Search Results (139)

In this study, a novel Bi₂O₃/BiOBr_0.9I_0.1 (BO0.9−BBI0.1) composite photocatalyst was successfully synthesized via a single-pot solvothermal method for the efficient degradation of 2,4-dichlorophenoxyacetic acid (2,4-D) under visible light. The structure, morphology, and optical properties of the photocatalyst were characterized through X-ray diffraction (XRD), Scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), UV–vis diffuse reflectance spectra (DRS), Steady-state photoluminescence (PL), and Electrochemical Impedance Spectroscopy (EIS). The composite exhibits a 3D hierarchical morphology with increased specific surface area and optimized pore structure, enhancing pollutant adsorption and providing more active sites. Under visible light irradiation, BO0.9−BBI0.1 achieved a 92.4% removal rate of 2,4-D within 2 h, with a reaction rate constant 5.3 and 4.6 times higher than that of pure BiOBr and BiOI, respectively. Mechanism studies confirm that photogenerated holes (h⁺) and superoxide radicals (·O₂⁻) are the primary active species, and the Z-scheme charge transfer pathway significantly promotes the separation of electron-hole pairs while maintaining strong redox capacity. The catalyst also demonstrated good stability over multiple cycles. This work provides a feasible dual-modification strategy for designing efficient bismuth-based photocatalysts for pesticide wastewater treatment. Full article

A transformation method was applied to the biconfluent (BHE), doubly confluent (DHE), and triconfluent (THE) Heun equations to generate and classify exactly solvable quantum mechanical potentials derived from them. With this, the range of potentials solvable in terms of the confluent hypergeometric function can be extended. The resulting potentials contained five independently tunable terms and two terms originating from the Schwartzian derivative that depended only on the parameters of the $z\left(x\right)$ transformation function. The polynomial solutions of these potentials contain expansion coefficients obtained from three-term (BHE and DHE) and four-term (THE) recurrence relations. For the simplest $z\left(x\right)$ transformation functions, the Lemieux–Bose potentials have been recovered for the BHE and DHE. The coupling parameters of these potentials and also of five potentials derived from the THE have been expressed in terms of the parameters of the respective differential equations. The present scheme offers a general framework into which a number of earlier results can be integrated in a systematic way. These include special cases of potentials obtained from less general versions of the Heun-type equations and individual solvable potentials obtained from various methods that do not necessarily refer to the Heun-type equations considered here. Several potentials derived here were found to coincide with or reduce to potentials found earlier from the quasi-exactly solvable (QES) formalism. Based on their mathematical form, their physically relevant features (domain of definition, asymptotic behaviour, single- or multi-well structure) were discussed, and possible fields of applications were pointed out. Full article

