Giant Barocaloric Effects in Natural Rubber: A Relevant Step toward Solid-State Cooling.

Solid-state cooling based on i-caloric effects has shown to be a promising alternative to the conventional refrigeration devices. Only very recently, the research on barocaloric materials is receiving a deal of attention due to the demonstration of giant barocaloric effects in shape-memory alloys. Regarding polymers, there is still a lack of literature, despite their high caloric potential. Thus, we present here giant barocaloric effects in natural rubber, a low-cost and environmental friendly elastomer polymer. The maximum values of entropy and temperature changes are larger than those previously reported for any promising barocaloric material. Moreover, the huge normalized temperature change and refrigerant capacity exhibited by natural rubber confirm its high potential for cooling applications. We also verify a relevant dependence of the barocaloric effect on the glass transition in natural rubber. Our findings suggest that commercial refrigeration devices based on barocaloric effects from elastomer polymers can be envisaged in the near future.

Note: Experimental setup for measuring the barocaloric effect in polymers: Application to natural rubber.

Barocaloric materials have shown to be promising alternatives to the conventional vapor-compression refrigeration technologies. Nevertheless, barocaloric effect (σb-CE) has not been extensively examined for many classes of materials up to now. Aiming at fulfilling this gap, the present paper describes the development of a high-pressure experimental setup for measuring the σb-CE in polymers. The design allows simultaneous measurements of temperature, pressure, and strain during the barocaloric cycle. The system proved to be fully functional through basic experiments using natural rubber. Samples exhibited large temperature variations associated with the σb-CE. Strain-temperature curves were also obtained, which could allow indirect measurements of the isothermal entropy change.

X-ray powder diffraction at the XRD1 beamline at LNLS.

Various upgrades have been completed at the XRD1 beamline at the Brazilian synchrotron light source (LNLS). The upgrades are comprehensive, with changes to both hardware and software, now allowing users of the beamline to conduct X-ray powder diffraction experiments with faster data acquisition times and improved quality. The main beamline parameters and the results obtained for different standards are presented, showing the beamline ability of performing high-quality experiments in transmission geometry. XRD1 operates in the 5.5-14 keV range and has a photon flux of 7.8 × 109 photons s-1 (with 100 mA) at 12 keV, which is one of the typical working energies. At 8 keV (the other typical working energy) the photon flux at the sample position is 3.4 × 1010 photons s-1 and the energy resolution ΔE/E = 3 × 10-4.

Chemical disorder determines the deviation of the Slater-Pauling rule for Fe2MnSi-based Heusler alloys: evidences from neutron diffraction and density functional theory.

Fe2MnSi fails to follow the Slater-Pauling rule. This phenomenon is thought to originate from either: (i) an antiferromagnetic arrangement of Mn ions at low temperature and/or (ii) chemical disorder. An important insight on this issue could be achieved by considering Fe2MnSi1-x Ga x compounds, thoroughly studied here by means of magnetization, neutron diffraction and density functional calculations (DFT). Our results indicate that chemical disorder (and not the antiferromagnetic arrangement) is responsible for the deviation of the Slater-Pauling rule on Fe2MnSi-based Heusler alloys. Furthermore, evidences suggest that Ga substitution into Si site favors the Fe/Mn disorder, further enhancing the observed deviation.