Colossal barocaloric effects in the complex hydride Li 2 B 12 H 12

Traditional refrigeration technologies based on compression cycles of greenhouse gases pose serious threats to the environment and cannot be downscaled to electronic device dimensions. Solid-state cooling exploits the thermal response of caloric materials to changes in the applied external fields (i...

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Detalles Bibliográficos
Autores: Sau, Kartik, Ikeshoji, Tamio, Takagi, Shigeyuki, Orimo, Shin-ichi, Errandonea Ponce, Daniel, Chu, Dewei, Cazorla Silva, Claudio|||0000-0002-6501-4513
Tipo de recurso: artículo
Fecha de publicación:2021
País:España
Institución:Universitat Politècnica de Catalunya (UPC)
Repositorio:UPCommons. Portal del coneixement obert de la UPC
Idioma:inglés
OAI Identifier:oai:upcommons.upc.edu:2117/355950
Acceso en línea:https://hdl.handle.net/2117/355950
https://dx.doi.org/10.1038/s41598-021-91123-4
Access Level:acceso abierto
Palabra clave:Condensed Matter Physics
Materials science
Ciència dels materials
Matèria condensada
Àrees temàtiques de la UPC::Física
Descripción
Sumario:Traditional refrigeration technologies based on compression cycles of greenhouse gases pose serious threats to the environment and cannot be downscaled to electronic device dimensions. Solid-state cooling exploits the thermal response of caloric materials to changes in the applied external fields (i.e., magnetic, electric and/or mechanical stress) and represents a promising alternative to current refrigeration methods. However, most of the caloric materials known to date present relatively small adiabatic temperature changes (|¿T|~1 to 10 K) and/or limiting irreversibility issues resulting from significant phase-transition hysteresis. Here, we predict by using molecular dynamics simulations the existence of colossal barocaloric effects induced by pressure (isothermal entropy changes of |¿S|~100 J K-1 kg-1) in the energy material Li2B12H12. Specifically, we estimate |¿S|=367 J K-1 kg-1 and |¿T|=43 K for a small pressure shift of P = 0.1 GPa at T=480 K. The disclosed colossal barocaloric effects are originated by a fairly reversible order–disorder phase transformation involving coexistence of Li+ diffusion and (BH)-212 reorientational motion at high temperatures.