Sodium (Na)-ion batteries offer an attractive option for low cost grid scale storage due to the abundance of Na. Tin (Sn) is touted as a high capacity anode for Na-ion batteries with a high theoretical capacity of 847 mAh/g, but it has several limitations such as large volume expansion with cycling, slow kinetics, and unstable solid electrolyte interphase (SEI) formation. In this article, we demonstrate that an anode consisting of a Sn thin film deposited on a hierarchical wood fiber substrate simultaneously addresses all the challenges associated with Sn anodes. The soft nature of wood fibers effectively releases the mechanical stresses associated with the sodiation process, and the mesoporous structure functions as an electrolyte reservoir that allows for ion transport through the outer and inner surface of the fiber. These properties are confirmed experimentally and computationally. A stable cycling performance of 400 cycles with an initial capacity of 339 mAh/g is demonstrated; a significant improvement over other reported Sn nanostructures. The soft and mesoporous wood fiber substrate can be utilized as a new platform for low cost Na-ion batteries.

Electronics on flexible and transparent substrates have received much interest due to their new functionalities and high-speed roll-toroll manufacturing processes. The properties of substrates are crucial, including flexibility, surface roughness, optical transmittance, mechanical strength, maximum processing temperature, etc.Although plastic substrates have been used widely in flexible macroelectronics, there is still a need for next-generation sustainable, high-performance substrates which are thermally stable with tunable optical properties and a higher handling temperature. In this communication, we focus on cellulose-based transparent, biodegradable substrates incorporating either nanopaper or a regenerated cellulose film (RCF). We found that both their optical and mechanical properties are dramatically different due to the difference of their building blocks. Highly flexible organic-light-emitting diodes (OLEDs) are also demonstrated on the biodegradable substrates, paving the way for next-generation green and flexible electronics.

The concept of water-in-salt electrolytes was introduced recently, and these systems have been successfully applied to yield extended operation voltage and hence significantly improved energy density in aqueous Li-ion batteries. In the present work, results of X-ray scattering and Fourier-transform infrared spectra measurements over a wide range of temperatures and salt concentrations are reported for the LiTFSI (lithium bis­(trifluoro­methane sulfonyl)­imide)-based water-in-salt electrolyte. Classical molecular dynamics simulations are validated against the experiments and used to gain additional information about the electrolyte structure. Based on our analyses, a new model for the liquid structure is proposed. Specifically, we demonstrate that at the highest LiTFSI concentration of 20 m the water network is disrupted, and the majority of water molecules exist in the form of isolated monomers, clusters, or small aggregates with chain-like configurations. On the other hand, TFSI– anions are connected to each other and form a network. This description is fundamentally different from those proposed in earlier studies of this system.