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1.
ChemSusChem ; 16(10): e202202323, 2023 May 19.
Artículo en Inglés | MEDLINE | ID: mdl-36716248

RESUMEN

Safer-by-design and sustainable energy storage devices are envisioned to be among the required 2.0 solutions to satisfy the fast growing energy demands. Responding to this evolution cannot be freed from a global and synergetic approach to design the requisite electrolytes taking into account the toxicity, the eco-compatibility and the cost of their constituents. To target low-temperature applications, a non-toxic and cost-efficient eutectic system comprising LiNO3 in water with 1,3-propylene glycol as co-solvent was selected to design a ternary electrolyte with a wide liquid range. By using this electrolyte in an electrochemical double-layer capacitor (EDLC), the operating voltage of the device reaches an optimum of 2.0 V at -40 °C over more than 100 h of floating. Moreover, after being set up at 20 °C, the temperature resilience of the capacitance is near total, demonstrating thus a promising feature related to the suitable thermal and electrochemical behaviours of the tested EDLC devices.

2.
Chem Commun (Camb) ; 56(68): 9830-9833, 2020 Aug 25.
Artículo en Inglés | MEDLINE | ID: mdl-32716427

RESUMEN

The redefinition of the commonly named "water-in-salt" clarifies the operating temperatures of the state-of-the-art LiTFSI-based aqueous solutions. An in-depth study shows its mismatch for low temperature applications. In contrast, the recommended strategy is to design an electrolyte with an invariant composition, as exemplified by the eutectic water/LiNO3 that is able to electrochemically cycle down to -23 °C.


Asunto(s)
Electrólitos/química , Técnicas Electroquímicas , Sales (Química)/química , Soluciones/química , Temperatura , Compuestos de Trimetilsililo/química , Agua/química
3.
Org Lett ; 17(7): 1720-3, 2015 Apr 03.
Artículo en Inglés | MEDLINE | ID: mdl-25763595

RESUMEN

A new rhodium-catalyzed asymmetric arylative cyclization of nitrogen-tethered alkyne-enoate with arylboronic acids is described. In this process two new carbon-carbon bonds and one stereocenter are formed, providing access to pyrrolidines and piperidines with good enantioselectivities by to the use of C1-symmetric chiral monosubstituted diene ligands.

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