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Abstract: Li2Ti6O13 has been prepared from Na2Ti6O13 by Li ion exchange in molten LiNO3 at 325°C. Chemical analysis and powder X-ray diffraction study of the reaction product respectively indicate that total Na/Li exchange takes place and the Ti–O framework of the Na2Ti6O13 parent structure is kept under those experimental conditions. Therefore, Li2Ti6O13 has been obtained with the mentioned parent structure. An important change is that particle size is decreased significantly which is favoring lithium insertion. Electrochemical study shows that Li2Ti6O13 inserts ca. 5 Li per formula unit in the voltage range 1.5–1.0V vs. Li+/Li, yielding a specific discharge capacity of 250mAhg−1 under equilibrium conditions. Insertion occurs at an average equilibrium voltage of 1.5V which is observed for oxides and titanates where Ti(IV)/Ti(III) is the active redox couple. However, a capacity loss of ca. 30% is observed due to a phase transformation occurring during the first discharge. After the first redox cycle a high reversible capacity is obtained (ca. 160mAhg−1 at C/12) and retained upon cycling. Taking into consideration these results, we propose Li2Ti6O13 as an interesting material to be further investigated as the anode of lithium ion batteries. [ABSTRACT FROM AUTHOR]

Abstract: The α-polymorph of Li3FeF6 has been obtained at room temperature by a precipitation reaction from aqueous solution. This easy procedure that does not require any further annealing at high temperature yields a white powder with particles sizes ranging from 250 to 400nm. After proper processing by mechanical milling, particle sizes clearly below 100nm are achieved and this fluoride reacts reversibly with lithium at an average voltage of 3.1V, which is expected for the Fe3+/Fe2+ redox couple. After 12h of ball milling observed average particle size is ca. 50nm and a reversible capacity of 100mAhg−1 is obtained. This corresponds to 70% of the theoretical capacity expected for the one electron reduction of Fe3+. The mentioned capacity is fairly kept upon cycling making the new material useful as the positive electrode in lithium batteries. This is the very first time that a material for cathode application in lithium batteries is prepared at room temperature and from aqueous solution, a procedure which is easily scalable and hence of high industrial interest. [Copyright &y& Elsevier]

Abstract: We present an electrochemical study of BiSbO4, an opened layered oxide having a structure related to Aurivillius phases. Li//BiSbO4 cells show a large specific capacity as high as 1250mAhg−1 during reduction down to 0.5V. This reaction involves 18Li atoms per formula unit, pointing it towards a very promising cathode material for primary lithium batteries, in particular for ICD devices. The characterization of the reduction products indicates that the reduction of BiSbO4 with lithium presumably goes along firstly with the formation of metallic Sb and Bi to follow the formation of the alloys Li3Bi and Li3Sb dispersed in a lithium oxide matrix. In situ X-ray diffraction experiments proved the amorphous nature of both metals and final alloys. On the other hand when Li//BiSbO4 cells are limited to discharge down to 1.2V, BiSbO4 reacts with 5Li atoms. After the first discharge, that develops a specific capacity of 350mAhg−1, high cyclability has been observed. [Copyright &y& Elsevier]

Abstract: New olivines LiMAsO4 (M=Mn, Fe, Co, and Ni) have been tested as positive electrode in lithium cells. Under the used experimental conditions we did not succeed to remove lithium ions from LiFeAsO4, LiMnAsO4 or LiNiAsO4. More work is needed in order to verify whether the lack of electrochemical activity is intrinsic to these materials, or it is due to kinetical limitations such as particle size and poor conductivity. On the contrary lithium ions could be reversibly deinserted/inserted from/into LiCoAsO4 at average voltages of 4.8 and 4.6V respectively; the delithiated compound maintaining the olivine structural framework. The high pressure polymorph of LiMAsO4 (M=Fe, Co, Ni) crystallizing with the spinel structure did not show any electrochemical activity potentially useful in rechargeable lithium batteries. [Copyright &y& Elsevier]

The effect of mechanical grinding (MG) on the electrochemical properties of Si3N4 is studied as the processing produces different particle size. The evolution of the amorphisation stage has been monitored by X-ray diffraction (XRD), although particle size has also been studied through transmission electron microscopy experiments. Processed Si3N4 has been used as the positive electrode in electrochemical cells, where the negative electrode is lithium. We do not expect an intercalation process during the discharge step of such a type of cell, but a behaviour similar to that named as “convertible compounds”. As the main result, the specific capacity of these lithium cells is increased up to 34% in relation to the starting, non-milled material. However, even though the size of the Si3N4 particles has been reduced, from micrometer to nanometer scale, no appreciable changes in the cycling behaviour is observed when compared with the pristine material. [Copyright &y& Elsevier]