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This study presents the fabrication of a Mg-doped Si/Al2O3/ZnO nanowall heterojunction ultraviolet (UV) detector via magnetron sputtering, electron beam evaporation, and a hydrothermal method. The effects of Mg doping on the crystal structure, surface morphology, Raman characteristics, photoluminescence, and UV detection performance of the ZnO nanowall are investigated, demonstrating the high stability of the Si/Al2O3/ZnO nanowall heterojunction UV detector. Notably, when the Mg doping concentration is 2 mol %, the detector exhibits a total current of 0.030 A. When the Mg doping concentration is increased from 0 to 2 mol %, the responsivity increases from 0.165 to 2.001 A/W. Moreover, the sensitivity increases from 11.45 to 76.77, whereas the response time reduces by 80%. These findings demonstrate the promising performance enhancement of UV detectors facilitated by Mg doping, expanding their application scope in the realm of UV detection. The Mg-doped Si/Al2O3/ZnO nanowall heterojunction UV detector demonstrates considerably improved responsiveness and response speed, emphasizing its broad application scope in various fields, such as energy conservation and carbon reduction and information technology. [ABSTRACT FROM AUTHOR]

In the search for two‐dimensional (2D) magnets operating under ambient conditions, quasi‐2D non‐van der Waals (vdW) materials have attracted considerable research interest over the last five years. In addition to their high Curie temperature (TC), their superior air stability to that of vdW 2D magnets has made them potential candidates for future room‐temperature spintronics applications. Furthermore, recent progress in the thickness‐dependent crystal lattice and magnetic properties of non‐vdW Cr2X3 (X = S, Se, or Te) has brought them to areas that are once set aside for 2D vdW magnets in fundamental research and applications. Despite covalent bonding between magnetic layers, various bottom‐up synthesis methods produced thickness‐controlled flakes of Cr2X3. Moreover, layer‐dependent structural and magnetic properties are among the novel research directions in these materials. This review systematically summarizes recent studies on Cr2X3 crystal structure, their controllable synthesis, and their respective magnetic properties. A summary of some significant results on thickness‐controlled synthesis in Cr2X3 and thickness‐dependent magnetism in Cr2Te3 is presented. Additionally, experimental and theoretical reports are presented to explain interlayer magnetic interaction. The work reveals the interaction between synthesis, structure, and magnetism. Finally, future research directions of new Cr2X3‐based materials, rich magnetism in Cr2X3, and their potential application are discussed. [ABSTRACT FROM AUTHOR]

A series of SrZrO3 : Eu3+ nano phosphors synthesized by a modified high‐temperature solid‐state reaction method. The structural, functional vibration groups, optical, morphological, luminescence and quantum yield studies were characterized through XRD, FTIR, UV, 'SEM & HR‐TEM' and PL analyses respectively. The SrZrO3 : Eu3+ phosphor has a perovskite orthorhombic structure and emits intense red emission around 612 nm when it is excited under 465 nm and covers NUV light range. The calculated average lifetime indicates the nature of the allowed emission transition in Eu3+ (2.44 μs). The calculated colour purity and Commission International del' Eclairagethe (CIE) chromaticity coordinates are 97.9 % and (0.5894, 0.4031) respectively. The observed quantum yield and thermal stability for the SrZrO3 : Eu3+ (9 mol %) phosphor are 22 % and 87 % at 423 K, respectively. These obtained results suggest that SrZrO3 : Eu3+ (9 mol %) phosphor would meliorate for red‐emitting phosphor in profound RGB‐based pc‐WLED applications. [ABSTRACT FROM AUTHOR]

Environmental contamination by hexavalent chromium (Cr(VI)) and antibiotic drug residues pose significant challenges to public health and ecosystems. This study investigates the application of CoTiO3/BiVO4@MIL-Fe(53) (CT/BV@Fe-MOF) for the reduction of Cr(VI) and degradation of tetracycline (TCL) under visible light. After grafting an iron-based metal–organic framework MIL-Fe(53) on a modified CoTiO3/BiVO4 composite, the photogenerated electrons could easily be transferred from CoTiO3 to BiVO4/Fe-MOF species via interfacial charge transfer. UV–vis diffuse reflectance spectroscopy showed that charge carriers were formed in response to visible light absorption. The effect of different operating parameters, including catalyst load, pH, initial Cr(VI), and TCL concentration, was systematically evaluated during the photocatalytic process. The CT/BV@Fe-MOF composite exhibited 98.7% reduction efficiency in Cr(VI) (50 ppm) and 97.5% degradation efficiency towards TCL (30 ppm) within 90 min, resulting in a greater efficiency than the pristine CoTiO3, BiVO4, and Fe-MOF materials. The CT/BV@Fe-MOF composite displayed excellent stability over six cycles, highlighting its potential for practical applications. In addition, the plausible degradation pathway of TCL was evaluated using LC-ESI/MS analysis, while the TEST program was utilized to investigate the toxicity of the products generated during the degradation process. [ABSTRACT FROM AUTHOR]