Organic semiconductors and organic–inorganic hybrids are promising materials for spintronic‐based memory devices. Recently, an alternative route to organic spintronic based on chiral‐induced spin selectivity (CISS) is suggested. In the CISS effect, the chirality of the molecular system itself acts as a spin filter, thus avoiding the use of magnets for spin injection. Here, spin filtering in excess of 85% in helical π‐conjugated materials based on supramolecular nanofibers at room temperature is reported. The high spin‐filtering efficiency can even be observed in nanofibers assembled from mixtures of chiral and achiral molecules through chiral amplification effect. Furthermore and most excitingly, it is shown that both “up” and “down” orientations of filtered spins can be obtained in a single enantiopure system via the temperature‐dependent helicity (P and M) inversion of supramolecular nanofibers. The findings showcase that materials based on helical noncovalently assembled systems are modular platforms with an emerging structure–property relationship for spintronic applications.

In this manuscript, we report our investigation of anode materials for Li-ion batteries based on silicon-graphene oxide composites. Previous reports in the literature on silicon-graphene oxide (GO) composites as anodes have shown a large discrepancy between the electrochemical properties, mainly capacity and coulombic efficiency. In our research, the surface chemistry of Si nanoparticles has been functionalized to yield a chemical bond between the Si and GO, a further annealing step yields a Si-reduced GO (Si-rGO) composite while controlled experiments have been carried on mechanical mixing of GO and Si. For all samples, including a simple mixing of Si nanoparticles and GO, a high specific capacity of 2000 mA h g(Si)(-1) can be achieved for 50 cycles. The main difference between the samples can be observed in terms of coulombic efficiency, which will determine the future of these composites in full Li-ion cells. The Si-rGO composite shows a very low capacity fading and a coulombic efficiency above 99%. Furthermore, the Si-rGO composite can be cycled at very high rate to 20 C (charge in 3 minutes).

Nanomaterials have triggered a lot of attention as potential triggers for a technological breakthrough in Energy Storage Devices and specifically Li-ion batteries. Herein, we report the original synthesis of well-defined silicon/iron oxide nanoparticles and its application as anode materials for Li-ion batteries. This model compound is based on earth abundant elements and allows for a full investigation of the electrochemical reactions through its iron oxide magnetic phase. The elaboration of silicon with iron oxide grown on its surface has been achieved by reacting an organometallic precursor Fe(CO) 5 with Si nanopowder and subsequent slow oxidation step in air yields hollow γ-Fe 2 O 3 on the Si surface. This specific morphology results in an enhancement of the specific capacity from 2000 mAh/g Si up to 2600 mAh/g Si . Such a high specific capacity is achieved only for hollow γ-Fe 2 O 3 and demonstrates a novel approach toward the modification of electrode materials with an earth abundant transition metal like iron. This result further emphasizes the need for precisely designed nanoparticles in achieving significant progress in energy storage.

Using chemical vapor deposition, we grew carbon nanotubes (CNTs) on the surface of Si nanoparticles (NPs) that were coated with a thin iron shell. We studied the CNT growth mechanisms and analyzed the influence of (1) varying annealing times and (2) varying growth times. We show that an initial annealing is necessary to reduce the iron oxide shell and to start the formation of Fe NPs and their consequent coarsening. We characterize the evolution of the catalyst morphology and its influence of the morphology and structure of the CNTs grown. We studied this nanocomposite of Si NPs interconnected by CNTs grown on them as anode material for Li-ion batteries. Compared to the pristine Si NPs, the Si-CNT nanocomposite brings an increase of 40% in specific capacity after 100 cycles at 1800 mA/gSi with a high stability and a very low capacity loss per cycle of 0.06%. The electrochemical performance demonstrates how efficient the CNT shell on the Si NP is to mitigate the usual failure mechanism of Si NPs. Thus, the in situ growth of CNTs on Si anode materials can be an efficient route toward the synthesis of more stable Si anode composites for a Li-ion battery.

No abstract