Stabilization of Li-Rich Disordered Rocksalt Oxyfluoride Cathodes by Particle Surface Modification.

Promising theoretical capacities and high voltages are offered by Li-rich disordered rocksalt oxyfluoride materials as cathodes in lithium-ion batteries. However, as has been discovered for many other Li-rich materials, the oxyfluorides suffer from extensive surface degradation, leading to severe capacity fading. In the case of Li2VO2F, we have previously determined this to be a result of detrimental reactions between an unstable surface layer and the organic electrolyte. Herein, we present the protection of Li2VO2F particles with AlF3 surface modification, resulting in a much-enhanced capacity retention over 50 cycles. While the specific capacity for the untreated material drops below 100 mA h g-1 after only 50 cycles, the treated materials retain almost 200 mA h g-1. Photoelectron spectroscopy depth profiling confirms the stabilization of the active material surface by the surface modification and reveals its suppression of electrolyte decomposition.

Insights into Structural Transformations in the Local Structure of Li2VO2F Using Operando X-ray Diffraction and Total Scattering: Amorphization and Recrystallization.

Disordered rock salt Li2VO2F cathode material for lithium-ion batteries was investigated using operando X-ray diffraction and total scattering to gain insight into the structural changes of the short-range and long-range orders during electrochemical cycling. The X-ray powder diffraction data show the well-known pattern of the disordered rock salt cubic structure, whereas the pair distribution function (PDF) analysis reveals significant deviations from the ideal cubic structure. During battery operation, a reversible rock salt-to-amorphous phase transformation is observed, upon Li extraction and reinsertion. The X-ray total scattering data show strong indications of the formation of tetrahedrally coordinated V in a nondisordered rock salt phase of the charged electrode material. The results show that the disordered rock salt Li2VO2F material undergoes a hidden structural rearrangement during battery operation.

Calcined chicken eggshell electrode for battery and supercapacitor applications.

Biowaste eggshell can be used as a cathode while in its calcined form and it is found to be suitable as an anode in an electrochemical cell. This not only enables energy to be stored reversibly but also achieves waste management and sustainability goals by redirecting material away from landfill. Biowaste eggshell comprises 94% calcium carbonate (CaCO3; calcite), an attractive divalent ion source as a viable option for energy storage. X-ray diffraction and electron microscopy coupled with energy dispersive analyses of the calcined (thermally decomposed) biowaste eggshell show that CaO has been formed and the reaction is topotactic. Field emission scanning electron microscopy (FESEM) images of the textural relationship show that the thermal decomposition of calcite resulted in a change in morphology. High-resolution XPS spectra of the C 1s core level from the CaCO3 and CaO shows that there is a chemical difference in the carbon environments and the total atomic fraction of Ca for each sample with that of carbonate and oxygen varies. In a three-electrode configuration, a working electrode of CaCO3 is found to be electrochemically active in the positive region, whereas a CaO electrode is active in the negative region. This indicates the potential use of eggshell-derived materials for both cathode and anode. Both the electrodes exhibited a quasi-box-shaped potentiostatic curve implying a capacitor-type behaviour. The CaCO3 cathode possesses a modest discharge capacitance of 10 F g-1 but the CaO anode showed excellent capacitance value of 47.5 F g-1. The CaO electrode in both positive and negative regions, at a current density of 0.15 A g-1 exhibited 55 F g-1 with a retention of nearly 100% after 1000 cycles. At a very low sweep rate of 0.5 mV s-1, the CaO electrode showed typical redox-type behaviour with well-defined peaks illustrating battery-type behaviour. The outcome of the calcite/CaO transformation, exhibiting technological importance for energy storage applications, may help to re-evaluate biowaste before throwing it away. The current work explores the viability of eggshell derived materials as a cathode/anode for use in batteries and capacitors.

Phase evolution in calcium molybdate nanoparticles as a function of synthesis temperature and its electrochemical effect on energy storage.

The design of a suitable electrode is an essential and fundamental research challenge in the field of electrochemical energy storage because the electronic structures and morphologies determine the surface redox reactions. Calcium molybdate (CaMoO4) was synthesized by a combustion route at 300 °C and 500 °C. We describe new findings on the behaviour of CaMoO4 and evaluate the influence of crystallinity on energy storage performance. A wide range of characterization techniques was used to obtain detailed information about the physical and morphological characteristics of CaMoO4. The characterization results enable the phase evolution as a function of the electrode synthesis temperature to be understood. The crystallinity of the materials was found to increase with increasing temperature but with no second phases observed. Molecular dynamics simulation of electronic structures correlated well with the experimental findings. These results show that to enable faster energy storage and release for a given surface area, amorphous CaMoO4 is required, while larger energy storage can be obtained by using crystalline CaMoO4. CaMoO4 has been evaluated as a cathode material in classical lithium-ion batteries recently. However, determining the surface properties in a sodium-ion system experimentally, combined with computational modelling to understand the results has not been reported. The superior electrochemical properties of crystalline CaMoO4 are attributed to its morphology providing enhanced Na+ ion diffusivity and electron transport. However, the presence of carbon in amorphous CaMoO4 resulted in excellent rate capability, suitable for supercapacitor applications.

Novel phenanthroline-diaryldiazadiene ligands with heteroditopic coordination spheres.

1,10-Phenanthroline-5,6-diaryldiazadienes are key structures for the development of novel heterodinuclear photocatalysts and for the construction of extended heterocycles of potential biological use. Herein, the first examples of this compound family are presented together with a wide range of initial reactivity studies. Synthetic strategies are presented to access the two first derivatives of the ligand and to accomplish subsequent metal coordination to the phenanthroline sphere.