A novel Z-scheme Dy₂TmSbO₇/BiHoO₃ heterostructure photocatalyst was synthesized with the ultrasound-assisted solvothermal method. The Dy₂TmSbO₇/BiHoO₃ heterojunction photocatalyst (DBHP) reflected wonderful separation efficiency of photogenerated electrons and photogenerated holes owing to the efficient direct Z-scheme heterojunction structure characteristic. The lattice parameter and the bandgap energy of the Dy₂TmSbO₇ were 10.52419 Å and 2.58 eV, simultaneously, the lattice parameter and the bandgap energy of the BiHoO₃ were 5.42365 Å and 2.25 eV, additionally, the bandgap energy of the DBHP was 2.32 eV. Above results indicated that DBHP, Dy₂TmSbO₇ or BiHoO₃ possessed an excellent ability for absorbing visible light energy, therefore, DBHP, Dy₂TmSbO₇ or BiHoO₃ owned superior photocatalytic activity for degrading the sulphamethoxypyridazine (SMP) under visible light irradiation. The removal rate of the SMP after visible light irradiation of 135 min with the DBHP was 99.47% for degrading the SMP during the photocatalytic degradation (PADA) process, correspondingly, the removal rate of the total organic carbon (TOC) concentration after visible light irradiation of 135 min with the DBHP was 98.02% for degrading the SMP during the PADA process. The removal rate of the SMP after visible light irradiation of 135 min with the DBHP was 1.15 times, 1.29 times or 2.60 times that with Dy₂TmSbO₇, BiHoO₃ or nitrogen-doped TiO₂ (N-T). Therefore, the DBHP displayed higher photocatalytic activity for degrading the SMP under visible light irradiation compared with Dy₂TmSbO₇, BiHoO₃ or N-T. Specifically, the mineralization rate for removing the TOC concentration during the PADA process of the SMP with the DBHP was 1.18 times, 1.32 times or 2.79 times that with Dy₂TmSbO₇, BiHoO₃ or N-T. In addition, the stability and reusability of the DBHP were systematically evaluated, confirming that the DBHP owned potential applicability for degrading the antibiotic pollutant, which derived from the practical industrial wastewater. Trapping radicals experiments and the electron paramagnetic resonance measurement experiments were conducted for identifying the reactive radicals, such as the hydroxyl radicals (•OH), the superoxide anions (•O₂⁻) and the photogenerated holes (h⁺), which were generated with the DBHP for degrading the SMP during the PADA process under visible light irradiation, as a result, the •O₂⁻ possessed the maximal oxidative capability compared with the •OH or the h⁺. Above results indicated the degradation mechanism and the degradation pathways which were related to the SMP. In conclusion, this study makes a significant contribution for the development of the efficient Z-scheme heterostructure photocatalysts and provides a key opinion to the development of the sustainable remediation method with the view of mitigating the antibiotic pollution. Full article

In this study, a novel photocatalytic nanomaterial BiTmFeSbO₇ was successfully synthesized for the first time by using the solvothermal method. On account of the effective Z-scheme mechanism, the BiTmFeSbO₇/BiTmO₃ heterojunction photocatalyst (BTBTHP) could effectively separate the photoinduced electrons and the photoinduced holes, concurrently, the high oxidation potential and reduction potential of the BiTmFeSbO₇ and the BiTmO₃ were retained. Additionally, a Z-scheme BTBTHP was synthesized by using an ultrasound-assisted solvothermal approach. As a result, the BTBTHP exhibited excellent photocatalytic performance during the degradation process of the sulfathiazole (STZ). The morphological features, composition distribution, photochemistry properties and photoelectric properties of the prepared samples were investigated by using the comprehensive characterization techniques. Under the condition of visible light irradiation, the BTBTHP demonstrated an excellent removal efficiency of 99.50% for degrading the STZ. Contrastive analysis results indicated that the removal efficiency of the STZ by using the BTBTHP was substantially higher than that by using the BiTmFeSbO₇, the BiTmO₃, and the N-doped TiO₂. The removal rate of the STZ by using the BTBTHP was 1.14 times that by using the BiTmFeSbO₇, 1.28 times that by using the BiTmO₃, and 2.71 times that by using the N-doped TiO₂. Moreover, the stability and the reusability of the BTBTHP were verified through five successive photocatalytic cyclic degradation experiments, indicating that the BTBTHP owned potential for the practical application. The active species which was produced by the BTBTHP were identified as hydroxyl radicals (•OH), superoxide anions (•O₂⁻), and photoinduced holes (h⁺) by capturing radicals experiments and electron paramagnetic resonance testing experiments. Therefore, the degradation mechanism and the pathway of the STZ could be more comprehensively elucidated. In summary, this study lays a solid foundation for the development and further research of high efficient Z-scheme heterojunction photocatalysts and offers novel insights into sustainable remediation strategies for the STZ pollution. Full article

