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A detailed investigation of the structural and magnetic properties, including magnetocaloric effect, re-entrant spin-glass behavior at low temperature, and critical behavior in polycrystalline Al$_2$MnFe Heusler alloy is reported. The prepared alloy crystallizes in a cubic CsCl-type crystal structure with Pm-3m space group. The temperature-dependent magnetization data reveals a second-order paramagnetic to ferromagnetic phase transition ($\sim$ 122.9 K), which is further supported by the analysis of the magnetocaloric effect. The isothermal magnetization loops show a soft ferromagnetic behavior of the studied alloy and also reveal an itinerant character of the underlying exchange interactions. In order to understand the nature of magnetic interactions, the critical exponents for spontaneous magnetization, initial magnetic susceptibility, and critical MH isotherm are determined using Modified Arrott plots, Kouvel-Fisher plots, and critical isotherm analysis. The derived critical exponents $\beta$ = 0.363(2), $\gamma$ = 1.384(3), and $\delta$ = 4.81(3) confirm the critical behavior similar to that of a 3D-Heisenberg-type ferromagnet with short-range exchange interactions that are found to decay with distance as J(r) $\approx$ r$^{-4.936}$. Moreover, the detailed analysis of the AC susceptibility data suggests that the frequency-dependent shifting of the peak temperatures is well explained using standard dynamic scaling laws such as the critical slowing down model and Vogel-Fulcher law, and confirms the signature of re-entrant spin-glass features in Al$_2$MnFe Heusler alloy. Furthermore, maximum magnetic entropy change of $\sim$ 1.92 J/kg-K and relative cooling power of $\sim$ 496 J/kg at 50 kOe applied magnetic field are determined from magnetocaloric studies that are comparable to those of other Mn-Fe-Al systems., Comment: 13 pages (main manuscript), 3 pages (supplementary material), 6 figures (main manuscript), 3 figures (supplementary material), 2 tables (main manuscript)

Liquid-phase exfoliation of two-dimensional materials is very attractive for large-scale applications. Although used extensively, isolating MoS2 layers (<10) with high efficiency is reported to be extremely difficult. Further, the importance of soaking has not yet been studied, and the surfactants' role in stabilizing MoS2 nanosheets is poorly understood1. Herein, we report a novel approach to exfoliating large quantities of MoS2 via high-pressure (HP) liquid-phase exfoliation (LPE) in deionized (DI) water. 4 to 7 layers of MoS2 nanosheets were obtained from 60 days-soaked samples and they were found to be stable in solvents for periods of up to six months. Studies on the effect of three surfactants, namely sodium dodecyl benzenesulfonate (SDBS), sodium cholate (SC), and tetra-butyl ammonium bromide (TBAB), indicate that exfoliation of MoS2 nanosheets in SDBS is highly efficient than the other two surfactants. The estimated yield reaches up to 7.25%, with a nanosheet concentration of 1.45 mg/ml, which is one of the highest ever reported. Our studies also suggest that the nanosheets' concentration and the lateral size depend on exfoliation cycles, applied pressure and surfactant concentration. Hydrogen evolution reaction (HER) and ion-transport study show that the nanosheets prepared by our method are stable in an acidic medium and free from surfactants. A high hydrogen evolution rate of 30.13 mmol g-1 h-1 was estimated under ambient laboratory conditions., Comment: 12 pages, 4 figures

Interlayer space in graphite is impermeable to ions and molecules, including protons. Its controlled expansion would find several applications in desalination, gas purification, high-density batteries, etc. In the past, metal intercalation has been used to modify graphitic interlayer spaces; however, resultant intercalation compounds are unstable in water. Here, we successfully expanded graphite interlayer spaces by intercalating aqueous KCl ions electrochemically. The water conductivity shows several orders of enhancement when compared to unintercalated graphite. Water evaporation experiments further confirm the high permeation rate. There is weak ion permeation through interlayer spaces, up to the highest chloride concentration of 1 M, an indication of sterically limited transport. In these very few transported ions, we observe hydration energy-dependent selectivity between salt ions. These strongly suggest a soft ball model of steric exclusion, which is rarely reported. Our spectroscopy studies provide clear evidence for cation-{\pi} interactions, though weak anion-{\pi} interactions were also detectable. These findings improve our understanding of molecular and ionic transport at the atomic scale., Comment: 21 pages, 4 main figures