SearcharxivSearch

arXiv subjects

Melony Dilshad

Publications and source records attributed to Melony Dilshad.

2 recordsLinked to original sources

Enhanced reversible barocaloric effect at low pressure in neopentyl plastic crystal solid solutions

The discovery of colossal barocaloric effects in neopentyl glycol (NPG) makes plastic crystals promising candidates for solid-state refrigerants with lower environmental impact than vapour compression fluids. Optimising operational temperatures and low-pressure operability remains challenging without compromising thermodynamic parameters. Here, we implement a strategy to improve the viability of NPG derivatives as barocaloric refrigerants. We blend pentaglycerine (PG) with NPG to lower the phase transition temperature, then dope the blend with 2% pentaerythritol (PE) to improve transition reversibility. In comparison with NPG under the same conditions, this ternary system has a seven-fold increase in reversible isothermal entropy change (|$ΔS_{(it,rev)}$ | = 13.4 J kg$^{-1}$ K$^{-1}$) and twenty-fold increase in operational temperature span ($ΔT_{span}$ = 18 K) at pressures of 1 kbar. Synchrotron x-ray diffraction and quasielastic neutron scattering reveal structural and dynamical effects that broaden the temperature range of the first-order phase transition due to intermolecular hydrogen bond network disruption by the molecular dopants. We propose that exploiting the compositional phase space of multi-component molecular blends is effective for designing practicable molecular BCs.

cond-mat.mtrl-sci

Direct observation of thermal hysteresis in the molecular dynamics of barocaloric neopentyl glycol

Barocalorics (BCs) are emerging as promising alternatives to vapour-phase refrigerants, which are problematic as they exacerbate climate change when they inevitably leak into the atmosphere. However, the commercialisation of BC refrigerants is significantly hindered by hysteresis in the solid-solid phase transition that would be exploited in a refrigeration cycle. Here, we provide new insight into the hysteresis that is a critical step towards the rational design of viable BCs. By studying the benchmark BC plastic crystal, neopentyl glycol (NPG), we observe directly the liberation of the hydroxyl rotational modes that unlock the hydrogen bond network, distinguishing for the first time the molecular reorientation and hydroxymethyl rotational modes. We showcase the use high-resolution inelastic fixed-window scans in combination with quasielastic neutron scattering (QENS) measurements to build a comprehensive microscopic understanding of the NPG phase transition, directly tracking the molecular dynamics of the phase transition. Hysteresis previously observed in calorimetric studies of NPG is now observed directly as hysteresis in molecular rotational modes, and hence in the formation and disruption of hydrogen bonding. Furthermore, by tracking the thermal activation of three main reorientation modes, we suggest that their fractional excitations may resolve an outstanding discrepancy between measured and calculated entropy change. These results allow for direct study of the molecular dynamics that govern the thermal hysteresis of small molecule energy materials. They will be broadly applicable, as many promising BC material families possess first-order transitions involving molecular reorientations.

cond-mat.mtrl-sci