The Rate of Penetration (ROP) during drilling is nonstationary and exhibits coupled local fluctuations, which makes it challenging to model for accurate prediction. To address the challenge of modeling multi-scale temporal dependencies in drilling, this study introduces a hybrid TCN–Informer framework. It integrates the causal dilated Temporal Convolutional Network (TCN) for capturing short-term patterns with the Informer’s ProbSparse attention mechanism for modeling long-range dependencies. A comprehensive methodology is adopted, which includes a four-stage data preprocessing pipeline featuring per-well z-score standardization and label concatenation, a sliding-window training scheme to address cold-start issues, and an Optuna-based Bayesian search for hyperparameter optimization. The prediction performance of the models was evaluated across various input sequence lengths using the Mean Absolute Error (MAE), Root Mean Square Error (RMSE), and Coefficient of Determination (R²). The results show that the proposed TCN–Informer demonstrates superior performance compared to Informer, Long Short-Term Memory (LSTM), Gated Recurrent Unit (GRU), and Transformer. Furthermore, the predictions of the TCN–Informer respond more rapidly to abrupt changes in the ROP and yield smoother, more stable results during intervals of stable ROP, validating its effectiveness in capturing both local and global temporal patterns. Full article

To enhance the precision, load capacity, disturbance rejection, and reliability of shipborne parallel stabilization platforms under complex sea conditions, this paper proposes a redundant, actuated, parasitic-motion-free 3-DOF 3RRS-RUS parallel stabilization platform. Based on the proposed 3RRS-RUS shipborne parallel stabilization platform, a Linear Active Disturbance Rejection Control (LADRC) approach, integrated with a Sliding Mode Disturbance Observer (SMDO), is developed. First, the mechanism is synthesized using screw theory, and its 2R1T 3-DOF characteristics are verified through parasitic motion analysis. Second, the inverse kinematics model is established. Third, the conventional LADRC is decoupled, and a new Linear Extended State Observer (LESO) together with its corresponding control law is designed. Moreover, an SMDO is incorporated into the motor’s three-loop control scheme to alleviate the estimation burden on the LESO and enhance the system’s disturbance rejection capability. Finally, experimental validations were carried out on both the CSPACE and SimMechanics platforms. The results demonstrate that the proposed SMDO–LADRC achieves superior tracking performance, high robustness, and strong disturbance rejection capability, The tracking errors along the RX, RY, and Z axes were reduced by 6.5%, 1.1%, and 16.6%, respectively, compared with the conventional LADRC, while also confirming the feasibility of the newly designed 3-DOF 3RRS-RUS shipborne parallel stabilization platform. Full article

This study presented the successful synthesis of a visible light responsive Z-scheme BiTmDySbO₇/BiEuO₃ heterojunction photocatalyst (BBHP) via the hydrothermal method, exhibiting outstanding removal efficiency for degrading the metronidazole (MNZ) in wastewater. The BBHP exhibited exceptional photocatalytic activity during the degradation process of the MNZ which was a widely detected pharmaceutical pollutant in aquatic environments. The key to the high photocatalytic activity of the BBHP was the formation of a Z-scheme photogenerated carrier transport channel which existed between BiTmDySbO₇ and BiEuO₃ within the heterojunction structure. This innovative structural design was experimentally confirmed for enhancing the separation efficiency of the photogenerated charge carriers significantly, thereby, the efficient photocatalytic activity of the BBHP was promoted. After visible light irradiation for 130 min, the BBHP achieved a removal efficiency of 99.56% for degrading MNZ and a mineralization rate of 98.11% for removing the total organic carbon (TOC) concentration. In contrast to a single photocatalyst, the removal rate of the MNZ by using the BBHP was 1.14 times that by using the BiEuO₃, 1.26 times that by using the BiTmDySbO₇, and 2.65 times that by using the nitrogen-doped TiO₂ (N-T) under visible light irradiation. The mineralization rate for removing the TOC concentration during the degradation process of the MNZ by using the BBHP was 1.17 times that by using the BiEuO₃, 1.29 times that by using the BiTmDySbO₇, and 2.86 times that by using the N-T under visible light irradiation. The photocatalytic degradation process of the MNZ by using the BBHP followed first-order kinetics model, concurrently, a dynamics rate constant of 0.0345 min⁻¹ was obtained. Furthermore, the BBHP demonstrated excellent stability and durability in accordance with multiple cyclic degradation experiments. According to the capturing radicals experiments and the electron paramagnetic resonance test experiments, it was determined that the hydroxyl radicals (•OH) and the superoxide anions (•O₂⁻) played key role during the photocatalytic degradation process of the MNZ by using the BBHP under visible light irradiation. Finally, the intermediate products that were produced during the degradation process of the MNZ were analyzed by using liquid chromatography-mass spectrometer, as a result, a potential degradation pathway for the MNZ was proposed. Overall, this study could provide valuable references for future research on composite photocatalysts and effectively maintain the safety and sustainable utilization of water resource. Full article

