorption simultaneously. Here, AlN/FeNi microwave-attenuating ceramics were synthesized via non–pressure sintering in a nitrogen atmosphere. The influence of FeNi content (0–20 wt%) on the density, phase composition, microstructure, microwave-absorption properties and thermal conductivity of the composites was investigated. AlN/FeNi composites consist primarily of an AlN phase with FeNi_0.0578, Fe, AlYO₃, and Al₅Y₃O₁₂ as secondary phases, and the microstructure is uniform and dense. As the FeNi content rises from 0 to 20 wt%, the density of the composites sintered at 1800 °C × 2 h increases from 3.3 to 3.7 g/cm³. Their X-band (2–18 GHz) dielectric constant goes up from 6.5 to 8.5, the dielectric loss factor rises from 0.1 to 0.9, and thermal conductivity diminishes from 130 to 123 W/m·K. Upon reaching an FeNi content of 20 wt%, the composite achieves a minimum reflection loss of −39.1 dB at 9.5 GHz, with over 90% absorption across an effective absorption bandwidth covering 2.5 GHz. It exhibits excellent impedance matching, electromagnetic wave-attenuation properties, a relative density of 98.6%, and a thermal conductivity of 123 W m⁻¹ K⁻¹. The prepared AlN/FeNi composites, with integrated outstanding microwave-absorption capabilities and thermal conductivity, holds great promise for applications in 5G communications, aerospace, and artificial intelligence.

Unilateral radiating antennas are widely studied due to their ability to provide lateral or unidirectional radiation patterns, which are especially suitable for indoor and office Wi-Fi router applications. In this letter, a unilateral radiating rectangular dielectric resonator antenna (DRA) without a ground plane is proposed. A temperature stable low-loss 0.8MgTiO3–0.2Mg2SiO4–0.06CaTiO3 (MT–MS–CT) composite ceramic prepared via solid-state reaction and sintered at 1380 °C is utilized for the proposed DRA. Notably, the MT–MS–CT composite ceramic shows good dielectric performance with a permittivity of εr∼13, a quality factor of Q×f0∼115,000, Q = 1/dielectric loss, f0 = 8.6 GHz, and a temperature coefficient of resonant frequency TCF∼+4.6ppm/°C. Its unilateral radiation pattern is based on the complementary magnetic dipole and electric dipole, where the excited dominant TE111 mode of the rectangular DRA serves as the magnetic dipole and a probe acts as an electric dipole. The proposed prototype antenna fabricated using the composite ceramic has a unilateral radiation pattern with wide impedance bandwidth, reasonable gain, and radiation efficiency of 95%.

The sintering of high-performance ceramics with complex shapes at low temperatures has a significant impact on the future application of ceramics. A joint process of digital light processing (DLP) 3D printing technology and a nitrogen-gas pressure-assisted sintering method were proposed to fabricate AlN ceramics in the present work. Printing parameters, including exposure energy and time, were optimized for the shaping of green bodies. The effects of sintering temperature, as well as nitrogen pressure, on the microstructure, density, and thermal conductivity of AlN ceramics were systematically discussed. A high thermal conductivity of 168 W·m⁻¹·K⁻¹ was achieved by sintering and holding at a significantly reduced temperature of 1720 °C with the assistance of a 0.6 MPa nitrogen-gas pressure. Further, a large-sized AlN ceramic plate and a heat sink with an internal mini-channel structure were designed and successfully fabricated by using the optimized printing and sintering parameters proposed in this study. The heat transfer performance of the ceramic heat sink was evaluated by infrared thermal imaging, showing excellent cooling abilities, which provides new opportunities for the development of ceramic heat dissipation modules with complex geometries and superior thermal management properties.

