Abstract
Molten carbonate fuel cell (MCFC) is one of the most advanced high-temperature devices to convert chemical energy into electrical energy without pollution. It can be used in cogeneration as electrical and thermal generator because of its high working temperature (650 °C). Nevertheless, its commercialization is still limited. In fact, its lifetime is mostly reduced by the dissolution of the cathode into the corrosive molten carbonate electrolyte. One of the ways to overcome this problem is to modify or protect the state-of-the-art cathode. In the last case, the deposit must present conductivity as good as the classical NiO porous cathode one but a lower solubility in the electrolyte. For this reason, thin films of cobalt(III) were electrodeposited. A classical three-electrode cell was used to deposit Co-based thin films by chronoamperometry in aqueous solution, at relatively high temperature (80 °C). The deposition conditions lead to homogeneous, covering, and crystallized films. The microstructure and the crystallinity of the deposits were characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD) measurements. Then, their electrochemical properties were studied in the molten carbonate electrolyte under a mixture of CO2 and air. In situ measurements such as chronopotentiometry at I = 0 (open-circuit potential) or impedance spectroscopy were carried out during 48 h. Moreover, ex situ measurements such as inductively coupled plasma atomic emission spectroscopy to evaluate the solubility, or SEM and XRD measurements were performed to characterize the thin Co-based films in such molten carbonate fuel cell working cathodic conditions.
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