Quality Factor Improvement of a Thin-Film Piezoelectric-on-Silicon Resonator Using a Radial Alternating Material Phononic Crystal.

This paper studies the radial alternating material phononic crystal (RAM-PnC). By simulating the band gap structure of the phononic crystal, a complete acoustic band gap was verified at the resonant frequency of 175.14 MHz, which can prevent the propagation of elastic waves in a specific direction. The proposed alternately arranged radial phononic crystal structure is applied to the thin-film piezoelectric-on-silicon (TPOS) MEMS resonator. The finite element simulation method increases the anchor quality factor (Qanchor) from 60,596 to 659,536,011 at the operating frequency of 175.14 MHz, which is about 10,000 times higher. The motion resistance of the RAM-PnC resonator is reduced from 156.25 Ω to 48.31 Ω compared with the traditional resonator. At the same time, the insertion loss of the RAM-PnC resonator is reduced by 1.1 dB compared with the traditional resonator.

The high photocatalytic efficiency and stability of LaNiO3/g-C3N4 heterojunction nanocomposites for photocatalytic water splitting to hydrogen.

A binary direct Z-scheme LaNiO3/g-C3N4 nanocomposite photocatalyst consisted with LaNiO3 nanoparticles and g-C3N4 nanosheets was successfully synthesized by means of mechanical mixing and solvothermal methods in order to improve the photocatalytic water splitting activity. The as-prepared materials were characterized by powder X-ray diffraction (XRD), Scanning Electron microscope (SEM), Transmission Electron microscope (TEM), X-ray photoelectron spectroscope (XPS), Fourier Transform Infrared Spectroscopy (FT-IR) and N2 adsorption-desorption experiments, respectively, demonstrating the formation of interfacial interaction and heterogeneous structure in LaNiO3/g-C3N4 nanocomposites. Under UV-light irradiation, the LaNiO3/g-C3N4 samples which without the addition of any noble metal as co-catalyst behaved enhanced photocatalytic water splitting activity compared with pure LaNiO3 and g-C3N4, owing to the Z-scheme charge carrier transfer pathway. Especially, the LaNiO3/70%g-C3N4 nanocomposite reach an optimal yield of up to 3392.50 µmol g-1 in 5 h and held a maximum H2 evolution rate of 678.5 µmol h-1 g-1 that was 5 times higher than that of pure LaNiO3.

Z-Scheme LaCoO3/g-C3N4 for Efficient Full-Spectrum Light-Simulated Solar Photocatalytic Hydrogen Generation.

Photocatalytic decomposition of water is the most attractive method for the sustainable production of hydrogen, but the development of a highly active and low-cost catalyst remains a major challenge. Here, we report the preparation of LaCoO3/g-C3N4 nanosheets and the utilization of LaCoO3 instead of noble metals to improve the photocatalytic activity for the production of hydrogen. First, LaCoO3 was successfully prepared by the sol-gel method, and then a series of highly efficient Z-scheme LaCoO3/g-C3N4 heterojunction photocatalysts were synthesized by the solvothermal method. Various characterization techniques (X-ray diffraction (XRD), Fourier transform infrared (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), ultraviolet-visible (UV-vis) diffuse reflectance spectroscopy (DRS), photoluminescence (PL), transient photocurrent response test, electron paramagnetic resonance (EPR)) confirm that the heterostructure and interfacial interaction had been formed between LaCoO3 nanoparticles and g-C3N4 nanosheets. In the photocatalytic water splitting test, LaCoO3/g-C3N4-20 wt % exhibited the highest photocatalytic activity of 1046.15 µmol h-1 g-1, which is 3.5 and 1.4 times higher than those of LaCoO3 and g-C3N4, respectively. This work leads to an inexpensive and efficient LaCoO3/g-C3N4 photocatalysis system for water splitting or other photocatalytic applications.