Two-dimensional (2D) hybrid organic-inorganic perovskite (HOIP) crystals show promise as scintillating materials for wide-energy radiation detection, outperforming their three-dimensional counterparts. In this study, we synthesized single crystals of (PEA_2-xBZA_x)PbBr₄ (x ranging from 0.1 to 2), utilizing phenethylammonium (C₆H₅CH₂CH₂NH₃⁺) and benzylammonium (C₆H₅CH₂NH₃⁺) cations. These materials exhibit favorable optical and scintillation properties, rendering them suitable for high light yield (LY) and fast-response scintillators. Our investigation, employing various techniques such as X-ray diffraction (XRD), photoluminescence (PL), time-resolved (TR) PL, Raman spectroscopy, radioluminescence (RL), thermoluminescence (TL), and scintillation measurements, unveiled lattice strain induced by dual-organic cations in powder X-ray diffraction. Density functional theory analysis demonstrated a maximal 0.13 eV increase in the band gap with the addition of BZA cation addition. Notably, the largest Stokes shift of 0.06 eV was observed in (BZA)₂PbBr₄. The dual-organic cation crystals displayed >80% fast component scintillation decay time, which is advantageous for the scintillating process. Furthermore, we observed a dual-organic cations-induced enhancement of electron-hole transfer efficiency by up to 60%, with a contribution of >70% to the fast component of scintillation decay. The crystal with the lowest BZA concentration, (PEA_1.9BZA_0.1)PbBr₄, demonstrated the highest LYs of 14.9 ± 1.5 ph/keV at room temperature. Despite a 55-70% decrease in LY for BZA concentrations >5%, simultaneous reductions in scintillation decay time (12-32%) may work for time-of-flight positron emission tomography and photon-counting computed tomography. Our work underscores the crucial role of dual-organic cations in advancing our understanding of 2D-HOIP crystals for materials science and radiation detection applications.

In this study, hydrothermally produced Fe-doped Co₃O₄ nanostructured particles are investigated as electrocatalysts for the water-splitting process and electrode materials for supercapacitor devices. The results of the experiments demonstrated that the surface area, specific capacitance, and electrochemical performance of Co₃O₄ are all influenced by Fe³⁺ content. The Fe_xCo_3-xO₄ with x = 1 sample exhibits a higher BET surface (87.45 m²/g) than that of the pristine Co₃O₄ (59.4 m²/g). Electrochemical measurements of the electrode carried out in 3 M KOH reveal a high specific capacitance of 153 F/g at a current density of 1 A/g for x = 0.6 and 684 F/g at a 2 mV/s scan rate for x = 1.0 samples. In terms of electrocatalytic performance, the electrode (x = 1.0) displayed a low overpotential of 266 mV (at a current density of 10 mA/cm²) along with 52 mV/dec Tafel slopes in the oxygen evolution reaction. Additionally, the overpotential of 132 mV (at a current density of 10 mA/cm²) and 109 mV with 52 mV/dec Tafel slope were obtained for x = 0.6 sample towards hydrogen evolution reaction (HER). According to electrochemical impedance spectroscopy (EIS) measurements and the density functional theory (DFT) study, the addition of Fe³⁺ increased the conductivity at the electrode–electrolyte interface, which substantially impacted the high activity of the iron-doped cobalt oxide. The electrochemical results revealed that the mesoporous Fe-doped Co₃O₄ nanostructure could be used as potential electrode material in the high-performance electrochemical capacitor and water-splitting catalysts.

In this work, we investigate magnetic monolayers of the form A ⁱ A ⁱⁱ B ₄ X ₈ based on the well-known intrinsic topological magnetic van der Waals (vdW) material MnBi ₂ Te ₄ (MBT) using first-principles calculations and machine learning techniques.

Strain-induced topological phase transition in the ferromagnetic Janus monolayer MnSbBiS₂Te₂ is displayed.

For electrochemical supercapacitors, nickel cobaltite (NiCo₂O₄) has emerged as a new energy storage material. The electrocapacitive performance of metal oxides is significantly influenced by their morphology and electrical characteristics. The synthesis route can modulate the morphological structure, while their energy band gaps and defects can vary the electrical properties. In addition to modifying the energy band gap, doping can improve crystal stability and refine grain size, providing much-needed surface area for high specific capacitance. This study evaluates the electrochemical performance of aluminum-doped Ni_1−xAl_xCo₂O₄ (0 ≤ x ≤ 0.8) compounds. The Ni_1−xAl_xCo₂O₄ samples were synthesized through a hydrothermal method by varying the Al to Ni molar ratio. The physical, morphological, and electrochemical properties of Ni_1−xAl_xCo₂O₄ are observed to vary with Al³⁺ content. A morphological change from urchin-like spheres to nanoplate-like structures with a concomitant increase in the surface area, reaching up to 189 m²/g for x = 0.8, was observed with increasing Al³⁺ content in Ni_1−xAl_xCo₂O₄. The electrochemical performance of Ni_1−xAl_xCo₂O₄ as an electrode was assessed in a 3M KOH solution. The high specific capacitance of 512 F/g at a 2 mV/s scan rate, 268 F/g at a current density of 0.5 A/g, and energy density of 12.4 Wh/kg was observed for the x = 0.0 sample, which was reduced upon further Al³⁺ substitution. The as-synthesized Ni_1−xAl_xCo₂O₄ electrode exhibited a maximum energy density of 12.4 W h kg⁻¹ with an outstanding high-power density of approximately 6316.6 W h kg⁻¹ for x = 0.0 and an energy density of 8.7 W h kg⁻¹ with an outstanding high-power density of approximately 6670.9 W h kg⁻¹ for x = 0.6. The capacitance retention of 97% and 108.52% and the Coulombic efficiency of 100% and 99.24% were observed for x = 0.0 and x = 0.8, respectively. First-principles density functional theory (DFT) calculations show that the band-gap energy of Ni_1−xAl_xCo₂O₄ remained largely invariant with the Al³⁺ substitution for low Al³⁺ content. Although the capacitance performance is reduced upon Al³⁺ doping, overall, the Al³⁺ doped Ni_1−xAl_xCo₂O₄ displayed good energy, powder density, and retention performance. Thus, Al³⁺ could be a cost-effective alternative in replacing Ni with the performance trade off.