Search

The channel in the marine environment is a time-varying and space-varying channel. Pulse-truncated continuous wave (PCW) speed measurement is often used in sonar, but the instability effect of PCW signal in the channel limits the effectiveness of speed measurement. Hyperbolic frequency modulation (HFM) signal is insensitive to Doppler; therefore, HFM signals are widely used in ranging and velocity measurement of sonar and radar. However, due to the filtering effect of the marine environment, the HFM signal of a single frequency band may cause excessive transmission loss, and the echo energy may be too weak to detect the target. Based on the analysis of the influence of speed on the distance measurement of HFM signal, a pulse sequence method based on HFM for speed measurement (PHS) is proposed, which uses HFM signals of different frequency bands and pulse widths in the pulse sequence to perform speed measurement. Extensive simulation results show that PHS method not only guarantees the speed measurement but also makes full use of the energy of the HFM sequence to improve the accuracy of the distance measurement. And PHS method is valuable to the practical application of engineering. [ABSTRACT FROM AUTHOR]

Atomically precise nanoclusters (NCs) provide opportunities for correlating the structure and electrocatalytic properties at atomic level. Herein, we report the single-atom doping effect and ligand effect on CO2 electroreduction (eCO2RR) by comparing monogold-doped Au1Cu24 and homocopper Cu25 NCs protected by triphenylphosphine or/and tris(4-fluorophenyl)phosphine. Catalytic results revealed that the electronic distribution of Cu25 NCs is enormously contracted by doping Au atoms, entitling it to exhibit the unique inhibition of hydrogen evolution reaction. And the inductive effect of ligand strongly favors the formation of formate in eCO2RR. Overall, this work will provide guidance for the rational design of the copper-based catalysts in the eCO2RR. Tuning the metal core and ligand environment of atomically precise nanoclusters enables the correlation of structural and electrocatalytic properties at an atomic level. Here, single-atom doping and ligand tuning of atomically precise copper clusters is shown to be an effective route to tuning CO2 electroreduction activity and selectivity. [ABSTRACT FROM AUTHOR]

In this brief, we consider the mean-field type H − index problem for stochastic Markovian jump systems. A sufficient condition is derived for stochastic Markovian jump systems with (x , u) -dependent noise based on generalized differential Riccati equations. Especially for stochastic Markovian jump systems with only x-dependent noise, a sufficient and necessary condition is developed to characterize H − index larger than some ξ > 0 . Finally, a numerical example is addressed to verify the effectiveness of our obtained results. [ABSTRACT FROM AUTHOR]

Silver-coated poly(methyl acrylic acid) (PSA) core–shell colloid particles were prepared by an in situ chemical reduction method. Crystalline silver/titania composite hollow spheres were obtained by coating the as-prepared PSA/silver particles with an amorphous titania layer and subsequently calcining in Ar atmosphere. SEM and TEM investigation indicated that the size of the as-prepared PSA/silver and PSA/silver/TiO2 core–shell particles and silver/titania composite hollow particles was fairly uniform and the wall thickness of the hollow spheres was in the range of 40–80 nm. UV–vis absorption spectra were recorded to investigate their optical properties. [Copyright &y& Elsevier]

Photocatalytic nitrogen reduction reaction (NRR) is a sustainable process for ammonia synthesis under mild conditions. However, photocatalytic NRR activity and are generally limited by inefficient carrier separation and transfer. Therefore, parallel engineering of bulk phase doping and surface coupling is critical to achieving the goal of efficient NRR. In this study, Cl doped BiOBr nanosheet assemblies (BiOBr/Cl) were constructed in delicately designed deep eutectic solvents (DESs), combined with ionothermal methods at low temperatures and Bi 3+ exsolution reduction strategy at high temperatures. The unique liquid state and reducibility of DESs induce the reduction of Bi 3+ and the in situ coupling of Bi quantum dots at the surface of BiOBr/Cl nanosheets along with the construction of Bi-BiOBr/Cl nanosheet assemblies. The experimental results show that Cl doping could reduce the exciton dissociation energy and promote its dissociation to free carriers. Bi quantum dots could form tightly coupled Schottky junction with BiOBr/Cl enabling the efficient and unidirectional transmission of photogenerated electrons from BiOBr/Cl to metal Bi. The formed electron deficient region at Schottky interface promotes the adsorption and activation of N 2 . The hierarchical structure of Bi-BiOBr/Cl nanosheet assembly benefits to providing more N 2 adsorption active sites. The DFT calculation shows that the accumulation of high concentration of active hydrogen in Bi-BiOBr/Cl leads to a significant decrease of energy barrier of the first step hydrogenation of N 2 . Bi-BiOBr/Clis more inclined to adsorb nitrogen for NRR in comparison with H* for hydrogen production. The synergistic effect of Cl doping and Bi coupling result in a high NRR activity of Bi-BiOBr/Cl photocatalyst of 6.67 mmol·g -1 ·h -1 , which was 11.3 times higher than that of initial BiOBr. This study provides a promising strategy for designing highly active NRR photocatalysts with high efficiency carrier dissociation and transport., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Oxygen vacancy (V o ) creation and morphology controlling make significant contributions to the electronic and structural regulation of metal oxide semiconductors, yet an investigation about convenient approaches for fabricating hierarchical catalyst with abundant oxygen vacancies still has significant challenges. Here, we report a unique method to create abundant oxygen vacancies in hierarchical Ag/TiO 2 nanoflowers during photocatalytic reaction, which is accompanied by light absorption variation and surface plasmon resonance (SPR) enhancement. Its high efficiency of photocatalytic H 2 evolution (the highest apparent quantum yield reaches 3.2% at 365 nm) and rhodamine B degradation can be considered as benefits from the synergistic effects of the well-arranged hierarchical structure, the photogenerated oxygen vacancies, and the SPR of cocatalyst Ag. This work proposes an effective strategy to optimize the synthesis of regular hierarchical structures and enriches the research on the vital function of oxygen vacancies in photocatalytic reactions., Competing Interests: The authors declare no competing financial interest., (Copyright © 2020 American Chemical Society.)

Hollow spheres and thin films of Ni(OH)(2) and NiO with unusual form and hierarchical structures have been synthesized by a simple solution chemistry method. First, in situ formed Ni(OH)(2) nanoflakelets organized on the surface of styrene-acrylic acid copolymer (PSA) latex particles to form core/shell structures. Ni(OH)(2) hollow shells built up with nanoflakelets were obtained after subsequent removal of the core latex particles by dissolving PSA latex in toluene; the removal of the cores by calcinations would result in NiO hollow shells, also with hierarchical structures. BET calculation showed the surface area of the NiO hollow spheres was 156 m(2)/g. The nanoflakelets could also organize themselves into thin films with hierarchical structures. It is anticipated that these novel structures will have some unique applications in Ni-based batteries and other potentials.