Addressing the challenges of energy production and environmental sustainability necessitates the development of advanced materials capable of facilitating both photocatalytic reduction and oxidation processes. Here, we report a Z-scheme Ag₃PO₄/CuBi₂O₄ heterojunction photocatalyst, which was fabricated via the in situ anisotropic growth of Ag₃PO₄ nanoparticles on the ends of CuBi₂O₄ microrods. The prepared heterojunction exhibits a low lattice mismatch (~3%) and features a covalently bonded interface, anchored by oxygen atoms, with the formation of P-O-Cu bonds. This interface synergizes with the built-in electric field to drive an efficient Z-scheme charge transfer mechanism, significantly enhancing the separation and migration of carriers. Furthermore, the interfacial chemical bonds induce electron redistribution that effectively weakens the Ag-O bond, thereby activating surface lattice oxygen. As a result, the photocatalyst shows remarkably improved performance for photocatalytic oxygen evolution synchronized with Cr(VI) reduction by enabling both the conventional adsorbate evolution mechanism and the lattice oxygen mechanism. This work provides critical insights into the design of efficient photocatalysts. Full article

Gap-protected topological channels are a promising way to realize robust and high-fidelity state transfer in quantum networks. Although various topological transfer protocols based on the Su-Schrieffer-Heeger (SSH) model or its variants have been proposed, the phase accumulation during the evolution, as an essential aspect, is underestimated. Here, by numerically studying the phase information of quantum state transfer (QST) in one-dimensional (1D) topological spin chains, we uncover a universal phase correction ${\varphi }_0=(N-1)\pi /2$ for both adiabatic and diabatic topological schemes. Interestingly, the site-number-dependent phase correction satisfies ${\mathbb{Z}}_4$ symmetry and is equally effective for perfect mirror transmission in spin chains. Our work reveals a universal phase correction in 1D topologically protected QST, which will prompt a reevaluation of the topological protection mechanism in quantum systems. Full article

You Only Look Once (YOLO) is a convolutional neural network-based object detection algorithm widely used in real-time vision applications. However, its high computational demand leads to significant power consumption and cost when deployed in graphics processing units. Field-programmable gate arrays offer a low-power alternative. However, their efficient implementation requires architecture-level optimization tailored to limited device resources. This study presents an optimized YOLOv2 accelerator for the Zynq-7000 system-on-chip (SoC). The design employs 16-bit integer quantization, a filter reuse structure, an input feature map reuse scheme using a line buffer, and tiling parameter optimization for the convolution and max pooling layers to maximize resource efficiency. In addition, a stall-based control mechanism is introduced to prevent structural hazards in the pipeline. The proposed accelerator was implemented on the Zynq-7000 SoC board, and a system-level evaluation confirmed a negligible accuracy drop of only 0.2% compared with the 32-bit floating-point baseline. Compared with previous YOLO accelerators on the same SoC, the design achieved up to 26% and 15% reductions in flip-flop and digital signal processor usage, respectively. This result demonstrates feasible deployment on XC7Z020 with DSP 57.27% and FF 16.55% utilization. Full article

