This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain. State-of-the-art and perspectives of the catalytic and electrocatalytic reduction of aqueous nitrates.
This work provides a critical review of the progress in the use of Room Temperature Ionic Liquids (RTILs) as Proton Exchange Membrane (PEM) electrolytes in Fuel Cells (FCs). It is well-known that for an efficient early commercialisation of this technology it is necessary to develop a proton exchange membrane with high proton conductivity without water dependency capable of working at temperatures above 100 ºC. The use of ionic liquids as electrolytes in electrochemical devices is an emerging field due to their high conductivity, as well as their thermal, chemical and electrochemical stability under anhydrous conditions. This paper attempts to give a general overview of the state-of-the-art, identifies the key factors for future research and summarises the recent progress in the use of ionic liquids as an innovative type of PEMs.
In this paper, we investigate the molecular dynamics and ions transport properties of polymerized imidazolium-based protic ionic liquid [HSO 3 −BVIm][OTf]a new material with potential applications in energy storage and electrochemical devices. The results of dielectric measurements, analyzed in modulus M*(f) and conductivity σ*(f) formalisms, combined with temperature-modulated differential scanning calorimetry experiments, have revealed a fundamental difference between the conducting properties of the examined polymer membrane and its low-molecular weight counterpart. Our findings indicated a strong decoupling between conductivity relaxation times τ σ (related to the ions migration through the polymer matrix) and segmental dynamics when the ionic transport is controlled by fast proton hopping through the dense hydrogen-bond network. Finally, we also discuss, for the first time, the effect of water content on the glass transition temperature value, relation between the charge and mass diffusion, reflected in the decoupling phenomenon, and the conductivity mechanism of examined poly[HSO 3 −BVIm][OTf].
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.