Adrian Brandt

An investigation about the use of mixtures of sulfonium-based ionic liquids and propylene carbonate as electrolytes for supercapacitors

This study describes the use of mixtures of the ionic liquid (IL) trimethyl-sulfonium bis[(trifluoromethyl)sulfonyl]imide (Me3STFSI) and propylene carbonate (PC) as electrolytes for carbon-based electrochemical double layer capacitors (EDLCs). Two different mixtures have been investigated. The first one contained the maximum amount of Me3STFSI (3.8 mol L−1) soluble in PC at room temperature (RT). The second one contained 1.9 mol L−1 of Me3STFSI, which is the concentration featuring the highest conductivity among all possible mixtures between PC and Me3STFSI at RT. The physicochemical properties, including conductivity, viscosity, and electrochemical and thermal stability of both mixtures, have been initially investigated. Afterward, the use of these mixtures as electrolytes for EDLCs has been considered. This study showed that by using these innovative electrolytes, it is possible to develop EDLCs with an operative voltage as high as 3.0 V. It was clearly demonstrated that the EDLC cycle life strongly depends on the concentration of Me3STFSI present in the mixture. Moreover, it was also proved that mixtures containing high concentrations of IL are able to suppress anodic oxidation of the Al current collector at high potential. When a solution with a high salt concentration is used, an EDLC with high energy, high cycle life and a broad temperature range of operation can be realized.

An investigation of the electrochemical delithiation process of carbon coated α-Fe2O3 nanoparticles

The electrochemical lithiation–delithiation of iron oxide is a rather complex process, which is still not fully understood. In this study we investigated the electrochemical lithiation–delithiation mechanism of hematite by means of X-ray diffraction (XRD), 57Fe Mossbauer spectroscopy, high-resolution transmission electron microscopy (HRTEM) and X-ray absorption spectroscopy (XAS). Since the delithiation process has been so far less investigated, particular attention was dedicated to the characterization of the chemical species that are formed during this process. The results of this investigation indicated that at the end of the delithiation process lithium iron oxide α-LiFeO2 is formed. The formation of this compound may be the explanation for the irreversible capacity loss in the first cycle, which is usually assigned to the formation of an organic gel-like layer. Based on these results a new charge–discharge mechanism of hematite in lithium-ion batteries (LIBs) is proposed and discussed.