The efficient degradation of antibiotics in pharmaceutical wastewater remains a critical challenge against environmental contaminants. Conventional photocatalysts face potential limitations such as narrow visible-light absorption, rapid carrier recombination, and reliance on precious metal cocatalysts. This review investigates the coordination structure of MXene as a cocatalyst to synergistically enhance photocatalytic antibiotic degradation efficiency and the coordination structure modification mechanisms. MXene’s tunable bandgap (0.92–1.75 eV), exceptional conductivity (100–20,000 S/cm), and abundant surface terminations (-O, -OH, -F) enable the construction of Schottky or Z-scheme heterojunctions with semiconductors (Cu₂O, TiO₂, g-C₃N₄), achieving 50–70% efficiency improvement compared to pristine semiconductors. The “electron sponge” effect of MXene suppresses electron-hole recombination by 3–5 times, while its surface functional groups dynamically optimize pollutant adsorption. Notably, MXene’s localized surface plasmon resonance extends light harvesting from visible (400–800 nm) to near-infrared regions (800–2000 nm), tripling photon utilization efficiency. Theoretical simulations demonstrate that d-orbital electronic configurations and terminal groups cooperatively regulate catalytic active sites at atomic scales. The MXene composites demonstrate remarkable environmental stability, maintaining over 90% degradation efficiency of antibiotic under high salinity (2 M NaCl) and broad pH range (4–10). Future research should prioritize green synthesis protocols and mechanistic investigations of interfacial dynamics in multicomponent wastewater systems to facilitate engineering applications. This work provides fundamental insights into designing MXene-based photocatalysts for sustainable water purification. Full article

Photocatalytic technology offers significant potential for pollutant remediation through efficient, cost-effective mineralization but faces inherent limitations, including catalyst agglomeration and rapid charge recombination. To address these challenges, we developed activated carbon-modified porous graphitic carbon nitride (APCN) synthesized through the co-polycondensation of dicyandiamide with NH₄Cl and fir-wood-derived activated carbon (AC). The incorporated AC effectively prevented the agglomeration of carbon nitride frameworks, thereby enhancing the specific surface area (S_BET) of APCN. This matrix was subsequently composited with hydrothermally prepared (1T/2H) mixed-phase MoS₂ through ultrasonication, forming a MoS₂/APCN heterostructure. Characterizations including Scanning electron microscopy (SEM), Transmission electron microscopy (TEM), and N₂ adsorption–desorption isotherms (BET) confirmed that MoS₂ was successfully loaded onto APCN via an ultrasonic synthesis method. The composite exhibited outstanding photocatalytic activity, degrading 95.5% RhB in 40 min (pH = 7) and 97.4% in 25 min (pH = 3.5), with 87.3% efficiency retention after four cycles (pH = 7). Crucially, AC enhanced visible-light absorption and functioned as an electron-mediating component. Photoelectrochemical analyses and radical-trapping experiments confirmed a direct Z-scheme charge transfer mechanism, wherein conductive AC accelerates electron transport and suppresses carrier recombination. This study establishes both an efficient RhB degradation photocatalyst and a sustainable strategy for valorizing agricultural waste in advanced material design. Full article

