ABSTRACT
Solid-state sodium ion conductors are crucial for the next generation of all-solid-state sodium batteries with high capacity, low cost, and improved safety. Sodium closo-carbadodecaborate (NaCB11 H12 ) is an attractive Na-ion conductor owing to its high thermal, electrochemical, and interfacial stability. Mechanical milling has recently been shown to increase conductivity by five orders of magnitude at room temperature, making it appealing for application in all-solid-state sodium batteries. Intriguingly, milling longer than 2 h led to a significant decrease in conductivity. In this study, X-ray Raman scattering (XRS) spectroscopy is used to probe the origin of the anomalous impact of mechanical treatment on the ionic conductivity of NaCB11 H12 . The B, C, and Na K-edge XRS spectra are successfully measured for the first time, and ab initio calculations are employed to interpret the results. The experimental and computational results reveal that the decrease in ionic conductivity upon prolonged milling is due to the increased proximity of Na to the CB11 H12 cage, caused by severe distortion of the long-range structure. Overall, this work demonstrates how the XRS technique, allowing investigation of low Z elements such as C and B in the bulk, can be used to acquire valuable information on the electronic structure of solid electrolytes and battery materials in general.
ABSTRACT
A calorimeter was built to measure the heat from a porous capacitive working electrode connected in a three-electrode configuration. This makes it possible to detect differences between cathodic and anodic heat production. The electrochemical cell contains a large electrolyte solution reservoir, ensuring a constant concentration of the salt solution probed by the reference electrode via a Luggin tube. A heat flux sensor is used to detect the heat, and its calibration as a gauge of the total amount of heat produced by the electrode is done based on the net electrical work performed on the working electrode during a full charging-discharging cycle. In principle, from the measured heat and the electrical work, the change in the internal energy of the working electrode can be determined as a function of the applied potential. Such measurements inform about the potential energy and average electric potential of ions inside the pores, giving insight into the electrical double layer inside electrode micropores. Example measurements of the heat are shown for porous carbon electrodes in an aqueous salt solution.
ABSTRACT
The internal energy of capacitive porous carbon electrodes was determined experimentally as a function of applied potential in aqueous salt solutions. Both the electrical work and produced heat were measured. The potential dependence of the internal energy is explained in terms of two contributions, namely the field energy of a dielectric layer of water molecules at the surface and the potential energy of ions in the pores. The average electric potential of the ions is deduced, and its dependence on the type of salt suggests that the hydration strength limits how closely ions can approach the surface.
ABSTRACT
The crystal structure of 5-fluorosalicylic acid is known from the literature [Choudhury & Guru Row (2004). Acta Cryst. E60, o1595-o1597] as crystallizing in the monoclinic crystal system with space-group setting P21/n and with one molecule in the asymmetric unit (polymorph I). We describe here a new polymorph which is again monoclinic but with different unit-cell parameters (polymorph II). Polymorph II has two molecules in the asymmetric unit. Its structure was modelled as a twin, with a pseudo-orthorhombic C-centred twin cell.
