The current environmental and potable water crisis requires technological advancement to tackle the issues caused by different organic pollutants. Herein, we report the degradation of organic pollutants such as Congo Red and acetophenone from aqueous media using visible light irradiation. To harvest the solar energy for photocatalysis, we fabricated a nanohybrid system composed of bismuth ferrite nanoparticles with two-dimensional (2D) MXene sheets, namely, the BiFeO₃ (BFO)/Ti₃C₂ (MXene) nanohybrid, for enhanced photocatalytic activity. The hybrid BFO/MXene is fabricated using a simple and low-cost double-solvent solvothermal method. The SEM and TEM images showed that the BFO nanoparticles are attached onto the surface of 2D MXene sheets. The photocatalytic degradation achieved by the hybrid is found to be 100% in 42 min for the organic dye (Congo Red) and 100% for the colorless aqueous pollutant (acetophenone) in 150 min. The BFO/MXene hybrid system exhibited a large surface area of 147 m² g^–1 measured via the Brunauer–Emmett–Teller sorption–desorption technique, which is found to be the largest among all BFO nanoparticles and derivatives. The photoluminescence spectra indicate a low electron–hole recombination rate. Fast and efficient degradation of organic molecules is caused by two factors: larger surface area and lower electron–hole recombination rate, which makes the BFO/MXene nanohybrid a highly efficient photocatalyst and a promising candidate for many future applications.

Over the years, scarcity of fresh potable water has increased the demand for clean water. Meanwhile, with the advent of nanotechnology, the use of nanomaterials for photocatalytic degradation of pollutants in wastewaters has increased. Herein, a new type of nanohybrids of La- and Mn-codoped bismuth ferrite (BFO) nanoparticles embedded into transition-metal carbide sheets (MXene–Ti₃C₂) were prepared by a low-cost double-solvent sol–gel method and investigated for their catalytic activity in dark and photoinduced conditions. The photoluminescence results showed that pure BFO has the highest electron hole recombination rate as compared to all the codoped BFO/Ti₃C₂ nanohybrids. The higher electron–hole pair generation rate of the nanohybrids provides a suitable environment for fast degradation of organic dye molecules. The band gap of the prepared nanohybrid was tuned to 1.73 eV. Moreover, the BLFO/Ti₃C₂ and BLFMO-5/Ti₃C₂ degraded 92 and 93% of the organic pollutant, respectively, from water in dark and remaining in the light spectrum. Therefore, these synthesized nanohybrids could be a promising candidate for catalytic and photocatalytic applications in future.

Over the years, scarcity of fresh potable water has increased the demand for clean water. Meanwhile, with the advent of nanotechnology, the use of nanomaterials for photocatalytic degradation of pollutants in wastewaters has increased. Herein, a new type of nanohybrids of La and Mn co-doped bismuth ferrite (BiFeO3) nanoparticles embedded into transition metal carbide sheets (MXene) were prepared by a low-cost double solvent sol-gel method, and investigated for their photocatalytic activity. The photoluminescence results showed that pure BFO has highest electron hole recombination rate as compared to all the co-doped BFO/MXene nanohybrids. The larger surface area and higher electron-hole pair generation rate provides suitable environment for fast photo-degradation of organic molecules. The band gap of the prepared nanohybrids was tuned to 1.96 eV having largest BiFeO3 surface area (147 m2g−1) reported till date. Moreover, the BLFO/MXene and BLFMO-5/Mxene degraded the 92% organic pollutant from water in dark and remaining in light spectrum as compare to undoped BFO/Mxene due to enhancement of the surface area and electron-hole recombination rate upon doping. Therefore, these synthesized nanohybrids could be a promising candidate for photocatalytic applications in future.

We investigated the structural, magnetic, magnetocaloric, and magnetotransport properties of Ni₅₀Mn₃₅In₁₅ Heusler alloys via partial substitution of Ni with 3 at.% Bi (Ni₄₇Bi₃Mn₃₅In₁₅) and 3 at.% Si (Ni₄₇Si₃Mn₃₅In₁₅) synthesized by arc melting. X-ray diffraction confirms a predominantly L2₁ cubic structure (space group Fm-3m), while SEM/EDX analysis verifies compositional homogeneity. Temperature-dependent magnetization measurements reveal that the Bi-substituted alloy exhibits a first-order magnetostructural transition associated with the martensitic transformation, followed by a second-order magnetic phase transition from ferromagnetic to paramagnetic behavior near the Curie temperature. In contrast, the Si-substituted alloy shows a single second-order transition with negligible thermal hysteresis, indicating suppression of the martensitic phase. The Curie temperature decreases from 324 K for the parent alloy to 313 K and 286 K for the Bi- and Si-substituted alloys, respectively. A maximum magnetic entropy change of 6.0 Jkg⁻¹K⁻¹ and 4.5 Jkg⁻¹K⁻¹ is observed for the Bi- and Si-substituted alloys, respectively, under an applied magnetic field change of 50 kOe, with corresponding relative cooling power values of 303 Jkg⁻¹ and 345 Jkg⁻¹. These results demonstrate that lattice expansion (Bi) and contraction (Si) distinctly modify Mn–Mn exchange interactions, enabling tunable magnetocaloric performance in Ni–Mn–In Heusler alloys.

Nanohybrids, made up of Bismuth ferrites/Carbon allotropes, are extensively used in photocatalytic applications nowadays. Our work proposes a nanohybrid system composed of Bismuth ferrite nanoparticles with two-dimensional (2D) MXene sheets namely, the BiFeO3 (BFO)/Ti3C2 (MXene) nanohybrid for enhanced photocatalytic activity. We have fabricated the BFO/MXene nanohybrid using simple and low cost double solvent solvothermal method. The SEM and TEM images show that the BFO nanoparticles were attached onto the MXene surface and in the inter-layers of two-dimensional (2D) MXene sheets. The photocatalytic application is tested for the visible light irradiation which showed the highest efficiency among all pure-BFO based photocatalysts, i.e. 100% degradation in 42 min for organic dye (Congo Red) and colorless aqueous pollutant (acetophenone) in 150 min, respectively. The present BFO-based hybrid system exhibited the large surface area of 147 m2g-1measured via Brunauer-Emmett-Teller (BET) sorption-desorption technique, and is found to be largest among BFO and its derivatives. Also, the photoluminescence (PL) spectra indicate large electron-hole pair generation. Fast and efficient degradation of organic molecules is supported by both factors; larger surface area and lower electron-hole recombination rate. The BFO/MXene nanohybrid presented here is a highly efficient photocatalyst compared to other nanostructures based on pure BiFeO3 which makes it a promising candidate for many future applications.