Thermodynamics and cell chemistry of room temperature sodium/sulfur cells with liquid and liquid/solid electrolyte
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Highlights
•
The Na/S battery operating at room temperature is assessed and studied.
•
XPS studies on the electrodes prove Na2S formation and decomposition.
•
Using a solid electrolyte prevents the shuttle mechanism and increases capacity.
•
Side reactions of standard PVDF binder are identified as possible ageing mechanism.
•
A comparison with state of the art knowledge on Li/S cells is provided.
Abstract
The cell chemistry of sodium/sulfur cells operating at room temperature (RT-Na/S cells) is being studied electrochemically and structurally. We show by means of X-ray photoelectron spectroscopy that the cell reaction is incomplete but prove that the end members of the cell reaction (S and Na2S) form among the expected polysulfide species Na2Sx. The sulfur utilization can be improved by employing a solid electrolyte membrane (beta″-alumina) that prevents the diffusion of the soluble polysulfide species toward the sodium side. As an important finding, the Na+ conduction within the solid electrolyte phase and across the two liquid/solid interfaces results in only small overpotentials. Nevertheless the utilization of sulfur in the present RT-Na/S (475 mAh g−1) cells is lower than the theoretical value (1675 mAh g−1). One probable reason is the chemical instability of the widely used PVDF binder. Also, the thermodynamic properties of RT-Na/S cells operating at room temperature are discussed and compared with the currently much more studied RT-Li/S cells.
•
The Na/S battery operating at room temperature is assessed and studied.
•
XPS studies on the electrodes prove Na2S formation and decomposition.
•
Using a solid electrolyte prevents the shuttle mechanism and increases capacity.
•
Side reactions of standard PVDF binder are identified as possible ageing mechanism.
•
A comparison with state of the art knowledge on Li/S cells is provided.
Abstract
The cell chemistry of sodium/sulfur cells operating at room temperature (RT-Na/S cells) is being studied electrochemically and structurally. We show by means of X-ray photoelectron spectroscopy that the cell reaction is incomplete but prove that the end members of the cell reaction (S and Na2S) form among the expected polysulfide species Na2Sx. The sulfur utilization can be improved by employing a solid electrolyte membrane (beta″-alumina) that prevents the diffusion of the soluble polysulfide species toward the sodium side. As an important finding, the Na+ conduction within the solid electrolyte phase and across the two liquid/solid interfaces results in only small overpotentials. Nevertheless the utilization of sulfur in the present RT-Na/S (475 mAh g−1) cells is lower than the theoretical value (1675 mAh g−1). One probable reason is the chemical instability of the widely used PVDF binder. Also, the thermodynamic properties of RT-Na/S cells operating at room temperature are discussed and compared with the currently much more studied RT-Li/S cells.
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