2021, Weng, Qunhong, Wang, Sitao, Liu, Lixiang, Lu, Xueyi, Zhu, Minshen, Li, Yang, Gabler, Felix, Schmidt, Oliver G.

Independent and well-packaged miniaturized energy storage devices (MESDs) are indispensable as power sources or backup units for integrated circuits and many dispersive electronics applications. Challenges associated with MESD development relate to their low packaged areal energy density and poor battery performance. Here, we propose a compact tube-in-tube battery configuration to overcome the areal energy density and packaging problems in microbatteries. Compact microtubular microelectrodes rolled up from patterned nanomembranes are sealed in an inert glass capillary with a thin tube wall. The resultant tube-in-tube microsized lithium-ion batteries (micro-LIBs), based on various active materials, exhibit very high and scalable packaged areal energy densities up to 605 microampere hours per square centimeter (μAh cm−2) or 313 μWh cm−2 with footprints as small as 0.39–0.79 mm2. This approach is a practical alternative for microbattery microelectrode, packaging, and configuration innovations.

2020, Budak, Ö., Geißler, M., Becker, D., Kruth, A., Quade, A., Haberkorn, R., Kickelbick, G., Etzold, B. J. M., Presser, V.

Nb2O5 has been explored as a promising anode material for use as lithium-ion batteries (LIBs), but depending on the crystal structure, the specific capacity was always reported to be usually around or below 200 mAh/g. For the first time, we present coarse-grained Nb2O5 materials that significantly overcome this capacity limitation with the promise of enabling high power applications. Our work introduces coarse-grained carbide-derived Nb2O5 phases obtained either by a one-step or a two-step bulk conversion process. By in situ production of chlorine gas from metal chloride salt at ambient pressure, we obtain in just one step directly orthorhombic Nb2O5 alongside carbide-derived carbon (o-Nb2O5/CDC). In situ formation of chlorine gas from metal chloride salt under vacuum conditions yields CDC covering the remaining carbide core, which can be transformed into metal oxides covered by a carbon shell upon thermal treatment in CO2 gas. The two-step process yielded a mixed-phase tetragonal and monoclinic Nb2O5 with CDC (m-Nb2O5/CDC). Our combined diffraction and spectroscopic data confirm that carbide-derived Nb2O5 materials show disordering of the crystallographic planes caused by oxygen deficiency in the structural units and, in the case of m-Nb2O5/CDC, severe stacking faults. This defect engineering allows access to a very high specific capacity exceeding the two-electron transfer process of conventional Nb2O5. The charge storage capacities of the resulting m-Nb2O5/CDC and o-Nb2O5/CDC are, in both cases, around 300 mAh/g at a specific current of 10 mA/g, thereby, the values are significantly higher than that of the state-of-the-art for Nb2O5 as a LIB anode. Carbide-derived Nb2O5 materials also show robust cycling stability over 500 cycles with capacity fading only 24% for the sample m-Nb2O5/CDC and 28% for o-Nb2O5/CDC, suggesting low degree of expansion/compaction during lithiation and delithiation.