Ultrathin oxide coatings are demonstrated to offer multiple functions for improving the cycling performance of lithium ion batteries. The coatings can serve as an artificial solid electrolyte interphase layer, which significantly suppresses electrolyte decomposition as well as mitigates mechanical degradation. Structure modification is critical for increasing the ion conductivity, and therefore leads to improved current efficiency.

W-doping produced the two-phase (Fm3̄m and R3̄m) structure which improved the cycling and thermal stability of the Ni-rich layered cathodes.

We demonstrate that the Mott metal-insulator transition (MIT) in single crystalline VO(2) nanowires is strongly mediated by surface stress as a consequence of the high surface area to volume ratio of individual nanowires. Further, we show that the stress-induced antiferromagnetic Mott insulating phase is critical in controlling the spatial extent and distribution of the insulating monoclinic and metallic rutile phases as well as the electrical characteristics of the Mott transition. This affords an understanding of the relationship between the structural phase transition and the Mott MIT.

We report a 3.8 V manganese-based mixed-phosphate cathode material for applications in sodium rechargeable batteries; i.e., Na4Mn3(PO4)2(P2O7).

In response to the ever-increasing global demand for viable energy-storage systems, sodium and potassium batteries appear to be promising alternatives to lithium ion batteries because of the abundance, low cost and environmental benignity of sodium/ potassium. Electrical energy storage via ion-intercalation reactions in crystalline electrodes is critically dependent on the sizes of the guest ions. Herein, we report on the use of a porous amorphous iron phosphate synthesized using ambient temperature strategies as a potential host that stores electrical energy through the feasible insertion of mono-/di-/tri-valent ions. A combination of ex situ studies reveals the existence of a reversible amorphous-to-crystalline transition in this versatile electrode during electrochemical reactions with monovalent sodium, potassium and lithium. This reconstitutive reaction contributes to realizing specific capacities of 179 and 156 mAhg − 1 versus sodium and potassium at current densities of 10 and 5 mAg − 1 , respectively. This finding facilitates the feasible development of several amorphous electrodes with similar phase behavior for energy-storage applications. NPG Asia Materials (2014) 6, e138; doi:10.1038/am.2014.98; published online 17 October 2014 INTRODUCTIONSince 1990, the global demand for electricity has increased twice as much as the demand for energy overall, and the demand for electricity is expected to further increase by more than two-thirds over the next 20 years. Energy storage/conversion technologies have therefore become a crucial research topic as we seek to make society sustainable. In particular, electrical energy storage is critical not only for supporting electronic, vehicular and load-leveling applications but also for efficiently commercializing renewable solar and wind power. Rechargeable Li-ion batteries with an output energy exceeding 90% have emerged as one of the most effective electrochemical energystorage technologies, and these batteries power most modern-day electronic devices. 1 Despite substantial research to enhance Li-ion batteries for high-power applications, aspects such as their availability, cost and safety still remain to be fully addressed. 2 The controversies surrounding the accessible global lithium reserves and the anticipated energy demand may greatly impact the cost of Li-ion batteries in the long term. 3 Although advancing Li-ion battery technologies for electric vehicle applications is attractive, the quest for alternative energy sources for smart grid-scale storage applications has recently gained significant momentum. Rechargeable sodium and potassium batteries offer tremendous potential because they utilize inexpensive, abundant and environmentally benign sodium/potassium elements. [4][5][6][7][8][9] However,

In this study, we report in situ measurements of lithium diffusion induced stress in patterned amorphous Si negative electrodes. This configuration was used as a model system to understand how the gap between islands can accommodate the large volume expansion and stress generation that occurs during the lithiation of Si. The effect of pattern size was studied systematically with 7 μm, 17 μm and 40 μm square islands. Experimentally measured stresses were then compared to a continuum model that describes stress accommodation due to interfacial sliding or plastic deformation in the underlying current collector. These results indicate that engineering an appropriately sized Si island is an effective method for mitigating lithiation-induced stress and mechanical degradation in Si based electrodes.

Natural gas hydrates are solid hydrogen-bonded water crystals containing small molecular gases. The amount of natural gas stored as hydrates in permafrost and ocean sediments is twice that of all other fossil fuels combined. However, hydrate blockages also hinder oil/gas pipeline transportation, and, despite their huge potential as energy sources, our insufficient understanding of hydrates has limited their extraction. Here, we report how the presence of amino acids in water induces changes in its structure and thus interrupts the formation of methane and natural gas hydrates. The perturbation of the structure of water by amino acids and the resulting selective inhibition of hydrate cage formation were observed directly. A strong correlation was found between the inhibition efficiencies of amino acids and their physicochemical properties, which demonstrates the importance of their direct interactions with water and the resulting dissolution environment. The inhibition of methane and natural gas hydrate formation by amino acids has the potential to be highly beneficial in practical applications such as hydrate exploitation, oil/gas transportation, and flow assurance. Further, the interactions between amino acids and water are essential to the equilibria and dynamics of many physical, chemical, biological, and environmental processes.

No abstract