A high-performance Z-scheme heterojunction photocatalytic compound, ZnBiGdO₄/SnS₂ (ZS), was prepared for the first time using a microwave-assisted solvothermal method. ZS significantly improved the separation efficiency of photoinduced carriers and effectively broadened the response range to visible light through the unique mechanism of the Z-type heterojunction. Therefore, ZS exhibited an excellent photocatalytic performance during the degradation process of tinidazole (TNZ). Specifically, the removal rate of TNZ by ZS reached 99.63%, and the removal rate of total organic carbon (TOC) reached 98.37% with ZS as catalyst under visible light irradiation (VLIN). Compared to other photocatalysts, the photocatalytic performance of ZS was significantly better than that of ZnBiGdO₄, SnS₂, or N-doped TiO₂ (N-T). The removal rate of TNZ by ZS was 1.12 times, 1.26 times, or 2.41 times higher than that by ZnBiGdO₄, SnS₂, or N-T, respectively. The mineralization efficiency of TNZ for TOC with ZS as a catalyst was 1.15 times, 1.28 times, or 2.57 times higher than that with ZnBiGdO₄, SnS₂, or N-T as a catalyst, respectively. Free radical scavenging experiments and the electron paramagnetic resonance experiments confirmed that ZS could generate multiple reactive species such as hydroxyl radicals (•OH), superoxide anions (•O₂⁻), and photoinduced holes (h⁺) during the photocatalytic degradation process of TNZ. The photocatalytic degradation performance of ZS on TNZ under VLIN was evaluated, concurrently, the reliability, reproducibility, and stability of ZS were verified by five cycle experiments. This study explored the degradation mechanism and degradation pathway of TNZ with ZS as a catalyst under VLIN. This study not only provides new ideas for the design and preparation of Z-type heterojunction photocatalysts but also lays an important foundation for the development of efficient environmental remediation technologies for TNZ pollution. Full article

Background: Vancomycin-resistant Enterococcus faecium (VREfm), particularly vanA-positive strains, represents a growing threat in hospital settings worldwide. These bacteria are able to survive under severe environmental conditions, including high temperatures and saline concentrations. High genome plasticity and advanced ability of inheriting antimicrobial resistance determinants defined the success of E. faecium as a hospital pathogen. Methods: This study presents the whole genomic characterization of vanA-positive VREfm isolates, analyzing 10 clinical isolates collected from three tertiary care hospitals in Moscow, Russia. Several typing approaches, including two MLST schemes and cgMLST profiles, were used to elucidate the relationship between the isolates. Phylogenetic analysis placed the isolates in context with global VREfm populations, demonstrating both local clonal expansion and possible international connections. Phenotypic and genomic antimicrobial resistance profiles were obtained, as well as data regarding the repertoire of virulence factors and plasmid content. Results: Whole genome sequencing revealed that all isolates belonged to the clinically significant CC17 lineage, specifically sequence types ST80 and ST552. Notably, two isolates possessed truncated Tn1546-type transposons lacking vanY and vanZ genes, representing a potentially emerging variant of the vanA operon in Russian clinical settings. A plasmid carrying a truncated vanA operon was reconstructed using long-read sequencing. Conclusions: The study highlights the utility of genomic investigation for tracking resistance mechanisms and strain dissemination, providing crucial baseline data for epidemiological surveillance of infections caused by VREfm in Russia. These findings emphasize the need for continued genomic monitoring to understand the evolution and spread of antimicrobial resistance in clinically important enterococcal lineages. Full article

Fenton oxidation technology utilizing hydrogen peroxide is recognized as an effective method for producing reactive oxygen species (ROS) to facilitate the degradation of antibiotics. However, the requirement for strongly acidic conditions during this process significantly restricts its broader applicability. In this study, we synthesized black phosphorus (BP) nanosheets by exposing the {010} crystal planes and then constructed a 0D/2D BP/Bi₂MoO₆ (PBMO) heterojunction to function as a Fenton catalyst. The PBMO-75 heterojunction exhibited a remarkable increase in photo-Fenton catalytic activity towards oxytetracycline (OTC) under neutral conditions, achieving catalytic efficiencies that were 20 and 8 times greater than those of BP and Bi₂MoO₆ (BMO), respectively. This can be attributed to its strong absorption of visible light, the establishment of an internal electric field (IEF) at the interface, and the implementation of a Z-scheme catalytic mechanism. Additionally, the photo-Fenton system was further improved in OTC degradation through the continuous conversion of Mo⁶⁺/Mo⁵⁺ under visible light irradiation in conjunction with H₂O₂. Based on ERS, XPS, and active species trapping experiments, we propose a Z-scheme charge transfer mechanism for PBMO. This research offers compelling evidence that 0D/2D Z-scheme heterojunctions are promising candidates for the photo-Fenton treatment of antibiotic contaminants. Full article