In this paper, the high-quality factor mullite microwave dielectric ceramic is employed to introduce in dielectric resonator antenna (DRA). The microwave dielectric properties of ɛr ∼ 5.8, Q × f ∼ 31 240 at 9.66 GHz, and loss tangent tanδ = 1/Q ∼ 2.7 × 10−4 can be obtained by the solid-state reaction method in mullite microwave dielectric ceramic sintered at 1700 °C. On this basis, the resonant modes of the proposed broadband high-gain rectangular DRA are analyzed by using a dielectric waveguide theoretical model and the antenna performance is evaluated by a commercial CST Microwave Studio 2021® software. It has been found that the proposed rectangular DRA can provide a broad bandwidth of 35.9%, a maximum gain of 10 dBi at 3.61 GHz, and a radiation efficiency of 90% in the range of 3.13–4.42 GHz. For demonstration, adequate consistency between the simulation results and the measurement results was achieved. The proposed DRA has great application potential and value in 5G communication scenarios requiring wideband and high-gain antenna.

Ce-doped gadolinium gallium aluminum oxide (Ce: GGAG) precursors were first prepared by the microwave-assisted homogeneous precipitation method (MAHP). Thermal gravity-differential thermal analysis (TG-DTA), X-ray diffraction (XRD), specific surface area analysis (BET) and field emission scanning electron microscopy (FE-SEM) were employed to investigate the crystal structure, phase evolution and morphologies of the Ce: GGAG precursors and powders. The influence of Ga ion concentration in the salt solution on the properties of Ce: GGAG powders was investigated. All the precursors were transformed into single-phase GGAG after being calcined at 950 °C in a furnace for 3 h. Monodispersed Ce: GGAG powders were obtained as the Ga ion concentration was lower than 0.06 mol/L. Single-phase and dense Ce: GGAG ceramics were obtained after sintering at 1600 °C in a flowing oxygen atmosphere for 10 h. Specifically, the Ce: GGAG ceramic reached its maximum density of ~6.68 g/cm³, which was close to its theoretical density of 6.70 g/cm³, and exhibited the highest optical transmittance of 65.2% at 800 nm after hot isostatic pressing sintering (HIP) as the Ga ion concentration was 0.02 mol/L. The decay time and light yield of the GGAG ceramic were 35 ns and 35,000 ± 1250 ph/MeV, respectively, suggesting that Ce: GGAG ceramics prepared using MAHP-synthesized nanopowders are promising for scintillation applications.

Highly transparent Ho:Y₂O₃ ceramics for laser diode lighting were prepared using the vacuum sintering method with 0.3 at.% Nb₂O₅ as a sintering additive. The microstructures, transmittance, and luminescence properties of the Ho:Y₂O₃ ceramic samples were investigated in detail. The transmittance levels of all samples with various Ho³⁺ concentrations reached ~81.5% (2 mm thick) at 1100 nm. Under the excitation of 363 nm (ultraviolet) or 448 nm (blue) light, Ho:Y₂O₃ transparent ceramic samples showed that green emission peaked at 550 nm. The emission intensity was strongly affected by the concentration of Ho³⁺ ions, reaching its highest level in the sample doped with 1 at.% Ho³⁺. The CIE coordinates of the luminescence were in the green region (i.e., the CIE coordinates of the sample doped with 1 at.% Ho³⁺ were [0.27, 0.53] and [0.30, 0.69], under the excitation of 363 nm and 448 nm light, respectively). The possibility of its application as laser diode lighting was reported. Under the excitation of 450 nm blue laser, the sample doped with 0.5 at.% Ho³⁺ had the best performance: the saturated luminous flux, lumen efficiency, and the luminescence saturation power densities were 800 lm, 57.7 lm/W, and 17.6 W/mm², respectively. Furthermore, the materials have high thermal conductivity and mechanical strength due to their host of rare-earth sesquioxide. Thus, Ho:Y₂O₃ transparent ceramics are expected to be a promising candidate for green-light-emitting devices for solid-state lighting, such as laser diode lighting.

Preparation of ZnO-NH ₂ @SiO ₂ QDs and the sensitive detection of dissolved oxygen in water.